Chromosome synapsis defects and sexually dimorphic meiotic progression in mice lacking Spo11. (Q50720785)

18 March 2018

title

Chromosome synapsis defects and sexually dimorphic meiotic progression in mice lacking Spo11. (English)

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18 March 2018

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Baudat F

1

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18 March 2018

Manova K

2

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18 March 2018

Yuen JP

3

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18 March 2018

Jasin M

4

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18 March 2018

Keeney S

5

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18 March 2018

publication date

1 November 2000

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18 March 2018

published in

Molecular Cell

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18 March 2018

volume

6

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18 March 2018

issue

5

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18 March 2018

page(s)

989-998

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18 March 2018

RecA-like proteins are components of early meiotic nodules in lily

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An atypical topoisomerase II from Archaea with implications for meiotic recombination

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RecA homologs Dmc1 and Rad51 interact to form multiple nuclear complexes prior to meiotic chromosome synapsis

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Multiple roles of Spo11 in meiotic chromosome behavior

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Identification and characterization of an SPO11 homolog in the mouse

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Sex-chromosome pairing and male fertility

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Histones H1 and H4 of surface-spread meiotic chromosomes

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Rad51 immunocytology in rat and mouse spermatocytes and oocytes

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Structure and function of an archaeal topoisomerase VI subunit with homology to the meiotic recombination factor Spo11

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7 January 2021

The mouse Spo11 gene is required for meiotic chromosome synapsis

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7 January 2021

Differential gene expression of mammalian SPO11/TOP6A homologs during meiosis

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7 January 2021

Recombination at work for meiosis

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Mouse testes contain two size classes of actin mRNA that are differentially expressed during spermatogenesis

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The Mouse RecA-like Gene Dmc1 Is Required for Homologous Chromosome Synapsis during Meiosis

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7 January 2021

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Identifiers

DOI

1 reference

18 March 2018

1 reference

18 March 2018