From owner-ageing@net.bio.net Tue Nov 01 22:00:00 1994
Path: biosci!daresbury!not-for-mail
From: draye@gena.ucl.ac.be (Xavier DRAYE)
Newsgroups: bionet.molbio.ageing
Subject: Re: Extended ageing in Microchiroptera
Date: 2 Nov 1994 08:21:22 -0000
Lines: 31
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
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X-Sender: draye@sci1.sri.ucl.ac.be
Original-To: ageing@dl.ac.uk

Sydney SHALL wrote:

>RESPONSE
>Is there any reason to suppose that there is a correlation between body
>size and longevity?

In mammals, Sacher (1978) found a functional relation between longevity and
some anatomical and physiological dimensions (body size, body weight, brain
size, etc). As a noticable exception, Peromyscus leucopus lives 2.5 times
as long as Mus musculus, although both have similar body sizes.

Sacher G.A. Evolution of longevity and survival characteristics in mammals.
In: The genetics of ageing, Schneider E.L. (Ed), Plenum press, NY, 1978.
Sacher G.A. and Hart R.W. Longevity, aging and the comparative cellular and
molecular biology of the house mouse, Mus musculus, and the white-footed
mouse, Peromyscus leucopus. In: Genetic effects on aging, Harrison D.H.
(Ed), R. Liss, NY, 1977.




Xavier DRAYE
_______________________________________________________________________
Unite de Genetique                                  Tel: (32) 10 473671 
Universite catholique de Louvain                    Fax: (32) 10 473031
Croix du Sud 2/14
1348 Louvain-la-Neuve
Belgium                                    E-mail: draye@gena.ucl.ac.be
_______________________________________________________________________



From owner-ageing@net.bio.net Wed Nov 02 22:00:00 1994
Path: biosci!daresbury!bioftp.unibas.ch!citi2.fr!jussieu.fr!cea.fr!usenet
From: cisitm@albert.cad.cea.fr (Pierre Didierjean)
Newsgroups: bionet.molbio.ageing
Subject: *** Q: WHAT KIND OF PEOPLE ON THE NET ?
Date: 3 Nov 1994 16:17:01 GMT
Organization: SSII
Lines: 28
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Message-ID: <39b2dt$9pb@anemone.saclay.cea.fr>
NNTP-Posting-Host: nyassa.cad.cea.fr

I'd like to know what kind of people i find on the net.

Students, Commercials, Adminitrations, Scientifics or what ??

Is anybody knows that or have statistical results ?


What are YOU doing in life ?

I am a system administrator.


Thanks for the answers and sorry for my english .....



Bye


+-----------------------------------------------------------------------------+
|		Pierre DIDIERJEAN 					      |
|									      |
|		Administrateur Systeme UNIX				      |
|		Cisi, Aix-en-Provence 					      |
|		France							      |
+-----------------------------------------------------------------------------+
|	email : 	cisitm@albert.cad.cea.fr 			      |
+-----------------------------------------------------------------------------+

From owner-ageing@net.bio.net Wed Nov 02 22:00:00 1994
Path: biosci!galaxy.ucr.edu!library.ucla.edu!agate!dog.ee.lbl.gov!overload.lbl.gov!lll-winken.llnl.gov!uwm.edu!news.alpha.net!news.mathworks.com!europa.eng.gtefsd.com!howland.reston.ans.net!math.ohio-state.edu!magnus.acs.ohio-state.edu!csn!mehalek
From: mehalek@teal.csn.org (Stephen Mehalek)
Newsgroups: bionet.molbio.ageing,sci.life-extension
Subject: CR side meeting at the AAMBT2010 conference
Date: 3 Nov 1994 19:32:52 GMT
Organization: Colorado SuperNet, Inc.
Lines: 27
Message-ID: <39bdt4$lsg@burgundy.csn.net>
NNTP-Posting-Host: 199.117.27.22
Xref: biosci bionet.molbio.ageing:996 sci.life-extension:2597



I have been practicing Caloric Restriction (CR) for the last 4
years, and I will be attending the "2nd Annual Conference on Anti-Aging
Medicine & Biomedical Technology" in Las Vegas (Dec 4-6).  I think
this would be a good time to start the foundations of a CR Society.
I know of at least on other CR practioner who would like to hold a
small side meeting at the Conference dedicated to CR and forming a
CR society.  I suspect a number of other CR practioners, among them
Dr. Walford, will be attending.

If you are interested in meeting with other CR practioners at the
Conference or forming a CR Society, please send your email address
to mehalek@csn.org.  I will be the defacto coordinator for
scheduling the CR side meeting(s) at the Conference, I'll will query
all of you for the best initial time and place.

All email addresses will be kept confidential.


Stephen Mehalek




--
Stephen Mehalek     mehalek@csn.org

From owner-ageing@net.bio.net Thu Nov 03 22:00:00 1994
Path: biosci!URIACC.URI.EDU!DPEARL
From: DPEARL@URIACC.URI.EDU
Newsgroups: bionet.molbio.ageing
Subject: Re: *** Q: WHAT KIND OF PEOPLE ON THE NET ?
Date: 3 Nov 1994 16:30:22 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 5
Sender: daemon@net.bio.net
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To Pierre Didierjean, as to what kind of people are on the net:

On trouve ici toutes sortes de gens, Di'jean, j'en suis sur,
ici comme en Suisse sur.
                        Dan Pearlman

From owner-ageing@net.bio.net Thu Nov 03 22:00:00 1994
Path: biosci!rutgers!gatech!howland.reston.ans.net!news2.near.net!news.delphi.com!usenet
From: jarice@delphi.com
Newsgroups: bionet.molbio.ageing
Subject: Re: Extended ageing in Microchiroptera
Date: Thu, 3 Nov 94 20:01:17 -0500
Organization: Delphi (info@delphi.com email, 800-695-4005 voice)
Lines: 29
Message-ID: <py4VjHF.jarice@delphi.com>
References: <397i62$d8b@mserv1.dl.ac.uk>
NNTP-Posting-Host: bos1f.delphi.com
X-To: Xavier DRAYE <draye@gena.ucl.ac.be>

Xavier DRAYE <draye@gena.ucl.ac.be> writes:
 
>>RESPONSE
>>Is there any reason to suppose that there is a correlation between body
>>size and longevity?
>
>In mammals, Sacher (1978) found a functional relation between longevity and
>some anatomical and physiological dimensions (body size, body weight, brain
>size, etc). As a noticable exception, Peromyscus leucopus lives 2.5 times
>as long as Mus musculus, although both have similar body sizes.
 
The correlation between body size and maximum life span potential
(mlp) was studied in a paper entitled "Antioxidants and Aging", by
Richard G Cutler, Am J Clin Nutr 1991;53:373S-9S.
Quoting from the abstract, "...a positive correlation in the tissue
concentration of specific antioxidants with life span of mammals was
found. These antioxidants include superoxide dismutase, carotenoids,
vitamin E, and uric acid."
 
The paper included many graphs showing different mammals levels of
antioxidants vs life span. Most animals with low levels of antioxidants
were small animals. There were numerous exceptions to the proposed
correlation between body size and longeveity. Example: horses and cows
are larger than humans yet live less than half as long.
 
I think any observed trend toward larger body size leading to longer
life is secondary to plasma antioxidant level.
 
Jim Rice

From owner-ageing@net.bio.net Fri Nov 04 22:00:00 1994
Path: biosci!FREENET.COLUMBUS.OH.US!acaudy
From: acaudy@FREENET.COLUMBUS.OH.US (Amy Caudy)
Newsgroups: bionet.molbio.ageing
Subject: Free Radicals- where should I go?
Date: 5 Nov 1994 14:13:20 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 24
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <Pine.3.07.9411051746.A7568-b100000@acme>
NNTP-Posting-Host: net.bio.net

I am a high school student.  After a science fair project treating poultry
projects with NaClO to kill bacteria, I became very interested in free
radical reactions.  I developed an experiment where I tested the effect of
the xanthine-xanthine oxidase system on plasmid pBR322.  I sucessfully
(and unknowingly) duplicated M. Rozenberg-Arska et. al.'s work published
in the Journal of General Microbiology 131,3325-3330 -- in 1985 =(  
	I learned that I should have gone back more than 5 years in
my journal search (access to Biosis or Medline or any such thing is
difficult for me) but I still want to continue my work.  I have been
looking at the xanthine-xo system on viruses, but those protein coats are
tough stuff.  (It is still interesting, though, because of the immune
system implications.)  
	Anyway, I have considered purifying flavanoids from various foods
and using them in my DNA system to see how they affect the time-loss of
transformation curve. However, I know little about flavanoid metabolism in
the body.  Do they cross the nuclear membrane?  Is there any flavanoid
interaction with DNA?  Am I totally off base?  Also, how would I determine
appropriate flavanoid concentrations?  I realize that I would be examining
a mixture of compounds, but there has certainly been debate that Vitamin
A, C, and E are not the enterity of our dietary protectants.
	I would greatly appreciate any suggestions that anyone might have.
 Thank you very much.



