DNA repair interest group: lectures via web/jobs/meetings

Charles Miller rellim at tulane.edu
Mon Dec 18 14:03:16 EST 2000


DNA Repair Interest Group -UPDATE - December 15, 2000

1.      VIDEOCONFERENCE -Tues, Dec 19, 2000 -Dr. Patrick Sung - University
of Texas Health Science Center at San Antonio - Functional Interactions
Among RAD52 Group Proteins in Recombination and Repair

2.      ANNOUNCEMENTS: BIORECRUIT website; HUMAN GENOME ON THE WEB; NEW
JOURNAL - MITOCHONDRION

3.      CONFERENCES - INTERNET PHOTOCHEMISTRY AND PHOTOBIOLOGY CONFERENCE;
GORDON RESEARCH CONFERENCE ON DNA REPAIR; DNA REPAIR CONF,
NOORDWIJKERHOUT, THE NETHERLANDS;  EMS ANNUAL MEETING; MIDWEST DNA REPAIR
MEETING; FASEB HELICASE MEETING

4.      XP SUPPORT GROUPS - UK and US

5.      POST DOC OPPORTUNITIES: Bethesda, MD; Sussex, UK; Bethesda, MD x2;
Smithville, TX; Bethesda; Seattle; Boston; Duarte, CA
6.      Electronic Contacts


1.0     DNA REPAIR VIDEOCONFERENCE:
        Tues, Dec 19, 2000 - 12:30 PM -Dr. Patrick Sung - University of
Texas Health Science Center at San Antonio - Functional Interactions Among
RAD52 Group Proteins in Recombination and Repair

VIDEOCONFERENCE LOCATIONS: MD Anderson, Smithville, TX (origin); Univ of
Kentucky, Lexington, KY; Building 45 (NATCHER) Room H, Bethesda, MD ; Room
1E03 GRC Baltimore, MD; Building 101 Room B200, NIEHS, Research Triangle
Park,  NC; Building 549, Conference Room A,  FCRDC, Frederick, MD; State
University of New York, Stony Brook, NY; ; Lawrence Livermore Labs,
Livermore, CA; Univ of Michigan, Ann Arbor; and Brookhaven National Labs,
Upton, NY. [WELCOME TO OUR 10TH SITE!]  MBONE ACCESS (NIH ONLY) and in the
internet at http://videocast.nih.gov

1.1     DNA REPAIR VIDEOCONFERENCE - FUTURE DATES AND VIDEO ARCHIVE
[Note: A larger and more up to date list of future and past
videoconferences can be found on the DNA Repair Interest Group web site:
http://www.nih.gov:80/sigs/dna-rep/ ]

1.1.1 FUTURE VIDEOCONFERENCES:
Tues, JAN 16, 2001- Dr. Mats Ljungman - Univ of Michigan, Ann Arbor, MI
-Stopped in its tracks - RNA polymerase II as a sensor for DNA damage
Tues, FEB 20, 2001 - Dr. Vilhelm Bohr - LMG, NIA, Baltimore, MD -  DNA
repair defects in premature aging disorders
Tues, Mar 20, 2001 - Short talks by post-doctoral fellows at 3 sites:
Peter Beernink, LLNL - A Second Divalent Metal Ion in the Active Site of a
New Crystal Form of Human Apurinic/Apyridinimic Endonuclease, Ape1, and
its Implications for the Catalytic Mechanism
Yong Hwan Jin, NIEHS - The 3'-5' Exonuclease of DNA Polymerase d is
Redundant with
5'-flap Endonuclease Rad27/Fen1 for Processing of Okazaki Fragments

Robert M. Brosh, NIA - Molecular Interactions of the Werner Syndrome
Protein

Tues, Apr 17, 2001 - Dr. Arthur Grollman -SUNY Stony Brook, NY -
Recognition of Oxidative damage by DNA Glycosylases

