Generation of induced pluripotent stem cells from a patient with X-linked juvenile retinoschisis
Author:
Funder
Ministry of Science and Technology
MOST
National Chiao Tung University
Academia Sinica
MOHW
NHRI
TVGH
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,General Medicine
Reference3 articles.
1. X-linked juvenile retinoschisis: clinical diagnosis, genetic analysis, and molecular mechanisms;Molday;Prog. Retin. Eye Res.,2012
2. Molecular modeling of retinoschisin with functional analysis of pathogenic mutations from human X-linked retinoschisis;Sergeev;Hum. Mol. Genet.,2010
3. Molecular mechanisms leading to null-protein product from retinoschisin (RS1) signal-sequence mutants in X-linked retinoschisis (XLRS) disease;Vijayasarathy;Hum. Mutat.,2010
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1. Application of patient-derived induced pluripotent stem cells and organoids in inherited retinal diseases;Stem Cell Research & Therapy;2023-11-27
2. Recognizing the Differentiation Degree of Human Induced Pluripotent Stem Cell-Derived Retinal Pigment Epithelium Cells Using Machine Learning and Deep Learning-Based Approaches;Cells;2023-01-04
3. Morphological and Molecular Defects in Human Three-Dimensional Retinal Organoid Model of X-Linked Juvenile Retinoschisis;Stem Cell Reports;2019-11
4. Human iPSC banking: barriers and opportunities;Journal of Biomedical Science;2019-10-28
5. Corrigendum to “Generation of induced pluripotent stem cells from a patient with X-linked juvenile retinoschisis” [Stem Cell Res. 29(2018): 152–156];Stem Cell Research;2019-01
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