AC T25652
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ID T25652
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DT 11.11.2009 (created); jig.
DT 22.08.2012 (updated); yre.
CO Copyright (C), QIAGEN.
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FA MCT
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SY BRIT1; FLJ12847; MCPH1; MCT; microcephalin 1; microcephaly, primary autosomal recessive 1.
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OS human, Homo sapiens
OC eukaryota; animalia; metazoa; chordata; vertebrata; tetrapoda; mammalia; eutheria; primates
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GE G034966 MCPH1; HGNC: MCPH1.
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IN T22426 BAF170; human, Homo sapiens.
IN T01542 E2F-1; human, Homo sapiens.
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DR TRANSPATH: MO000164839.
DR UniProtKB: Q8NEM0;
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RN [1]; RE0065412.
RX PUBMED: 19525936.
RA Peng G., Yim E. K., Dai H., Jackson A. P., Burgt I., Pan M. R., Hu R., Li K., Lin S. Y.
RT BRIT1/MCPH1 links chromatin remodelling to DNA damage response.
RL Nat. Cell Biol. 11:865-872 (2009).
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