Mitochondrial disease (Q34543745)

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Language	Label	Description	Also known as
English	Mitochondrial disease	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

1 reference

Europe PubMed Central

Mitochondrial disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

1 reference

based on heuristic

inferred from title

Anthony H V Schapira

1

object named as

Anthony H V Schapira

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

language of work or name

0 references

publication date

1 July 2006

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

368

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

9529

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

70-82

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Mitochondrial respiratory chain disorders I: mitochondrial DNA defects

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7 January 2021

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Mitochondrial respiratory chain disorders II: neurodegenerative disorders and nuclear gene defects

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7 January 2021

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The "new" mitochondrial disorders

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7 January 2021

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Mitochondrial respiratory-chain diseases

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7 January 2021

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1 reference

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7 January 2021

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Mitochondrial DNA depletion can be prevented by dGMP and dAMP supplementation in a resting culture of deoxyguanosine kinase-deficient fibroblasts

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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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Mitochondrial DNA variation in human evolution and disease

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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

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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Maintenance of human rearranged mitochondrial DNAs in long-term cultured transmitochondrial cell lines

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7 January 2021

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Heterologous mitochondrial DNA recombination in human cells

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7 January 2021

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Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease

1 reference

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7 January 2021

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Paternal inheritance of mitochondrial DNA

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7 January 2021

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No evidence for paternal mtDNA transmission to offspring or extra-embryonic tissues after ICSI

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7 January 2021

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Evaluation of parental mitochondrial inheritance in neonates born after intracytoplasmic sperm injection

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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Is paternal mitochondrial DNA transferred to the offspring following intracytoplasmic sperm injection?

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Ubiquitin tag for sperm mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Degradation of paternal mitochondria after fertilization: implications for heteroplasmy, assisted reproductive technologies and mtDNA inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Failure of elimination of paternal mitochondrial DNA in abnormal embryos

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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Genotypes from patients indicate no paternal mitochondrial DNA contribution

1 reference

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7 January 2021

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MELAS and MERRF. The relationship between maternal mutation load and the frequency of clinically affected offspring

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22

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7 January 2021

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A novel intronic mutation in the DDP1 gene in a family with X-linked dystonia-deafness syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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The epidemiology of pathogenic mitochondrial DNA mutations

1 reference

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7 January 2021

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Minimum birth prevalence of mitochondrial respiratory chain disorders in children

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Risk of developing a mitochondrial DNA deletion disorder

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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Mitochondrial encephalomyopathies: gene mutation

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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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A cluster of metabolic defects caused by mutation in a mitochondrial tRNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Familial myopathy: new insights into the T14709C mitochondrial tRNA mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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The epidemiology of Leber hereditary optic neuropathy in the North East of England

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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Suppression of complex I gene expression induces optic neuropathy

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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Optic neuropathy induced by reductions in mitochondrial superoxide dismutase

1 reference

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7 January 2021

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SOD2 gene transfer protects against optic neuropathy induced by deficiency of complex I.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell lines.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Role of adenine nucleotide translocator 1 in mtDNA maintenance

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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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TWINKLE Has 5' -> 3' DNA helicase activity and is specifically stimulated by mitochondrial single-stranded DNA-binding protein

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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy number

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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Two families with autosomal dominant progressive external ophthalmoplegia

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https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Sensory ataxic neuropathy due to a novel C10Orf2 mutation with probable germline mosaicism

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase gamma

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Mutations at the mitochondrial DNA polymerase (POLG) locus associated with male infertility

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Frequent polymorphism of the mitochondrial DNA polymerase gamma gene (POLG) in patients with normal spermiograms and unexplained subfertility

1 reference

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7 January 2021

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The Clinical Significance of the POLG Gene Polymorphism in Male Infertility

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7 January 2021

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POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion

1 reference

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7 January 2021

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Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-gammaA.

1 reference

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7 January 2021

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Familial spongiform glioneuronal dystrophy (author's transl)

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7 January 2021

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Progressive neuronal degeneration of childhood with liver disease (Alpers' disease) presenting in young adults

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and Parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Cytochrome oxidase in health and disease.

1 reference

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7 January 2021

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Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

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Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Cytochrome c oxidase biogenesis in a patient with a mutation in COX10 gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Studies of COX16, COX19, and PET191 in Human Cytochrome-c Oxidase Deficiency

1 reference

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7 January 2021

based on heuristic

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A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial cerebellar ataxia with muscle coenzyme Q10 deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Cerebellar ataxia and coenzyme Q10 deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial complex I deficiency in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Abnormalities of the electron transport chain in idiopathic Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Mitochondrial oxidative phosphorylation defects in Parkinson's disease

1 reference

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7 January 2021

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Platelet mitochondrial function in Parkinson's disease. The Royal Kings and Queens Parkinson Disease Research Group

1 reference

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7 January 2021

based on heuristic

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Dysfunction of mitochondrial complex I and the proteasome: interactions between two biochemical deficits in a cellular model of Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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alpha-synuclein promotes mitochondrial deficit and oxidative stress

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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alpha-synuclein aggregation: a link between mitochondrial defects and Parkinson's disease?

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Mitochondrial dysfunction and oxidative damage in parkin-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Mitochondrial complex I and IV activities in leukocytes from patients with parkin mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Hereditary early-onset Parkinson's disease caused by mutations in PINK1

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Mutations in PTEN-induced putative kinase 1 associated with recessive parkinsonism have differential effects on protein stability

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Variability and validity of polymorphism association studies in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

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Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD.

1 reference

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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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Beta-amyloid inhibits integrated mitochondrial respiration and key enzyme activities

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Brain Cytochrome Oxidase in Alzheimer's Disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Electron transport chain defects in Alzheimer's disease brain

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytochrome c oxidase in Alzheimer's disease brain: purification and characterization

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial function in Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytochrome oxidase deficiency in Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Marked changes in mitochondrial DNA deletion levels in Alzheimer brains

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

ABAD directly links Abeta to mitochondrial toxicity in Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Neuronal degeneration and mitochondrial dysfunction

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Amyotrophic lateral sclerosis: a proposed mechanism

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Friedreich ataxia: the oxidative stress paradox

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Idebenone and reduced cardiac hypertrophy in Friedreich's ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Antioxidant treatment of patients with Friedreich ataxia: four-year follow-up

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Premature ageing in mice expressing defective mitochondrial DNA polymerase

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Somatic mutations of the mitochondrial genome in human colorectal tumours

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

mtDNA mutations increase tumorigenicity in prostate cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Strategies for treating disorders of the mitochondrial genome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Reversal of a mitochondrial DNA defect in human skeletal muscle.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2806%2968970-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0140-6736(06)68970-8

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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