Gene Expression Analyses Identify Narp Contribution in the Development of l-DOPA-Induced Dyskinesia | Journal of Neuroscience
NARP - Neurogenic Weakness, Ataxia and Retinitis Pigmentosa - The Charlie Gard Foundation | Because Mito Matters
Neuropathy, Ataxia and Retinitis Pigmentosa (NARP Syndrome)
Frontiers | Non-Cell-Autonomous Factors Implicated in Parvalbumin Interneuron Maturation and Critical Periods
Gene Expression Analyses Identify Narp Contribution in the Development of l-DOPA-Induced Dyskinesia | Journal of Neuroscience
Sustained Increase in Narp Protein Expression Following Repeated Electroconvulsive Seizure | Neuropsychopharmacology
A schematic of the novel strategy for gene therapy of NARP disease... | Download Scientific Diagram
RegulonDB
Neuropathy, ataxia, and retinitis pigmentosa - Wikipedia
Progress and prospects: gene therapy for mitochondrial DNA disease | Gene Therapy
Narp and NP1 Form Heterocomplexes that Function in Developmental and Activity-Dependent Synaptic Plasticity
Neuropathy, ataxia, and retinitis pigmentosa: MedlinePlus Genetics
Definition of a Bidirectional Activity-Dependent Pathway Involving BDNF and Narp - ScienceDirect
Frontiers | The Role of Neuronal Pentraxin 2 (NP2) in Regulating Glutamatergic Signaling and Neuropathology
The neurology of mitochondrial DNA disease - The Lancet Neurology
Neuropathy, ataxia, and retinitis pigmentosa: MedlinePlus Genetics
Strategy for targeting the m.8993T>G NARP mutation using mtZFN and... | Download Scientific Diagram
div id="textblankwhite"><p>Engineering Success</p></div> | CUHKSZ - iGEM 2022
Novel Pathogenic Sequence Variation m.5789T>C Causes NARP Syndrome and Promotes Formation of Deletions of the Mitochondrial Genome | Neurology Genetics
Frontiers | Mitochondrial Medicine: Genetic Underpinnings and Disease Modeling Using Induced Pluripotent Stem Cell Technology
Structural basis for the pathogenesis of NARP/MILS due to mutations at... | Download Scientific Diagram
Part:BBa K3411020 - parts.igem.org
Neuropathy, Ataxia, and Retinitis Pigmentosa | Hereditary Ocular Diseases
Pentraxin - an overview | ScienceDirect Topics
Neuropathy, ataxia, and retinitis pigmentosa: MedlinePlus Genetics
A 2 bp deletion in the mitochondrial ATP 6 gene responsible for the NARP (neuropathy, ataxia, and retinitis pigmentosa) syndrome - ScienceDirect
Solved NARP syndrome is a genetic disease characterized by | Chegg.com
Part:BBa K3411020 - parts.igem.org
A schematic of the novel strategy for gene therapy of NARP disease... | Download Scientific Diagram