From owner-chromosomes@net.bio.net Sat Mar 02 22:00:00 1996
Path: biosci!agate!howland.reston.ans.net!math.ohio-state.edu!jussieu.fr!rain.fr!news
From: dgieff@mail.sdv.fr (Didier Georgieff)
Newsgroups: bionet.genome.chromosomes,sci.med
Subject: Looking for Trisomy 1 info
Date: Sun, 03 Mar 1996 21:43:17 GMT
Organization: Christian Debs (Strasbourg Medical University - France)
Lines: 21
Message-ID: <4hd7j7$gvr@obelix.rain.fr>
NNTP-Posting-Host: sdvip09.sdv.fr
Keywords: health trisomy
X-Newsreader: Forte Free Agent 1.0.82
Xref: biosci bionet.genome.chromosomes:1055 sci.med:113300

Hi,

I'm involved in research for trisomy 1 (q 32 q ter) for completing a
case study.

I looked a www pages via search engine, but found nothing.
So i try usenet.

I'm particulary interested in biography, article reference ans
especially in  case study.
If any physician had such patient, i greatly appreciate any info on
the age, the patology, and any special thing with that trisomy.

If you are interested in such case, i can (when the article will be
over) send clinical observations about the case we are studing.

PS : I'm french so .... don't pay attention to that special kind of
english :-)
-- 
Didier Georgieff -/-  dgieff@mail.sdv.fr  -/-  DDAF du Bas-Rhin, France


From owner-chromosomes@net.bio.net Sat Mar 02 22:00:00 1996
Path: biosci!biosci!not-for-mail
From: BIOSCI Administrator <biosci-help@net.bio.net>
Newsgroups: bionet.genome.chromosomes
Subject: AUTOMATED-SEQUENCING/bionet.genome.autosequencing PASSES: 197-3
Date: 3 Mar 1996 15:32:52 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 96
Sender: biohelp@net.bio.net
Distribution: world
Message-ID: <4hda74$lq@net.bio.net>
NNTP-Posting-Host: net.bio.net

I am pleased to announce that the proposal to create the mailing list
& newsgroup

AUTOMATED-SEQUENCING/bionet.genome.autosequencing (moderated)

passed by 197 YES votes to 3 NO votes.  We will proceed to create this
group as soon as possible.

E-mail users: please wait until you see an announcement in
BIONEWS/bionet.announce that the group is ready for operation before
you request an e-mail subscription.

				Sincerely,

				Dave Kristofferson
				BIOSCI/bionet Manager

				biosci-help@net.bio.net

----------------------------------------------------------------------
Proposal to create AUTOMATED-SEQUENCING/bionet.genome.autosequencing (moderated)

USENET newsgroup name:	bionet.genome.autosequencing

Status:			Moderated

One line Description:	Research and support on automated DNA sequencing

Moderation address:	bionet-genome-autosequencing@net.bio.net
			(autoseq-moderator@net.bio.net is an
			 alias for bionet-genome-autosequencing@net.bio.net)

Administrator:		David Cain

Mailing list name:	AUTOMATED-SEQUENCING

E-mail addresses:	autoseq@net.bio.net
			autoseq@daresbury.ac.uk

Newsgroup character:    

AUTOMATED-SEQUENCING/bionet.genome.autosequencing is a forum for the
concentrated discussion and source of assistance on issues relating to
automated DNA sequencing and fragment analysis such as microsatellite
analysis and SSCP . AUTOMATED-SEQUENCING has been chosen as the name
to represent the many different systems currently avaliable .

Functions of the newsgroup:

The newsgroup will offer a well needed focus for the discussion of
automated DNA sequencing / fragment analysis which has until now been
spread across a number of newsgroups resulting in many cross postings
.  The newsgroup will replace the one currently running on mailbase
which has been running for just under a year and proaved to be well
supported .

Topics for discussion will include sequencing chemistries , template
preparation methods , hints and tips for optimisation , recommended
protocols for both large and small scale projects as well as providing
a forum for support between scientists. Other aspects of the
post-sequencing process will also be dealt with, for example, sequence
troubleshooting and software issues.

The newsgroup will also serve as a bulletin board for the announcement
of meetings , conferences , job opportunities within the rapidly
expanding sequencing market .

Subscriptions are welcome from all academic institutions , hospitals ,
government agencies and other research facilities as well as
commercial and industrial organisations . Contributions which support
the outlined functions of the newsgroup will be actively encouraged .

Moderation Policy:

Chain letters , mass posted commercial messages and other messages
deemed to be "Junk mail" will be deleted without comment .
Inappropriate messages for commercial or legal reasons will be
returned to the originator for editing and re-submission . Messages
which are not strictly within the terms of the charter but still
deemed to be of interest to the subscribers will be accepted as long
as they do not breach any of the terms and conditions of the charter .
Due to the commercial competitive nature of the subject companies with
a vested interest will be encouraged to limit their activities on the
newsgroup to replying directly to questions posted or clearing an
article with the moderators prior posting to the list.  Advertisements
for commercial products are prohibited on the BIOSCI/bionet newsgroups.

Proposed Moderators

David Cain
DNA sequencing Unit , Institute of Cancer Research , Chester Beatty
Labs , London , UK

Robert Feakes
Department of Genetics , University of Cambridge , Cambridge , UK
----------------------------------------------------------------------

From owner-chromosomes@net.bio.net Mon Mar 04 22:00:00 1996
Path: biosci!ODYSSEE.NET!dellaire
From: dellaire@ODYSSEE.NET (Graham Dellaire)
Newsgroups: bionet.genome.chromosomes
Subject: FISH probes for Murine alpha satellite DNA?  WHo sells them (or reference)
Date: 4 Mar 1996 19:44:15 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 14
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <313BB74B.53C5@odyssee.net>
NNTP-Posting-Host: net.bio.net

Hello,

I am trying to do a karyotype of a murine cells line (LTA(a derivative 
of L M tk- ) that appears to have quite a few anomolies.  Does anyone 
know of a company ( or the ref on a paper) that sells paints for alphoid 
DNA or for murine centromeres?


Thanks 


Graham

dellaire@odyssee.net

From owner-chromosomes@net.bio.net Wed Mar 06 22:00:00 1996
Path: biosci!SURGERY.BSD.UCHICAGO.EDU!ewhite
From: ewhite@SURGERY.BSD.UCHICAGO.EDU (Eileen White)
Newsgroups: bionet.genome.chromosomes
Subject: mouse chr 11and human chr 17
Date: 7 Mar 1996 09:56:14 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 5
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199603071756.LAA19772@surgery.bsd.uchicago.edu>
NNTP-Posting-Host: net.bio.net

I am trying to locate any individuals or labs that are currently studying
the region of mouse chr 11 that shares homology with human chr 17p.  Any
e-mail addresses or phone numbers would be greatly appreciated. 
Eileen White


From owner-chromosomes@net.bio.net Wed Mar 06 22:00:00 1996
Path: biosci!genetics.adelaide.edu.au!rsaint
From: rsaint@genetics.adelaide.edu.au
Newsgroups: bionet.genome.chromosomes
Subject: Faculty Positions in Genetics
Date: 6 Mar 1996 23:15:55 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 50
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <01I22DGMTQNAB7CCXL@mulga.itd.adelaide.edu.au>
NNTP-Posting-Host: net.bio.net

TWO LECTURESHIPS IN GENETICS

Applications are invited for two Lectureships in genetics in the Department of 
Genetics, University of Adelaide, Australia.

Lecturer (tenurable) (Ref: 8893)

Lecturer (limited term, 3 years) (Ref: 8892)


  The successful applicants, who will have an appropriate doctoral degree (or 
equivalent qualification) and a record of productive and innovative research, 
will be expected to establish vibrant research programs and teach in various 
undergraduate genetics courses.  Research areas of particular interest are those 
that strengthen or extend current areas of expertise within the Department and 
that will provide high quality training for postgraduate students.  These 
include (but are not limited to) any aspect of human genetics, neurogenetics, 
behavioural genetics, genome and chromosome structure and function, gene 
expression and developmental genetics.  It is expected that one of the two 
appointees will be actively involved in human genetics research.  

  The Department of Genetics has excellent postgraduate and research programs 
with strengths in gene expression, chromosome structure, developmental genetics, 
cell cycle genetics, evolutionary genetics and genetic engineering of plants and 
microbes.  Affiliates include members of the Department of Cytogenetics and 
Molecular Genetics, the Women's and Children's Hospital, the Evolutionary 
Biology Unit of the South Australian Museum and the South Australian Forensic 
Science Centre.

  The positions are available from 1 July 1996.

  Further details about the Department and duties of the positions, including a 
selection criteria, may be obtained from Professor Robert Saint, Department of 
Genetics, telephone 61-8-303 4043, facsimile 61-8-303 4399 or via http://
www.science.adelaide.edu.au/genetics/home.html.

Salary per annum:   Lecturer (Level B): Aust$42,198 - $50,111

  Applications, in duplicate, quoting reference numbers 8893/8892 and giving 
full personal particulars (including whether candidates hold Australian 
permanent residency status), details of qualifications, current salary and names 
and full addresses of three referees should reach the Director, Personnel 
Services, University of Adelaide, Australia 5005, no later than 12 April 1996.  
Applicants should clearly address the selection criteria in their applications.

  The University reserves the right to make enquiries of any person regarding 
any candidate's suitability for appointment, not to make an appointment or to 
appoint by invitation.

The university of adelaide is an equal opportunity employer.

From owner-chromosomes@net.bio.net Wed Mar 06 22:00:00 1996
Path: biosci!lhc.nlm.nih.gov!darwin.sura.net!news.sesqui.net!news.ti.com!news.dseg.ti.com!news	
From: shelton@adrs1.dseg.ti.com (Anne Shelton)
Newsgroups: bionet.genome.chromosomes
Subject: Genetics questions
Date: 7 Mar 1996 18:55:01 GMT
Lines: 22
Distribution: world
Message-ID: <4hnbe5$l4g@mksrv1.dseg.ti.com>
Reply-To: shelton@adrs1.dseg.ti.com
NNTP-Posting-Host: adr15.dseg.ti.com

1) In another newsgroup, the question of eye color came up. How many
genes does it take to determine eye color. I know there's more than
1 because there are  many shades and different eye colors. Some 
people can't get over high school biology: Brown is dominant over
blue.  Some references and quotable sources would help.

