1. Adelaide Research & Scholarship

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Results 31-40 of 104 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2010Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidanceTischfield, M.; Baris, H.; Wu, C.; Rudolph, G.; van Maldergem, L.; He, W.; Chan, W.; Andrews, C.; Demer, J.; Robertson, R.; Mackey, D.; Ruddle, J.; Bird, T.; Gottlob, I.; Pieh, C.; Traboulsi, E.; Pomeroy, S.; Hunter, D.; Soul, J.; Newlin, A.; et al.
1995The CEPH consortium linkage map of human chromosome 16Kozman, H.; Keith, T.; Donis-Keller, H.; White, R.; Weissenbach, J.; Sutherland, G.
2003Development of a diagnostic PCR assay that targets a heat-shock protein gene (groES) for detection of Pseudomonas spp. in cystic fibrosis patientsClarke, L.; Moore, J.; Millar, B.; Garske, L.; Xu, J.; Heuzenroeder, M.; Crowe, M.; Elborn, J.
2000Cytochrome P450 4A, peroxisomal enzymes and nicotinamide cofactors in koala liverNgo, S.; Kong, S.; Kirlich, A.; McKinnon, R.; Stupans, I.
1995Apert syndrome results from localised mutations of FGFR2 and is allelic with Crouzon syndromeWilkie, A.; Slaney, S.; Oldridge, M.; Poole, M.; Ashworth, G.; Hockley, A.; Hayward, R.; David, D.; Pulleyn, L.; Rutland, P.; Malcolm, S.; Winter, R.; Reardon, W.
2010DNA methylation-mediated Down-regulation of DNA methyltransferase-1 (DNMT1) is coincident with, but not essential for, global hypomethylation in human placentaNovakovic, B.; Wong, N.; Sibson, M.; Ng, H.; Morley, R.; Manuelpillai, U.; Down, T.; Rakyan, V.; Beck, S.; Hiendleder, S.; Roberts, C.; Craig, J.; Saffery, R.
2013HIV non-B subtype distribution: Emerging trends and risk factors for imported and local infections newly diagnosed in South AustraliaHawke, K.; Waddell, R.; Gordon, D.; Ratcliff, R.; Ward, P.; Kaldor, J.
1996Further characterization of proteins associated with elastic fiber microfibrils including the molecular cloning of MAGP-2 (MP25)Gibson, M.; Hatzinikolas, G.; Kumaratilake, J.; Sandberg, L.; Nicholl, J.; Sutherland, G.; Cleary, E.
2004Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardationFreude, K.; Hoffmann, K.; Jensen, L.; Delatycki, M.; des Portes, V.; Moser, B.; Hamel, B.; van Bokhoven, H.; Moraine, C.; Fryns, J.; Chelly, J.; Gecz, J.; Lenzner, S.; Kalscheuer, V.; Ropers, H.
1998Two-dimensional mapping and microsequencing of lysosomal proteins from human placentaChataway, T.; Whittle, A.; Lewis, M.; Bindloss, C.; Davey, R.; Moritz, R.; Simpson, R.; Hopwood, J.; Meikle, P.

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