Generation of HEXA-deficient hiPSCs from fibroblasts of a Tay

Human iPSC line TSD-01-hiPSC was generated from fibroblasts of a patient with infantile Tay-Sachs disease (TSD). The patient is compound heterozygous …

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iPSCs for modeling lysosomal storage diseases - ScienceDirect

Sandhoff disease cerebral organoids display increased proliferation.

Models to study basic and applied aspects of lysosomal storage disorders - ScienceDirect

Nonviral Cell Labeling and Differentiation Agent for Induced Pluripotent Stem Cells Based on Mesoporous Silica Nanoparticles

The C-Mannosylome of Human Induced Pluripotent Stem Cells Implies a Role for ADAMTS16 C-Mannosylation in Eye Development - ScienceDirect

Novel HEXA variants in Korean children with Tay–Sachs disease with regression of neurodevelopment from infancy - Park - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library

Nanog Antibody [Unconjugated] (AF1997): Novus Biologicals

Identification of mutations in HEXA and HEXB in Sandhoff and Tay-Sachs diseases: a new large deletion caused by Alu elements in HEXA