From owner-ageing@net.bio.net Sat Nov 05 22:00:00 1994
Path: biosci!bloom-beacon.mit.edu!gatech!europa.eng.gtefsd.com!news.umbc.edu!haven.umd.edu!cville-srv.wam.umd.edu!theoblit
From: theoblit@wam.umd.edu (M.D. Lover)
Newsgroups: bionet.molbio.ageing
Subject: Re: Request: Information on Current Research
Date: 6 Nov 1994 03:55:30 GMT
Organization: University of Maryland College Park
Lines: 33
Message-ID: <39hk3i$2bh@cville-srv.wam.umd.edu>
References: <393jh0$ed4@quartz.ucs.ualberta.ca>
NNTP-Posting-Host: rac3.wam.umd.edu
X-Newsreader: TIN [version 1.2 PL0]

Alec Oskin (ooskin@gpu.srv.ualberta.ca) wrote:
: Does anyone have a list of labs currently working in this field (i.e. 
: telomerase characterization / function) and what, specifically these labs 
: are doing?  I would appreciate it if you could either post such a list 
: here or e-mail me directly.  Also, can anyone recommend any 
: reviews/current papers that would bring me "up to par" on the research 
: being done in this field.  

This is just a repost of what Suresh Rattan was nice enough to write:

>Sender: lpddist@mserv1.dl.ac.uk
>Once again there h ve been enquiries about some basic information about
>telomeres. For those of you who want to have a very general introduction
>to telomere research and progress, a well-written simple article by a 
>science-journalist Jean Marx is available in the journal SCIENCE, vol. 265,
>pp 1656, issue dated 16 September 1994, titled CHROMOSOME ENDS CATCH FIRE.
.. 
>Wish you a good reading.
..
>In the previous posting, I forgot to mention two more interesting
>write-ups on telomeres:
>1, by T.R. Cech in SCIENCE, vol. 266, pp 387, 21st October 1994 issue: giving
>enough background and discussing the publication of a paper in the same
>issue of SCIENCE, pp 404 reporting the discovery of the gene for
>telomerase RNA in the yeast.
>
>These two papers should bring any one up-to-date in telomere research.
>Wishing you good reading,
>Suresh Rattan/Aarhus/Denmark

Hope that helps.

--Jason Taylor

From owner-ageing@net.bio.net Sat Nov 05 22:00:00 1994
Path: biosci!bloom-beacon.mit.edu!senator-bedfellow.mit.edu!athena.mit.edu!naustria
From: naustria@athena.mit.edu (Nicanor R. Austriaco Jr.)
Newsgroups: bionet.molbio.ageing
Subject: lipofuscin
Date: 6 Nov 1994 19:50:47 GMT
Organization: Massachusetts Institute of Technology
Lines: 10
Distribution: world
Message-ID: <39jc2n$h89@senator-bedfellow.MIT.EDU>
NNTP-Posting-Host: m66-080-6.mit.edu
Keywords: lipofuscin, aging pigment

Hello,

	I have recently been reading a lot about lipofuscin - the ubiquitous
aging pigment which is found in many aging organisms.  What is the most up-to-date
info. on the content of this pigment and its source?  I heard somewhere that
a large fraction of the pigment was made up of a component of the mitochondrial
ATP synthase.  Is this correct?

	Nick Austriaco
	naustria@mit.edu

From owner-ageing@net.bio.net Sun Nov 06 22:00:00 1994
Path: biosci!REDVAX1.DGSCA.UNAM.MX!caviedes
From: caviedes@REDVAX1.DGSCA.UNAM.MX (Caviedes Contreras Francisco-EST)
Newsgroups: bionet.molbio.ageing
Subject: Hipertention and Krebs cicle
Date: 6 Nov 1994 16:54:31 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 5
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <Pine.SUN.3.90.941106184936.22591A-100000@redvax1.dgsca.unam.mx>
NNTP-Posting-Host: net.bio.net

	Hi
	Does anyone have information about Krebs cicle and hipertention?
	any information will be appreciated
	Best regards
	Francisco

From owner-ageing@net.bio.net Sun Nov 06 22:00:00 1994
Path: biosci!Oberon.HSC.Colorado.edu!BRUCKLIER-J
From: BRUCKLIER-J@Oberon.HSC.Colorado.edu ("John Brucklier")
Newsgroups: bionet.molbio.ageing
Subject: subscribe
Date: 7 Nov 1994 15:45:59 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 1
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <MAILQUEUE-101.941107164412.480@Oberon.HSC.Colorado.edu>
NNTP-Posting-Host: net.bio.net

subscribe ageing

From owner-ageing@net.bio.net Sun Nov 06 22:00:00 1994
Path: biosci!agate!howland.reston.ans.net!pipex!uunet!Germany.EU.net!news.dfn.de!news.belwue.de!zib-berlin.de!workm6!bzbkowal
From: bzbkowal@workm6.NoSubdomain.NoDomain (Axel Kowald)
Newsgroups: bionet.molbio.ageing
Subject: Re: Extended ageing in Microchiroptera
Date: 7 Nov 1994 11:29:19 GMT
Organization: Konrad-Zuse-Zentrum fuer Informationstechnik Berlin
Lines: 26
Distribution: world
Message-ID: <39l32f$hk1@newsserv.zib-berlin.de>
References: <9410260221.AA08400@possum.murdoch.edu.au>
NNTP-Posting-Host: workm6.zib-berlin.de

Well, back to the original question of Jim Cummins

In article <9410260221.AA08400@possum.murdoch.edu.au>, cummins@POSSUM.MURDOCH.EDU.AU (Dr Jim Cummins) writes:
|> A recent report in a local journal (Tideman, CR "Meat Markets and Chastity
|> Belts" Australian Natural History 1994 p 66-67) suggests that
|> Microchiropteran bats, with body masses equivalent to mice, can
|> nevertheless live more than 30 years.  
|>  
|> (1) Does anyone in this group know of active research on ageing in bats;
|> 
|> (2) Any ideas as to the possible mechanism(s)?
|> 


According to the 'Disposable Soma' theory of Tom Kirkwood, the optimal life-span
for a species has something to do with the environmental risk of the ecological
niche the species has occupied.

The safer the environment the higher the optimal life-span. According to this the
explanation would be: bats (and birds) have a lower environmental risk compared
to similar sized on the ground living mammals (they can fly). Therefore they have
evolved a longer lifespan. ... simple, isn't it ?


	Axel Kowald


From owner-ageing@net.bio.net Sun Nov 06 22:00:00 1994
Path: biosci!POSSUM.MURDOCH.EDU.AU!cummins
From: cummins@POSSUM.MURDOCH.EDU.AU (Dr Jim Cummins)
Newsgroups: bionet.molbio.ageing
Subject: Re: lipofuscin
Date: 6 Nov 1994 18:31:33 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 56
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <9411070235.AA28268@possum.murdoch.edu.au>
NNTP-Posting-Host: net.bio.net

Hi:

>        I have recently been reading a lot about lipofuscin - the ubiquitous
>aging pigment which is found in many aging organisms.  What is the most
>up-to-date
>info. on the content of this pigment and its source?  I heard somewhere that
>a large fraction of the pigment was made up of a component of the mitochondrial
>ATP synthase.  Is this correct?

