无精子症因子候选基因DAZ在人类精原细胞中的表达。 - Suppr

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超能文献

Expression of DAZ, an azoospermia factor candidate, in human spermatogonia.

作者信息

Menke D B, Mutter G L, Page D C

出版信息

Am J Hum Genet. 1997 Jan;60(1):237-41.

PMID:8981970

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1712565/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52d3/1712565/ddc294198e20/ajhg00001-0265-a.jpg

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本文引用的文献

The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned.人类Y染色体上的DAZ基因簇起源于一个常染色体基因，该基因经过转座、多次扩增和修剪。

Nat Genet. 1996 Nov;14(3):292-9. doi: 10.1038/ng1196-292.

A murine homologue of the human DAZ gene is autosomal and expressed only in male and female gonads.

Hum Mol Genet. 1996 Apr;5(4):513-6. doi: 10.1093/hmg/5.4.513.

Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11.人类Y染色体无精子症因子（AZF）定位于Yq11的不同亚区域。

Hum Mol Genet. 1996 Jul;5(7):933-43. doi: 10.1093/hmg/5.7.933.

Mouse autosomal homolog of DAZ, a candidate male sterility gene in humans, is expressed in male germ cells before and after puberty.DAZ（人类中一个候选的雄性不育基因）的小鼠常染色体同源物在青春期前后的雄性生殖细胞中表达。

Genomics. 1996 Jul 15;35(2):346-52. doi: 10.1006/geno.1996.0366.

Meiotic cell cycle requirement for a fly homologue of human Deleted in Azoospermia.人类无精子症缺失基因的果蝇同源物在减数分裂细胞周期中的需求。

Nature. 1996 Jun 27;381(6585):783-5. doi: 10.1038/381783a0.

Substantial prevalence of microdeletions of the Y-chromosome in infertile men with idiopathic azoospermia and oligozoospermia detected using a sequence-tagged site-based mapping strategy.采用基于序列标签位点的定位策略检测到，特发性无精子症和少精子症的不育男性中Y染色体微缺失的发生率很高。

J Clin Endocrinol Metab. 1996 Apr;81(4):1347-52. doi: 10.1210/jcem.81.4.8636331.

Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome.

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Am J Hum Genet. 1993 Jan;52(1):152-66.

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