Complex mitochondrial DNA rearrangements in individual cells from patients with sporadic inclusion body myositis. (Q42578650)

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3 April 2020

title

Complex mitochondrial DNA rearrangements in individual cells from patients with sporadic inclusion body myositis (English)

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3 April 2020

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3

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3 April 2020

Amy E Vincent

4

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3 April 2020

Martin Picard

8

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Douglass Matthew Turnbull

3 April 2020

10

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3 April 2020

Robert William Taylor

7

object named as

Robert W Taylor

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3 April 2020

5

Emma L Blakely

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3 April 2020

2

Helen A Tuppen

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1

Karolina A Rygiel

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author name string

Amy K Reeve

6

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3 April 2020

James Miller

9

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3 April 2020

language of work or name

English

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publication date

30 April 2016

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3 April 2020

published in

Nucleic Acids Research

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volume

44

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3 April 2020

page(s)

5313-5329

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issue

11

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Creative Commons Attribution 4.0 International

3 April 2020

copyright license

start time

11 November 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families

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High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

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Single-molecule PCR: an artifact-free PCR approach for the analysis of somatic mutations

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Molecular analyses of mtDNA deletion mutations in microdissected skeletal muscle fibers from aged rhesus monkeys.

28 May 2018

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Mitochondrial DNA deletion in "identical" twin brothers

28 May 2018

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Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia.

28 May 2018

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Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR.

28 May 2018

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Mitochondrial DNA deletion mutations are concomitant with ragged red regions of individual, aged muscle fibers: analysis by laser-capture microdissection

28 May 2018

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Coupled leading- and lagging-strand synthesis of mammalian mitochondrial DNA.

28 May 2018

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Cell-by-cell scanning of whole mitochondrial genomes in aged human heart reveals a significant fraction of myocytes with clonally expanded deletions

28 May 2018

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Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?

28 May 2018

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https://api.crossref.org/works/10.1093%2FNAR%2FGKW382

Multiple deletions of mtDNA remove the light strand origin of replication

21 January 2018

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12 December 2020

Inclusion body myositis

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12 December 2020

Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy

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12 December 2020

Clinical implications of duplicated mtDNA in Pearson syndrome

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Inclusion body myositis: MRC Centre for Neuromuscular Diseases, IBM workshop, London, 13 June 2008

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Duplication and triplication with staggered breakpoints in human mitochondrial DNA

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

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Maternally transmitted partial direct tandem duplication of mitochondrial DNA associated with diabetes mellitus

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Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy

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12 December 2020

Analysis of multiple mitochondrial DNA deletions in inclusion body myositis

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12 December 2020

Pathogenic role of mtDNA duplications in mitochondrial diseases associated with mtDNA deletions

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12 December 2020

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12 December 2020

Human mtDNA sublimons resemble rearranged mitochondrial genoms found in pathological states

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Association of age-related mitochondrial abnormalities with skeletal muscle fiber atrophy

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12 December 2020

Quantification and sequencing of somatic deleted mtDNA in single cells: evidence for partially duplicated mtDNA in aged human tissues

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12 December 2020

A multiplex real-time PCR method to detect and quantify mitochondrial DNA deletions in individual cells

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12 December 2020

Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients

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12 December 2020

Identifiers

DOI

10.1093/NAR/GKW382

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27131788%20AND%20SRC:MED&resulttype=core&format=json

3 April 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27131788%20AND%20SRC:MED&resulttype=core&format=json

3 April 2020

1 reference

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