AAAAAA

   
Results: 1-7 |
Results: 7
A novel mutation (N233K) in the transactivating domain and the N756S mutation in the ligand binding domain of the androgen receptor gene are associated with male infertility
Authors: Giwercman, YL Nikoshkov, A Bystrom, B Pousette, A Arver, S Wedell, A
Citation: Yl. Giwercman et al., A novel mutation (N233K) in the transactivating domain and the N756S mutation in the ligand binding domain of the androgen receptor gene are associated with male infertility, CLIN ENDOCR, 54(6), 2001, pp. 827-834
Insulin-degrading enzyme identified as a candidate diabetes susceptibilitygene in GK rats
Authors: Fakhrai-Rad, H Nikoshkov, A Kamel, A Fernstrom, M Zierath, JR Norgren, S Luthman, H Galli, J
Citation: H. Fakhrai-rad et al., Insulin-degrading enzyme identified as a candidate diabetes susceptibilitygene in GK rats, HUM MOL GEN, 9(14), 2000, pp. 2149-2158
Response to treatment in patients with partial androgen insensitivity due to mutations in the DNA-binding domain of the androgen receptor
Authors: Giwercman, YL Nikoshkov, A Lindsten, K Bystrom, B Pousette, A Knudtzon, J Alm, J Wedell, A
Citation: Yl. Giwercman et al., Response to treatment in patients with partial androgen insensitivity due to mutations in the DNA-binding domain of the androgen receptor, HORMONE RES, 53(2), 2000, pp. 83-88
A new locus for autosomal recessive hypercholesterolemia maps to human chromosome 15q25-q26
Authors: Ciccarese, M Pacifico, A Tonolo, G Pintus, P Nikoshkov, A Zuliani, G Fellin, R Luthman, H Maioli, M
Citation: M. Ciccarese et al., A new locus for autosomal recessive hypercholesterolemia maps to human chromosome 15q25-q26, AM J HU GEN, 66(2), 2000, pp. 453-460
A conformation-dependent epitope in Addison's disease and other endocrinological autoimmune diseases maps to a carboxyl-terminal functional domain ofhuman steroid 21-hydroxylase
Authors: Nikoshkov, A Falorni, A Lajic, S Laureti, S Wedell, A Lernmark, A Luthman, H
Citation: A. Nikoshkov et al., A conformation-dependent epitope in Addison's disease and other endocrinological autoimmune diseases maps to a carboxyl-terminal functional domain ofhuman steroid 21-hydroxylase, J IMMUNOL, 162(4), 1999, pp. 2422-2426
Effects of missense mutations and deletions on membrane anchoring and enzyme function of human steroid 21-hydroxylase (P450c21)
Authors: Lajic, S Nikoshkov, A Holst, M Wedell, A
Citation: S. Lajic et al., Effects of missense mutations and deletions on membrane anchoring and enzyme function of human steroid 21-hydroxylase (P450c21), BIOC BIOP R, 257(2), 1999, pp. 384-390
Functional characterisation of mutations in the ligand-binding domain of the androgen receptor gene in patients with androgen insensitivity syndrome
Authors: Giwercman, YL Nikoshkov, A Lindsten, K Bystrom, B Pousette, A Chibalin, AV Arvidsson, S Tiulpakov, A Semitcheva, TV Peterkova, V Hagenfeldt, K Ritzen, EM Wedell, A
Citation: Yl. Giwercman et al., Functional characterisation of mutations in the ligand-binding domain of the androgen receptor gene in patients with androgen insensitivity syndrome, HUM GENET, 103(4), 1998, pp. 529-531
Risultati: 1-7 |