This is an intriguing suggestion but I haven't come across any
corroborating evidence. Do you have a reference to this? Lipofuscins are a
range of fluorescent lipopigments.  The following turned up in a Current
Contents search:-

VONZGLINICKI T (Reprint)
AU  - BRUNK UT
AD  - CHARITE BERLIN, INST PATHOL, SCHUMANNSTR 20-21, D-10117 BERLIN,
      GERMANY (Reprint).  UNIV LINKOPING, INST PATHOL, LINKOPING, SWEDEN
SO  - ZEITSCHRIFT FUR GERONTOLOGIE 1993 JUL-AUG;26(4):215-220
AB  - Oxygen-derived free radicals may result from various reactions, both
      intra- and extracellularly, but generation of oxygen free radicals
      from electrons escaping from the electron transport chain in
      mitochondria is by far the predominant process during the lifetime of
      a normal'', healthy cell.
      There is clear evidence that mitochondria are also an important
      target for oxygen-derived free radicals, and the resulting
      mitochondrial malfunction has long been suggested as the
      intracellular basis of aging. Moreover, there is clear evidence that
      free radical-dependent reactions lead to lipofuscin formation and its
      accumulation in Lysomes of post-mitotic cells. Lipofuscin
      accumulation was demonstrated to be dependent on the probability of
      iron-catalyzed Fenton reactions.
      A hypothesis is presented which assumes free radical dependent
      reactions in mitochondria and lysosomes to be interdependent.
      Production of hydrogen peroxide in mitochondria and its subsequent
      diffusion in the cytoplasm, and Fenton reactions in lysosomes,
      transferring hydrogen peroxide intralysosomally to the highly
      cytotoxic hydroxyl radical, are thought to be necessary intermediary
      steps in the generation of mitochondrial damage. On the other hand,
      damage to mitochondria increases both mitochondrial output of
      hydrogen peroxide and lipofuscin accumulation.

Yours, virtually:-

Jim "Spermatology rules o~ o~ o~ o~" Cummins

Associate Professor in Veterinary Anatomy
Murdoch University,
Murdoch Western Australia 6150
Tel +61-9-360 2668
Fax +61-9-310 4144
E mail cummins@possum.murdoch.edu.au





From owner-ageing@net.bio.net Sun Nov 06 22:00:00 1994
Path: biosci!Oberon.HSC.Colorado.edu!BRUCKLIER-J
From: BRUCKLIER-J@Oberon.HSC.Colorado.edu ("John Brucklier")
Newsgroups: bionet.molbio.ageing
Subject: subscribe
Date: 7 Nov 1994 15:54:08 -0800
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subscribe

From owner-ageing@net.bio.net Wed Nov 09 22:00:00 1994
Path: biosci!bloom-beacon.mit.edu!spool.mu.edu!howland.reston.ans.net!pipex!uunet!Germany.EU.net!netmbx.de!zrz.TU-Berlin.DE!math.fu-berlin.de!cs.tu-berlin.de!kaikuh
From: kaikuh@cs.tu-berlin.de (Kai)
Newsgroups: bionet.molbio.ageing
Subject: Genetic Engineering
Date: 10 Nov 1994 11:15:39 GMT
Organization: Technical University of Berlin, Germany
Lines: 26
Message-ID: <39svcr$ee2@news.cs.tu-berlin.de>
NNTP-Posting-Host: manelaq.cs.tu-berlin.de
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Content-Type: text/plain; charset=iso-8859-1
Content-Transfer-Encoding: 8bit
Summary: Genetic Engineering
Keywords: Genetic Engineering

Hello out there,
================

I don't know if this is the right group to post but I have the following
problem:
a friend of mine will have to read a report on genetic engineering in a few
weeks. Unfortunately she does not have access to the Internet; thus she
asked me to post some questions here because she has to mention something
about the United States.
She would like to know something of the party platform both of the democrats
and of the republicans, concerning genetic engineering and its laws in the
USA.
Furthermore she would appreciate it to get some statements of the economy/
business/trade and industry.
It would be great if anyone was able to send me some articles, drafts etc.
or just some information where we can find something like that (e-mail
preferred).

Thank you very much in advance,
                               Kai

-- 
                                    ,,,
                                   (o o)
-------------------------------oOO--(_)--OOo-----------------------------
  Make it as easy as possible, but not easier!   kaikuh@cs.tu-berlin.de

From owner-ageing@net.bio.net Fri Nov 11 22:00:00 1994
Path: biosci!agate!howland.reston.ans.net!news.sprintlink.net!sunserver.insinc.net!cato.Direct.CA!hookup!nic.hookup.net!sgaran.hookup.net!login_name
From: login_name@hookup.net
Newsgroups: bionet.molbio.ageing
Subject: The WWW site for biological aging and the Museum of Natural History
Date: Sat, 12 Nov 1994 17:10:42 GMT
Organization: HookUp Communication Corporation, Waterloo, Ontario, CANADA
Lines: 56
Message-ID: <login_name.11.2EC4F711@hookup.net>
NNTP-Posting-Host: sgaran.hookup.net
Keywords: WWW, aging,  Museum of Natural History
X-Newsreader: Trumpet for Windows [Version 1.0 Rev A]

  I maintain the WWW site for aging and on November the 9th I
recieved an E-Mail from the Museum of Natural History in New York City.
The Museum plans to include the information about the site in an
upcoming news letter. I would like to ask the people who are 
doing research in the field of biological aging if they would like
to include there lab on the WWW site. People who look at the 
site will be able to see where the lab is, what type of research is 
being done, who the members of the lab are,  etc.
  A copy of the E-Mail is provided below:


Return-Path: dan@www.itp.tsoa.nyu.edu
Date: Wed, 9 Nov 94 22:35:35 -0500
From: dan <dan@www.itp.tsoa.nyu.edu>
Sender: windeatr@www.itp.tsoa.nyu.edu
To: sgaran@hookup.net
Subject: http://www.hookup.net/mall/aging/agesit59.html
X-Url: http://www.hookup.net/mall/aging/agesit59.html

I saw yr page after starting research for
a project i am doing with the Museum of
Natural History in NYC. I am the Managing
Editor of the Electronic Newspaper at the museum.
Our next issue(january) will have a feature
piece on Aging. The Newspaper is available
via kiosk in the Hall of Human Biology and
evolution. I just wanted to make contact at
this early stage to see if you might wish
to participate in some way...

Thanks and please feel free to email me.
dan



                        END OF LETTER
________________________________________


If you have not seen our WWW site as yet please feel 
free to use it, the address is:

http://www.hookup.net/mall/aging/agesit59.html



Please send any details about your lab to Steven A. Garan,
my E-Mail address is        sgaran@hookup.net


Best Regards




  

From owner-ageing@net.bio.net Sun Nov 13 22:00:00 1994
Path: biosci!bloom-beacon.mit.edu!gatech!swrinde!pipex!sunsite.doc.ic.ac.uk!dundee.ac.uk!NewsWatcher
From: k.c.breen@dundee.ac.uk
Newsgroups: bionet.molbio.ageing
Subject: Lectureship
Followup-To: bionet.molbio.ageing
Date: 12 Nov 1994 12:13:26 GMT
Organization: University of Dundee
Lines: 27
Distribution: world
Message-ID: <3a2bh6$fnp@dux.dundee.ac.uk>
NNTP-Posting-Host: 134.36.198.60


Fixed-Term Lectureship in Pharmacology

Applications are invited for a Lectureship in Pharmacology at the
University of Dundee, Scotland, tenable from 1st January 1995. The
appointment will be made on a fixed-term basis for a period of three years.

The candidate will join a Department with a strong interest in Neuroscience
and will be expected to undertake an vigorous independent programme of
research. Applicants with an interest in the molecular basis of
neurodegeneration or glycobiology are particularly invited to apply. The
successful candidate will be encouraged to interact with a dynamic research
group with interests in these fields. The appointee will also be expected
to undertake general teaching duties for students of science and
pre-clinical medical students.  

Salary will be commensurate with experience and will be on the lecturer A
scale (£14,756-£19326).

Informal enquiries should be addressed to Dr. Kieran Breen at
+44-1382-633900 ext. 2522 (E-mail: k.c.breen@dundee.ac.uk).

CV (3 copies) together with the names and addresses of 3 referees should be
sent to Personnel Services, The University, Dundee DD1 4HN, Scotland, U.K.
quoting ref: est/16/45. 

The university is an Equal Opportunities Employer.

