Pages that link to "Q24313262"
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The following pages link to MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion (Q24313262):
Displaying 50 items.
- Mitochondrial inner membrane protein MPV17 (Q21120862) (← links)
- Mapping gene associations in human mitochondria using clinical disease phenotypes (Q21145361) (← links)
- MpV17 mitochondrial inner membrane protein (Q21985797) (← links)
- MPV17L2 is required for ribosome assembly in mitochondria (Q24299607) (← links)
- Identification of Rhit as a novel transcriptional repressor of human Mpv17-like protein with a mitigating effect on mitochondrial dysfunction, and its transcriptional regulation by FOXD3 and GABP (Q24304429) (← links)
- Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease (Q24308200) (← links)
- Mutations in FBXL4, encoding a mitochondrial protein, cause early-onset mitochondrial encephalomyopathy (Q24321305) (← links)
- AAV-mediated liver-specific MPV17 expression restores mtDNA levels and prevents diet-induced liver failure (Q24622009) (← links)
- Mutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenance (Q24625735) (← links)
- Kinetic properties of mutant deoxyguanosine kinase in a case of reversible hepatic mtDNA depletion (Q24675030) (← links)
- Deficiency of the alpha subunit of succinate-coenzyme A ligase causes fatal infantile lactic acidosis with mitochondrial DNA depletion (Q24678341) (← links)
- Navajo neurohepatopathy is caused by a mutation in the MPV17 gene (Q24678502) (← links)
- mitochondrial DNA depletion syndrome 6 (Q26492818) (← links)
- Genes and Pathways Involved in Adult Onset Disorders Featuring Muscle Mitochondrial DNA Instability (Q26801194) (← links)
- Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options (Q26865135) (← links)
- Mitochondrial genome changes and neurodegenerative diseases (Q27023750) (← links)
- The conserved translocase Tim17 prevents mitochondrial DNA loss (Q27931436) (← links)
- Assessing systems properties of yeast mitochondria through an interaction map of the organelle (Q27937134) (← links)
- The channel-forming Sym1 protein is transported by the TIM23 complex in a presequence-independent manner (Q27938469) (← links)
- Biochemical diagnosis of mitochondrial disorders (Q27990527) (← links)
- Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion (Q28301052) (← links)
- Thymidine kinase 2 (H126N) knockin mice show the essential role of balanced deoxynucleotide pools for mitochondrial DNA maintenance. (Q28504546) (← links)
- The peroxisome: still a mysterious organelle (Q28754736) (← links)
- A mutation in the gene encoding mitochondrial Mg²+ channel MRS2 results in demyelination in the rat. (Q29347166) (← links)
- Pxmp2 is a channel-forming protein in Mammalian peroxisomal membrane (Q29871130) (← links)
- MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: new patients and novel mutations. (Q30384428) (← links)
- Adult-onset leukodystrophies from respiratory chain disorders: do they exist? (Q30586606) (← links)
- Brain imaging in mitochondrial respiratory chain deficiency: combination of brain MRI features as a useful tool for genotype/phenotype correlations. (Q30813761) (← links)
- A novel transcriptional repressor, Rhit, is involved in heat-inducible and age-dependent expression of Mpv17-like protein, a participant in reactive oxygen species metabolism (Q31813066) (← links)
- Clinical and molecular features of mitochondrial DNA depletion syndromes. (Q33397750) (← links)
- Mitochondrial mosaics in the liver of 3 infants with mtDNA defects (Q33461789) (← links)
- Next generation sequencing with copy number variant detection expands the phenotypic spectrum of HSD17B4-deficiency (Q33587248) (← links)
- The in-depth evaluation of suspected mitochondrial disease (Q33608204) (← links)
- Inhibition of ATPIF1 ameliorates severe mitochondrial respiratory chain dysfunction in mammalian cells. (Q33696265) (← links)
- Mpv17 in mitochondria protects podocytes against mitochondrial dysfunction and apoptosis in vivo and in vitro (Q33701530) (← links)
- A critical analysis of the combined usage of protein localization prediction methods: Increasing the number of independent data sets can reduce the accuracy of predicted mitochondrial localization (Q33783130) (← links)
- Encephalomyopathies caused by abnormal nuclear-mitochondrial intergenomic cross-talk (Q33810387) (← links)
- Mitochondrial disorders of the nuclear genome (Q33810406) (← links)
- The role of mitochondrial DNA copy number in mammalian fertility. (Q33926626) (← links)
- Adult-Onset Fatal Neurohepatopathy in a Woman Caused by MPV17 Mutation (Q33947292) (← links)
- Deoxypyrimidine monophosphate bypass therapy for thymidine kinase 2 deficiency. (Q34131169) (← links)
- Prkdc participates in mitochondrial genome maintenance and prevents Adriamycin-induced nephropathy in mice. (Q34145974) (← links)
- Leukoencephalopathies in mitochondrial disorders: clinical and MRI findings. (Q34150287) (← links)
- Modifier genes and the plasticity of genetic networks in mice (Q34236664) (← links)
- MPV17 mutation causes neuropathy and leukoencephalopathy with multiple mtDNA deletions in muscle. (Q34268558) (← links)
- Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene (Q34347182) (← links)
- The myriad essential roles of microRNAs in cardiovascular homeostasis and disease (Q34356918) (← links)
- Mitochondrial depletion syndromes in children and adults (Q34365934) (← links)
- Individual exome analysis in diagnosis and management of paediatric liver failure of indeterminate aetiology (Q34373758) (← links)
- Onset and organ specificity of Tk2 deficiency depends on Tk1 down-regulation and transcriptional compensation (Q34399422) (← links)