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A Mackey

Showing results (621-630 of 763) with videos related to

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American Journal of Human Genetics|February 18, 2010
Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathyJames A Poulter, Manir Ali, David F Gilmour, et al.
Human Molecular Genetics|October 8, 2025
Genomic structural equation Modeling analysis of glaucoma Endophenotypes: investigating genetic architecture and non-intraocular pressure mechanismsMaryam Marzban, Santiago Diaz-Torres, Jackson Thorp, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|February 15, 2011
The Norfolk Island Eye Study (NIES): rationale, methodology and distribution of ocular biometry (biometry of the bounty)David A Mackey, Justin C Sherwin, Lisa S Kearns, et al.
Nature Genetics|June 16, 1999
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophyE M Stone, A J Lotery, F L Munier, et al.
American Journal of Human Genetics|September 2, 2017
Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative VitreoretinopathyJames A Poulter, Manir Ali, David F Gilmour, et al.
Human Molecular Genetics|January 25, 2024
High throughput functional profiling of genes at intraocular pressure loci reveals distinct networks for glaucomaConnor J Greatbatch, Qinyi Lu, Sandy Hung, et al.
Journal of the American Chemical Society|February 8, 2011
Poly(perfluoroalkylation) of metallic nitride fullerenes reveals addition-pattern guidelines: synthesis and characterization of a family of Sc3N@C80(CF3)n (n = 2-16) and their radical anionsNatalia B Shustova, Dmitry V Peryshkov, Igor V Kuvychko, et al.
Cell Reports|December 31, 2013
Hypomethylation of the IL17RC promoter in peripheral blood leukocytes is not a hallmark of age-related macular degenerationVerity F Oliver, Maria Franchina, Andrew E Jaffe, et al.
Science (New York, N.Y.)|January 31, 1997
Identification of a gene that causes primary open angle glaucomaE M Stone, J H Fingert, W L Alward, et al.
Investigative Ophthalmology & Visual Science|June 21, 2012
Association of genetic variants in the TMCO1 gene with clinical parameters related to glaucoma and characterization of the protein in the eyeShiwani Sharma, Kathryn P Burdon, Glyn Chidlow, et al.
Pageof 77

Showing results (621-630 of 763) with videos related to

Sort By:
Pageof 77
American Journal of Human Genetics|February 18, 2010
Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathyJames A Poulter, Manir Ali, David F Gilmour, et al.
Human Molecular Genetics|October 8, 2025
Genomic structural equation Modeling analysis of glaucoma Endophenotypes: investigating genetic architecture and non-intraocular pressure mechanismsMaryam Marzban, Santiago Diaz-Torres, Jackson Thorp, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|February 15, 2011
The Norfolk Island Eye Study (NIES): rationale, methodology and distribution of ocular biometry (biometry of the bounty)David A Mackey, Justin C Sherwin, Lisa S Kearns, et al.
Nature Genetics|June 16, 1999
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophyE M Stone, A J Lotery, F L Munier, et al.
American Journal of Human Genetics|September 2, 2017
Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative VitreoretinopathyJames A Poulter, Manir Ali, David F Gilmour, et al.
Human Molecular Genetics|January 25, 2024
High throughput functional profiling of genes at intraocular pressure loci reveals distinct networks for glaucomaConnor J Greatbatch, Qinyi Lu, Sandy Hung, et al.
Journal of the American Chemical Society|February 8, 2011
Poly(perfluoroalkylation) of metallic nitride fullerenes reveals addition-pattern guidelines: synthesis and characterization of a family of Sc3N@C80(CF3)n (n = 2-16) and their radical anionsNatalia B Shustova, Dmitry V Peryshkov, Igor V Kuvychko, et al.
Cell Reports|December 31, 2013
Hypomethylation of the IL17RC promoter in peripheral blood leukocytes is not a hallmark of age-related macular degenerationVerity F Oliver, Maria Franchina, Andrew E Jaffe, et al.
Science (New York, N.Y.)|January 31, 1997
Identification of a gene that causes primary open angle glaucomaE M Stone, J H Fingert, W L Alward, et al.
Investigative Ophthalmology & Visual Science|June 21, 2012
Association of genetic variants in the TMCO1 gene with clinical parameters related to glaucoma and characterization of the protein in the eyeShiwani Sharma, Kathryn P Burdon, Glyn Chidlow, et al.
Pageof 77