A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle
about
Mitochondrial DNA mutations in human diseaseMitochondrial geneticsMitochondrial genome changes and neurodegenerative diseasesA missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathyHeterogeneous tissue distribution of a mitochondrial DNA polymorphism in heteroplasmic subjects without mitochondrial disordersGimap3 regulates tissue-specific mitochondrial DNA segregationMitochondrial DNA disease and developmental implications for reproductive strategiesDissecting the mechanisms underlying the accumulation of mitochondrial DNA deletions in human skeletal muscle.Transmission of mitochondrial DNA diseases and ways to prevent them.Clinical mitochondrial genetics.Decrease of 3243 A-->G mtDNA mutation from blood in MELAS syndrome: a longitudinal study.Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene.Axial mitochondrial myopathy in a patient with rapidly progressive adult-onset scoliosis.Mitochondrial-nuclear epistasis: implications for human aging and longevity.Mitochondrial genetics '98 is the bottleneck cracked?Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy.Intracellular mitochondrial triplasmy in a patient with two heteroplasmic base changesQuantitative changes in Gimap3 and Gimap5 expression modify mitochondrial DNA segregation in mice.The awakening of an advanced malignant cancer: an insult to the mitochondrial genomeInduced pluripotent stem cells with a mitochondrial DNA deletionMitochondrial DNA deletions in muscle satellite cells: implications for therapiesClinical features of the pathogenic m.5540G>A mitochondrial transfer RNA tryptophan gene mutation.Relaxation of selective constraints on avian mitochondrial DNA following the degeneration of flight ability.The inheritance of pathogenic mitochondrial DNA mutations.Slowly progressive encephalopathy with hearing loss due to a mutation in the mtDNA tRNA(Leu(CUN)) gene.Synthesis of mitochondrial DNA in permeabilised human cultured cells.Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age.Myopathology of Adult and Paediatric Mitochondrial Diseases.Systematic segregation to mutant mitochondrial DNA and accompanying loss of mitochondrial DNA in human NT2 teratocarcinoma Cybrids.Limited locomotive ability relaxed selective constraints on molluscs mitochondrial genomes.Relaxed replication of mtDNA: A model with implications for the expression of disease.Age-related changes in skeletal muscle mitochondria: the role of exercise.
P2860
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P2860
A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle
description
1997 nî lūn-bûn
@nan
1997 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle
@ast
A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle
@en
type
label
A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle
@ast
A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle
@en
prefLabel
A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle
@ast
A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle
@en
P2093
P2860
P1476
A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle
@en
P2093
P2860
P304
P407
P577
1997-02-01T00:00:00Z