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Alan Shiels

Showing results (21-30 of 44) with videos related to

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Molecular Vision|December 19, 2007
X-linked idiopathic infantile nystagmus associated with a missense mutation in FRMD7Alan Shiels, Thomas M Bennett, Jessica B Prince, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 7, 2023
Charged multivesicular body protein 4b forms complexes with gap junction proteins during lens fiber cell differentiationYuefang Zhou, Thomas M Bennett, Thomas W White, et al.
Cells|October 23, 2021
Mutation of the EPHA2 Tyrosine-Kinase Domain Dysregulates Cell Pattern Formation and Cytoskeletal Gene Expression in the LensYuefang Zhou, Thomas M Bennett, Philip A Ruzycki, et al.
Plos One|December 22, 2017
Germ-line and somatic EPHA2 coding variants in lens aging and cataractThomas M Bennett, Oussama M'Hamdi, J Fielding Hejtmancik, et al.
Investigative Ophthalmology & Visual Science|January 26, 2007
Refractive defects and cataracts in mice lacking lens intrinsic membrane protein-2Alan Shiels, Jennifer M King, Donna S Mackay, et al.
Human Genomics|November 19, 2014
Exome sequencing identifies novel and recurrent mutations in GJA8 and CRYGD associated with inherited cataractDonna S Mackay, Thomas M Bennett, Susan M Culican, et al.
Investigative Ophthalmology & Visual Science|December 15, 2011
A role for epha2 in cell migration and refractive organization of the ocular lensYanrong Shi, Alicia De Maria, Thomas Bennett, et al.
Plos One|August 5, 2014
Mutation of the melastatin-related cation channel, TRPM3, underlies inherited cataract and glaucomaThomas M Bennett, Donna S Mackay, Carla J Siegfried, et al.
Molecular Vision|June 23, 2004
A novel missense mutation in the gene for gap-junction protein alpha3 (GJA3) associated with autosomal dominant "nuclear punctate" cataracts linked to chromosome 13qThomas M Bennett, Donna S Mackay, Harry L S Knopf, et al.
G3 (Bethesda, Md.)|March 9, 2023
Whole-exome sequencing prioritizes candidate genes for hereditary cataract in the Emory mouse mutantThomas M Bennett, Yuefang Zhou, Kacie J Meyer, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Molecular Vision|December 19, 2007
X-linked idiopathic infantile nystagmus associated with a missense mutation in FRMD7Alan Shiels, Thomas M Bennett, Jessica B Prince, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 7, 2023
Charged multivesicular body protein 4b forms complexes with gap junction proteins during lens fiber cell differentiationYuefang Zhou, Thomas M Bennett, Thomas W White, et al.
Cells|October 23, 2021
Mutation of the EPHA2 Tyrosine-Kinase Domain Dysregulates Cell Pattern Formation and Cytoskeletal Gene Expression in the LensYuefang Zhou, Thomas M Bennett, Philip A Ruzycki, et al.
Plos One|December 22, 2017
Germ-line and somatic EPHA2 coding variants in lens aging and cataractThomas M Bennett, Oussama M'Hamdi, J Fielding Hejtmancik, et al.
Investigative Ophthalmology & Visual Science|January 26, 2007
Refractive defects and cataracts in mice lacking lens intrinsic membrane protein-2Alan Shiels, Jennifer M King, Donna S Mackay, et al.
Human Genomics|November 19, 2014
Exome sequencing identifies novel and recurrent mutations in GJA8 and CRYGD associated with inherited cataractDonna S Mackay, Thomas M Bennett, Susan M Culican, et al.
Investigative Ophthalmology & Visual Science|December 15, 2011
A role for epha2 in cell migration and refractive organization of the ocular lensYanrong Shi, Alicia De Maria, Thomas Bennett, et al.
Plos One|August 5, 2014
Mutation of the melastatin-related cation channel, TRPM3, underlies inherited cataract and glaucomaThomas M Bennett, Donna S Mackay, Carla J Siegfried, et al.
Molecular Vision|June 23, 2004
A novel missense mutation in the gene for gap-junction protein alpha3 (GJA3) associated with autosomal dominant "nuclear punctate" cataracts linked to chromosome 13qThomas M Bennett, Donna S Mackay, Harry L S Knopf, et al.
G3 (Bethesda, Md.)|March 9, 2023
Whole-exome sequencing prioritizes candidate genes for hereditary cataract in the Emory mouse mutantThomas M Bennett, Yuefang Zhou, Kacie J Meyer, et al.
Pageof 5