1 - 25 of 49 results for author:"Mohrenweiser H." in Literature citations
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| Polymorphisms in XPC and ERCC2 genes, smoking and breast cancer risk. Shore R.E., Zeleniuch-Jacquotte A., Currie D., Mohrenweiser H., Afanasyeva Y., Koenig K.L., Arslan A.A., Toniolo P., Wirgin I. Int. J. Cancer 122:2101-2105(2008) · Mapped (14) |
| 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 expression system. Lee S.J., Perera L., Coulter S.J., Mohrenweiser H.W., Jetten A., Goldstein J.A. Pharmacogenet. Genomics 17:169-180(2007) · Mapped (1) |
| Identification and functional characterization of polymorphisms in human cyclooxygenase-1 (PTGS1). Lee C.R., Bottone F.G. Jr., Krahn J.M., Li L., Mohrenweiser H.W., Cook M.E., Petrovich R.M., Bell D.A., Eling T.E., Zeldin D.C. Pharmacogenet. Genomics 17:145-160(2007) · Mapped (7) |
| Analysis of the XRCC1 gene as a modifier of the cerebral response in ischemic stroke. Dutra A.V., Lin H.F., Juo S.H., Mohrenweiser H., Sen S., Grewal R.P. BMC Med. Genet. 7:78-78(2006) · Mapped (5) |
| Four human FANCG polymorphic variants show normal biological function in hamster CHO cells. Hinz J.M., Nham P.B., Yamada N.A., Tebbs R.S., Salazar E.P., Hinz A.K., Mohrenweiser H.W., Jones I.M., Thompson L.H. Mutat. Res. 602:34-42(2006) · Mapped (3) |
| Polymorphisms in nucleotide excision repair genes and risk of multiple primary melanoma: the Genes Environment and Melanoma Study. Millikan R.C., Hummer A., Begg C., Player J., de Cotret A.R., Winkel S., Mohrenweiser H., Thomas N., Armstrong B., Kricker A. et al. Carcinogenesis 27:610-618(2006) · Mapped (33) |
| Functional consequences of single nucleotide polymorphisms in the human organic anion transporter hOAT1 (SLC22A6). Bleasby K., Hall L.A., Perry J.L., Mohrenweiser H.W., Pritchard J.B. J. Pharmacol. Exp. Ther. 314:923-931(2005) · UniProtKB (1) |
| Discovery of new potentially defective alleles of human CYP2C9. Blaisdell J., Jorge-Nebert L.F., Coulter S., Ferguson S.S., Lee S.J., Chanas B., Xi T., Mohrenweiser H., Ghanayem B., Goldstein J.A. Pharmacogenetics 14:527-537(2004) · Mapped (7) |
| A prospective study of XRCC1 haplotypes and their interaction with plasma carotenoids on breast cancer risk. Han J., Hankinson S.E., De Vivo I., Spiegelman D., Tamimi R.M., Mohrenweiser H.W., Colditz G.A., Hunter D.J. Cancer Res. 63:8536-8541(2003) · Mapped (5) |
| DNA-repair genetic polymorphisms and breast cancer risk. Smith T.R., Levine E.A., Perrier N.D., Miller M.S., Freimanis R.I., Lohman K., Case L.D., Xu J., Mohrenweiser H.W., Hu J.J. Cancer Epidemiol. Biomarkers Prev. 12:1200-1204(2003) · Mapped (11) |
| Polymorphisms in the genes encoding members of the tristetraprolin family of human tandem CCCH zinc finger proteins. Blackshear P.J., Phillips R.S., Vazquez-Matias J., Mohrenweiser H. Prog. Nucleic Acid Res. Mol. Biol. 75:43-68(2003) · Mapped (6) |
| Genetic findings and functional studies of human CYP3A5 single nucleotide polymorphisms in different ethnic groups. Lee S.J., Usmani K.A., Chanas B., Ghanayem B., Xi T., Hodgson E., Mohrenweiser H.W., Goldstein J.A. Pharmacogenetics 13:461-472(2003) · UniProtKB (1) · Mapped (11) |
