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Preview	Issue Date	Title	Author(s)
	2009	Aire-Deficient C57BL/6 Mice Mimicking the Common Human 13-Base Pair Deletion Mutation Present with Only a Mild Autoimmune Phenotype	Hubert, F.; Kinkel, S.; Crewther, P.; Cannon, P.; Webster, K.; Link, M.; Uibo, R.; O'Bryan, M.; Meager, A.; Forehan, S.; Smyth, G.; Mittaz, L.; Antonarakis, S.; Peterson, P.; Heath, W.; Scott, H.
	2003	RegR, a global LacI/GalR family regulator, modulates virulence and competence in Streptococcus pneumoniae	Chapuy-Regaud, S.; Ogunniyi, A.; Diallo, N.; Huet, Y.; Desnottes, J.; Paton, J.; Escaich, S.; Trombe, M.
	1995	Comparative toxicity and virulence of Escherichia coli clones expressing variant and chimeric Shiga-like toxin type II operons	Paton, A.; Bourne, A.; Manning, P.; Paton, J.
	1995	Assignment of the human skeletal muscle a-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridization	Eyre, H.; Akkari, P.; Wilton, S.; Callen, D.; Baker, E.; Laing, N.
	1996	bcl-w, a novel member of the bcl-2 family, promotes cell survival	Gibson, L.; Holmgreen, S.; Huang, D.; Bernand, O.; Copeland, N.; Jenkins, N.; Sutherland, G.; Baker, E.; Adams, J.; Cory, S.
	1996	Expression of functional decay-accelerating factor (Cd55) in transgenic mice protects against human complement-mediated attack1	van Denderen, B.; Pearse, M.; Katerelos, M.; Nottle, M.; Du, Z.T.; Aminian, A.; Adam, W.; Shenoy-Scaria, A.; Lublin, D.; Shinkel, T.; d'Apice, A.
	1996	Physiological Levels of Calcitonin Regulate the Mouse Osteoclast Calcitonin Receptor by a Protein Kinase A-Mediated Mechanism	Wada, S.; Udagawa, N.; Nagata, N.; Martin, T.; Findlay, D.
	1997	A Novel Epithelial-Expressed ETS Gene, ELF3 - Human and Murine cDNA Sequences, Murine Genomic Organization, Human Mapping to 1q32.2 and Expression in Tissues and Cancer	Tymms, M.; Ng, A.; Thomas, R.; Schutte, B.; Zhou, J.; Eyre, H.; Sutherland, G.; Seth, A.; Rosenberg, M.; Papas, T.; Debouck, C.; Kola, I.
	1995	Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation	Hunt, C.; Eyre, H.; Akkari, P.; Meredith, C.; Dorosz, S.; Wilton, S.; Callen, D.; Laing, N.; Baker, E.
	2012	A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability	Huang, L.; Jolly, L.; Willis-Owen, S.; Gardner, A.; Sharma, R.; Douglas, E.; Shoubridge, C.; Wieczorek, D.; Tzschach, A.; Cohen, M.; Hackett, A.; Field, M.; Froyen, G.; Hu, H.; Haas, S.; Ropers, H.; Kalscheuer, V.; Corbett, M.; Gecz, J.