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Preview	Issue Date	Title	Author(s)
	2016	CXCR5⁺ follicular cytotoxic T cells control viral infection in B cell follicles	Leong, Y.; Chen, Y.; Ong, H.; Wu, D.; Man, K.; Deleage, C.; Minnich, M.; Meckiff, B.; Wei, Y.; Hou, Z.; Zotos, D.; Fenix, K.; Atnerkar, A.; Preston, S.; Chipman, J.; Beilman, G.; Allison, C.; Sun, L.; Wang, P.; Xu, J.; et al.
	2004	Proceedings of the Oxygen Homeostasis/Hypoxia Meeting	Kaufman, B.; Scharf, O.; Arbeit, J.; Ashcroft, M.; Brown, J.; Bruick, R.; Chapman, J.; Evans, S.; Giaccia, A.; Harris, A.; Huang, E.; Johnson, R.; Kaelin Jr., W.; Koch, C.; Maxwell, P.; Mitchell, J.; Neckers, L.; Powis, G.; Rajendran, J.; Semenza, G.; et al.
	2017	NAD deficiency, congenital malformations, and niacin supplementation	Shi, H.; Enriquez, A.; Rapadas, M.; Martin, E.; Wang, R.; Moreau, J.; Lim, C.; Szot, J.; Ip, E.; Hughes, J.; Sugimoto, K.; Humphreys, D.; McInerney-Leo, A.; Leo, P.; Maghzal, G.; Halliday, J.; Smith, J.; Colley, A.; Mark, P.; Collins, F.; et al.
	2018	Atypical chemokine receptor 4 shapes activated B cell fate	Kara, E.E.; Bastow, C.R.; McKenzie, D.R.; Whyte, C.E.; Fenix, K.A.; Babb, R.; Norton, T.S.; Zotos, D.; Rodda, L.B.; Hermes, J.R.; Bourne, K.; Gilchrist, D.S.; Nibbs, R.J.; Alsharifi, M.; Vinuesa, C.G.; Tarlinton, D.M.; Brink, R.; Hill, G.R.; Cyster, J.G.; Comerford, I.; et al.
	2023	Pharmacological inhibition of TBK1/IKKε blunts immunopathology in a murine model of SARS-CoV-2 infection	Ullah, T.R.; Johansen, M.D.; Balka, K.R.; Ambrose, R.L.; Gearing, L.J.; Roest, J.; Vivian, J.P.; Sapkota, S.; Jayasekara, W.S.N.; Wenholz, D.S.; Aldilla, V.R.; Zeng, J.; Miemczyk, S.; Nguyen, D.H.; Hansbro, N.G.; Venkatraman, R.; Kang, J.H.; Pang, E.S.; Thomas, B.J.; Alharbi, A.S.; et al.
	2013	Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse	Bellone, R.; Holl, H.; Sealuri, V.; Devi, S.; Maddodi, N.; Archer, S.; Sandmeyer, L.; Ludwig, A.; Foerster, D.; Pruvost, M.; Reissmann, M.; Bortfeldt, R.; Adelson, D.; Lim, S.; Nelson, J.; Haase, B.; Engensteiner, M.; Leeb, T.; Forsyth, G.; Mienaltowski, M.; et al.; Anderson, M.G.
	2008	Genome analysis of the platypus reveals unique signatures of evolution	Warren, W.; Hillier, L.; Graves, J.; Birney, E.; Ponting, C.; Grutzner, F.; Belov, K.; Miller, W.; Clarke, L.; Chinwall, A.; Yang, S.; Heger, A.; Locke, D.; Miethke, P.; Waters, P.; Veyrunes, F.; Fulton, L.; Fulton, B.; Graves, T.; Wallis, J.; et al.
	2011	Chromosomal rearrangements maintain a polymorphic supergene controlling butterfly mimicry	Joron, M.; Frezal, L.; Jones, R.; Chamberlain, N.; Lee, S.; Haag, C.; Whibley, A.; Becuwe, M.; Baxter, S.; Ferguson, L.; Wilkinson, P.; Salazar, C.; Davidson, C.; Clark, R.; Quail, M.; Beasley, H.; Glithero, R.; Lloyd, C.; Sims, S.; Jones, M.; et al.
	2013	Mutations in DEPDC5 cause familial focal epilepsy with variable foci	Dibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; et al.
	2002	Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome	Lower, K.; Turner, G.; Kerr, B.; Mathews, K.; Shaw, M.; Gedeon, A.; Schelley, S.; Hoyme, H.; White, S.; Delatycki, M.; Lampe, A.; Clayton-Smith, J.; Stewart, H.; van Ravenswaay, C.; de Vries, B.; Cox, B.; Grompe, M.; Ross, S.; Thomas, P.; Mulley, J.; et al.