Search research articles
Contact Us
Filters
Showing results (41-50 of 149) with videos related to
Page
of 15
Sort By:
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 ACTG1
Anne-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 retina
Irene 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 phenotype
Qin 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 1
Jeroen 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 dystrophies
Ralph 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 vasculature
Dyah 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>A
Nuria 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 POU4F3
F 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 POU4F3
Robert 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 Pigmentosa
Renske Schellens, Erik de Vrieze, Pam Graave, et al.
Page
of 15
Search research articles
Search
Showing results (41-50 of 149) with videos related to
Sort By:
Page
of 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 ACTG1
Anne-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 retina
Irene 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 phenotype
Qin 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 1
Jeroen 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 dystrophies
Ralph 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 vasculature
Dyah 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>A
Nuria 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 POU4F3
F 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 POU4F3
Robert 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 Pigmentosa
Renske Schellens, Erik de Vrieze, Pam Graave, et al.
Page
of 15