Tues, May 15, 2001- Dr. Bill Copeland - Laboratory of Molecular Genetics
NIEHS - Mitochondrial DNA Replication Fidelity and Mitochondrial Diseases

Tues, June 19, 2001 - Dr. James Cleaver -Univ of California, San
Francisco, CA - History of DNA Repair - Mending Human Genes

1.1.2 VIDEOARCHIVES: INTERNET ACCESS (WORLDWIDE):

Now 29 of these videoconferences have been archived and are available for
viewing at your leisure on the internet. You will need a web browser (with
a high speed link) and free Real Video software.  Setup details and access
are available at the NIH videocast website:  http://videocast.nih.gov. Go
to Unicast sessions; Past events; DNA Repair Interest Group Sessions.

Note: Technical improvements are made regularly on this site to increase
transmission speeds and ease of access. If you were not successful in
viewing these videos in the past it is worth trying again!
NOV 21, 2000 -Dr. Zhigang Wang - Univ of Kentucky -Translesion synthesis
by the UmuC family of DNA polymerase

OCT 17, 2000- Dr. Yoshihiro Matsumoto - Fox Chase Cancer Center,
Philadelphia, PA -Functions of PCNA in Base Excision Repair

SEPT 19, 2000 - Dr. Kenneth Kraemer, NCI, Bethesda, MD  -Clinical and
Molecular Features of Xeroderma Pigmentosum and Related Disorders of DNA
Repair

JUNE 20, 2000- Dr. Richard Setlow , Brookhaven National Lab- Reflections
on how I was led into and onto DNA Repair -  Host:  SUNY

MAY 16, 2000  Dr. Veronica Maher, Michigan State Univ - Role of DNA
Replication and Repair in Carcinogen-Induced Human Cell Mutagenesis  Host:
U of Michigan [Note: this talk will be posted after the data presented is
published]

APR 18, 2000 - Dr. Peter Glazer, Yale Univ - Targeted genome modification
via DNA triple helix formation

MAR 21, 2000 - Research reports by 3 Postdoctoral fellows:
Dr. Steffen Emmert, NCI - The xeroderma pigmentosum group C gene leads to
selective repair of cyclobutane pyrimidine dimers rather than 6-4
photoproducts. [See recent paper describing this work: Proc. Natl. Acad.
Sci. USA 97: 2151-2156, 2000]

Dr. Robert Sobol, NIEHS - Mutagenesis and dRP Lyase Activity in DNA
-Polymerase Dependent Base Excision Repair in Mouse Cells [See recent
paper by Dr. Sobol describing this work:  Nature 405, 807-810 (2000)]

Mr. Robert Levine, SUNY -Mutagenesis Induced by Endogenous DNA Adducts in
Human Cells

FEB 15, 2000  Dr Steve Matson, UNC - Two E. coli mismatch repair enzymes,
DNA helicase II and MutL, interact to catalyze efficient unwinding of
duplex DNA

JAN 18, 2000- Dr. John Essigman, MIT - Cellular responses to the DNA
damaging agent cisplatin

Through the miracle of vidotape we now have been able to post most of the
DNA Repair Interest Group videoconferences from 1998 and 1999 on the web
site.  These include talks by Drs. Bogenhagen, Sutherland, Kunkel,
Stefanini, Hanawalt, Matson, Sharan, Kashlev , Fornace, Anderson, Leadon,
Brooks, McKay, Drotschmann, Chu, Thompson, Woodgate,George, Liu and
Grossman

2. ANNOUNCEMENTS: BIORECRUIT website; HUMAN GENOME ON THE WEB; NEW JOURNAL
- MITOCHONDRION

2.1 Paul Heelis writes:
I would like to take this opportunity to inform you of a recently created
site at http://www.biorecruit.net

Biorecruit.net specialises in the biosciences area and already has links
from university bioscience departments from around the world.

I would like to offer you the chance to advertise as many postdoctoral,
fellowships and any other position that you feel appropriate completely
FREE of charge.

