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Results: 1-9 |
Results: 9

Authors: Hess, JF Hey, PJ Chen, TB O'Brien, J Omalley, SS Pettibone, DJ Chang, RSL
Citation: Jf. Hess et al., Molecular cloning and pharmacological characterization of the canine B1 and B2 bradykinin receptors, BIOL CHEM, 382(1), 2001, pp. 123-129

Authors: Twells, RCJ Metzker, ML Brown, SD Cox, R Garey, C Hammond, H Hey, PJ Levy, E Nakagawa, Y Philips, MS Todd, JA Hess, JF
Citation: Rcj. Twells et al., The sequence and gene characterization of a 400-kb candidate region for IDDM4 on chromosome 11q13, GENOMICS, 72(3), 2001, pp. 231-242

Authors: Hess, JF Casselman, JT FitzGerald, P
Citation: Jf. Hess et al., Modified version of pACT-2 that simplifies cloning with NdeI, BIOTECHNIQU, 30(6), 2001, pp. 1204

Authors: Blankenship, TN Hess, JF FitzGerald, PG
Citation: Tn. Blankenship et al., Development- and differentiation-dependent reorganization of intermediate filaments in fiber cells, INV OPHTH V, 42(3), 2001, pp. 735-742

Authors: Angelos, JA Hess, JF George, LW
Citation: Ja. Angelos et al., Cloning and characterization of a Moraxella bovis cytotoxin gene, AM J VET RE, 62(8), 2001, pp. 1222-1228

Authors: Lyons, PA Hancock, WW Denny, P Lord, CJ Hill, NJ Armitage, N Siegmund, T Todd, JA Phillips, MS Hess, JF Chen, SL Fischer, PA Peterson, LB Wicker, LS
Citation: Pa. Lyons et al., The NOD Idd9 genetic interval influences the pathogenicity of insulitis and contains molecular variants of Cd30, Tnfr2, and Cd137, IMMUNITY, 13(1), 2000, pp. 107-115

Authors: Figueroa, DJ Hess, JF Ky, B Brown, SD Sandig, V Hermanowski-Vosatka, A Twells, RCJ Todd, JA Austin, CP
Citation: Dj. Figueroa et al., Expression of the Type I diabetes-associated gene LRP5 in macrophages, vitamin A system cells, and the islets of Langerhans suggests multiple potential roles in diabetes, J HIST CYTO, 48(10), 2000, pp. 1357-1368

Authors: Conley, YP Erturk, D Keverline, A Mah, TS Keravala, A Barnes, LR Bruchis, A Hess, JF FitzGerald, PG Weeks, DE Ferrell, RE Gorin, MB
Citation: Yp. Conley et al., A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2, AM J HU GEN, 66(4), 2000, pp. 1426-1431

Authors: Jakobs, PM Hess, JF FitzGerald, PG Kramer, P Weleber, RG Litt, M
Citation: Pm. Jakobs et al., Autosomal-dominant congenital cataract associated with a deletion mutationin the human beaded filament protein gene BFSP2, AM J HU GEN, 66(4), 2000, pp. 1432-1436
Risultati: 1-9 |