From owner-ageing@net.bio.net Sun Nov 13 22:00:00 1994
Path: biosci!bloom-beacon.mit.edu!spool.mu.edu!howland.reston.ans.net!pipex!sunsite.doc.ic.ac.uk!daresbury!not-for-mail
From: geriatri@c220.unimo.it (Alessandro  Pirani)
Newsgroups: bionet.molbio.ageing
Subject: Subscribe
Date: 14 Nov 1994 11:16:23 -0000
Lines: 1
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
Message-ID: <3a7gu7$12e@mserv1.dl.ac.uk>
Original-To: ageing@dl.ac.uk

Subscribe ageing@daresbury.ac.uk Prof. Salvioli

From owner-ageing@net.bio.net Mon Nov 14 22:00:00 1994
Path: biosci!bloom-beacon.mit.edu!spool.mu.edu!howland.reston.ans.net!gatech!udel!news.sprintlink.net!pipex!sunsite.doc.ic.ac.uk!daresbury!not-for-mail
From: Graham Pawelec <olxpa01@mailserv.zdv.uni-tuebingen.de>
Newsgroups: bionet.molbio.ageing
Subject: Meeting: Molecular bases of immunosenescence
Date: 15 Nov 1994 12:25:23 -0000
Lines: 42
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
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Original-To: "bionet discussion group imm. & ageing" <ageing@dl.ac.uk>, immuno@dl.ac.uk

FIRST ANNOUNCEMENT

The second EUCAMBIS International Meeting on the Molecular Biology of 
Immunosenescence will take place at the Max-Planck Institutes Campus in 
Tuebingen, Southern Germany, from 30.3. - 2.4.1995.

EUCAMBIS (European Union Concerted Action on the Molecular Biology of 
Immunosenescence) consists of a small group of cellular 
immunogerontologists and molecular biologists interested in the ageing of 
T cells and NK cells in the human system (see previous posting to the 
newsgroup). 

The EUCAMBIS core participants will speak during the plenary session of 
the meeting. They are:

Carlo Bartoloni, Rome
Kurt Schaudt, Tuebingen
Gerard Ligthart, Leiden
Erminia Mariani, Bologne
Chris Paraskeva, Bristol
Graham Pawelec, Tuebingen
Sydney Shall, Brighton
Rafael Solana, Cordoba
Malcolm Taylor, Manchester
Vincenzo Sorrentino, Milan

In addition, a number of other invited speakers will be present, and free 
communications from those interested in participating are welcome 
(abstract deadline 15th February 1995). Total number of participants will 
be limited to ca. 50.

Further details on the development of this program are available on 
request by E-mail at
                          pawelec@mailserv.zdv.uni-tuebingen.de
or after 1.1.1995 at      graham.pawelec@uni-tuebingen.de


We hope to see some of you in the attractive old University City of Tuebingen
for this meeting in the Spring!


Graham Pawelec, Coordinator, EUCAMBIS

From owner-ageing@net.bio.net Fri Nov 18 22:00:00 1994
Path: biosci!agate!spool.mu.edu!uwm.edu!msuinfo!netnews.upenn.edu!netnews.CC.Lehigh.EDU!ns1.CC.Lehigh.EDU!not-for-mail
From: x011@ns1.CC.Lehigh.EDU
Newsgroups: bionet.molbio.ageing
Subject: Gold and aging?
Date: 19 Nov 1994 13:57:09 -0500
Organization: Lehigh University
Lines: 5
Message-ID: <3alhq5$1hmb@ns1.CC.Lehigh.EDU>
NNTP-Posting-Host: ns1.cc.lehigh.edu

A lot of my relatives live in Ruby, South Carolina.  Gold is currently
being striped mined.  Most of the people are given the comment don't
you ever age?  Could gold be a reason for their long life.

Ron Blue

From owner-ageing@net.bio.net Sun Nov 20 22:00:00 1994
Path: biosci!agate!howland.reston.ans.net!spool.mu.edu!caen!msuinfo!harbinger.cc.monash.edu.au!news.uwa.edu.au!newsman.csu.murdoch.edu.au!Jim.Cummins
From: cummins@possum.murdoch.edu.au (Jim Cummins)
Newsgroups: bionet.molbio.ageing
Subject: mt DNA inheritance
Date: 21 Nov 1994 06:24:43 GMT
Organization: Murdoch University, Western Australia
Lines: 27
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Xdisclaimer: No attempt was made to authenticate the sender's name.

According to Hurst (Proc R Soc B 128: 135-140, 1992) uniparental
inheritance of mitochondrial DNA has evolved as a means of avoiding
potentially lethal intragenomic conflict.  Another possibility is the
limitation of mtDNA mutations.  
In human females, there's an estimated 24 cell divisions between zygote
and egg, whereas for males the number of precursor cell divisions is
around 36 for sperm produced at puberty, increasing at a constant rate
of 23 per year.  
Thus the sperm produced by a 45-year old man have been through c. 770
cell divisions, with a concomitant increase in the rate of mutations. 
This undoubtedly underlies the well-known disproportionate
contributions of male parents to mutations (first pointed out by
Haldane: Ann Eugen 13: 262-271, 1947).  
As the mitochondrial DNA mutates c 10x faster than nuclear DNA, the
effect is likely to be even more disproportionate. As the average
nuclear DNA mutation causes about 2% reduction in fitness, it seems
that the effects of any paternal mitochondrial DNA inheritance would be
rapid and lethal. Of course, this argument can't apply to those
organisms (eg Sequoia) where paternal inheritance of mtDNA is the rule.
However, in these cases there may be different patterns of mitotic
proliferation leading up to meiosis.  Anyone know?

Jim "I refuse to have a signature" Cummins                   
School of Veterinary Studies
Murdoch University
Western Australia 6150  Tel +61-9-360 2668 Fax +61-9-310 4144
E-mail cummins@possum.murdoch.edu.au

From owner-ageing@net.bio.net Mon Nov 21 22:00:00 1994
Path: biosci!bloom-beacon.mit.edu!gatech!howland.reston.ans.net!EU.net!uunet!zib-berlin.de!fauern!news.th-darmstadt.de!news
From: dh7y@.pop.th-darmstadt.de (Inst. f. Biochemistry)
Newsgroups: bionet.molbio.ageing
Subject: Apoptosis vio flow-cytometry??
Date: 22 Nov 1994 15:19:16 GMT
Organization: TH Darmstadt
Lines: 18
Message-ID: <3at25k$148g@rs18.hrz.th-darmstadt.de>
NNTP-Posting-Host: bc3.bc.chemie.th-darmstadt.de
X-Newsreader: WinVN 0.90.6

Hello world!

In the moment I´m working on the exciting field of apoptosis.
I´m trying to detect a small amount of apoptotic cells and I 
can use a flow cytometer. I tried some techniques to detect
the apoptotic cells as mentioned in several papers (ethanol fixation
and DAPI-staining afterwards) but I still wasn´t succesful to detect the
apoptotic cells. Is there anybody working on a similar problem and is able
to give me some useful hints or another good method?
I think of another method as well, the DNA end labeling. Are there some good
hints as well or can I use the protocols descirpted in papers by Gavrieli
(Journal of Cell Biol.) or Gorczyca (Cytometry) or Hotz (Cytometry).

I thank everybody for useful hints because in the moment I´m a little bit 
frustrated.

Gangolf Schrimpf
e-mail: dh7y@pop.th-darmstadt.de

From owner-ageing@net.bio.net Tue Nov 22 22:00:00 1994
Path: biosci!bloom-beacon.mit.edu!gatech!howland.reston.ans.net!vixen.cso.uiuc.edu!uchinews!apollo!jerikse
From: jerikse@news.luc.edu (Jason L. Eriksen)
Newsgroups: bionet.molbio.ageing
Subject: Re: Gold and aging?
Date: 22 Nov 1994 18:56:13 GMT
Organization: Loyola University of Chicago
Lines: 7
Message-ID: <3atesd$p39@apollo.it.luc.edu>
References: <3alhq5$1hmb@ns1.CC.Lehigh.EDU>
NNTP-Posting-Host: bsd.meddean.luc.edu
X-Newsreader: TIN [version 1.2 PL2]

x011@ns1.CC.Lehigh.EDU wrote:
: A lot of my relatives live in Ruby, South Carolina.  Gold is currently
: being striped mined.  Most of the people are given the comment don't
: you ever age?  Could gold be a reason for their long life.

Uh, don't think so.


