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Article

Functional interaction of monoubiquitinated FANCD2 and BRCA2/FANCD1 in chromatin.

Molecular and cellular biology - 1 Jul 2004

Wang XiaoZhe, Andreassen Paul R, D'Andrea Alan D

Abstract excerpt

Fanconi anemia (FA) is an autosomal recessive cancer susceptibility syndrome with at least 11 complementation groups (A, B, C, D1, D2, E, F, G, I, J, and L), and eight FA genes have been cloned. The FANCD1 gene is identical to the breast cancer susceptibility gene, BRCA2. The FA proteins cooperate in a common pathway, but the function of BRCA2/FANCD1 in this pathway remains unknown. Here we show that...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 15199141
DOI: 10.1128/MCB.24.13.5850-5862.2004
PMCID: PMC480901

Genes

BRCA2
FANCD2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Functional interaction of monoubiquitinated FANCD2 and BRCA2/FANCD1 in chromatin.PMID 15199141Read ↗

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The Fanconi anemia proteins FANCD2 and FANCJ interact and regulate each other's chromatin localization.Semantic proximity Read ↗

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Regulation of the Fanconi anemia pathway by a CUE ubiquitin-binding domain in the FANCD2 protein.Semantic proximity Read ↗

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