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European Journal of Human Genetics : EJHG|February 20, 2024
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, et al.Stem Cell Research|July 2, 2026
Establishment and characterization of three human pluripotent stem cell lines from patients with spinocerebellar ataxia 27B (SCA27B)David Pellerin, Adriana Rebelo, Mohammad Faraz Zafeer, et al.JCI Insight|June 18, 2026
Distal enhancer-insulator module of GDF6 is essential for cochlear formationMohammad Faraz Zafeer, Clemer Abad, Havva Ortabozkoyun, et al.Journal of Medical Genetics|March 19, 2026
CDK4 and CDK6 variants in patients with primary microcephaly lead to cell cycle defects and mitochondria-induced apoptosisEsra Isik, Mohammad Faraz Zafeer, Guney Bademci, et al.Human Genomics|November 23, 2023
Dispersed DNA variants underlie hearing loss in South Florida's minority populationLéShon Peart, Joanna Gonzalez, Dayna Morel Swols, et al.Stem Cell Research|June 29, 2026
Establishment and characterization of two human pluripotent stem cell lines from patients with ATX-FGF14/spinocerebellar ataxia 27A (SCA27A)David Pellerin, Adriana Rebelo, Mohammad Faraz Zafeer, et al.Proceedings of the National Academy of Sciences of the United States of America|June 21, 2022
Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and miceGuney Bademci, María Lachgar-Ruiz, Mangesh Deokar, et al.The Journal of Clinical Investigation|September 30, 2025
Carboxypeptidase D deficiency causes hearing loss amenable to treatmentMemoona Ramzan, Natalie Ortiz-Vega, Mohammad Faraz Zafeer, et al.Pageof 2