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Clamping down on mammalian meiosis.

Clamping down on mammalian meiosis.

http://www.wikidata.org/entity/Q37396828

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Functional compartmentalization of Rad9 and Hus1 reveals diverse assembly of the 9-1-1 complex components during the DNA damage response in Leishmania.The meiotic checkpoint network: step-by-step through meiotic prophase

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Clamping down on mammalian meiosis.

http://www.wikidata.org/entity/Q37396828

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 26 August 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Clamping down on mammalian meiosis.

@en

Clamping down on mammalian meiosis.

@nl

type

label

Clamping down on mammalian meiosis.

@en

Clamping down on mammalian meiosis.

@nl

prefLabel

Clamping down on mammalian meiosis.

@en

Clamping down on mammalian meiosis.

@nl

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Clamping down on mammalian meiosis.

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Amy M Lyndaker

http://www.w3.org/2001/XMLSchema#string

Ana Vasileva

http://www.w3.org/2001/XMLSchema#string

Debra J Wolgemuth

http://www.w3.org/2001/XMLSchema#string

Howard B Lieberman

http://www.w3.org/2001/XMLSchema#string

Robert S Weiss

http://www.w3.org/2001/XMLSchema#string

P2860

HDAC1, a histone deacetylase, forms a complex with Hus1 and Rad9, two G2/M checkpoint Rad proteins

Expression of mammalian paralogues of HRAD9 and Mrad9 checkpoint control genes in normal and cancerous testicular tissue

The human checkpoint sensor and alternative DNA clamp Rad9-Rad1-Hus1 modulates the activity of DNA ligase I, a component of the long-patch base excision repair machinery

A DNA damage response screen identifies RHINO, a 9-1-1 and TopBP1 interacting protein required for ATR signaling

Crystal structure of the human rad9-hus1-rad1 clamp

Human and mouse homologs of Schizosaccharomyces pombe rad1(+) and Saccharomyces cerevisiae RAD17: linkage to checkpoint control and mammalian meiosis

Surveillance of different recombination defects in mouse spermatocytes yields distinct responses despite elimination at an identical developmental stage.

Conditional inactivation of the DNA damage response gene Hus1 in mouse testis reveals separable roles for components of the RAD9-RAD1-HUS1 complex in meiotic chromosome maintenance

Hormad1 mutation disrupts synaptonemal complex formation, recombination, and chromosome segregation in mammalian meiosis

Crystal structure of the rad9-rad1-hus1 DNA damage checkpoint complex--implications for clamp loading and regulation

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3135-3145

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scholarly article

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10.4161/CC.26061

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