From owner-ageing@net.bio.net Wed Nov 23 22:00:00 1994
Path: biosci!sjubiol.stjohns.edu!rick
From: rick@sjubiol.stjohns.edu (Richard Lockshin)
Newsgroups: bionet.molbio.ageing
Subject: Re:  Apoptosis vio flow-cytometry??
Date: 23 Nov 1994 20:40:49 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 8
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For end labeling, try the Apoptag kit (Oncor).  Although it has some ability
to pick up DNA repair, it generally is pretty good for in situ end labeling.
For chemical end labeling, see paper by Zakeri....Lockshin in FASEB J,
1993 and references cited therein.
Richard A. Lockshin Dept. Biol. Sci. St. John's U. 8000 Utopia Pkwy

Jamaica NY 11439 USA/Phone 718: 990-1854/ Fax 718: 380-8543


From owner-ageing@net.bio.net Thu Nov 24 22:00:00 1994
Path: biosci!agate!howland.reston.ans.net!news.sprintlink.net!malgudi.oar.net!mercury.wright.edu!desire!s006sef
From: s006sef@desire.wright.edu
Newsgroups: bionet.molbio.ageing
Subject: ha just playin with ya
Message-ID: <1994Nov24.235616.28593@desire>
Date: 24 Nov 94 23:56:16 EST
Organization:  Wright State University 
Lines: 12

hello i am a fool just trying this information highway stuff out


cool dudes jammin'

ok cold out see ya now


peace




From owner-ageing@net.bio.net Fri Nov 25 22:00:00 1994
Newsgroups: bionet.molbio.ageing
Path: biosci!bloom-beacon.mit.edu!gatech!swrinde!sgiblab!sgigate.sgi.com!enews.sgi.com!decwrl!tribune.usask.ca!quartz.ucs.ualberta.ca!mercury.arc.ab.ca!skyler.arc.ab.ca!morgan
From: morgan@skyler.arc.ab.ca
Subject: Current odds of Immortality by 2050 at 30 to 49%
Message-ID: <785806366.173571@skyler.arc.ab.ca>
Sender: news@arc.ab.ca (USENET News System)
Nntp-Posting-Host: skyler.arc.ab.ca
Organization: Alberta Research Council
Date: Fri, 25 Nov 1994 23:32:46 GMT
Lines: 43

The full description of this claim is as follows:

The death rate (per hundred thousand persons) will drop by 90%, relative to 1994, in any year through 2050. The measurement population is people in the United States, who are at least one year old. Persons in suspended animation (or cryonic suspension, reduced metabolism, etc.), if they are expected to remain suspended for a month or more, count as dead while suspended; they are omitted from the calculation after the year of "death".

This claim will be judged 12/31/2053.

The odds shown in the subject line are the consensus of participants in an
Idea Futures market (the two prices are the buy and sell prices for 'funny
money' bets).  You can learn more about this market by pointing your world
wide web browser to

     http://skyler.arc.ab.ca/~morgan/IF/IF.shtml

To participate in the market, a web browser with forms support is mandatory
(e.g., Mosaic2alpha or later, Lynx).  Instructions for accessing the web
(including email and plain text browsers) are in the WWW FAQ, posted to
news.answers, and the various comp.infosystems.www groups.

The current odds for all questions on the market are as follows:

     $Cdn [misc] 25 - 87%  Cdn$ below $.65 US by June 95
     3SAT [sci]  35 - 40%  Good 3SAT Algorithm by 2020
     Am30 [misc] 20 - 40%  30 amends. to US Const by 2000
     CFsn [sci]   8 - 15%  Cold Fusion
     Canc [sci]  30 - 40%  Cancer Cured by 2010
     Cryo [sci]  15 - 19%  Cryonics Catches On by 2000
     Ferm [sci]   1 - 70%  Fermat's Last Theorem resolved
     Immo [sci]  30 - 49%  Immortality by 2050
     Moon [sci]  30 - 36%  Moonbase by 2025
     Neut [sci]  15 - 25%  Neutrino mass >0
     QueS [misc] 15 - 25%  Quebec separation
     SLvl [sci]  15 - 25%  1 m rise in Sea Level
     SSTO [sci]  25 - 30%  Single Stage to Orbit
     Stew [sci]  13 - 15%  Nanotech Stewart platform
     Terr [misc] 45 - 46%  Nuke capable Terrorists
     Time [sci]   5 - 15%  Time Travel
     Univ [sci]  14 - 30%  Eventual Collapse of Universe

Full descriptions and conditions of these claims are available at

     http://skyler.arc.ab.ca/~morgan/IF/claim.shtml

This message is automatically posted to this newsgroup on a quarterly basis

From owner-ageing@net.bio.net Mon Nov 28 22:00:00 1994
Newsgroups: bionet.molbio.ageing
Path: biosci!rutgers!gatech!swrinde!pipex!uunet!zib-berlin.de!news.th-darmstadt.de!terra.wiwi.uni-frankfurt.de!zeus.rbi.informatik.uni-frankfurt.de!news.dfn.de!scsing.switch.ch!swidir.switch.ch!news.unige.ch!NewsWatcher!user
From: lhuber@sc2a.unige.ch (Lukas A. Huber)
Subject: Re: Apoptosis vio flow-cytometry??
Message-ID: <lhuber-2911941756530001@129.194.51.207>
Sender: usenet@news.unige.ch
Organization: University of Geneva, Dept. Biochemistry
References: <3at25k$148g@rs18.hrz.th-darmstadt.de>
Date: Tue, 29 Nov 1994 16:56:53 GMT
Lines: 13

contact george Wick , University of Innsbruck Austria, tel
+43-512-507-3100, he is a leading expertz on that.
best
Lukas A. Huber

OFFICE:
Département de Biochimie      
Université de Genève, Sciences II   
30, quai Ernest-Ansermet            
1211 Genève 4                       
FAX:  +41 22 702 6464
PH:   +41 22 702 6467 (office), +41 22 702 6468 (lab) e-mail: 
LHUBER@sc2a.unige.ch

From owner-ageing@net.bio.net Wed Nov 30 22:00:00 1994
Newsgroups: bionet.molbio.ageing
Path: biosci!rutgers!gatech!howland.reston.ans.net!pipex!uknet!cix.compulink.co.uk!not-for-post
From: mrobert@cix.compulink.co.uk ("Maurice Robert")
Subject: Longevity genes?
Message-ID: <D04rMH.2xG@cix.compulink.co.uk>
Organization: Phase 1                       
Date: Thu, 1 Dec 1994 11:51:52 GMT
X-News-Software: Ameol
Lines: 9

It appears that longevity runs in some families just as the tendency to 
suffer the diseases that shorten life runs in others.  Do people who live 
long have healthier versions of the genes which, in others, increase the 
risk of vascular disease, cancer etc?  Or is there evidence that people 
that are still healthy in their 90's have a range of genes which equip 
them to live longer? 
Can anyone supply references of reviews on this? 

Lesley Newson

From owner-ageing@net.bio.net Wed Nov 30 22:00:00 1994
Path: biosci!rutgers!uwm.edu!vixen.cso.uiuc.edu!howland.reston.ans.net!pipex!uknet!daresbury!not-for-mail
From: <mbtm@lf3.cuni.cz 3>
Newsgroups: bionet.molbio.ageing
Subject: BIOTECHNOLOGY CONFERENCE - PRAGUE 1995
Date: 1 Dec 1994 10:20:38 -0000
Lines: 348
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
Message-ID: <3bk81m$hl9@mserv1.dl.ac.uk>
X-Mts: smtp
X-Char-Esc: 29
X-Charset: ASCII
Original-To: admin-l@albnydh2.bitnet, ageing@dl.ac.uk, clan@frmop11.bitnet,
 cocamed@utoronto.bitnet, health-L@irlearn.bitnet, lpn-l@brownvm.bitnet,
 mbtm@decsys.lf3.cuni.cz, medinf-l@dearn.bitnet, pharm@dmu.ac.uk,
 telemed@leon.nrcps.ariadne-T.gr, wmn-hlth@uwavm.bitnet

    +*************************************************************+
    *                                                             *
    *        M E D I C A L        B I O T E C H N O L O G Y       *
    *                                                             *
    *          T O W A R D S   T H E    M I L L E N I U M         *
    *                                                             *
    *                    WORLD CONFERENCE                         *
    *                                                             *
    *                         held                                *
    *                                                             *
    *       September 5-8, 1995  in Prague, Czech Republic        *
    *                                                             *
    *                                                             *
    *               *   1st Announcement   *                      *
    *                                                             *
    *      Plenary lectures    Papers     Short Papers            *
    *  Panel Discussions  Symposia  Demonstrations  Posters       *
    *                                                             *
    +*************************************************************+

                        ----------
                        INVITATION
                        ----------

World Conference Medical Biotechnology towards  the Millenium is an
international meeting,  organized  by  the  3rd  Medical Faculty of
Charles Universityin Prague, Biocon Ltd. and partially supported by 
governmental  and  non-governmental  organizations. This conference 
serves  as  a  multi-disciplinary  forum  for the  dissemination of 
information on  the  research,  development and applications on all 
topics related to medical biotechnology.

