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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	Interlaboratory comparison of results of susceptibility testing with caspofungin against candida and aspergillus species	Odds, F.; Motyl, M.; Andrade, R.; Bille, J.; Canton, E.; Cuenca-Estrella, M.; Davidson, A.; Durussel, C.; Ellis, D.; Foraker, E.; Fothergill, A.; Ghannoum, M.; Giacobbe, R.; Gobernado, M.; Handke, R.; Laverdiere, M.; Lee-Yang, W.; Merz, W.; Ostrosky-Zeichner, L.; Peman, J.; et al.
	2007	Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly	Field, M.; Tarpey, P.; Smith, R.; Edkins, S.; O'Meara, S.; Stevens, C.; Tofts, C.; Teague, J.; Butler, A.; Dicks, E.; Barthorpe, S.; Buck, G.; Cole, J.; Gray, K.; Halliday, K.; Hills, K.; Jenkinson, A.; Jones, D.; Menzies, A.; Mironenko, T.; 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.
	2007	Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation	Tarpey, P.; Raymond, F.; Nguyen, L.; Rodriguez, J.; Hackett, A.; Vandeleur, L.; Smith, R.; Shoubridge, C.; Edkins, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Hills, K.; Jones, D.; Mironenko, T.; Perry, J.; 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.
	2019	Alternative splicing in a presenilin 2 variant associated with Alzheimer disease	Braggin, J.E.; Bucks, S.A.; Course, M.M.; Smith, C.L.; Sopher, B.; Osnis, L.; Shuey, K.D.; Domoto-Reilly, K.; Caso, C.; Kinoshita, C.; Scherpelz, K.P.; Cross, C.; Grabowski, T.; Nik, S.H.M.; Newman, M.; Garden, G.A.; Leverenz, J.B.; Tsuang, D.; Latimer, C.; Gonzalez-Cuyar, L.F.; et al.
	2023	Sulfonylpiperazine compounds prevent Plasmodium falciparum invasion of red blood cells through interference with actin-1/profilin dynamics	Dans, M.G.; Piirainen, H.; Nguyen, W.; Khurana, S.; Mehra, S.; Razook, Z.; Geoghegan, N.D.; Dawson, A.T.; Das, S.; Parkyn Schneider, M.; Jonsdottir, T.K.; Gabriela, M.; Gancheva, M.R.; Tonkin, C.J.; Mollard, V.; Goodman, C.D.; McFadden, G.I.; Wilson, D.W.; Rogers, K.L.; Barry, A.E.; et al.; Kim, K.
	2023	TP53 mutation variant allele frequency of ≥10% is associated with poor prognosis in therapy-related myeloid neoplasms	Shah, M.V.; Tran, E.N.H.; Shah, S.; Chhetri, R.; Baranwal, A.; Ladon, D.; Shultz, C.; Al-Kali, A.; Brown, A.L.; Chen, D.; Scott, H.S.; Greipp, P.; Thomas, D.; Alkhateeb, H.B.; Singhal, D.; Gangat, N.; Kumar, S.; Patnaik, M.M.; Hahn, C.N.; Kok, C.H.; et al.
	2013	Rare variants in single-minded 1 (SIM1) are associated with severe obesity	Ramachandrappa, S.; Raimondo, A.; Cali, A.; Keogh, J.; Henning, E.; Saeed, S.; Thompson, A.; Garg, S.; Bochukova, E.; Brage, S.; Trowse, V.; Wheeler, E.; Sullivan, A.; Dattani, M.; Clayton, P.; Datta, V.; Bruning, J.; Wareham, N.; O'Rahilly, S.; Peet, D.; et al.