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PreviewIssue DateTitleAuthor(s)
1996bcl-w, a novel member of the bcl-2 family, promotes cell survivalGibson, L.; Holmgreen, S.; Huang, D.; Bernand, O.; Copeland, N.; Jenkins, N.; Sutherland, G.; Baker, E.; Adams, J.; Cory, S.
1998Identification of a human HECT family protein with homology to the Drosophila tumor suppressor gene hyperplastic discsCallaghan, M.; Russell, A.; Woollatt, E.; Sutherland, G.; Sutherland, R.; Watts, C.
1996Characterization and chromosomal localization of the human A2a adenosine receptor gene - ADORA2ALe, F.; Townsend-Nicholson, A.; Baker, E.; Sutherland, G.; Schofield, P.
1998PAK3 mutation in nonsyndromic X-linked mental retardationAllen, K.; Gleeson, J.; Bagrodia, S.; Partington, M.; MacMillan, J.; Cerione, R.; Mulley, J.; Walsh, C.
1998The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.Kortschak, R.; Reimann, H.; Zimmer, M.; Eyre, H.; Saint, R.; Jenne, D.
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.
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.