2) Second Question: is the X sex chromosome required for viability? A
single X (Turner's Syndrome) is a sterile female but are there any single
Y syndromes (living)? If so, what is it called and what are the syndrome
effects?

3) Third Question:  In the Trisomy combinations of the sex chromosomes,
XXX, XXY, XYY, (YYY?) what are the different effects of these genetic
combinations? (i.e. XYY = aggressive male)

I hope someone with firsthand knowledge out there can provide the
answers to the above questions. Thanks in advance.

Regards,
Anne Shelton



From owner-chromosomes@net.bio.net Thu Mar 07 22:00:00 1996
Path: biosci!daresbury!nntp-trd.UNINETT.no!nntp.uio.no!usenet
From: line.roed@kjemi.uio.no (Line R|ed)
Newsgroups: bionet.genome.chromosomes
Subject: Primers for PCR?
Date: 8 Mar 1996 10:01:26 GMT
Organization: Universitet i Oslo
Lines: 18
Message-ID: <4hp0hm$l5f@ratatosk.uio.no>
NNTP-Posting-Host: pckjemi103.uio.no
Mime-Version: 1.0
Content-Type: Text/Plain; charset=US-ASCII
X-Newsreader: WinVN 0.99.7

Hi!

We are to do PCR on whole blood from dogs. We have no information on 
sequences, 
restriction maps or anything - all we want is to get a PCR product of 
reasonable
length (1000-2000 bp).

Is there anyone who could suggest what primers to use? We have considered 
using
random primers of ca. length 12 bp. Are there any other suggestions?

Please mail us directly: line.roed@kjemi.uio.no

Regards,

Irina Arsky and Line Roed


From owner-chromosomes@net.bio.net Fri Mar 08 22:00:00 1996
Path: biosci!agate!howland.reston.ans.net!news-e2a.gnn.com!newstf01.news.aol.com!newsbf02.news.aol.com!not-for-mail
From: rcjohnsen@aol.com (Rcjohnsen)
Newsgroups: bionet.genome.chromosomes
Subject: Re: Genetics questions
Date: 8 Mar 1996 18:41:45 -0500
Organization: America Online, Inc. (1-800-827-6364)
Lines: 21
Sender: root@newsbf02.news.aol.com
Message-ID: <4hqgjp$fiq@newsbf02.news.aol.com>
References: <4hnbe5$l4g@mksrv1.dseg.ti.com>
Reply-To: rcjohnsen@aol.com (Rcjohnsen)
NNTP-Posting-Host: newsbf02.mail.aol.com

Reply to  asking 3 genetics questions:
 I doubt there's an answer to the first question about the number of genes
controlling eye color.  Eye color appears to dependent upon the number,
shape, and size of pigment granules in the iris as well as the type and
amount of pigment deposited on them.  The number of genes controlling this
is speculative.
 On the second question about the X chromosome necessary for viability,
the answer is, most definitely yes.  Research in Drosophila and mice where
0/Y zygotes can be produced experimentally shows that such zygotes die in
the early stages of zygotic division.  Hence, most scientists feel this is
true for 0/Y human zygotes too and you might find something more concrete
about it in a University or good community library with journals on in
vitro fertilization research.  The NY Academy of Sciences has published a
couple of volumes on this research.
 On the third question,  there is a lot of literature on the various
syndromes you had questions about.  I suggest you try searching
Searching OMIM Using Fill-In Forms
http://gdbwww.gdb.org/omim-bin/omim/bin/omimq

an online searchable database in human genetics.
Rcjohnsen@aol.com

From owner-chromosomes@net.bio.net Sat Mar 09 22:00:00 1996
Path: biosci!CS.Arizona.EDU!noao!ennfs.eas.asu.edu!gatech!newsfeed.internetmci.com!usenet.eel.ufl.edu!psgrain!nntp.teleport.com!usenet
From: saramac@teleport.com
Newsgroups: bionet.genome.chromosomes
Subject: Congenital Hypothyroidism
Date: 10 Mar 1996 03:16:30 GMT
Organization: Teleport - Portland's Public Access (503) 220-1016
Lines: 8
Distribution: world
Message-ID: <4hthie$fgh@nadine.teleport.com>
NNTP-Posting-Host: ip-pdx04-22.teleport.com
X-Newsreader: AIR News 3.X (SPRY, Inc.)

I'm looking for information on this one.

The symptoms: an underdeveloped/atrophied thyroid gland, unable to produce any thyroxine.

What chromosome does it happen on????

Poly


From owner-chromosomes@net.bio.net Sat Mar 09 22:00:00 1996
Path: biosci!biosci!not-for-mail
From: BIOSCI Administrator <biosci-help@net.bio.net>
Newsgroups: bionet.genome.chromosomes
Subject: AUTOMATED-SEQUENCING/bionet.genome.autosequencing is ready!
Date: 10 Mar 1996 14:29:23 -0800
Organization: BIOSCI International Newsgroups for Biology
Lines: 330
Sender: biohelp@net.bio.net
Distribution: world
Message-ID: <4hvl43$nc5@net.bio.net>
NNTP-Posting-Host: net.bio.net

The AUTOMATED-SEQUENCING/bionet.genome.autosequencing newsgroup is
ready for operation.  This newsgroup is moderated, i.e., all postings
are forwarded to a moderator/editor and are reviewed prior to
distribution.  The newsgroup charter is appended below followed by
detailed usage instructions and information on how to search the
newsgroup archives.  *Please save* this message for future reference
if you intend to participate in this newsgroup.

IMPORTANT - All member's of David Cain's autoseq mailing list
(regardless of their geographical location) have been added to the
autoseq mailing list at net.bio.net.  If you were on that mailing list
and would prefer to access this group through USENET (check first and
make sure that it has been set up properly at your site!!) or through
the WWW at http://www.bio.net, you can cancel your e-mail subscription
by sending a message addressed to

biosci-server@net.bio.net

containing the line

unsubscribe autoseq

Please put the command in the body of the message.  The server ignores
the Subject: line of your mail.  This will only succeed if the address
on your mail matches the address on the mailing list at net.bio.net.
If you have problems or get a message saying that you were not on the
list (because the addresses did not match exactly), please contact
biosci-help@net.bio.net for human assistance.

If you want to receive messages by e-mail, but reside in Europe,
Africa, or Central Asia, you may want to cancel your e-mail
subscription as described above, and sign up at our UK distribution
site as detailed further below.

----------------------------------------------------------------------
Information for AUTOMATED-SEQUENCING/bionet.genome.autosequencing (moderated)

USENET newsgroup name:	bionet.genome.autosequencing

Status:			Moderated

One line Description:	Research and support on automated DNA sequencing

Moderation address:	bionet-genome-autosequencing@net.bio.net
			(autoseq-moderator@net.bio.net is an
			 alias for bionet-genome-autosequencing@net.bio.net)

Moderator:		David Cain

Mailing list name:	AUTOMATED-SEQUENCING

E-mail addresses:	autoseq@net.bio.net
			autoseq@daresbury.ac.uk

Newsgroup character:    

AUTOMATED-SEQUENCING/bionet.genome.autosequencing is a forum for the
concentrated discussion and source of assistance on issues relating to
automated DNA sequencing and fragment analysis such as microsatellite
analysis and SSCP. AUTOMATED-SEQUENCING has been chosen as the name
to represent the many different systems currently avaliable.

Functions of the newsgroup:

The newsgroup will offer a well needed focus for the discussion of
automated DNA sequencing / fragment analysis which has until now been
spread across a number of newsgroups resulting in many cross postings.
The newsgroup will replace the one currently running on mailbase which
has been running for just under a year and proaved to be well
supported.

Topics for discussion will include sequencing chemistries , template
preparation methods , hints and tips for optimisation , recommended
protocols for both large and small scale projects as well as providing
a forum for support between scientists. Other aspects of the
post-sequencing process will also be dealt with, for example, sequence
troubleshooting and software issues.

The newsgroup will also serve as a bulletin board for the announcement
of meetings , conferences , job opportunities within the rapidly
expanding sequencing market.

Subscriptions are welcome from all academic institutions , hospitals ,
government agencies and other research facilities as well as
commercial and industrial organisations. Contributions which support
the outlined functions of the newsgroup will be actively encouraged.

Moderation Policy:

Chain letters , mass posted commercial messages and other messages
deemed to be "Junk mail" will be deleted without comment.
Inappropriate messages for commercial or legal reasons will be
returned to the originator for editing and re-submission.  Messages
which are not strictly within the terms of the charter but still
deemed to be of interest to the subscribers will be accepted as long
as they do not breach any of the terms and conditions of the charter.
Due to the commercial competitive nature of the subject companies with
a vested interest will be encouraged to limit their activities on the
newsgroup to replying directly to questions posted or clearing an
article with the moderators prior posting to the list.  Advertisements
for commercial products are prohibited on the BIOSCI/bionet
newsgroups.

Moderators:

David Cain
DNA sequencing Unit , Institute of Cancer Research , Chester Beatty
Labs , London , UK

Robert Feakes
Department of Genetics , University of Cambridge , Cambridge , UK

----------------------------------------------------------------------

		    SUBSCRIPTION/USAGE INFORMATION

All BIOSCI/bionet newsgroups are now accessible via the World Wide
Web.  Please go to URL http://www.bio.net, click on the "Access the
BIOSCI/bionet Newsgroups" option, and then click on the
AUTOMATED-SEQUENCING/bionet.genome.autosequencing hyperlink.  You can
read, reply to, or post new messages through our Web site if your Web
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If you prefer to use your local USENET newsreader, PLEASE NOTE that
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ftp://net.bio.net/pub/BIOSCI/doc/bionet-checkgroups-msg

This file contains the latest list of bionet USENET newsgroups and can
be used to update your bionet distribution.  If the newgroup did not
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Subscribing to this group:
--------------------------

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----------------------

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How to look at archives of the list:
------------------------------------

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available on the World Wide Web at URL http://www.bio.net.  Please
look under the "Access the BIOSCI/bionet Newsgroups" hypertext link
and then click on the
AUTOMATED-SEQUENCING/bionet.genome.autosequencing hyperlink.  Each
monthly archive directory is assigned a date such as 9509 for
September 1995.  You can read, reply to, or post new messages through
our Web site if your Web browser is configured properly to send
e-mail.  Postings to bionet.genome.autosequencing are also indexed and
can be searched at our site.

