10 results for author:"Harrison W.R." in Literature citations
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| Intracorneal positioning of the lens in Pax6-GAL4/VP16 transgenic mice. Govindarajan V., Harrison W.R., Xiao N., Liang D., Overbeek P.A. Mol. Vis. 11:876-886(2005) · Mapped (20) |
| Genetic mapping of an insertional hydrocephalus-inducing mutation allelic to hy3. Robinson M.L., Allen C.E., Davy B.E., Durfee W.J., Elder F.F., Elliott C.S., Harrison W.R. Mamm. Genome 13:625-632(2002) · Mapped (1) |
| A transgenic insertion causing cryptorchidism in mice. Overbeek P.A., Gorlov I.P., Sutherland R.W., Houston J.B., Harrison W.R., Boettger-Tong H.L., Bishop C.E., Agoulnik A.I. |
| Smcy transgene does not rescue spermatogenesis in sex-reversed mice. Agulnik A.I., Harrison W.R., Bishop C.E. Mamm. Genome 12:112-116(2001) · Mapped (7) |
| A transgenic insertion upstream of sox9 is associated with dominant XX sex reversal in the mouse. Bishop C.E., Whitworth D.J., Qin Y., Agoulnik A.I., Agoulnik I.U., Harrison W.R., Behringer R.R., Overbeek P.A. Nat. Genet. 26:490-494(2000) · Mapped (22) |
| Mutations in a novel photoreceptor-pineal gene on 17p cause Leber congenital amaurosis. Sohocki M.M., Bowne S.J., Sullivan L.S., Blackshaw S., Cepko C.L., Payne A.M., Bhattacharya S.S., Khaliq S., Mehdi Q., Birch D.G. et al. Nat. Genet. 24:79-83(2000) · UniProtKB (3) |
| Insertional mutation of the collagen genes Col4a3 and Col4a4 in a mouse model of Alport syndrome. Lu W., Phillips C.L., Killen P.D., Hlaing T., Harrison W.R., Elder F.F.B., Miner J.H., Overbeek P.A., Meisler M.H. |
| Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sites. Sohocki M.M., Sullivan L.S., Harrison W.R., Sodergren E.J., Elder F.F.B., Weinstock G., Tanase S., Daiger S.P. Genomics 40:247-252(1997) · UniProtKB (1) |
| Characterization of human DSPG3, a small dermatan sulfate proteoglycan. Deere M., Johnson H.J., Garza S., Harrison W.R., Yoon S.-J., Elder F.F.B., Kucherlapati R., Hoeoek M., Hecht J.T. Genomics 38:399-404(1996) · UniProtKB (1) |
| Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia. Hecht J.T., Nelson L.D., Crowder E., Wang Y., Elder F.F.B., Harrison W.R., Francomano C.A., Prange C.K., Lennon G.G., Deere M. et al. |