2.2     SPECIAL ANNOUNCEMENT - HUMAN GENOME ON THE WEB
Dr Francis Collins, head of the NHGRI writes:
        A few weeks ago, the international human genome sequencing
consortium described (in a letter published in the Sept. 1 issue of
Science and in a news brief published in the Aug. 31 issue of Nature) a
number of electronic sites where the public working draft version of the
human sequence can be found in its most useable forms. However, it is
clear from a number of recent interactions with investigators, that many
are still not aware of the accessibility of this important information. I
am writing to make sure that you are aware that the working draft sequence
is available and to ask your assistance in helping to make the
entirescientific community aware of this valuable resource, by
distributing the attached information describing three sites that display
the entire
working draft sequence and provide tools for its use.

The following links will take investigators directly to three different
(but complementary) assembled views of the human genome,together with
useful browsing tools that provide a wide variety ofannotations of the
sequence. These sites are updated very frequently,
indeed almost continually.

U. Calif. at Santa Cruz
http://genome.ucsc.edu/

National Center for Biotechnology Information (NCBI)
http://www.ncbi.nlm.nih.gov/genome/guide/
and click "Map Viewer"

European Bioinformatics Institute (EBI)
http://www.ensembl.org/

2.3 New journal: MITOCHONDRION
Dr. Keshav Singh <singhke at JHMI.EDU> writes:
Dear Colleague:
        I invite you to submit your research articles to a new journal
"Mitochondrion" dedicated to research on mitochondria. The scope of this
journal is broad, from reporting on the basic science of mitochondria in
all model systems to reporting on pathology and clinical aspects of
mitochondrial diseases. The journal welcomes articles for publication by
investigators working in diverse disciplines such as aging, cancer,
biophysics, biochemistry, cell biology, evolution, genetics, molecular
biology, neurobiology, pharmacology, plant biology, program cell death,
toxicology, and clinical aspects of mitochondrial diseases. Detailed
instructions to authors can be found either www.mitoresearch.org or
www.elsevier.com/locate/mito.


Please join us and make the "Mitochondrion" journal the best journal on
mitochondria devoted to mitochondria research.
Sincerely,
Keshav Singh
Editor-in-Chief
Mitochondrion

Johns Hopkins Oncology Center
Bunting-Blaustein Cancer Research Building
1650 Orleans Street, Room 143
Baltimore, MD 21231
TEL: 410-614-5128  Fax: 410-502-7234


3.    CONFERENCES - INTERNET PHOTOCHEMISTRY AND PHOTOBIOLOGY CONFERENCE;
GORDON RESEARCH CONFERENCE ON DNA REPAIR; DNA REPAIR CONF,
NOORDWIJKERHOUT, THE NETHERLANDS;  EMS ANNUAL MEETING; MIDWEST DNA REPAIR
MEETING; FASEB HELICASE MEETING

[Note: A larger and more up-to-date list of conferences can be found on
the DNA Repair Interest Group web site:
http://www.nih.gov:80/sigs/dna-rep/ ]

3.1 2001 GRC CONFERENCE ON DNA REPAIR - VENTURA, CA JAN 21-26, 2001
        The 2001 Gordon Research Conference on MAMMALIAN DNA REPAIR,
Chaired by Dr. Samuel Wilson of the National Institute of Environmental
Health Sciences, will be held January 21 - 26, 2001 at the Clarion Beach
Hotel in Ventura, California.

        As this conference has been oversubscribed in the past, applicants
are encouraged to apply soon; as it is possible that later applicants will
be turned away.

