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PreviewIssue DateTitleAuthor(s)
2001Gene structure, alternative splicing, and chromosomal localization of pro-apoptotic Bcl-2 relative BimBouillet, P.; Zhang, L.; Huang, D.; Webb, G.; Bottema, C.; Shore, P.; Eyre, H.; Sutherland, G.; Adams, J.
2001Fcα/μ receptor is a single gene-family member closely related to polymeric immunoglobulin receptor encoded on Chromosome 1Shimizu, Y.; Honda, S.; Yotsumoto, K.; Tahara-Hanaoka, S.; Eyre, H.; Sutherland, G.; Endo, Y.; Shibuya, K.; Koyama, A.; Nakauchi, H.; Shibuya, A.
2000Y-receptor-like genes GPR72 and GPR73: molecular cloning, genomic organisation and assignment to human chromosome 11q21.1 and 2p14 and mouse chromosome 9 and 6Parker, R.; Liu, M.; Eyre, H.; Copeland, N.; Gilbert, D.; Crawford, J.; Sutherland, G.; Jenkins, N.; Herzog, H.
2004HLS5, a novel RBCC (ring finger, B box, coiled-coil) family member isolated from a hemopoietic lineage switch, is a candidate tumor suppressorLalonde, J.; Lim, R.; Ingley, E.; Tilbrook, P.; Thompson, M.; McCulloch, R.; Beaumont, J.; Wicking, C.; Eyre, H.; Sutherland, G.; Howe, K.; Solomon, E.; Williams, J.; Klinken, S.
2001CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsyPhillips, H.; Favre, I.; Kirkpatrick, M.; Zuberi, S.; Goudie, D.; Heron, S.; Scheffer, I.; Sutherland, G.; Berkovic, S.; Bertrand, D.; Mulley, J.
2002Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsyStromme, P.; Mangelsdorf, M.; Shaw, M.; Lower, K.; Lewis, S.; Bruyere, H.; Lutcherath, V.; Gedeon, A.; Wallace, R.; Scheffer, I.; Turner, G.; Partington, M.; Frints, S.; Fryns, J.; Sutherland, G.; Mulley, J.; Gecz, J.
2001TTYH2, a human homologue of the Drosophila melanogaster gene tweety, is located on 17q24 and upregulated in renal cell carcinomaRae, F.; Hooper, J.; Eyre, H.; Sutherland, G.; Nicol, D.; Clements, J.
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.

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