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J Collin

Showing results (281-290 of 449) with videos related to

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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.
Cancer|July 22, 2022
Drivers of racial, regional, and socioeconomic disparities in late-stage breast cancer mortalityLeah Moubadder, Lindsay J Collin, Rebecca Nash, 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.
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.
Audiology & Neuro-Otology|November 14, 2008
Flat threshold and mid-frequency hearing impairment in a Dutch DFNA8/12 family with a novel mutation in TECTA. Some evidence for protection of the inner earA R de Heer, R J Pauw, P L M Huygen, et al.
Epidemiology (Cambridge, Mass.)|June 3, 2020
Adaptive Validation Design: A Bayesian Approach to Validation Substudy Design With Prospective Data CollectionLindsay J Collin, Richard F MacLehose, Thomas P Ahern, 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.
Annals of Surgery|October 1, 1984
Removal of gastrinomas for control of Zollinger-Ellison syndromeJ W Harmon, J A Norton, M J Collin, et al.
American Journal of Medical Genetics. Part A|July 13, 2006
Identification of a novel COCH mutation, G87W, causing autosomal dominant hearing impairment (DFNA9)Rob W J Collin, Robert J Pauw, Jeroen Schoots, 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.
Pageof 45

Showing results (281-290 of 449) with videos related to

Sort By:
Pageof 45
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.
Cancer|July 22, 2022
Drivers of racial, regional, and socioeconomic disparities in late-stage breast cancer mortalityLeah Moubadder, Lindsay J Collin, Rebecca Nash, 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.
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.
Audiology & Neuro-Otology|November 14, 2008
Flat threshold and mid-frequency hearing impairment in a Dutch DFNA8/12 family with a novel mutation in TECTA. Some evidence for protection of the inner earA R de Heer, R J Pauw, P L M Huygen, et al.
Epidemiology (Cambridge, Mass.)|June 3, 2020
Adaptive Validation Design: A Bayesian Approach to Validation Substudy Design With Prospective Data CollectionLindsay J Collin, Richard F MacLehose, Thomas P Ahern, 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.
Annals of Surgery|October 1, 1984
Removal of gastrinomas for control of Zollinger-Ellison syndromeJ W Harmon, J A Norton, M J Collin, et al.
American Journal of Medical Genetics. Part A|July 13, 2006
Identification of a novel COCH mutation, G87W, causing autosomal dominant hearing impairment (DFNA9)Rob W J Collin, Robert J Pauw, Jeroen Schoots, 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.
Pageof 45