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Results 71-79 of 79 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1997Structural organization of the mouse and human GALR1 Galanin receptor genes (Galnr and GALNR) and chromosomal localization of the mouse geneJacoby, A.; Webb, G.; Liu, M.; Kofler, B.; Hort, Y.; Fathi, Z.; Bottema, C.; Shine, J.; Iismaa, T.
1999Identification, functional characterization, and chromosomal localization of USP15, a novel human ubiquitin-specific protease related to the UNP oncoprotein, and a systematic nomenclature for human ubiquitin-specific proteasesBaker, R.; Wang, X.W.; Woollatt, E.; White, J.; Sutherland, G.
1998SOLH, a human homologue of the Drosophila melanogaster small optic lobes gene is a member of the Calpain and Zinc-Finger gene families and maps to human chromosome 16p13.3 near CATM (cataract with microphthalmia)Kamei, M.; Webb, G.; Young, I.; Campbell, H.
2000Human and mouse homologues of the Drosophila melanogaster tweety (tty) gene: A novel gene family encoding predicted transmembrane proteinsCampbell, H.; Kamei, M.; Claudianos, C.; Woollatt, E.; Sutherland, G.; Suzuki, Y.; Hida, M.; Sugano, S.; Young, I.
2001Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia proteinKremmidiotis, G.; Gardner, A.; Settasatian, C.; Savoia, A.; Sutherland, G.; Callen, D.
2000Solh, the mouse homologue of the Drosophila melanogaster small optic lobes gene: organization, chromosomal mapping, and localization of gene product to the olfactory bulbKamei, M.; Webb, G.; Heydon, K.; Hendry, I.; Young, I.; Campbell, H.
1995Cloning and sequence analysis of caprine N-acetylglucosamine 6-sulfatase cDNAFriderici, K.; Cavanagh, K.; Leipprandt, J.; Traviss, C.; Anson, D.; Hopwood, J.; Jones, M.
1994Isolation and characterization of ovine IGFBP-4: protein purification and cDNA sequenceCARR, J.M.; GRANT, P.A.; FRANCIS, G.L.; OWENS, J.A.; WALLACE, J.C.; WALTON, P.E.
2009Aire-Deficient C57BL/6 Mice Mimicking the Common Human 13-Base Pair Deletion Mutation Present with Only a Mild Autoimmune PhenotypeHubert, F.; Kinkel, S.; Crewther, P.; Cannon, P.; Webster, K.; Link, M.; Uibo, R.; O'Bryan, M.; Meager, A.; Forehan, S.; Smyth, G.; Mittaz, L.; Antonarakis, S.; Peterson, P.; Heath, W.; Scott, H.