Trinucleotide (CAG) repeat polymorphisms in the androgen receptor gene: molecular markers of risk for male infertility
- 1 February 2001
- journal article
- research article
- Published by Elsevier in Fertility and Sterility
- Vol. 75 (2) , 275-281
- https://doi.org/10.1016/s0015-0282(00)01693-9
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Analysis of the transactivation domain of the androgen receptor in patients with male infertilitvClinical Genetics, 2008
- Oligospermic infertility associated with an androgen receptor mutation that disrupts interdomain and coactivator (TIF2) interactionsJournal of Clinical Investigation, 1999
- Absence of DAZ gene mutations in cases of non-obstructed azoospermiaMolecular Human Reproduction, 1997
- The length and location of CAG trinucleotide repeats in the androgen receptor N-terminal domain affect transactivation functionNucleic Acids Research, 1994
- Reduced transcriptional regulatory competence of the androgen receptor in X–linked spinal and bulbar muscular atrophyNature Genetics, 1993
- Kennedy's diseaseNeurology, 1993
- Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groupsGenomics, 1992
- Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophyNature, 1991
- Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.Proceedings of the National Academy of Sciences, 1989
- A family with adult spinal and bulbar muscular atrophy, X-linked inheritance and associated testicular failureJournal of the Neurological Sciences, 1983