(Q30320769)

English

Mitochondrial respiratory rates and activities of respiratory chain complexes correlate linearly with heteroplasmy of deleted mtDNA without threshold and independently of deletion size

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scholarly article

1 reference

Europe PubMed Central

17 June 2017

Mitochondrial respiratory rates and activities of respiratory chain complexes correlate linearly with heteroplasmy of deleted mtDNA without threshold and independently of deletion size (English)

1 reference

Europe PubMed Central

17 June 2017

1 reference

based on heuristic

inferred from title

author name string

Frank Norbert Gellerich

1

1 reference

Europe PubMed Central

17 June 2017

Marcus Deschauer

2

1 reference

Europe PubMed Central

17 June 2017

Ying Chen

3

1 reference

Europe PubMed Central

17 June 2017

Tobias Müller

4

1 reference

Europe PubMed Central

17 June 2017

Stephan Neudecker

5

1 reference

Europe PubMed Central

17 June 2017

Stephan Zierz

6

1 reference

Europe PubMed Central

17 June 2017

language of work or name

0 references

publication date

1 October 2002

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Europe PubMed Central

17 June 2017

number of pages

12

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inferred from page(s)

Biochimica et Biophysica Acta

1 reference

Europe PubMed Central

17 June 2017

1556

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Europe PubMed Central

17 June 2017

1

1 reference

Europe PubMed Central

17 June 2017

41-52

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Europe PubMed Central

17 June 2017

The development of mitochondrial medicine

1 reference

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Heteroplasmy in chronic external ophthalmoplegia: clinical and molecular observations

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Autosomal dominant progressive external ophthalmoplegia: distribution of multiple mitochondrial DNA deletions.

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A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies

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Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA

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[Familial mitochondrial chronic progressive external ophthalmoplegia. Five families with differing genetics]

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MELAS- and kearns-sayre-type with myopathy and autoimmune polyendocrinopahy

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A novel mitochondrial DNA point mutation in the tRNA(Ile) gene is associated with progressive external ophtalmoplegia.

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Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

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Defects of intergenomic communication: autosomal disorders that cause multiple deletions and depletion of mitochondrial DNA.

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Biochemical and molecular investigations in respiratory chain deficiencies

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Small scale preparation of skeletal muscle mitochondria, criteria of integrity, and assays with reference to tissue function.

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Aging selectively decreases oxidative capacity in rat heart interfibrillar mitochondria

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Characterisation of oxidative phosphorylation in skeletal muscle mitochondria subpopulations in pig: a study using top-down elasticity analysis.

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Twitch-potentiation increases calcium in peripheral more than in central mitochondria of guinea-pig ventricular myocytes.

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Functional characterization of mitochondrial oxidative phosphorylation in saponin-skinned human muscle fibers

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Different sensitivity of rabbit heart and skeletal muscle to endotoxin-induced impairment of mitochondrial function

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Mitochondrial respiratory parameters in cardiac tissue: a novel method of assessment by using saponin-skinned fibers

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A respirometer for investigating oxidative cell metabolism: toward optimization of respiratory studies

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High resolution respirometry of permeabilized skeletal muscle fibers in the diagnosis of neuromuscular disorders.

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Mitochondrial Myopathy Studies on Permeabilized Muscle Fibers1

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Function of the mitochondrial outer membrane as a diffusion barrier in health and diseases

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Distribution of flux control among the enzymes of mitochondrial oxidative phosphorylation in calcium-activated saponin-skinned rat musculus soleus fibers

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Muscle fatigue, lactate, and pyruvate in mitochondrial myopathy with progressive external ophthalmoplegia

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Exogenous coenzyme Q (coq) fails to increase coq in skeletal muscle of two patients with mitochondrial myopathies

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Assay conditions for the mitochondrial NADH:coenzyme Q oxidoreductase

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

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Development and evaluation of a spectrophotometric assay for complex III in isolated mitochondria, tissues and fibroblasts from rats and humans

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Oxidative capacity of muscle and mitochondria: correlation of physiological, biochemical, and morphometric characteristics

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HEAT repeats mediate plasma membrane localization of Tor2p in yeast

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Control of oxidative phosphorylation in skeletal muscle

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Inborn errors of complex II--unusual human mitochondrial diseases

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Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia

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Succinate-cytochrome c reductase: assessment of its value in the investigation of defects of the respiratory chain

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Molecular histology of mitochondrial and nuclear transcripts in the muscle of patients harbouring a single mitochondrial DNA deletion

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Chronic progressive external ophthalmoplegia: a correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsies

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Identifiers

10.1016/S0005-2728(02)00305-5

1 reference

Europe PubMed Central

17 June 2017

1 reference

Europe PubMed Central

17 June 2017

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