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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.234-238

1998

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The Use of Androgen Receptor Amino/Carboxyl-Terminal Interaction Assays to Investigate Androgen Receptor Gene Mutations in Subjects with Varying Degrees of Androgen Insensitivity

The journal of clinical endocrinology and metabolism, 2003-05, Vol.88 (5), p.2185-2193

2003

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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 androgen receptor gene mutations database

Nucleic acids research, 1997-01, Vol.25 (1), p.158-162

1997

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The androgen receptor gene mutations database

Nucleic acids research, 1996-01, Vol.24 (1), p.151-154

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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The androgen receptor gene mutations database

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

1994

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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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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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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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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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The state transitions of normal and mutant androgen-receptor complexes in human genital skin fibroblasts

Journal of steroid biochemistry, 1990-08, Vol.36 (6), p.651-657

1990

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Androgen insensitivity

American journal of medical genetics, 1999-12, Vol.89 (4), p.210-217

1999

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Amber mutation creates a diagnostic MaeI site in the androgen receptor gene of a family with complete androgen insensitivity

American journal of medical genetics, 1991-09, Vol.40 (4), p.493-499

1991

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Multiplexed identification, quantification and genotyping of infectious agents using a semiconductor biochip

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

The Androgen Receptor Gene Mutations Database

The Use of Androgen Receptor Amino/Carboxyl-Terminal Interaction Assays to Investigate Androgen Receptor Gene Mutations in Subjects with Varying Degrees of Androgen Insensitivity

Update of the androgen receptor gene mutations database

The androgen receptor gene mutations database

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

The androgen receptor gene mutations database

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

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

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

The state transitions of normal and mutant androgen-receptor complexes in human genital skin fibroblasts

Androgen insensitivity

Amber mutation creates a diagnostic MaeI site in the androgen receptor gene of a family with complete androgen insensitivity

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