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Ercc3
excision repair cross-complementing rodent repair deficiency, complementation group 3
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On chromosome: 18
Known also as: XPB; Ercc-3; BTF2 p89;
Mus musculus excision repair cross-complementing rodent repair deficiency, complementation group 3 (Ercc3).
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Gene sequence:
Proteins coded by this gene:
References:
Authors
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Title
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Journal
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Weeda G, Ma L, van Ham RC, Bootsma D, van der Eb AJ, Hoeijmakers JH
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Characterization of the mouse homolog of the XPBC/ERCC-3 gene implicated in xeroderma pigmentosum and Cockayne's syndrome.
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Carcinogenesis
Dec. 1, 1991
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Sano M, Izumi Y, Helenius K, Asakura M, Rossi DJ, Xie M, Taffet G, Hu L, Pautler RG, Wilson CR, Boudina S, Abel ED, Taegtmeyer H, Scaglia F, Graham BH, Kralli A, Shimizu N, Tanaka H, Makela TP, Schneider MD
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Menage-a-trois 1 is critical for the transcriptional function of PPARgamma coactivator 1.
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Cell Metab
Jan. 1, 2007
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Andressoo JO, Weeda G, de Wit J, Mitchell JR, Beems RB, van Steeg H, van der Horst GT, Hoeijmakers JH
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An Xpb mouse model for combined xeroderma pigmentosum and cockayne syndrome reveals progeroid features upon further attenuation of DNA repair.
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Mol Cell Biol
March 1, 2009
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Giglia-Mari G, Theil AF, Mari PO, Mourgues S, Nonnekens J, Andrieux LO, de Wit J, Miquel C, Wijgers N, Maas A, Fousteri M, Hoeijmakers JH, Vermeulen W
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Differentiation driven changes in the dynamic organization of Basal transcription initiation.
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PLoS Biol
Oct. 1, 2009
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Sasaki K, Hamazaki J, Koike M, Hirano Y, Komatsu M, Uchiyama Y, Tanaka K, Murata S
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PAC1 gene knockout reveals an essential role of chaperone-mediated 20S proteasome biogenesis and latent 20S proteasomes in cellular homeostasis.
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Mol Cell Biol
Aug. 1, 2010
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Last modification of this entry: Oct. 6, 2010.
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