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Andrew J Waskiewicz

Showing results (31-40 of 38) with videos related to

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Genes|February 3, 2021
The Axenfeld-Rieger Syndrome Gene <i>FOXC1</i> Contributes to Left-Right PatterningPaul W Chrystal, Curtis R French, Francesca Jean, et al.
Neurobiology of Disease|March 26, 2013
Targeted mutation of the gene encoding prion protein in zebrafish reveals a conserved role in neuron excitabilityValerie C Fleisch, Patricia L A Leighton, Hao Wang, et al.
Zebrafish|June 21, 2013
Evaluating the mutagenic activity of targeted endonucleases containing a Sharkey FokI cleavage domain variant in zebrafishLaura M Pillay, Lyndsay G Selland, Valerie C Fleisch, et al.
Human Molecular Genetics|October 30, 2009
Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomaliesMing Ye, Karyn M Berry-Wynne, Mika Asai-Coakwell, et al.
Human Molecular Genetics|January 12, 2013
Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophiesMika Asai-Coakwell, Lindsey March, Xiao Hua Dai, et al.
The Journal of Clinical Investigation|September 25, 2014
Mutation of FOXC1 and PITX2 induces cerebral small-vessel diseaseCurtis R French, Sudha Seshadri, Anita L Destefano, et al.
Human Molecular Genetics|January 9, 2009
Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypesMika Asai-Coakwell, Curtis R French, Ming Ye, et al.
Zebrafish|June 2, 2016
Restrictions on the Importation of Zebrafish into Canada Associated with Spring Viremia of Carp VirusDavid Hanwell, Sarah A Hutchinson, Chereen Collymore, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Genes|February 3, 2021
The Axenfeld-Rieger Syndrome Gene <i>FOXC1</i> Contributes to Left-Right PatterningPaul W Chrystal, Curtis R French, Francesca Jean, et al.
Neurobiology of Disease|March 26, 2013
Targeted mutation of the gene encoding prion protein in zebrafish reveals a conserved role in neuron excitabilityValerie C Fleisch, Patricia L A Leighton, Hao Wang, et al.
Zebrafish|June 21, 2013
Evaluating the mutagenic activity of targeted endonucleases containing a Sharkey FokI cleavage domain variant in zebrafishLaura M Pillay, Lyndsay G Selland, Valerie C Fleisch, et al.
Human Molecular Genetics|October 30, 2009
Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomaliesMing Ye, Karyn M Berry-Wynne, Mika Asai-Coakwell, et al.
Human Molecular Genetics|January 12, 2013
Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophiesMika Asai-Coakwell, Lindsey March, Xiao Hua Dai, et al.
The Journal of Clinical Investigation|September 25, 2014
Mutation of FOXC1 and PITX2 induces cerebral small-vessel diseaseCurtis R French, Sudha Seshadri, Anita L Destefano, et al.
Human Molecular Genetics|January 9, 2009
Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypesMika Asai-Coakwell, Curtis R French, Ming Ye, et al.
Zebrafish|June 2, 2016
Restrictions on the Importation of Zebrafish into Canada Associated with Spring Viremia of Carp VirusDavid Hanwell, Sarah A Hutchinson, Chereen Collymore, et al.
Pageof 4