Once again, if you have any administrative questions that require
personal assistance, please address them to biosci-help@net.bio.net in
the U.S. or biosci@daresbury.ac.uk in the UK.

Best wishes for a successful newsgroup!

				Sincerely,

				Dave Kristofferson
				BIOSCI/bionet Manager

				biosci-help@net.bio.net

From owner-chromosomes@net.bio.net Sun Mar 10 22:00:00 1996
Path: biosci!rutgers!uwm.edu!lll-winken.llnl.gov!fnnews.fnal.gov!nntp-server.caltech.edu!news
From: "Dr. Ung-Jin Kim" <ung@ash.tree.caltech.edu>
Newsgroups: bionet.genome.chromosomes
Subject: Caltech: lab assistants and a bioinformatician
Date: Mon, 11 Mar 1996 10:46:06 -0800
Organization: Division of Biology, Caltech
Lines: 48
Message-ID: <314474EE.5BC1@ash.tree.caltech.edu>
NNTP-Posting-Host: apple.tree.caltech.edu
Mime-Version: 1.0
Content-Type: text/plain; charset=us-ascii
Content-Transfer-Encoding: 7bit
X-Mailer: Mozilla 2.0 (X11; I; SunOS 5.4 sun4m)

Genome Research Laboratory at Caltech: Please see our WEB page,
  http://www.tree.caltech.edu
 
 
Job 1: We are looking for a few lab assistants
 
  
Caltech Genome Resaerch Laboratory is looking for qualified
full time technicians with experiences in laboratory works 
involving recombinant DNA procedures. Works will require 
skills in colony hybridization, PCR screening of genomic 
libraries, DNA preparation, restriction fingerprint analysis, 
and more.
 
Positions are open immediately. College or higher degrees in
Biological sciences or other sciences required. Interested 
parties should send cv to Dr. Ung-Jin Kim.
Electronic submissions are welcome.
 
 
 
Job 2: We are looking for a bioinformatician
 
 
Caltech Genome Research Laboratory is looking for a full time
informatician to manage and analyze laboratory data, and help 
operate robotic workstations. Knowledge and experieince in 
handling biological information, especially in the analysis 
and management of physcal mapping and DNA sequence data is 
essential. We also expect the person to be familiar with Unix 
server/workstations and PC/MacIntosh platforms. 
Interested parties should send CV to Dr. Ung-Jin Kim. 
Electronic submissions are welcome.
 
  
 
We will notify the applicants if an interview is necessary soon
after reviewing their applications.


Ung-Jin Kim, Ph.D.
147-75, Division of Biology,
Caltech, Pasadena,
CA 91125
ung@caltech.edu
(818)395-4901 (office)
(818)395-4154 (lab)
(818)796-7066 (fax)

From owner-chromosomes@net.bio.net Mon Mar 11 22:00:00 1996
Path: biosci!rutgers!uwm.edu!vixen.cso.uiuc.edu!howland.reston.ans.net!gatech!newsfeed.internetmci.com!news.sprintlink.net!news.nis.net!slip-ppp5.paramus.nis.net!sengelke
From: sengelke@nycradio.com (Stuart engelke)
Newsgroups: bionet.genome.chromosomes
Subject: Chromosome 17
Date: Tue, 12 Mar 1996 15:06:21 UNDEFINED
Organization: National Internet Source, Inc.
Lines: 4
Message-ID: <sengelke.6.0006FC47@nycradio.com>
NNTP-Posting-Host: slip-ppp5.paramus.nis.net
Summary: want info
Keywords: newborn
X-Newsreader: Trumpet for Windows [Version 1.0 Rev B]

I am considering adoption of a little girl that "had her #17 chromosome flip". 
The doctors do not know if any of the chromosome "broke off" or not. 
I am wondering what implications this may have to her future health.The 
doctors tell me she passes all her 6 month milestones now.

From owner-chromosomes@net.bio.net Mon Mar 11 22:00:00 1996
Path: biosci!rutgers!gatech!newsfeed.internetmci.com!in2.uu.net!brighton.openmarket.com!decwrl!lll-winken.llnl.gov!fnnews.fnal.gov!nntp-server.caltech.edu!news
From: "Dr. Ung-Jin Kim" <ung@ash.tree.caltech.edu>
Newsgroups: bionet.genome.chromosomes
Subject: Caltech: lab assistants and a bioinformatician
Date: Mon, 11 Mar 1996 17:20:11 -0800
Organization: California Institute of Technology
Lines: 51
Message-ID: <3144D14B.3558@ash.tree.caltech.edu>
NNTP-Posting-Host: apple.tree.caltech.edu
Mime-Version: 1.0
Content-Type: text/plain; charset=us-ascii
Content-Transfer-Encoding: 7bit
X-Mailer: Mozilla 2.0 (X11; I; SunOS 5.4 sun4m)

Genome Research Laboratory at Caltech: Please see our WEB page,
  http://www.tree.caltech.edu
 
 
Job 1: We are looking for a few lab assistants -------
   
Caltech Genome Resaerch Laboratory is looking for qualified
full time technicians with at least 1 year experience in 
laboratory works involving recombinant DNA procedures. 
Works will require skills in colony hybridization, PCR 
screening of genomic libraries, DNA preparation, restriction 
fingerprint analysis, and more.
 
Positions are open immediately. A college degree in Biological 
sciences or other sciences required. Interested parties should 
send and salary requirement to Dr. Ung-Jin Kim.
Electronic submissions are welcome.
 
 
 
Job 2: We are looking for a bioinformatician -------
 
Caltech Genome Research Laboratory is looking for a full time
informatician to manage and analyze laboratory data, and help 
operate robotic workstations. Knowledge and experieince in 
handling biological information, especially in the analysis 
and management of physcal mapping and DNA sequence data is 
essential. We also expect the person to be familiar with Unix 
server/workstations and PC/MacIntosh platforms. 
 
Interested parties should send CV and salary history to 
Dr. Ung-Jin Kim. 
Electronic submissions are welcome.
 
  
 
We will notify the applicants if an interview is necessary soon
after reviewing their applications.
 
Caltech provides employees with excellent work environment and 
benefit plans.
 
 
Ung-Jin Kim, Ph.D.
147-75, Division of Biology,
Caltech, Pasadena,
CA 91125
ung@caltech.edu
(818)395-4901 (office)
(818)395-4154 (lab)
(818)796-7066 (fax)

From owner-chromosomes@net.bio.net Wed Mar 13 22:00:00 1996
Path: biosci!rutgers!gatech!newsfeed.internetmci.com!sgigate.sgi.com!nntp.coast.net!swidir.switch.ch!scsing.switch.ch!elna.ethz.ch!usenet
From: Alexander Kraev <kraev@bc.biol.ethz.ch>
Newsgroups: bionet.genome.chromosomes
Subject: Re: Primers for PCR? (Dog genomic)
Date: 14 Mar 1996 18:12:38 GMT
Organization: ETH Zentrum Zurich, Switzerland
Lines: 25
Message-ID: <4i9nim$3k8@elna.ethz.ch>
References: <4hp0hm$l5f@ratatosk.uio.no>
NNTP-Posting-Host: bcmac6.ethz.ch
Mime-Version: 1.0
Content-Type: multipart/mixed;
	boundary="-------------------------------320131692358"
X-Mailer: Mozilla 1.1N (Macintosh; I; PPC)
X-URL: news:4hp0hm$l5f@ratatosk.uio.no

This is a multi-part message in MIME format.

---------------------------------320131692358
Content-Transfer-Encoding: 7bit
Content-Type: text/plain; charset=us-ascii

Hi there,
Dog sodium-calcium exchanger gene NCX1 happens to have two very large
exons, so that the primers can be inferred from the cDNA sequence.
Accession M36119 contains the coding sequence, bases from 11 to 1840
can be used for PCR from genomic DNA, since this is an  exon. 

Good luck,


---------------------------------320131692358
Content-Transfer-Encoding: 7bit
Content-Type: text/plain

Alexander Kraev, PhD                     Internet:    kraev@bc.biol.ethz.ch
> Lab.of Biochemistry III                            Phone:   0041-1-632-31-47
> Swiss Federal Inst. Of Technology           FAX:      0041-1-632-12-13
> Universitaetsstr. 16                    Home Page: http://www.bc.biol.ethz.ch/BiochemistryIII/                                 
> CH-8092 Zurich                                     /Sasha/kraev.html
---------------------------------320131692358--

From owner-chromosomes@net.bio.net Wed Mar 13 22:00:00 1996
Path: biosci!rutgers!gatech!news.jsums.edu!news2.cais.net!news.cais.net!news.ac.net!imci4!newsfeed.internetmci.com!in2.uu.net!news.accessone.com!not-for-mail
From: rivero@accessone.com (Michael Rivero)
Newsgroups: bionet.genome.chromosomes
Subject: Question about eye color.
Date: 14 Mar 1996 06:51:28 -0800
Organization: Accessone
Lines: 14
Message-ID: <4i9bpg$fv0@pulm1.accessone.com>
NNTP-Posting-Host: pulm1.accessone.com

There doesn't seem to be a newsgroup specific to questions of heredity.
 
  What is the likelyhood that two blued parents will produce a brown
eyed child?  
 
 
  Thanks.
 

