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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.
2020
Genetic comorbidity between major depression and cardio-metabolic traits, stratified by age at onset of major depression
Hagenaars, S.P.
;
Coleman, J.R.I.
;
Choi, S.W.
;
Gaspar, H.
;
Adams, M.J.
;
Howard, D.M.
;
Hodgson, K.
;
Traylor, M.
;
Air, T.M.
;
Andlauer, T.F.M.
;
Arolt, V.
;
Baune, B.T.
;
Binder, E.B.
;
Blackwood, D.H.R.
;
Boomsma, D.I.
;
Campbell, A.
;
Cearns, M.
;
Czamara, D.
;
Dannlowski, U.
;
Domschke, K.
;
et al.
2018
A global cline in a colour polymorphism suggests a limited contribution of gene flow towards the recovery of a heavily exploited marine mammal
Hoffman, J.I.
;
Bauer, E.
;
Paijmans, A.J.
;
Humble, E.
;
Beckmann, L.M.
;
Kubetschek, C.
;
Christaller, F.
;
Kröcker, N.
;
Fuchs, B.
;
Moreras, A.
;
Shihlomule, Y.D.
;
Bester, M.N.
;
Cleary, A.C.
;
De Bruyn, P.J.N.
;
Forcada, J.
;
Goebel, M.E.
;
Goldsworthy, S.D.
;
Guinet, C.
;
Hoelzel, A.R.
;
Lydersen, C.
;
et al.
2017
YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction
Gabriele, M.
;
Vulto-van Silfhout, A.
;
Germain, P.
;
Vitriolo, A.
;
Kumar, R.
;
Douglas, E.
;
Haan, E.
;
Kosaki, K.
;
Takenouchi, T.
;
Rauch, A.
;
Steindl, K.
;
Frengen, E.
;
Misceo, D.
;
Pedurupillay, C.
;
Stromme, P.
;
Rosenfeld, J.
;
Shao, Y.
;
Craigen, W.
;
Schaaf, C.
;
Rodriguez-Buritica, D.
;
et al.
2020
Repurposing a neurodegenerative disease drug to treat Gram-negative antibiotic-resistant bacterial sepsis
De Oliveira, D.M.P.
;
Bohlmann, L.
;
Conroy, T.
;
Jen, F.E.-C.
;
Everest-Dass, A.
;
Hansford, K.A.
;
Bolisetti, R.
;
El-Deeb, I.M.
;
Forde, B.M.
;
Phan, M.-D.
;
Lacey, J.A.
;
Tan, A.
;
Rivera-Hernandez, T.
;
Brouwer, S.
;
Keller, N.
;
Kidd, T.J.
;
Cork, A.J.
;
Bauer, M.J.
;
Cook, G.M.
;
Davies, M.R.
;
et al.
Discover
Author
3
Dinger, M.E.
3
Espinel-Ingroff, A.
3
Fernandes, D.
3
Ferry, M.
3
Fothergill, A.
3
Geoghegan, N.D.
3
Hughes, J.
3
Kassahn, K.
3
Kidd, S.
3
Kvarnung, M.
.
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Subject
48
Humans
26
Animals
22
Female
22
Male
15
Mice
11
Mutation
10
Molecular Sequence Data
9
Adult
8
Genetic Predisposition to Disease
8
Mice, Inbred C57BL
.
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Date issued
28
2020 - 2023
79
2010 - 2019
15
2000 - 2009
5
1997 - 1999