| Polymorphisms in human soluble epoxide hydrolase. Przybyla-Zawislak B.D., Srivastava P.K., Vazquez-Matias J., Mohrenweiser H.W., Maxwell J.E., Hammock B.D., Bradbury J.A., Enayetallah A.E., Zeldin D.C., Grant D.F. Mol. Pharmacol. 64:482-490(2003) · UniProtKB (1) |
| Polymorphisms of XRCC1 and XRCC3 genes and susceptibility to breast cancer. Smith T.R., Miller M.S., Lohman K., Lange E.M., Case L.D., Mohrenweiser H.W., Hu J.J. Cancer Lett. 190:183-190(2003) · Mapped (7) |
| Identification and functional characterization of new potentially defective alleles of human CYP2C19. Blaisdell J., Mohrenweiser H., Jackson J., Ferguson S., Coulter S., Chanas B., Xi T., Ghanayem B., Goldstein J.A. Pharmacogenetics 12:703-711(2002) · UniProtKB (1) |
| Cloning of CYP2J2 gene and identification of functional polymorphisms. King L.M., Ma J., Srettabunjong S., Graves J., Bradbury J.A., Li L., Spiecker M., Liao J.K., Mohrenweiser H., Zeldin D.C. Mol. Pharmacol. 61:840-852(2002) · UniProtKB (1) |
| Modulation of repair of ultraviolet damage in the host-cell reactivation assay by polymorphic XPC and XPD/ERCC2 genotypes. Qiao Y., Spitz M.R., Shen H., Guo Z., Shete S., Hedayati M., Grossman L., Mohrenweiser H., Wei Q. Carcinogenesis 23:295-299(2002) · Mapped (23) |
| Identification of variants of CYP3A4 and characterization of their abilities to metabolize testosterone and chlorpyrifos. Dai D., Tang J., Rose R., Hodgson E., Bienstock R.J., Mohrenweiser H.W., Goldstein J.A. J. Pharmacol. Exp. Ther. 299:825-831(2001) · UniProtKB (1) · Mapped (7) |
| Polymorphisms in the DNA repair gene XRCC1 and breast cancer. Duell E.J., Millikan R.C., Pittman G.S., Winkel S., Lunn R.M., Tse C.K., Eaton A., Mohrenweiser H.W., Newman B., Bell D.A. Cancer Epidemiol. Biomarkers Prev. 10:217-222(2001) · Mapped (5) |
| Modulation of nucleotide excision repair capacity by XPD polymorphisms in lung cancer patients. Spitz M.R., Wu X., Wang Y., Wang L.E., Shete S., Amos C.I., Guo Z., Lei L., Mohrenweiser H., Wei Q. |
| Cloning and characterization of HARP/SMARCAL1: a prokaryotic HepA-related SNF2 helicase protein from human and mouse. Coleman M.A., Eisen J.A., Mohrenweiser H.W. |
| ANOVA, a putative astrocytic RNA binding protein gene that maps to chromosome 19q13.3. Ueki K., Ramaswamy S., Billings S.J., Mohrenweiser H.W., Louis D.N. Neurogenetics 1:31-36(1997) · UniProtKB (1) |
| A transcript map of the chromosome 19q-Arm glioma tumor suppressor region. Smith J.S., Tachibana I., Pohl U., Lee H.K., Thanarajasingam U., Portier B.P., Ueki K., Billings S., Ramaswamy S., Mohrenweiser H.W. et al. Genomics 64:44-50(2000) · UniProtKB (2) |
| EHD2, EHD3, and EHD4 encode novel members of a highly conserved family of EH domain-containing proteins. Pohl U., Smith J.S., Tachibana I., Ueki K., Lee H.K., Ramaswamy S., Wu Q., Mohrenweiser H.W., Jenkins R.B., Louis D.N. |
| Human hydroxysteroid sulfotransferase SULT2B1: two enzymes encoded by a single chromosome 19 gene. Her C., Wood T.C., Eichler E.E., Mohrenweiser H.W., Ramagli L.S., Siciliano M.J., Weinshilboum R.M. Genomics 53:284-295(1998) · UniProtKB (1) |