221 related articles for article (PubMed ID: 2332504)
21. Mutations of the androgen receptor coding sequence are infrequent in patients with isolated hypospadias.
Alléra A; Herbst MA; Griffin JE; Wilson JD; Schweikert HU; McPhaul MJ
J Clin Endocrinol Metab; 1995 Sep; 80(9):2697-9. PubMed ID: 7673412
[TBL] [Abstract][Full Text] [Related]
22. Partial androgen insensitivity caused by an androgen receptor mutation at amino acid 907 (Gly-->Arg) that results in decreased ligand binding affinity and reduced androgen receptor messenger ribonucleic acid levels.
Choong CS; Sturm MJ; Strophair JA; McCulloch RK; Tilley WD; Leedman PJ; Hurley DM
J Clin Endocrinol Metab; 1996 Jan; 81(1):236-43. PubMed ID: 8550758
[TBL] [Abstract][Full Text] [Related]
23. Extreme androgen resistance in a kindred with a novel insertion/deletion mutation in exon 5 of the androgen receptor gene.
Vilchis F; Ramos L; Kofman-Alfaro S; Zenteno JC; Méndez JP; Chávez B
J Hum Genet; 2003; 48(7):346-51. PubMed ID: 12908100
[TBL] [Abstract][Full Text] [Related]
24. Mutant androgen receptor detected in an advanced-stage prostatic carcinoma is activated by adrenal androgens and progesterone.
Culig Z; Hobisch A; Cronauer MV; Cato AC; Hittmair A; Radmayr C; Eberle J; Bartsch G; Klocker H
Mol Endocrinol; 1993 Dec; 7(12):1541-50. PubMed ID: 8145761
[TBL] [Abstract][Full Text] [Related]
25. Amino acid substitutions in the hormone-binding domain of the human androgen receptor alter the stability of the hormone receptor complex.
Marcelli M; Zoppi S; Wilson CM; Griffin JE; McPhaul MJ
J Clin Invest; 1994 Oct; 94(4):1642-50. PubMed ID: 7929841
[TBL] [Abstract][Full Text] [Related]
26. A single base deletion in the Tfm androgen receptor gene creates a short-lived messenger RNA that directs internal translation initiation.
Gaspar ML; Meo T; Bourgarel P; Guenet JL; Tosi M
Proc Natl Acad Sci U S A; 1991 Oct; 88(19):8606-10. PubMed ID: 1924321
[TBL] [Abstract][Full Text] [Related]
27. Point mutations detected in the androgen receptor gene of three men with partial androgen insensitivity syndrome.
Saunders PT; Padayachi T; Tincello DG; Shalet SM; Wu FC
Clin Endocrinol (Oxf); 1992 Sep; 37(3):214-20. PubMed ID: 1424203
[TBL] [Abstract][Full Text] [Related]
28. A novel substitution (Leu707Arg) in exon 4 of the androgen receptor gene causes complete androgen resistance.
Lumbroso S; Lobaccaro JM; Georget V; Leger J; Poujol N; Térouanne B; Evain-Brion D; Czernichow P; Sultan C
J Clin Endocrinol Metab; 1996 May; 81(5):1984-8. PubMed ID: 8626869
[TBL] [Abstract][Full Text] [Related]
29. Differential display RT PCR of total RNA from human foreskin fibroblasts for investigation of androgen-dependent gene expression.
Nitsche EM; Moquin A; Adams PS; Guenette RS; Lakins JN; Sinnecker GH; Kruse K; Tenniswood MP
Am J Med Genet; 1996 May; 63(1):231-8. PubMed ID: 8723115
[TBL] [Abstract][Full Text] [Related]
30. A single-base substitution in exon 6 of the androgen receptor gene causing complete androgen insensitivity: the mutated receptor fails to transactivate but binds to DNA in vitro.
