6
results
for author:"Tan M.-H."
in Literature Citations
| Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectors. Tan M.H., Smith A.J., Pawlyk B., Xu X., Liu X., Bainbridge J.B., Basche M., McIntosh J., Tran H.V., Nathwani A. et al. Hum. Mol. Genet. 18:2099-2114(2009) · Mapped (2) |
| Somatic pairing of chromosome 19 in renal oncocytoma is associated with deregulated EGLN2-mediated oxygen-sensing response. Koeman J.M., Russell R.C., Tan M.H., Petillo D., Westphal M., Koelzer K., Metcalf J.L., Zhang Z., Matsuda D., Dykema K.J. et al. PLoS Genet. 4:e1000176-e1000176(2008) · Mapped (2) |
| Identification of MEN1 and HRPT2 somatic mutations in paraffin-embedded (sporadic) parathyroid carcinomas. Haven C.J., van Puijenbroek M., Tan M.H., Teh B.T., Fleuren G.J., van Wezel T., Morreau H. Clin. Endocrinol. (Oxf) 67:370-376(2007) · Mapped (14) |
| Patterns of somatic mutation in human cancer genomes. Greenman C., Stephens P., Smith R., Dalgliesh G.L., Hunter C., Bignell G., Davies H., Teague J., Butler A., Stevens C. et al. Nature 446:153-158(2007) · UniProtKB (453) |
| Parafibromin inhibits cancer cell growth and causes G1 phase arrest. Zhang C., Kong D., Tan M.H., Pappas D.L. Jr., Wang P.F., Chen J., Farber L., Zhang N., Koo H.M., Weinreich M. et al. Biochem. Biophys. Res. Commun. 350:17-24(2006) · Mapped (2) |
| Deletion of the alternatively spliced fibronectin EIIIA domain in mice reduces atherosclerosis. Tan M.H., Sun Z., Opitz S.L., Schmidt T.E., Peters J.H., George E.L. Blood 104:11-18(2004) · Mapped (25) |
