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Mitochondrial disease
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
16815381
retrieved
2 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Mitochondrial disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
16815381
retrieved
2 August 2017
main subject
mitochondrion
1 reference
based on heuristic
inferred from title
author
Anthony H V Schapira
series ordinal
1
object named as
Anthony H V Schapira
1 reference
stated in
Europe PubMed Central
PubMed ID
16815381
retrieved
2 August 2017
language of work or name
English
0 references
publication date
1 July 2006
1 reference
stated in
Europe PubMed Central
PubMed ID
16815381
retrieved
2 August 2017
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed ID
16815381
retrieved
2 August 2017
volume
368
1 reference
stated in
Europe PubMed Central
PubMed ID
16815381
retrieved
2 August 2017
page(s)
70-82
1 reference
stated in
Europe PubMed Central
PubMed ID
16815381
retrieved
2 August 2017
issue
9529
1 reference
stated in
Europe PubMed Central
PubMed ID
16815381
retrieved
2 August 2017
cites work
Mitochondrial respiratory chain disorders I: mitochondrial DNA defects
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
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7 January 2021
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inferred from DOI database lookup
Mitochondrial respiratory chain disorders II: neurodegenerative disorders and nuclear gene defects
1 reference
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Crossref
reference URL
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7 January 2021
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The "new" mitochondrial disorders
1 reference
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Crossref
reference URL
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7 January 2021
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inferred from DOI database lookup
Mitochondrial respiratory-chain diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondria
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA depletion can be prevented by dGMP and dAMP supplementation in a resting culture of deoxyguanosine kinase-deficient fibroblasts
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
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7 January 2021
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Discovery of a major D-loop replication origin reveals two modes of human mtDNA synthesis
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
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7 January 2021
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Mitochondrial DNA variation in human evolution and disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
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7 January 2021
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Behaviour of a population of partially duplicated mitochondrial DNA molecules in cell culture: segregation, maintenance and recombination dependent upon nuclear background
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
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7 January 2021
based on heuristic
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Maintenance of human rearranged mitochondrial DNAs in long-term cultured transmitochondrial cell lines
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Heterologous mitochondrial DNA recombination in human cells
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Paternal inheritance of mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
No evidence for paternal mtDNA transmission to offspring or extra-embryonic tissues after ICSI
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evaluation of parental mitochondrial inheritance in neonates born after intracytoplasmic sperm injection
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Is paternal mitochondrial DNA transferred to the offspring following intracytoplasmic sperm injection?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ubiquitin tag for sperm mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Degradation of paternal mitochondria after fertilization: implications for heteroplasmy, assisted reproductive technologies and mtDNA inheritance
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Failure of elimination of paternal mitochondrial DNA in abnormal embryos
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genotypes from patients indicate no paternal mitochondrial DNA contribution
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MELAS and MERRF. The relationship between maternal mutation load and the frequency of clinically affected offspring.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel intronic mutation in the DDP1 gene in a family with X-linked dystonia-deafness syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The epidemiology of pathogenic mitochondrial DNA mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Minimum birth prevalence of mitochondrial respiratory chain disorders in children.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Risk of developing a mitochondrial DNA deletion disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial encephalomyopathies: gene mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
A cluster of metabolic defects caused by mutation in a mitochondrial tRNA.
