Cytogenetic and molecular analysis of the Y chromosome: absence of a significant relationship between CAG repeat length in exon 1 of the androgen receptor gene and infertility in Indian men (Q44597376)

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scientific article published on October 1, 2003

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English	Cytogenetic and molecular analysis of the Y chromosome: absence of a significant relationship between CAG repeat length in exon 1 of the androgen receptor gene and infertility in Indian men	scientific article published on October 1, 2003

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scholarly article

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4 December 2017

Cytogenetic and molecular analysis of the Y chromosome: absence of a significant relationship between CAG repeat length in exon 1 of the androgen receptor gene and infertility in Indian men (English)

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10.1046/J.1365-2605.2003.00425.X

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trinucleotide repeats

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Varinderpal S. Dhillon

1

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Syed A. Husain

2

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publication date

1 October 2003

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https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2605.2003.00425.x

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International Journal of Andrology

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286-295

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4 December 2017

A family with adult spinal and bulbar muscular atrophy, X-linked inheritance and associated testicular failure

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Detection of azoospermic factor genes in Chinese men with azoospermia or severe oligozoospermia

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The size of the CAG repeat in exon 1 of the androgen receptor gene shows no significant relationship to impaired spermatogenesis in an infertile Caucasoid sample of German origin

1 reference

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Linkage between male infertility and trinucleotide repeat expansion in the androgen-receptor gene

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High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia

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DAZ (Deleted in AZoospermia) genes encode proteins located in human late spermatids and in sperm tails

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Transmission of Y chromosomal microdeletions from father to son through intracytoplasmic sperm injection.

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Association of oestrogen receptor alpha polymorphisms and androgen receptor CAG trinucleotide repeats with male infertility: a study in 109 Greek infertile men.

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Y chromosome microdeletions, in azoospermic or near-azoospermic subjects, are located in the AZFc (DAZ) subregion

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Genotyping of Israeli infertile men with idiopathic oligozoospermia

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CAG repeat length in androgen-receptor gene and reproductive variables in fertile and infertile men.

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Molecular analysis of the Y chromosome AZFc region in Japanese infertile males with spermatogenic defects.

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A comparative study of Y chromosome microdeletions in infertile males from two Chinese populations

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Human chromosome deletions in Yq11, AZF candidate genes and male infertility: history and update

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Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11

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Rapid and accurate determination of (CAG)n repeats in the androgen receptor gene using polymerase chain reaction and automated fragment analysis

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Transmission of de novo mutations of the deleted in azoospermia genes from a severely oligozoospermic male to a son via intracytoplasmic sperm injection

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Genetic screening for patients with azoospermia and severe oligo-asthenospermia

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Screening for deletions in interval D16-22 of the Y chromosome in azoospermic and oligozoospermic Japanese men

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CAG repeat length in the androgen receptor gene is enhanced in patients with idiopathic azoospermia

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Microdeletions within the azoospermia factor subregions of the Y chromosome in patients with idiopathic azoospermia

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CAG repeat length in the androgen receptor gene of infertile Japanese males with oligozoospermia

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Association between CAG repeat number in the androgen receptor and male infertility in a Belgian study

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Absence of cyclic adenosine 3':5' monophosphate responsive element modulator expression at the spermatocyte arrest stage

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Manifestation of Y-chromosomal deletions in the human testis: a morphometrical and immunohistochemical evaluation

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Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits

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Trinucleotide (CAG) repeat polymorphisms in the androgen receptor gene: molecular markers of risk for male infertility

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Low number of Y-chromosome deletions in infertile azoospermic men at a Swedish andrology centre

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Men with infertility caused by AZFc deletion can produce sons by intracytoplasmic sperm injection, but are likely to transmit the deletion and infertility

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Screening for Y chromosome microdeletions in 226 Slovenian subfertile men

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Microdeletions in the Y chromosome of infertile men

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Laboratory guidelines for molecular diagnosis of Y-chromosomal microdeletions

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Absence of DAZ gene mutations in cases of non-obstructed azoospermia

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Structure and evolution of human Y chromosome DNA

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10.1046/J.1365-2605.2003.00425.X

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

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