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Rob W J Collin

Showing results (81-90 of 149) with videos related to

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Cellular and Molecular Life Sciences : CMLS|January 13, 2026
Exploring extracellular vesicle MicroRNAs in Usher syndrome type 1B: Tear-Derived EVs as potential indicators of retinal healthSander Bervoets, Lonneke Duijkers, Hedwig M Velde, et al.
Molecular Vision|June 6, 2012
Identification of recurrent and novel mutations in TULP1 in Pakistani families with early-onset retinitis pigmentosaMuhammad Ajmal, Muhammad Imran Khan, Shazia Micheal, et al.
Scientific Reports|September 17, 2017
Therapeutic effects of the mitochondrial ROS-redox modulator KH176 in a mammalian model of Leigh DiseaseRia de Haas, Devashish Das, Alejandro Garanto, et al.
American Journal of Human Genetics|April 20, 2010
Mutations in C2ORF71 cause autosomal-recessive retinitis pigmentosaRob W J Collin, Christine Safieh, Karin W Littink, et al.
Ophthalmology|August 20, 2023
Study of Late-Onset Stargardt Type 1 Disease: Characteristics, Genetics, and ProgressionCatherina H Z Li, Jeroen A A H Pas, Zelia Corradi, et al.
Ophthalmology|February 12, 2011
CLRN1 mutations cause nonsyndromic retinitis pigmentosaMuhammad Imran Khan, Ferry F J Kersten, Maleeha Azam, et al.
Molecular Vision|June 28, 2012
Novel mutations in RDH5 cause fundus albipunctatus in two consanguineous Pakistani familiesMuhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, et al.
Orphanet Journal of Rare Diseases|January 30, 2013
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophyIvana Peluso, Ivan Conte, Francesco Testa, et al.
Ophthalmology Science|June 19, 2023
Evaluation of Sleep Quality and Fatigue in Patients with Usher Syndrome Type 2aJessie M Hendricks, Juriaan R Metz, Hedwig M Velde, et al.
Molecular Therapy. Methods & Clinical Development|June 12, 2023
CRISPR-Cas9 correction of a nonsense mutation in <i>LCA5</i> rescues lebercilin expression and localization in human retinal organoidsTess A V Afanasyeva, Dimitra Athanasiou, Pedro R L Perdigao, et al.
Pageof 15

Showing results (81-90 of 149) with videos related to

Sort By:
Pageof 15
Cellular and Molecular Life Sciences : CMLS|January 13, 2026
Exploring extracellular vesicle MicroRNAs in Usher syndrome type 1B: Tear-Derived EVs as potential indicators of retinal healthSander Bervoets, Lonneke Duijkers, Hedwig M Velde, et al.
Molecular Vision|June 6, 2012
Identification of recurrent and novel mutations in TULP1 in Pakistani families with early-onset retinitis pigmentosaMuhammad Ajmal, Muhammad Imran Khan, Shazia Micheal, et al.
Scientific Reports|September 17, 2017
Therapeutic effects of the mitochondrial ROS-redox modulator KH176 in a mammalian model of Leigh DiseaseRia de Haas, Devashish Das, Alejandro Garanto, et al.
American Journal of Human Genetics|April 20, 2010
Mutations in C2ORF71 cause autosomal-recessive retinitis pigmentosaRob W J Collin, Christine Safieh, Karin W Littink, et al.
Ophthalmology|August 20, 2023
Study of Late-Onset Stargardt Type 1 Disease: Characteristics, Genetics, and ProgressionCatherina H Z Li, Jeroen A A H Pas, Zelia Corradi, et al.
Ophthalmology|February 12, 2011
CLRN1 mutations cause nonsyndromic retinitis pigmentosaMuhammad Imran Khan, Ferry F J Kersten, Maleeha Azam, et al.
Molecular Vision|June 28, 2012
Novel mutations in RDH5 cause fundus albipunctatus in two consanguineous Pakistani familiesMuhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, et al.
Orphanet Journal of Rare Diseases|January 30, 2013
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophyIvana Peluso, Ivan Conte, Francesco Testa, et al.
Ophthalmology Science|June 19, 2023
Evaluation of Sleep Quality and Fatigue in Patients with Usher Syndrome Type 2aJessie M Hendricks, Juriaan R Metz, Hedwig M Velde, et al.
Molecular Therapy. Methods & Clinical Development|June 12, 2023
CRISPR-Cas9 correction of a nonsense mutation in <i>LCA5</i> rescues lebercilin expression and localization in human retinal organoidsTess A V Afanasyeva, Dimitra Athanasiou, Pedro R L Perdigao, et al.
Pageof 15