CRISPR-Cas9 correction of OPA1 c.1334G>A: p.R445H restores mitochondrial homeostasis in dominant optic atrophy patient-derived iPSCs: Molecular Therapy - Nucleic Acids
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Descrição
CRISPR-AsCas12a Efficiently Corrects a GPR143 Intronic Mutation in
Enhanced genome editing in human iPSCs with CRISPR-CAS9 by co
Characterisation of a novel OPA1 splice variant resulting in
IJMS, Free Full-Text
Metabolic rescue ameliorates mitochondrial encephalo
Functional genomics and the future of iPSCs in disease modeling
PDF) Modelling autosomal dominant optic atrophy associated with
CRISPR/Cas9-mediated A4GALT suppression rescues Fabry disease
Retinal Ganglion Cells in a Dish: Current Strategies and
OPA1 Mutation and Late‐Onset Cardiomyopathy: Mitochondrial
Retinal Ganglion Cells in a Dish: Current Strategies and
OPA1 regulation of mitochondrial dynamics in skeletal and cardiac
OPA1 Mutation and Late‐Onset Cardiomyopathy: Mitochondrial
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