Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation.

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Hypocrellin B in hepatocellular carcinoma cells: Subcellular localization and sonodynamic damage.Targeting autophagy and mitophagy for mitochondrial diseases treatment.

P2860

Q35539246-971C83BE-0CEF-4424-A7A2-750783F910CA Q38622293-ADFFEC4A-D662-4377-804F-D14B00F8B2DC

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Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation.

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http://www.wikidata.org/entity/Q44645048

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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2013年學術文章

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name

Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation.

@en

Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation.

@nl

type

Item

label

Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation.

@en

Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation.

@nl

prefLabel

Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation.

@en

Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation.

@nl

P1476

Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation.

@en

P2093

Akihiro Hashiguchi

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

Akiko Yoshimura

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

Hiroshi Takashima

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

Itsuro Higuchi

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Jun-Hui Yuan

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

Keiko Higashi

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

Yujiro Higuchi

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

Yukie Inamori

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

Yusuke Sakiyama

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P2860

PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1

Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

Selective degradation of mitochondria by mitophagy

Wobble modification defect in tRNA disturbs codon-anticodon interaction in a mitochondrial disease

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

Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.

A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy.

Second generation sequencing allows for mtDNA mixture deconvolution and high resolution detection of heteroplasmy.

An oligonucleotide microarray for high-throughput sequencing of the mitochondrial genome

What can mitochondrial heterogeneity tell us about mitochondrial dynamics and autophagy?

P304

659-664

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P31

scholarly article

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10.1136/JCLINPATH-2012-201431

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English

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

P478

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

P577

2013-04-04T00:00:00Z

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P698

23559353

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Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation.

about

P2860

P2860

Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation.

description

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type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698