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MPV17
Ejhg2013112.Pdf
MPV17-Related Hepatocerebral Mitochondrial DNA Depletion Syndrome
Clinical and Molecular Basis of Hepatocerebral Mitochondrial DNA
Clinical and Molecular Characterization of Three Patients
MPV17 Gene Mitochondrial Inner Membrane Protein MPV17
A Functional Enrichment Test for Molecular Convergent Evolution Finds a Clear Protein-Coding Signal in Echolocating Bats and Whales
Prkdc Participates in Mitochondrial Genome Maintenance and Prevents Adriamycin-Induced Nephropathy in Mice
A Monoclonal Antibody Raised Against Bacterially Expressed MPV17
The Zebrafish Orthologue of the Human Hepatocerebral Disease
Opa1 Overexpression Protects from Early Onset Mpv17-/--Related Mouse Kidney Disease
MPV17-Associated Hepatocerebral Mitochondrial DNA Depletion Syndrome: New Patients and Novel Mutations
REPORT Navajo Neurohepatopathy Is Caused by a Mutation in the MPV17 Gene
Quantitative Trait Loci Mapping of Macrophage Atherogenic Phenotypes
Imbalanced Mitochondrial Function Provokes Heterotaxy Via Aberrant Ciliogenesis
Analyzing the Mirna-Gene Networks to Mine the Important Mirnas Under Skin of Human and Mouse
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Signatures of Adaptive Evolution in Platyrrhine Primate Genomes 5 6 Hazel Byrne*, Timothy H
MPV17 Loss Causes Deoxynucleotide Insufficiency and Slow DNA Replication in Mitochondria
Top View
Navajo Neurohepatopathy : a Case Report and Literature Review Emphasizing Clinicopathologic Diagnosis
Detection of Uniparental Isodisomy in Autosomal Recessive Mitochondrial DNA Depletion Syndrome by High-Density SNP Array Analysis
This Report Contains Confidential Information That Should Not Be Placed in the Public Domain Until the Work Has Been Accepted for Publication
Peripheral Neuropathy in Mitochondrial Disorders
Blueprint Genetics Mitochondrial DNA Depletion Syndrome Panel
Platform Abstracts
FGF21 Is a Biomarker for Mitochondrial Translation and Mtdna Maintenance Disorders
MPV17-Related Mitochondrial DNA Maintenance Defect: New Cases and Review of Clinical, Biochemical, and Molecular Aspects
First Cases of MPV17 Related Mitochondrial DNA Depletion Syndrome with Compound Heterozygous Mutations in P.R50Q/P.R50W: a Case Report
Therapeutic Approaches to Treat Mitochondrial Diseases: “One-Size-Fits-All” and “Precision Medicine” Strategies
MPV17-Related Mitochondrial DNA Maintenance Defect: New Cases and Review of Clinical, Biochemical, and Molecular Aspects
Therapeutical Management and Drug Safety in Mitochondrial Diseases—Update 2020
Drp1 Regulates Mitochondrial Dysfunction And
MPV17 Encodes an Inner Mitochondrial Membrane Protein and Is Mutated in Infantile Hepatic Mitochondrial DNA Depletion
The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
Integrated Computational Analysis of Genes Associated with Human Hereditary Insensitivity to Pain
MPV17 Sirna (H): Sc-94662
MPV17 Mutations Causing Adult-Onset Multisystemic Disorder with Multiple Mitochondrial DNA Deletions