Literature DB >> 11283700

To err (meiotically) is human: the genesis of human aneuploidy.

T Hassold1, P Hunt.   

Abstract

Aneuploidy (trisomy or monosomy) is the most commonly identified chromosome abnormality in humans, occurring in at least 5% of all clinically recognized pregnancies. Most aneuploid conceptuses perish in utero, which makes this the leading genetic cause of pregnancy loss. However, some aneuploid fetuses survive to term and, as a class, aneuploidy is the most common known cause of mental retardation. Despite the devastating clinical consequences of aneuploidy, relatively little is known of how trisomy and monosomy originate in humans. However, recent molecular and cytogenetic approaches are now beginning to shed light on the non-disjunctional processes that lead to aneuploidy.

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Year:  2001        PMID: 11283700     DOI: 10.1038/35066065

Source DB:  PubMed          Journal:  Nat Rev Genet        ISSN: 1471-0056            Impact factor:   53.242


  759 in total

1.  Patterns of meiotic recombination in human fetal oocytes.

Authors:  Charles Tease; Geraldine M Hartshorne; Maj A Hultén
Journal:  Am J Hum Genet       Date:  2002-05-01       Impact factor: 11.025

2.  Crossover distribution and high interference for both the X chromosome and an autosome during oogenesis and spermatogenesis in Caenorhabditis elegans.

Authors:  Philip M Meneely; Anna F Farago; Tate M Kauffman
Journal:  Genetics       Date:  2002-11       Impact factor: 4.562

3.  Multiple independent evolutionary losses of XY pairing at meiosis in the grey voles.

Authors:  Pavel M Borodin; Ekaterina A Basheva; Anna A Torgasheva; Olesya A Dashkevich; Fedor N Golenishchev; Irina V Kartavtseva; Kazuyuki Mekada; Beth L Dumont
Journal:  Chromosome Res       Date:  2011-12-13       Impact factor: 5.239

Review 4.  Chromosomal translocations and palindromic AT-rich repeats.

Authors:  Takema Kato; Hiroki Kurahashi; Beverly S Emanuel
Journal:  Curr Opin Genet Dev       Date:  2012-03-06       Impact factor: 5.578

5.  Meiotic errors activate checkpoints that improve gamete quality without triggering apoptosis in male germ cells.

Authors:  Aimee Jaramillo-Lambert; Yuriko Harigaya; Jeffrey Vitt; Anne Villeneuve; JoAnne Engebrecht
Journal:  Curr Biol       Date:  2010-10-21       Impact factor: 10.834

6.  Trisomy recurrence: a reconsideration based on North American data.

Authors:  Dorothy Warburton; Louis Dallaire; Maya Thangavelu; Lori Ross; Bruce Levin; Jennie Kline
Journal:  Am J Hum Genet       Date:  2004-07-08       Impact factor: 11.025

Review 7.  Male infertility: establishing sperm aneuploidy thresholds in the laboratory.

Authors:  Elena García-Mengual; Juan Carlos Triviño; Alba Sáez-Cuevas; Juan Bataller; Miguel Ruíz-Jorro; Xavier Vendrell
Journal:  J Assist Reprod Genet       Date:  2019-01-02       Impact factor: 3.412

8.  Analysis of Chromosome Segregation, Histone Acetylation, and Spindle Morphology in Horse Oocytes.

Authors:  Federica Franciosi; Irene Tessaro; Rozenn Dalbies-Tran; Cecile Douet; Fabrice Reigner; Stefan Deleuze; Pascal Papillier; Ileana Miclea; Valentina Lodde; Alberto M Luciano; Ghylene Goudet
Journal:  J Vis Exp       Date:  2017-05-11       Impact factor: 1.355

9.  Inadequate histone deacetylation during oocyte meiosis causes aneuploidy and embryo death in mice.

Authors:  Tomohiko Akiyama; Masao Nagata; Fugaku Aoki
Journal:  Proc Natl Acad Sci U S A       Date:  2006-05-01       Impact factor: 11.205

10.  Chromatin Spread Preparations for the Analysis of Mouse Oocyte Progression from Prophase to Metaphase II.

Authors:  Grace H Hwang; Jessica L Hopkins; Philip W Jordan
Journal:  J Vis Exp       Date:  2018-02-26       Impact factor: 1.355

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