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Results: 1-8 |
Results: 8

Authors: Winterton, DL Kaufman, J Keener, CV Quigley, S Farin, FM Williams, PV Koenig, JQ
Citation: Dl. Winterton et al., Genetic polymorphisms as biomarkers of sensitivity to inhaled sulfur dioxide in subjects with asthma, ANN ALLER A, 86(2), 2001, pp. 232-238

Authors: Kim, HS Newcomb, PA Ulrich, CM Keener, CL Bigler, J Farin, FM Bostick, RM Potter, JD
Citation: Hs. Kim et al., Vitamin D receptor polymorphism and the risk of colorectal adenomas: Evidence of interaction with dietary vitamin D and calcium, CANC EPID B, 10(8), 2001, pp. 869-874

Authors: Farin, FM Janssen, P Quigley, S Abbott, D Hassett, C Smith-Weller, T Franklin, GM Swanson, PD Longstreth, WT Omiecinski, CJ Checkoway, H
Citation: Fm. Farin et al., Genetic polymorphisms of microsomal and soluble epoxide hydrolase and the risk of Parkinson's disease, PHARMACOGEN, 11(8), 2001, pp. 703-708

Authors: Farin, FM Hitosis, Y Hallagan, SE Kushleika, J Woods, JS Janssen, PS Smith-Weller, T Franklin, GM Swanson, PD Checkoway, H
Citation: Fm. Farin et al., Genetic polymorphisms of superoxide dismutase in Parkinson's disease, MOVEMENT D, 16(4), 2001, pp. 705-707

Authors: Diaz, D Krejsa, CM White, CC Keener, CL Farin, FM Kavanagh, TJ
Citation: D. Diaz et al., Tissue specific changes in the expression of glutamate-cysteine ligase mRNAs in mice exposed to methylmercury, TOX LETT, 122(2), 2001, pp. 119-129

Authors: Ulrich, CM Yasui, Y Storb, R Schubert, MM Wagner, JL Bigler, J Ariail, KS Keener, CL Li, S Liu, H Farin, FM Potter, JD
Citation: Cm. Ulrich et al., Pharmacogenetics of methotrexate: toxicity among marrow transplantation patients varies with the methylenetetrahydrofolate reductase C677T polymorphism, BLOOD, 98(1), 2001, pp. 231-234

Authors: Ulrich, CM Bigler, J Velicer, CM Greene, EA Farin, FM Potter, JD
Citation: Cm. Ulrich et al., Searching expressed sequence tag databases: Discovery and confirmation of a common polymorphism in the Thymidylate synthase gene, CANC EPID B, 9(12), 2000, pp. 1381-1385

Authors: Kirchner, SC Hallagan, SE Farin, FM Dilley, J Costa-Mallen, P Smith-Weller, T Franklin, GM Swanson, PD Checkoway, H
Citation: Sc. Kirchner et al., Mitochondrial ND1 sequence analysis and association of the T4216C mutationwith Parkinson's disease, NEUROTOXICO, 21(4), 2000, pp. 441-445
Risultati: 1-8 |