Generation of HEXA-deficient hiPSCs from fibroblasts of a Tay
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 …
Models to study basic and applied aspects of lysosomal storage disorders - ScienceDirect
Human Nanog Antibody AF1997: R&D Systems
Cells, Free Full-Text
Novel bicistronic lentiviral vectors correct β-Hexosaminidase deficiency in neural and hematopoietic stem cells and progeny: implications for in vivo and ex vivo gene therapy of GM2 gangliosidosis - ScienceDirect
Hexosaminidase a deficiency hi-res stock photography and images - Alamy
Cells, Free Full-Text
IJMS, Free Full-Text
Adult mouse fibroblasts retain organ-specific transcriptomic identity
Frontiers Therapeutic Strategies For Tay-Sachs Disease
Frontiers The Linkage Phase of the Polymorphism KCNH2-K897T Influences the Electrophysiological Phenotype in hiPSC Models of LQT2
46 Beta Hexosaminidase Royalty-Free Images, Stock Photos & Pictures
Human Nanog Antibody AF1997: R&D Systems
Tay-Sachs Disease - The Medical Biochemistry Page
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
Tay-Sachs disease, illustration - Stock Image - F034/4334 - Science Photo Library
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