uniprot:Q562F6 in Computationally mapped citations

2 results for uniprot:Q562F6 in Computationally mapped citations

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Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy. CPNDS Consortium Ross C.J., Katzov-Eckert H., Dube M.P., Brooks B., Rassekh S.R., Barhdadi A., Feroz-Zada Y., Visscher H., Brown A.M., Rieder M.J. et al. Nat. Genet. 41:1345-1349(2009) GeneRIF 151246 · Mapped (250) Observational study of gene-disease association. (HuGE Navigator) GeneRIF 151246
Phosphorylation of mammalian Sgo2 by Aurora B recruits PP2A and MCAK to centromeres. Tanno Y., Kitajima T.S., Honda T., Ando Y., Ishiguro K., Watanabe Y. Genes Dev. 24:2169-2179(2010) GeneRIF 151246 · Mapped (25) identified the phosphorylation of hSgo2 by Aurora B at the N-terminal coiled-coil region and the middle region and showed that these phosphorylations separately promote binding of hSgo2 to PP2A and MCAK GeneRIF 151246