Yalan Zhou
Paraguay
Last Updated: 09/26/2026
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Found 11 publications
PRPF8 Mutation-Induced Defects in Human iPSC-Derived RPE Are Rescued by Adenine Base Editing.
Journal: Investigative ophthalmology & visual science
Published: January 14, 2026
CRB1 mutations cause structural and molecular defects in patient-derived retinal pigment epithelium cells.
Journal: Experimental eye research
Published: March 26, 2025
Generation of a gene-corrected isogenic human iPSC line (CSUASOi006-A-1) from a retinitis pigmentosa patient with heterozygous c.5792C > T mutation in the PRPF8 gene.
Journal: Stem cell research
Published: January 07, 2024
Generation of a gene-corrected human iPSC line (CSUASOi004-A-1) from a retinitis pigmentosa patient with heterozygous c.2699 G>A mutation in the PRPF6 gene.
Journal: Stem cell research
Published: August 29, 2022
Establishment of a human induced pluripotent stem cell line (CSUASOi010-A) by reprogramming peripheral blood mononuclear cells of a type 2 diabetic mellitus patient.
Journal: Stem cell research
Published: April 19, 2022
Establishment of non-integrate induced pluripotent stem cell line CSUASOi006-A, from urine-derived cells of a PRPF8-related dominant retinitis pigmentosa patient.
Journal: Stem cell research
Published: June 19, 2020
Transcriptomic Analysis of the Developmental Similarities and Differences Between the Native Retina and Retinal Organoids.
Journal: Investigative ophthalmology & visual science
Published: March 10, 2020
Establishment of a human induced pluripotent stem cell line (CSUASOi005-A), from peripheral blood mononuclear cells of a patient with X-linked juvenile retinoschisis carrying a novel mutation in RS1 gene.
Journal: Stem cell research
Published: December 20, 2019
Establishment of induced pluripotent stem cell line CSUASOi004-A by reprogramming peripheral blood mononuclear cells of a PRPF6-related dominant retinitis pigmentosa patient.
Journal: Stem cell research
Published: November 20, 2019
Establishment of induced pluripotent stem cell line CSUASOi003- A from an autosomal recessive retinitis pigmentosa patient carrying compound heterozygous mutations in CRB1 gene.
Journal: Stem cell research
Published: November 09, 2019
Establishment of a non-integrate iPS cell line CSUASOi002-A, from urine-derived cells of a female patient with macular corneal dystrophy carrying compound heterozygous CHST6 mutations.
Journal: Stem cell research
Published: August 15, 2019
Showing 1-11 of 11
Last Updated: 09/26/2026