Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J Collin

Showing results (321-330 of 449) with videos related to

Pageof 45
Sort By:
American Journal of Ophthalmology|July 27, 2025
The Visual Acuity Course in Stargardt DiseaseJeroen A A H Pas, Dyon Valkenburg, Catherina H Z Li, et al.
Investigative Ophthalmology & Visual Science|February 26, 2020
Modeling ZNF408-Associated FEVR in Zebrafish Results in Abnormal Retinal VasculatureDyah W Karjosukarso, Zaheer Ali, Theo A Peters, et al.
Molecular Vision|December 24, 2010
Missense mutations at homologous positions in the fourth and fifth laminin A G-like domains of eyes shut homolog cause autosomal recessive retinitis pigmentosaMuhammad Imran Khan, Rob W J Collin, Kentar Arimadyo, et al.
American Journal of Epidemiology|January 13, 2025
A registry-based approach for estimating county-level race disparities in breast cancer mortality: an analysis in GeorgiaRebecca Nash, Jeffrey M Switchenko, Kevin C Ward, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 3, 2020
Neighborhood-Level Redlining and Lending Bias Are Associated with Breast Cancer Mortality in a Large and Diverse Metropolitan AreaLindsay J Collin, Anne H Gaglioti, Kristen M Beyer, et al.
European Journal of Human Genetics : EJHG|December 3, 2015
Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in DenmarkGaluh D N Astuti, Mette Bertelsen, Markus N Preising, et al.
Investigative Ophthalmology & Visual Science|April 28, 2025
Progression of Atrophy as a Function of ABCA4 Variants and Age of Onset in Stargardt DiseaseJeroen A A H Pas, Catherina H Z Li, Filip Van den Broeck, et al.
Molecular Therapy. Nucleic Acids|March 13, 2023
Antisense oligonucleotide therapy corrects splicing in the common Stargardt disease type 1-causing variant <i>ABCA4</i> c.5461-10T>CMelita Kaltak, Petra de Bruijn, Davide Piccolo, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|August 16, 2021
Receipt of Guideline-Concordant Care Does Not Explain Breast Cancer Mortality Disparities by Race in Metropolitan AtlantaLindsay J Collin, Ming Yan, Renjian Jiang, et al.
Audiology & Neuro-Otology|January 22, 2011
Progressive sensorineural hearing loss and normal vestibular function in a Dutch DFNB7/11 family with a novel mutation in TMC1Anne-Martine R de Heer, Rob W J Collin, Patrick L M Huygen, et al.
Pageof 45

Showing results (321-330 of 449) with videos related to

Sort By:
Pageof 45
American Journal of Ophthalmology|July 27, 2025
The Visual Acuity Course in Stargardt DiseaseJeroen A A H Pas, Dyon Valkenburg, Catherina H Z Li, et al.
Investigative Ophthalmology & Visual Science|February 26, 2020
Modeling ZNF408-Associated FEVR in Zebrafish Results in Abnormal Retinal VasculatureDyah W Karjosukarso, Zaheer Ali, Theo A Peters, et al.
Molecular Vision|December 24, 2010
Missense mutations at homologous positions in the fourth and fifth laminin A G-like domains of eyes shut homolog cause autosomal recessive retinitis pigmentosaMuhammad Imran Khan, Rob W J Collin, Kentar Arimadyo, et al.
American Journal of Epidemiology|January 13, 2025
A registry-based approach for estimating county-level race disparities in breast cancer mortality: an analysis in GeorgiaRebecca Nash, Jeffrey M Switchenko, Kevin C Ward, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 3, 2020
Neighborhood-Level Redlining and Lending Bias Are Associated with Breast Cancer Mortality in a Large and Diverse Metropolitan AreaLindsay J Collin, Anne H Gaglioti, Kristen M Beyer, et al.
European Journal of Human Genetics : EJHG|December 3, 2015
Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in DenmarkGaluh D N Astuti, Mette Bertelsen, Markus N Preising, et al.
Investigative Ophthalmology & Visual Science|April 28, 2025
Progression of Atrophy as a Function of ABCA4 Variants and Age of Onset in Stargardt DiseaseJeroen A A H Pas, Catherina H Z Li, Filip Van den Broeck, et al.
Molecular Therapy. Nucleic Acids|March 13, 2023
Antisense oligonucleotide therapy corrects splicing in the common Stargardt disease type 1-causing variant <i>ABCA4</i> c.5461-10T>CMelita Kaltak, Petra de Bruijn, Davide Piccolo, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|August 16, 2021
Receipt of Guideline-Concordant Care Does Not Explain Breast Cancer Mortality Disparities by Race in Metropolitan AtlantaLindsay J Collin, Ming Yan, Renjian Jiang, et al.
Audiology & Neuro-Otology|January 22, 2011
Progressive sensorineural hearing loss and normal vestibular function in a Dutch DFNB7/11 family with a novel mutation in TMC1Anne-Martine R de Heer, Rob W J Collin, Patrick L M Huygen, et al.
Pageof 45