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Results 71-80 of 80 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1999Characterization of copine VII, a new member of the copine family, and its exclusion as a candidate in sporadic breast cancers with loss of heterozygosity at 16q24.3Savino, M.; d'Apolito, M.; Centra, M.; van Beerendonk, H.; Cleton-Jansen, A.M.; Whitmore, S.; Crawford, J.; Callen, D.; Zelante, L.; Savoia, A.
2001Molecular cloning of a human Vent-like homeobox geneMoretti, P.; Davidson, A.; Baker, E.; Lilley, B.; Zon, L.; D'Andrea, R.
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.
1997The Mouse Homeobox Gene, Gbx2: Genomic Organisation and Expression in Pluripotent Cells in Vitro and in VivoChapman, G.; Remiszewski, J.; Webb, G.; Schulz, T.; Bottema, C.; Rathjen, P.
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.
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.