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Issue Date
Title
Author(s)
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.
2014
Reduced polyalanine-expanded Arx mutant protein in developing mouse subpallium alters Lmo1 transcriptional regulation
Lee, K.
;
Mattiske, T.
;
Kitamura, K.
;
Gecz, J.
;
Shoubridge, C.
2013
The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth
Jolly, L.
;
Homan, C.
;
Jacob, R.
;
Barry, S.
;
Gecz, J.
2015
Oocyte induction of EGF responsiveness in somatic cells is associated with the acquisition of porcine oocyte developmental competence
Ritter, L.
;
Sugimura, S.
;
Gilchrist, R.
2015
Gestational dietary protein is associated with sex specific decrease in blood flow, fetal heart growth and post-natal blood pressure of progeny
Hernandez-Medrano, J.
;
Copping, K.
;
Hoare, A.
;
Wapanaar, W.
;
Grivell, R.
;
Kuchel, T.
;
Miguel-Pacheco, G.
;
McMillen, I.
;
Rodgers, R.
;
Perry, V.
;
Crispi-Brillas, F.
2012
A possible murine model for investigation of pathogenesis of Sudden Infant Death Syndrome
Bettelheim, K.
;
Luke, R.
;
Johnston, N.
;
Pearce, J.
;
Goldwater, P.
2010
Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes
Dimasi, D.
;
Chen, J.
;
Hewitt, A.
;
Klebe, S.
;
Davey, R.
;
Stirling, J.
;
Thompson, E.
;
Forbes, R.
;
Tan, T.
;
Savarirayan, R.
;
Mackey, D.
;
Healey, P.
;
Mitchell, P.
;
Burdon, K.
;
Craig, J.
2009
Interaction of dietary zinc and intracellular binding protein metallothionein in postnatal bone growth
Fong, L.
;
Tan, K.
;
Tran, C.
;
Cool, J.
;
Scherer, M.
;
Elovaris, R.
;
Coyle, P.
;
Foster, B.
;
Rofe, A.
;
Xian, C.
2008
Behavioural characterisation of the alpha-mannosidosis guinea pig
Robinson, A.
;
Crawley, A.
;
Auclair, D.
;
Weston, P.
;
Hirte, C.
;
Hemsley, K.
;
Hopwood, J.
2010
Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly
Giannandrea, M.
;
Bianchi, V.
;
Mignogna, M.
;
Sirri, A.
;
Carrabino, S.
;
D'Elia, E.
;
Vecellio, M.
;
Russo, S.
;
Cogliati, F.
;
Larizza, L.
;
Ropers, H.
;
Tzschach, A.
;
Kalscheuer, V.
;
Oehl-Jaschkowitz, B.
;
Skinner, C.
;
Schwartz, C.
;
Gecz, J.
;
Van Esch, H.
;
Raynaud, M.
;
Chelly, J.
;
et al.
Discover
Author
13
Hopwood, J.
10
Gecz, J.
9
Sutherland, G.
6
et al.
6
Jolly, L.
6
Makrides, M.
5
Gilchrist, R.
5
Shoubridge, C.
4
Barry, S.
4
Byers, S.
.
next >
Subject
62
Male
59
Humans
42
Mice
23
Pregnancy
17
Mutation
16
Disease Models, Animal
15
Molecular Sequence Data
13
Amino Acid Sequence
13
Pedigree
12
Mice, Inbred C57BL
.
next >
Date issued
43
2010 - 2019
40
2000 - 2009
17
1995 - 1999