-- 
============== P I X E L O D E O N   P R O D U C T I O N S   ==============
|  Mike & Claire - The Rancho Runnamukka http://www.accessone.com/~rivero |
=========================================================================== 


From owner-chromosomes@net.bio.net Thu Mar 14 22:00:00 1996
Path: biosci!daresbury!bioftp.unibas.ch!infobiogen.fr!jussieu.fr!oleane!tank.news.pipex.net!pipex!usenet.eel.ufl.edu!gatech!newsfeed.internetmci.com!hookup!news.nstn.ca!news.dal.ca!news
From: "A. WILSON" <WILSON_A94@cox.nsac.ns.ca>
Newsgroups: bionet.genome.chromosomes
Subject: Re: Question about eye color.
Date: 15 Mar 1996 13:20:33 GMT
Organization: Nova Scotia Agricultural College
Lines: 10
Message-ID: <4ibqr1$ojd@News.Dal.Ca>
References: <4i9bpg$fv0@pulm1.accessone.com>
NNTP-Posting-Host: cox-23-7b.nsac.ns.ca
Mime-Version: 1.0
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To: rivero@accessone.com

The chances of two blue-eyed parents producing a brown-eyed child is 
about one in many many million.  Brown eyes are dominant to blue. The 
only way this could happen could be through mutation (very rare).

                 ---------------------------------
                 |A microbiologist is someone who|
                 |won't say that a restaurant was|
                 |  good for at least 24 hours.  |
                 ---------------------------------


From owner-chromosomes@net.bio.net Thu Mar 14 22:00:00 1996
Path: biosci!daresbury!nntp-trd.UNINETT.no!newsfeed.sunet.se!news00.sunet.se!sunic!mn6.swip.net!plug.news.pipex.net!pipex!tank.news.pipex.net!pipex!newsfeed.internetmci.com!gatech!rutgers!csn!news-1.csn.net!csn!nntp-xfer-2.csn.net!tali.UCHSC.edu!essex.UCHSC.edu!binstoct
From: Teresa Binstock <binstoct@essex.UCHSC.edu>
Newsgroups: bionet.molbio.yeast,bionet.molbio.proteins,bionet.molbio.evolution,bionet.genome.chromosomes,bionet.general
Subject: DATA BASE?: STE2 & STE3: yeast & humans.
Date: Thu, 14 Mar 1996 18:08:09 -0700
Organization: University of Colorado, Health Sciences Center
Lines: 39
Message-ID: <Pine.ULT.3.91.960314175949.13504E-100000-100000@essex.UCHSC.edu>
References: <Bilha001-1403961141500001@dialup-2-155.gw.umn.edu> <Pine.ULT.3.91.960314174357.13504C-100000@essex.UCHSC.edu>
NNTP-Posting-Host: essex.uchsc.edu
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Xref: biosci bionet.molbio.yeast:4953 bionet.molbio.proteins:7346 bionet.molbio.evolution:4329 bionet.genome.chromosomes:1073 bionet.general:20426

On Thu, 14 Mar 1996, Teresa Binstock wrote:

> QUESTION about data base, if any:
> 
> In one study findable via OVID search of Medline, STE2 and STE3 are 
> described as occurring in the human thymic epithelium. Otherwise, all the 
> other STE2 and STE3 studies refer to cell-surface receptors occurring in 
> Saccharomyces Cerevisiae. Many S. Cerevisiae genes and molecules have 
> homologues in mammals including humans. In fact, some human molecules 
> function in yeast and vice versa.
> 	I would like to "pin-down" whether or not the human STE2 and STE3 
> molecules reported by Patel et al are homologous to S. Cerevisiae 
> molecules with the same nomenclature. 
> 	Are there data bases other than Medline that would yield such 
> information? 
> 
> I would be very appreciative of being informed about such data bases and 
> how to access them. E-mails directly to me would be appreciated and/or to 
> the newsgroups if such distribution is appropriate.
> 
> 
> 
> au: Patel et al
> so: Journal of Clinical Immunology 15.2.80-92 1995
> ti: Characterization of human thymic epithelial cell surface antigens:
>        phenotypic similarity of thymic epithelial cells to epidermal 
>           keratinocytes.
> 
> 
> Thank you,
> 
> 
> Teresa 
> 
> 
> Teresa C. Binstock, Researcher
> Developmental & Behavioral Neuroanatomy
> Denver CO USA
> 			Teresa.Binstock@uchsc.edu


From owner-chromosomes@net.bio.net Thu Mar 14 22:00:00 1996
Path: biosci!MENDEL.LLNL.GOV!greg
From: greg@MENDEL.LLNL.GOV
Newsgroups: bionet.genome.chromosomes
Subject: Re: Question about eye color
Date: 15 Mar 1996 12:47:30 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 40
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <9603152044.AA01035@mendel.llnl.gov>
NNTP-Posting-Host: net.bio.net


This is incorrect. As stated in OMIM, "eye color is likely to
be a polygenic trait. The early view that blue is a simple
recessive has been repeatedly shown to be wrong by observation
of brown-eyed offspring of 2 blue-eyed parents."

To access the OMIM (Online Mendelian Inheritance in Man) database
through the WWW, go to either the current URL:
http://www3.ncbi.nlm.nih.gov/Omim/
or to the now historic URL:
http://gdbwww.gdb.org/gdb-bin/omim/bin/omimq

Greg Lennon
Lawrence Livermore National Laboratory

> From BIOSCI-REQUEST@net.bio.net Fri Mar 15 06:11:15 1996
> To: biochrom@net.bio.net
> From: "A. WILSON" <WILSON_A94@cox.nsac.ns.ca>
> Subject: Re: Question about eye color.
> Date: 15 Mar 1996 13:20:33 GMT
> Nntp-Posting-Host: cox-23-7b.nsac.ns.ca
> Mime-Version: 1.0
> Content-Type> : > text/plain> ; > charset=us-ascii> 
> Content-Transfer-Encoding: 7bit
> X-Mailer: Mozilla 1.22 (Windows; I; 16bit)
> To: rivero@accessone.com
> Content-Length: 465
> 
> The chances of two blue-eyed parents producing a brown-eyed child is 
> about one in many many million.  Brown eyes are dominant to blue. The 
> only way this could happen could be through mutation (very rare).
> 
>                  ---------------------------------
>                  |A microbiologist is someone who|
>                  |won't say that a restaurant was|
>                  |  good for at least 24 hours.  |
>                  ---------------------------------
> 
> 
> 

From owner-chromosomes@net.bio.net Fri Mar 15 22:00:00 1996
Path: biosci!AIX1.UOTTAWA.CA!s060965
From: s060965@AIX1.UOTTAWA.CA
Newsgroups: bionet.genome.chromosomes
Subject: Re: methylation of DNA in mice
Date: 16 Mar 1996 06:08:21 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 35
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <Pine.A32.3.91.960316085943.100818A-100000@aix1.uottawa.ca>
References: <mrtour-1503961736210001@ski-h-99-094.ski.mskcc.org>
NNTP-Posting-Host: net.bio.net

Expensive??????   Relative to what???  I've been using HpaII and MspI for 
years and doing similar experiments.

I suspect it is one of the cheaper pairs.  Certainly it is more expensive 
than things like BamHI or EcoRI .... but not much .... compare it to the 
price of Taq polymerase or some of the other stranger restriction enzymes.

And considering that almost everyone using these two enzymes for 
methylation studies, it probably would be unwise to alter from this.

Cris Martin

On 15 Mar 1996 mrtour@stud.med.cornell.edu wrote:

> I want to examine DNA methylation differences in two types of mice....i
> plan to do this by utilizing 2 restriction enzymes which are isoschizomers
> (recognize the same cut site) but one is sensitive to methylation at the
> site and the other isn't...
> 
> one pair of which i am absolute sure of is MspI and HpaII...but these are
> expensive....would anyone know of another pair which would do the same
> thing but perhaps be cheaper?
> 
> thank you for your help.
> 
> please post here or to mrtour@stud.med.cornell.edu
> 
> michelle
> 
> -- 
> db
> 
> or Michelle
> 
> 

From owner-chromosomes@net.bio.net Fri Mar 15 22:00:00 1996
Path: biosci!CS.Arizona.EDU!noao!ennfs.eas.asu.edu!gatech!newsfeed.internetmci.com!howland.reston.ans.net!vixen.cso.uiuc.edu!uwm.edu!msunews!netnews.upenn.edu!sanger.bcm.tju.edu!tromp
From: tromp@sanger.bcm.tju.edu (Gerard Tromp)
Newsgroups: bionet.genome.chromosomes
Subject: Re: Question about eye color.
Date: 15 Mar 1996 19:48:34 GMT
Organization: Biochemistry
Lines: 24
Distribution: world
Message-ID: <4ichii$qli@netnews.upenn.edu>
References: <4i9bpg$fv0@pulm1.accessone.com> <4ibqr1$ojd@News.Dal.Ca>
NNTP-Posting-Host: sanger.bcm.tju.edu

In article <4ibqr1$ojd@News.Dal.Ca>, "A. WILSON" <WILSON_A94@cox.nsac.ns.ca> writes:
> The chances of two blue-eyed parents producing a brown-eyed child is 
> about one in many many million.  Brown eyes are dominant to blue. The 
> only way this could happen could be through mutation (very rare).
> 


Patently false. Assumes that eye color is inherited as a simple single-locus
mendelian trait, it is not. Also, in some simple single-locus mendelian traits 
which are caused predominantly by de novo mutations, the mutation rate can be much
higher, in the range of 1 in 10 or 20 thousand. Simply put, it is not possible to
give and estimate without considerable additional information (data).

Gerard Tromp
-- 
=======================================================================
Gerard Tromp, Ph.D.
Assistant Professor                     Vox:  313-577-8773
Center for Molecular Medicine 
   and Genetics                         Fax:  313-577-5218
Wayne State University
540 East Canfield Ave., Room 3116    E-mail:  tromp@sanger.med.wayne.edu
Detroit, MI 48201                             gtromp@cmb.biosci.wayne.edu
U.S.A.

