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Preview	Issue Date	Title	Author(s)
	2010	Effect of parity on lymphocytes in peripheral blood and colostrum of healthy holstein dairy cows	Ohtsuka, H.; Terasawa, S.; Watanabe, C.; Kohiruimaki, M.; Mukai, M.; Ando, T.; Petrovski, K.; Morris, S.
	2010	An odontometric study of the maxillary molars in Australian marsupials. I. The koala (Phascolarctos cinereus).	Ueno, R.; Iimura, A.; Yoshida, S.; Kondo, K.; Sato, I.; Henneberg, M.; Townsend, G.
	2010	In vitro and in vivo characterization of putative porcine embryonic stem cells	Vassiliev, I.; Vassilieva, S.; Beebe, L.; Harrison, S.; McIlfatrick, S.; Nottle, M.
	2010	GM-CSF is an essential regulator of T cell activation competence in uterine dendritic cells during early pregnancy in mice	Moldenhauer, L.; Keenihan, S.; Hayball, J.; Robertson, S.
	2010	Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes	Dimasi, D.; Chen, J.; Hewitt, A.; Klebe, S.; Davey, R.; Stirling, J.; Thompson, E.; Forbes, R.; Tan, T.; Savarirayan, R.; Mackey, D.; Healey, P.; Mitchell, P.; Burdon, K.; Craig, J.
	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	A new species of Neoheterocotyle Hargis, 1955 (Monogenea: Monocotylidae) from the gills of Rhinobatos annulatus Müller & Henle (Rhinobatidae) off the southern tip of Africa	Vaughan, D.; Chisholm, L.
	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.