Generation of HEXA-deficient hiPSCs from fibroblasts of a Tay
Por um escritor misterioso
Last updated 22 outubro 2024
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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PDF) New Approaches to Tay-Sachs Disease Therapy
Frontiers New Approaches to Tay-Sachs Disease Therapy
Dynamic Pluripotent Stem Cell States and Their Applications - 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
Delineating the Neuropathology of Lysosomal Storage Diseases Using Patient-Derived Induced Pluripotent Stem Cells
Models to study basic and applied aspects of lysosomal storage disorders - ScienceDirect
Illustration of Tay-Sachs disease, a genetic disorder that progressively destroys brain neurons. It is caused by a mutation in the HEXA gene of chromo Stock Photo - Alamy
PDF) New Approaches to Tay-Sachs Disease Therapy
Adult mouse fibroblasts retain organ-specific transcriptomic identity
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