(Q33459245)

27 July 2017

title

Sensory ataxic neuropathy in golden retriever dogs is caused by a deletion in the mitochondrial tRNATyr gene (English)

1 reference

27 July 2017

9

Ake Hedhammar

0 references

Nadja Heidrich

object named as

Nadja Heidrich

5

0 references

Nils-Göran Larsson

6

object named as

Nils-Göran Larsson

1 reference

27 July 2017

7

Göran Andersson

1 reference

27 July 2017

11

Leif Andersson

1 reference

27 July 2017

8

E Gerhart H Wagner

1 reference

27 July 2017

10

Rolf Wibom

1 reference

27 July 2017

Izabella Baranowska

1

1 reference

27 July 2017

Karin Hultin Jäderlund

2

1 reference

27 July 2017

Inger Nennesmo

3

1 reference

27 July 2017

Erik Holmqvist

4

1 reference

27 July 2017

language of work or name

1 reference

29 May 2009

1 reference

27 July 2017

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27 July 2017

volume

5

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27 July 2017

issue

5

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27 July 2017

page(s)

e1000499

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Creative Commons Attribution 4.0 International

27 July 2017

copyright license

start time

29 May 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

ImageQuant

object named as

ImageQuant

2 references

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2683749/fullTextXML

inferred from PubMed Central ID database lookup

CZ Software Mentions: A large dataset of software mentions in the biomedical literature

cites work

Inherited mitochondrial optic neuropathies

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Age-associated mosaic respiratory chain deficiency causes trans-neuronal degeneration

21 June 2018

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Strong purifying selection in transmission of mammalian mitochondrial DNA

21 June 2018

1 reference

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Human mitochondrial transfer RNAs: role of pathogenic mutation in disease

21 June 2018

1 reference

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Hfq-dependent regulation of OmpA synthesis is mediated by an antisense RNA.

21 June 2018

1 reference

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Mitochondrial DNA and disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683749

Mitochondrial DNA mutations in human disease

21 June 2018

1 reference

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Premature ageing in mice expressing defective mitochondrial DNA polymerase

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683749

Impact of disease-related mitochondrial mutations on tRNA structure and function

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683749

Mitochondrial respiratory-chain diseases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683749

Increased mitochondrial mass in mitochondrial myopathy mice

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683749

Primer3 on the WWW for general users and for biologist programmers

21 June 2018

1 reference

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Multiple defects of the mitochondrial respiratory chain in a mitochondrial encephalopathy (MERRF): a clinical, biochemical and molecular study.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683749

Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients harboring the A3243G point mutation or large-scale deletions of mitochondrial DNA.

21 June 2018

1 reference

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Pathology of skeletal muscle in mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000499

Biochemical evaluation of mitochondrial respiratory chain enzymes in canine skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000499

A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.

21 January 2018

1 reference

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Canine spongiform leukoencephalomyelopathy is associated with a missense mutation in cytochrome b.

21 January 2018

1 reference

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Functional characterisation of mitochondrial tRNA(Tyr) mutation (5877-->GA) associated with familial chronic progressive external ophthalmoplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000499

Measurement of ATP production and respiratory chain enzyme activities in mitochondria isolated from small muscle biopsy samples

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000499

A Neurologic Syndrome in Golden Retrievers Presenting as a Sensory Ataxic Neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000499

Episodic weakness associated with exertional lactic acidosis and myopathy in Old English sheepdog littermates

21 January 2018

1 reference

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31 October 2018

Mitochondrial diseases

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000499

Suspected mitochondrial myopathy in a Jack Russell terrier

21 January 2018

1 reference

12 December 2020

Fatal neonatal lactic acidosis with respiratory insufficiency due to complex I and IV deficiency

1 reference

12 December 2020

Novel homoplasmic mutation in the mitochondrial tRNATyr gene associated with atypical mitochondrial cytopathy presenting with focal segmental glomerulosclerosis

1 reference

12 December 2020

Mitochondrial DNA mutations in human disease

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12 December 2020

Canine mitochondrial myopathy associated with reduced mitochondrial mRNA and altered cytochrome c oxidase activities in fibroblasts and skeletal muscle

1 reference

12 December 2020

The epidemiology of pathogenic mitochondrial DNA mutations

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12 December 2020

CPEO associated with a single nucleotide deletion in the mitochondrial tRNA(Tyr) gene

1 reference

12 December 2020

A novel mutation in the mitochondrial tRNA(TYr) gene associated with exercise intolerance

1 reference

12 December 2020

10.1371/JOURNAL.PGEN.1000499

Identifiers

DOI

1 reference

27 July 2017

1 reference

27 July 2017

1 reference