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Results 1-10 of 15 (Search time: 0.001 seconds).
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Issue Date
Title
Author(s)
2015
Acute inhibition of casein kinase 1δ/ε rapidly delays peripheral clock gene rhythms
Kennaway, D.
;
Varcoe, T.
;
Voultsios, A.
;
Salkeld, M.
;
Rattanatray, L.
;
Boden, M.
2015
Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis
Ramos-Brossier, M.
;
Montani, C.
;
Lebrun, N.
;
Gritti, L.
;
Martin, C.
;
Seminatore-Nole, C.
;
Toussaint, A.
;
Moreno, S.
;
Poirier, K.
;
Dorseuil, O.
;
Chelly, J.
;
Hackett, A.
;
Gecz, J.
;
Bieth, E.
;
Faudet, A.
;
Heron, D.
;
Kooy, R.
;
Loeys, B.
;
Humeau, Y.
;
Sala, C.
;
et al.
2015
Incidence of curable sexually transmissible infections among adolescents and young adults in remote Australian Aboriginal communities: analysis of longitudinal clinical service data
Silver, B.
;
Guy, R.
;
Wand, H.
;
Ward, J.
;
Rumbold, A.
;
Fairley, C.
;
Donovan, B.
;
Maher, L.
;
Dyda, A.
;
Garton, L.
;
Hengel, B.
;
Knox, J.
;
McGregor, S.
;
Taylor-Thomson, D.
;
Kaldor, J.
2015
Brain structural and microstructural alterations associated with cerebral palsy and motor impairments in adolescents born extremely preterm and/or extremely low birthweight
Kelly, C.E.
;
Chan, L.
;
Burnett, A.C.
;
Lee, K.J.
;
Connelly, A.
;
Anderson, P.J.
;
Doyle, L.W.
;
Cheong, J.L.Y.
;
Thompson, D.K.
2015
Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioral problems
Kumar, R.
;
Corbett, M.
;
Van Bon, B.
;
Gardner, A.
;
Woenig, J.
;
Jolly, L.
;
Douglas, E.
;
Friend, K.
;
Tan, C.
;
Van Esch, H.
;
Holvoet, M.
;
Raynaud, M.
;
Field, M.
;
Leffler, M.
;
Budny, B.
;
Wisniewska, M.
;
Badura-Stronka, M.
;
Latos-Bieleńska, A.
;
Batanian, J.
;
Rosenfeld, J.
;
et al.
2015
Pharmacological management of low milk supply with domperidone: separating fact from fiction
Grzeskowiak, L.E.
;
Amir, L.H.
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.
2015
Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity
Brookes, E.
;
Laurent, B.
;
Õunap, K.
;
Carroll, R.
;
Moeschler, J.
;
Field, M.
;
Schwartz, C.
;
Gecz, J.
;
Shi, Y.
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.
2015
Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder
Kumar, R.
;
Corbett, M.
;
Smith, N.
;
Jolly, L.
;
Tan, C.
;
Keating, D.
;
Duffield, M.
;
Utsumi, T.
;
Moriya, K.
;
Smith, K.
;
Hoischen, A.
;
Abbott, K.
;
Harbord, M.
;
Compton, A.
;
Woenig, J.
;
Arts, P.
;
Kwint, M.
;
Wieskamp, N.
;
Gijsen, S.
;
Veltman, J.
;
et al.
Discover
Author
5
Corbett, M.
5
Gecz, J.
3
et al.
3
Jolly, L.
2
Anderson, P.J.
2
Cheong, J.L.Y.
2
Doyle, L.W.
2
Field, M.
2
Kumar, R.
2
Lee, K.J.
.
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Subject
13
Humans
10
Female
5
Animals
4
Intellectual Disability
4
Mutation
3
Adolescent
3
Adult
3
Child
3
Child, Preschool
3
Infant
.
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