Preview
Sign-in for full Details 
Sign-in free and Explore the Exciting World of BiomedExperts:
- Over 1.500.000 Profiles
- More than 1.800 Organizations worldwide
- State of the Art Network Visualizations
- Manage your own Profile
- Locate Experts in your Country/Region
- Locate Experts in your 1. and 2. Level Network
- Connect to Experts Worldwide
NetworkView
Larry Thompson
This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers
together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles
free of charge to researchers worldwide.
Research Profile (preview)
Physiology
Living Beings
Chemicals & Drugs
Anatomy
Procedures
Phenomena
Disorders
Concepts & Ideas
Sign-in to see full Profile
Network (preview)
23
Salazar, Edmund
14
Hinz, John
14
Tucker, James
13
Tebbs, Robert
10
Felton, James
8
Lamerdin, Jane
8
Schild, David
7
Takata, Minoru
6
Jones, Nigel
6
Wu, Rebekah
5
Yamada, Alice
5
Takeda, Shunichi
5
Urbin, Salustra
5
Nham, Peter
5
Albala, Joanna
Sign-in to see all Coauthors
Publications
Sign-in to see all Publications
Sign in free and see...
Visualized networks:
See your personal network in
sophisticated graphical views
GeoTargeted Searches:
Locate experts around the world
and connect with global collaborators
Research Profiles:
See the visualized research activity
of experts around the globe
Sign-in to see more
Geonetwork of Larry Thompson (preview)
Cities where this author has publications
Cities where co-authors of this author have publications
Sign-in to see more
All Publications
-
2009: Thompson Larry H; Hinz John M
Cellular and molecular consequences of defective Fanconi anemia proteins in replication-coupled DNA repair: mechanistic insights.
Mutation research 2009;668(1-2):54-72.
-
2009: Hinz John M; Urbin Salustra S; Thompson Larry H
RAD51D- and FANCG-dependent base substitution mutagenesis at the ATP1A1 locus in mammalian cells.
Mutation research 2009;665(1-2):61-6.
-
2008: Wilson J B; Yamamoto K; Marriott A S; Hussain S; Sung P; Hoatlin M E; Mathew C G; Takata M; Thompson L H; Kupfer G M; Jones N J
FANCG promotes formation of a newly identified protein complex containing BRCA2, FANCD2 and XRCC3.
Oncogene 2008;27(26):3641-52.
-
2008: Nagasawa Hatsumi; Wilson Paul F; Chen David J; Thompson Larry H; Bedford Joel S; Little John B
Low doses of alpha particles do not induce sister chromatid exchanges in bystander Chinese hamster cells defective in homologous recombination.
DNA repair 2008;7(3):515-22.
-
2007: Stackpole Megan M; Wise Sandra S; Goodale Britton C; Duzevik Eliza Grlickova; Munroe Ray C; Thompson W Douglas; Thacker John; Thompson Larry H; Hinz John M; Wise John Pierce
Homologous recombination repair protects against particulate chromate-induced chromosome instability in Chinese hamster cells.
Mutation research 2007;625(1-2):145-54.
-
2007: Fan Jinshui; Wilson Paul F; Wong Heng-Kuan; Urbin Salustra S; Thompson Larry H; Wilson David M
XRCC1 down-regulation in human cells leads to DNA-damaging agent hypersensitivity, elevated sister chromatid exchange, and reduced survival of BRCA2 mutant cells.
Environmental and molecular mutagenesis 2007;48(6):491-500.
-
2007: Wilson David M; Thompson Larry H
Molecular mechanisms of sister-chromatid exchange.
Mutation research 2007;616(1-2):11-23.
-
2007: Savery Laura C; Grlickova-Duzevik Eliza; Wise Sandra S; Thompson W Douglas; Hinz John M; Thompson Larry H; Wise John Pierce
Role of the Fancg gene in protecting cells from particulate chromate-induced chromosome instability.
Mutation research 2007;626(1-2):120-7.
