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Preview	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	Accuracy of two motor assessments during the first year of life in preterm infants for predicting motor outcome at preschool age	Spittle, A.J.; Lee, K.J.; Spencer-Smith, M.; Lorefice, L.E.; Anderson, P.J.; Doyle, L.W.; Parikh, N.A.
	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.