序列家族变体对识别人类Y染色体缺失是否有用？ - Suppr

Are sequence family variants useful for identifying deletions in the human Y chromosome?

作者信息

Repping Sjoerd, Korver Cindy M, Oates Robert D, Silber Sherman, van der Veen Fulco, Page David C, Rozen Steve

出版信息

Am J Hum Genet. 2004 Sep;75(3):514-7; author reply 517-9. doi: 10.1086/423394.

DOI:10.1086/423394

PMID:15284951

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1182031/

Abstract

摘要

相似文献

Are sequence family variants useful for identifying deletions in the human Y chromosome?

Am J Hum Genet. 2004 Sep;75(3):514-7; author reply 517-9. doi: 10.1086/423394.

A novel partial deletion of the Y chromosome azoospermia factor c region is caused by non-homologous recombination between palindromes and may be associated with increased sperm counts.

Hum Reprod. 2011 Mar;26(3):713-23. doi: 10.1093/humrep/deq386. Epub 2011 Jan 11.

Y chromosome assessment and its implications for the development of ICSI children.

Reprod Biomed Online. 2004 Mar;8(3):307-18. doi: 10.1016/s1472-6483(10)60911-x.

MSY Breakpoint Mapper, a database of sequence-tagged sites useful in defining naturally occurring deletions in the human Y chromosome.

Nucleic Acids Res. 2008 Jan;36(Database issue):D809-14. doi: 10.1093/nar/gkm849. Epub 2007 Oct 26.

Y chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairment.

Hum Reprod. 2008 Sep;23(9):2167-72. doi: 10.1093/humrep/den229. Epub 2008 Jun 25.

The human Y chromosome: a 43-interval map based on naturally occurring deletions.

Science. 1992 Oct 2;258(5079):52-9. doi: 10.1126/science.1439769.

Y chromosome microdeletions: are they implicated in teratozoospermia?

Hum Reprod. 2005 Dec;20(12):3505-9. doi: 10.1093/humrep/dei254. Epub 2005 Aug 25.

[Y chromosome and spermatogenesis].

Gynecol Obstet Fertil. 2009 Nov-Dec;37(11-12):901-7. doi: 10.1016/j.gyobfe.2009.09.009. Epub 2009 Oct 12.

Prenatal diagnosis of mos46,X,del(Y)(q11.2)/45,X by cytogenetic and molecular studies with multiplex STR analysis.

Prenat Diagn. 2004 Feb;24(2):121-4. doi: 10.1002/pd.817.

Ring (Y) in two azoospermic men.

Am J Med Genet A. 2004 Jul 15;128A(2):209-13. doi: 10.1002/ajmg.a.30097.

引用本文的文献

Discrimination of Deletion and Duplication Subtypes of the Deleted in Azoospermia Gene Family in the Context of Frequent Interloci Gene Conversion.

PLoS One. 2016 Oct 10;11(10):e0163936. doi: 10.1371/journal.pone.0163936. eCollection 2016.

Impact of Y chromosome AZFc subdeletion shows lower risk of fertility impairment in Siddi tribal men, Western Ghats, India.

Basic Clin Androl. 2015 Jan 22;25:1. doi: 10.1186/s12610-014-0017-5. eCollection 2015.

Molecular dissection of the basal clades in the human Y chromosome phylogenetic tree.

PLoS One. 2012;7(11):e49170. doi: 10.1371/journal.pone.0049170. Epub 2012 Nov 7.

A revised root for the human Y chromosomal phylogenetic tree: the origin of patrilineal diversity in Africa.

Am J Hum Genet. 2011 Jun 10;88(6):814-818. doi: 10.1016/j.ajhg.2011.05.002. Epub 2011 May 27.

The Y deletion gr/gr and susceptibility to testicular germ cell tumor.

Am J Hum Genet. 2005 Dec;77(6):1034-43. doi: 10.1086/498455. Epub 2005 Oct 24.

本文引用的文献

Online Mendelian Inheritance in Man 'OMIM'.

Indian J Dermatol Venereol Leprol. 2003 Nov-Dec;69(6):423-4.

A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region.

Genomics. 2004 Jun;83(6):1046-52. doi: 10.1016/j.ygeno.2003.12.018.

A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N.

Am J Hum Genet. 2004 Jan;74(1):180-7. doi: 10.1086/381132. Epub 2003 Nov 21.

Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection.

Nat Genet. 2003 Nov;35(3):247-51. doi: 10.1038/ng1250. Epub 2003 Oct 5.

Abundant gene conversion between arms of palindromes in human and ape Y chromosomes.

Nature. 2003 Jun 19;423(6942):873-6. doi: 10.1038/nature01723.

The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes.

Nature. 2003 Jun 19;423(6942):825-37. doi: 10.1038/nature01722.

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

Mol Hum Reprod. 2002 Mar;8(3):286-98. doi: 10.1093/molehr/8.3.286.

A nomenclature system for the tree of human Y-chromosomal binary haplogroups.

Genome Res. 2002 Feb;12(2):339-48. doi: 10.1101/gr.217602.

The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men.

Nat Genet. 2001 Nov;29(3):279-86. doi: 10.1038/ng757.

Y chromosome sequence variation and the history of human populations.

Nat Genet. 2000 Nov;26(3):358-61. doi: 10.1038/81685.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

Are sequence family variants useful for identifying deletions in the human Y chromosome?

作者信息

出版信息

相似文献

引用本文的文献

本文引用的文献

文献AI研究员

用中文搜PubMed

文档翻译

Suppr 超能文献

相似文献

引用本文的文献

本文引用的文献