Dedicated to the core: understanding the Fanconi anemia complex.

No abstract is available for this paper.

• Publication year

  2006

• Venue

  DNA Repair

• Publication date

  2006-09-08

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/J.DNAREP.2006.05.009PMID 16784902
• 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.

• Fanconi Anemia Proteins Are Required To Prevent Accumulation of Replication-Associated DNA Double-Strand Breaks

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• The WD40 Repeats of FANCL Are Required for Fanconi Anemia Core Complex Assembly*

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• Ubiquitin-Binding Domains in Y-Family Polymerases Regulate Translesion Synthesis

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• Direct DNA Binding Activity of the Fanconi Anemia D2 Protein*

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• Structural analysis of the anaphase-promoting complex reveals multiple active sites and insights into polyubiquitylation.

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• The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia

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

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• The Fanconi anemia core complex associates with chromatin during S phase.

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• The vertebrate Hef ortholog is a component of the Fanconi anemia tumor-suppressor pathway

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• The Fanconi Anemia/BRCA pathway: new faces in the crowd.

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• Localization of the coactivator Cdh1 and the cullin subunit Apc2 in a cryo-electron microscopy model of vertebrate APC/C.

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• FANCC, FANCE, and FANCD2 Form a Ternary Complex Essential to the Integrity of the Fanconi Anemia DNA Damage Response Pathway*

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

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• A FancD2-monoubiquitin fusion reveals hidden functions of Fanconi anemia core complex in DNA repair.

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

  2005cited by this paper
• The anaphase-promoting complex: a key factor in the regulation of cell cycle

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

  2005cited by this paper
• Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes.

  2004cited by this paper
• ATR couples FANCD2 monoubiquitination to the DNA-damage response.

  2004cited by this paper
• Phosphorylation of Fanconi Anemia (FA) Complementation Group G Protein, FANCG, at Serine 7 Is Important for Function of the FA Pathway*

  2004cited by this paper
• Functional Interaction of Monoubiquitinated FANCD2 and BRCA2/FANCD1 in Chromatin

  2004cited by this paper
• The Fanconi Anemia Gene Product FANCF Is a Flexible Adaptor Protein*

  2004cited by this paper
• X-linked inheritance of Fanconi anemia complementation group B

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• Crosslinks and crosstalk: human cancer syndromes and DNA repair defects.

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• The Fanconi anaemia gene FANCC promotes homologous recombination and error-prone DNA repair.

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• Cooperation of the N-terminal Helicase and C-terminal Endonuclease Activities of Archaeal Hef Protein in Processing Stalled Replication Forks*

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• FANCG Is Phosphorylated at Serines 383 and 387 during Mitosis

  2004cited by this paper
• The Fanconi Anemia Core Complex Forms Four Complexes of Different Sizes in Different Subcellular Compartments*

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• A hitchhiker's guide to the cullin ubiquitin ligases: SCF and its kin.

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• Multiple TPR motifs characterize the Fanconi anemia FANCG protein.

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• Fanconi anaemia

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• The Bloom's syndrome helicase suppresses crossing over during homologous recombination

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• An alternative to FISH: detecting deletion and duplication carriers within 24 hours

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• A novel ubiquitin ligase is deficient in Fanconi anemia

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• A Multiprotein Nuclear Complex Connects Fanconi Anemia and Bloom Syndrome

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• The Fanconi anemia protein, FANCE, promotes the nuclear accumulation of FANCC.

  2002cited by this paper
• The Bloom's syndrome helicase stimulates the activity of human topoisomerase IIIalpha.

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• Biallelic Inactivation of BRCA2 in Fanconi Anemia

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• Interaction of FANCD2 and NBS1 in the DNA damage response

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• FANCE: the link between Fanconi anaemia complex assembly and activity

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• Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway.

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• Ubiquitin and proteasomes: Protein regulation by monoubiquitin

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• Fanconi Anemia Proteins Localize to Chromatin and the Nuclear Matrix in a DNA Damage- and Cell Cycle-regulated Manner*

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• Positional cloning of a novel Fanconi anemia gene, FANCD2.

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• Structure of a c-Cbl-UbcH7 complex: RING domain function in ubiquitin-protein ligases.

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• DNA Replication Is Required To Elicit Cellular Responses to Psoralen-Induced DNA Interstrand Cross-Links

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• Isolation of a cDNA representing the Fanconi anemia complementation group E gene.

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• The APC11 RING-H2 finger mediates E2-dependent ubiquitination.

  2000cited by this paper
• Replication Protein A Physically Interacts with the Bloom's Syndrome Protein and Stimulates Its Helicase Activity*

  2000cited by this paper
• The Bloom's syndrome gene product promotes branch migration of holliday junctions.

  2000cited by this paper
• The fanconi anemia proteins FANCA and FANCG stabilize each other and promote the nuclear accumulation of the Fanconi anemia complex.

  2000cited by this paper
• The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM

  2000cited by this paper
• The fanconi anemia pathway requires FAA phosphorylation and FAA/FAC nuclear accumulation.

  1998cited by this paper
• The Fanconi anaemia group G gene FANCG is identical with XRCC9

  1998cited by this paper
• The Fanconi anemia polypeptide, FAC, binds to the cyclin-dependent kinase, cdc2.

  1997cited by this paper
• Involvement of the Fanconi's anemia protein FAC in a pathway that signals to the cyclin B/cdc2 kinase.

  1997cited by this paper
• Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA

  1996cited by this paper
• Erratum: Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA

  1996cited by this paper
• Cloning of cDNAs for Fanconi's anaemia by functional complementation

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• Cloning of cDNAs for Fanconi's anaemia by functional complementation

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