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Nucleic Acids Research|August 6, 2024
The characteristics of CTCF binding sequences contribute to enhancer blocking activityFelice H Tsang, Rosa J Stolper, Muhammad Hanifi, et al.
Human Mutation|August 13, 2019
CAPN5 genetic inactivation phenotype supports therapeutic inhibition trialsKatherine J Wert, Susanne F Koch, Gabriel Velez, et al.
Retina (Philadelphia, Pa.)|July 9, 2009
Structural assessment of hyperautofluorescent ring in patients with retinitis pigmentosaLuiz H Lima, Wener Cella, Vivienne C Greenstein, et al.
Scientific Reports|July 26, 2019
Multimodal structural disease progression of retinitis pigmentosa according to mode of inheritanceRuben Jauregui, Vitor K L Takahashi, Karen Sophia Park, et al.
Translational Vision Science & Technology|October 2, 2018
Personalized Proteomics for Precision Health: Identifying Biomarkers of Vitreoretinal DiseaseGabriel Velez, Peter H Tang, Thiago Cabral, et al.
Regenerative Medicine|January 24, 2018
Autologous stem cell therapy for inherited and acquired retinal diseaseMary Ben L Apatoff, Jesse D Sengillo, Eugenia C White, et al.
Scientific Reports|August 29, 2022
Foveolar thickness as potential standardized structural outcome measurement in studies of Bietti crystalline dystrophyLaura A Jenny, Pei-Kang Liu, Masha Kolesnikova, et al.
Ophthalmic Surgery, Lasers & Imaging Retina|August 29, 2023
Venous Tortuosity in <i>COL4A2</i>-Associated Gould SyndromeJin Kyun Oh, Sarah R Levi, Jose Ronaldo Lima de Carvalho, et al.
Advances in Experimental Medicine and Biology|July 13, 2023
Prime Editing Strategy to Install the PRPH2 c.828+1G>A MutationSalvatore Marco Caruso, Yi-Ting Tsai, Bruna Lopes da Costa, et al.
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