1. Adelaide Research & Scholarship

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Results 21-30 of 35 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1995A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsySteinlein, O.; Mulley, J.; Propping, P.; Wallace, R.; Phillips, H.; Sutherland, G.; Scheffer, I.; Berkovic, S.
1995Molecular cloning of the cDNA encoding human skeletal muscle triadin and its localisation to chromosome 6q22-6q23Taske, N.; Eyre, H.; O'Brien, R.; Sutherland, G.; Denborough, M.; Foster, P.
1995Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a 'hot-spot' for recombination at 16p12Callen, D.; Lane, S.; Kozman, H.; Kremmidiotis, G.; Whitmore, S.; Lowenstein, M.; Doggett, N.; Kenmochi, N.; Page, D.; Maglott, D.; Nierman, W.; Murakawa, K.; Sikela, J.; Houlgatte, R.; Auffray, C.; Sutherland, G.
1996Characterization and chromosomal localization of the human A2a adenosine receptor gene - ADORA2ALe, F.; Townsend-Nicholson, A.; Baker, E.; Sutherland, G.; Schofield, P.
1995Localization of the gene encoding the human heat shock cognate protein, HSP73 to chromosome 11Tavaria, M.; Gabriele, T.; Anderson, R.; Mirault, M.E.; Baker, E.; Sutherland, G.; Kola, I.
1995Bovine latent transforming growth factor β1-binding protein 2: molecular cloning, identification of tissue isoforms, and immunolocalization to elastin-associated microfibrilsGibson, M.; Hatzinikolas, G.; Davis, E.; Baker, E.; Sutherland, G.; Mecham, R.
1999GPR56, a novel secretin-like human G-protein-coupled receptor geneLiu, M.; Parker, R.; Darby, K.; Eyre, H.; Copeland, N.; Crawford, J.; Gilbert, D.; Sutherland, G.; Jenkins, N.; Herzog, H.
1996Cloning of human lymphocyte-specific interferon regulatory factor (hLSIRF/hIRF4) and mapping of the gene to 6p23-p25Grossman, A.; Mittrucker, H.W.; Nicholl, J.; Suzuki, A.; Chung, S.; Antonio, L.; Suggs, S.; Sutherland, G.; Siderovski, D.; Mak, T.
1998Localisation of the human NMDAR2D receptor subunit gene (GRIN2D) to 19q13.1-qter, the NMDAR2A subunit gene to 16p13.2 (GRIN2A), and the NMDAR2C subunit gene (GRIN2C) to 17q24-q25 using somatic cell hybrid and radiation hybrid mapping panels.Kalsi, G.; Whiting, P.; Bourdelles, B.; Callen, D.; Barnard, E.; Gurling, H.
1996Molecular Characterization of a Nonneuronal Human Unc18 HomologZiegler, S.; Mortrud, M.; Swartz, A.; Baker, E.; Sutherland, G.; Burmeister, M.; Mulligan, J.

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