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Curtis R French

Showing results (21-30 of 29) with videos related to

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Scientific Reports|August 31, 2024
Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signalingSerhiy Havrylov, Paul Chrystal, Suey van Baarle, et al.
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.
Developmental Biology|June 15, 2019
foxc1 is required for embryonic head vascular smooth muscle differentiation in zebrafishThomas R Whitesell, Paul W Chrystal, Jae-Ryeon Ryu, 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.
Human Genetics|March 12, 2022
Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase geneJustin A Pater, Cindy Penney, Darren D O'Rielly, et al.
Human Genetics|October 11, 2021
A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) geneNelly Abdelfatah, Ahmed A Mostafa, Curtis R French, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Scientific Reports|August 31, 2024
Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signalingSerhiy Havrylov, Paul Chrystal, Suey van Baarle, et al.
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.
Developmental Biology|June 15, 2019
foxc1 is required for embryonic head vascular smooth muscle differentiation in zebrafishThomas R Whitesell, Paul W Chrystal, Jae-Ryeon Ryu, 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.
Human Genetics|March 12, 2022
Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase geneJustin A Pater, Cindy Penney, Darren D O'Rielly, et al.
Human Genetics|October 11, 2021
A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) geneNelly Abdelfatah, Ahmed A Mostafa, Curtis R French, et al.
Pageof 3