Adeyemo O; Kallio PJ; Palvimo JJ; Kontula K; Jänne OA
Hum Mol Genet; 1993 Nov; 2(11):1809-12. PubMed ID: 8281140
[TBL] [Abstract][Full Text] [Related]
31. Substitution of arginine-839 by cysteine or histidine in the androgen receptor causes different receptor phenotypes in cultured cells and coordinate degrees of clinical androgen resistance.
Beitel LK; Kazemi-Esfarjani P; Kaufman M; Lumbroso R; DiGeorge AM; Killinger DW; Trifiro MA; Pinsky L
J Clin Invest; 1994 Aug; 94(2):546-54. PubMed ID: 8040309
[TBL] [Abstract][Full Text] [Related]
32. 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.
Giwercman YL; Nikoshkov A; Byström B; Pousette A ; Arver S; Wedell A
Clin Endocrinol (Oxf); 2001 Jun; 54(6):827-34. PubMed ID: 11422119
[TBL] [Abstract][Full Text] [Related]
33. Premature termination mutation (772Glu-->stop) in the hormone-binding domain of the androgen receptor in a patient with the receptor-negative form of complete androgen insensitivity syndrome.
Imasaki K; Okabe T; Murakami H; Fujita K; Takayanagi R; Nawata H
Endocr J; 1995 Oct; 42(5):643-8. PubMed ID: 8574287
[TBL] [Abstract][Full Text] [Related]
34. Correlation of clinical, endocrine and molecular abnormalities with in vivo responses to high-dose testosterone in patients with partial androgen insensitivity syndrome.
Tincello DG; Saunders PT; Hodgins MB; Simpson NB; Edwards CR; Hargreaves TB; Wu FC
Clin Endocrinol (Oxf); 1997 Apr; 46(4):497-506. PubMed ID: 9196614
[TBL] [Abstract][Full Text] [Related]
35. Phenotypic variation in a family with partial androgen insensitivity syndrome explained by differences in 5alpha dihydrotestosterone availability.
Boehmer AL; Brinkmann AO; Nijman RM; Verleun-Mooijman MC; de Ruiter P; Niermeijer MF; Drop SL
J Clin Endocrinol Metab; 2001 Mar; 86(3):1240-6. PubMed ID: 11238515
[TBL] [Abstract][Full Text] [Related]
36. Heterogeneous mutations in the gene encoding the alpha-subunit of the stimulatory G protein of adenylyl cyclase in Albright hereditary osteodystrophy.
Miric A; Vechio JD; Levine MA
J Clin Endocrinol Metab; 1993 Jun; 76(6):1560-8. PubMed ID: 8388883
[TBL] [Abstract][Full Text] [Related]
37. Immunoreactive androgen receptor expression in subjects with androgen resistance.
Wilson CM; Griffin JE; Wilson JD; Marcelli M; Zoppi S; McPhaul MJ
J Clin Endocrinol Metab; 1992 Dec; 75(6):1474-8. PubMed ID: 1464650
[TBL] [Abstract][Full Text] [Related]
38. Altered mRNA expression due to insertion or substitution of thymine at position +3 of two splice-donor sites in the androgen receptor gene.
Trifiro MA; Lumbroso R; Beitel LK; Vasiliou DM; Bouchard J; Deal C; Van Vliet G; Pinsky L
Eur J Hum Genet; 1997; 5(1):50-8. PubMed ID: 9156321
[TBL] [Abstract][Full Text] [Related]
39. Genetic basis of endocrine disease. 4. The spectrum of mutations in the androgen receptor gene that causes androgen resistance.
McPhaul MJ; Marcelli M; Zoppi S; Griffin JE; Wilson JD
J Clin Endocrinol Metab; 1993 Jan; 76(1):17-23. PubMed ID: 8421085
[TBL] [Abstract][Full Text] [Related]
40. Complete androgen insensitivity syndrome due to a new frameshift deletion in exon 4 of the androgen receptor gene: functional analysis of the mutant receptor.
Lobaccaro JM; Lumbroso S; Poujol N; Georget V; Brinkmann AO; Malpuech G; Sultan C
Mol Cell Endocrinol; 1995 Apr; 111(1):21-8. PubMed ID: 7649349
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
