Interaction between the helicases genetically linked to Fanconi anemia group J and Bloom's syndrome
about
The Werner syndrome protein is distinguished from the Bloom syndrome protein by its capacity to tightly bind diverse DNA structuresHuman single-stranded DNA binding proteins are essential for maintaining genomic stabilityGetting Ready for the Dance: FANCJ Irons Out DNA WrinklesCellular response to DNA interstrand crosslinks: the Fanconi anemia pathwayFunctions and regulation of the multitasking FANCM family of DNA motor proteinsClose encounters for the first time: Helicase interactions with DNA damageDisease-causing missense mutations in human DNA helicase disordersMolecular functions and cellular roles of the ChlR1 (DDX11) helicase defective in the rare cohesinopathy Warsaw breakage syndromeBLM protein mitigates formaldehyde-induced genomic instabilityDefining the molecular interface that connects the Fanconi anemia protein FANCM to the Bloom syndrome dissolvasomeFancJ (Brip1) loss-of-function allele results in spermatogonial cell depletion during embryogenesis and altered processing of crossover sites during meiotic prophase I in miceBLM helicase facilitates telomere replication during leading strand synthesis of telomeresInsight into the roles of helicase motif Ia by characterizing Fanconi anemia group J protein (FANCJ) patient mutationsNovel function of the Fanconi anemia group J or RECQ1 helicase to disrupt protein-DNA complexes in a replication protein A-stimulated manner.Regulation of DNA cross-link repair by the Fanconi anemia/BRCA pathwayFANCJ/BACH1 acetylation at lysine 1249 regulates the DNA damage responseMolecular and cellular functions of the FANCJ DNA helicase defective in cancer and in Fanconi anemiaHeterozygous mutations in DNA repair genes and hereditary breast cancer: a question of power.Impact of age-associated cyclopurine lesions on DNA repair helicases.Mechanistic insight into the interaction of BLM helicase with intra-strand G-quadruplex structuresFanconi anemia group J helicase and MRE11 nuclease interact to facilitate the DNA damage response.Fanconi anemia and Bloom's syndrome crosstalk through FANCJ-BLM helicase interaction.Rescue of replication failure by Fanconi anaemia proteins.Protein degradation pathways regulate the functions of helicases in the DNA damage response and maintenance of genomic stabilityhMSH5 Facilitates the Repair of Camptothecin-induced Double-strand Breaks through an Interaction with FANCJ.DNA helicases involved in DNA repair and their roles in cancerDNA helicases associated with genetic instability, cancer, and aging.DNA repair and replication fork helicases are differentially affected by alkyl phosphotriester lesion.DNA helicase and helicase-nuclease enzymes with a conserved iron-sulfur cluster.The Q motif of Fanconi anemia group J protein (FANCJ) DNA helicase regulates its dimerization, DNA binding, and DNA repair function.Human RecQ helicases in DNA repair, recombination, and replication.The human RecQ helicases BLM and RECQL4 cooperate to preserve genome stability.FANCD2, FANCJ and BRCA2 cooperate to promote replication fork recovery independently of the Fanconi Anemia core complex.FANCJ couples replication past natural fork barriers with maintenance of chromatin structure.FANCJ at the FORK.FANCD2 regulates BLM complex functions independently of FANCI to promote replication fork recovery.The BLM dissolvasome in DNA replication and repair.Specialization among iron-sulfur cluster helicases to resolve G-quadruplex DNA structures that threaten genomic stability.FANCP/SLX4: a Swiss army knife of DNA interstrand crosslink repair.HP1 regulates the localization of FANCJ at sites of DNA double-strand breaks.
P2860
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P2860
Interaction between the helicases genetically linked to Fanconi anemia group J and Bloom's syndrome
description
2011 nî lūn-bûn
@nan
2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Interaction between the helica ...... a group J and Bloom's syndrome
@ast
Interaction between the helica ...... a group J and Bloom's syndrome
@en
Interaction between the helica ...... a group J and Bloom's syndrome
@en-gb
Interaction between the helica ...... a group J and Bloom's syndrome
@nl
type
label
Interaction between the helica ...... a group J and Bloom's syndrome
@ast
Interaction between the helica ...... a group J and Bloom's syndrome
@en
Interaction between the helica ...... a group J and Bloom's syndrome
@en-gb
Interaction between the helica ...... a group J and Bloom's syndrome
@nl
prefLabel
Interaction between the helica ...... a group J and Bloom's syndrome
@ast
Interaction between the helica ...... a group J and Bloom's syndrome
@en
Interaction between the helica ...... a group J and Bloom's syndrome
@en-gb
Interaction between the helica ...... a group J and Bloom's syndrome
@nl
P2093
P2860
P3181
P356
P1433
P1476
Interaction between the helica ...... a group J and Bloom's syndrome
@en
P2093
Avvaru N Suhasini
Georgina Mosedale
Ian D Hickson
Joshua A Sommers
Nina A Rawtani
Phillip S North
Robert M Brosh
Sharon B Cantor
Yuliang Wu
P2860
P304
P3181
P356
10.1038/EMBOJ.2010.362
P407
P50
P577
2011-01-14T00:00:00Z