-
2007: Hinz John M; Nham Peter B; Urbin Salustra S; Jones Irene M; Thompson Larry H
Disparate contributions of the Fanconi anemia pathway and homologous recombination in preventing spontaneous mutagenesis.
Nucleic acids research 2007;35(11):3733-40.
-
2006: Hinz John M; Nham Peter B; Yamada N Alice; Tebbs Robert S; Salazar Edmund P; Hinz Angela K; Mohrenweiser Harvey W; Jones Irene M; Thompson Larry H
Four human FANCG polymorphic variants show normal biological function in hamster CHO cells.
Mutation research 2006;602(1-2):34-42.
-
2006: Hinz John M; Nham Peter B; Salazar Edmund P; Thompson Larry H
The Fanconi anemia pathway limits the severity of mutagenesis.
DNA repair 2006;5(8):875-84.
-
2006: Hussain Shobbir; Wilson James B; Blom Eric; Thompson Larry H; Sung Patrick; Gordon Susan M; Kupfer Gary M; Joenje Hans; Mathew Christopher G; Jones Nigel J
Tetratricopeptide-motif-mediated interaction of FANCG with recombination proteins XRCC3 and BRCA2.
DNA repair 2006;5(5):629-40.
-
2006: Wiese Claudia; Hinz John M; Tebbs Robert S; Nham Peter B; Urbin Salustra S; Collins David W; Thompson Larry H; Schild David
Disparate requirements for the Walker A and B ATPase motifs of human RAD51D in homologous recombination.
Nucleic acids research 2006;34(9):2833-43.
-
2006: Hinz John M; Tebbs Robert S; Wilson Paul F; Nham Peter B; Salazar Edmund P; Nagasawa Hatsumi; Urbin Salustra S; Bedford Joel S; Thompson Larry H
Repression of mutagenesis by Rad51D-mediated homologous recombination.
Nucleic acids research 2006;34(5):1358-68.
-
2005: Hinz John M; Yamada N Alice; Salazar Edmund P; Tebbs Robert S; Thompson Larry H
Influence of double-strand-break repair pathways on radiosensitivity throughout the cell cycle in CHO cells.
DNA repair 2005;4(7):782-92.
-
2005: Thompson Larry H; Hinz John M; Yamada N Alice; Jones Nigel J
How Fanconi anemia proteins promote the four Rs: replication, recombination, repair, and recovery.
Environmental and molecular mutagenesis 2005;45(2-3):128-42.
-
2005: Miller Kristi A; Hinz John M; Yamada N Alice; Thompson Lawrence H; Albala Joanna S
Nuclear localization of Rad51B is independent of Rad51C and BRCA2.
Mutagenesis 2005;20(1):57-63.
-
2005: Hirano Seiki; Yamamoto Kazuhiko; Ishiai Masamichi; Yamazoe Mitsuyoshi; Seki Masayuki; Matsushita Nobuko; Ohzeki Mioko; Yamashita Yukiko M; Arakawa Hiroshi; Buerstedde Jean-Marie; Enomoto Takemi; Takeda Shunichi; Thompson Larry H; Takata Minoru
Functional relationships of FANCC to homologous recombination, translesion synthesis, and BLM.
The EMBO journal 2005;24(2):418-27.
-
2005: Yamamoto Kazuhiko; Hirano Seiki; Ishiai Masamichi; Morishima Kenichi; Kitao Hiroyuki; Namikoshi Keiko; Kimura Masayo; Matsushita Nobuko; Arakawa Hiroshi; Buerstedde Jean-Marie; Komatsu Kenshi; Thompson Larry H; Takata Minoru
Fanconi anemia protein FANCD2 promotes immunoglobulin gene conversion and DNA repair through a mechanism related to homologous recombination.
Molecular and cellular biology 2005;25(1):34-43.
-
2005: Tebbs Robert S; Hinz John M; Yamada N Alice; Wilson James B; Salazar Edmund P; Thomas Cynthia B; Jones Irene M; Jones Nigel J; Thompson Larry H
New insights into the Fanconi anemia pathway from an isogenic FancG hamster CHO mutant.
