(Q37775585)

23 August 2017

1 reference

title

Assessing the link between BACH1/FANCJ and MLH1 in DNA crosslink repair (English)

1 reference

23 August 2017

Sharon B Cantor

1

1 reference

PubMed ID

20658644

23 August 2017

Jenny Xie

series ordinal

2

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23 August 2017

1 July 2010

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Environmental and Molecular Mutagenesis

23 August 2017

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23 August 2017

51

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23 August 2017

500-507

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23 August 2017

6

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Repair of DNA interstrand cross-links

23 August 2017

1 reference

Cellular and molecular consequences of defective Fanconi anemia proteins in replication-coupled DNA repair: mechanistic insights

21 January 2018

1 reference

RTEL1 maintains genomic stability by suppressing homologous recombination

21 January 2018

1 reference

7 January 2021

Functional interactions and signaling properties of mammalian DNA mismatch repair proteins

1 reference

7 January 2021

The BRIP1 helicase functions independently of BRCA1 in the Fanconi anemia pathway for DNA crosslink repair

1 reference

7 January 2021

The mismatch repair system is required for S-phase checkpoint activation

1 reference

7 January 2021

The BRCA1-associated protein BACH1 is a DNA helicase targeted by clinically relevant inactivating mutations

1 reference

7 January 2021

BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function

1 reference

7 January 2021

A rapid method for retrovirus-mediated identification of complementation groups in Fanconi anemia patients.

1 reference

7 January 2021

Mismatch-, MutS-, MutL-, and helicase II-dependent unwinding from the single-strand break of an incised heteroduplex

1 reference

7 January 2021

A novel breast cancer-associated BRIP1 (FANCJ/BACH1) germ-line mutation impairs protein stability and function

1 reference

7 January 2021

Dependence on RAD52 and RAD1 for anticancer drug resistance mediated by inactivation of mismatch repair genes.

1 reference

7 January 2021

Multifactorial contributions to an acute DNA damage response by BRCA1/BARD1-containing complexes

1 reference

7 January 2021

Inhibition of BACH1 (FANCJ) helicase by backbone discontinuity is overcome by increased motor ATPase or length of loading strand.

1 reference

7 January 2021

Analysis of the DNA substrate specificity of the human BACH1 helicase associated with breast cancer

1 reference

7 January 2021

FANCJ (BACH1) helicase forms DNA damage inducible foci with replication protein A and interacts physically and functionally with the single-stranded DNA-binding protein

1 reference

7 January 2021

Biallelic inactivation of BRCA2 in Fanconi anemia

1 reference

7 January 2021

DNA mismatch repair: functions and mechanisms

1 reference

7 January 2021

The multifaceted mismatch-repair system

1 reference

7 January 2021

The interacting domains of three MutL heterodimers in man: hMLH1 interacts with 36 homologous amino acid residues within hMLH3, hPMS1 and hPMS2

1 reference

7 January 2021

Activation of BRCA1/BRCA2-associated helicase BACH1 is required for timely progression through S phase

1 reference

7 January 2021

Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes

1 reference

7 January 2021

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

1 reference

7 January 2021

The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia

1 reference

7 January 2021

An Msh2 point mutation uncouples DNA mismatch repair and apoptosis

1 reference

7 January 2021

DNA polymerase zeta accounts for the reduced cytotoxicity and enhanced mutagenicity of cisplatin in human colon carcinoma cells that have lost DNA mismatch repair

1 reference

7 January 2021

BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ.

1 reference

7 January 2021

DNA interstrand crosslink repair in mammalian cells

1 reference

7 January 2021

Escherichia coli MutL loads DNA helicase II onto DNA.

1 reference

7 January 2021

The mismatch-repair protein hMSH2 binds selectively to DNA adducts of the anticancer drug cisplatin

1 reference

7 January 2021

PCNA, the maestro of the replication fork

1 reference

7 January 2021

Fanconi anemia (cross)linked to DNA repair

1 reference

7 January 2021

Signalling cell cycle arrest and cell death through the MMR System

1 reference

7 January 2021

Crosstalk between SUMO and ubiquitin on PCNA is mediated by recruitment of the helicase Srs2p

1 reference

7 January 2021

BACH1 is a DNA repair protein supporting BRCA1 damage response

1 reference

7 January 2021

The FANCJ/MutLalpha interaction is required for correction of the cross-link response in FA-J cells

1 reference

7 January 2021

The DNA repair helicases XPD and FancJ have essential iron-sulfur domains

1 reference

7 January 2021

Physical and functional interactions between Werner syndrome helicase and mismatch-repair initiation factors

1 reference

7 January 2021

Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

1 reference

7 January 2021

Recruitment of fanconi anemia and breast cancer proteins to DNA damage sites is differentially governed by replication

1 reference

7 January 2021

Human MutL-complexes monitor homologous recombination independently of mismatch repair

1 reference

7 January 2021

FANCJ uses its motor ATPase to destabilize protein-DNA complexes, unwind triplexes, and inhibit RAD51 strand exchange

1 reference

7 January 2021

Mismatch repair-dependent G2 checkpoint induced by low doses of SN1 type methylating agents requires the ATR kinase

1 reference

7 January 2021

Mismatch repair proteins: key regulators of genetic recombination

1 reference

7 January 2021

How Fanconi anemia proteins promote the four Rs: replication, recombination, repair, and recovery

1 reference

7 January 2021

Recovery from checkpoint-mediated arrest after repair of a double-strand break requires Srs2 helicase

1 reference

7 January 2021

Ten genes for inherited breast cancer.

1 reference

7 January 2021

Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins

1 reference

7 January 2021

Mismatch repair participates in error-free processing of DNA interstrand crosslinks in human cells

1 reference

7 January 2021

Human MLH1 protein participates in genomic damage checkpoint signaling in response to DNA interstrand crosslinks, while MSH2 functions in DNA repair

1 reference

7 January 2021

FANCJ helicase defective in Fanconia anemia and breast cancer unwinds G-quadruplex DNA to defend genomic stability

1 reference

7 January 2021

MutS and MutL activate DNA helicase II in a mismatch-dependent manner

1 reference

7 January 2021

DOG-1 is the Caenorhabditis elegans BRIP1/FANCJ homologue and functions in interstrand cross-link repair

1 reference

7 January 2021

The BRCT Domain Is a Phospho-Protein Binding Domain

1 reference

7 January 2021

Double-strand breaks induce homologous recombinational repair of interstrand cross-links via cooperation of MSH2, ERCC1-XPF, REV3, and the Fanconi anemia pathway

1 reference

7 January 2021

hMutSbeta is required for the recognition and uncoupling of psoralen interstrand cross-links in vitro

1 reference

7 January 2021

Identifiers

DOI

10.1002/EM.20568

1 reference

23 August 2017

1 reference

PubMed ID

20658644