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Results: 1-14 |
Results: 14

Authors: Haider, NB Naggert, JK Nishina, PM
Citation: Nb. Haider et al., Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice, HUM MOL GEN, 10(16), 2001, pp. 1619-1626

Authors: Ikeda, A Ikeda, S Gridley, T Nishina, PM Naggert, JK
Citation: A. Ikeda et al., Neural tube defects and neuroepithelial cell death in Tulp3 knockout mice, HUM MOL GEN, 10(12), 2001, pp. 1325-1334

Authors: Kim, JH Sen, S Avery, CS Simpson, E Chandler, P Nishina, PM Churchill, GA Naggert, JK
Citation: Jh. Kim et al., Genetic analysis of a new mouse model for non-insulin-dependent diabetes, GENOMICS, 74(3), 2001, pp. 273-286

Authors: Bronson, RT Donahue, LR Samples, R Naggert, JK
Citation: Rt. Bronson et al., Mice with mutations in the mahogany gene Atrn have cerebral spongiform changes, J NE EXP NE, 60(7), 2001, pp. 724-730

Authors: Ikeda, S Shiva, N Ikeda, A Smith, RS Nusinowitz, S Yan, G Lin, TR Chu, S Heckenlively, JR North, MA Naggert, JK Nishina, PM Duyao, MP
Citation: S. Ikeda et al., Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene, HUM MOL GEN, 9(2), 2000, pp. 155-163

Authors: He, W Ikeda, S Bronson, RT Yan, G Nishina, PM North, MA Naggert, JK
Citation: W. He et al., GFP-tagged expression and immunohistochemical studies to determine the subcellular localization of the tubby gene family members, MOL BRAIN R, 81(1-2), 2000, pp. 109-117

Authors: Leiter, EH Kintner, J Flurkey, K Beamer, WG Naggert, JK
Citation: Eh. Leiter et al., Physiologic and endocrinologic characterization of male sex-biased diabetes in C57BLKS/J mice congenic for the fat mutation at the carboxypeptidease E locus, ENDOCRINE, 10(1), 1999, pp. 57-66

Authors: Ikeda, A Zheng, QY Rosenstiel, P Maddatu, T Zuberi, AR Roopenian, DC North, MA Naggert, JK Johnson, KR Nishina, PM
Citation: A. Ikeda et al., Genetic modification of heaving in tubby mice: evidence for the existence of a major gene (moth1) which protects tubby mice from hearing loss, HUM MOL GEN, 8(9), 1999, pp. 1761-1767

Authors: York, B Truett, AA Monteiro, MP Barry, SJ Warden, CH Naggert, JK Maddatu, TP West, DB
Citation: B. York et al., Gene-environment interaction: a significant diet-dependent obesity locus demonstrated in a congenic segment on mouse Chromosome 7, MAMM GENOME, 10(5), 1999, pp. 457-462

Authors: Collin, GB Marshall, JD Boerkoel, CF Levin, AV Weksberg, R Greenberg, J Michaud, JL Naggert, JK Nishina, PM
Citation: Gb. Collin et al., Alstrom syndrome: further evidence for linkage to human chromosome 2p13, HUM GENET, 105(5), 1999, pp. 474-479

Authors: Ikeda, S He, W Ikeda, A Naggert, JK North, MA Nishina, PM
Citation: S. Ikeda et al., Cell-specific expression of tubby gene family members (tub, Tulp1, 2, and 3) in the retina, INV OPHTH V, 40(11), 1999, pp. 2706-2712

Authors: Mu, JL Naggert, JK Svenson, KL Collin, GB Kim, JH McFarland, C Nishina, PM Levine, DM Williams, KJ Paigen, B
Citation: Jl. Mu et al., Quantitative trait loci analysis for the differences in susceptibility to atherosclerosis and diabetes between inbred mouse strains C57BL/6J and C57BLKS/J, J LIPID RES, 40(7), 1999, pp. 1328-1335

Authors: Collin, GB Marshall, JD Naggert, JK Nishina, PM
Citation: Gb. Collin et al., TGFA: exon-intron structure and evaluation as a candidate gene for Alstromsyndrome, CLIN GENET, 55(1), 1999, pp. 61-62

Authors: Nishina, PM North, MA Ikeda, A Yan, YZ Naggert, JK
Citation: Pm. Nishina et al., Molecular characterization of a novel tubby gene family member, TULP3, in mouse and humans, GENOMICS, 54(2), 1998, pp. 215-220
Risultati: 1-14 |