Title : Point mutation in the DNA binding domain of the androgen receptor in two families with Reifenstein syndrome.

Pub. Date : 1992 Jun

PMID : 1598912






7 Functional Relationships(s)
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1 We have analyzed the androgen receptor (AR) gene in male pseudohermaphrodites with normal specific binding of dihydrotestosterone in their genital skin fibroblasts. Dihydrotestosterone androgen receptor Homo sapiens
2 We have analyzed the androgen receptor (AR) gene in male pseudohermaphrodites with normal specific binding of dihydrotestosterone in their genital skin fibroblasts. Dihydrotestosterone androgen receptor Homo sapiens
3 The mutation is a guanine-to-adenine transition at nucleotide 2314, which changes the alanine codon (GCC) immediately after the first cysteine of the second zinc finger motif of the AR into a threonine codon (ACC). Guanine androgen receptor Homo sapiens
4 The mutation is a guanine-to-adenine transition at nucleotide 2314, which changes the alanine codon (GCC) immediately after the first cysteine of the second zinc finger motif of the AR into a threonine codon (ACC). Adenine androgen receptor Homo sapiens
5 The mutation is a guanine-to-adenine transition at nucleotide 2314, which changes the alanine codon (GCC) immediately after the first cysteine of the second zinc finger motif of the AR into a threonine codon (ACC). Alanine androgen receptor Homo sapiens
6 The mutation is a guanine-to-adenine transition at nucleotide 2314, which changes the alanine codon (GCC) immediately after the first cysteine of the second zinc finger motif of the AR into a threonine codon (ACC). Cysteine androgen receptor Homo sapiens
7 The mutation is a guanine-to-adenine transition at nucleotide 2314, which changes the alanine codon (GCC) immediately after the first cysteine of the second zinc finger motif of the AR into a threonine codon (ACC). Threonine androgen receptor Homo sapiens