1. Adelaide Research & Scholarship

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Results 1-10 of 43 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2014Aberrant GDF9 expression and activation are associated with common human ovarian disordersSimpson, C.; Robertson, D.; Al-Musawi, S.; Heath, D.; McNatty, K.; Ritter, L.; Mottershead, D.; Gilchrist, R.; Harrison, C.; Stanton, P.
2013Phl p 1-Specific Human Monoclonal IgE and Design of a Hypoallergenic Group 1 Grass Pollen Allergen FragmentLevin, M.; Rydnert, F.; Kallstrom, E.; Tan, L.; Wormald, P.; Lindstedt, M.; Greiff, L.; Ohlin, M.
2015p84 forms a negative regulatory complex with p110γ to control PI3Kγ signalling during cell migrationTurvey, M.; Klingler-Hoffmann, M.; Hoffmann, P.; McColl, S.
2013The genomic landscape of hypodiploid acute lymphoblastic leukemiaTo, L.
2010The structure of the talin/integrin complex at a lipid bilayer: an NMR and MD simulation studyKalli, A.; Wegener, K.; Goult, B.; Anthis, N.; Campbell, I.; Sansom, M.
2011Defining the substrate specificity determinants recognized by the active site of C-terminal Src kinase-homologous kinase (CHK) and identification of β-synuclein as a potential CHK physiological substrateIa, K.; Jeschke, G.; Deng, Y.; Kamaruddin, M.; Williamson, N.; Scanlon, D.; Culvenor, J.; Hossain, M.; Purcell, A.; Liu, S.; Zhu, H.; Turk, B.; Catimel, B.; Cheng, H.
2013H-NS plays a role in expression of Acinetobacter baumannii virulence featuresEijkelkamp, B.; Stroeher, U.; Hassan, K.; Elbourne, L.; Paulsen, I.; Brown, M.; Payne, S.M.
2013Yunis-Varón Syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphataseCampeau, P.; Lenk, G.; Lu, J.; Bae, Y.; Burrage, L.; Turnpenny, P.; Corona-Rivera, J.; Morandi, L.; Mora, M.; Reutter, H.; Vulto-van Silfhout, A.; Faivre, L.; Haan, E.; Gibbs, R.; Meisler, M.; Lee, B.
2011An MD2 hot-spot-mimicking peptide that suppresses TLR4-mediated inflammatory response in vitro and in vivoLiu, L.; Ghosh, N.; Slivka, P.; Fiorini, Z.; Hutchinson, M.; Watkins, L.; Yin, H.
2012A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disabilityHuang, 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.

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