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Proceedings of the National Academy of Sciences of the United States of America
|
April 15, 2026
Rhesus macaques with an <i>OPA1</i> mutation demonstrate features of autosomal dominant optic atrophy
Tracy N Jaggers, Ana Ripolles-Garcia, Ala Moshiri, et al.
BMC Biology
|
February 4, 2023
Genome-wide screening reveals the genetic basis of mammalian embryonic eye development
Justine M Chee, Louise Lanoue, Dave Clary, et al.
Scientific Reports
|
December 1, 2022
Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes
Kendall Higgins, Bret A Moore, Zorana Berberovic, et al.
American Journal of Ophthalmology
|
June 17, 2026
SEARCHING FOR NEW GENES THAT CAUSE USHER SYNDROME
Ala Moshiri, Niusha Kasiri, Michael Shea, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 22, 2026
Genome-wide association and multi-omics functional screens reveal the genetic architecture of foveal development
Callum Hunt, Manjiri Patil, Hammad Syed, et al.
Investigative Ophthalmology & Visual Science
|
May 5, 2025
Systematic Ocular Phenotyping of Knockout Mouse Lines Identifies Genes Associated With Age-Related Corneal Dystrophies
Andrew Briere, Peter Vo, Benjamin Yang, et al.
Investigative Ophthalmology & Visual Science
|
June 23, 2025
Ocular Phenotyping of Knockout Mice Identifies Genes Associated With Late Adult Retinal Phenotypes
Abraham Hang, Andy Shao, Michael Shea, et al.
Nature Communications
|
January 20, 2018
Identification of genetic elements in metabolism by high-throughput mouse phenotyping
Jan Rozman, Birgit Rathkolb, Manuela A Oestereicher, et al.
Plos Genetics
|
December 28, 2020
Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density
Anna L Swan, Christine Schütt, Jan Rozman, et al.
BMC Genomics
|
January 20, 2025
Systematic ocular phenotyping of 8,707 knockout mouse lines identifies genes associated with abnormal corneal phenotypes
Peter Vo, Denise M Imai-Leonard, Benjamin Yang, et al.
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of 10
Search research articles
Search
Showing results (81-90 of 92) with videos related to
Sort By:
Page
of 10
Proceedings of the National Academy of Sciences of the United States of America
|
April 15, 2026
Rhesus macaques with an <i>OPA1</i> mutation demonstrate features of autosomal dominant optic atrophy
Tracy N Jaggers, Ana Ripolles-Garcia, Ala Moshiri, et al.
BMC Biology
|
February 4, 2023
Genome-wide screening reveals the genetic basis of mammalian embryonic eye development
Justine M Chee, Louise Lanoue, Dave Clary, et al.
Scientific Reports
|
December 1, 2022
Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes
Kendall Higgins, Bret A Moore, Zorana Berberovic, et al.
American Journal of Ophthalmology
|
June 17, 2026
SEARCHING FOR NEW GENES THAT CAUSE USHER SYNDROME
Ala Moshiri, Niusha Kasiri, Michael Shea, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 22, 2026
Genome-wide association and multi-omics functional screens reveal the genetic architecture of foveal development
Callum Hunt, Manjiri Patil, Hammad Syed, et al.
Investigative Ophthalmology & Visual Science
|
May 5, 2025
Systematic Ocular Phenotyping of Knockout Mouse Lines Identifies Genes Associated With Age-Related Corneal Dystrophies
Andrew Briere, Peter Vo, Benjamin Yang, et al.
Investigative Ophthalmology & Visual Science
|
June 23, 2025
Ocular Phenotyping of Knockout Mice Identifies Genes Associated With Late Adult Retinal Phenotypes
Abraham Hang, Andy Shao, Michael Shea, et al.
Nature Communications
|
January 20, 2018
Identification of genetic elements in metabolism by high-throughput mouse phenotyping
Jan Rozman, Birgit Rathkolb, Manuela A Oestereicher, et al.
Plos Genetics
|
December 28, 2020
Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density
Anna L Swan, Christine Schütt, Jan Rozman, et al.
BMC Genomics
|
January 20, 2025
Systematic ocular phenotyping of 8,707 knockout mouse lines identifies genes associated with abnormal corneal phenotypes
Peter Vo, Denise M Imai-Leonard, Benjamin Yang, et al.
Page
of 10