The will-o'-the-wisp of genetics--hunting for the azoospermia factor gene.
作者信息
Tyler-Smith Chris, Krausz Csilla
出版信息
N Engl J Med. 2009 Feb 26;360(9):925-7. doi: 10.1056/NEJMe0900301.
Abstract
摘要
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The will-o'-the-wisp of genetics--hunting for the azoospermia factor gene.遗传学的鬼火——寻找无精子症因子基因。
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本文引用的文献
1
Spermatogenesis in a man with complete deletion of USP9Y.一名USP9Y完全缺失男性的精子发生情况
N Engl J Med. 2009 Feb 26;360(9):881-5. doi: 10.1056/NEJMoa0806218.
2
The AZF proteins.无精子因子蛋白
Int J Androl. 2008 Aug;31(4):383-94. doi: 10.1111/j.1365-2605.2008.00890.x.
3
The evolutionary history of human and chimpanzee Y-chromosome gene loss.人类和黑猩猩Y染色体基因丢失的进化史。
Mol Biol Evol. 2007 Mar;24(3):853-9. doi: 10.1093/molbev/msm002. Epub 2007 Jan 11.
4
Natural transmission of USP9Y gene mutations: a new perspective on the role of AZFa genes in male fertility.USP9Y基因突变的自然传递：AZFa基因在男性生育中作用的新视角。
Hum Mol Genet. 2006 Sep 15;15(18):2673-81. doi: 10.1093/hmg/ddl198. Epub 2006 Aug 7.
5
Y chromosome and male infertility: update, 2006.Y染色体与男性不育：2006年最新进展
Front Biosci. 2006 Sep 1;11:3049-61. doi: 10.2741/2032.
6
Two long homologous retroviral sequence blocks in proximal Yq11 cause AZFa microdeletions as a result of intrachromosomal recombination events.近端Yq11中两个长的同源逆转录病毒序列块由于染色体内重组事件导致AZFa微缺失。
Hum Mol Genet. 2000 Oct 12;9(17):2563-72. doi: 10.1093/hmg/9.17.2563.
7
An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y.一名患有Y染色体基因USP9Y新生点突变的无精子症男性。
Nat Genet. 1999 Dec;23(4):429-32. doi: 10.1038/70539.
8
Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxrb interval of the mouse Y chromosome of the Dffry gene.人类DFFRY基因编码序列的特征分析与精细定位，以及Dffry基因的比较表达分析及其在小鼠Y染色体Sxrb区间的定位。
Hum Mol Genet. 1998 Jan;7(1):97-107. doi: 10.1093/hmg/7.1.97.
9
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.
10
Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location.基于染色体定位克隆一种遗传性人类疾病——慢性肉芽肿病——的基因。
Nature. 1986;322(6074):32-8. doi: 10.1038/322032a0.
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