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 …

Frontiers The Linkage Phase of the Polymorphism KCNH2-K897T Influences the Electrophysiological Phenotype in hiPSC Models of LQT2

IJMS, Free Full-Text

PDF) New Approaches to Tay-Sachs Disease Therapy

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

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

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

Human Nanog Antibody AF1997: R&D Systems

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

The science and engineering of stem cell‐derived organoids‐examples from hepatic, biliary, and pancreatic tissues - Ogoke - 2021 - Biological Reviews - Wiley Online Library

PDF) New Approaches to Tay-Sachs Disease Therapy

Rui Zhao's research works University of Alabama at Birmingham, AL (UAB) and other places

Role of induced pluripotent stem cells in lysosomal storage diseases - ScienceDirect

Frontiers Human Motor Neurons With SOD1-G93A Mutation Generated From CRISPR/Cas9 Gene-Edited iPSCs Develop Pathological Features of Amyotrophic Lateral Sclerosis