Literature DB >> 16192713

Male infertility in reciprocal translocation carriers: the sex body affair.

M Oliver-Bonet1, E Ko, R H Martin.   

Abstract

Previous reports have linked chromosomal reorganization and spermatogenic failure. In this context, it has long been known that reciprocal translocation carriers are more likely to have anomalies in the meiotic process, including fertility failures. It has also been proposed that this fertility failure may be a consequence of an association between the translocated chromosomes and the sex body. In this work, we review different hypotheses explaining meiotic failure in these carriers, and propose a model that relates meiotic abnormalities with both sex body-translocation association and different checkpoints that are known to operate during meiosis. Copyright 2005 S. Karger AG, Basel.

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Year:  2005        PMID: 16192713     DOI: 10.1159/000086908

Source DB:  PubMed          Journal:  Cytogenet Genome Res        ISSN: 1424-8581            Impact factor:   1.636


  13 in total

1.  Positioning of chromosome 15, 18, X and Y centromeres in sperm cells of fertile individuals and infertile patients with increased level of aneuploidy.

Authors:  Marta Olszewska; Ewa Wiland; Maciej Kurpisz
Journal:  Chromosome Res       Date:  2008-08-15       Impact factor: 5.239

2.  Human male meiotic sex chromosome inactivation.

Authors:  Marieke de Vries; Sanne Vosters; Gerard Merkx; Kathleen D'Hauwers; Derick G Wansink; Liliana Ramos; Peter de Boer
Journal:  PLoS One       Date:  2012-02-15       Impact factor: 3.240

3.  Failure of homologous synapsis and sex-specific reproduction problems.

Authors:  Hiroki Kurahashi; Hiroshi Kogo; Makiko Tsutsumi; Hidehito Inagaki; Tamae Ohye
Journal:  Front Genet       Date:  2012-06-18       Impact factor: 4.599

Review 4.  Cytogenetic determinants of male fertility.

Authors:  R H Martin
Journal:  Hum Reprod Update       Date:  2008-06-04       Impact factor: 15.610

5.  Meiotic outcome in two carriers of Y autosome reciprocal translocations: selective elimination of certain segregants.

Authors:  Harita Ghevaria; Roy Naja; Sioban SenGupta; Paul Serhal; Joy Delhanty
Journal:  Mol Cytogenet       Date:  2017-02-02       Impact factor: 2.009

6.  Meiotic defects and decreased expression of genes located around the chromosomal breakpoint in the testis of a patient with a novel 46,X,t(Y;1)(p11.3;p31) translocation.

Authors:  Guangyuan Li; Furhan Iqbal; Liu Wang; Zhipeng Xu; Xiaoyan Che; Wen Yu; Liang Shi; Tonghang Guo; Guixiang Zhou; Xiaohua Jiang; Huan Zhang; Yuanwei Zhang; Dexin Yu
Journal:  Int J Mol Med       Date:  2017-06-14       Impact factor: 4.101

7.  Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.

Authors:  M De Gregori; R Ciccone; P Magini; T Pramparo; S Gimelli; J Messa; F Novara; A Vetro; E Rossi; P Maraschio; M C Bonaglia; C Anichini; G B Ferrero; M Silengo; E Fazzi; A Zatterale; R Fischetto; C Previderé; S Belli; A Turci; G Calabrese; F Bernardi; E Meneghelli; M Riegel; M Rocchi; S Guerneri; F Lalatta; L Zelante; C Romano; M Fichera; T Mattina; G Arrigo; M Zollino; S Giglio; F Lonardo; A Bonfante; A Ferlini; F Cifuentes; H Van Esch; L Backx; A Schinzel; J R Vermeesch; O Zuffardi
Journal:  J Med Genet       Date:  2007-08-31       Impact factor: 6.318

8.  Cytogenetic and molecular analyses of de novo translocation dic(9;13)(p11.2;p12) in an infertile male.

Authors:  Ewa Wiland; Marta Olszewska; Andrew Georgiadis; Nataliya Huleyuk; Barbara Panasiuk; Danuta Zastavna; Svetlana A Yatsenko; Piotr Jedrzejczak; Alina T Midro; Alexander N Yatsenko; Maciej Kurpisz
Journal:  Mol Cytogenet       Date:  2014-02-21       Impact factor: 2.009

9.  Meiotic Recombination Analyses in Pigs Carrying Different Balanced Structural Chromosomal Rearrangements.

Authors:  Nicolas Mary; Harmonie Barasc; Stéphane Ferchaud; Aurélia Priet; Anne Calgaro; Anne-Marie Loustau-Dudez; Nathalie Bonnet; Martine Yerle; Alain Ducos; Alain Pinton
Journal:  PLoS One       Date:  2016-04-28       Impact factor: 3.240

10.  Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism.

Authors:  Juliana Dourado Grzesiuk; Ciro Silveira Pereira; Carlos Henrique Paiva Grangeiro; Clarissa Gondim Picanço-Albuquerque; Flávia Gaona Oliveira-Gennaro; Filipe Brum Machado; Enrique Medina-Acosta; Ester Silveira Ramos; Maisa Yoshimoto; Lucia Martelli
Journal:  Mol Cytogenet       Date:  2016-06-15       Impact factor: 2.009

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