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Preview	Issue Date	Title	Author(s)
	2017	Dominant protection from HLA-linked autoimmunity by antigen-specific regulatory T cells	Ooi, J.; Petersen, J.; Tan, Y.; Huynh, M.; Willett, Z.; Ramarathinam, S.; Eggenhuizen, P.; Loh, K.; Watson, K.; Gan, P.; Alikhan, M.; Dudek, N.; Handel, A.; Hudson, B.; Fugger, L.; Power, D.; Holt, S.; Coates, P.; Gregersen, J.; Purcell, A.; et al.
	2018	Matrix stiffness controls lymphatic vessel formation through regulation of a GATA2-dependent transcriptional program	Frye, M.; Taddei, A.; Dierkes, C.; Martinez-Corral, I.; Fielden, M.; Ortsäter, H.; Kazenwadel, J.; Calado, D.P.; Ostergaard, P.; Salminen, M.; He, L.; Harvey, N.L.; Kiefer, F.; Mäkinen, T.
	2018	Plasmacytoid dendritic cells protect from viral bronchiolitis and asthma through semaphorin 4a-mediated T reg expansion	Lynch, J.; Werder, R.; Loh, Z.; Sikder, M.; Curren, B.; Zhang, V.; Rogers, M.; Lane, K.; Simpson, J.; Mazzone, S.; Spann, K.; Hayball, J.; Diener, K.; Everard, M.; Blyth, C.; Forstner, C.; Dennis, P.; Murtaza, N.; Morrison, M.; Cuív, P.; et al.
	2013	A novel prion disease associated with diarrhea and autonomic neuropathy	Mead, S.; Gandhi, S.; Beck, J.; Caine, D.; Gallujipali, D.; Carswell, C.; Hyare, H.; Joiner, S.; Ayling, H.; Lashley, T.; Linehan, J.M.; Al-Doujaily, H.; Sharps, B.; Revesz, T.; Sandberg, M.K.; Reilly, M.M.; Koltzenburg, M.; Forbes, A.; Rudge, P.; Brandner, S.; et al.
	2015	Overexpression of catalase diminishes oxidative cysteine modifications of cardiac proteins	Yao, C.; Behring, J.; Shao, D.; Sverdlov, A.; Whelan, S.; Elezaby, A.; Yin, X.; Siwik, D.; Seta, F.; Costello, C.; Cohen, R.; Matsui, R.; Colucci, W.; McComb, M.; Bachschmid, M.; Franco, R.
	2013	Macrophages regulate corpus luteum development during embryo implantation in mice	Care, A.; Diener, K.; Jasper, M.; Brown, H.; Ingman, W.; Robertson, S.
	2014	Reduced polyalanine-expanded Arx mutant protein in developing mouse subpallium alters Lmo1 transcriptional regulation	Lee, K.; Mattiske, T.; Kitamura, K.; Gecz, J.; Shoubridge, C.
	2013	The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth	Jolly, L.; Homan, C.; Jacob, R.; Barry, S.; Gecz, J.
	2012	Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature	Kazenwadel, J.; Secker, G.; Liu, Y.; Rosenfeld, J.; Wildin, R.; Cuellar-Rodriguez, J.; Hsu, A.; Dyack, S.; Fernandez, C.; Chong, C.; Babic, M.; Bardy, P.; Shimamura, A.; Zhang, M.; Walsh, T.; Holland, S.; Hickstein, D.; Horwitz, M.; Hahn, C.; Scott, H.; et al.
	2011	Identification of SOX3 as an XX male sex reversal gene in mice and humans	Sutton, E.; Hughes, J.; White, S.; Sekido, R.; Tan, J.; Arboleda, V.; Rogers, N.; Knower, K.; Rowley, L.; Eyre, H.; Rizzoti, K.; McAninch, D.; Golcalves, J.; Slee, J.; Turbitt, E.; Bruno, D.; Bengtsson, H.; Harley, V.; Vilain, E.; Sinclair, A.; et al.