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Literature DB >> 2828763

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

S Miyabayashi¹, T Ito, D Abukawa, K Narisawa, K Tada, M Tanaka, T Ozawa, M Droste, B Kadenbach.

Abstract

Entities: Disease Species

Mesh：

Year: 1987 PMID： 2828763 DOI： 10.1007/BF01800084

Source DB: PubMed Journal: J Inherit Metab Dis ISSN： 0141-8955 Impact factor: 4.982

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12 in total

1. Biochemistry of dystrophic muscle. Mitochondrial succinate-tetrazolium reductase and adenosine triphosphatase.

Authors: R J PENNINGTON
Journal: Biochem J Date: 1961-09 Impact factor: 3.857

2. Leigh's encephalomyelopathy in a patient with cytochrome c oxidase deficiency in muscle tissue.

Authors: J L Willems; L A Monnens; J M Trijbels; J H Veerkamp; A E Meyer; K van Dam; U van Haelst
Journal: Pediatrics Date: 1977-12 Impact factor: 7.124

3. Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy.

Authors: S Miyabayashi; T Ito; K Narisawa; K Iinuma; K Tada
Journal: Eur J Pediatr Date: 1985-03 Impact factor: 3.183

4. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.

Authors: H Towbin; T Staehelin; J Gordon
Journal: Proc Natl Acad Sci U S A Date: 1979-09 Impact factor: 11.205

5. Analysis of products of mitochondrial protein synthesis in yeast: genetic and biochemical aspects.

Authors: M Douglas; D Finkelstein; R A Butow
Journal: Methods Enzymol Date: 1979 Impact factor: 1.600

6. Oxidative phosphorylation in mitochondria isolated from human fibroblasts.

Authors: A J Millis; D A Pious
Journal: Biochim Biophys Acta Date: 1973-01-18

7. Tissue-specific genes code for polypeptide VIa of bovine liver and heart cytochrome c oxidase.

Authors: B Kadenbach; R Hartmann; R Glanville; G Buse
Journal: FEBS Lett Date: 1982-02-22 Impact factor: 4.124

8. Two siblings with cytochrome c oxidase deficiency.

Authors: S Miyabayashi; K Narisawa; K Tada; K Sakai; K Kobayashi; Y Kobayashi
Journal: J Inherit Metab Dis Date: 1983 Impact factor: 4.982

9. Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle.

Authors: N Bresolin; M Zeviani; E Bonilla; R H Miller; R W Leech; S Shanske; M Nakagawa; S DiMauro
Journal: Neurology Date: 1985-06 Impact factor: 9.910

10. Lactic acidosis and mitochondrial myopathy associated with deficiency of several components of complex III of the respiratory chain.

Authors: N G Kennaway; N R Buist; V M Darley-Usmar; A Papadimitriou; S Dimauro; R I Kelley; R A Capaldi; N K Blank; A D'Agostino
Journal: Pediatr Res Date: 1984-10 Impact factor: 3.756

8 in total

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

1. Biochemistry of dystrophic muscle. Mitochondrial succinate-tetrazolium reductase and adenosine triphosphatase.

2. Leigh's encephalomyelopathy in a patient with cytochrome c oxidase deficiency in muscle tissue.

3. Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy.

4. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.

5. Analysis of products of mitochondrial protein synthesis in yeast: genetic and biochemical aspects.

6. Oxidative phosphorylation in mitochondria isolated from human fibroblasts.

7. Tissue-specific genes code for polypeptide VIa of bovine liver and heart cytochrome c oxidase.

8. Two siblings with cytochrome c oxidase deficiency.

9. Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle.

10. Lactic acidosis and mitochondrial myopathy associated with deficiency of several components of complex III of the respiratory chain.

1. Defective pattern of mitochondrial respiratory enzymes in mitochondrial myopathy.

2. Cytochrome c oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome).

3. Cytochrome c oxidase deficiency in infancy.

4. Influence of ageing on onset of mitochondrial disease.

5. Complementation analysis of systemic cytochrome oxidase deficiency presenting as Leigh syndrome.

Review 6. Mutations of mitochondrial DNA and human death.

7. Quantitative evaluation of electron transport system proteins in mitochondrial encephalomyopathy.

8. Immunohistochemical analysis of muscle cytochrome c oxidase deficiency in children.