(Q36796199)

16 August 2017

1 reference

title

Optical imaging techniques (histochemical, immunohistochemical, and in situ hybridization staining methods) to visualize mitochondria (English)

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16 August 2017

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1 reference

Kurenai Tanji

1

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16 August 2017

Eduardo Bonilla

series ordinal

2

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16 August 2017

publication date

1 January 2007

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16 August 2017

published in

Methods in Cell Biology

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16 August 2017

volume

80

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16 August 2017

page(s)

135-154

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Cytopathies involving mitochondrial complex II.

16 August 2017

cites work

1 reference

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7 January 2021

Sequence and organization of the human mitochondrial genome

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7 January 2021

Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: A new approach to the study of mitochondrial myopathies

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7 January 2021

Biogenesis of mitochondria

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7 January 2021

Immunocytochemical demonstration of cytochrome c oxidase with an immunoperoxidase method: a specific stain for mitochondria in formalin-fixed and paraffin-embedded human tissues

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7 January 2021

Electron cytochemistry of crystalline inclusions in human skeletal muscle mitochondria

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7 January 2021

New morphological approaches to the study of mitochondrial encephalomyopathies

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7 January 2021

Mitochondrial involvement in Alzheimer's disease

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7 January 2021

Structure and assembly of cytochrome c oxidase

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7 January 2021

Cytochrome c oxidase: structure, function, and membrane topology of the polypeptide subunits

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7 January 2021

RAPID EXAMINATION OF MUSCLE TISSUE. AN IMPROVED TRICHROME METHOD FOR FRESH-FROZEN BIOPSY SECTIONS

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7 January 2021

Maternal inheritance of human mitochondrial DNA

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7 January 2021

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

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7 January 2021

A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

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7 January 2021

Deficiency of skeletal muscle succinate dehydrogenase and aconitase. Pathophysiology of exercise in a novel human muscle oxidative defect

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7 January 2021

The mitochondrial electron transport and oxidative phosphorylation system

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7 January 2021

Immunohistochemical studies on complexes I, II, III, and IV of mitochondria in Parkinson's disease

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7 January 2021

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

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7 January 2021

Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures

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7 January 2021

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

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7 January 2021

Immunocytochemical studies of cytochrome oxidase subunits in skeletal muscle of patients with partial cytochrome oxidase deficiencies

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7 January 2021

Nuclear functions required for cytochrome c oxidase biogenesis in Saccharomyces cerevisiae: multiple trans-acting nuclear genes exert specific effects on expression of each of the cytochrome c oxidase subunits encoded on mitochondrial DNA.

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7 January 2021

Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?

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7 January 2021

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

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7 January 2021

Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions

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7 January 2021

Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia

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7 January 2021

Protein import into mitochondria

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7 January 2021

Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

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7 January 2021

The identification of 18 nuclear genes required for the expression of the yeast mitochondrial gene encoding cytochrome c oxidase subunit 1

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7 January 2021

Microphotometric measurement of initial maximum reaction rates in quantitative enzyme histochemistry in situ

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7 January 2021

Organization of multiple nucleoids and DNA molecules in mitochondria of a human cell

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7 January 2021

The histochemical demonstration of succinic dehydrogenase.

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Nuclear genetic defects of oxidative phosphorylation

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7 January 2021

Myoclonic Epilepsy with Ragged‐red Fibers (MERRF): An Immunohistochemical Study of the Brain

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7 January 2021

Mitochondrial DNA deletion: a cause of chronic tubulointerstitial nephropathy

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7 January 2021

Human cytochrome c oxidase: structure, function, and deficiency.

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7 January 2021

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

1 reference

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7 January 2021

Kearns-Sayre syndrome: unusual pattern of expression of subunits of the respiratory chain in the cerebellar system

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7 January 2021

The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunction

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7 January 2021

Deficiency of complex II of the mitochondrial respiratory chain in late-onset optic atrophy and ataxia

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7 January 2021

Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency

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7 January 2021

Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA

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7 January 2021

Mitochondrial DNA depletion in a patient with long survival

1 reference

https://api.crossref.org/works/10.1016%2FS0091-679X%2806%2980006-3

7 January 2021

Analysis of mtDNA deletions in muscle by in situ hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS0091-679X%2806%2980006-3

7 January 2021

Diseases of the mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0091-679X%2806%2980006-3

7 January 2021

Cytochrome oxidase: an endogenous metabolic marker for neuronal activity

1 reference

https://api.crossref.org/works/10.1016%2FS0091-679X%2806%2980006-3

7 January 2021

SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0091-679X%2806%2980006-3

7 January 2021

10.1016/S0091-679X(06)80006-3

Identifiers

DOI

1 reference

16 August 2017

1 reference