From owner-chromosomes@net.bio.net Fri Mar 15 22:00:00 1996
Path: biosci!rutgers!csn!news-1.csn.net!magnus.acs.ohio-state.edu!lerc.nasa.gov!purdue!haven.umd.edu!hecate.umd.edu!research-01.ski.mskcc.org!ski-h-99-094.ski.mskcc.org!user
From: mrtour@stud.med.cornell.edu,dburtrum@ski.mskcc.org (michelle or doug......)
Newsgroups: bionet.molbio.methds-reagnts,bionet.genome.chromosomes,
Subject: methylation of DNA in mice
Date: 15 Mar 1996 22:33:25 GMT
Organization: Memorial Sloan-Kettering Cancer Center
Lines: 19
Message-ID: <mrtour-1503961736210001@ski-h-99-094.ski.mskcc.org>
NNTP-Posting-Host: ski-h-99-094.ski.mskcc.org
Xref: biosci bionet.molbio.methds-reagnts:41917 bionet.genome.chromosomes:1077

I want to examine DNA methylation differences in two types of mice....i
plan to do this by utilizing 2 restriction enzymes which are isoschizomers
(recognize the same cut site) but one is sensitive to methylation at the
site and the other isn't...

one pair of which i am absolute sure of is MspI and HpaII...but these are
expensive....would anyone know of another pair which would do the same
thing but perhaps be cheaper?

thank you for your help.

please post here or to mrtour@stud.med.cornell.edu

michelle

-- 
db

or Michelle

From owner-chromosomes@net.bio.net Sat Mar 16 22:00:00 1996
Path: biosci!ns1.faseb.org!lamarck.sura.net!newsfeed.internetmci.com!howland.reston.ans.net!newsjunkie.ans.net!newsfeeds.ans.net!news.rmii.com!estreet.com!user
From: kcollins@estreet.com (Kent F. Collins)
Newsgroups: bionet.genome.chromosomes
Subject: HELP< HELP
Date: Sat, 16 Mar 96 16:24:09 -0700
Organization: E Street Denver
Lines: 5
Message-ID: <4949566.ensmtp@estreet.com>
NNTP-Posting-Host: news.estreet.com
X-Newsreader: ExpressNet/SMTP v1.1.5

I need some clip art of cell miosis, mitosis and  fertilization of 2 haploid
cells. Thanks 

E-mail to kcollins@estreet.com


From owner-chromosomes@net.bio.net Sat Mar 16 22:00:00 1996
Path: biosci!UCRAC1.UCR.EDU!judelson
From: judelson@UCRAC1.UCR.EDU (Howard S. Judelson)
Newsgroups: bionet.genome.chromosomes
Subject: postdoc positions: fungal genetics/map-based cloning/gene analysis
Date: 17 Mar 1996 14:23:05 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 43
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199603172220.OAA07602@click.ucr.edu>
NNTP-Posting-Host: net.bio.net

POSTDOCTORAL POSITIONS

Molecular genetics of the oomycete fungus, Phytophthora infestans

        Candidates are sought for two postdoctoral positions in a
laboratory investing the molecular genetics of Phytophthora infestans, an
oomycete fungus that causes the important late blight diseases of potato
and tomato.  Successful applicants can join either of several on-going
projects.  These include the positional cloning of genes determining mating
type (sexual compatibility type; see Judelson et al. 1995, Genetics
141:503-512); the analysis of genome rearrangements associated with a
system of balanced lethals in Phytophthora; the characterization of
mating-induced genes (isolated by differential display and subtraction
cloning); and the analysis of genes determining resistance to fungicides. 
Major funding for these positions comes from grants from the USDA and NSF.

        Applicants should have a Ph.D. and some experience in molecular
biology.  Depending on the project, the experiments will involve techniques
such as genetic mapping, long-range restriction mapping, chromosome walking
in cosmid and BAC libraries, and fungal transformation; experience with
these would be helpful but is not required.  

        Please sent a curriculum vitae and the names of three references
(including addresses and telephone numbers) to: 

Howard Judelson
Department of Plant Pathology
University of California
Riverside, California 92521 USA
email: judelson@ucrac1.ucr.edu
fax: 909-787-4294

Howard Judelson (judelson@ucrac1.ucr.edu)
Assistant Professor
Department of Plant Pathology
University of California
Riverside, California 92521
USA

Tel: 909-787-4199
Fax: 909-787-4294



From owner-chromosomes@net.bio.net Sun Mar 17 22:00:00 1996
Path: biosci!rutgers!uwm.edu!cs.utexas.edu!howland.reston.ans.net!newsfeed.internetmci.com!in1.uu.net!news.epix.net!usenet
From: wild@epix.net (Wild Dude)
Newsgroups: bionet.genome.chromosomes
Subject: a biology students wants your help
Date: Mon, 18 Mar 1996 00:35:23 GMT
Organization: epix.net
Lines: 16
Message-ID: <4iib1m$egf@guava.epix.net>
NNTP-Posting-Host: lsptppp68.epix.net
X-Newsreader: Forte Free Agent 1.0.82

Dear scientists,
	I'm a 16 year old high school biology student. In class, we are
studying genetics, and your project came up in discussion. I admire
your work, and wish you well in it. My teacher said, jokingly, that
she'd give an "A" to anyone who could put together a Punnett Square
for a human being, showing all chromosomes and possible crosses. I
know that creating a Punnett Square of this size would be impossible
to do with a pencil and paper, but I thought that there might be a way
to do it with a computer. I'd really like to do this, just to see what
my teacher says about it. Please respond to me by email at
WILD@EPIX.NET . Thank you VERY much for your valuable time.

Sincerely,
Brian Snyder
wild@epix.net


From owner-chromosomes@net.bio.net Sun Mar 17 22:00:00 1996
Path: biosci!daresbury!bioftp.unibas.ch!infobiogen.fr!jussieu.fr!oleane!tank.news.pipex.net!pipex!swrinde!howland.reston.ans.net!nntp.coast.net!swidir.switch.ch!scsing.switch.ch!elna.ethz.ch!smac.ethz.ch!user
From: tan@mol.biol.ethz.ch (Song Tan)
Newsgroups: bionet.molbio.yeast,bionet.molbio.proteins,bionet.molbio.evolution,bionet.genome.chromosomes,bionet.general
Subject: Re: DATA BASE?: STE2 & STE3: yeast & humans.
Date: Mon, 18 Mar 1996 16:38:54 +0100
Organization: ETH-Honggerberg (Swiss Federal Institute of Technology)
Lines: 43
Message-ID: <tan-1803961638540001@smac.ethz.ch>
References: <Bilha001-1403961141500001@dialup-2-155.gw.umn.edu> <Pine.ULT.3.91.960314174357.13504C-100000@essex.UCHSC.edu> <Pine.ULT.3.91.960314175949.13504E-100000-100000@essex.UCHSC.edu>
NNTP-Posting-Host: smac.ethz.ch
Xref: biosci bionet.molbio.yeast:4969 bionet.molbio.proteins:7367 bionet.molbio.evolution:4345 bionet.genome.chromosomes:1082 bionet.general:20514

In article
<Pine.ULT.3.91.960314175949.13504E-100000-100000@essex.UCHSC.edu>, Teresa
Binstock <binstoct@essex.UCHSC.edu> wrote:

> On Thu, 14 Mar 1996, Teresa Binstock wrote:
> 
> > QUESTION about data base, if any:
> > 
> > In one study findable via OVID search of Medline, STE2 and STE3 are 
> > described as occurring in the human thymic epithelium. Otherwise, all the 
> > other STE2 and STE3 studies refer to cell-surface receptors occurring in 
> > Saccharomyces Cerevisiae. Many S. Cerevisiae genes and molecules have 
> > homologues in mammals including humans. In fact, some human molecules 
> > function in yeast and vice versa.
> >       I would like to "pin-down" whether or not the human STE2 and STE3 
> > molecules reported by Patel et al are homologous to S. Cerevisiae 
> > molecules with the same nomenclature. 
> > 
> > au: Patel et al
> > so: Journal of Clinical Immunology 15.2.80-92 1995
> > ti: Characterization of human thymic epithelial cell surface antigens:
> >        phenotypic similarity of thymic epithelial cells to epidermal 
> >           keratinocytes.

I find Entrez <http://atlas.nlm.nih.gov:5700/Entrez/index.html> to be the
best tool for tracking down sequences.  However, I didn't find any
non-yeast STE2 or STE3 sequences in the GenBank database that Entrez uses,
nor any relevant epithelial sequences from authors named Patel.   Since I
don't have access to the article you cited, I wasn't able to figure out if
the authors published the sequences of the human STE2 and STE3 genes.  If
they did, it would be easy to compare them against the yeast STE2 and STE3
genes.  If they didn't publish any sequence, I'm not sure you will find
any other publicly available databases that might answer whether the human
and yeast genes are related. 

Hope this helps.

-- 
Song Tan
Institute for Molecular Biology and Biophysics
ETH-Honggerberg (Swiss Federal Institute of Technology)
8093 Zurich, Switzerland
email:  tan@mol.bio.ethz.ch

From owner-chromosomes@net.bio.net Sun Mar 17 22:00:00 1996
Path: biosci!lhc.nlm.nih.gov!borduas!francis
From: francis@borduas.nlm.nih.gov (Francis Ouellette)
Newsgroups: bionet.molbio.yeast,bionet.molbio.proteins,bionet.molbio.evolution,bionet.genome.chromosomes,bionet.general
Subject: Re: DATA BASE?: STE2 & STE3: yeast & humans.
Followup-To: bionet.molbio.yeast,bionet.molbio.proteins,bionet.molbio.evolution,bionet.genome.chromosomes,bionet.general
Date: 18 Mar 1996 22:06:52 GMT
Organization: National Library of Medicine
Lines: 18
Message-ID: <4ikmps$lkg@lhc.nlm.nih.gov>
References: <Bilha001-1403961141500001@dialup-2-155.gw.umn.edu> <Pine.ULT.3.91.960314174357.13504C-100000@essex.UCHSC.edu> <Pine.ULT.3.91.960314175949.13504E-100000-100000@essex.UCHSC.edu> <tan-1803961638540001@smac.ethz.ch>
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Xref: biosci bionet.molbio.yeast:4971 bionet.molbio.proteins:7372 bionet.molbio.evolution:4348 bionet.genome.chromosomes:1083 bionet.general:20525

