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Results: 1-8 |
Results: 8
A G577R mutation in the human AR P box results in selective decreases in DNA binding and in partial androgen insensitivity syndrome
Authors: Nguyen, D Steinberg, SV Rouault, E Chagnon, S Gottlieb, B Pinsky, L Trifiro, M Mader, S
Citation: D. Nguyen et al., A G577R mutation in the human AR P box results in selective decreases in DNA binding and in partial androgen insensitivity syndrome, MOL ENDOCR, 15(10), 2001, pp. 1790-1802
Post-zygotic mutations and somatic mosaicism in androgen insensitivity syndrome - Response
Authors: Gottlieb, B Beltel, LK Trifiro, M
Citation: B. Gottlieb et al., Post-zygotic mutations and somatic mosaicism in androgen insensitivity syndrome - Response, TRENDS GEN, 17(11), 2001, pp. 628-628
Testosterone-mediated neuroprotection through the androgen receptor in human primary neurons
Authors: Hammond, J Le, Q Goodyer, C Gelfand, M Trifiro, M LeBlanc, A
Citation: J. Hammond et al., Testosterone-mediated neuroprotection through the androgen receptor in human primary neurons, J NEUROCHEM, 77(5), 2001, pp. 1319-1326
Human androgen receptor mutation disrupts ternary interactions between ligand, receptor domains, and the coactivator TIF2 (transcription intermediaryfactor 2)
Authors: Lim, J Ghadessy, FJ Abdullah, AAR Pinsky, L Trifiro, M Yong, EL
Citation: J. Lim et al., Human androgen receptor mutation disrupts ternary interactions between ligand, receptor domains, and the coactivator TIF2 (transcription intermediaryfactor 2), MOL ENDOCR, 14(8), 2000, pp. 1187-1197
Update of the androgen receptor gene mutations database
Authors: Gottlieb, B Beitel, LK Lumbroso, R Pinsky, L Trifiro, M
Citation: B. Gottlieb et al., Update of the androgen receptor gene mutations database, HUM MUTAT, 14(2), 1999, pp. 103-114
Androgen insensitivity
Authors: Gottlieb, B Pinsky, L Beitel, LK Trifiro, M
Citation: B. Gottlieb et al., Androgen insensitivity, AM J MED G, 89(4), 1999, pp. 210-217
A missense mutation in both hMSH2 and APC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening
Authors: Yuan, ZQ Wong, N Foulkes, WD Alpert, L Manganaro, F Andreutti-Zaugg, C Iggo, R Anthony, K Hsieh, E Redston, M Pinsky, L Trifiro, M Gordon, PH Lasko, D
Citation: Zq. Yuan et al., A missense mutation in both hMSH2 and APC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening, J MED GENET, 36(10), 1999, pp. 790-793
The effect of the I1307K APC polymorphism on the clinicopathological features and natural history of breast cancer
Authors: Yuan, ZQ Begin, LR Wong, N Brunet, JS Trifiro, M Gordon, PH Pinsky, L Foulkes, WD
Citation: Zq. Yuan et al., The effect of the I1307K APC polymorphism on the clinicopathological features and natural history of breast cancer, BR J CANC, 81(5), 1999, pp. 850-854
Risultati: 1-8 |