Multimodal MRI and (31)P-MRS investigations of the ACTA1(Asp286Gly) mouse model of nemaline myopathy provide evidence of impaired in vivo muscle function, altered muscle structure and disturbed energy metabolism (Q34973774)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	Multimodal MRI and (31)P-MRS investigations of the ACTA1(Asp286Gly) mouse model of nemaline myopathy provide evidence of impaired in vivo muscle function, altered muscle structure and disturbed energy metabolism	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Multimodal MRI and (31)P-MRS investigations of the ACTA1(Asp286Gly) mouse model of nemaline myopathy provide evidence of impaired in vivo muscle function, altered muscle structure and disturbed energy metabolism (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

nemaline myopathy

1 reference

based on heuristic

inferred from title

Guillaume Duhamel

object named as

Guillaume Duhamel

2

0 references

author name string

Charlotte Gineste

1

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Yann Le Fur

3

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Christophe Vilmen

4

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Patrick J Cozzone

5

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Kristen J Nowak

6

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

David Bendahan

7

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Julien Gondin

8

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

language of work or name

0 references

publication date

20 August 2013

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

e72294

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

copyright license

Creative Commons Attribution 4.0 International

20 August 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Combined MRI and ³¹P-MRS investigations of the ACTA1(H40Y) mouse model of nemaline myopathy show impaired muscle function and altered energy metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Constitutive activation of the calcium sensor STIM1 causes tubular-aggregate myopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Nemaline myopathy-related skeletal muscle α-actin (ACTA1) mutation, Asp286Gly, prevents proper strong myosin binding and triggers muscle weakness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Clinical utility gene card for: nemaline myopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Consensus statement on standard of care for congenital myopathies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

A myopathy-related actin mutation increases contractile function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Use of skeletal muscle MRI in diagnosis and monitoring disease progression in Duchenne muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Actin nemaline myopathy mouse reproduces disease, suggests other actin disease phenotypes and provides cautionary note on muscle transgene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Muscle imaging in congenital myopathies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Lower leg muscle involvement in Duchenne muscular dystrophy: an MR imaging and spectroscopy study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Changes in muscle T2 and tissue damage after downhill running in mdx mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Changes in cross-bridge cycling underlie muscle weakness in patients with tropomyosin 3-based myopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Quantification of fat infiltration in oculopharyngeal muscular dystrophy: comparison of three MR imaging methods

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

T2 mapping in Duchenne muscular dystrophy: distribution of disease activity and correlation with clinical assessments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Grid-free interactive and automated data processing for MR chemical shift imaging data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Ca2+ sensitizers: An emerging class of agents for counterbalancing weakness in skeletal muscle diseases?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Nebulin plays a direct role in promoting strong actin-myosin interactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Mouse models for thin filament disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Magnetic resonance imaging of mouse skeletal muscle to measure denervation atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Sarcoplasmic reticulum calcium uptake and speed of relaxation are depressed in nebulin-free skeletal muscle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Nebulin-deficient mice exhibit shorter thin filament lengths and reduced contractile function in skeletal muscle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Tubular aggregates: sarcoplasmic reticulum origin, calcium storage ability, and functional implications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Noninvasive monitoring of gene correction in dystrophic muscle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Functional investigations of exercising muscle: a noninvasive magnetic resonance spectroscopy-magnetic resonance imaging approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Tubular aggregates are from whole sarcoplasmic reticulum origin: alterations in calcium binding protein expression in mouse skeletal muscle during aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Expression profiling reveals altered satellite cell numbers and glycolytic enzyme transcription in nemaline myopathy muscle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Clinical course correlates poorly with muscle pathology in nemaline myopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Mice lacking skeletal muscle actin show reduced muscle strength and growth deficits and die during the neonatal period

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Reduced oxidative phosphorylation and proton efflux suggest reduced capillary blood supply in skeletal muscle of patients with dermatomyositis and polymyositis: a quantitative 31P-magnetic resonance spectroscopy and MRI study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

'An artefact gone awry': identification of the first case of nemaline myopathy by Dr R.D.K. Reye

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

MR spectroscopy in clinical research.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Determination of Intracellular pH by 31P Magnetic Resonance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Skeletal Muscle Energetics and Metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

8 July 2018

Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutations

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0072294

21 January 2018

Comparative MRI analysis of T2 changes associated with single and repeated bouts of downhill running leading to eccentric-induced muscle damage

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0072294

21 January 2018

Skeletal muscle degeneration and regeneration after femoral artery ligation in mice: monitoring with diffusion MR imaging.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0072294

21 January 2018

Segmentation of fascias, fat and muscle from magnetic resonance images in humans: the DISPIMAG software.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0072294

21 January 2018

A quantitative study of bioenergetics in skeletal muscle lacking utrophin and dystrophin.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0072294

21 January 2018

The origin of tubular aggregates in human myopathies

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0072294

21 January 2018

Contraction duration affects metabolic energy cost and fatigue in skeletal muscle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748127

26 October 2018

Genotype?phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle ?-actin

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0072294

21 January 2018

Magnetic resonance imaging of muscle in nemaline myopathy

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0072294

21 January 2018

Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathy

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0072294

21 January 2018

In vivo and in vitro investigations of heterozygous nebulin knock-out mice disclose a mild skeletal muscle phenotype

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0072294

21 January 2018

Muscular involvement assessed by MRI correlates to motor function measurement values in oculopharyngeal muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/23977274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three-point technique of fat quantification of muscle tissue as a marker of disease progression in Duchenne muscular dystrophy: preliminary study

1 reference

https://pubmed.ncbi.nlm.nih.gov/23977274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant nemaline myopathy caused by a novel alpha-tropomyosin 3 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/23977274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A strictly noninvasive MR setup dedicated to longitudinal studies of mechanical performance, bioenergetics, anatomy, and muscle recruitment in contracting mouse skeletal muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/23977274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mouse models of dominant ACTA1 disease recapitulate human disease and provide insight into therapies

1 reference

https://pubmed.ncbi.nlm.nih.gov/23977274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0072294

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

2013PLoSO...872294G

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34973774&oldid=1864163307"