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A comprehensive analysis of chromosomal anomalies in metaphase II spermatocytes from infertile patients.

作者信息

Sarrate Zaida, Blanco Joan, Valero Oliver, Vidal Francesca

机构信息

Genetics of Male Fertility Group, Unitat de Biologia Cel·lular, Departament de Biologia Cel·lular, Fisiologia i Immunologia, Facultat de Biociències, Universitat Autònoma de Barcelona, Bellaterra (Cerdanyola del Vallès) 08193, Spain.

Servei d'Estadística Aplicada, Universitat Autònoma de Barcelona, Bellaterra (Cerdanyola del Vallès) 08193, Spain.

出版信息

Asian J Androl. 2018 Jan-Feb;20(1):105-106. doi: 10.4103/1008-682X.194819.

DOI:10.4103/1008-682X.194819
PMID:28230004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5753547/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41be/5753547/cb379b97dadb/AJA-20-105-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41be/5753547/cb379b97dadb/AJA-20-105-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41be/5753547/cb379b97dadb/AJA-20-105-g001.jpg

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本文引用的文献

1
Meiotic abnormalities in metaphase I human spermatocytes from infertile males: frequencies, chromosomes involved, and the relationships with polymorphic karyotype and seminal parameters.不育男性减数分裂中期I人类精母细胞的减数分裂异常：频率、涉及的染色体以及与多态核型和精液参数的关系。
Asian J Androl. 2014 Nov-Dec;16(6):838-44. doi: 10.4103/1008-682X.135126.
2
Premature separation of sister chromatids in human male meiosis.人类男性减数分裂中姐妹染色单体的过早分离。
Hum Reprod. 2008 Apr;23(4):982-7. doi: 10.1093/humrep/dem427. Epub 2008 Feb 11.
3
Bi-orientation of achiasmatic chromosomes in meiosis I oocytes contributes to aneuploidy in mice.
减数分裂I期卵母细胞中无交叉染色体的双定向导致小鼠非整倍体。
Nat Genet. 2007 Aug;39(8):966-8. doi: 10.1038/ng2065. Epub 2007 Jul 8.
4
Centromere-proximal crossovers are associated with precocious separation of sister chromatids during meiosis in Saccharomyces cerevisiae.着丝粒近端交叉与酿酒酵母减数分裂过程中姐妹染色单体的过早分离有关。
Genetics. 2006 Dec;174(4):1745-54. doi: 10.1534/genetics.106.058933. Epub 2006 Oct 8.
5
The occurrence of aneuploidy in human: lessons from the cytogenetic studies of human oocytes.人类非整倍体的发生：来自人类卵母细胞细胞遗传学研究的经验教训。
Eur J Med Genet. 2006 Mar-Apr;49(2):103-16. doi: 10.1016/j.ejmg.2005.08.001. Epub 2005 Sep 26.
6
Meiotic abnormalities in infertile males.不育男性的减数分裂异常。
Cytogenet Genome Res. 2005;111(3-4):337-42. doi: 10.1159/000086907.
7
Identification of meiotic anomalies with multiplex fluorescence in situ hybridization: Preliminary results.
Fertil Steril. 2004 Sep;82(3):712-7. doi: 10.1016/j.fertnstert.2004.02.122.
8
To err (meiotically) is human: the genesis of human aneuploidy.（减数分裂时）犯错乃人之常情：人类非整倍体的起源。
Nat Rev Genet. 2001 Apr;2(4):280-91. doi: 10.1038/35066065.
9
Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21.增加21号染色体母体不分离风险的易感性交叉构型的特征分析。
Hum Mol Genet. 1997 Sep;6(9):1391-9. doi: 10.1093/hmg/6.9.1391.
10
Y chromosome aneuploidy, micronuclei, kinetochores and aging in men.
Chromosoma. 1995 Jul;103(10):725-31. doi: 10.1007/BF00344234.