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Results 1-10 of 42 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2006
Suppression of androgen receptor signaling in prostate cancer cells by an inhibitory receptor variant
Butler, L.
;
Centenera, M.
;
Neufing, P.
;
Buchanan, G.
;
Choong, C.
;
Ricciardelli, C.
;
Saint, K.
;
Lee, M.
;
Ochnik, A.
;
Yang, M.
;
Brown, M.
;
Tilley, W.
1995
Fragile X syndrome and other dynamic mutation diseases
Sutherland, G.
;
Richards, R.
2004
Effect of β₂‐glycoprotein I null mutation on reproductive outcome and antiphospholipid antibody‐mediated pregnancy pathology in mice
Robertson, S.
;
Roberts, C.
;
van Beijering, E.
;
Pensa, K.
;
Sheng, Y.
;
Shi, T.
;
Krilis, S.
2008
Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform
Sharma, S.
;
Burdon, K.
;
Dave, A.
;
Jamieson, R.
;
Yaron, Y.
;
Billson, F.
;
van Maldergem, L.
;
Lorenz, B.
;
Gecz, J.
;
Craig, J.
2001
Bovine spongiform encephalopathy and variant Creutzfeldt-Jakob disease: implications for Australia
Goldwater, P.
2017
Knockout of the epilepsy gene Depdc5 in mice causes severe embryonic dysmorphology with hyperactivity of mTORC1 signalling
Hughes, J.
;
Dawson, R.
;
Tea, M.
;
McAninch, D.
;
Piltz, S.
;
Jackson, D.
;
Stewart, L.
;
Ricos, M.
;
Dibbens, L.
;
Harvey, N.
;
Thomas, P.
2012
CDP-diacylglycerol synthetase-controlled phosphoinositide availability limits VEGFA signaling and vascular morphogenesis
Pan, W.
;
Pham, V.
;
Stratman, A.
;
Castranova, D.
;
Kamei, M.
;
Kidd, K.
;
Lo, B.
;
Shaw, K.
;
Torres-Vazquez, J.
;
Mikelis, C.
;
Gutkind, J.
;
Davis, G.
;
Weinstein, B.
2004
Transport, enzymatic activity, and stability of mutant sulfamidise (SGSH) identified in patients with mucopolysaccharidosis type III A
Muschol, N.
;
Storch, S.
;
Balhausen, D.
;
Beesley, C.
;
Westermann, J.
;
Gal, A.
;
Ullrich, K.
;
Hopwood, J.
;
Winchester, B.
;
Braulke, T.
2004
Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and forebrain GABAergic neurons
Colombo, E.
;
Galli, R.
;
Cossu, G.
;
Gecz, J.
;
Broccoli, V.
2013
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity
Hirata, H.
;
McMichael, G.
;
Haan, E.
;
MacLennan, A.
;
Yap, T.
;
Nguyen, L.
;
Shaw, M.
;
Gecz, J.
Discover
Author
18
Gecz, J.
13
Hopwood, J.
6
Brooks, D.
6
Yogalingam, G.
5
et al.
4
Kalscheuer, V.
4
Shoubridge, C.
3
Beesley, C.
3
Haan, E.
3
Jolly, L.
.
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Subject
19
Male
17
Female
17
Mice
12
Pedigree
11
Molecular Sequence Data
10
Intellectual Disability
10
Phenotype
9
Amino Acid Sequence
9
Transcription Factors
8
Base Sequence
.
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Date issued
13
2010 - 2018
26
2000 - 2009
3
1995 - 1999