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Showing results (131-140 of 183) with videos related to

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Investigative Ophthalmology & Visual Science|February 27, 2004
Characterization and prevalence of PITX2 microdeletions and mutations in Axenfeld-Rieger malformationsMatthew A Lines, Kathy Kozlowski, Stephen C Kulak, et al.
Molecular Vision|December 20, 2008
Optineurin coding variants in Ghanaian patients with primary open-angle glaucomaYutao Liu, Stephen Akafo, Cecile Santiago-Turla, et al.
Molecular Vision|May 10, 2011
Myocilin mutations in black South Africans with POAGBenjamin T Whigham, Susan E I Williams, Yutao Liu, et al.
Molecular Vision|January 5, 2013
The role of lysyl oxidase-like 1 DNA copy number variants in exfoliation glaucomaYutao Liu, Benjamin T Whigham, Joshua Wheeler, et al.
Investigative Ophthalmology & Visual Science|May 26, 2006
Distribution of WDR36 DNA sequence variants in patients with primary open-angle glaucomaMichael A Hauser, R Rand Allingham, Kevin Linkroum, et al.
Journal of Glaucoma|September 22, 2006
Distribution of optineurin sequence variations in an ethnically diverse population of low-tension glaucoma patients from the United StatesMichael A Hauser, Dayse Figueiredo Sena, Jason Flor, et al.
Plos Genetics|January 26, 2018
Genomic locus modulating corneal thickness in the mouse identifies POU6F2 as a potential risk of developing glaucomaRebecca King, Felix L Struebing, Ying Li, et al.
Investigative Ophthalmology & Visual Science|April 19, 2008
Lack of association between LOXL1 variants and primary open-angle glaucoma in three different populationsYutao Liu, Silke Schmidt, Xuejun Qin, et al.
Investigative Ophthalmology & Visual Science|March 31, 2017
VEGF as a Paracrine Regulator of Conventional Outflow FacilityEster Reina-Torres, Joanne C Wen, Katy C Liu, et al.
Human Molecular Genetics|February 11, 2020
Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1Heather M Schmitt, William M Johnson, Inas F Aboobakar, et al.
Pageof 19

Showing results (131-140 of 183) with videos related to

Sort By:
Pageof 19
Investigative Ophthalmology & Visual Science|February 27, 2004
Characterization and prevalence of PITX2 microdeletions and mutations in Axenfeld-Rieger malformationsMatthew A Lines, Kathy Kozlowski, Stephen C Kulak, et al.
Molecular Vision|December 20, 2008
Optineurin coding variants in Ghanaian patients with primary open-angle glaucomaYutao Liu, Stephen Akafo, Cecile Santiago-Turla, et al.
Molecular Vision|May 10, 2011
Myocilin mutations in black South Africans with POAGBenjamin T Whigham, Susan E I Williams, Yutao Liu, et al.
Molecular Vision|January 5, 2013
The role of lysyl oxidase-like 1 DNA copy number variants in exfoliation glaucomaYutao Liu, Benjamin T Whigham, Joshua Wheeler, et al.
Investigative Ophthalmology & Visual Science|May 26, 2006
Distribution of WDR36 DNA sequence variants in patients with primary open-angle glaucomaMichael A Hauser, R Rand Allingham, Kevin Linkroum, et al.
Journal of Glaucoma|September 22, 2006
Distribution of optineurin sequence variations in an ethnically diverse population of low-tension glaucoma patients from the United StatesMichael A Hauser, Dayse Figueiredo Sena, Jason Flor, et al.
Plos Genetics|January 26, 2018
Genomic locus modulating corneal thickness in the mouse identifies POU6F2 as a potential risk of developing glaucomaRebecca King, Felix L Struebing, Ying Li, et al.
Investigative Ophthalmology & Visual Science|April 19, 2008
Lack of association between LOXL1 variants and primary open-angle glaucoma in three different populationsYutao Liu, Silke Schmidt, Xuejun Qin, et al.
Investigative Ophthalmology & Visual Science|March 31, 2017
VEGF as a Paracrine Regulator of Conventional Outflow FacilityEster Reina-Torres, Joanne C Wen, Katy C Liu, et al.
Human Molecular Genetics|February 11, 2020
Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1Heather M Schmitt, William M Johnson, Inas F Aboobakar, et al.
Pageof 19