DNA repair 2005;4(1):11-22.
-
2004: Lamerdin Jane E; Yamada Nazumi A; George James W; Souza Brian; Christian Allen T; Jones Nigel J; Thompson Larry H
Characterization of the hamster FancG/Xrcc9 gene and mutations in CHO UV40 and NM3.
Mutagenesis 2004;19(3):237-44.
-
2004: Yamada Nazumi Alice; Hinz John M; Kopf Vicki L; Segalle Kathryn D; Thompson Larry H
XRCC3 ATPase activity is required for normal XRCC3-Rad51C complex dynamics and homologous recombination.
The Journal of biological chemistry 2004;279(22):23250-4.
-
2003: Tebbs Robert S; Thompson Larry H; Cleaver James E
Rescue of Xrcc1 knockout mouse embryo lethality by transgene-complementation.
DNA repair 2003;2(12):1405-17.
-
2003: Yamamoto Kazuhiko; Ishiai Masamichi; Matsushita Nobuko; Arakawa Hiroshi; Lamerdin Jane E; Buerstedde Jean-Marie; Tanimoto Mitsune; Harada Mine; Thompson Larry H; Takata Minoru
Fanconi anemia FANCG protein in mitigating radiation- and enzyme-induced DNA double-strand breaks by homologous recombination in vertebrate cells.
Molecular and cellular biology 2003;23(15):5421-30.
-
2002: Thompson Larry H; Schild David
Recombinational DNA repair and human disease.
Mutation research 2002;509(1-2):49-78.
-
2002: Takata Minoru; Tachiiri Seiji; Fujimori Akira; Thompson Larry H; Miki Yoshio; Hiraoka Masahiro; Takeda Shunichi; Yamazoe Mitsuyoshi
Conserved domains in the chicken homologue of BRCA2.
Oncogene 2002;21(7):1130-4.
-
2002: Liu Nan; Schild David; Thelen Michael P; Thompson Larry H
Involvement of Rad51C in two distinct protein complexes of Rad51 paralogs in human cells.
Nucleic acids research 2002;30(4):1009-15.
-
2002: Wiese Claudia; Collins David W; Albala Joanna S; Thompson Larry H; Kronenberg Amy; Schild David
Interactions involving the Rad51 paralogs Rad51C and XRCC3 in human cells.
Nucleic acids research 2002;30(4):1001-8.
-
2001: George J W; Salazar E P; Vreeswijk M P; Lamerdin J E; Reardon J T; Zdzienicka M Z; Sancar A; Kadkhodayan S; Tebbs R S; Mullenders L H; Thompson L H
Restoration of nucleotide excision repair in a helicase-deficient XPD mutant from intragenic suppression by a trichothiodystrophy mutation.
Molecular and cellular biology 2001;21(21):7355-65.
-
2001: Fujimori A; Tachiiri S; Sonoda E; Thompson L H; Dhar P K; Hiraoka M; Takeda S; Zhang Y; Reth M; Takata M
Rad52 partially substitutes for the Rad51 paralog XRCC3 in maintaining chromosomal integrity in vertebrate cells.
The EMBO journal 2001;20(19):5513-20.
-
2001: Thompson L H; Schild D
Homologous recombinational repair of DNA ensures mammalian chromosome stability.
Mutation research 2001;477(1-2):131-53.
-
2001: Takata M; Sasaki M S; Tachiiri S; Fukushima T; Sonoda E; Schild D; Thompson L H; Takeda S
Chromosome instability and defective recombinational repair in knockout mutants of the five Rad51 paralogs.
Molecular and cellular biology 2001;21(8):2858-66.
-
2001: Kadkhodayan S; Coin F; Salazar E P; George J W; Egly J M; Thompson L H
Codominance associated with overexpression of certain XPD mutations.
Mutation research 2001;485(2):153-68.