        The Gordon Research Conference Winter 2001 brochure will be mailed
in September.  If you wish to attend the conference you may apply on line
at our Web Site now <http://www.grc.uri.edu/>

3.2   DNA REPAIR: INTERPLAY WITH OTHER CELLULAR PROCESSES -
NOORDWIJKERHOUT, THE NETHERLANDS FEB 25 - MAR 2, 2001

The Concerted Action on "Genetic Disorders associated with defects in DNA
repair" (a project of the European Union) will be funding a workshop on
"DNA repair: interplay with other cellular processes" in Noordwijkerhout,
The Netherlands from February 25 to March 2, 2001. The participants will
be members from European laboratories that are part of the Concerted
Action, as well as scientists from outside the EU. The total number of
participants is limited to maximally 250. The Workshop can be regarded  as
the European counterpart of the UCLA and Gordon Conferences on DNA repair
in the U.S.A.

We invite applicants for a limited number of about 80 places. These places
will be distributed on the basis of abstracts submitted for poster
presentations. The deadline for the submission is November 15. The
Organising Committee hopes to inform applicants about acceptances in the
first half of December.

The format of the meeting is similar to that of previous DNA Repair
meetings in Noordwijkerhout (in 1996 and 1991 and before), i.e. plenary
talks in the mornings, posters with intensive discussion sessions in the
afternoons, and evenings. The last day will be mainly devoted to a special
Symposium in which we will focus on new technology that we anticipate to
be relevant for future research in DNA repair.

Extensive information about the Workshop including a preliminary
programme, costs etc. can be found at the conference website:
http://www.medgencentre.nl/Workshop2001/

To apply: fill in the electronic registration form at the website not
later than November 15, 2000.  Send us an abstract for your poster not
later than November 15, 2000 (by e-mail to the meeting secretary
ferro at lumc.nl ; see instructions at the website).

3.3      EMS ANNUAL MEETING - SAN DIEGO, MAR 16-21, 2001

The Environmental Mutagen Society annual meeting will be held on March
16-21, 2001 in San Diego, CA, at the Paradise Point Resort Hotel. The
entire meeting is organized and the complete program and all registration
details are available from David M. DeMarini, Ph.D. (See below for contact
information  for obtaining a PDF file of the6 page brochure).  We have 3
symposia on DNA repair, and we have Stephen J. Gould as our keynote
speaker.  Information is also available on the EMS website:
http://www.ems-us.org/

For more information contact:

David M. DeMarini, Ph.D.
Environmental Carcinogenesis Division (MD-68)
U.S. Environmental Protection Agency
Research Triangle Park, North Carolina 27711, USA
TEL 1-919-541-1510
FAX 1-919-541-0694
demarini.david at epa.gov

3.4     THIRD ANNUAL MIDWEST DNA REPAIR SYMPOSIUM: JUNE 2-3, 2001 INDIANA
UNIVERSITY SCHOOL OF MEDICINE, INDIANAPOLIS, IN
        Keynote speakers: Dr. Samuel H. Wilson, NIEHS, Dr. Stanton L.
Gerson, Case Western Reserve Univ.
        Contact information:
        Drs Mark Kelley and David A. Williams
        TEL: 317-274-2755;      FAX; 317-274-5378;
        e-mail:  mkelley at iupui.edu

3.5     HELICASES: STRUCTURE, FUNCTION AND ROLES IN HUMAN DISEASE  -JULY
7-12, 2001  VERMONT ACADEMY,  SAXTONS RIVER VERMONT

A FASEB helicase meeting to be held July 7-12, 2001 at the Vermont
Academy, Saxtons River Vermont.

Session subtopics include:
Helicase Structure
Helicase Function and Mechanism
Helicases in DNA Replication
Helicases in DNA Repair and Recombination
RNA Helicases in Transcription, Splicing, RNA stability and transport
RNA Helicases in Translation and  Ribosome Biogenesis
Helicases as part of macromolecular machines
Helicases in Viral Replication
Helicases in Cancer and Aging.

This will be the first meeting held in the United States dedicated
entirely to helicases.   Further information can be obtained from meeting
organizers:  Sandy Weller, University of Connecticut HealthCenter,
weller at nso2.uchc.edu, 860-679-2310 and Steve Matson, Univeristy of North
Carolina smatson at bio.unc.edu, 919-962-0005.  Vice-chairs will be Anna
Marie Pyle (amp11 at columbia.edu) and Smita Patel (patelss at umdnj.edu).
Please pass on to colleagues who may be interested.

