Many amino acid substitution variants identified in DNA repair genes during human population screenings are predicted to impact protein function von TONG XI, JONES, Irene M, MOHRENWEISER, Harvey W

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Challenges and complexities in estimating both the functional impact and the disease risk associated with the extensive genetic variation in human DNA repair genes von MOHRENWEISER, Harvey W, WILSON, David M, JONES, Irene M

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Polymorphisms in the DNA Repair Gene XRCC1 and Breast Cancer von DUELL, Eric J, MILLIKAN, Robert C, PITTMAN, Vary S, WINKEL, Scott, LUNN, Ruth M, TSE, Chiu-Kit J, EATON, Allison, MOHRENWEISER, Harvey W, NEWMAN, Beth, BELL, Douglas A

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Amino acid substitution variants of APE1 and XRCC1 genes associated with ionizing radiation sensitivity von Hu, Jennifer J., Smith, Tasha R., Miller, Mark Steven, Mohrenweiser, Harvey W., Golden, Andrea, Case, L.Douglas

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DNA-Repair Genetic Polymorphisms and Breast Cancer Risk von SMITH, Tasha R, LEVINE, Edward A, PERRIER, Nancy D, MILLER, Mark Steven, FREIMANIS, Rita I, LOHMAN, Kurt, CASE, L. Douglas, XU, Jianfeng, MOHRENWEISER, Harvey W, HU, Jennifer J

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Functional characterization of Ape1 variants identified in the human population von Hadi, M Z, Coleman, M A, Fidelis, K, Mohrenweiser, H W, Wilson, 3rd, D M

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Modulation of repair of ultraviolet damage in the host-cell reactivation assay by polymorphic XPC and XPD/ERCC2 genotypes von Qiao, Yawei, Spitz, Margaret R., Shen, Hongbing, Guo, Zhaozheng, Shete, Sanjay, Hedayati, Mohammad, Grossman, Lawrence, Mohrenweiser, Harvey, Wei, Qingyi

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Polymorphisms in Human Soluble Epoxide Hydrolase von Przybyla-Zawislak, Beata D, Srivastava, Punit K, Vazquez-Matias, Johana, Mohrenweiser, Harvey W, Maxwell, Joseph E, Hammock, Bruce D, Bradbury, J Alyce, Enayetallah, Ahmed E, Zeldin, Darryl C, Grant, David F

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Identification of 127 amino acid substitution variants in screening 37 DNA repair genes in humans von Mohrenweiser, Harvey W, Xi, Tong, Vázquez-Matías, Johana, Jones, Irene M

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Polymorphisms of XRCC1 and XRCC3 genes and susceptibility to breast cancer von Smith, Tasha R., Miller, Mark Steven, Lohman, Kurt, Lange, Ethan M., Case, L.Douglas, Mohrenweiser, Harvey W., Hu, Jennifer J.

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Genetic variability in susceptibility and response to toxicants von Miller, Merrill C., Mohrenweiser, Harvey W., Bell, Douglas A.

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A prospective study of XRCC1 haplotypes and their interaction with plasma carotenoids on breast cancer risk von HAN, Jiali, HANKINSON, Susan E, DE VIVO, Immaculata, SPIEGELMAN, Donna, TAMIMI, Rulla M, MOHRENWEISER, Harvey W, COLDITZ, Graham A, HUNTER, David J

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Genetic Variation and Exposure Related Risk Estimation: Will Toxicology Enter a New Era? DNA Repair and Cancer as a Paradigm von Mohrenweiser, Harvey W.

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Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4 von Ophoff, R A, Terwindt, G M, Vergouwe, M N, van Eijk, R, Oefner, P J, Hoffman, S M, Lamerdin, J E, Mohrenweiser, H W, Bulman, D E, Ferrari, M, Haan, J, Lindhout, D, van Ommen, G J, Hofker, M H, Ferrari, M D, Frants, R R

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Identification and functional characterization of polymorphisms in human cyclooxygenase-1 (PTGS1) von Lee, Craig R, Bottone, Frank G, Krahn, Joseph M, Li, Leping, Mohrenweiser, Harvey W, Cook, Molly E, Petrovich, Robert M, Bell, Douglas A, Eling, Thomas E, Zeldin, Darryl C

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Cloning of CYP2J2 Gene and Identification of Functional Polymorphisms von King, Lorraine M, Ma, Jixiang, Srettabunjong, Supawon, Graves, Joan, Bradbury, J Alyce, Li, Leping, Spiecker, Martin, Liao, James K, Mohrenweiser, Harvey, Zeldin, Darryl C

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The discovery of new coding alleles of human CYP26A1 that are potentially defective in the metabolism of all-trans retinoic acid and their assessment in a recombinant cDNA expressi... von Lee, Su-Jun, Perera, Lalith, Coulter, Sherry J, Mohrenweiser, Harvey W, Jetten, Anton, Goldstein, Joyce A

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Exploration of methods to identify polymorphisms associated with variation in DNA repair capacity phenotypes von Jones, I M, Thomas, C B, Xi, T, Mohrenweiser, H W, Nelson, DO

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Production and processing of erythropoietin receptor transcripts in brain von Chin, Kyung, Yu, Xiaobing, Beleslin-Cokic, Bojana, Liu, Chun, Shen, Kun, Mohrenweiser, Harvey W, Noguchi, Constance Tom

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Survey of polymorphic sequence variation in the immediate 5' region of human DNA repair genes von Mohrenweiser, H

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