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DNAREPAIR-L archives -- November 2000, week 3 (#1)

Content-Type: TEXT/PLAIN; charset=US-ASCII Message-ID: <[log in to unmask]> Date: Fri, 17 Nov 2000 14:26:16 -0500 Reply-To: Ken Kraemer <[log in to unmask]> Sender: DNA Repair Interest Group <[log in to unmask]> From: "Kenneth H. Kraemer" <[log in to unmask]> Subject: DNA Repair Interest Group -UPDATE - November 17, 2000

DNA Repair Interest Group -UPDATE - November 17, 2000 1. VIDEOCONFERENCE -Tues, Nov 21, 2000 -12:30 PM -Dr. Zhigang Wang - Univ of Kentucky -Translesion synthesis by the UmuC family of DNA polymerases 2. SPECIAL ANNOUNCEMENTS - HUMAN GENOME ON THE WEB; MITOCHONDRIA JOURNAL 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, Nov 21, 2000 - Dr. Zhigang Wang - Univ of Kentucky -Translesion synthesis by the UmuC family of DNA polymerases VIDEOCONFERENCE LOCATIONS: Univ of Kentucky, Lexington, KY (origin); 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; MD Anderson, Smithville, TX; Lawrence Livermore Labs, Livermore, CA; Univ of Michigan, Ann Arbor; and Brookhaven National Labs, Upton, NY. [A WARM 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, 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 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 2 more talks TBA 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! 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: HUMAN GENOME ON THE WEB; NEW JOURNAL - MITOCHONDRION 2.1 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/ 2.2 New journal: MITOCHONDRION Dr. Keshav Singh <[log in to unmask]> 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 FIRST NOTICE: THIRD INTERNET PHOTOCHEMISTRY AND PHOTOBIOLOGY CONFERENCE NOVEMBER 13 TO DECEMBER 10 2000 Paul Heelis <[log in to unmask]> writes: As in previous virtual meeting there will be the opportunity to present posters and papers. Papers should be finished works. They will be considered for publication by J.Photochem.Photobiol:B Posters can be any length and can either be incomplete works or finished work that the authors prefer to publish elsewhere after the meeting. Register (FREE) at http://www.photobiology.com/photobiology2000/register.htm 3.2 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/> 3.3 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 [log in to unmask] ; see instructions at the website). 3.4 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 [log in to unmask] 3.5 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: [log in to unmask] 3.6 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, [log in to unmask], 860-679-2310 and Steve Matson, Univeristy of North Carolina [log in to unmask], 919-962-0005. Vice-chairs will be Anna Marie Pyle ([log in to unmask]) and Smita Patel ([log in to unmask]). 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: [log in to unmask] 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 [log in to unmask] 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: [log in to unmask] 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: [log in to unmask] 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: [log in to unmask] 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: [log in to unmask] 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) [log in to unmask] 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 [log in to unmask] 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: [log in to unmask] 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 ([log in to unmask]) 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: [log in to unmask] DNA Repair Interest Group web site: http://www.nih.gov:80/sigs/dna-rep/

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