Song Tan (tan@mol.biol.ethz.ch) wrote:

> I find Entrez <http://atlas.nlm.nih.gov:5700/Entrez/index.html> to be the

the proper URL for Entrez is:

http://www3.ncbi.nlm.nih.gov/Entrez/

regards,

francis


--
| B.F. Francis Ouellette  
| GenBank
|
| francis@ncbi.nlm.nih.gov   

From owner-chromosomes@net.bio.net Mon Mar 18 22:00:00 1996
Path: biosci!rutgers!uwm.edu!vixen.cso.uiuc.edu!howland.reston.ans.net!newsfeed.internetmci.com!in2.uu.net!fdn.fr!r2d2.fdn.org!med.univ-tours.fr!news.univ-angers.fr!jussieu.fr!univ-lyon1.fr!news
From: 4BC <bio4insa@insa.insa-lyon.fr>
Newsgroups: bionet.genome.chromosomes
Subject: help RETROTRANSPOSONS
Date: 19 Mar 1996 18:38:26 GMT
Organization: insa-lyon.fr
Lines: 7
Message-ID: <4imuv2$g74@tempo.univ-lyon1.fr>
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Sorry I sent an article named "re : retrotransposon" but I made a mistake 
I'm actually looking for synthetic easy to understand paper or book on 
this topic
Thanks to email me

Eric


From owner-chromosomes@net.bio.net Mon Mar 18 22:00:00 1996
Path: biosci!rutgers!uwm.edu!vixen.cso.uiuc.edu!howland.reston.ans.net!newsfeed.internetmci.com!in2.uu.net!fdn.fr!med.univ-tours.fr!news.univ-angers.fr!jussieu.fr!univ-lyon1.fr!news
From: 4BC <bio4insa@insa.insa-lyon.fr>
Newsgroups: bionet.genome.chromosomes
Subject: RE : retrotransposon
Date: 19 Mar 1996 18:31:01 GMT
Organization: insa-lyon.fr
Lines: 9
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I'm a student in biochemistry and I have to work on retrotransposon to 
make a presentation in my course of genetic of microorganisms.
If you know a good,easy to understand reference on this topic could you 
please email me.
I'm looking for synthetic book or paper
thank you in advance

Eric


From owner-chromosomes@net.bio.net Mon Mar 18 22:00:00 1996
Path: biosci!ns1.faseb.org!lamarck.sura.net!newsfeed.internetmci.com!tank.news.pipex.net!pipex!lade.news.pipex.net!pipex!bbc!news
From: KathyBarnby <Kathy.Barnby@bbc.co.UK>
Newsgroups: bionet.genome.chromosomes
Subject: BBC TV  Natural History of Human Body
Date: 19 Mar 1996 12:25:28 GMT
Organization: BBC
Lines: 26
Message-ID: <4im93o$22c@bbcnews.rd.bbc.co.uk>
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BBC Needs Help With Natural History of Human Body


The BBC are making a series of programmes about the Human Body. 
They will illustrate what science can currently tell us about how 
the human body works and how it evolved. If you have research 
that you think would help us to visualise human biological 
processes in a new and enlightening way, 
please contact me at kathy.barnby@bbc.co.uk
*+44.181.752.6210 and fax +44.181.752 6810 in London.

I would love to see examples of images created by new 
technologies such as magnetic resonance imaging, ultrasound, 
computer analysis of X-ray and PET scans. Also film or video 
images, no matter how old, which show the processes of our 
bodies. We want to illustrate human life from conception, 
through foetal development, into babyhood, childhood, before and 
after puberty, the ageing process, death and beyond. Examples of 
the moments we might capture on film are: 

1 Meiosis    
2 SEM images of chromosomes     
3 how small can you go?   




From owner-chromosomes@net.bio.net Mon Mar 18 22:00:00 1996
Path: biosci!rutgers!uwm.edu!vixen.cso.uiuc.edu!newsfeed.internetmci.com!in2.uu.net!fdn.fr!r2d2.fdn.org!med.univ-tours.fr!news.univ-angers.fr!jussieu.fr!univ-lyon1.fr!news
From: 4eme annee biochimie <bio4insa@insa.insa-lyon.fr>
Newsgroups: bionet.genome.chromosomes
Subject: heterologous expression
Date: 19 Mar 1996 19:14:09 GMT
Organization: Biochimie
Lines: 9
Message-ID: <4in121$j8k@tempo.univ-lyon1.fr>
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hi!
I'm student in national institut of applied science of lyon (France), in 
biochemistry department. I have to work on heterologous expression for my 
course of molecular genetic.
I'm looking for documents about it. It would be very nice of you if you 
email me some informations.
Thank you
Nico.


From owner-chromosomes@net.bio.net Mon Mar 18 22:00:00 1996
Path: biosci!CGNET.COM!A.VALLADOLID
From: A.VALLADOLID@CGNET.COM ("Valladolid, Andres")
Newsgroups: bionet.genome.chromosomes
Subject: (none)
Date: 19 Mar 1996 14:22:22 -0800
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Lines: 2
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subscribe chromosomes

From owner-chromosomes@net.bio.net Tue Mar 19 22:00:00 1996
Path: biosci!rutgers!gatech!newsfeed.internetmci.com!hookup!news.nstn.ca!coranto.ucs.mun.ca!leif!pallderdice
From: pallderdice@kean.ucs.mun.ca
Newsgroups: bionet.genome.chromosomes
Subject: Is there anyone who has two translocation chromosomes from #21 & #22?
Date: 19 Mar 96 21:07:14 -0330
Organization: Memorial University. St.John's Nfld, Canada
Lines: 19
Message-ID: <1996Mar19.210714.1@leif>
NNTP-Posting-Host: leif.ucs.mun.ca

I know a mother and daughter who are physically and mentally normal
and each has two translocation chromosomes.  
One includes the long arm of chromosome 21 and the long arm of chromosome 
22.
The second is formed by the short arm of chromosome 21 and the short arm
of chromosome 22.
I am writing the karytoype: 46,XX,-21,-22,+t(21q22q),+t(21p22p).
The mother had a normal daughter, and then repeated apontaneous abortions.
The daughter had a spontaneous abortion, with a karyotype like the mothers'
.Her next pregnancy was a Down syndrome (trisomy 21).
The chromosomes for the Down syndrome were the same as the mothers' plus
another chromosome 21.

The daughter would like to correspond with someone else who has the
same balanced chromosome rearrangement as her own.
Specifically, she would like to hear that this unknown person, has had
some normal liveborn infants.

Thank you, Penny

From owner-chromosomes@net.bio.net Tue Mar 19 22:00:00 1996
Path: biosci!agate!howland.reston.ans.net!newsfeed.internetmci.com!uwm.edu!news.inap.net!news
From: Nick Golas <nickg@wi.net>
Newsgroups: bionet.genome.chromosomes
Subject: Smith's Lemli Opitz Syndrome
Date: 20 Mar 1996 10:44:09 GMT
Organization: NAP.NET -- Milwaukee, WI
Lines: 3
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To: ALl

My friend's little boy has this (he's 14). Are there any other parents who have children 
diagnosed with SLO out there?


From owner-chromosomes@net.bio.net Tue Mar 19 22:00:00 1996
Path: biosci!agate!howland.reston.ans.net!news.moneng.mei.com!uwm.edu!news.inap.net!news
From: Nick Golas <nickg@wi.net>
Newsgroups: bionet.genome.chromosomes
Subject: Smith's Lemli Opitz Syndrome
Date: 20 Mar 1996 10:44:46 GMT
Organization: NAP.NET -- Milwaukee, WI
Lines: 24
Message-ID: <4ioniu$2ct@news.inap.net>
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To: ALl

My friend's little boy has this (he's 14). Are there any other parents who have children 
diagnosed with SLO out the> 
> --------------------------------------------------------------------
> 
> Newsgroup: bionet.genome.chromosomes
> 
>    * HELP< HELP - Kent F. Collins (5)
>    * postdoc positions: fungal genetics/map-based cloning/gene
>      analysis - Howard S. Judelson (43)
>    * a biology students wants your help - Wild Dude (16)
>    * Re: DATA BASE?: STE2 & STE3: yeast & humans. - Song Tan (43)
>         o Francis Ouellette (18)
>    * BBC TV Natural History of Human Body - KathyBarnby (26)
>    * RE : retrotransposon - 4BC (9)
>    * help RETROTRANSPOSONS - 4BC (7)
>    * heterologous expression - 4eme annee biochimie (9)
>    * (none) - "Valladolid, Andres" (2)
>    * Is there anyone who has two translocation chromosomes from #21
>      & #22? - pallderdice@kean.ucs.mun.ca (19)
> 
> --------------------------------------------------------------------
> 
re?


From owner-chromosomes@net.bio.net Wed Mar 20 22:00:00 1996
Path: biosci!rutgers!uwm.edu!vixen.cso.uiuc.edu!newsfeed.internetmci.com!in2.uu.net!newsfeed.pitt.edu!news
From: jcard+@pitt.edu (John J. Cardamone Jr.)
Newsgroups: bionet.genome.chromosomes
Subject: Used Dupont Genesis DNA Sequencers FOR SALE
Date: 21 Mar 1996 20:31:18 GMT
Organization: University of Pittsburgh
Lines: 10
Sender: jcard@pop.pitt.edu
Message-ID: <4iseam$hef@usenet.srv.cis.pitt.edu>
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University of Pittsburgh, Dept. of Molecular Genetics & Biochemistry,
Research Support Facilities.

  We have 2 Genesis Automated DNA sequencers in good condition.
Please contact 


John Cardamone
412-383-9769
jcard+@pitt.edu

From owner-chromosomes@net.bio.net Wed Mar 20 22:00:00 1996
Newsgroups: bionet.genome.chromosomes
Path: biosci!ns1.faseb.org!lamarck.sura.net!fconvx.ncifcrf.gov!tobin
From: tobin@ncifcrf.gov (Greg Tobin)
Subject: in situ hybridization
Message-ID: <DoMr57.Bnt@ncifcrf.gov>
Organization: Frederick Cancer Research and Development Center
Date: Thu, 21 Mar 1996 18:24:43 GMT
Lines: 16

Our lab is getting into in situ hybridization to identify tissues containing
specific DNA or RNA.  This would entail standard in situ hybridization, 
PCR in situ, and RT-PCR in situ.  There are many, many protocols out there
for doing these experiments.  At first, I would like to try in situ hyb with
a radioactive probe and then move to a fluorescent probe.  The PCR-based assays
would be fluorescent.