We invite you cordially to attend the Conference and submit proposals 
for papers,  panels and demonstrations/posters. All proposals will be
reviewed for inclusion to the conference program.

                ------------------
                Scientific Program
                ------------------

      The preliminary program outlines are as follows:

PLENARY LECTURES
----------------
  * impact of the modern biotechnology to medicine
  * research development and research tools
  * diseases of important socio-economic impact
  * overlapping of medical biotechnology with other fields of biotechnology

SYMPOSIA
--------
  * gene therapy
  * advanced informatics in medicine
  * new drugs and antibiotics
  * diagnostics
  * artificial organs
  * futuristic aspects (ageing, neurobiomedicine, cancer, AIDS, vaccines)

PANEL DISCUSSIONS
-----------------
   * link between fundamental research and medical applications
   * political and economic aspects of medical biotechnology
   * legal and social aspects of medical biotechnology

                   ------------------------
                   Date, Venue and Language
                   ------------------------

The Conference Medical Biotechnology toward the Millenium (MBTM) will
be held from 5-8 September 1995 at the Hotel Atrium, Prague, Czech Republic.
The official language of the Conference will be English.

            --------------------------
            Information for Presenters
            --------------------------

Details of presentation formats are given on the following pages.
The general principles applying to all are:

o  All communication will be with the principal presenters who are
   responsible for communicating with co-presenters of a particular session.
o  The conference will attempt to provide with all equipments needed for
   presenters.  However, where special equipment is needed, presenters may
   be asked to provide it on their own.
o  All presenters must pay the registration fee.

Proceedings
-----------
Accepted papers will be publishedin proceedings. In addition, selected papers may be
invited for publication in the topics-related Journals and/or in a book
to be published by a major international publisher.

Exhibition
----------
Exhibits  are  expected  to  be  an  integral  part of the conference.
The  exhibition  will  give  companies and  research institutions the
opportunity  to  present  their  activities, specific  know  how  and
biotechniology products associated with the issues of the Conference.
Companies or institutions interested are invited to complete and return
the Request for Information form below.

            ----------------------------------
            INTERNATIONAL CONFERENCE COMMITTEE
            ----------------------------------

  * Prof.C.Hoeschl,M.D., Chairman
    Dean of the 3rd Medical Faculty, Charles University, Czech Republic

  * Prof.F.T.de Dombal, University of Leeds, United Kingdom

  * Prof.L.Ernster, Stockholm University, Sweden

  * Prof.D.Loisance, Faculte de Medicine, Creteil, France

  * Dr.V.Lungagnani, ASSOBIOTEC, Italy

  * Prof.J.F.Martin, Universidad de Leon, Spain

  * Dr.P.Patel, University of Birmingham, United Kingdom

  * Prof.E.Skamene, McGill University, Canada

  * Doc.M.Jira, M.D., Charles University, Prague, Czech Republic

  * Dr.Weigl, Olomouc University, Czech Republic


                  -----------------
                  TECHNICAL PROGRAM
                  -----------------

The Technical Program includes a wide range of interesting and useful
activities designed to facilitate the exchange of ideas and information.
These include keynote and invited talks, full and short paper
presentations, demonstrations, poster sessions and panel discussions.

Papers (25 minutes)
-------------------
Papers present reports of significant work or integrative reviews in
research, development, and applications related to medical biotechnologies.

Submissions: Papers should include a cover page and an extended
abstract of at least 2500 words or should be submitted as full paper of not over
words (4-8 pages). The cover page should include the title of the paper
with names of each author, their affiliations, complete addresses, phone
numbers, and suggested conference topic area(s).  Papers may be submitted
in either hard copy (send 5 copies) or by FAX or in electronic form.
Electronic proposals are preferred and MUST BE pure ASCII
text.  Final versions of accepted papers must be submitted in photo-
reproducible form according to specifications available upon acceptance and
will have a length of 4-8 pages. Final papers also submitted as ASCII,
will also be published on a CD-ROM.

Each full paper will be presented in a 25-minute session. This includes 5
minutes for discussion.


Short Papers (15 minutes)
-------------------------
Short papers are brief, more condensed presentations and will be published
as 1 page in the conference proceedings volume.  Use above Full Paper
submission guidelines except submission length should be 2-6 pages.

Panels ( 1.5 hours)
-----------------------
A panel offers an opportunity for 3-5 people to present their views or
results on a common theme, issue, or question. Panels should cover timely
topics related to the conference areas of interest. Panel selection will be
based on the importance, originality, focus and timeliness of the topic;
expertise of proposed panelists; as well as the potential for informative
(and even controversial) discussion. Panels should have no more than 5
members, including the chair. A panel summary and position statements will
be included in the proceedings.

Submissions: Panel proposals should include:

- A brief position statement and qualifications of each panelist; no more
  than 1 page each.

A cover sheet should include the panel title, panelists' names and
affiliations, and the panel organizer's name, affiliation, address, e-mail
address, Fax and phone number. Electronic proposals are preferred and
must be in ASCII format.

Submit to:
----------
MBTM Secretariat, Minska 9, 101 00 Praha 10, Czech Republic
attn.Dr.Beata Lejtnarova
Phone:  +42-2-725469, +42-2-7248356
Fax:    +42-2-724417
E-mail: mbtm@LF3.cuni.cz

Demonstrations/Posters 
-------------------------------
Demonstration/Poster sessions enable researchers and non-commercial
developers to demonstrate and discuss their latest results and development
in progress in order to gain feedback and to establish contact with similar
projects. Demonstration/Poster sessions do not involve a formal
presentation but will be included in the proceedings.

Submissions: Demonstration/Poster proposals should include a 2-3 page
written description of the planned demonstration/poster and should
emphasize the problem; what was done, and why the work is important. The
proposal should make clear the advantages of presenting the material in the
form of a demonstration/poster rather than a paper. The cover page should
include the session title with presenter names, affiliations, complete
addresses, phone and FAX numbers of the principal presenter.
Electronic proposals are preferred and must be in ASCII format.


Submit to:
----------
MBTM Secretariat, Minska 9, 101 00 Praha 10, Czech Republic
attn.Dr.Beata Lejtnarova
Phone: +42-2-725469, +42-2-7248356
Fax:   +42-2-724417
E-mail: mbtm@LF3.cuni.cz

            ---------------------------------------------
             About Prague - the Capital of Czech Republic
            ---------------------------------------------

The Conference  will  be held  in  Prague, the capital of the Czech Republic
situated in the very heart of Europe.  Prague  is one of  the most beautiful
cities in the world,  it is  one of the biggest  administrative and economic
points in Central Europe. Prague  is also the  heart of  the most  important
political, cultural and scientific events going on in this area.

The " Golden city "  provides the visitors with innumerable opportunities to
enjoy their stay with all  the conveniences  they are looking for. There are
plenty of places of interest such as galleries, museums,historical buildings,
parks and gardens and also a wide choice of cultural events.

The City also offers fine restaurants and many shops of high quality. There
is a possibility to make  a day trip to the castles Karlstejn and Konopiste
and to see Prague's  surroundings and beautiful Czech countryside.

Prague  has  an  international  airport  and  is  connected  with almost all
the European countries. There are daily flights to and from most of European
capitals and other cities. There exist  rapid railway connections to Prague,
with a  typical  3  hour travel time from the borders of the Czech Republic.
By car it is possible to reach Prague by E12, E14 and E15 motorway routes.


