Generation of HEXA-deficient hiPSCs from fibroblasts of a Tay
Por um escritor misterioso
Descrição
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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Adult mouse fibroblasts retain organ-specific transcriptomic identity
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
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Intranasal Delivery of CRISPR-Cas9 Edited HEXA Gene to Treat Tay Sachs Disease in Newborn HEXA/NEU3-Deficient Mice — Le Pouls
Role of induced pluripotent stem cells in lysosomal storage diseases - ScienceDirect
Generation of HEXA-deficient hiPSCs from fibroblasts of a Tay-Sachs disease patient - ScienceDirect
Nanog Antibody [Unconjugated] (AF1997): Novus Biologicals
Presynaptic Dysfunction in Neurons Derived from Tay–Sachs iPSCs - ScienceDirect
Sandhoff disease cerebral organoids display increased proliferation.
Chemical mutagenesis of a GPCR ligand: Detoxifying “inflammo-attraction” to direct therapeutic stem cell migration
Generation of HEXA-deficient hiPSCs from fibroblasts of a Tay-Sachs disease patient - ScienceDirect
Rui Zhao's research works University of Alabama at Birmingham, AL (UAB) and other places
Generation and characterization of patient-specific induced pluripotent
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