15 results for author:"Chan A.Y." in Literature citations
Results Customize
› Repeat search in UniProtKB (1)
| Cdc42 GTPase and Rac1 GTPase act downstream of p120 catenin and require GTP exchange during gastrulation of zebrafish mesoderm. Hsu C.L., Muerdter C.P., Knickerbocker A.D., Walsh R.M., Zepeda-Rivera M.A., Depner K.H., Sangesland M., Cisneros T.B., Kim J.Y., Sanchez-Vazquez P. et al. Dev. Dyn. 241:1545-1561(2012) · Mapped (20) |
| Treatment of erythropoietin deficiency in mice with systemically administered siRNA. Querbes W., Bogorad R.L., Moslehi J., Wong J., Chan A.Y., Bulgakova E., Kuchimanchi S., Akinc A., Fitzgerald K., Koteliansky V. et al. Blood 120:1916-1922(2012) · Mapped (7) |
| Genetic diagnosis of severe myoclonic epilepsy of infancy (Dravet syndrome) with SCN1A mutations in the Hong Kong Chinese patients. Mak C.M., Chan K.Y., Yau E.K., Chen S.P., Siu W.K., Law C.Y., Lam C.W., Chan A.Y. Hong Kong Med J 17:500-502(2011) · Mapped (7) |
| Novel nonsense CDC73 mutations in Chinese patients with parathyroid tumors. Siu W.K., Law C.Y., Lam C.W., Mak C.M., Wong G.W., Ho A.Y., Ho K.Y., Loo K.T., Chiu S.C., Chow L.T. et al. Fam. Cancer 10:695-699(2011) · Mapped (2) |
| Fatal viral infection-associated encephalopathy in two Chinese boys: a genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants. Mak C.M., Lam C.W., Fong N.C., Siu W.K., Lee H.C., Siu T.S., Lai C.K., Law C.Y., Tong S.F., Poon W.T. et al. J. Hum. Genet. 56:617-621(2011) · UniProtKB (1) · Mapped (1) |
| Molecular basis of von Hippel-Lindau syndrome in Chinese patients. Siu W.K., Ma R.C., Lam C.W., Mak C.M., Yuen Y.P., Lo F.M., Chan K.W., Lam S.F., Ling S.C., Tong S.F. et al. Chin. Med. J. 124:237-241(2011) · Mapped (3) |
| A novel duplication at the putative DNA polymerase alpha arrest site and a founder mutation in Chinese in the IVD gene underlie isovaleric acidaemia. Lee H.H., Lee R.S., Lai C.K., Yuen Y.P., Siu T.S., Chan A.Y., Lam C.W. Hong Kong Med J 16:219-222(2010) · Mapped (7) |
| Distinct early signaling events resulting from the expression of the PRKAG2 R302Q mutant of AMPK contribute to increased myocardial glycogen. Folmes K.D., Chan A.Y., Koonen D.P., Pulinilkunnil T.C., Baczko I., Hunter B.E., Thorn S., Allard M.F., Roberts R., Gollob M.H. et al. Circ Cardiovasc Genet 2:457-466(2009) · Mapped (3) |
| Hereditary spastic paraplegia: identification of an SPG3A gene mutation in a Chinese family. Chan K.Y., Ching C.K., Mak C.M., Lam C.W., Chan A.Y. Hong Kong Med J 15:304-307(2009) · Mapped (3) |
| Resveratrol inhibits cardiac hypertrophy via AMP-activated protein kinase and Akt. Chan A.Y., Dolinsky V.W., Soltys C.L., Viollet B., Baksh S., Light P.E., Dyck J.R. J. Biol. Chem. 283:24194-24201(2008) · Mapped (27) |
| The lack of association between JAK2 V617F mutation and myelodysplastic syndrome with or without myelofibrosis. Yip S.F., So C.C., Chan A.Y., Liu H.Y., Wan T.s.K., Chan L.C. Leukemia 20:1165-1165(2006) · Mapped (6) |
| Roles of the Rac1 and Rac3 GTPases in human tumor cell invasion. Chan A.Y., Coniglio S.J., Chuang Y.Y., Michaelson D., Knaus U.G., Philips M.R., Symons M. Oncogene 24:7821-7829(2005) · Mapped (1) |
| Role of Rho family GTPases in CCR1- and CCR5-induced actin reorganization in macrophages. Di Marzio P., Dai W.W., Franchin G., Chan A.Y., Symons M., Sherry B. Biochem. Biophys. Res. Commun. 331:909-916(2005) · Mapped (27) |
| Association of extensive polymorphisms in the SLAM/CD2 gene cluster with murine lupus. Wandstrat A.E., Nguyen C., Limaye N., Chan A.Y., Subramanian S., Tian X.H., Yim Y.S., Pertsemlidis A., Garner H.R. Jr., Morel L. et al. Immunity 21:769-780(2004) · Mapped (41) |
| Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia? Chan L.C., Ma S.K., Chan A.Y., Ha S.Y., Waye J.S., Lau Y.L., Chui D.H. J. Clin. Pathol. 54:317-320(2001) · Mapped (14) |