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 …

PDF) Generation of HEXA-deficient hiPSCs from fibroblasts of a Tay-Sachs disease patient

Engineering of Human-Induced Pluripotent Stem Cells for Precise Disease Modeling

Hexosaminidase a deficiency hi-res stock photography and images - Alamy

Myelination and Node of Ranvier Formation in a Human Motoneuron–Schwann Cell Serum-Free Coculture

PDF) Generation of HEXA-deficient hiPSCs from fibroblasts of a Tay-Sachs disease patient

Presynaptic Dysfunction in Neurons Derived from Tay–Sachs iPSCs - 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

PDF) New Approaches to Tay-Sachs Disease Therapy

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

iPSCs for modeling lysosomal storage diseases - ScienceDirect

Presynaptic Dysfunction in Neurons Derived from Tay–Sachs iPSCs - ScienceDirect

Human Induced Pluripotent Stem Cells as a Platform for Personalized and Precision Cardiovascular Medicine

FOXP1 protein (human) - STRING interaction network

Adult mouse fibroblasts retain organ-specific transcriptomic identity