-
2001: Tebbs R S; Salazar E P; Thompson L H
Identification of ICR170-induced XPD mutations in UV-sensitive CHO cells.
Environmental and molecular mutagenesis 2001;38(2-3):111-7.
-
2000: Takata M; Sasaki M S; Sonoda E; Fukushima T; Morrison C; Albala J S; Swagemakers S M; Kanaar R; Thompson L H; Takeda S
The Rad51 paralog Rad51B promotes homologous recombinational repair.
Molecular and cellular biology 2000;20(17):6476-82.
-
2000: Thompson L H; West M G
XRCC1 keeps DNA from getting stranded.
Mutation research 2000;459(1):1-18.
-
1999: Schild L J; Brookman K W; Thompson L H; Wilson D M
Effects of Ape1 overexpression on cellular resistance to DNA-damaging and anticancer agents.
Somatic cell and molecular genetics 1999;25(5-6):253-62.
-
1999: Tebbs R S; Flannery M L; Meneses J J; Hartmann A; Tucker J D; Thompson L H; Cleaver J E; Pedersen R A
Requirement for the Xrcc1 DNA base excision repair gene during early mouse development.
Developmental biology 1999;208(2):513-29.
-
1999: Thompson L H; Schild D
The contribution of homologous recombination in preserving genome integrity in mammalian cells.
Biochimie 1999;81(1-2):87-105.
-
1999: Cleaver J E; Thompson L H; Richardson A S; States J C
A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy.
Human mutation 1999;14(1):9-22.
-
1998: Liu N; Lamerdin J E; Tebbs R S; Schild D; Tucker J D; Shen M R; Brookman K W; Siciliano M J; Walter C A; Fan W; Narayana L S; Zhou Z Q; Adamson A W; Sorensen K J; Chen D J; Jones N J; Thompson L H
XRCC2 and XRCC3, new human Rad51-family members, promote chromosome stability and protect against DNA cross-links and other damages.
Molecular cell 1998;1(6):783-93.
-
1998: Shen M R; Zdzienicka M Z; Mohrenweiser H; Thompson L H; Thelen M P
Mutations in hamster single-strand break repair gene XRCC1 causing defective DNA repair.
Nucleic acids research 1998;26(4):1032-7.
-
1997: Albala J S; Thelen M P; Prange C; Fan W; Christensen M; Thompson L H; Lennon G G
Identification of a novel human RAD51 homolog, RAD51B.
Genomics 1997;46(3):476-9.
-
1997: Wilson D M; Thompson L H
Life without DNA repair.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(24):12754-7.
-
1997: Liu N; Lamerdin J E; Tucker J D; Zhou Z Q; Walter C A; Albala J S; Busch D B; Thompson L H
The human XRCC9 gene corrects chromosomal instability and mutagen sensitivities in CHO UV40 cells.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(17):9232-7.
-
1997: Wu R W; Tucker J D; Sorensen K J; Thompson L H; Felton J S
Differential effect of acetyltransferase expression on the genotoxicity of heterocyclic amines in CHO cells.
Mutation research 1997;390(1-2):93-103.
-
1997: Busch D B; van Vuuren H; de Wit J; Collins A; Zdzienicka M Z; Mitchell D L; Brookman K W; Stefanini M; Riboni R; Thompson L H; Albert R B; van Gool A J; Hoeijmakers J
Phenotypic heterogeneity in nucleotide excision repair mutants of rodent complementation groups 1 and 4.
Mutation research 1997;383(2):91-106.
-
1997: Reardon J T; Thompson L H; Sancar A
Rodent UV-sensitive mutant cell lines in complementation groups 6-10 have normal general excision repair activity.
Nucleic acids research 1997;25(5):1015-21.
-
1997: Bessho T; Sancar A; Thompson L H; Thelen M P
Reconstitution of human excision nuclease with recombinant XPF-ERCC1 complex.
The Journal of biological chemistry 1997;272(6):3833-7.
