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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.
1998
Construction of an ~700-kb transcript map around the Familial Mediterranean Fever locus on human chromosome 16p13.3
Centola, M.
;
Chen, X.
;
Sood, R.
;
Deng, Z.
;
Aksentijevich, I.
;
Blake, T.
;
Ricke, D.
;
Chen, X.
;
Wood, G.
;
Zaks, N.
;
Richards, N.
;
Krizman, D.
;
Mansfield, E.
;
Apostolou, S.
;
Liu, J.
;
Shafran, N.
;
Vedula, A.
;
Hamon, M.
;
Cercek, A.
;
Kahan, 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.
2021
The androgen receptor is a tumor suppressor in estrogen receptor-positive breast cancer
Hickey, T.E.
;
Selth, L.A.
;
Chia, K.M.
;
Laven-Law, G.
;
Milioli, H.H.
;
Roden, D.
;
Jindal, S.
;
Hui, M.
;
Finlay-Schultz, J.
;
Ebrahimie, E.
;
Birrell, S.N.
;
Stelloo, S.
;
Iggo, R.
;
Alexandrou, S.
;
Caldon, C.E.
;
Abdel-Fatah, T.M.
;
Ellis, I.O.
;
Zwart, W.
;
Palmieri, C.
;
Sartorius, C.A.
;
et al.
2017
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
Geisheker, M.
;
Heymann, G.
;
Wang, T.
;
Coe, B.
;
Turner, T.
;
Stessman, H.
;
Hoekzema, K.
;
Kvarnung, M.
;
Shaw, M.
;
Friend, K.
;
Liebelt, J.
;
Barnett, C.
;
Thompson, E.
;
Haan, E.
;
Guo, H.
;
Anderlid, B.
;
Nordgren, A.
;
Lindstrand, A.
;
Vandeweyer, G.
;
Alberti, A.
;
et al.
2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing
Jansen, I.E.
;
Ye, H.
;
Heetveld, S.
;
Lechler, M.C.
;
Michels, H.
;
Seinstra, R.I.
;
Lubbe, S.J.
;
Drouet, V.
;
Lesage, S.
;
Majounie, E.
;
Gibbs, J.R.
;
Nalls, M.A.
;
Ryten, M.
;
Botia, J.A.
;
Vandrovcova, J.
;
Simon-Sanchez, J.
;
Castillo-Lizardo, M.
;
Rizzu, P.
;
Blauwendraat, C.
;
Chouhan, A.K.
;
et al.
Discover
Author
5
Aksentijevich, I.
5
Centola, M.
5
Wood, G.
4
Blake, T.
4
Chen, X.
4
Deng, Z.
4
Sood, R.
4
Zaks, N.
3
Canton, E.
3
Coe, B.
.
next >
Subject
20
Male
19
Female
17
Animals
10
Mice
9
Adult
9
Mutation
8
Molecular Sequence Data
7
Genetic Predisposition to Disease
7
Pedigree
7
Sequence Analysis, DNA
.
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Date issued
12
2020 - 2023
19
2010 - 2019
12
2000 - 2009
5
1997 - 1999