Different in situ hybridization patterns of mitochondrial DNA in cytochrome c oxidase-deficient extraocular muscle fibres in the elderly (Q72071043)

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scientific article published on 01 January 1993

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English	Different in situ hybridization patterns of mitochondrial DNA in cytochrome c oxidase-deficient extraocular muscle fibres in the elderly	scientific article published on 01 January 1993

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PubMed publication ID

7679851

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23 October 2019

title

Different in situ hybridization patterns of mitochondrial DNA in cytochrome c oxidase-deficient extraocular muscle fibres in the elderly (English)

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Europe PubMed Central

PubMed publication ID

7679851

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23 October 2019

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J. Müller-Höcker

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1

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Europe PubMed Central

PubMed publication ID

7679851

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P. Seibel

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2

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PubMed publication ID

7679851

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K. Schneiderbanger

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3

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PubMed publication ID

7679851

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B. Kadenbach

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4

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Europe PubMed Central

PubMed publication ID

7679851

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English

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National Center for Biotechnology Information

PubMed publication ID

7679851

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publication date

1 January 1993

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PubMed publication ID

7679851

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23 October 2019

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http://link.springer.com/content/pdf/10.1007/BF01605127.pdf

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10.1007/BF01605127

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Crossref

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10.1007/BF01605127

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http://link.springer.com/content/pdf/10.1007/BF01605127

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Crossref

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10.1007/BF01605127

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https://api.crossref.org/works/10.1007/BF01605127

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12 August 2024

published in

Virchows Archiv. A, Pathological Anatomy and Histopathology

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Europe PubMed Central

PubMed publication ID

7679851

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23 October 2019

volume

422

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Europe PubMed Central

PubMed publication ID

7679851

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23 October 2019

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1

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Europe PubMed Central

PubMed publication ID

7679851

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23 October 2019

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7-15

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Europe PubMed Central

PubMed publication ID

7679851

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23 October 2019

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An integrated theory of aging as the result of mitochondrial-DNA mutation in differentiated cells

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12 December 2020

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Sequence and organization of the human mitochondrial genome

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/7679851

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12 December 2020

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Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNALeu(UUR) ]

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Oxidative energy failure in post-mitotic cells: a major factor in senescence.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/7679851

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12 December 2020

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Mutations of mitochondrial DNA and human death

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PubMed

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12 December 2020

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Focal deficiency of cytochrome c oxidase and of mitochondrial ATPase with histochemical evidence of loosely coupled oxidative phosphorylation in a mitochondrial myopathy of a patient with bilateral ptosis. An enzyme histochemical, immunocytochemical

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In situ hybridization of mitochondrial DNA in the heart of a patient with Kearns-Sayre syndrome and dilatative cardiomyopathy

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12 December 2020

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Partial cytochrome oxidase (aa3) deficiency in chronic progressive external ophthalmoplegia

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12 December 2020

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Cytochrome c oxidase deficient fibres in the limb muscle and diaphragm of man without muscular disease: an age-related alteration

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Ageing-associated 5 kb deletion in human liver mitochondrial DNA.

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https://pubmed.ncbi.nlm.nih.gov/7679851

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12 December 2020

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Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescence

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https://pubmed.ncbi.nlm.nih.gov/7679851

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12 December 2020

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Mitochondrial gene mutation: the ageing process and degenerative diseases

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12 December 2020

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Fatal mitochondrial cardiomyopathy in Kearns-Sayre syndrome with deficiency of cytochrome-c-oxidase in cardiac and skeletal muscle. An enzymehistochemical--ultra-immunocytochemical--fine structural study in longterm frozen autopsy tissue.

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12 December 2020

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Different copy numbers of apparently identically deleted mitochondrial DNA in tissues from a patient with Kearns-Sayre syndrome detected by PCR.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndrome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathy

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/7679851

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA mutations and neuromuscular disease

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular pathology of respiratory-chain dysfunction in human mitochondrial myopathies

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial encephalomyopathies

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common mitochondrial DNA mutation in the t-RNA(Lys) of patients with myoclonus epilepsy associated with ragged-red fibers

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytochrome oxidase deficiency: clinical and biochemical heterogeneity

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial role in cell aging

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondria and ageing

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal mitochondrial myopathy with cytochrome-c-oxidase deficiency and subunit-restricted reduction of enzyme protein in two siblings: an autopsy-immunocytochemical study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A specific point mutation in the mitochondrial genome of Caucasians with MELAS

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial genome distribution in histochemically cytochrome c oxidase-negative muscle fibres in patients with a mixture of deleted and wild type mitochondrial DNA

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: Genetic, biochemical and morphological studies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of a specific mitochondrial DNA deletion in tissues of older humans

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is cell aging caused by respiration-dependent injury to the mitochondrial genome?

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive loss of cytochrome c oxidase in the human extraocular muscles in ageing--a cytochemical-immunohistochemical study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple mitochondrial DNA deletions in an elderly human individual

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Focal deficiency of cytochrome-c-oxidase in skeletal muscle of patients with progressive external ophthalmoplegia. Cytochemical-fine-structural study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kearns-Sayre syndrome with muscle mitochondrial DNA deletion

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative analysis of age-associated accumulation of mitochondrial DNA with deletion in human hearts

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytochrome-c-oxidase deficient cardiomyocytes in the human heart--an age-related phenomenon. A histochemical ultracytochemical study.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseases

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Age-dependent increase in deleted mitochondrial DNA in the human heart: possible contributory factor to presbycardia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Skeletal muscle pathology in chronic progressive external ophthalmoplegia with ragged-red fibers

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical features of mitochondrial myopathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Age-associated accumulation of 8-hydroxydeoxyguanosine in mitochondrial DNA of human diaphragm

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marked decrease of mitochondrial DNA with multiple deletions in a patient with familial mitochondrial myopathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A partial deficiency of cytochrome c oxidase in chronic progressive external ophthalmoplegia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biogenesis of mitochondria

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathy caused by long-term zidovudine therapy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bioenergetics in aging

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple deletions in mitochondrial DNA at direct repeats of non-D-loop regions in cases of familial mitochondrial myopathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deleted mitochondrial DNA in the skeletal muscle of aged individuals

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurological disease and mitochondrial genes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DECLINE IN SKELETAL MUSCLE MITOCHONDRIAL RESPIRATORY CHAIN FUNCTION: POSSIBLE FACTOR IN AGEING

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscle

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7679851

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETION

series ordinal

35

1 reference

stated in

Crossref

DOI

10.1007/BF01605127

reference URL

https://api.crossref.org/works/10.1007/BF01605127

retrieved

12 August 2024

Identifiers

DOI

10.1007/BF01605127

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7679851

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7679851%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 October 2019

PubMed publication ID

7679851

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7679851

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7679851%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 October 2019

 

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