               ------------------------------------------
               HOTEL ATRIUM - THE VENUE OF THE CONFERENCE
               ------------------------------------------

The hotel Atrium is a modern four star hotel located very close to the centre
of the City. It  can  offer to its visitors  nice reastaurants, bars, fitness
centre and other sport facilities including an inner swimming-pool.
English is used as the main communication language there.


For more information on Prague turn to:

MBTM Secretariat, Minska 9, 101 00 Prague 10, Czech Republic
attn.Dr.Beata Lejtnarova
Phone : +42-2-725469, +42-2-7248356
Fax :   +42-2-724417
E-mail: mbtm@LF3.cuni.cz


       

       +-----------------------------------------------------+
       |       Congress Deadlines (postmark dates)           |
       |                                                     |
       |   Submissions Due:              March 31, 1995      |
       |   Authors Notified:             May 15, 1995        |
       |   Pre-Registration Deadline:    June 30, 1995       |
       |   Post-registration Fee:        after June 30, 1995 |
       +-----------------------------------------------------+

                  -----------------
                  REGISTRATION FEES
                  -----------------
    The  registration  fee will be $ 600 before  July 1, 1995;  it will
include admission to all scientific sessions, the commercial exhibition,
copy of the final programme and  the  abstract book,  the Proceedings of
the Conference, work lunches, and welcome and farewell parties.

    Students will be eligible for a reduced rates at $ 450.

    After July 1,1995, the fees will be $ 680 (full registration) and $ 500
    (student registration).

    Limited  amount  of  fellowships will be available for participants from
technically-emerged countries of Central and Eastern Europe countries or NIS.
Application for the above mentioned fellowships must include:

    * C.V. of the applicant (incl. list of publications etc.)
    * references if applicable
    * estimated support requested (in US $)

The  applications  should  reach  the  Conference   Secretariat   before
January 31, 1995. The review Commitee will notify succesfull  applicants
before April 30, 1995. The required documents should be send in 5 copies,
Faxed, or e-mailed (in ASCII) to:

MBTM Conference Secretariat
attn. Dr. Beata Lejtnarova
Minska 9, 101 00 Praha 10
Phone: +42-2-725469, +42-2-7248356
Fax:   +42-2-724417
E-mail: mbtm@LF3.cuni.cz

-------------- x  ----------  Cut Here  ---------- x -------------------
                   -------------------
                   INFORMATION REQUEST
                   -------------------

To receive future Conference announcements, please complete this form
and return to the address below.

  Name: _________________________________________________________

  Address: ______________________________________________________

  _______________________________________________________________

  City/State/Code: ______________________________________________

  Country: ______________________________________________________

  Fax:  _________________________________________________________

  E-Mail: _______________________________________________________

Please send me:
 __  Conference registration form and further information
 __  Proceedings order
 __  Information for Exhibitor/Sponsor 
 --  Information calendar of 3rd MF of Charles University in Prague

Return to: MBTM Conference Secretariat
         Minska 9
         Praha 10, 101 00, Czech Republic
Fax: +42-2-724417
E-mail: mtbm@LF3.cuni.cz

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From owner-ageing@net.bio.net Wed Nov 30 22:00:00 1994
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From: magnesum@ix.netcom.com (Paul Mason)
Newsgroups: bionet.molbio.ageing
Subject: Breakthrough!   Now what do we do?
Date: 1 Dec 1994 03:34:50 GMT
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There has been a breakthrough in the correlation of cardiovascular death 
with magnesium deficiency.  Dr. C. Everett Koop, retired Surgeon General 
of the United States, writes, "A good case can be made for the 
correlation of cardiovascular death with magnesium deficient water."

Now what do we do?

Attached is a petition to the FDA for the voluntary fortification of 
beverages with magnesium.  It is a starting point, and other 
well-reasoned suggestions are welcome at this address.

