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Rob W J Collin

Showing results (41-50 of 149) with videos related to

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The Annals of Otology, Rhinology, and Laryngology|June 25, 2009
Audiometric and vestibular features in a second Dutch DFNA20/26 family with a novel mutation in ACTG1Anne-Martine R de Heer, Patrick L M Huygen, Rob W J Collin, et al.
Nucleic Acids Research|August 9, 2024
Efficacy, biodistribution and safety comparison of chemically modified antisense oligonucleotides in the retinaIrene Vázquez-Domínguez, Alejandro Allo Anido, Lonneke Duijkers, et al.
Plos One|August 29, 2012
Expression of wild-type Rp1 protein in Rp1 knock-in mice rescues the retinal degeneration phenotypeQin Liu, Rob W J Collin, Frans P M Cremers, et al.
Ophthalmology Science|January 22, 2026
A Comparison of Randomizing Either One Eye or Both Eyes in Clinical Trials for Stargardt Disease Type 1Jeroen A A H Pas, Patty P A Dhooge, Catherina H Z Li, et al.
Progress in Retinal and Eye Research|May 5, 2015
The pros and cons of vertebrate animal models for functional and therapeutic research on inherited retinal dystrophiesRalph W N Slijkerman, Fei Song, Galuh D N Astuti, et al.
Human Molecular Genetics|July 9, 2018
An FEVR-associated mutation in ZNF408 alters the expression of genes involved in the development of vasculatureDyah W Karjosukarso, Sebastianus H C van Gestel, Jieqiong Qu, et al.
Stem Cell Research|November 18, 2023
Generation of an iPSC line (RMCGENi020-A) from a patient with Stargardt disease harboring the recurrent intronic ABCA4 variant c.4253+43G>ANuria Suárez-Herrera, Nico Leijsten, Silvia Albert, et al.
Audiology & Neuro-Otology|April 18, 2009
Vestibular impairment in a Dutch DFNA15 family with an L289F mutation in POU4F3F J Wendy van Drunen, Robert J Pauw, Rob W J Collin, et al.
Archives of Otolaryngology--Head & Neck Surgery|March 19, 2008
Audiometric characteristics of a Dutch family linked to DFNA15 with a novel mutation (p.L289F) in POU4F3Robert J Pauw, F J Wendy van Drunen, Rob W J Collin, et al.
International Journal of Molecular Sciences|September 10, 2021
Zebrafish as a Model to Evaluate a CRISPR/Cas9-Based Exon Excision Approach as a Future Treatment Option for <i>EYS</i>-Associated Retinitis PigmentosaRenske Schellens, Erik de Vrieze, Pam Graave, et al.
Pageof 15

Showing results (41-50 of 149) with videos related to

Sort By:
Pageof 15
The Annals of Otology, Rhinology, and Laryngology|June 25, 2009
Audiometric and vestibular features in a second Dutch DFNA20/26 family with a novel mutation in ACTG1Anne-Martine R de Heer, Patrick L M Huygen, Rob W J Collin, et al.
Nucleic Acids Research|August 9, 2024
Efficacy, biodistribution and safety comparison of chemically modified antisense oligonucleotides in the retinaIrene Vázquez-Domínguez, Alejandro Allo Anido, Lonneke Duijkers, et al.
Plos One|August 29, 2012
Expression of wild-type Rp1 protein in Rp1 knock-in mice rescues the retinal degeneration phenotypeQin Liu, Rob W J Collin, Frans P M Cremers, et al.
Ophthalmology Science|January 22, 2026
A Comparison of Randomizing Either One Eye or Both Eyes in Clinical Trials for Stargardt Disease Type 1Jeroen A A H Pas, Patty P A Dhooge, Catherina H Z Li, et al.
Progress in Retinal and Eye Research|May 5, 2015
The pros and cons of vertebrate animal models for functional and therapeutic research on inherited retinal dystrophiesRalph W N Slijkerman, Fei Song, Galuh D N Astuti, et al.
Human Molecular Genetics|July 9, 2018
An FEVR-associated mutation in ZNF408 alters the expression of genes involved in the development of vasculatureDyah W Karjosukarso, Sebastianus H C van Gestel, Jieqiong Qu, et al.
Stem Cell Research|November 18, 2023
Generation of an iPSC line (RMCGENi020-A) from a patient with Stargardt disease harboring the recurrent intronic ABCA4 variant c.4253+43G>ANuria Suárez-Herrera, Nico Leijsten, Silvia Albert, et al.
Audiology & Neuro-Otology|April 18, 2009
Vestibular impairment in a Dutch DFNA15 family with an L289F mutation in POU4F3F J Wendy van Drunen, Robert J Pauw, Rob W J Collin, et al.
Archives of Otolaryngology--Head & Neck Surgery|March 19, 2008
Audiometric characteristics of a Dutch family linked to DFNA15 with a novel mutation (p.L289F) in POU4F3Robert J Pauw, F J Wendy van Drunen, Rob W J Collin, et al.
International Journal of Molecular Sciences|September 10, 2021
Zebrafish as a Model to Evaluate a CRISPR/Cas9-Based Exon Excision Approach as a Future Treatment Option for <i>EYS</i>-Associated Retinitis PigmentosaRenske Schellens, Erik de Vrieze, Pam Graave, et al.
Pageof 15