-
1996: Brookman K W; Lamerdin J E; Thelen M P; Hwang M; Reardon J T; Sancar A; Zhou Z Q; Walter C A; Parris C N; Thompson L H
ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs.
Molecular and cellular biology 1996;16(11):6553-62.
-
1996: Busch D B; Zdzienicka M Z; Natarajan A T; Jones N J; Overkamp W J; Collins A; Mitchell D L; Stefanini M; Botta E; Albert R B; Liu N; White D A; van Gool A J; Thompson L H
A CHO mutant, UV40, that is sensitive to diverse mutagens and represents a new complementation group of mitomycin C sensitivity.
Mutation research 1996;363(3):209-21.
-
1996: Thompson L H
Evidence that mammalian cells possess homologous recombinational repair pathways.
Mutation research 1996;363(2):77-88.
-
1996: Takayama K; Salazar E P; Broughton B C; Lehmann A R; Sarasin A; Thompson L H; Weber C A
Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophy.
American journal of human genetics 1996;58(2):263-70.
-
1996: Thompson L H
Identifying genes and proteins involved in human DNA repair processes using somatic cell and molecular genetics.
Progress in clinical and biological research 1996;395():175-99.
-
1995: Thompson L H; Wu R W; Felton J S
Genetically modified Chinese hamster ovary (CHO) cells for studying the genotoxicity of heterocyclic amines from cooked foods.
Toxicology letters 1995;82-83():883-9.
-
1995: Caldecott K W; Tucker J D; Stanker L H; Thompson L H
Characterization of the XRCC1-DNA ligase III complex in vitro and its absence from mutant hamster cells.
Nucleic acids research 1995;23(23):4836-43.
-
1995: Takayama K; Salazar E P; Lehmann A; Stefanini M; Thompson L H; Weber C A
Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D.
Cancer research 1995;55(23):5656-63.
-
1995: Thompson L H; Jeggo P A
Nomenclature of human genes involved in ionizing radiation sensitivity.
Mutation research 1995;337(2):131-4.
-
1995: Tebbs R S; Zhao Y; Tucker J D; Scheerer J B; Siciliano M J; Hwang M; Liu N; Legerski R J; Thompson L H
Correction of chromosomal instability and sensitivity to diverse mutagens by a cloned cDNA of the XRCC3 DNA repair gene.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(14):6354-8.
-
1995: Wu R W; Wu E M; Thompson L H; Felton J S
Identification of aprt gene mutations induced in repair-deficient and P450-expressing CHO cells by the food-related mutagen/carcinogen, PhIP.
Carcinogenesis 1995;16(5):1207-13.
-
1995: Jones N J; Zhao Y; Siciliano M J; Thompson L H
Assignment of the XRCC2 human DNA repair gene to chromosome 7q36 by complementation analysis.
Genomics 1995;26(3):619-22.
-
1995: Lamerdin J E; Montgomery M A; Stilwagen S A; Scheidecker L K; Tebbs R S; Brookman K W; Thompson L H; Carrano A V
Genomic sequence comparison of the human and mouse XRCC1 DNA repair gene regions.
Genomics 1995;25(2):547-54.
-
1995: Felton J S; Wu R; Knize M G; Thompson L H; Hatch F T
Heterocyclic amine mutagenicity/carcinogenicity: influence of repair, metabolism, and structure.
Princess Takamatsu symposia 1995;23():50-8.
-
1994: Walter C A; Lu J; Bhakta M; Zhou Z Q; Thompson L H; McCarrey J R
Testis and somatic Xrcc-1 DNA repair gene expression.
Somatic cell and molecular genetics 1994;20(6):451-61.
-
1994: Caldecott K W; Thompson L H
Partial correction of the single-strand break repair defect in the CHO mutant EM9 by electroporated recombinant XRCC1 protein.
Annals of the New York Academy of Sciences 1994;726():336-9.
-
1994: Thompson L H; Brookman K W; Weber C A; Salazar E P; Reardon J T; Sancar A; Deng Z; Siciliano M J
Molecular cloning of the human nucleotide-excision-repair gene ERCC4.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(15):6855-9.
