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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.
Breast Cancer Research : BCR|November 5, 2021
Hypoxia-inducible factor-1α expression and breast cancer recurrence in a Danish population-based case control studyLindsay J Collin, Maret L Maliniak, Deirdre P Cronin-Fenton, et al.
Orphanet Journal of Rare Diseases|January 30, 2013
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophyIvana Peluso, Ivan Conte, Francesco Testa, et al.
Ophthalmology Science|June 19, 2023
Evaluation of Sleep Quality and Fatigue in Patients with Usher Syndrome Type 2aJessie M Hendricks, Juriaan R Metz, Hedwig M Velde, et al.
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