1. Adelaide Research & Scholarship

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Results 1-10 of 17 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1995Molecular cloning of cDNA encoding a novel platelet-endothelial cell tetra-span antigen, PETA-3Fitter, S.; Tetaz, T.J.; Berndt, M.C.; Ashman, L.K.
1995Activating point mutations in the common beta subunit of the human GM-CSF, IL-3 and IL-5 receptors suggest the involvement of beta subunit dimerization and cell type-specific molecules in signallingJenkins, B.; D'Andrea, R.; Gonda, T.
1996Two novel frameshift mutations causing premature stop codons in a patient with the severe form of Maroteaux-Lamy syndromeIsbrandt, D.; Hopwood, J.; von Figura, K.; Peters, C.
1999Splice variants of the mouse Tec gene are differentially expressed in vivoMerkel, A.; Atmosukarto, I.; Stevens, K.; Rathjen, P.; Booker, G.
1999A single limit dextrinase gene is expressed both in the developing endosperm and in germinated grains of barleyBurton, R.; Zhang, X.Q.; Hrmova, M.; Fincher, G.
1996DNA binding by the coliphage 186 repressor protein C1Dodd, I.; Egan, J.
1995A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathyLaing, N.; Wilton, S.; Akkari, P.; Dorosz, S.; Boundy, K.; Kneebone, C.; Blumbergs, P.; White, S.; Watkins, H.; Love, D.; Haan, E.
1996A novel X-linked gene, G4.5. is responsible for Barth SyndromeBione, S.; D'Adamo, P.; Maestrini, E.; Gedeon, A.; Bolhuis, P.; Toniolo, D.
1996Identification of the gene FMR2, associated with FRAXE mental retardationGecz, J.; Gedeon, A.; Sutherland, G.; Mulley, J.
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.

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