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Preview	Issue Date	Title	Author(s)
	2010	Boron toxicity tolerance in barley through reduced expression of the multifunctional aquaporin HvNIP2;1	Schnurbusch, T.; Hayes, J.; Hrmova, M.; Baumann, U.; Ramesh, S.; Tyerman, S.; Langridge, P.; Sutton, T.
	2010	The structure of the talin/integrin complex at a lipid bilayer: an NMR and MD simulation study	Kalli, A.; Wegener, K.; Goult, B.; Anthis, N.; Campbell, I.; Sansom, M.
	2010	Poor outcome after liver transplantation for transthyretin amyloid neuropathy in a family with an Ala36Pro transthyretin mutation: Case report	Muller, K.; Padbury, R.; Jeffrey, G.; Poplawski, N.; Thompson, P.; Tonkin, A.; Harley, H.
	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.
	2010	Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly	Giannandrea, M.; Bianchi, V.; Mignogna, M.; Sirri, A.; Carrabino, S.; D'Elia, E.; Vecellio, M.; Russo, S.; Cogliati, F.; Larizza, L.; Ropers, H.; Tzschach, A.; Kalscheuer, V.; Oehl-Jaschkowitz, B.; Skinner, C.; Schwartz, C.; Gecz, J.; Van Esch, H.; Raynaud, M.; Chelly, J.; et al.
	2010	Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndrome	Gecz, J.
	2010	Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination	Pearlman, A.; Loke, J.; Le Caignec, C.; White, S.; Chin, L.; Friedman, A.; Warr, N.; Willan, J.; Brauer, D.; Farmer, C.; Brooks, E.; Oddoux, C.; Riley, B.; Shajahan, S.; Camerino, G.; Homfray, T.; Crosby, A.; Couper, J.; David, A.; Greenfield, A.; et al.
	2010	The RON1/FRY1/SAL1 gene is required for leaf morphogenesis and venation patterning in Arabidopsis1,[W],[OA]	Fleury, D.
	2010	Poor prognosis in familial acute myeloid leukaemia with combined biallelic CEBPA mutations and downstream events affecting the ATM, FLT3 and CDX2 genes	Carmichael, C.; Wilkins, E.; Bengtsson, H.; Horwitz, M.; Speed, T.; Vincent, P.; Young, G.; Hahn, C.; Escher, J.; Scott, H.
	2010	CLE peptides control medicago truncatula nodulation locally and systemically	Mortier, V.; Den Herder, G.; Whitford, R.; Van de Velde, W.; Rombauts, S.; D'haeseleer, K.; Holsters, M.; Goormachtig, S.