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Cellular and Molecular Life Sciences : CMLS
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January 13, 2026
Exploring extracellular vesicle MicroRNAs in Usher syndrome type 1B: Tear-Derived EVs as potential indicators of retinal health
Sander 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 adults
Rachel 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 pigmentosa
Muhammad 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 Disease
Ria de Haas, Devashish Das, Alejandro Garanto, et al.
American Journal of Human Genetics
|
April 20, 2010
Mutations in C2ORF71 cause autosomal-recessive retinitis pigmentosa
Rob 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 lead
David 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 Progression
Catherina 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 Equity
Lindsay J Collin, Renjian Jiang, Kevin C Ward, et al.
Ophthalmology
|
February 12, 2011
CLRN1 mutations cause nonsyndromic retinitis pigmentosa
Muhammad 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 families
Muhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, et al.
Page
of 45
Search research articles
Search
Showing results (351-360 of 449) with videos related to
Sort By:
Page
of 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 health
Sander 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 adults
Rachel 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 pigmentosa
Muhammad 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 Disease
Ria de Haas, Devashish Das, Alejandro Garanto, et al.
American Journal of Human Genetics
|
April 20, 2010
Mutations in C2ORF71 cause autosomal-recessive retinitis pigmentosa
Rob 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 lead
David 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 Progression
Catherina 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 Equity
Lindsay J Collin, Renjian Jiang, Kevin C Ward, et al.
Ophthalmology
|
February 12, 2011
CLRN1 mutations cause nonsyndromic retinitis pigmentosa
Muhammad 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 families
Muhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, et al.
Page
of 45