Pathological mechanisms underlying single large-scale mitochondrial DNA deletions.

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Pathological mechanisms underlying single large-scale mitochondrial DNA deletions.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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2018年學術文章

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Pathological mechanisms underlying single large-scale mitochondrial DNA deletions.

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Pathological mechanisms underlying single large-scale mitochondrial DNA deletions.

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Pathological mechanisms underlying single large-scale mitochondrial DNA deletions.

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Pathological mechanisms underlying single large-scale mitochondrial DNA deletions.

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Pathological mechanisms underlying single large-scale mitochondrial DNA deletions.

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Pathological mechanisms underlying single large-scale mitochondrial DNA deletions.

@nl

P1476

Pathological mechanisms underlying single large-scale mitochondrial DNA deletions.

@en

P2093

Emma L Blakely

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Helen A Tuppen

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Jane Newman

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Langping He

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Nadine Romain

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Robert W Taylor

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Ronald G Haller

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P2860

A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I

Denervation causes fiber atrophy and myosin heavy chain co-expression in senescent skeletal muscle

Retinitis pigmentosa, external ophthalmophegia, and complete heart block: unusual syndrome with histologic study in one of two cases

A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction

Mitochondrial respiratory rates and activities of respiratory chain complexes correlate linearly with heteroplasmy of deleted mtDNA without threshold and independently of deletion size.

Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO.

Chronic progressive external ophthalmoplegia: a correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsies.

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.

Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome

Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesis

P304

115-130

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P31

scholarly article

P356

10.1002/ANA.25127

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P433

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P478

http://www.w3.org/2001/XMLSchema#string

P50

P577

2018-01-01T00:00:00Z

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P698

29283441

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P921

mitochondrial DNA

P932

5893934

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