-
1994: Busch D; Greiner C; Rosenfeld K L; Ford R; de Wit J; Hoeijmakers J H; Thompson L H
Complementation group assignments of moderately UV-sensitive CHO mutants isolated by large-scale screening (FAECB).
Mutagenesis 1994;9(4):301-6.
-
1994: Brookman K W; Tebbs R S; Allen S A; Tucker J D; Swiger R R; Lamerdin J E; Carrano A V; Thompson L H
Isolation and characterization of mouse Xrcc-1, a DNA repair gene affecting ligation.
Genomics 1994;22(1):180-8.
-
1994: Caldecott K W; McKeown C K; Tucker J D; Ljungquist S; Thompson L H
An interaction between the mammalian DNA repair protein XRCC1 and DNA ligase III.
Molecular and cellular biology 1994;14(1):68-76.
-
1993: Liu P; Siciliano J; White B; Legerski R; Callen D; Reeders S; Siciliano M J; Thompson L H
Regional mapping of human DNA excision repair gene ERCC4 to chromosome 16p13.13-p13.2.
Mutagenesis 1993;8(3):199-205.
-
1992: Caldecott K W; Tucker J D; Thompson L H
Construction of human XRCC1 minigenes that fully correct the CHO DNA repair mutant EM9.
Nucleic acids research 1992;20(17):4575-9.
-
1992: Yoo H; Li L; Sacks P G; Thompson L H; Becker F F; Chan J Y
Alterations in expression and structure of the DNA repair gene XRCC1.
Biochemical and biophysical research communications 1992;186(2):900-10.
-
1991: Buonarati M H; Tucker J D; Minkler J L; Wu R W; Thompson L H; Felton J S
Metabolic activation and cytogenetic effects of 2-amino-1-methyl-6-phenylimidazo[4,5-b] pyridine (PhIP) in Chinese hamster ovary cells expressing murine cytochrome P450 IA2.
Mutagenesis 1991;6(4):253-9.
-
1991: Thompson L H; Wu R W; Felton J S
Introduction of cytochrome P450IA2 metabolic capability into cell lines genetically matched for DNA repair proficiency/deficiency.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(9):3827-31.
-
1991: Thompson L H
Properties and applications of human DNA repair genes.
Mutation research 1991;247(2):213-9.
-
1991: Tucker J D; Jones N J; Allen N A; Minkler J L; Thompson L H; Carrano A V
Cytogenetic characterization of the ionizing radiation-sensitive Chinese hamster mutant irs1.
Mutation research 1991;254(2):143-52.
-
1991: Felton J S; Knize M K; Turteltaub K W; Buonarati M H; Taylor R T; Vanderlaan M; Watkins B E; Tucker J D; Thompson L H
Mutagens and carcinogens in cooked foods: concentration, potency, and risk.
Advances in experimental medicine and biology 1991;289():133.
-
1991: Trinidad A C; Wu R W; Thompson L H; Felton J S
Expression of mouse cytochrome P450IA1 cDNA in repair-deficient and repair-proficient CHO cells.
Molecular carcinogenesis 1991;4(6):510-8.
-
1990: Thompson L H; Brookman K W; Jones N J; Allen S A; Carrano A V
Molecular cloning of the human XRCC1 gene, which corrects defective DNA strand break repair and sister chromatid exchange.
Molecular and cellular biology 1990;10(12):6160-71.
-
1990: Olson E; Edmondson D; Wright W E; Lin V K; Guenet J L; Simon-Chazottes D; Thompson L H; Stallings R L; Schroeder W T; Duvic M
Myogenin is in an evolutionarily conserved linkage group on human chromosome 1q31-q41 and unlinked to other mapped muscle regulatory factor genes.
Genomics 1990;8(3):427-34.
-
1990: Regan J D; Thompson L H; Carrier W L; Weber C A; Francis A A; Zdzienicka M Z
Cyclobutane-pyrimidine dimer excision in UV-sensitive CHO mutants and the effect of the human ERCC2 repair gene.
