FANCJ helicase operates in the Fanconi Anemia DNA repair pathway and the response to replicational stress.

No abstract is available for this paper.

• Publication year

  2009

• Venue

  Current molecular medicine

• Publication date

  2009-05-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.2174/156652409788167159PMID 19519404PMCID PMC2763586
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Spectrum of mutational events in the absence of DOG-1/FANCJ in Caenorhabditis elegans.

  2008cited by this paper
• Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD

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• Mutagenic capacity of endogenous G4 DNA underlies genome instability in FANCJ-defective C. elegans.

  2008cited by this paper
• Fanconi anemia proteins stabilize replication forks.

  2008cited by this paper
• FANCJ Helicase Defective in Fanconia Anemia and Breast Cancer Unwinds G-Quadruplex DNA To Defend Genomic Stability

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• The Fanconi anemia protein FANCM can promote branch migration of Holliday junctions and replication forks.

  2008cited by this paper
• FANCM of the Fanconi anemia core complex is required for both monoubiquitination and DNA repair.

  2008cited by this paper
• Expression of the BRCA1-interacting protein Brip1/BACH1/FANCJ is driven by E2F and correlates with human breast cancer malignancy

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• Structure of the DNA repair helicase XPD.

  2008cited by this paper
• Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins

  2007cited by this paper
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  2007cited by this paper
• FAAP100 is essential for activation of the Fanconi anemia‐associated DNA damage response pathway

  2007cited by this paper
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  2007cited by this paper
• Fanconi anemia is associated with a defect in the BRCA2 partner PALB2

  2007cited by this paper
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  2007cited by this paper
• Loss of ChlR1 Helicase in Mouse Causes Lethality Due to the Accumulation of Aneuploid Cells Generated by Cohesion Defects and Placental Malformation

  2007cited by this paper
• Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM.

  2007cited by this paper
• Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair.

  2007cited by this paper
• Chk1-Mediated Phosphorylation of FANCE Is Required for the Fanconi Anemia/BRCA Pathway

  2007cited by this paper
• An Iron-Sulfur Cluster in the C-terminal Domain of the p58 Subunit of Human DNA Primase*

  2007cited by this paper
• FANCI is a second monoubiquitinated member of the Fanconi anemia pathway

  2007cited by this paper
• Molecular genetics of RecQ helicase disorders

  2007cited by this paper
• DOG-1 Is the Caenorhabditis elegans BRIP1/FANCJ Homologue and Functions in Interstrand Cross-Link Repair

  2007cited by this paper
• The FANCJ/MutLα interaction is required for correction of the cross‐link response in FA‐J cells

  2007cited by this paper
• The DinG Protein from Escherichia coli Is a Structure-specific Helicase*

  2007cited by this paper
• ATM and ATR Substrate Analysis Reveals Extensive Protein Networks Responsive to DNA Damage

  2007cited by this paper
• Identification of the Fanconi Anemia Complementation Group I Gene, FANCI

  2007cited by this paper
• FANCJ (BACH1) helicase forms DNA damage inducible foci with replication protein A and interacts physically and functionally with the single-stranded DNA-binding protein.

  2007cited by this paper
• Inducibility of nuclear Rad51 foci after DNA damage distinguishes all Fanconi anemia complementation groups from D1/BRCA2.

  2006cited by this paper
• The Fanconi Anemia Pathway of Genomic Maintenance

  2006cited by this paper
• Assessing the Link between BACH1 and BRCA1 in the FA Pathway

  2006cited by this paper
• Gene function correlates with potential for G4 DNA formation in the human genome

  2006cited by this paper
• Homologous Recombination Is Required for Genome Stability in the Absence of DOG-1 in Caenorhabditis elegans

  2006cited by this paper
• The DNA repair helicases XPD and FancJ have essential iron-sulfur domains.

  2006cited by this paper
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  2006cited by this paper
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  2006cited by this paper
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• Mechanisms of RecQ helicases in pathways of DNA metabolism and maintenance of genomic stability.

  2006cited by this paper
• Molecular pathogenesis of Fanconi anemia: recent progress.

  2006cited by this paper
• Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

  2006cited by this paper
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  2006cited by this paper
• Inhibition of BACH1 (FANCJ) helicase by backbone discontinuity is overcome by increased motor ATPase or length of loading strand

  2006cited by this paper
• Chemically modified DNA substrates implicate the importance of electrostatic interactions for DNA unwinding by Dda helicase.

  2005cited by this paper
• The Fanconi anemia pathway is required for the DNA replication stress response and for the regulation of common fragile site stability.

  2005cited by this paper
• Fanconi anemia (cross)linked to DNA repair.

  2005cited by this paper
• The BRIP1 helicase functions independently of BRCA1 in the Fanconi anemia pathway for DNA crosslink repair

  2005cited by this paper
• The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

  2005cited by this paper
• A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M

  2005cited by this paper
• How Fanconi anemia proteins promote the four Rs: Replication, recombination, repair, and recovery

  2005cited by this paper
• A role for iron-sulfur clusters in DNA repair.

  2005cited by this paper
• The Fanconi Anemia/BRCA pathway: new faces in the crowd.

  2005cited by this paper
• Analysis of the DNA Substrate Specificity of the Human BACH1 Helicase Associated with Breast Cancer*

  2005cited by this paper
• BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ.

  2005cited by this paper
• The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia

  2005cited by this paper
• BRCA1 and BRCA2: 1994 and beyond

  2004cited by this paper
• Backbone tracking by the SF2 helicase NPH-II

  2004cited by this paper
• The DNA crosslink‐induced S‐phase checkpoint depends on ATR–CHK1 and ATR–NBS1–FANCD2 pathways

  2004cited by this paper
• Structural basis of BACH1 phosphopeptide recognition by BRCA1 tandem BRCT domains.

  2004cited by this paper
• The DNA-unwinding mechanism of the ring helicase of bacteriophage T7.

  2004cited by this paper
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  2004cited by this paper
• The BRCA1-associated protein BACH1 is a DNA helicase targeted by clinically relevant inactivating mutations.

  2004cited by this paper
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  2004cited by this paper
• The DNA double-strand break response pathway: becoming more BRCAish than ever.

  2004cited by this paper
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  2004cited by this paper
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  2004cited by this paper
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• [Telomerase inhibitor, telomestatin, a specific mechanism to interact with telomere structure].

  2004cited by this paper
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  2002cited by this paper
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  2001cited by this paper
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  2001cited by this paper
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  2000cited by this paper
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  1999cited by this paper
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  1999cited by this paper
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  1999cited by this paper
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  1998cited by this paper
• The Bloom’s Syndrome Helicase Unwinds G4 DNA*

  1998cited by this paper
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  1997cited by this paper
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  1996cited by this paper
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  1996cited by this paper
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  1995cited by this paper
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  2017cites this paper
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  2016cites this paper
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