About: The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

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rdf:type	Item
description	article (en) ലേഖനം (ml) artículu científicu (ast) wetenschappelijk artikel (nl) article scientifique publié en 2005 (fr) наукова стаття, опублікована у вересні 2005 (uk) im September 2005 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q55671102-30426E1B-F19C-4458-B13B-81C8CDBF6BD8
publication date	2005-09-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q55671102-A52A6C8D-41C0-4444-9E12-FD1DDEF2F98E
language of work or name	English
exact match	wds:Q55671102-05798FFC-8709-4346-850B-CFD53CAAF852
exact match	https://scigraph.springernature.com/pub.10.1038/ng1625
cites work	wds:Q55671102-0222FD6F-70A7-4FBD-9EEC-020ED3713E89 wds:Q55671102-1406D22A-6151-4281-A134-2222B3192F9E wds:Q55671102-1A48DE29-719A-405B-9492-3209276C1FC3 wds:Q55671102-362FA9B8-BA3B-45A0-939B-141BCEF72F01 wds:Q55671102-45518D40-61E4-4453-B345-21F24269D3A5 wds:Q55671102-6142280B-85ED-4D91-BC74-68C2A32F55CD wds:Q55671102-BAAC4127-DCBD-47B9-86ED-0D4E32908292 wds:Q55671102-C33416FB-40EC-492A-AFA7-F77C41EC3C5A wds:Q55671102-EA1C832B-8BEC-4ADD-9E47-7EAD9CF088F8
cites work	Cloning of cDNAs for Fanconi's anaemia by functional complementation The BRCA1-associated protein BACH1 is a DNA helicase targeted by clinically relevant inactivating mutations The BRCT Domain Is a Phospho-Protein Binding Domain A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M The BRIP1 helicase functions independently of BRCA1 in the Fanconi anemia pathway for DNA crosslink repair BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes The emerging genetic and molecular basis of Fanconi anaemia Microcell-mediated chromosome transfer (MMCT): small cells with huge potential
author name string	wds:Q55671102-0A63AF7D-966A-45FD-BCCF-2982926B66B6 wds:Q55671102-2D0163DF-1599-4202-A7E9-00BE04A0173E wds:Q55671102-637B75DA-D016-4BE8-918E-D0F2475112E5 wds:Q55671102-71EB74BD-3199-433E-AD2C-3C36C80F4547 wds:Q55671102-F1449962-074A-417E-83AE-61CC036B7CEB wds:Q55671102-F9D08C25-B07D-4B6A-B60D-0EEB9A25401C
author name string	Shobbir Hussain Kevin Hiom Jûrgen Steltenpool Marieke Levitus Yne de Vries Johan P De Winter
rdfs:label	The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J (en) The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J (nl)
skos:prefLabel	The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J (en) The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J (nl)
name	The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J (en) The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J (nl)
author	wds:Q55671102-2110FC64-8143-48B9-B8F0-1523487A4EF6 wds:Q55671102-40C322C1-A764-40D5-8B46-076A5150BABF wds:Q55671102-8162E668-C8BC-4724-90CE-938A87679F7C wds:Q55671102-82182695-74F2-4B52-AB98-6363CA229ECB wds:Q55671102-89B430F2-2CED-4BE8-85E9-D41AFA9CD465 wds:Q55671102-CC720386-41FF-4BA0-921E-FD7B9D87358B wds:Q55671102-D5D66259-DC4E-4592-AE24-45EF568FF1DA wds:Q55671102-E72653E9-AAE6-4A90-B3AB-5DBA8421CF5E wds:Q55671102-E7BC7983-D3C2-4B77-898C-C1A6CEBE199E wds:Q55671102-ECDF6FDA-E8E9-429C-9AE0-2BD34CC282C1
author	Christopher G. Mathew Wouter W Wiegant Hans Joenje Quinten Waisfisz Gerard Pals Barbara C Godthelp Małgorzata Z Zdzienicka Martin A Rooimans Elhaam Elghalbzouri-Maghrani Fré Arwert
title	wds:Q55671102-559DE412-E34A-4DFD-B2DF-43F3A6F09EAD
title	The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J (en)
page(s)	wds:Q55671102-86E52B80-D8D2-431C-A592-454C88A76DC0
page(s)	934-5
instance of	wds:Q55671102-9AC9DD7C-4279-4254-A431-C8E85CC437A0
instance of	scholarly article
main subject	wds:Q55671102-53C98BBA-3524-4DF0-973F-9142098B9D44
main subject	Fanconi anemia complementation group J
PubMed ID	wds:Q55671102-6513C167-CB79-428C-9133-EF3D7A0A2516
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16116423
PubMed ID	16116423
published in	wds:Q55671102-5A134A01-CA87-4D58-97F5-8A5ABC55AE20
published in	Nature Genetics
issue	wds:Q55671102-D88222F6-2F35-413F-B2C9-EA6D0784FD0A
volume	wds:Q55671102-32217EFB-85A3-4CA4-9B81-09D2CC1ACB8D
issue	9
volume	37
DOI	wds:Q55671102-902EA1D9-2146-4505-8340-65A3FE4420FD
DOI	http://dx.doi.org/10.1038/NG1625
DOI	10.1038/NG1625
ResearchGate publication ID	wds:Q55671102-99E73B5B-DBB5-4624-BAA5-DF5BB1C7EBE0
ResearchGate publication ID	7645182
Dimensions Publication ID	wds:Q55671102-48FE6C41-86F3-4BBB-91A1-005CBB057223
Dimensions Publication ID	1048817934
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55671102
is cites work of	MRE11-RAD50-NBS1 is a critical regulator of FANCD2 stability and function during DNA double-strand break repair FancJ (Brip1) loss-of-function allele results in spermatogonial cell depletion during embryogenesis and altered processing of crossover sites during meiotic prophase I in mice Germline mutations in RAD51D confer susceptibility to ovarian cancer RAD51C is a susceptibility gene for ovarian cancer FAVL elevation in human tumors disrupts Fanconi anemia pathway signaling and promotes genomic instability and tumor growth

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