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

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

Frontiers New Approaches to Tay-Sachs Disease Therapy

Delineating the Neuropathology of Lysosomal Storage Diseases Using Patient-Derived Induced Pluripotent Stem Cells

Sandhoff disease cerebral organoids display increased proliferation.

Adult mouse fibroblasts retain organ-specific transcriptomic identity

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

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

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

Frontiers Therapeutic Strategies For Tay-Sachs Disease

Chemical mutagenesis of a GPCR ligand: Detoxifying “inflammo-attraction” to direct therapeutic stem cell migration

Generation and characterization of patient-specific induced pluripotent

Delineating the Neuropathology of Lysosomal Storage Diseases Using Patient-Derived Induced Pluripotent Stem Cells