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J Collin

Showing results (351-360 of 449) 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.
Research Square|September 11, 2024
Associations of demographic, health, and risk-taking behaviors with tattooing in a population-based cross-sectional study of ~18,000 US adultsRachel D McCarty, Britton Trabert, Morgan M Millar, 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.
Bioorganic & Medicinal Chemistry Letters|September 27, 2008
Discovery of small molecule agonists for the bombesin receptor subtype 3 (BRS-3) based on an omeprazole leadDavid L Carlton, Lissa J Collin-Smith, Alejandro J Daniels, 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.
JNCI Cancer Spectrum|April 25, 2020
Racial Disparities in Breast Cancer Outcomes in the Metropolitan Atlanta Area: New Insights and Approaches for Health EquityLindsay J Collin, Renjian Jiang, Kevin C Ward, 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.
Pageof 45

Showing results (351-360 of 449) with videos related to

Sort By:
Pageof 45
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.
Research Square|September 11, 2024
Associations of demographic, health, and risk-taking behaviors with tattooing in a population-based cross-sectional study of ~18,000 US adultsRachel D McCarty, Britton Trabert, Morgan M Millar, 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.
Bioorganic & Medicinal Chemistry Letters|September 27, 2008
Discovery of small molecule agonists for the bombesin receptor subtype 3 (BRS-3) based on an omeprazole leadDavid L Carlton, Lissa J Collin-Smith, Alejandro J Daniels, 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.
JNCI Cancer Spectrum|April 25, 2020
Racial Disparities in Breast Cancer Outcomes in the Metropolitan Atlanta Area: New Insights and Approaches for Health EquityLindsay J Collin, Renjian Jiang, Kevin C Ward, 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.
Pageof 45