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Vinit B Mahajan

Showing results (151-160 of 259) with videos related to

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Journal of Clinical Medicine|December 11, 2022
Conjunctival Swabs Reveal Higher Detection Rate Compared to Schirmer Strips for SARS-CoV-2 RNA Detection in Tears of Hospitalized COVID-19 PatientsLuís Expedito Sabage, Young Joo Sun, Julian Wolf, et al.
American Journal of Ophthalmology Case Reports|April 11, 2020
Phenotypic variance in Calpain-5 retinal degenerationPeter H Tang, Teja Chemudupati, Katherine J Wert, et al.
Investigative Ophthalmology & Visual Science|October 13, 2020
Retinal Manifestations of Mitochondrial Oxidative Phosphorylation DisordersJin Kyun Oh, Jose Ronaldo Lima de Carvalho, Yan Nuzbrokh, et al.
Molecular Genetics & Genomic Medicine|May 27, 2017
Structural modeling of a novel <i>SLC38A8</i> mutation that causes foveal hypoplasiaMarcus A Toral, Gabriel Velez, Katherine Boudreault, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 13, 2011
Seroreactivity against aqueous-soluble and detergent-soluble retinal proteins in posterior uveitisAudrey C Ko, Jason P Brinton, Vinit B Mahajan, et al.
Biofabrication|February 24, 2026
Implantable ocular therapeutic systems: an insight into their clinical potential in the long-term treatment of ocular diseasesHyeonji Kim, Nae-Won Kang, Wen Hong, et al.
Diagnostics (Basel, Switzerland)|July 27, 2022
Predicting Systemic Health Features from Retinal Fundus Images Using Transfer-Learning-Based Artificial Intelligence ModelsNergis C Khan, Chandrashan Perera, Eliot R Dow, et al.
Nature Communications|February 26, 2022
Investigation of Cas9 antibodies in the human eyeMarcus A Toral, Carsten T Charlesworth, Benjamin Ng, et al.
Cold Spring Harbor Molecular Case Studies|December 15, 2019
Compound heterozygous novel frameshift variants in the <i>PROM1</i> gene result in Leber congenital amaurosisSara D Ragi, Jose Ronaldo Lima de Carvalho, Akemi J Tanaka, et al.
Orphanet Journal of Rare Diseases|August 3, 2019
Comparison of structural progression between ciliopathy and non-ciliopathy associated with autosomal recessive retinitis pigmentosaVitor K L Takahashi, Christine L Xu, Júlia T Takiuti, et al.
Pageof 26

Showing results (151-160 of 259) with videos related to

Sort By:
Pageof 26
Journal of Clinical Medicine|December 11, 2022
Conjunctival Swabs Reveal Higher Detection Rate Compared to Schirmer Strips for SARS-CoV-2 RNA Detection in Tears of Hospitalized COVID-19 PatientsLuís Expedito Sabage, Young Joo Sun, Julian Wolf, et al.
American Journal of Ophthalmology Case Reports|April 11, 2020
Phenotypic variance in Calpain-5 retinal degenerationPeter H Tang, Teja Chemudupati, Katherine J Wert, et al.
Investigative Ophthalmology & Visual Science|October 13, 2020
Retinal Manifestations of Mitochondrial Oxidative Phosphorylation DisordersJin Kyun Oh, Jose Ronaldo Lima de Carvalho, Yan Nuzbrokh, et al.
Molecular Genetics & Genomic Medicine|May 27, 2017
Structural modeling of a novel <i>SLC38A8</i> mutation that causes foveal hypoplasiaMarcus A Toral, Gabriel Velez, Katherine Boudreault, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 13, 2011
Seroreactivity against aqueous-soluble and detergent-soluble retinal proteins in posterior uveitisAudrey C Ko, Jason P Brinton, Vinit B Mahajan, et al.
Biofabrication|February 24, 2026
Implantable ocular therapeutic systems: an insight into their clinical potential in the long-term treatment of ocular diseasesHyeonji Kim, Nae-Won Kang, Wen Hong, et al.
Diagnostics (Basel, Switzerland)|July 27, 2022
Predicting Systemic Health Features from Retinal Fundus Images Using Transfer-Learning-Based Artificial Intelligence ModelsNergis C Khan, Chandrashan Perera, Eliot R Dow, et al.
Nature Communications|February 26, 2022
Investigation of Cas9 antibodies in the human eyeMarcus A Toral, Carsten T Charlesworth, Benjamin Ng, et al.
Cold Spring Harbor Molecular Case Studies|December 15, 2019
Compound heterozygous novel frameshift variants in the <i>PROM1</i> gene result in Leber congenital amaurosisSara D Ragi, Jose Ronaldo Lima de Carvalho, Akemi J Tanaka, et al.
Orphanet Journal of Rare Diseases|August 3, 2019
Comparison of structural progression between ciliopathy and non-ciliopathy associated with autosomal recessive retinitis pigmentosaVitor K L Takahashi, Christine L Xu, Júlia T Takiuti, et al.
Pageof 26