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Results 1-10 of 19 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2012
TGF-β mediates proinflammatory seminal fluid signaling in human cervical epithelial cells
Sharkey, D.
;
Macpherson, A.
;
Tremellen, K.
;
Mottershead, D.
;
Gilchrist, R.
;
Robertson, 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
Macrophages regulate corpus luteum development during embryo implantation in mice
Care, A.
;
Diener, K.
;
Jasper, M.
;
Brown, H.
;
Ingman, W.
;
Robertson, S.
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.
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.
2012
A possible murine model for investigation of pathogenesis of Sudden Infant Death Syndrome
Bettelheim, K.
;
Luke, R.
;
Johnston, N.
;
Pearce, J.
;
Goldwater, P.
Discover
Author
8
Gecz, J.
4
et al.
3
Corbett, M.
3
Haan, E.
3
Jolly, L.
3
Kalscheuer, V.
3
Nguyen, L.
2
Brown, H.
2
Field, M.
2
Gardner, A.
.
next >
Subject
16
Female
9
Mutation
6
Intellectual Disability
5
Pedigree
4
Cells, Cultured
4
Transcription Factors
3
Brain
3
Carrier Proteins
3
Child, Preschool
3
Disease Models, Animal
.
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Date issued
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2018
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2015
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2014
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2013
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2012
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2010