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Stephen W Wilson

Showing results (81-90 of 107) with videos related to

Pageof 11
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Plos One|January 30, 2019
Abrogation of Stem Loop Binding Protein (Slbp) function leads to a failure of cells to transition from proliferation to differentiation, retinal coloboma and midline axon guidance deficitsKatherine J Turner, Jacqueline Hoyle, Leonardo E Valdivia, et al.
Development (Cambridge, England)|June 7, 2002
Retinoic acid signalling in the zebrafish embryo is necessary during pre-segmentation stages to pattern the anterior-posterior axis of the CNS and to induce a pectoral fin budHeiner Grandel, Klaus Lun, Gerd-Jörg Rauch, et al.
Development (Cambridge, England)|August 25, 2011
Lef1-dependent Wnt/β-catenin signalling drives the proliferative engine that maintains tissue homeostasis during lateral line developmentLeonardo E Valdivia, Rodrigo M Young, Thomas A Hawkins, et al.
Development (Cambridge, England)|February 8, 2008
The ATPase-dependent chaperoning activity of Hsp90a regulates thick filament formation and integration during skeletal muscle myofibrillogenesisThomas A Hawkins, Anna-Pavlina Haramis, Christelle Etard, et al.
Nature|May 14, 2015
Recursive splicing in long vertebrate genesChristopher R Sibley, Warren Emmett, Lorea Blazquez, et al.
Development (Cambridge, England)|September 19, 2013
Daam1a mediates asymmetric habenular morphogenesis by regulating dendritic and axonal outgrowthAlicia Colombo, Karina Palma, Lorena Armijo, et al.
Elife|January 8, 2021
A simple and effective F0 knockout method for rapid screening of behaviour and other complex phenotypesFrançois Kroll, Gareth T Powell, Marcus Ghosh, et al.
Disease Models & Mechanisms|May 6, 2022
Loss of slc39a14 causes simultaneous manganese hypersensitivity and deficiency in zebrafishKarin Tuschl, Richard J White, Chintan Trivedi, et al.
Human Genetics|August 18, 2009
Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulatorsGaia Gestri, Robert J Osborne, Alexander W Wyatt, et al.
Neuron|August 5, 2003
Local tissue interactions across the dorsal midline of the forebrain establish CNS lateralityMiguel L Concha, Claire Russell, Jennifer C Regan, et al.
Pageof 11

Showing results (81-90 of 107) with videos related to

Sort By:
Pageof 11
Plos One|January 30, 2019
Abrogation of Stem Loop Binding Protein (Slbp) function leads to a failure of cells to transition from proliferation to differentiation, retinal coloboma and midline axon guidance deficitsKatherine J Turner, Jacqueline Hoyle, Leonardo E Valdivia, et al.
Development (Cambridge, England)|June 7, 2002
Retinoic acid signalling in the zebrafish embryo is necessary during pre-segmentation stages to pattern the anterior-posterior axis of the CNS and to induce a pectoral fin budHeiner Grandel, Klaus Lun, Gerd-Jörg Rauch, et al.
Development (Cambridge, England)|August 25, 2011
Lef1-dependent Wnt/β-catenin signalling drives the proliferative engine that maintains tissue homeostasis during lateral line developmentLeonardo E Valdivia, Rodrigo M Young, Thomas A Hawkins, et al.
Development (Cambridge, England)|February 8, 2008
The ATPase-dependent chaperoning activity of Hsp90a regulates thick filament formation and integration during skeletal muscle myofibrillogenesisThomas A Hawkins, Anna-Pavlina Haramis, Christelle Etard, et al.
Nature|May 14, 2015
Recursive splicing in long vertebrate genesChristopher R Sibley, Warren Emmett, Lorea Blazquez, et al.
Development (Cambridge, England)|September 19, 2013
Daam1a mediates asymmetric habenular morphogenesis by regulating dendritic and axonal outgrowthAlicia Colombo, Karina Palma, Lorena Armijo, et al.
Elife|January 8, 2021
A simple and effective F0 knockout method for rapid screening of behaviour and other complex phenotypesFrançois Kroll, Gareth T Powell, Marcus Ghosh, et al.
Disease Models & Mechanisms|May 6, 2022
Loss of slc39a14 causes simultaneous manganese hypersensitivity and deficiency in zebrafishKarin Tuschl, Richard J White, Chintan Trivedi, et al.
Human Genetics|August 18, 2009
Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulatorsGaia Gestri, Robert J Osborne, Alexander W Wyatt, et al.
Neuron|August 5, 2003
Local tissue interactions across the dorsal midline of the forebrain establish CNS lateralityMiguel L Concha, Claire Russell, Jennifer C Regan, et al.
Pageof 11