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Preview	Issue Date	Title	Author(s)
	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.
	2012	Relaxin increases human endothelial progenitor cell NO and migration and vasculogenesis in mice	Segal, M.S.; Sautina, L.; Li, S.; Diao, Y.; Agoulnik, A.I.; Kielczewski, J.; McGuane, J.T.; Grant, M.B.; Conrad, K.P.
	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	Comparative assessment of the osteoconductive properties of different biomaterials in vivo seeded with human or ovine mesenchymal stem/stromal cells	Zannettino, A.; Paton, S.; Itescu, S.; Gronthos, S.
	2012	Congenital hydrocephalus and abnormal subcommissural organ development in Sox3 transgenic mice	Lee, K.; Tan, J.; Morris, M.; Rizzoti, K.; Hughes, J.; Cheah, P.; Felquer, F.; Liu, X.; Piltz, S.; Lovell-Badge, R.; Thomas, P.; Schmidt, J.V.
	2010	Canal cristae growth and fiber extension to the outer hair cells of the mouse ear require Prox1 activity	Fritzsch, B.; Dillard, M.; Lavado, A.; Harvey, N.; Israt, J.; Koch, K.-W.
	2011	Successful in vitro culture of pre-antral follicles derived from vitrified murine ovarian tissue: oocyte maturation, fertilization, and live births	Wang, X.; Catt, S.; Pangesto, M.; Temple-Smith, P.
	2018	Differential effects on gene transcription and hematopoietic differentiation correlate with GATA2 mutant disease phenotypes	Chong, C.-E.; Venugopal, P.; Stokes, P.; Lee, Y.; Brautigan, P.; Yeung, D.; Babic, M.; Engler, G.; Lane, S.; Klingler-Hoffmann, M.; Matthews, J.; D'Andrea, R.; Brown, A.; Hahn, C.; Scott, H.
	2010	Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down Syndrome	Hewitt, C.; Ling, K.; Merson, T.; Simpson, K.; Ritchie, M.; King, S.; Pritchard, M.; Smyth, G.; Thomas, T.; Scott, H.; Voss, A.; Aziz, S.A.