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Results 1-10 of 36 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2017
A novel embryo culture media supplement that improves pregnancy rates in mice
Highet, A.
;
Bianco-Miotto, T.
;
Pringle, K.
;
Peura, A.
;
Bent, S.
;
Zhang, J.
;
Nottle, M.
;
Thompson, J.
;
Roberts, C.
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.
2010
Genome-wide identification of human FOXP3 target genes in natural regulatory T cells
Sadlon, T.
;
Wilkinson, B.
;
Pederson, S.
;
Brown, C.
;
Bresatz, S.
;
Gargett, T.
;
Melville, E.
;
Peng, K.
;
D'Andrea, R.
;
Glonek, G.
;
Goodall, G.
;
Zola, H.
;
Shannon, F.
;
Barry, S.
2014
Modifications of human growth differentiation factor 9 to improve the generation of embryos from low competence oocytes
Li, J.
;
Sugimura, S.
;
Mueller, T.
;
White, M.
;
Martin, G.
;
Ritter, L.
;
Liang, X.
;
Gilchrist, R.
;
Mottershead, D.
2015
shRNA off-target effects in vivo: impaired endogenous siRNA expression and spermatogenic defects
Song, H.
;
Bettegowda, A.
;
Oliver, D.
;
Yan, W.
;
Phan, M.
;
De Rooij, D.
;
Corbett, M.
;
Wilkinson, M.
;
White-Cooper, H.
2013
A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome
Buchovecky, C.
;
Turley, S.
;
Brown, H.
;
Kyle, S.
;
McDonald, J.
;
Liu, B.
;
Pieper, A.
;
Huang, W.
;
Katz, D.
;
Russell, D.
;
Shendure, J.
;
Justice, M.
2012
A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability
Huang, L.
;
Jolly, L.
;
Willis-Owen, S.
;
Gardner, A.
;
Sharma, R.
;
Douglas, E.
;
Shoubridge, C.
;
Wieczorek, D.
;
Tzschach, A.
;
Cohen, M.
;
Hackett, A.
;
Field, M.
;
Froyen, G.
;
Hu, H.
;
Haas, S.
;
Ropers, H.
;
Kalscheuer, V.
;
Corbett, M.
;
Gecz, J.
2015
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain.
Jolly, L.
;
Nguyen, L.
;
Domingo, D.
;
Sun, Y.
;
Barry, S.
;
Hancarova, M.
;
Plevova, P.
;
Vlckova, M.
;
Havlovicova, M.
;
Kalscheuer, V.
;
Graziano, C.
;
Pippucci, T.
;
Bonora, E.
;
Sedlacek, Z.
;
Gecz, J.
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.
Discover
Author
10
Gecz, J.
6
Jolly, L.
5
Barry, S.
4
Corbett, M.
4
Cowin, A.
4
et al.
4
Shoubridge, C.
3
Field, M.
3
Kalscheuer, V.
3
Melville, E.
.
next >
Subject
24
Humans
21
Female
19
Male
11
Disease Models, Animal
11
Mutation
9
Mice, Knockout
7
Intellectual Disability
6
Brain
5
Carrier Proteins
5
HEK293 Cells
.
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2010