4.      XP SUPPORT GROUPS - UK and US

4.1     UNITED KINGDOM XERODERMA PIGMENTOSUM SUPPORT GROUP
        We are pleased to announce the opening of the UK XP Support Group
Website at http://xpsupportgroup.org.uk The site gives up to date
information that is held by the Support Group as well as details of
forthcoming events and Newsletters.

4.2     XP SOCIETY
        The US XP Society is an active group involved in education, fund
raising, and providing information for XP patients worldwide. They run
Camp Sundown a summer camp with activities in the evening and night for XP
patients and their families. Their website is http://www.xps.org


5.      POST DOC OPPORTUNITIES: Bethesda, MD; Sussex, UK; Bethesda, MD x2;
Smithville, TX; Bethesda; Seattle; Boston
[Note: Check the list for more Job Opportunities on the DNA Repair
Interest Group web site: http://www.nih.gov:80/sigs/dna-rep/ ]

5.1     HUMAN DISEASES WITH DEFECTIVE DNA REPAIR - POST-DOCTORAL
FELLOWSHIP - BETHESDA, MD
        We are studying molecular, cellular and clinical abnormalities in
patients with defective DNA repair and possible links of these genes to
disease in the general population. Current emphasis is on xeroderma
pigmentosum, Cockayne syndrome and trichothiodystrophy.  A postdoctoral
position is available for a talented individual (M.D., Ph.D. or MD-PhD)
with less than 5 years of postdoctoral experience who has knowledge of
molecular biology and DNA repair.

To apply, send CV and bibliography and names (with contact information) of
3 references to:

Kenneth H. Kraemer, M.D.
Basic Research Laboratory
National Cancer Institute, NIH
Building 37 Room 3E24
Bethesda,  MD 20892
TEL: 301-496-9033    FAX: 301-496-8419
e-mail: kraemerk at nih.gov
http://rex.nci.nih.gov/RESEARCH/basic/lmc/khk.htm

NIH is an equal opportunity employer.

5.2      POSTDOCTORAL FELLOWSHIP, MRC CELL MUTATION UNIT, UNIVERSITY  OF
SUSSEX, UK
        A postdoc position is available for a protein biochemist to work
in Alan Lehmann's lab at the University of Sussex on the structure and
function of the S.pombe Rad18 protein family, which we are studying in
both yeast and man. Rad18 is of importance for two reasons. First it is
involved in several repair pathways (repair of double-strand breaks and
tolerance of DNA damage), as well as having an essential function,
probably in DNA replication. Second, structurally the protein is a member
of the very important SMC family. SMC proteins from the cores of the
cohesins and condensins, respectively involved in sister chromatid
cohesion and chromosome condensation. Rad18 and its SMC partner Spr18 form
the core of a third SMC protein complex in S. pombe. We have purified this
protein complex and found that it contains at least five other
polypeptides, which we are currently trying to identify. We have also
isolated and characterised the human homologues of both Rad18 and Spr18,
showing that these proteins are conserved. The function of these proteins
in mammalian cells is currently under investigation.

        The work will include identifying activities of the complex, eg
DNA-binding, helicase activities,determining how the different components
interact, and understanding their individual functions. This work will
give insights into the way in which this important protein is involved in
the different repair processes.
        Send applications with CV, or e-mail for more information, to
a.r.lehmann at sussex.ac.uk
Also visit our Website on http://www.biols.susx.ac.uk/biols/MRC/labs.html

5.3 TENURE-TRACK POSITION - DNA REPAIR - NIAAA, BETHESDA, MD
        The Division of Intramural Clinical and Biological Research of the
National Institute on Alcohol Abuse and Alcoholism, NIH, is recruiting an
individual into a tenure-track position to develop and direct an
independent research program focused on the role of DNA damage and repair
in function and in relation to human disease.  This includes
carcinogenesis, teratogenesis and/or degenerative diseases in response to
genotoxic agents such as ethanol.  Candidates should have an outstanding
publication record and, when applicable, a history of independent research
funding.  The successful candidate will be provided with sufficient
resources in the form of personnel and funds to conduct original basic
research in DNA modification and repair.

