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 …
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Models to study basic and applied aspects of lysosomal storage disorders - ScienceDirect
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Human Nanog Antibody AF1997: R&D Systems
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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
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Hexosaminidase a deficiency hi-res stock photography and images - Alamy
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Adult mouse fibroblasts retain organ-specific transcriptomic identity
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Frontiers Therapeutic Strategies For Tay-Sachs Disease
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Frontiers The Linkage Phase of the Polymorphism KCNH2-K897T Influences the Electrophysiological Phenotype in hiPSC Models of LQT2
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46 Beta Hexosaminidase Royalty-Free Images, Stock Photos & Pictures
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Human Nanog Antibody AF1997: R&D Systems
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Tay-Sachs Disease - The Medical Biochemistry Page
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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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Tay-Sachs disease, illustration - Stock Image - F034/4334 - Science Photo Library
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