Mutation research 1990;235(3):157-63.
-
1990: Weber C A; Salazar E P; Stewart S A; Thompson L H
ERCC2: cDNA cloning and molecular characterization of a human nucleotide excision repair gene with high homology to yeast RAD3.
The EMBO journal 1990;9(5):1437-47.
-
1990: Jones N J; Stewart S A; Thompson L H
Biochemical and genetic analysis of the Chinese hamster mutants irs1 and irs2 and their comparison to cultured ataxia telangiectasia cells.
Mutagenesis 1990;5(1):15-23.
-
1989: Thompson L H; Bachinski L L; Stallings R L; Dolf G; Weber C A; Westerveld A; Siciliano M J
Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19.
Genomics 1989;5(4):670-9.
-
1989: Thompson L H; Mitchell D L; Regan J D; Bouffler S D; Stewart S A; Carrier W L; Nairn R S; Johnson R T
CHO mutant UV61 removes (6-4) photoproducts but not cyclobutane dimers.
Mutagenesis 1989;4(2):140-6.
-
1989: Thompson L H
Somatic cell genetics approach to dissecting mammalian DNA repair.
Environmental and molecular mutagenesis 1989;14(4):264-81.
-
1989: Mohrenweiser H W; Carrano A V; Fertitta A; Perry B; Thompson L H; Tucker J D; Weber C A
Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19.
Cytogenetics and cell genetics 1989;52(1-2):11-4.
-
1988: Thompson L H; Shiomi T; Salazar E P; Stewart S A
An eighth complementation group of rodent cells hypersensitive to ultraviolet radiation.
Somatic cell and molecular genetics 1988;14(6):605-12.
-
1988: Stallings R L; Olson E; Strauss A W; Thompson L H; Bachinski L L; Siciliano M J
Human creatine kinase genes on chromosomes 15 and 19, and proximity of the gene for the muscle form to the genes for apolipoprotein C2 and excision repair.
American journal of human genetics 1988;43(2):144-51.
-
1988: Weber C A; Salazar E P; Stewart S A; Thompson L H
Molecular cloning and biological characterization of a human gene, ERCC2, that corrects the nucleotide excision repair defect in CHO UV5 cells.
Molecular and cellular biology 1988;8(3):1137-46.
-
1987: Thompson L H; Tucker J D; Stewart S A; Christensen M L; Salazar E P; Carrano A V; Felton J S
Genotoxicity of compounds from cooked beef in repair-deficient CHO cells versus Salmonella mutagenicity.
Mutagenesis 1987;2(6):483-7.
-
1987: Thompson L H; Carrano A V; Sato K; Salazar E P; White B F; Stewart S A; Minkler J L; Siciliano M J
Identification of nucleotide-excision-repair genes on human chromosomes 2 and 13 by functional complementation in hamster-human hybrids.
Somatic cell and molecular genetics 1987;13(5):539-51.
-
1987: Thompson L H
Dissecting human DNA repair.
Photo-dermatology 1987;4(2):63-5.
-
1987: Thompson L H; Salazar E P; Brookman K W; Collins C C; Stewart S A; Busch D B; Weber C A
Recent progress with the DNA repair mutants of Chinese hamster ovary cells.
Journal of cell science. Supplement 1987;6():97-110.
-
1986: Carrano A V; Minkler J L; Dillehay L E; Thompson L H
Incorporated bromodeoxyuridine enhances the sister-chromatid exchange and chromosomal aberration frequencies in an EMS-sensitive Chinese hamster cell line.
Mutation research 1986;162(2):233-9.
-
1986: Thompson L H; Brookman K W; Salazar E P; Fuscoe J C; Weber C A
DNA repair genes of mammalian cells.
Basic life sciences 1986;39():349-58.
-
1985: Hoy C A; Thompson L H; Salazar E P; Stewart S A
Different genetic alterations underlie dual hypersensitivity of CHO mutant UV-1 to DNA methylating and cross-linking agents.
