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American Journal of Ophthalmology
|
October 7, 2014
Copy number variations of TBK1 in Australian patients with primary open-angle glaucoma
Mona S Awadalla, John H Fingert, Benjamin E Roos, et al.
Science (New York, N.Y.)
|
January 31, 1997
Identification of a gene that causes primary open angle glaucoma
E M Stone, J H Fingert, W L Alward, et al.
Plos One
|
March 29, 2013
A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel Loci
Todd E Scheetz, John H Fingert, Kai Wang, et al.
Human Mutation
|
January 13, 2015
Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 in patients with cavitary optic disc anomaly
Ralph J Hazlewood, Benjamin R Roos, Frances Solivan-Timpe, et al.
Investigative Ophthalmology & Visual Science
|
August 19, 2021
Diffusion Tensor Imaging of Visual Pathway Abnormalities in Five Glaucoma Animal Models
Max K Colbert, Leon C Ho, Yolandi van der Merwe, et al.
JAMA Ophthalmology
|
March 1, 2019
Myocilin Mutations in Patients With Normal-Tension Glaucoma
Wallace L M Alward, Carly van der Heide, Cheryl L Khanna, et al.
Human Molecular Genetics
|
April 10, 1999
Analysis of myocilin mutations in 1703 glaucoma patients from five different populations
J H Fingert, E Héon, J M Liebmann, et al.
Human Genetics
|
October 29, 2010
Genome-wide analysis of copy number variants in age-related macular degeneration
Kacie J Meyer, Lea K Davis, Emily I Schindler, et al.
Investigative Ophthalmology & Visual Science
|
February 12, 2011
Copy number variations and primary open-angle glaucoma
Lea K Davis, Kacie J Meyer, Emily I Schindler, et al.
Investigative Ophthalmology & Visual Science
|
June 30, 2001
Glucocorticoid induction of the glaucoma gene MYOC in human and monkey trabecular meshwork cells and tissues
A F Clark, H T Steely, J E Dickerson, et al.
Page
of 16
Search research articles
Search
Showing results (131-140 of 159) with videos related to
Sort By:
Page
of 16
American Journal of Ophthalmology
|
October 7, 2014
Copy number variations of TBK1 in Australian patients with primary open-angle glaucoma
Mona S Awadalla, John H Fingert, Benjamin E Roos, et al.
Science (New York, N.Y.)
|
January 31, 1997
Identification of a gene that causes primary open angle glaucoma
E M Stone, J H Fingert, W L Alward, et al.
Plos One
|
March 29, 2013
A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel Loci
Todd E Scheetz, John H Fingert, Kai Wang, et al.
Human Mutation
|
January 13, 2015
Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 in patients with cavitary optic disc anomaly
Ralph J Hazlewood, Benjamin R Roos, Frances Solivan-Timpe, et al.
Investigative Ophthalmology & Visual Science
|
August 19, 2021
Diffusion Tensor Imaging of Visual Pathway Abnormalities in Five Glaucoma Animal Models
Max K Colbert, Leon C Ho, Yolandi van der Merwe, et al.
JAMA Ophthalmology
|
March 1, 2019
Myocilin Mutations in Patients With Normal-Tension Glaucoma
Wallace L M Alward, Carly van der Heide, Cheryl L Khanna, et al.
Human Molecular Genetics
|
April 10, 1999
Analysis of myocilin mutations in 1703 glaucoma patients from five different populations
J H Fingert, E Héon, J M Liebmann, et al.
Human Genetics
|
October 29, 2010
Genome-wide analysis of copy number variants in age-related macular degeneration
Kacie J Meyer, Lea K Davis, Emily I Schindler, et al.
Investigative Ophthalmology & Visual Science
|
February 12, 2011
Copy number variations and primary open-angle glaucoma
Lea K Davis, Kacie J Meyer, Emily I Schindler, et al.
Investigative Ophthalmology & Visual Science
|
June 30, 2001
Glucocorticoid induction of the glaucoma gene MYOC in human and monkey trabecular meshwork cells and tissues
A F Clark, H T Steely, J E Dickerson, et al.
Page
of 16