Cytochrome C oxidase-deficient mitochondria in mitochondrial myopathy (Q48601404)

13 February 2018

title

Cytochrome C oxidase-deficient mitochondria in mitochondrial myopathy (English)

1 reference

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3 December 2023

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3 December 2023

author name string

K. Haginoya

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1313674

3 December 2023

S. Miyabayashi

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1313674

3 December 2023

K. Iinuma

3

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3 December 2023

E. Okino

4

1 reference

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3 December 2023

H. Maesaka

5

1 reference

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3 December 2023

K. Tada

6

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3 December 2023

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1313674

3 December 2023

publication date

1 January 1992

1 reference

13 February 2018

full work available at URL

https://api.elsevier.com/content/article/PII:0887899492900462?httpAccept=text/xml

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https://api.crossref.org/works/10.1016/0887-8994(92)90046-2

https://api.elsevier.com/content/article/PII:0887899492900462?httpAccept=text/plain

3 December 2023

1 reference

https://api.crossref.org/works/10.1016/0887-8994(92)90046-2

3 December 2023

1 reference

13 February 2018

volume

8

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13 February 2018

issue

1

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13 February 2018

page(s)

13-18

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13 February 2018

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

cites work

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1 reference

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Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

3 December 2023

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KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETION

3 December 2023

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Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy

3 December 2023

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

3 December 2023

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1 reference

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Tissue specificity in cytochrome c oxidase deficient myopathy

3 December 2023

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Mosaicism of mitochondria in mitochondrial myopathy: an electronmicroscopic analysis of cytochrome c oxidase

3 December 2023

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Comparative appraisal of CT scan and MRI in the diagnosis of Leigh encephalomyelopathy in two siblings

3 December 2023

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Cytochrome C oxidase deficiency in two siblings with leigh encephalomyelopathy

3 December 2023

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Immunochemical study in three patients with cytochrome c oxidase deficiency presenting Leigh's encephalomyelopathy

3 December 2023

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Multiple cytochrome deficiency and deteriorated mitochondrial polypeptide composition in fatal infantile mitochondrial myopathy and renal dysfunction

3 December 2023

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Nondroplet ultrastructural demonstration of cytochrome oxidase activity with a polymerizing osmiophilic reagent, diaminobenzidine (DAB).

3 December 2023

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The use of skin fibroblast cultures in the detection of respiratory chain defects in patients with lacticacidemia

3 December 2023

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Subacute necrotizing encephalomyelopathy in an infant

3 December 2023

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Cytochrome c oxidase deficiency in Leigh syndrome

3 December 2023

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Cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence for a nuclear DNA-encoded mutation.

3 December 2023

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Cytochrome c oxidase deficiency

3 December 2023

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Mitochondrial mutation in fatal infantile cardiomyopathy

3 December 2023

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Mitotic segregation of cytoplasmic determinants for chloramphenicol resistance in mammalian cells II: Fusions with human cell lines

3 December 2023

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3 December 2023

Identifiers

1 reference

13 February 2018

1 reference

13 February 2018