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Evidence for a repressive function of the long polyglutamine tract in the human androgen receptor: possible pathogenetic relevance for the (CAG)n-expanded neuronopathies

Human molecular genetics, 1995-04, Vol.4 (4), p.523-527

1995

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Interactions between androgen and estrogen receptors and the effects on their transactivational properties

Molecular and cellular endocrinology, 2000-09, Vol.167 (1), p.139-150

2000

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Reduced transcriptional regulatory competence of the androgen receptor in X-linked spinal and bulbar muscular atrophy

Nature genetics, 1993-10, Vol.5 (2), p.184-188

1993

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The Androgen Receptor Gene Mutations Database

Nucleic acids research, 1998-01, Vol.26 (1), p.234

1998

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Kennedy's disease : Caspase cleavage of the androgen receptor is a crucial event in cytotoxicity

Journal of neurochemistry, 1999, Vol.72 (1), p.185-195

1999

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Update of the androgen receptor gene mutations database

Human mutation, 1999, Vol.14 (2), p.103-114

1999

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The polymorphic CAG repeat of the androgen receptor gene: a potential role in breast cancer in women over 40

Breast cancer research and treatment, 2001-11, Vol.70 (2), p.109-116

2001

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The androgen receptor gene mutations database

Nucleic acids research, 1997-01, Vol.25 (1), p.158

1997

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Cytochrome c oxidase subunit Vb interacts with human androgen receptor: A potential mechanism for neurotoxicity in spinobulbar muscular atrophy

Brain research bulletin, 2001-11, Vol.56 (3-4), p.285-297

2001

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Oligospermic infertility associated with an androgen receptor mutation that disrupts interdomain and coactivator (TIF2) interactions

The Journal of clinical investigation, 1999-06, Vol.103 (11), p.1517-1525

1999

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Spinobulbar Muscular Atrophy: Polyglutamine-expanded Androgen Receptor Is Proteolytically Resistant in Vitro and Processed Abnormally in Transfected Cells

Human molecular genetics, 1998-03, Vol.7 (3), p.379-384

1998

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The androgen receptor gene mutations database

Nucleic acids research, 1996-01, Vol.24 (1), p.151

1996

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A G577R Mutation in the Human AR P Box Results in Selective Decreases in DNA Binding and in Partial Androgen Insensitivity Syndrome

Molecular endocrinology (Baltimore, Md.), 2001-10, Vol.15 (10), p.1790-1802

2001

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Analysis of exon 1 mutations in the androgen receptor gene

Human mutation, 1999-01, Vol.14 (6), p.527-539

1999

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Discordant measures of androgen-binding kinetics in two mutant androgen receptors causing mild or partial androgen insensitivity, respectively

The journal of clinical endocrinology and metabolism, 1999-02, Vol.84 (2), p.805-810

1999

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The androgen receptor gene mutations database

Nucleic acids research, 1994-09, Vol.22 (17), p.3560-3562

1994

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Replacement of arginine 773 by cysteine of histidine in the human androgen receptor causes complete androgen insensitivity with different receptor phenotypes

American journal of human genetics, 1992-07, Vol.51 (1), p.143-155

1992

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Substitution of valine-865 by methionine or leucine in the human androgen receptor causes complete or partial androgen insensitivity, respectively with distinct androgen receptor phenotypes

Molecular endocrinology (Baltimore, Md.), 1993, Vol.7 (1), p.37-46

1993

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Complete androgen insensitivity due to mutations in the probable α-helical segments of the DNA-binding domain in the human androgen receptor

Human molecular genetics, 1994-01, Vol.3 (1), p.21-27

1994

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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

The Journal of clinical investigation, 1994-08, Vol.94 (2), p.546-554

1994

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Codon-usage variants in the polymorphic (GGN)n trinucleotide repeat of the human androgen receptor gene

Human genetics, 1997-11, Vol.101 (1), p.43-46

1997

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An exonic point mutation of the androgen receptor gene in a family with complete androgen insensitivity

American journal of human genetics, 1990-06, Vol.46 (6), p.1095-1100

1990

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Altered mRNA expression due to insertion or substitution of thymine at position +3 of two splice-donor sites in the androgen receptor gene

European journal of human genetics : EJHG, 1997-01, Vol.5 (1), p.50-58

1997

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Characterization of alternative amino acid substitutions at arginine 830 of the androgen receptor that cause complete androgen insensitivity in three families

Human molecular genetics, 1995-04, Vol.4 (4), p.515-521

1995

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The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene

Molecular and cellular endocrinology, 1991, Vol.75 (1), p.37-47

1991

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Evidence for a repressive function of the long polyglutamine tract in the human androgen receptor: possible pathogenetic relevance for the (CAG)n-expanded neuronopathies

Interactions between androgen and estrogen receptors and the effects on their transactivational properties

Reduced transcriptional regulatory competence of the androgen receptor in X-linked spinal and bulbar muscular atrophy

The Androgen Receptor Gene Mutations Database

Kennedy's disease : Caspase cleavage of the androgen receptor is a crucial event in cytotoxicity

Update of the androgen receptor gene mutations database

The polymorphic CAG repeat of the androgen receptor gene: a potential role in breast cancer in women over 40

The androgen receptor gene mutations database

Cytochrome c oxidase subunit Vb interacts with human androgen receptor: A potential mechanism for neurotoxicity in spinobulbar muscular atrophy

Oligospermic infertility associated with an androgen receptor mutation that disrupts interdomain and coactivator (TIF2) interactions

Spinobulbar Muscular Atrophy: Polyglutamine-expanded Androgen Receptor Is Proteolytically Resistant in Vitro and Processed Abnormally in Transfected Cells

The androgen receptor gene mutations database

A G577R Mutation in the Human AR P Box Results in Selective Decreases in DNA Binding and in Partial Androgen Insensitivity Syndrome

Analysis of exon 1 mutations in the androgen receptor gene

Discordant measures of androgen-binding kinetics in two mutant androgen receptors causing mild or partial androgen insensitivity, respectively

The androgen receptor gene mutations database

Replacement of arginine 773 by cysteine of histidine in the human androgen receptor causes complete androgen insensitivity with different receptor phenotypes

Substitution of valine-865 by methionine or leucine in the human androgen receptor causes complete or partial androgen insensitivity, respectively with distinct androgen receptor phenotypes

Complete androgen insensitivity due to mutations in the probable α-helical segments of the DNA-binding domain in the human androgen receptor

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

Codon-usage variants in the polymorphic (GGN)n trinucleotide repeat of the human androgen receptor gene

An exonic point mutation of the androgen receptor gene in a family with complete androgen insensitivity

Altered mRNA expression due to insertion or substitution of thymine at position +3 of two splice-donor sites in the androgen receptor gene

Characterization of alternative amino acid substitutions at arginine 830 of the androgen receptor that cause complete androgen insensitivity in three families

The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene

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