Paul Mason
Researcher
USA (408) 897-3023

========================================================================
=======     October 3, 1994
     Dockets Management Branch                     DOCKET 94P-0361/CP1  
   Food and Drug Administration     Room 1-23     12420 Park Lawn Drive 
    Rockville, MD  20857
PAGE 21                                CITIZEN PETITION
     The undersigned submits this petition under the relevant statutory 
    sections of the Federal Food, Drug, and Cosmetic Act or the Public  
   Health Service Act, or under any other statutory provision for which 
    authority has been delegated to the Commissioner of Food and Drugs  
   under 21 CFR 5.10 to request the Commissioner of Food and Drugs to   
  make a public recommendation announced to the media.
                                ACTION REQUESTED
     I request that the Commissioner of Food and Drugs make the 
following     public announcement to the media:
     "A good case can be made for the correlation of cardiovascular 
death     with magnesium deficient water.  Numerous studies show that 
many     Americans get less than the Recommended Daily Intake of 
magnesium.  To     correct that deficiency, the FDA recommends that 
bottlers fortify     bottled or canned water and water-based beverages, 
including soft     drinks and beer, to provide at least 90 mg of 
bio-available magnesium     per liter of beverage.  The recommended 
additive is magnesium     carbonate because it has been more widely 
tested in practice than     other compounds.  Excluded beverages are 
naturally magnesium-rich     beverages which need no fortification, such 
as orange juice (110     mg/L), milk (140 mg/L), and grape juice (130 
mg/L).  Bottlers who wish     to fortify to more than 90 mg magnesium 
per liter of beverage are     cautioned to be aware that excessive 
magnesium may cause a laxative     effect in some individuals.  
Individuals having kidney failure are     advised to consult their 
doctor before consuming fortified beverages.
     Consumers are urged to use only magnesium-rich water in all cooking 
or     boiling of food, as magnesium is leached out of foods boiled in 
soft     water."                              STATEMENT OF GROUNDS
     1.  Mg deficiency is widespread in the United States         
(1,7,24,44,45,54,61,68,70,73,82,88,93)
     2.  Mg deficiency causes atherosclerosis, ischemic heart disease,  
       arrhythmias, and cardiovascular death.         
(5,7,9,20,25,51,78,79,80,81,82,85,87)
     3.  A global pattern exists which positively correlates 
cardiovascular         death with magnesium-deficient water supplies.   
      (8,9,10,11,13,18,19,20,57,58,66,74,75,76,85).
     4.  Supplementation has been shown by intervention or cohort 
studies         to be effective in lowering the rate of cardio-vascular 
death.         (69,85)         Mg intake predicted future IHD events 
(35).
     5.  Extensive data suggests that if the Ca/Mg ratio exceeds 2/1,   
      cardiovascular death is positively correlated with the rising PAGE 
22
         Ca/Mg ratio.    (45, also: Karpannen; Minerals, coronary heart 
        disease, and sudden coronary death.   Advances in Cardiology    
     25:9-24, 1978.
     6.  The NIH has recently recommended a calcium intake of 1500 mg 
per         day.  Studies show American Mg intake is 300 mg/day, which 
would         make an unprecedented ratio of Ca/Mg of 5/1, with the 
possibility         of a much increased rate of cardiovascular death.  
(expert: Dr.         Mildred Seelig).
     7.  Boiling food in soft water leaches out more magnesium than does 
        boiling of food in magnesium-rich water (40,50).
     8.  Mg in water is absorbed 30% better and much faster than Mg in  
       food.  (23,25,27,40,50)
     9.  Mg may be toxic to persons with kidney dysfunction, but at 
levels         above what is normally found in wine (110 mg/L Mg).  
METAL CONTENT         OF CALIFORNIA WINES ; OUGH, C. S., CROWELL, E. A., 
BENZ. J.; 1985,         JUNE
     Besides the references cited above, Dr. Burton Altura has informed 
me     that he will be submitting a written comment in support of this  
   petition within two weeks which will include additional citations of 
    the literature of magnesium.
                              ENVIRONMENTAL IMPACT
     I claim a categorical exclusion under paragraph 25.24 of 21 CFR.
                             UNFAVORABLE INFORMATION
     1.  Magnesium is commonly sold over-the-counter as a laxative.     
    Hearsay indicates that the bottled water from a spring in         
Bartlett, California, sometimes has a laxative effect due to its        
 360 mg/L magnesium content.  Bottled water from the Adobe Springs      
   in California contains 96 mg/L magnesium, and no laxative effect     
    has been reported to the bottler.  If assorted brands of foods and  
       beverages are voluntarily fortified with various amounts of      
   magnesium without guidelines, there is a strong chance of some       
  consumers experiencing a laxative effect while other consumers        
 remain deficient in magnesium.
     2.  Consumers having kidney failure may tolerate only mineral-free 
        water.
                                   OTHER VIEWS
     Dr. C. Everett Koop, retired Surgeon General of the United States, 
has     written me, "A good case can be made for the correlation of     
cardiovascular death with magnesium-deficient water."
PAGE 23
     Dr. Mildred Seelig has identified a new health hazard caused by a 
new     policy of the NIH which may vastly increase the number of 
cardiac     deaths in this country:
     To explain the problem, Dr. Seelig first quotes Karpannen's 
article,     "Minerals, Coronary Heart Disease, And Sudden Coronary 
Death"     published in ADVANCES IN CARDIOLOGY in 1978.  Abstract:  Loss 
of     myocardial K and Mg and increased myocardial Ca predispose to    
 ventricular arrhythmias and Sudden Coronary Death.  Reference to animal 
    studies and epidemiological studies.  Finland has highest Ca/Mg 
ratio     (4/1) and SCD rate.  Line graph showing direct correlation of 
rising     IHD with increasing Ca/Mg ratio.  USA is next with ratio of 
3/1.     Japan, Greece, and Yugoslavia have lowest IHD rate and lowest 
Ca/Mg     ratio.
               "As the Ca/Mg ratio rises, so does the heart             
  attack death rate.
               "Now that the NIH has recommended a Ca intake of         
      1500 mg/day, the ratio of Ca/Mg will be about 5/1               
since large scale surveys have shown that               Americans (on 
average) consume no more than 300 mg               Mg/day.
               "Providing Mg in water or soft drinks (especially        
       sports drinks--since surveys show that Mg is               likely 
to be deficient in athletes, and that this               may cause 
sub-optimal performance) may well be a               practical means to 
correct the Mg deficiency."
          It appears that the NIH's recommendation of a Ca intake of    
      1500 mg/day may increase substantially the cardiac death          
rate in this country because it destroys the proper Ca/Mg          
ratio.
          Dr. Burton Altura's view is:  "The mean value of about 0.60   
       mM for ionized Mg2+ is approximately one-half what it is for     
     Ca2+ and thus represents a Ca2+/Mg2+ ratio in human blood of       
   about 2.0.  This ratio may be of more than passing interest          
considering that Mg2+ acts as a natural Ca channel blocker          and 
that variability in either of their concentrations could          
influence the interpretation of the effects of the other on          
conduction, contraction, vasomotor tone, and numerous          functions 
of cells and tissues."
          ANOTHER VIEW:  Most companies selling bottled spring water    
      in America advertise their water's "purity",  and are loath       
   to admit that the lack of magnesium in their spring water is         
 a problem.  The bottled water industry has been hostile to          
foreign medical journal articles examining the correlation          
between cardiovascular death rates and the magnesium content          of 
tap water.  I have repeatedly brought the problem to the PAGE 24
          attention of senior officers of the International Bottled     
     Water Association, but they have expressed no interest          
whatever, and some IBWA members have been overtly hostile to          
the study of magnesium in water.  Over dinner at a meeting          of 
the California Bottled Water Association a couple years          ago I 
was told most emphatically that bread should be          fortified 
instead of beverages.
          The problem with the Mg-fortification of food is the dosage.  
        The most common foods are bread and salt, yet some people       
   eat almost no bread or salt and other people eat a lot.  To          
get a uniform Mg intake without resorting to pills, there          are 
only three possibilities:
               1.  Fortify all processed foods with "X"* Mg per         
          Kg of food.  (This method penalizes people who                
   don't eat processed foods, but maybe they                   don't 
need fortification as much, depending on                   which 
unprocessed foods they eat.   Processing                   often removes 
Mg.)
               2.  Fortify all processed foods/beverages with "X"       
            Mg per Kg of food/beverage.
               3.  Fortify beverages with "X" Mg per liter.
          *"X" = an adequate amount of Mg fortification to prevent      
    deficiency without triggering a laxative effect.
          Any other method than one of the three above will result in   
       uneven dosages, with the possibility of some consumers          
getting the runs and other consumers not getting enough Mg.          Of 
the three alternatives above, beverage-borne Mg is 30%          more 
bio-available, and the cheapest to implement, as there          are far 
fewer beverages than foods.   Undissolved magnesium          carbonate 
in foods might wear the enamel off teeth.
          Mr. John Albers, Chairman and CEO of the Dr. Pepper/Seven-Up  
        Cos., wrote me a letter that was friendly and open to the       
   possibility of fortifying beverages with magnesium,          
contingent on a favorable reaction from the FDA and other          
agencies.
          Discussions with isotonic bottlers have also been friendly.   
       I have supplied all interested parties with a copy of my         
 paper, "The Economics of Magnesium Fortification of          Beverages" 
(60).
          Dr. Arthur Marx at the California Environmental Health        
  Investigations Branch (510) 540-3657, has voiced his opinion          
to me that magnesium chloride, magnesium oxide, magnesium          
citrate, and many other magnesium compounds have not been PAGE 25
          tested on a large scale for possible unwanted effects.  It    
      is common knowledge that magnesium carbonate is natural in        
  nearly all ground waters, and magnesium carbonate is found          in 
some historic European bottled waters at concentrations          
yielding more than 90 mg/L magnesium content:
          Apollinaris             122 mg/L          Gerolsteiner        
    112 mg/L          St. Gero                120 mg/L          
Adelheidquelle          107 mg/L          Rosbacher               128 
mg/L
          (ref: The Best Bottled Waters In The World, by M & T Green,   
       1985).
          Natural magnesium carbonate in water has been so widely       
   tested in practice for so many centuries that there is          
negligible chance of any problem with it.
          To test the feasibility of fortifying with magnesium          
carbonate, I obtained a pound of USP grade magnesium          carbonate 
in light powder form, 4MgCO3 * Mg(OH)2 * 5H2O.  I          mixed .5 
teaspoon of it with one cup of distilled water, and          got these 
results:
               1.  One hour after adding Mg, there was no flavor,       
            but it did end the flatness of the distilled                
   water.  The water was clear.  I thought I                   detected 
some sweetness, but it was not as                   sweet as Adobe 
Springs.  It tasted OK to me,                   about the same as a good 
grade of tap water.
               2.  The mouth-feel was a little bit slippery,            
       which some people also notice in the Adobe                   
Springs' water.
               3.  I tested the TDS using a Myron L "DS" meter.         
          One hour after adding the Mg, the meter read                  
 110 ppm TDS, and the undissolved white residue                   lay in 
the bottom of the cup.  Three days                   later, the meter 
read 220 ppm TDS, and there                   was noticeably less 
residue in the bottom.                   The flavor was unchanged.  
After one week, the                   TDS levelled off at 350 ppm, with 
some residue                   still left in the bottom.  With a lesser 
                  amount of magnesium carbonate, dissolution is         
          complete.
          More views are contained in the 94 articles listed in the     
     Enclosures section of this petition.
 PAGE 26
                                  CERTIFICATION
          The Undersigned certifies, that, to the best knowledge and    
      belief of the Undersigned, this petition includes all          
information and views on which the petition relies, and that          it 
includes representative data and information known to the          
petitioner which are unfavorable to the petition.
          (Signature)_________________________________________________
          PAUL W. MASON          P O Box 1199          Livermore, Ca. 
94551          tel: (408) 897-3023          fax: (408) 897-3028
                            REFERENCES AND ENCLOSURES
          1.   Absorption and Excretion of Magnesium; Gastrointestinal  
             Absorption of Magnesium; Renal Excretion of Magnesium;     
          etc.: 1984.
          2.   Alfrey, A. C.; Miller, N. L.; Butkus,  D.: Evaluation    
           of body magnesium stores: The Journal of Laboratory and      
         Clinical Medicine: Aug., 1974.
          3.   Alpers, D.; Clouse, R.: Magnesium: Manual of             
  Nutritional Therapeutics: 1979?.
          4.   Altura, B. M.; Altura, B. T.: Cardiovascular risk        
       factors and magnesium: relationships to               
atherosclerosis, ischemic heart disease and               hypertension: 
Magnesium and Trace Elements: 1991-92;               10:182-192.
          5.   Altura, B. M.: Sudden-death ischemic heart disease and   
            dietary magnesium intake: is the target site coronary       
        vascular smooth muscle?: Medical Hypotheses: 

