Generation of Leber congenital amaurosis, type 12 patient-specific induced pluripotent stem cell line (LVPEIi006-A), harboring a homozygous mutation in RD3-Reference-Cited by-同舟云学术

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Generation of Leber congenital amaurosis, type 12 patient-specific induced pluripotent stem cell line (LVPEIi006-A), harboring a homozygous mutation in RD3

Published:2024-06 Issue: Volume:77 Page:103380
ISSN:1873-5061
Container-title:Stem Cell Research
language:en
Short-container-title:Stem Cell Research

Author:

Mahato Sudipta,Maddileti Savitri,Naik Milind,Kannabiran Chitra,Jalali Subhadra,Mariappan Indumathi

Funder

Science and Engineering Research Board

Department of Biotechnology, Ministry of Science and Technology, India

Department of Science and Technology, Ministry of Science and Technology, India

Indian Council of Medical Research

Publisher

Elsevier BV

Reference6 articles.

1. RD3, the protein associated with leber congenital amaurosis type 12, is required for guanylate cyclase trafficking in photoreceptor cells;Azadi;Proc. Natl. Acad. Sci. USA.,2010

2. Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration;Friedman;Am. J. Hum. Genet.,2006

3. Generation of retinal organoids from healthy and retinal disease-specific human-induced pluripotent stem cells;Mahato;J. Vis. Exp.,2022

4. A more efficient method to generate integration-free human iPS cells;Okita;Nature Methods.,2011

5. Functional study and mapping sites for interaction with the target enzyme in retinal degeneration 3 (RD3) protein;Peshenko;J. Biol. Chem.,2016

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