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Severe myopathy in mice lacking the MEF2/SRF-dependent gene leiomodin-3
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scholarly article
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PubMed
PubMed ID
25774500
retrieved
21 March 2017
title
Severe myopathy in mice lacking the MEF2/SRF-dependent gene leiomodin-3
(English)
1 reference
stated in
PubMed
PubMed ID
25774500
retrieved
21 March 2017
main subject
Leiomodin 3 (fetal)
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GOA release 2020-03-11
author
James A. Richardson
series ordinal
5
object named as
James A. Richardson
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PubMed
PubMed ID
25774500
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21 March 2017
author name string
Bercin K. Cenik
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1
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PubMed
PubMed ID
25774500
retrieved
21 March 2017
Ankit Garg
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2
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PubMed
PubMed ID
25774500
retrieved
21 March 2017
John R. McAnally
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3
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PubMed
PubMed ID
25774500
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21 March 2017
John M. Shelton
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4
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PubMed
PubMed ID
25774500
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21 March 2017
Rhonda Bassel-Duby
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6
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PubMed
PubMed ID
25774500
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21 March 2017
Eric N. Olson
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7
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PubMed
PubMed ID
25774500
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21 March 2017
Ning Liu
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8
1 reference
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PubMed
PubMed ID
25774500
retrieved
21 March 2017
language of work or name
English
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publication date
1 April 2015
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PubMed
PubMed ID
25774500
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21 March 2017
published in
Journal of Clinical Investigation
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PubMed
PubMed ID
25774500
retrieved
21 March 2017
volume
125
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PubMed
PubMed ID
25774500
retrieved
21 March 2017
page(s)
1569–1578
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PubMed
PubMed ID
25774500
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21 March 2017
issue
4
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PubMed
PubMed ID
25774500
retrieved
21 March 2017
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ImageJ
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Europe PubMed Central
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11 June 2022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4396495/fullTextXML
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KLHL40 deficiency destabilizes thin filament proteins and promotes nemaline myopathy
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PubMed Central
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23 March 2017
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Modulation of adverse cardiac remodeling by STARS, a mediator of MEF2 signaling and SRF activity
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Muscle-specific signaling mechanism that links actin dynamics to serum response factor
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Actin dynamics control SRF activity by regulation of its coactivator MAL
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23 March 2017
Potentiation of serum response factor activity by a family of myocardin-related transcription factors
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Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin gene
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Leiomodin 3 and tropomodulin 4 have overlapping functions during skeletal myofibrillogenesis
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3 June 2018
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy
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Prevention of muscular dystrophy in mice by CRISPR/Cas9-mediated editing of germline DNA
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Nebulin interactions with actin and tropomyosin are altered by disease-causing mutations.
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Rho-actin signaling to the MRTF coactivators dominates the immediate transcriptional response to serum in fibroblasts
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Muscle histopathology in nebulin-related nemaline myopathy: ultrastrastructural findings correlated to disease severity and genotype.
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Requirement of MEF2A, C, and D for skeletal muscle regeneration
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3 June 2018
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy
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In vivo genome editing using a high-efficiency TALEN system
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Mice lacking microRNA 133a develop dynamin 2–dependent centronuclear myopathy
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3 June 2018
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3 June 2018
Leiomodin-2 is an antagonist of tropomodulin-1 at the pointed end of the thin filaments in cardiac muscle
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Linking actin dynamics and gene transcription to drive cellular motile functions
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New players in actin polymerization--WH2-domain-containing actin nucleators
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3 June 2018
Protein kinase D1 stimulates MEF2 activity in skeletal muscle and enhances muscle performance
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Nuclear actin regulates dynamic subcellular localization and activity of the SRF cofactor MAL.
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Serum response factor: master regulator of the actin cytoskeleton and contractile apparatus
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Clinical course correlates poorly with muscle pathology in nemaline myopathy.
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3 June 2018
WH2 domain: a small, versatile adapter for actin monomers.
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'An artefact gone awry': identification of the first case of nemaline myopathy by Dr R.D.K. Reye
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3 June 2018
Stimulation of slow skeletal muscle fiber gene expression by calcineurin in vivo.
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3 June 2018
Synergistic interactions between heterologous upstream activation elements and specific TATA sequences in a muscle-specific promoter
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3 June 2018
Identification of upstream and intragenic regulatory elements that confer cell-type-restricted and differentiation-specific expression on the muscle creatine kinase gene
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3 June 2018
Inducible expression of an hsp68-lacZ hybrid gene in transgenic mice
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3 June 2018
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Filament assembly by Spire: key residues and concerted actin binding
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26 November 2018
Leiomodins: larger members of the tropomodulin (Tmod) gene family.
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In situ hybridization of whole-mount embryos.
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26 November 2018
Binding of TFIID and MEF2 to the TATA element activates transcription of the Xenopus MyoDa promoter
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26 November 2018
Congenital myopathies
1 reference
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PubMed
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https://pubmed.ncbi.nlm.nih.gov/25774500
retrieved
12 December 2020
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Regulation of mitochondrial biogenesis in skeletal muscle by CaMK
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12 December 2020
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inferred from PubMed ID database lookup
Identifiers
DOI
10.1172/JCI80115
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1040077
Fatcat ID
release_pre4bzylhjbhldfgewvw3fby2y
0 references
OpenCitations bibliographic resource ID
1040077
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1040077
PMCID
4396495
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1040077
PubMed ID
25774500
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1040077
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