Skip navigation
Home
Browse
Communities
& Collections
Browse Items by:
Issue Date
Author
Title
Advisor
Help
Sign on to:
My DSpace
Receive email
updates
Edit Profile
Adelaide Research & Scholarship
Adelaide Research & Scholarship
Search
Search:
All collections
University Library
Adelaide Festival of Ideas
Barr Smith Press
Friends of the University of Adelaide Library
Library Publications
Internal documents (Library staff only)
Library images
Library reports and papers
for
Current filters:
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Start a new search
Add filters:
Use filters to refine the search results.
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Results 21-30 of 56 (Search time: 0.002 seconds).
previous
1
2
3
4
5
6
next
Item hits:
Preview
Issue Date
Title
Author(s)
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.
2013
Pyrimidyn compounds: dual-action small molecule pyrimidine-based dynamin inhibitors
McGeachie, A.
;
Odell, L.
;
Quan, A.
;
Daniel, J.
;
Chau, N.
;
Hill, T.
;
Gorgani, N.
;
Keating, D.
;
Cousin, M.
;
van Dam, E.
;
Mariana, A.
;
Whiting, A.
;
Perera, S.
;
Novelle, A.
;
Young, K.
;
Deane, F.
;
Gilbert, J.
;
Sakoff, J.
;
Chircop, M.
;
McCluskey, A.
;
et al.
2013
Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndrome
Aoki, Y.
;
Niihori, T.
;
Banjo, T.
;
Okamoto, N.
;
Mizuno, S.
;
Kurosawa, K.
;
Ogata, T.
;
Takada, F.
;
Yano, M.
;
Ando, T.
;
Hoshika, T.
;
Barnett, C.
;
Ohashi, H.
;
Kawame, H.
;
Hasegawa, T.
;
Okutani, T.
;
Nagashima, T.
;
Hasegawa, S.
;
Funayama, R.
;
Nagashima, T.
;
et al.
2013
Regulation of vascular leak and recovery from ischemic injury by general and VE-cadherin-restricted miRNA antagonists of miR-27
Young, J.
;
Ting, K.
;
Li, J.
;
Moller, T.
;
Dunn, L.
;
Lu, Y.
;
Moses, J.
;
Prado-Lourenco, L.
;
Khachigian, L.
;
Ng, M.
;
Gregory, P.
;
Goodall, G.
;
Tsykin, A.
;
Lichtenstein, I.
;
Hahn, C.
;
Tran, N.
;
Shackel, N.
;
Kench, J.
;
McCaughan, G.
;
Vadas, M.
;
et al.
2016
A syntenic cross species aneuploidy genetic screen links RCAN1 expression to β-Cell mitochondrial dysfunction in type 2 diabetes
Peiris, H.
;
Duffield, M.D.
;
Fadista, J.
;
Jessup, C.F.
;
Kashmir, V.
;
Genders, A.J.
;
McGee, S.L.
;
Martin, A.M.
;
Saiedi, M.
;
Morton, N.
;
Carter, R.
;
Cousin, M.A.
;
Kokotos, A.C.
;
Oskolkov, N.
;
Volkov, P.
;
Hough, T.A.
;
Fisher, E.M.C.
;
Tybulewicz, V.L.J.
;
Busciglio, J.
;
Coskun, P.E.
;
et al.
;
Scott, H.S.
2015
Progesterone receptor modulates ERα action in breast cancer
Mohammed, H.
;
Russell, I.
;
Stark, R.
;
Rueda, O.
;
Hickey, T.
;
Tarulli, G.
;
Serandour, A.
;
Birrell, S.
;
Bruna, A.
;
Saadi, A.
;
Menon, S.
;
Hadfield, J.
;
Pugh, M.
;
Raj, G.
;
Brown, G.
;
D'Santos, C.
;
Robinson, J.
;
Silva, G.
;
Launchbury, R.
;
Perou, C.
;
et al.
2012
Death adder envenoming causes neurotoxicity not reversed by antivenom - Australian snakebite project (ASP-16)
Johnston, C.
;
O'Leary, M.
;
Brown, S.
;
Currie, B.
;
Halkidis, L.
;
Whitaker, R.
;
Close, B.
;
Isbister, G.
;
Nagree, Y.
;
Ker, F.
;
Greene, S.
;
Taylor, M.
;
Macrokanis, C.
;
Wilke, G.
;
Coulson, A.
;
Barnes, C.
;
Bonni, R.
;
Whitake, R.
;
Halkidis, L.
;
Isbiste, G.
;
et al.
;
de Silva, J.
2013
Distinctive expansion of potential virulence genes in the genome of the oomycete fish pathogen Saprolegnia parasitica
Jiang, R.
;
de Bruijn, I.
;
Haas, B.
;
Belmonte, R.
;
Löbach, L.
;
Christie, J.
;
van den Ackerveken, G.
;
Bottin, A.
;
Bulone, V.
;
Díaz-Moreno, S.
;
Dumas, B.
;
Fan, L.
;
Gaulin, E.
;
Govers, F.
;
Grenville-Briggs, L.
;
Horner, N.
;
Levin, J.
;
Mammella, M.
;
Meijer, H.
;
Morris, P.
;
et al.
;
McDowell, J.
2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
Heron, S.
;
Grinton, B.
;
Kivity, S.
;
Afawi, Z.
;
Zuberi, S.
;
Hughes, J.
;
Pridmore, C.
;
Hodgson, B.
;
Iona, X.
;
Sadleir, L.
;
Pelekanos, J.
;
Herlenius, E.
;
Goldberg-Stern, H.
;
Bassan, H.
;
Haan, E.
;
Korczyn, A.
;
Gardner, A.
;
Corbett, M.
;
Gecz, J.
;
Thomas, P.
;
et al.
2011
Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma
Khan, K.
;
Rudkin, A.
;
Parry, D.
;
Burdon, K.
;
McKibbin, M.
;
Logan, C.
;
Abdelhamed, Z.
;
Muecke, J.
;
Fernandez-Fuentes, N.
;
Laurie, K.
;
Shires, M.
;
Fogarty, R.
;
Carr, I.
;
Poulter, J.
;
Morgan, J.
;
Mohamed, M.
;
Jafri, H.
;
Raashid, Y.
;
Meng, N.
;
Piseth, H.
;
et al.
Discover
Author
4
Hughes, J.
3
Gecz, J.
3
Hahn, C.
2
Amat, J.
2
Babic, M.
2
Baker, A.
2
Burdon, K.
2
Chelly, J.
2
Chong, C.
2
Corbett, M.
.
next >
Subject
41
Humans
34
Mice
29
Male
25
Female
13
Mutation
11
Mice, Inbred C57BL
9
Child
9
Signal Transduction
8
Adult
8
Child, Preschool
.
next >
Date issued
5
2018
8
2017
7
2016
5
2015
3
2014
10
2013
9
2012
6
2011
3
2010