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Cellular and Molecular Life Sciences : CMLS|April 13, 2019
Mechanisms of neurodegeneration in a preclinical autosomal dominant retinitis pigmentosa knock-in model with a RhoD190N mutationJavier Sancho-Pelluz, Xuan Cui, Winston Lee, et al.
EMBO Molecular Medicine|January 16, 2023
HIF2α activation and mitochondrial deficit due to iron chelation cause retinal atrophyYang Kong, Pei-Kang Liu, Yao Li, et al.
The Journal of Clinical Investigation|November 15, 2016
Reprogramming metabolism by targeting sirtuin 6 attenuates retinal degenerationLijuan Zhang, Jianhai Du, Sally Justus, et al.
Child Abuse & Neglect|March 11, 2017
Risk factors for child physical abuse and neglect among Chinese young mothersCamilla K M Lo, Keith T S Tung, Ko Ling Chan, et al.
Cell Stem Cell|September 7, 2019
Distinct Imprinting Signatures and Biased Differentiation of Human Androgenetic and Parthenogenetic Embryonic Stem CellsIdo Sagi, Joao C De Pinho, Michael V Zuccaro, et al.
Human Molecular Genetics|February 23, 2022
Long-term vitamin A supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosaXuan Cui, Hye Jin Kim, Chia-Hua Cheng, et al.
Investigative Ophthalmology & Visual Science|June 5, 2012
Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 geneTomas R Burke, Gerald A Fishman, Jana Zernant, et al.
Investigative Ophthalmology & Visual Science|May 7, 2016
Calpain-5 Expression in the Retina Localizes to Photoreceptor SynapsesKellie A Schaefer, Marcus A Toral, Gabriel Velez, et al.
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