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Results 11-20 of 29 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1999Isolation and characterisation of a cDNA encoding a Zona Pellucida Protein (ZPB) from the marsupial Trichosurus vulpecula (Brushtail Possum)Haines, B.; Rathjen, P.; Hope, R.; Whyatt, L.; Holland, M.; Breed, W.
1999Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patientGecz, J.; Baker, E.; Donnelly, A.; Ming, J.; McDonald-McGinn, D.; Spinner, N.; Zackai, E.; Sutherland, G.; Mulley, J.
1999Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHMFriend, K.; Crimmins, D.; Phan, T.; Sue, C.; Colley, A.; Fung, V.; Morris, J.; Sutherland, G.; Richards, R.
1999The Salmonella typhi melittin resistance gene pqaB affects intracellular growth in PMA-differentiated U937 cells, polymyxin B resistance, and lipopolysaccharide.Baker, S.; Gunn, J.; Morona, R.
1999A cell type-specific constitutive point mutant of the common β-subunit of the human granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin (IL)-3, and IL-5 receptors requires the GM-CSF receptor α-subunit for activationJenkins, B.; Le, F.; Gonda, T.
1999Cloning, characterization, and chromosomal location of a novel human K+-C1- cotransporterHiki, K.; D'Andrea, R.; Furze, J.; Crawford, J.; Woollatt, E.; Sutherland, G.; Vadas, M.; Gamble, J.
1999Microfibril-associated glycoprotein-2 specifically interacts with a range of bovine and human cell types via αVβ3 integrinGibson, M.; Leavesley, D.; Ashman, L.
1999Characterization and chromosomal localization of USP3, a novel human ubiquitin-specific proteaseSloper-Mould, K.; Eyre, H.; Wang, X.W.; Sutherland, G.; Baker, R.
1999Molecular cloning and characterization of a cDNA encoding the human leucocyte vacuolar protein sorting (h1Vps45)Rajasekariah, P.; Eyre, H.; Stanley, K.; Walls, R.; Sutherland, G.
1999Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromesMcDermott, M.; Aksentijevich, I.; Galon, J.; McDermott, E.; Ogunkolade, B.; Centola, M.; Mansfield, E.; Gadina, M.; Karenko, L.; Petterson, T.; McCarthy, J.; Frucht, D.; Aringer, M.; Torosyan, Y.; Teppo, A.M.; Wilson, M.; Karaarslan, H.; Wan, Y.; Todd, I.; Wood, G.; et al.