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4 results for author:"Paulding C." in Literature citations

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Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056.

Jacquemont S., Curie A., des Portes V., Torrioli M.G., Berry-Kravis E., Hagerman R.J., Ramos F.J., Cornish K., He Y., Paulding C. et al.

Sci Transl Med 3:64ra1-64ra1(2011) · Mapped (8)

A genome-wide study identifies HLA alleles associated with lumiracoxib-related liver injury.

Singer J.B., Lewitzky S., Leroy E., Yang F., Zhao X., Klickstein L., Wright T.M., Meyer J., Paulding C.A.

Nat. Genet. 42:711-714(2010) · Mapped (808)

DOCK4, a GTPase activator, is disrupted during tumorigenesis.

Yajnik V., Paulding C., Sordella R., McClatchey A.I., Saito M., Wahrer D.C.R., Reynolds P., Bell D.W., Lake R., van den Heuvel S. et al.

Cell 112:673-684(2003) · UniProtKB (3) · Mapped (1)

The Tre2 (USP6) oncogene is a hominoid-specific gene.

Paulding C.A., Ruvolo M., Haber D.A.

Proc. Natl. Acad. Sci. U.S.A. 100:2507-2511(2003) · UniProtKB (17) · Mapped (2)

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