Can I get some opinions on how to make the best probe?  How long should it be
for in situ hyb?  Would a random primed or PCR-generated probe have higher
sp. activity than the nick-translation probes?  If the target is 2.5 kb, 
would it be better to use a 2.5 kb probe or an 0.5 kb probe (the smaller probe
might penetrate and bind better).

Any advice would be appreciated.



From owner-chromosomes@net.bio.net Wed Mar 20 22:00:00 1996
Path: biosci!rutgers!uwm.edu!vixen.cso.uiuc.edu!newsfeed.internetmci.com!tank.news.pipex.net!pipex!oleane!jussieu.fr!univ-compiegne.fr!u-picardie.fr!usenet
From: ghislaine.grenier@isab.fr
Newsgroups: bionet.genome.chromosomes
Subject: Lipid Transfer Protein cDNAs
Date: Thu, 21 Mar 1996 18:23:36 GMT
Organization: Universite de Picardie-Jules Verne - Amiens - France
Lines: 9
Distribution: inet
Message-ID: <4ir7gs$phv@gip.u-picardie.fr>
NNTP-Posting-Host: pc3.isab.fr
X-Newsreader: Forte Free Agent 1.0.82

I'd like to know if there is a data base about LTP cDNAs.

I would be very appreciative of being informed about such data bases
and  how to access them. E-mails directly to me would be appreciated
and/or to the newsgroups if such distribution is appropriate.

E-mail : ghislaine.grenier@isab.fr



From owner-chromosomes@net.bio.net Wed Mar 20 22:00:00 1996
Path: biosci!rutgers!uwm.edu!vixen.cso.uiuc.edu!newsfeed.internetmci.com!in2.uu.net!newsfeed.pitt.edu!news
From: jcard+@pitt.edu (John J. Cardamone Jr.)
Newsgroups: bionet.genome.chromosomes
Subject: University of Pittsburgh, Dept. of Molecular Genetics & 
 Biochemistry's New Home Page
Date: 21 Mar 1996 20:32:03 GMT
Organization: University of Pittsburgh
Lines: 5
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Please visit our new Home Page

http://www.pitt.edu/~rsup/mgb

  

From owner-chromosomes@net.bio.net Wed Mar 20 22:00:00 1996
Path: biosci!rutgers!uwm.edu!vixen.cso.uiuc.edu!newsfeed.internetmci.com!in2.uu.net!newsfeed.pitt.edu!news
From: jcard+@pitt.edu (John J. Cardamone Jr.)
Newsgroups: bionet.genome.chromosomes
Subject: University of Pittsburgh, Dept. of Molecular Genetics & 
 Biochemistry's New Home Page
Date: 21 Mar 1996 20:32:23 GMT
Organization: University of Pittsburgh
Lines: 5
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Please visit our new Home Page

http://www.pitt.edu/~rsup/mgb

  

From owner-chromosomes@net.bio.net Thu Mar 21 22:00:00 1996
Path: biosci!rutgers!uwm.edu!vixen.cso.uiuc.edu!chi-news.cic.net!news.compuserve.com!news.production.compuserve.com!news
From: Mark Langan <100071.3213@CompuServe.COM>
Newsgroups: bionet.genome.chromosomes
Subject: Chromosomes 7 & 8. Translocation Pr
Date: 22 Mar 1996 19:17:48 GMT
Organization: CompuServe, Inc. (1-800-689-0736)
Lines: 13
Message-ID: <4iuucs$h2$1@mhafc.production.compuserve.com>

I am not sure I have the right newsgroup.  I am looking for 
information on an unbalanced translocation of chromosomes 7 and 8.

It has caused a physical development to slow in the body of a male 
2 year old child. The head is growing normally and is as it should 
be. 

I would appreciate any information on, or treatments for this 
condition or sources of information etc.

TIA

Mark Langan 

From owner-chromosomes@net.bio.net Fri Mar 22 22:00:00 1996
Path: biosci!biosci!not-for-mail
From: white@pobox.upenn.edu (Peter White)
Newsgroups: bionet.genome.chromosomes
Subject: Human chromosome 1 WWW site
Date: 22 Mar 1996 21:00:35 -0800
Organization: Children's Hospital of Philadelphia
Lines: 25
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <white-2203961728550001@159.14.43.8>
NNTP-Posting-Host: net.bio.net

Human chromosome 1 WWW site

Announcing the opening of a human chromosome 1 World Wide Web site. This
resource is available on-line at:

http://linkage.cpmc.columbia.edu/chr1/

The WWW site contains pertinent information regarding cytogenetic,
genetic, physical, and transcript mapping exclusively of or including the
largest human chromosome. Current resources include:

   -Repository of meeting information and report of the September 1995 
    chromosome 1 workshop

   -Directory of links to available chromosome 1-specific mapping information

   -On-line forum for discussion of chromosome 1 mapping and sequencing issues

This resource is sponsored by a collaboration between the Statistical
Genetics Group at Columbia University and the Division of Oncology at the
Children's Hospital of Philadelphia, with guidance from much of the
chromosome 1 mapping community. For further information, please contact
Pete White at white@kermit.oncol.chop.edu or Tara Matise at
tara.matise@columbia.edu.


From owner-chromosomes@net.bio.net Tue Mar 26 22:00:00 1996
Message-ID: <190328Z26031996@anon.penet.fi>
Path: biosci!galaxy.ucr.edu!ihnp4.ucsd.edu!usc!elroy.jpl.nasa.gov!swrinde!howland.reston.ans.net!EU.net!news.eunet.fi!anon.penet.fi
Newsgroups: alt.drugs.pot.cultivation,alt.hemp,bionet.plants,bionet.genome.chromosomes,alt.sustainable.agriculture,rec.gardens,carleton.clubs.cannabis,sdnet.hemp
From: an307269@anon.penet.fi (Alien Anthropologist)
X-Anonymously-To: alt.drugs.pot.cultivation,,alt.hemp,bionet.plants,bionet.genome.chromosomes,alt.sustainable.agriculture,rec.gardens,carleton.clubs.cannabis,sdnet.hemp
Organization: Anonymous forwarding service
Reply-To: an307269@anon.penet.fi
Date: Tue, 26 Mar 1996 18:57:40 UTC
Subject: Re: (fwd) Botany of Skunk/Northern-Lights/Kush cross
Lines: 20
Xref: biosci bionet.plants:10675 bionet.genome.chromosomes:1099 rec.gardens:103584


People with a moral problem with a plant, please read no further (get an
education while you're at it)
 
Cannabis:

 Last year AFOAF had the most amazing hybrid (what they say was a
 Northern Lights x Skunk hybrid. Unfortunately his/her last clone died, but
 not before s/he had a chance to cross with a Kush male. My questions
 stemming (no punn intended) purely from a curiosity standpoint, and a
 haphazard genetic education are as follows:
 
 1) Why did the plant seem to remain with only 3 blades per leaf, long
 after reverting from flowering cycle - would it ever have changed back to 5?

--****ATTENTION****--****ATTENTION****--****ATTENTION****--***ATTENTION***
Your e-mail reply to this message WILL be *automatically* ANONYMIZED.
Please, report inappropriate use to                abuse@anon.penet.fi
For information (incl. non-anon reply) write to    help@anon.penet.fi
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From owner-chromosomes@net.bio.net Tue Mar 26 22:00:00 1996
Path: biosci!internet!biosci!not-for-mail
From: biohelp (BIOSCI Administrator)
Newsgroups: bionet.genome.chromosomes
Subject: IMPORTANT - BIOSCI Fundraising Update!
Date: 27 Mar 1996 02:00:38 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 149
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199603271000.CAA20959@net.bio.net>
NNTP-Posting-Host: net.bio.net


I'm interrupting the usual monthly posting of the BIOSCI miniFAQ to
bring you up to date on BIOSCI fundraising progress, a topic of
concern to your future use of this resource.  Thank you in advance for
taking the time to read this message carefully.

Last year we announced that BIOSCI was going to adopt the U.S. Public
Broadcasting System model to fund its operations after our DOE/NSF
grant runs out later this year.  Unlike PBS, we are not soliciting
contributions from users; we are only selling ads on our Web pages
solely to cover our operating costs.  Our goal is to seek sponsorships
until we build up an operating reserve of about $100,000 and then
cease further promotions until we need to build the reserve back up.
(The accountants among our readership will be familiar with the
problem of deferred revenue which we can not safely utilize until ads
have been displayed for a period of time.)  We have three sponsors to
date with a couple more pending.  The process is time-consuming,
however, and we need your help as explained further below.

Our operating costs consist of our network connection, phone lines,
hardware maintenance (we hope to have new and faster hardware soon!),
plus 0.7 FTE of salaries covering UNIX systems admin, technical
support, quality assurance, i.e., testing, of our system, and
administrative costs (such as the time it takes to actually
find/write/call potential sponsors and raise money!).  Although the
BIOSCI staff does get compensated for a portion of the work that they
do, this project has always received a lot of free after-hours and
"vacation" time labor, so we hope that no one will begrudge the time
that we do charge to the project to serve you.  All of the three
part-time staff members, Dave Mack, Julie Lawrence, and myself, have
full time day jobs and families in addition to working hard to keep
this service running for all of you.  Julie and Dave Mack are
subcontractors for BIOSCI; my time that is charged to the project
defrays a portion of my regular salary instead of adding to my income.

Besides having to relocate the project, we were very busy this last
year building new infrastructure such as our WWW hypermail interface
to the system.  This was released last December along with scores of
WAIS indices for the newsgroups.  Virtually everything is complete,
although we do continue to find and fix bugs (many through your
helpful feedback!).  We are still having some problems with our WAIS
indexing.  The archives continue to grow rapidly.  We are running over
100 indexes now versus three previously and any systems crashes cause
greater havoc with the indexing than before!  We are still working to
fix this as fast as our resources permit and appreciate your patience,
but we have been able to automate a lot of the infrastructure to
reduce labor as compared to past requirements.

