Carboxy terminal region of the Fanconi anemia protein, FANCG/XRCC9, is required for functional activity

Blood

Volumn 96, Issue 5, 2000, Pages 1625-1632

  Kuang, Y ^a   Garcia Higuera, I ^a   Moran, A ^a   Mondoux, M ^a   Digweed, M ^a   D'Andrea, A D ^a  

^a HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOMYCIN C; MUTANT PROTEIN;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CARBOXY TERMINAL SEQUENCE; FANCONI ANEMIA; GENE SEQUENCE; GENE TRANSLOCATION; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; MOLECULAR CLONING; NUCLEAR LOCALIZATION SIGNAL; PRIORITY JOURNAL; PROTEIN BINDING;

EID: 0034283708     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v96.5.1625.h8001625a_1625_1632     Document Type: Article

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32. Selective G protein coupling by chemokine receptors
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34. Characterization of regions functional in the nuclear localization of the Fanconi anemia group A protein
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36. The retinoblastoma protein associates with the protein phosphatase type I catalytic subunit
37. The Atr and Arm protein kinases associate with different sites along meiotically pairing chromosomes
38. Deletion analysis of GAL4 defines two transcriptional activating segments
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45. Resistance to mitomycin C requires direct interaction between the Fanconi anemia protein FANCA and FANCG in the nucleus through an arginine-rich domain