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Proceedings of the National Academy of Sciences of the United States of America|May 26, 2004
Gene knockout of glycine transporter 1: characterization of the behavioral phenotypeGuochuan Tsai, Rebecca J Ralph-Williams, Marzia Martina, et al.
Translational Vision Science & Technology|March 29, 2022
Assessing Variant Causality and Severity Using Retinal Pigment Epithelial Cells Derived from Stargardt Disease PatientsAnna Matynia, Jun Wang, Sangbae Kim, et al.
Synapse (New York, N.Y.)|April 7, 2009
Phenotypic characterization of mice heterozygous for a null mutation of glutamate carboxypeptidase IILiqun Han, Jonathan D Picker, Laura R Schaevitz, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 16, 2021
Lipofuscin causes atypical necroptosis through lysosomal membrane permeabilizationChendong Pan, Kalpita Banerjee, Guillermo L Lehmann, et al.
Theranostics|March 15, 2019
Abnormal mTORC1 signaling leads to retinal pigment epithelium degenerationJiancheng Huang, Shun Gu, Meng Chen, et al.
Investigative Ophthalmology & Visual Science|January 1, 2016
Monoallelic ABCA4 Mutations Appear Insufficient to Cause Retinopathy: A Quantitative Autofluorescence StudyPhilipp L Müller, Martin Gliem, Elisabeth Mangold, et al.
Nature Communications|July 23, 2024
Mutant mice with rod-specific VPS35 deletion exhibit retinal α-synuclein pathology-associated degenerationCheng Fu, Nan Yang, Jen-Zen Chuang, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 8, 2014
Beta cyclodextrins bind, stabilize, and remove lipofuscin bisretinoids from retinal pigment epitheliumMarcelo M Nociari, Guillermo L Lehmann, Andres E Perez Bay, et al.
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