We have also implemented new software to make moderation of
BIOSCI/bionet newsgroups much easier and combat the growing problem of
Internet junk mail and USENET "spamming."  About 20% of our groups are
now moderated, many of them by the BIOSCI staff!  This, for example,
made a major difference last year in the quality of content in our
EMPLOYMENT/bionet.jobs.offered newsgroup which many commercial
concerns and recruiting firms are using **without charge** to recruit
candidates for positions in the biological sciences.

We are also now in a position to have sponsors for individual
newsgroups as you will have noticed if you have visited
http://www.bio.net/ and clicked on "Access the BIOSCI/bionet
newsgroups" recently.

So, how can you help??
----------------------

As noted above it can take a lot of time to contact potential sponsors
if I have to do it all myself.  Our request is quite simple.  You can
do two important things which will take very little time for you
individually.  

First, please use our WWW system at http://www.bio.net/ to access the
archives.  You can now post or reply to messages via your Web browser.
Your usage helps attract sponsors.  If you contact any of our
sponsors, please be sure to thank them for supporting BIOSCI.  It is
critical for them to get this feedback if they are to continue their
sponsorship for the long term.

Second, if you work for a company or organization that provides
products or services of interest to the biology community, please pass
this message on to your marketing or marketing communications
department or other appropriate group.  Please ask them to help
support BIOSCI by sponsoring our Web site and explain the uses and
benefits of the system to the biology community.  If they are
interested, they can then contact us for further information at our
tech support address, biosci-help@net.bio.net.

Our hope is to quickly raise several large corporate/institutional
sponsors on our heavily-used WWW locations (some stats appended
below), and then end this sponsorship campaign so that our resources
can continue to be used for service provision, not fundraising.  Many
of our specialty newsgroup WWW archives are still used by small
communities of scientists (and they haven't been heavily promoted
yet).  While these may be valuable niche markets to some advertisers,
it will generate more labor and overhead having to find these
sponsors, fairly price the locations, and deal with lots of smaller
sponsorships than fewer mid-to large sponsors.  We are striving to
keep our operation as lean and efficient as possible since we are not
trying to make careers out of running BIOSCI.  We are trying if at all
possible to avoid the administrative overhead entailed with processing
lots of small payments to reach our fundraising goals.

I'd like to thank all of you for your help in advance. In helping us,
you are also helping yourselves, not only in keeping this resource
available for all of the both large and small research communities
that we serve, but also by alleviating the need for us to go back and
compete with researchers for tight grant dollars!  We promised NSF
when we were awarded the BIOSCI grant that we would carry out this
mission to make the service self-supporting.  With your help, we will
succeed in continuing BIOSCI's work into its second decade.  Thank you
very much!

				Sincerely,

				Dave Kristofferson
				BIOSCI/bionet Manager

				biosci-help@net.bio.net


A list of our prime WWW sponsorship locations follow.  Statistics are
for the four week period from 22 Jan. - 18 Feb. 1996 and usage
continues to grow.
----------------------------------------------------------------------

The overall BIOSCI WWW pages are currently visited by users from close
to 5000 unique computer hosts per week.  Web servers only log the
Internet computer/host name and frequently more than one individual
can connect to us from a particular host.

Main home page, http://www.bio.net, visited recently by about 2100
unique hosts per week

Main Newsgroups archives page, http://www.bio.net/archives.html,
visited recently by about 1200 Unique hosts per week

BIO-JOURNALS archive page, http://www.bio.net/BIO-JOURNALS.html,
visited recently by about 1000 unique hosts per week.

EMPLOYMENT archive pages: http://www.bio.net:80/hypermail/EMPLOYMENT/ 
and monthly header pages, visited recently by about 600 unique hosts
per week.

Address database search page, http://www.bio.net/addrsearch.html,
visited recently by about 450 unique hosts per week.

Methods newsgroup archive pages, http://www.bio.net:80/hypermail/METHDS-
REAGNTS/ and monthly header pages, visited recently by about 350
unique hosts per week.
----------------------------------------------------------------------

From owner-chromosomes@net.bio.net Wed Mar 27 22:00:00 1996
Path: biosci!MAIL.MED.UPENN.EDU!dnaseq
From: dnaseq@MAIL.MED.UPENN.EDU (Vahe Bedian)
Newsgroups: bionet.genome.chromosomes
Subject: Position at Penn
Date: 28 Mar 1996 07:55:07 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 37
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <v01530505ad806669054a@[130.91.204.127]>
NNTP-Posting-Host: net.bio.net

University of Pennsylvania              Department of Genetics

                        DNA Sequencing Facility

                455 CRB, Philadelphia, PA 19104-6145

Phone: 573-7407    Fax: 573-9327      E-mail:dnaseq@mail.med.upenn.edu
--------------------------------------------------------------------
Position Available:  Research Specialist I or II

The facility has two ABI 373 Stretch Automated Sequencers, one ABI 377
Automated Sequencer,  and one ABI 394 Oligonucleotide Synthesizer.  It
provides template preparation, DNA sequencing, primer walking, GeneScan
(fragment sizing), oligonucleotide synthesis, sequence assembly and
analysis, and other molecular biological services.  Applicants should have
a B.S. in a biological field or equivalent; 1-2 years experience also
required for Research Specialist I level, 2-3 years of experience for the
Research Specialist II level.  Previous experience in DNA sequencing,
molecular biology, and computers desirable.

Duties include:

Prepare templates and samples for automated sequencing
Pour  & run DNA sequencing and GeneScan gels
Operate ABI 373 and 377 sequencers with Sequencing and GeneScan software
Synthesize oligonucleotides on the ABI 394 synthesizer
Manage large sequencing projects
Provide technical support and consultation to facility users
Perform sequence analysis and computerized searches


If interested send resume' to Dr. Vahe Bedian at the above address
or fax resume' to 215-573-9327

 Call 215-573-7407 or e-mail dnaseq@mail.med.upenn.edu for inquiries



From owner-chromosomes@net.bio.net Thu Mar 28 22:00:00 1996
Path: biosci!rutgers!gatech!swrinde!newsfeed.internetmci.com!news.dacom.co.kr!nntp.coast.net!fu-berlin.de!rag2.rz-berlin.mpg.DE!leser
From: Ulf Leser <leser@mpimg-berlin-dahlem.mpg.de>
Newsgroups: bionet.genome.chromosomes
Subject: An X chromosome YAC map
Date: Fri, 29 Mar 1996 18:31:54 +0100
Organization: MPI: "Molekulare Genetik", Berlin, Dahlem
Lines: 51
Message-ID: <315C1E8A.2781@mpimg-berlin-dahlem.mpg.de>
NNTP-Posting-Host: rag2.rz-berlin.mpg.de (141.14.130.102)
Mime-Version: 1.0
Content-Type: text/plain; charset=us-ascii
Content-Transfer-Encoding: 7bit
NNTP-Posting-User: leser
X-Access: 16 25 816
X-Mailer: Mozilla 2.0 (X11; I; OSF1 V3.0 alpha)

Max-Planck-Institut fuer Molekulare Genetik

                            ANNOUNCEMENT

                      An X chromosome YAC map
                       -  IXDB release 1.0  -


The X chromosome YAC map constructed at the ICRF Genome Analysis lab
(London) and later at the Max-Planck-Institut fr Molekulare Genetik
(Berlin) is now available. Approximately 125 Mb are covered (80 %) in 25
contigs, and include 906 YAC clones.  The data is stored and graphically
displayed in an acedb database (version 4.1) named IXDB release 1.0. To
facilitate the integration and comparison with other maps from the X
chromosome community, we have kept the same scale and banding pattern as
for the consensus map constructed at the last X chromosome workshop. 

To access the data, simply connect to
http://www.mpimg-berlin-dahlem.mpg.de/~xteam using a World Wide Web
browser.  Follow the instructions to first install the acedb program on
your local computer, and then download the X chromosome data from our
server. 
 
The database contains results from about 2000 hybridisations, 972 gel
fingerprints of Alu-PCR products and 172 FISH mapping experiments.  We
strongly encourage you to also download the X chromosome subset of the
Integrated Genome Database (IGD), fully compatible with our dataset.
This
will enable you to merge the experimental YAC mapping data with
information from GDB, OMIM, EMBL, RLDB, and other genome related
databases
in a single step. 


Dept. H. Lehrach
Max-Planck-Institut fuer Molekulare Genetik
Ihnestrasse 73
14195 Berlin
Germany



_____________________________________________________________________
Hugues Roest Crollius                           Tel: +49 30 8413 1612
Abt. Lehrach                                    FAX: +49 30 8413 1380
Max-Planck-Institut fuer Molekulare Genetik
Ihnestrasse 73
14195 Berlin
Germany
e-mail: roest@mpimg-berlin-dahlem.mpg.de
_____________________________________________________________________

From owner-chromosomes@net.bio.net Sun Mar 31 23:00:00 1996
Path: biosci!rutgers!gatech!newsfeed.internetmci.com!in2.uu.net!brighton.openmarket.com!decwrl!waikato!midland.co.nz!newsource.ihug.co.nz!usenet
From: anghara@ihug.co.nz (Alma Hromic)
Newsgroups: bionet.genome.chromosomes
Subject: long arm of fourth chromosome
Date: 1 Apr 1996 07:52:25 GMT
Organization: The Internet Group
Lines: 8
Message-ID: <4jo1vp$91u@newsource.ihug.co.nz>
Reply-To: anghara@ihug.co.nz
NNTP-Posting-Host: ppp183.ihug.co.nz
Mime-Version: 1.0
X-Newsreader: WinVN 0.99.4

Help!
I have a friend with a learning-impaired daughter who has just had a blood 
test and has been diagnosed as having the long arm of chromosome 4 deleted. 
Does anyone know anything about this deletion and what effect it might have on 
people? Any information gratefully received.

Alma


