9 results for author:"Beck J.S." in Literature citations
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| Primary cilia membrane assembly is initiated by Rab11 and transport protein particle II (TRAPPII) complex-dependent trafficking of Rabin8 to the centrosome. Westlake C.J., Baye L.M., Nachury M.V., Wright K.J., Ervin K.E., Phu L., Chalouni C., Beck J.S., Kirkpatrick D.S., Slusarski D.C. et al. Proc. Natl. Acad. Sci. U.S.A. 108:2759-2764(2011) · Mapped (10) |
| The N-terminal region of centrosomal protein 290 (CEP290) restores vision in a zebrafish model of human blindness. Baye L.M., Patrinostro X., Swaminathan S., Beck J.S., Zhang Y., Stone E.M., Sheffield V.C., Slusarski D.C. Hum. Mol. Genet. 20:1467-1477(2011) · Mapped (3) |
| Genome-wide analysis of copy number variants in age-related macular degeneration. Meyer K.J., Davis L.K., Schindler E.I., Beck J.S., Rudd D.S., Grundstad A.J., Scheetz T.E., Braun T.A., Fingert J.H., Alward W.L. et al. Hum. Genet. 129:91-100(2011) · Mapped (4) |
| BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly. Seo S., Baye L.M., Schulz N.P., Beck J.S., Zhang Q., Slusarski D.C., Sheffield V.C. Proc. Natl. Acad. Sci. U.S.A. 107:1488-1493(2010) · UniProtKB (11) · Mapped (31) |
| A BBSome subunit links ciliogenesis, microtubule stability and acetylation. Loktev A.V., Zhang Q., Beck J.S., Searby C.C., Scheetz T.E., Bazan F., Slusarski D.C., Sheffield V.C., Jackson P.K., Nachury M.V. |
| Genetic interaction between Bardet-Biedl syndrome genes and implications for limb patterning. Tayeh M.K., Yen H.J., Beck J.S., Searby C.C., Westfall T.A., Griesbach H., Sheffield V.C., Slusarski D.C. Hum. Mol. Genet. 17:1956-1967(2008) · Mapped (14) |
| Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11). Chiang A.P., Beck J.S., Yen H.-J., Tayeh M.K., Scheetz T.E., Swiderski R.E., Nishimura D.Y., Braun T.A., Kim K.-Y.A., Huang J. et al. Proc. Natl. Acad. Sci. U.S.A. 103:6287-6292(2006) · UniProtKB (1) · Mapped (2) |
| Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome. Mykytyn K., Nishimura D.Y., Searby C.C., Shastri M., Yen H., Beck J.S., Braun T., Streb L.M., Cornier A.S., Cox G.F. et al. Nat. Genet. 31:435-438(2002) · UniProtKB (1) |
| Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresis. Sheffield V.C., Fishman G.A., Beck J.S., Kimura A.E., Stone E.M. Am. J. Hum. Genet. 49:699-706(1991) · UniProtKB (1) |