Somatic cell and molecular genetics 1985;11(6):523-32.
-
1985: Thompson L H; Mooney C L; Brookman K W
Genetic complementation between UV-sensitive CHO mutants and xeroderma pigmentosum fibroblasts.
Mutation research 1985;150(1-2):423-9.
-
1985: Thompson L H; Brookman K W; Minkler J L; Fuscoe J C; Henning K A; Carrano A V
DNA-mediated transfer of a human DNA repair gene that controls sister chromatid exchange.
Molecular and cellular biology 1985;5(4):881-4.
-
1985: Brookman K W; Salazar E P; Thompson L H
Comparative mutagenic efficiencies of the DNA adducts from the cooked-food-related mutagens Trp-P-2 and IQ in CHO cells.
Mutation research 1985;149(2):249-55.
-
1985: Hoy C A; Thompson L H; Mooney C L; Salazar E P
Defective DNA cross-link removal in Chinese hamster cell mutants hypersensitive to bifunctional alkylating agents.
Cancer research 1985;45(4):1737-43.
-
1984: Hoy C A; Salazar E P; Thompson L H
Rapid detection of DNA-damaging agents using repair-deficient CHO cells.
Mutation research 1984;130(5):321-32.
-
1984: Thompson L H; Brookman K W; Mooney C L
Repair of DNA adducts in asynchronous CHO cells and the role of repair in cell killing and mutation induction in synchronous cells treated with 7-bromomethylbenz[a]anthracene.
Somatic cell and molecular genetics 1984;10(2):183-94.
-
1983: Thompson L H; Salazar E P; Brookman K W; Hoy C A
Hypersensitivity to cell killing and mutation induction by chemical carcinogens in an excision repair-deficient mutant of CHO cells.
Mutation research 1983;112(6):329-44.
-
1983: Dillehay L E; Thompson L H; Minkler J L; Carrano A V
The relationship between sister-chromatid exchange and perturbations in DNA replication in mutant EM9 and normal CHO cells.
Mutation research 1983;109(2):283-96.
-
1983: Thompson L H; Carrano A V; Salazar E; Felton J S; Hatch F T
Comparative genotoxic effects of the cooked-food-related mutagens Trp-P-2 and IQ in bacteria and cultured mammalian cells.
Mutation research 1983;117(3-4):243-57.
-
1982: Thompson L H; Brookman K W; Dillehay L E; Mooney C L; Carrano A V
Hypersensitivity to mutation and sister-chromatid-exchange induction in CHO cell mutants defective in incising DNA containing UV lesions.
Somatic cell genetics 1982;8(6):759-73.
-
1982: Thompson L H; Brookman K W; Dillehay L E; Carrano A V; Mazrimas J A; Mooney C L; Minkler J L
A CHO-cell strain having hypersensitivity to mutagens, a defect in DNA strand-break repair, and an extraordinary baseline frequency of sister-chromatid exchange.
Mutation research 1982;95(2-3):427-40.
-
1982: Thompson L H; Brookman K W; Carrano A V; Dillehay L E
Role of DNA repair in mutagenesis of Chinese hamster ovary cells by 7-bromomethylbenz[a]anthracene.
Proceedings of the National Academy of Sciences of the United States of America 1982;79(2):534-8.
-
1981: Thompson L H; Busch D B; Brookman K; Mooney C L; Glaser D A
Genetic diversity of UV-sensitive DNA repair mutants of Chinese hamster ovary cells.
Proceedings of the National Academy of Sciences of the United States of America 1981;78(6):3734-7.
-
1980: Thompson L H; Baker R M; Carrano A V; Brookman K W
Failure of the phorbol ester 12-O-tetradecanoylphorbol-13-acetate to enhance sister chromatid exchange, mitotic segregation, or expression of mutations in Chinese hamster cells.
Cancer research 1980;40(9):3245-51.
Sign-in to see more
