(Q74439857)

English

Expression of mtDNA and nDNA encoded respiratory chain proteins in chemically and genetically-derived Rho0 human fibroblasts: a comparison of subunit proteins in normal fibroblasts treated with ethidium bromide and fibroblasts from a patient with mt

scientific article published on 01 December 1997

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10 November 2019

Expression of mtDNA and nDNA encoded respiratory chain proteins in chemically and genetically-derived Rho0 human fibroblasts: a comparison of subunit proteins in normal fibroblasts treated with ethidium bromide and fibroblasts from a patient with mtDNA depletion syndrome (English)

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10 November 2019

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10 November 2019

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M F Marusich

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10 November 2019

B H Robinson

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10 November 2019

S J Kim

4

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10 November 2019

R Schillace

5

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10 November 2019

J L Smith

6

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10 November 2019

R A Capaldi

7

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10 November 2019

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1 December 1997

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10 November 2019

Biochimica et Biophysica Acta

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10 November 2019

1362

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10 November 2019

2-3

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10 November 2019

145-159

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10 November 2019

Determination of the structures of respiratory enzyme complexes from mammalian mitochondria

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Diseases of the mitochondrial DNA.

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Cytochrome oxidase: an endogenous metabolic marker for neuronal activity

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Mitochondrial myopathies and respiratory chain proteins

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Cytochrome c oxidase deficiency

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Mitochondrial encephalomyopathies

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Mitochondrial DNA sequence variation in human evolution and disease.

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Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease

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MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts

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Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systems

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Subunit specific monoclonal antibodies show different steady-state levels of various cytochrome-c oxidase subunits in chronic progressive external ophthalmoplegia

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Tissue distribution of cytochrome c oxidase isoforms in mammals. Characterization with monoclonal and polyclonal antibodies

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7 January 2021

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Mammalian cytochrome-c oxidase: characterization of enzyme and immunological detection of subunits in tissue extracts and whole cells

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Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency

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Investigation of mitochondrial metabolism in small human skeletal muscle biopsy specimens. Improvement of preparation procedure.

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Efficient hybridoma production using previously frozen splenocytes

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Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

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An Antisense Oligodeoxynucleotide Approach to Investigate the Function of the Nuclear-Encoded Subunits of Human Cytochrome c Oxidase

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Disorders associated with depletion of mitochondrial DNA

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Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA

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Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: a morphological, biochemical and molecular-genetic study

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Mitochondrial DNA depletion: prevalence in a pediatric population referred for neurologic evaluation.

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

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Expression and fate of the nuclearly encoded subunits of cytochrome-c oxidase in cultured human cells depleted of mitochondrial gene products

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The whole structure of the 13-subunit oxidized cytochrome c oxidase at 2.8 A

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NRF-1: a trans-activator of nuclear-encoded respiratory genes in animal cells

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The rat cytochrome c oxidase subunit IV gene family: tissue-specific and hormonal differences in subunit IV and cytochrome c mRNA expression

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Molecular cloning and characterization of the rat cytochrome c oxidase subunit Vb gene

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Respiratory-deficient human fibroblasts exhibiting defective mitochondrial DNA replication

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Fatal infantile liver failure associated with mitochondrial DNA depletion

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Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts

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

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

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Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemia

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Identifiers

10.1016/S0925-4439(97)00061-6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9540845%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9540845%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

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