Applicants must have a Ph.D. and/or M.D. degree and should submit a
curriculum vitae, bibliography, the names and addresses of three
individuals who can be contacted for a reference, and a statement of
research goals to:

Ms. Kathleen Hanratty
NIAAA, NIH
Bldg. 31, Room 1B58
31 Center Drive MSC 2088
Bethesda, MD 20892-2088
Tel: 301/402-2997 Fax: 301/402-0016
e-mail: kh54d at nih.gov

Applications should be received by December 15, 2000.  Candidates rated
highly qualified will be invited to present a seminar.  NIH is an equal
opportunity employer.

Candidates rated as highly qualified will be invited to present a seminar.


5.4     POST-DOCTORAL POSITION - BETHESDA, MD: DNA REPLICATION
        A postdoctoral position is available in the laboratory of Dr.
Mirit I. Aladjem at the National Cancer Institute, Bethesda, MD to study
the regulation of  DNA replication origins in mammalian cells.  The aim of
the research program is understanding how information from the cell cycle
machinery leads to the initiation of DNA replication.  The proposed
project is based on the observation (1) that in some mammalian loci,
initiation sites are determined by interaction between local sequences at
the origin of replication and distant regulatory sequences.   A recently
developed intrachromosomal initiation assay (2), combining biochemical
analysis with recombinase-mediated gene targeting (3) will be used to
evaluate the local and distant requirements for initiation.  We will then
be able to determine the cell cycle regulatory pathways that interact with
these sequences in normal and malignant cells.

The position is located in Bethesda, Maryland, a suburb of Washington,
D.C.  Applicants with a background in molecular biology and an interest in
DNA replication, cell cycle and mechanisms of carcinogenesis are
encouraged to contact the email address or the phone number below, or
Email:  aladjemm at mail.nih.gov

Mirit I. Aladjem, Ph.D.
Laboratory of Molecular Pharmacology
DBS/NCI/NIH
Bldg. 37,  Rm 5D09
37 Convent Dr.
Bethesda, MD 20892-4255
Tel. 301-435-2848; Fax  301-402-0752

5.5     POSTDOCTORAL POSITION- UNIVERSITY OF TEXAS M.D. ANDERSON CANCER
CENTER, SCIENCE PARK-RESEARCH DIVISION, DEPARTMENT OF CARCINOGENESIS
      A postdoctoral position is available immediately to study the
molecular mechanisms of DNA damage recognition and the role of unusual DNA
structures in genomic instability.  The studies involve techniques in
biochemistry, protein expression and purification, cell culture, and
molecular biology.

        Please send a current CV, a letter of research interests, and a
list of references (including phone numbers and email addresses) to the
following address:

Dr. Karen M. Vasquez
Assistant Professor
U.T. M.D. Anderson Cancer Center
Science Park-Research Division
P.O. Box 389
Smithville, TX 78957
Email:  kvasquez at sprd1.mdacc.tmc.edu
Phone: 512-237-9324, FAX:  512-237-2475

5.6     POST-DOCTORAL POSITION -BETHESDA, MD:  STRESS GENE AND CELL CYCLE
REGULATION
        A position is available for a doctoral scientist with interest and
experience in the study of the regulation of mammalian stress gene
responses and/or the study of cell cycle control in mammalian cells.  This
is a postdoctoral position for a talented individual with less than 5
years of postdoctoral experience. Applicants should send a letter of
interest, C.V., and a list  of references, including telephone numbers and
e-mail addresses, to the following address:
Dr. A. J. Fornace Jr.
Head, Gene Response Section, BRL, DBS, NCI
Building 37, Room 5C09
National Institutes of Health
37 CONVENT DR MSC 4255
Bethesda, Maryland 20892-4255
TEL:  301 402 0744
FAX:  301 480 1946 (preferred)
                    301 480 2514 (alternative)
email:    fornace at nih.gov
http://rex.nci.nih.gov/RESEARCH/basic/lbc/fornace.htm

