Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 73

1.

The androgen receptor gene mutations database.

Patterson MN, Hughes IA, Gottlieb B, Pinsky L.

Nucleic Acids Res. 1994 Sep;22(17):3560-2.

2.

The androgen receptor gene mutations database.

Gottlieb B, Trifiro M, Lumbroso R, Pinsky L.

Nucleic Acids Res. 1997 Jan 1;25(1):158-62.

3.

The androgen receptor gene mutations database.

Gottlieb B, Trifiro M, Lumbroso R, Vasiliou DM, Pinsky L.

Nucleic Acids Res. 1996 Jan 1;24(1):151-4.

4.

Update of the androgen receptor gene mutations database.

Gottlieb B, Beitel LK, Lumbroso R, Pinsky L, Trifiro M.

Hum Mutat. 1999;14(2):103-14.

PMID:
10425033
5.

The androgen receptor gene mutations database (ARDB): 2004 update.

Gottlieb B, Beitel LK, Wu JH, Trifiro M.

Hum Mutat. 2004 Jun;23(6):527-33. Erratum in: Hum Mutat. 2004 Jul;24(1):102.

PMID:
15146455
6.

The Androgen Receptor Gene Mutations Database.

Gottlieb B, Lehvaslaiho H, Beitel LK, Lumbroso R, Pinsky L, Trifiro M.

Nucleic Acids Res. 1998 Jan 1;26(1):234-8.

7.

Mutations of androgen receptor gene in androgen insensitivity syndromes.

Sultan C, Lumbroso S, Poujol N, Belon C, Boudon C, Lobaccaro JM.

J Steroid Biochem Mol Biol. 1993 Nov;46(5):519-30. Review.

PMID:
8240973
8.

[Androgen insensitivity syndrome. Clinical features and molecular genetics].

Sólyom J, Scheiber D, Fekete G.

Orv Hetil. 2001 Aug 5;142(31):1659-65. Review. Hungarian.

PMID:
11556259
9.

Variable expressivity and mutation databases: The androgen receptor gene mutations database.

Gottlieb B, Beitel LK, Trifiro MA.

Hum Mutat. 2001 May;17(5):382-8.

PMID:
11317353
10.

Correlation between genotype, phenotype and sex of rearing in 111 patients with partial androgen insensitivity syndrome.

Deeb A, Mason C, Lee YS, Hughes IA.

Clin Endocrinol (Oxf). 2005 Jul;63(1):56-62.

PMID:
15963062
11.

Novel androgen receptor gene mutations in Australian patients with complete androgen insensitivity syndrome.

MacLean HE, Ball EM, Rekaris G, Warne GL, Zajac JD.

Hum Mutat. 2004 Mar;23(3):287.

PMID:
14974091
12.

Comparison of the molecular consequences of different mutations at residue 754 and 690 of the androgen receptor (AR) and androgen insensitivity syndrome (AIS) phenotype.

Tadokoro R, Bunch T, Schwabe JW, Hughes IA, Murphy JC.

Clin Endocrinol (Oxf). 2009 Aug;71(2):253-60. doi: 10.1111/j.1365-2265.2008.03462.x. Epub 2008 Oct 26.

PMID:
19178528
13.

Eight novel mutations of the androgen receptor gene in patients with androgen insensitivity syndrome.

Chávez B, Méndez JP, Ulloa-Aguirre A, Larrea F, Vilchis F.

J Hum Genet. 2001;46(10):560-5.

PMID:
11587068
14.

The androgen receptor gene mutations database: 2012 update.

Gottlieb B, Beitel LK, Nadarajah A, Paliouras M, Trifiro M.

Hum Mutat. 2012 May;33(5):887-94. doi: 10.1002/humu.22046. Epub 2012 Mar 13.

PMID:
22334387
15.

Androgen receptor mutations and androgen insensitivity.

McPhaul MJ.

Mol Cell Endocrinol. 2002 Dec 30;198(1-2):61-7. Review.

PMID:
12573815
16.

Functional analysis of six androgen receptor mutations identified in patients with partial androgen insensitivity syndrome.

Bevan CL, Brown BB, Davies HR, Evans BA, Hughes IA, Patterson MN.

Hum Mol Genet. 1996 Feb;5(2):265-73.

PMID:
8824883
17.

Molecular basis of androgen insensitivity.

Brüggenwirth HT, Boehmer AL, Verleun-Mooijman MC, Hoogenboezem T, Kleijer WJ, Otten BJ, Trapman J, Brinkmann AO.

J Steroid Biochem Mol Biol. 1996 Aug;58(5-6):569-75.

PMID:
8918984
18.

Functional characterisation of mutations in the ligand-binding domain of the androgen receptor gene in patients with androgen insensitivity syndrome.

Lundberg Giwercman Y, Nikoshkov A, Lindsten K, Byström B, Pousette A, Chibalin AV, Arvidsson S, Tiulpakov A, Semitcheva TV, Peterkova V, Hagenfeldt K, Ritzén EM, Wedell A.

Hum Genet. 1998 Oct;103(4):529-31.

PMID:
9856504
19.

[Deletion of thymine at position 2298 in exon 5 of the androgenic receptor gene causing complete androgen insensitivity syndrome].

Soriano Guillén L, Muñoz Calvo MT, Martinez Pérez J, Pozo Román J, Martín Sobrino MA, González Medeiro I, Argente Oliver J.

An Esp Pediatr. 2002 Apr;56(4):347-52. Spanish.

PMID:
11927080
20.

The human FOXL2 mutation database.

Beysen D, Vandesompele J, Messiaen L, De Paepe A, De Baere E.

Hum Mutat. 2004 Sep;24(3):189-93.

PMID:
15300845

Supplemental Content

Support Center