(Q68453563)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2156958%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

title

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

1 reference

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24 September 2019

author name string

K D Gerbitz

1

1 reference

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24 September 2019

B Obermaier-Kusser

2

1 reference

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24 September 2019

S Zierz

3

1 reference

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24 September 2019

D Pongratz

4

1 reference

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24 September 2019

J Müller-Höcker

5

1 reference

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24 September 2019

P Lestienne

6

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24 September 2019

publication date

1 February 1990

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24 September 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2156958%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

volume

237

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24 September 2019

issue

1

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24 September 2019

page(s)

5-10

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https://scigraph.springernature.com/pub.10.1007/bf00319660

24 September 2019

exact match

0 references

cites work

Sequence and organization of the human mitochondrial genome

1 reference

12 December 2020

Maternal genes: mitochondrial diseases.

1 reference

12 December 2020

Mitochondrial morphometrics of histochemically identified human extraocular muscle fibers

1 reference

12 December 2020

Co-linear organization of Xenopus laevis and mouse mitochondrial genomes

1 reference

12 December 2020

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.

1 reference

12 December 2020

Retinitis pigmentosa, external ophthalmophegia, and complete heart block: unusual syndrome with histologic study in one of two cases

1 reference

12 December 2020

Transcription of the mammalian mitochondrial genome

1 reference

12 December 2020

Cloning of human mitochondrial DNA in Escherichia coli

1 reference

12 December 2020

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

12 December 2020

Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanisms.

1 reference

12 December 2020

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

12 December 2020

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

1 reference

12 December 2020

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

1 reference

12 December 2020

Chronic stimulation of rat skeletal muscle induces coordinate increases in mitochondrial and nuclear mRNAs of cytochrome-c-oxidase subunits

1 reference

12 December 2020

Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy

1 reference

12 December 2020

Kearns-Sayre syndrome with muscle mitochondrial DNA deletion

1 reference

12 December 2020

Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome

1 reference

12 December 2020

Decreased activities in mitochondrial inner membrane electron transport system in muscle from patients with Kearns-Sayre syndrome

1 reference

12 December 2020

Preparation and properties of succinate: ubiquinone oxidoreductase (complex II)

1 reference

12 December 2020

MTTOCHONDRIAL DNA DELETION IN ENCEPHALOMYOPATHY

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00319660

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2156958%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

1 reference