(Q33876294)

29 July 2017

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title

Mitochondrial biogenesis defects and neuromuscular disorders (English)

1 reference

29 July 2017

Marin-Garcia J

1

1 reference

PubMed ID

10738917

29 July 2017

Goldenthal MJ

series ordinal

2

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PubMed ID

10738917

29 July 2017

language of work or name

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1 February 2000

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29 July 2017

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29 July 2017

22

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29 July 2017

2

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29 July 2017

122-129

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Sequence and organization of the human mitochondrial genome

29 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Mouse L cell mitochondrial DNA molecules are selected randomly for replication throughout the cell cycle

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Mitochondrial DNA maintenance in vertebrates

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Cloning and characterization of the human mitochondrial DNA polymerase, DNA polymerase gamma

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Differential expression of mitochondrial DNA replication factors in mammalian tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Mitochondrial DNA mutations and pathogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Diseases of the mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Mitochondrial DNA sequence variation in human evolution and disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Specific mitochondrial DNA deletions in idiopathic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Whole mitochondrial genome amplification reveals basal level multiple deletions in mtDNA of patients with dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Kearns-Sayre syndrome with a novel mitochondrial DNA deletion

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Skeletal muscle mitochondrial defects in nonspecific neurologic disorders.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Depletion of mitochondrial deoxyribonucleic acid in a family with fatal neonatal liver disease

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Cardiac mitochondrial dysfunction and DNA depletion in children with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate form.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Mitochondria in neuromuscular disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Can mitochondrial clocks keep time?

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Excision sequences in the mitochondrial genome of yeast.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Mitochondrial toxicity of antiviral drugs

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Partial cytochrome c oxidase deficiency and cytoplasmic bodies in patients with zidovudine myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Amounts of mitochondrial DNA and abundance of some mitochondrial gene transcripts in early mouse embryos

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Localization of the Wilson's disease protein product to mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Deficiency of the voltage-dependent anion channel: a novel cause of mitochondriopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Neurodegeneration, myocardial injury, and perinatal death in mitochondrial superoxide dismutase-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Mitochondrial diseases in man and mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in human

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2899%2900117-4

7 January 2021

10.1016/S0887-8994(99)00117-4

Identifiers

DOI

1 reference

29 July 2017

1 reference

PubMed ID

10738917