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Issue Date
Title
Author(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.
1995
Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation
Hunt, C.
;
Eyre, H.
;
Akkari, P.
;
Meredith, C.
;
Dorosz, S.
;
Wilton, S.
;
Callen, D.
;
Laing, N.
;
Baker, E.
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.
2009
Characterisation and Developmental Potential of Ovine Bone Marrow Derived Mesenchymal Stem Cells
Mc Carty, R.
;
Gronthos, S.
;
Zannettino, A.
;
Foster, B.
;
Xian, C.
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.
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
26
Hopwood, J.
24
Sutherland, G.
18
Gecz, J.
11
Eyre, H.
8
Anson, D.
8
Baker, E.
8
et al.
7
Cowin, A.
7
Parsons, D.
6
Butler, R.
.
next >
Subject
90
Humans
44
Male
42
Female
38
Molecular Sequence Data
27
Base Sequence
26
Disease Models, Animal
24
Amino Acid Sequence
22
Chromosome Mapping
19
Brain
19
Mice, Knockout
.
next >
Date issued
36
2010 - 2018
69
2000 - 2009
28
1995 - 1999