5.7     POSTDOCTORAL POSITIONS IN SEATTLE
Our laboratory studies DNA recombination and repair in mammalian cells.We
focus on two processes that occur in activated B cells, class
switchrecombination and somatic hypermutation, and we also study the role
of general recombination/repair factors (Rad52, BLM helicase) in genomic
stability and instability.  We have just moved from Yale to the University
of Washington, and we seek to recruit talented, motivated, and interactive
individuals to postdoctoral positions in the laboratory.  Experience in
protein purification is useful, but not essential.

Please send c.v. and names of three references to:
Dr. Nancy Maizels
Departments of Immunology and Biochemistry
University of Washington Medical School, Room H474A HSB
1959 NE Pacific Street, Box 357650
Seattle, WA  98195-7650
206-221-6876 (phone); 206-221-6781 (fax)
maizels at u.washington.edu


5.8      POST-DOC POSITION -DEPT OF CANCER CELL BIOLOGY - HARVARD SCHOOL
OF PUBLIC HEALTH  - BOSTON, MA
Post-Doc position available immediately to study the ubiquitination,
stability, and localization of p53, p53 family members, and other cell
cycle regulatory  proteins.  One goal of the lab is to determine the
mechanisms which regulate p53 nuclear export in normal and  stressed
cells.  See Nature Cell Biology (Sept. 2000) for most recent work.
Send resume to:
Dr. Carl Maki
Harvard School of Public Health
Dept. of Cancer Cell Biology
665 Huntington Ave.
Bldg. I, second floor
Boston, MA 02115
cmaki at hsph.harvard.edu

6.      ELECTRONIC CONTACTS:
6.1     Check out the DNA Repair Interest Group web site:
http://www.nih.gov:80/sigs/dna-rep/
You can find the schedule for future DNA Repair Interest Group
videoconferences and a listing of past videoconferences (with links to the
videoarchive) as well as a current list of JOB OPPORTUNITIES in DNA repair
and MEETING NOTICES.

6.2     Encourage your colleagues who are interested in DNA Repair to
request that they be added to this DNA Repair Interest Group listserve
e-mail list by sending a request by e-mail to: listserv at list.nih.gov
Leave the subject  blank. In the message field, type in: subscribe
DNARepair-L your name
        Alternatively, by filling out the form on the website you can both
add your name to the e-mail list and have your name posted on the website.
If you want your name to be listed you can fill out the "Join the SIG"
form on the web site and add your name to the listing of members.  If you
are not at NIH then be sure to click the "other" box and then fill in the
name of your institution.

6.3     Archives of these listserve mailings can be found at
        http://list.nih.gov/archives/dnarepair-l.html
                or via links from the DNA Repair Interest Group web site:
http://www.nih.gov:80/sigs/dna-rep/

6.4     I will be happy to relay information about post-doctoral
positions, jobs and meetings and other information related to DNA Repair.
Please send me an e-mail message (kraemerk at nih.gov) and I will incorporate
it into the next announcement list and post it on the DNA Repair Interest
Group web site: http://www.nih.gov:80/sigs/dna-rep/ .
(This list goes to more than 650 scientists around the world who are
interested in DNA repair.)



Kenneth H. Kraemer, M.D.
Basic Research Laboratory
National Cancer Institute
Building 37 Room 3E24
Bethesda,  MD 20892
301-496-9033    FAX: 301-496-8419
e-mail: kraemerk at nih.gov
DNA Repair Interest Group web site:
http://www.nih.gov:80/sigs/dna-rep/



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