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S Amer Riazuddin

Showing results (1-10 of 125) with videos related to

Pageof 13
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Experimental Eye Research|November 7, 2020
Metabolome profiling of the developing murine lensShahid Y Khan, Muhammad Ali, S Amer Riazuddin
Cornea|March 19, 2016
Distinct Clinical Phenotype of Corneal Dystrophy Predicts the p.(Leu450Trp) Substitution in COL8A2Allen O Eghrari, S Amer Riazuddin, John D Gottsch
Progress in Molecular Biology and Translational Science|August 28, 2015
Overview of the Cornea: Structure, Function, and DevelopmentAllen O Eghrari, S Amer Riazuddin, John D Gottsch
American Journal of Human Genetics|May 8, 2012
Documenting the corneal phenotype associated with the MIR184 c.57C>T mutationBenjamin W Iliff, S Amer Riazuddin, John D Gottsch
Experimental Eye Research|January 26, 2016
Non-coding RNA profiling of the developing murine lensShahid Y Khan, Sean F Hackett, S Amer Riazuddin
Progress in Molecular Biology and Translational Science|August 28, 2015
Fuchs Corneal DystrophyAllen O Eghrari, S Amer Riazuddin, John D Gottsch
Investigative Ophthalmology & Visual Science|December 2, 2011
A single-base substitution in the seed region of miR-184 causes EDICT syndromeBenjamin W Iliff, S Amer Riazuddin, John D Gottsch
Expert Review of Ophthalmology|April 16, 2013
The genetics of Fuchs' corneal dystrophyBenjamin W Iliff, S Amer Riazuddin, John D Gottsch
Molecular Vision|September 9, 2008
Primary congenital glaucoma localizes to chromosome 14q24.2-24.3 in two consanguineous Pakistani familiesSabika Firasat, S Amer Riazuddin, J Fielding Hejtmancik, et al.
Molecular Vision|November 8, 2008
Novel CYP1B1 mutations in consanguineous Pakistani families with primary congenital glaucomaSabika Firasat, S Amer Riazuddin, Shaheen N Khan, et al.
Pageof 13

Showing results (1-10 of 125) with videos related to

Sort By:
Pageof 13
Experimental Eye Research|November 7, 2020
Metabolome profiling of the developing murine lensShahid Y Khan, Muhammad Ali, S Amer Riazuddin
Cornea|March 19, 2016
Distinct Clinical Phenotype of Corneal Dystrophy Predicts the p.(Leu450Trp) Substitution in COL8A2Allen O Eghrari, S Amer Riazuddin, John D Gottsch
Progress in Molecular Biology and Translational Science|August 28, 2015
Overview of the Cornea: Structure, Function, and DevelopmentAllen O Eghrari, S Amer Riazuddin, John D Gottsch
American Journal of Human Genetics|May 8, 2012
Documenting the corneal phenotype associated with the MIR184 c.57C>T mutationBenjamin W Iliff, S Amer Riazuddin, John D Gottsch
Experimental Eye Research|January 26, 2016
Non-coding RNA profiling of the developing murine lensShahid Y Khan, Sean F Hackett, S Amer Riazuddin
Progress in Molecular Biology and Translational Science|August 28, 2015
Fuchs Corneal DystrophyAllen O Eghrari, S Amer Riazuddin, John D Gottsch
Investigative Ophthalmology & Visual Science|December 2, 2011
A single-base substitution in the seed region of miR-184 causes EDICT syndromeBenjamin W Iliff, S Amer Riazuddin, John D Gottsch
Expert Review of Ophthalmology|April 16, 2013
The genetics of Fuchs' corneal dystrophyBenjamin W Iliff, S Amer Riazuddin, John D Gottsch
Molecular Vision|September 9, 2008
Primary congenital glaucoma localizes to chromosome 14q24.2-24.3 in two consanguineous Pakistani familiesSabika Firasat, S Amer Riazuddin, J Fielding Hejtmancik, et al.
Molecular Vision|November 8, 2008
Novel CYP1B1 mutations in consanguineous Pakistani families with primary congenital glaucomaSabika Firasat, S Amer Riazuddin, Shaheen N Khan, et al.
Pageof 13