Indumathi Mariappan
Bellary Road
Bengaluru, KA 560065, India
Bengaluru, KA 560065, India
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 33 publications
Charting the translational pathway: ISSCR best practices for the development of PSC-derived therapies.
Journal: Stem cell reports
Published: November 26, 2025
Charting the translational pathway: ISSCR best practices for the development of PSC-derived therapies.
Journal: Stem cell reports
Published: November 26, 2025
Creating a roadmap to fast-track human-centric non-animal methodologies via innovative funding mechanisms and strategic partnerships.
Journal: ALTEX
Published: September 01, 2025
Host-membrane lipid composition controls Cryptococcus neoformans cellular targets.
Journal: Frontiers in immunology
Published: August 16, 2025
Loss of retinal stem cell reserve and lipofuscin accumulation accelerates cone-rod degeneration and replicates Stargardt disease in abca4b null zebrafish.
Journal: Scientific reports
Published: August 11, 2025
Generation and validation of a Leber Congenital Amaurosis, Type 12 patient-specific iPSC line (LVPEIi006-B) with a splice-site mutation in RD3 and an isogenic mutation-corrected iPSC line (LVPEIi006-B-1).
Journal: Stem cell research
Published: March 01, 2025
PAM-flexible Engineered FnCas9 variants for robust and ultra-precise genome editing and diagnostics.
PAM-flexible Engineered FnCas9 variants for robust and ultra-precise genome editing and diagnostics.
Journal: Nature communications
Published: April 03, 2024
Generation and characterization of a Stargardt's disease-specific induced pluripotent stem cell line (LVPEIi008-A) with a homozygous nonsense mutation in exon 44 of ABCA4.
Journal: Stem cell research
Published: March 25, 2024
Generation of two induced pluripotent stem cell lines (LVPEIi007-B, LVPEIi008-B) from patients harboring homozygous mutation in ABCA4 (c.6088C>T) using non-integrative Sendai virus-based approach.
Journal: Stem cell research
Published: February 01, 2024
Generation of Leber congenital amaurosis, type 12 patient-specific induced pluripotent stem cell line (LVPEIi006-A), harboring a homozygous mutation in RD3.
Journal: Stem cell research
Published: January 29, 2024
Generation of two induced pluripotent stem cell lines (LVPEIi004-A and LVPEIi005-A) from probands with Leber Congenital Amaurosis 2 (LCA2) and harboring mutations in RPE65.
Journal: Stem cell research
Published: January 29, 2024
Last Updated: 09/26/2026