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PreviewIssue DateTitleAuthor(s)
2006Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardationHagens, O.; Dubos, A.; Abidi, F.; Barbi, G.; Van Zutven, L.; Hoeltzenbein, M.; Tommerup, N.; Moraine, C.; Fryns, J.; Chelly, J.; van Bokhoven, H.; Gecz, J.; Dollfus, H.; Ropers, H.; Schwartz, C.; de Cassia Stocco dos Santos, R.; Kalscheuer, V.; Hanauer, A.
2008The fallaxidin peptides from the skin secretion of the Eastern Dwarf Tree Frog Litoria fallax. Sequence determination by positive and negative ion electrospray mass spectrometry: antimicrobial activity and cDNA cloning of the fallaxidinsJackway, R.; Bowie, J.; Bilusich, D.; Musgrave, I.; Surinya, K.; Tyler, M.; Eichinger, P.
1995Gene duplication of the human peptide YY gene (PYY) generated the pancreatic polypeptide gene (PPY) on chromosome 17q21.1Hort, Y.; Baker, E.; Sutherland, G.; Shine, J.; Herzog, H.
1999A putative exchange factor for Rho1 GTPase is required for initiation of cytokinesis in DrosophilaProkopenko, S.; Brumby, A.; O'Keefe, L.; Prior, L.; He, Y.; Saint, R.; Bellen, H.
1998Inactivation of two haemolytic toxin genes in Aeromonas hydrophila attenuates virulence in a suckling mouse modelWong, C.; Heuzenroeder, M.; Flower, R.
2000Cytochrome P450 4A, peroxisomal enzymes and nicotinamide cofactors in koala liverNgo, S.; Kong, S.; Kirlich, A.; McKinnon, R.; Stupans, I.
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.
1996Feline mucopolysaccharidosis type VI - characterization of recombinant N-acetylgalactosamine 4-sulfatase and identification of a mutation causing the diseaseYogalingam, G.; Litjens, T.; Bielicki, J.; Crawley, A.; Muller, V.; Anson, D.; Hopwood, J.
1999Myeloid DAP12-associating lectin (MDL)-1 is a cell surface receptor involved in the activation of myeloid cellsBaker, E.; Sutherland, G.; Phillips, J.; Lanier, L.
1997Ancient missense mutations in a new member of the RoRet gene family are likely to cause Familial Mediterranean FeverAksentijevich, I.; Centola, M.; Deng, Z.; Sood, R.; Balow, J.; Wood, G.; Zaks, N.; Mansfield, E.; Chen, X.; Eisenberg, S.; Vedula, A.; Shafran, N.; Raben, N.; Pras, E.; Pras, M.; Kastner, D.; Blake, T.; Baxevanis, A.; Robbins, C.; Krizman, D.; et al.