1 reference
stated in
Crossref
reference URL
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retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial myopathy: new insights into the T14709C mitochondrial tRNA mutation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
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inferred from DOI database lookup
The epidemiology of Leber hereditary optic neuropathy in the North East of England
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Suppression of complex I gene expression induces optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Optic neuropathy induced by reductions in mitochondrial superoxide dismutase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
SOD2 gene transfer protects against optic neuropathy induced by deficiency of complex I.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell lines.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Role of adenine nucleotide translocator 1 in mtDNA maintenance
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
TWINKLE Has 5' -> 3' DNA helicase activity and is specifically stimulated by mitochondrial single-stranded DNA-binding protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy number
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two families with autosomal dominant progressive external ophthalmoplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sensory ataxic neuropathy due to a novel C10Orf2 mutation with probable germline mosaicism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase gamma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations at the mitochondrial DNA polymerase (POLG) locus associated with male infertility
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frequent polymorphism of the mitochondrial DNA polymerase gamma gene (POLG) in patients with normal spermiograms and unexplained subfertility.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Clinical Significance of the POLG Gene Polymorphism in Male Infertility
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-gammaA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial spongiform glioneuronal dystrophy (author's transl)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive neuronal degeneration of childhood with liver disease (Alpers' disease) presenting in young adults
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and Parkinsonism.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome oxidase in health and disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome c oxidase biogenesis in a patient with a mutation in COX10 gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Studies of COX16, COX19, and PET191 in Human Cytochrome-c Oxidase Deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial cerebellar ataxia with muscle coenzyme Q10 deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cerebellar ataxia and coenzyme Q10 deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial complex I deficiency in Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormalities of the electron transport chain in idiopathic Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial oxidative phosphorylation defects in Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Platelet mitochondrial function in Parkinson's disease. The Royal Kings and Queens Parkinson Disease Research Group
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dysfunction of mitochondrial complex I and the proteasome: interactions between two biochemical deficits in a cellular model of Parkinson's disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
alpha-synuclein promotes mitochondrial deficit and oxidative stress
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
alpha-synuclein aggregation: a link between mitochondrial defects and Parkinson's disease?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial dysfunction and oxidative damage in parkin-deficient mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial complex I and IV activities in leukocytes from patients with parkin mutations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parkin prevents mitochondrial swelling and cytochrome c release in mitochondria-dependent cell death.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Parkinson's disease protein DJ-1 is neuroprotective due to cysteine-sulfinic acid-driven mitochondrial localization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in PTEN-induced putative kinase 1 associated with recessive parkinsonism have differential effects on protein stability
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of the trinucleotide CAG repeat from the DNA polymerase gamma gene (POLG) in patients with Parkinson's disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Variability and validity of polymorphism association studies in Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the Irish
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of coenzyme Q10 in early Parkinson disease: evidence of slowing of the functional decline
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Beta-amyloid inhibits integrated mitochondrial respiration and key enzyme activities
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Altered metabolism of the amyloid beta precursor protein is associated with mitochondrial dysfunction in Down's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Brain Cytochrome Oxidase in Alzheimer's Disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Electron transport chain defects in Alzheimer's disease brain.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome c oxidase in Alzheimer's disease brain: purification and characterization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Decreased expression of nuclear and mitochondrial DNA-encoded genes of oxidative phosphorylation in association neocortex in Alzheimer disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial function in Alzheimer's disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analyses of energy metabolism and mitochondrial genome in post-mortem brain from patients with Alzheimer's disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome oxidase deficiency in Alzheimer's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in mitochondrial cytochrome c oxidase genes segregate with late-onset Alzheimer disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Marked changes in mitochondrial DNA deletion levels in Alzheimer brains
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
ABAD directly links Abeta to mitochondrial toxicity in Alzheimer's disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
scully, an essential gene of Drosophila, is homologous to mammalian mitochondrial type II L-3-hydroxyacyl-CoA dehydrogenase/amyloid-beta peptide-binding protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An intracellular protein that binds amyloid-beta peptide and mediates neurotoxicity in Alzheimer's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Role of ERAB/L-3-hydroxyacyl-coenzyme A dehydrogenase type II activity in Abeta-induced cytotoxicity.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuronal degeneration and mitochondrial dysfunction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Amyotrophic lateral sclerosis: a proposed mechanism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Friedreich ataxia: the oxidative stress paradox
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Idebenone delays the onset of cardiac functional alteration without correction of Fe-S enzymes deficit in a mouse model for Friedreich ataxia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Idebenone and reduced cardiac hypertrophy in Friedreich's ataxia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Antioxidant treatment improves in vivo cardiac and skeletal muscle bioenergetics in patients with Friedreich's ataxia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Antioxidant treatment of patients with Friedreich ataxia: four-year follow-up
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Premature ageing in mice expressing defective mitochondrial DNA polymerase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Extension of murine life span by overexpression of catalase targeted to mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Somatic mutations of the mitochondrial genome in human colorectal tumours
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: is there a common mechanism?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
mtDNA mutations increase tumorigenicity in prostate cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Impaired mitochondrial activity in the insulin-resistant offspring of patients with type 2 diabetes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Erralpha and Gabpa/b specify PGC-1alpha-dependent oxidative phosphorylation gene expression that is altered in diabetic muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mtDNA T8993G (NARP) mutation results in an impairment of oxidative phosphorylation that can be improved by antioxidants
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Strategies for treating disorders of the mitochondrial genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reversal of a mitochondrial DNA defect in human skeletal muscle.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
5 S rRNA and tRNA import into human mitochondria. Comparison of in vitro requirements
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nuclear DNA-encoded tRNAs targeted into mitochondria can rescue a mitochondrial DNA mutation associated with the MERRF syndrome in cultured human cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(06)68970-8
1 reference
stated in
Europe PubMed Central
PubMed ID
16815381
retrieved
2 August 2017
PubMed ID
16815381
1 reference
stated in
Europe PubMed Central
PubMed ID
16815381
retrieved
2 August 2017
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