Modulating myosin restores muscle function in a mouse model of nemaline myopathy (Q37107119)

18 August 2017

Modulating myosin restores muscle function in a mouse model of nemaline myopathy (English)

1 reference

18 August 2017

2

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13 June 2020

Paul Gregorevic

5

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13 June 2020

Julien Ochala

6

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13 June 2020

author name string

Johan Lindqvist

1

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13 June 2020

Alisha Pati-Alam

3

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13 June 2020

Edna C Hardeman

4

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13 June 2020

publication date

17 February 2016

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18 August 2017

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13 June 2020

volume

79

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13 June 2020

page(s)

717-725

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13 June 2020

issue

5

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Recent advances in nemaline myopathy

13 June 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Distinct underlying mechanisms of limb and respiratory muscle fiber weaknesses in nemaline myopathy.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Mammalian target of rapamycin (mTOR) signaling network in skeletal myogenesis

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Skeletal muscle α-actin diseases (actinopathies): pathology and mechanisms.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Follistatin-mediated skeletal muscle hypertrophy is regulated by Smad3 and mTOR independently of myostatin

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Activation of fast skeletal muscle troponin as a potential therapeutic approach for treating neuromuscular diseases

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Therapeutic approaches to muscular dystrophy.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Cytoskeletal protein kinases: titin and its relations in mechanosensing

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Cardiac myosin activation: a potential therapeutic approach for systolic heart failure

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Human essential myosin light chain isoforms revealed distinct myosin binding, sarcomeric sorting, and inotropic activity

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

A myopathy-linked tropomyosin mutation severely alters thin filament conformational changes during activation

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Molecular mechanisms of mechanosensing in muscle development.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

The sarcomere and the nucleus: functional links to hypertrophy, atrophy and sarcopenia

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Genotype-phenotype correlations in ACTA1 mutations that cause congenital myopathies

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Signaling in muscle atrophy and hypertrophy

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Effects of a R133W beta-tropomyosin mutation on regulation of muscle contraction in single human muscle fibres

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Functional characterization of the human atrial essential myosin light chain (hALC-1) in a transgenic rat model

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Regulation of contraction in striated muscle

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Maximum velocity of shortening in relation to myosin isoform composition in single fibres from human skeletal muscles

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Sarcomere length-tension relations of frog skinned muscle fibres during calcium activation at short lengths

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Prevalence and phenotypes of congenital myopathy due to α-actin 1 gene mutations.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

Efficient transduction of skeletal muscle using vectors based on adeno-associated virus serotype 6.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4950341

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

3 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FANA.24619

Defective regulation of contractile function in muscle fibres carrying an E41K beta-tropomyosin mutation

21 January 2018

1 reference

12 December 2020

Congenital myopathies – Clinical features and frequency of individual subtypes diagnosed over a 5-year period in the United Kingdom

1 reference

12 December 2020

Contractile studies of single human skeletal muscle fibers: a comparison of different muscles, permeabilization procedures, and storage techniques

1 reference

12 December 2020

Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy

1 reference

12 December 2020

Identifiers

DOI

10.1002/ANA.24619

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26891371%20AND%20SRC:MED&resulttype=core&format=json

13 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26891371%20AND%20SRC:MED&resulttype=core&format=json

13 June 2020

1 reference