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Preview	Issue Date	Title	Author(s)
	2014	Aberrant GDF9 expression and activation are associated with common human ovarian disorders	Simpson, C.; Robertson, D.; Al-Musawi, S.; Heath, D.; McNatty, K.; Ritter, L.; Mottershead, D.; Gilchrist, R.; Harrison, C.; Stanton, P.
	2013	Phl p 1-Specific Human Monoclonal IgE and Design of a Hypoallergenic Group 1 Grass Pollen Allergen Fragment	Levin, M.; Rydnert, F.; Kallstrom, E.; Tan, L.; Wormald, P.; Lindstedt, M.; Greiff, L.; Ohlin, M.
	2015	p84 forms a negative regulatory complex with p110γ to control PI3Kγ signalling during cell migration	Turvey, M.; Klingler-Hoffmann, M.; Hoffmann, P.; McColl, S.
	2011	An MD2 hot-spot-mimicking peptide that suppresses TLR4-mediated inflammatory response in vitro and in vivo	Liu, L.; Ghosh, N.; Slivka, P.; Fiorini, Z.; Hutchinson, M.; Watkins, L.; Yin, H.
	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.
	2013	The Guinea Pig as a model for sporadic Alzheimer's Disease (AD): the impact of cholesterol intake on expression of AD-related genes	Sharman, M.; Moussavi Nik, S.; Chen, M.; Ong, D.; Wijaya, L.; Laws, S.; Taddei, K.; Newman, M.; Lardelli, M.; Martins, R.; Verdile, G.; Götz, J.
	2015	HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain.	Jolly, L.; Nguyen, L.; Domingo, D.; Sun, Y.; Barry, S.; Hancarova, M.; Plevova, P.; Vlckova, M.; Havlovicova, M.; Kalscheuer, V.; Graziano, C.; Pippucci, T.; Bonora, E.; Sedlacek, Z.; Gecz, J.
	2014	Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human disease	Newman, M.; Wilson, L.; Verdile, G.; Lim, A.; Khan, I.; Nik, S.; Pursglove, S.; Chapman, G.; Martins, R.; Lardelli, M.
	2015	LRGUK-1 is required for basal body and manchette function during spermatogenesis and male fertility	Liu, Y.; DeBoer, K.; de Kretser, D.; O Donnell, L.; O Connor, A.; Merriner, D.; Okuda, H.; Whittle, B.; Jans, D.; Efthymiadis, A.; McLachlan, R.; Ormandy, C.; Goodnow, C.; Jamsai, D.; O Bryan, M.; Yan, W.
	2010	A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24	Bahlo, M.; Jolly, L.; Afawi, Z.; Gardner, A.; Oliver, K.; Tan, S.; Coffey, A.; Mulley, J.; Dibbens, L.; Simri, W.; Shalata, A.; Kivity, S.; Jackson, G.; Berkovic, S.; Gecz, J.; Corbett, M.