Actin isoform expression patterns during mammalian development and in pathology: insights from mouse models (Q37417675)

20 August 2017

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title

Actin isoform expression patterns during mammalian development and in pathology: insights from mouse models (English)

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20 August 2017

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Davina Tondeleir

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20 August 2017

Drieke Vandamme

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20 August 2017

Joël Vandekerckhove

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20 August 2017

Christophe Ampe

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20 August 2017

Anja Lambrechts

5

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20 August 2017

1 October 2009

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20 August 2017

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20 August 2017

66

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20 August 2017

798-815

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20 August 2017

10

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Congenital fiber type disproportion--30 years on.

20 August 2017

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Structure, chromosome location, and expression of the human gamma-actin gene: differential evolution, location, and expression of the cytoskeletal beta- and gamma-actin genes

21 January 2018

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alpha-skeletal and alpha-cardiac actin genes are coexpressed in adult human skeletal muscle and heart

21 January 2018

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Identification and developmental expression of a smooth-muscle gamma-actin in postmeiotic male germ cells of mice

21 January 2018

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Expression of transfected mutant beta-actin genes: alterations of cell morphology and evidence for autoregulation in actin pools

21 January 2018

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The development expression of the rat alpha-vascular and gamma-enteric smooth muscle isoactins: isolation and characterization of a rat gamma-enteric actin cDNA.

21 January 2018

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Upstream regions of the human cardiac actin gene that modulate its transcription in muscle cells: presence of an evolutionarily conserved repeated motif

21 January 2018

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Structure, chromosome location, and expression of the human smooth muscle (enteric type) gamma-actin gene: evolution of six human actin genes

21 January 2018

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Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.

21 January 2018

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Characterization of a beta-actin mRNA zipcode-binding protein

21 January 2018

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Clinical course correlates poorly with muscle pathology in nemaline myopathy.

21 January 2018

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Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy

21 January 2018

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Cellular Disorganization and Extensive Apoptosis in the Developing Heart of Mice that Lack Cardiac Muscle α-Actin: Apparent Cause of Perinatal Death

21 January 2018

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7 January 2021

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

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7 January 2021

Nemaline myopathy with minicores caused by mutation of the CFL2 gene encoding the skeletal muscle actin-binding protein, cofilin-2

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7 January 2021

Genetic analysis of the interaction between cardiac and skeletal actin gene expression in striated muscle of the mouse

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7 January 2021

Isolation and characterization of an avian myogenic cell line

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7 January 2021

Gene mutations in apical hypertrophic cardiomyopathy

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7 January 2021

Sorting of beta-actin mRNA and protein to neurites and growth cones in culture.

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7 January 2021

Developmental expression of the alpha-skeletal actin gene.

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7 January 2021

Developmental and tissue-specific regulation of the murine cardiac actin gene in vivo depends on distinct skeletal and cardiac muscle-specific enhancer elements in addition to the proximal promoter.

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7 January 2021

Skeletal actin mRNA increases in the human heart during ontogenic development and is the major isoform of control and failing adult hearts

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7 January 2021

Pathological situations characterized by altered actin isoform expression

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7 January 2021

The pathogenesis of ACTA1-related congenital fiber type disproportion

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7 January 2021

Actin isoform pattern expression: a tool for the diagnosis and biological characterization of human rhabdomyosarcoma

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7 January 2021

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

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7 January 2021

Myopathy mutations in alpha-skeletal-muscle actin cause a range of molecular defects.

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7 January 2021

Transcriptional regulation of actin and myosin genes during differentiation of a mouse muscle cell line

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7 January 2021

Gamma actin, spectrin, and intermediate filament proteins colocalize with vinculin at costameres, myofibril-to-sarcolemma attachment sites

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7 January 2021

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

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7 January 2021

Silenced RNA on the move

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7 January 2021

Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy

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7 January 2021

Localization of a beta-actin messenger ribonucleoprotein complex with zipcode-binding protein modulates the density of dendritic filopodia and filopodial synapses

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7 January 2021

Functional nonequivalence of Drosophila actin isoforms.

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7 January 2021

The myofibroblast in wound healing and fibrocontractive diseases

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7 January 2021

A 5' duplication of the alpha-cardiac actin gene in BALB/c mice is associated with abnormal levels of alpha-cardiac and alpha-skeletal actin mRNAs in adult cardiac tissue.

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7 January 2021

MicroRNA-mediated up-regulation of an alternatively polyadenylated variant of the mouse cytoplasmic {beta}-actin gene

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7 January 2021

Changes in the quantity of histone and actin messenger RNA during the development of preimplantation mouse embryos.

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7 January 2021

A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core-like lesions

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7 January 2021

A predominantly nuclear protein affecting cytoplasmic localization of beta-actin mRNA in fibroblasts and neurons

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7 January 2021

Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections.

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7 January 2021

Cytoplasmic gamma-actin contributes to a compensatory remodeling response in dystrophin-deficient muscle

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7 January 2021

Cellular localization of muscle and nonmuscle actin mRNAs in chicken primary myogenic cultures: the induction of alpha-skeletal actin mRNA is regulated independently of alpha-cardiac actin gene expression

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7 January 2021

Alpha-skeletal actin is associated with increased contractility in the mouse heart

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7 January 2021

Beta and gamma actin mRNAs are differentially located within myoblasts

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7 January 2021

Vertebrate myotome development

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7 January 2021

Beta actin and its mRNA are localized at the plasma membrane and the regions of moving cytoplasm during the cellular response to injury

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7 January 2021

Spatial regulation of beta-actin translation by Src-dependent phosphorylation of ZBP1.

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7 January 2021

Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin gene

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7 January 2021

Defining alpha-skeletal and alpha-cardiac actin expression in human heart and skeletal muscle explains the absence of cardiac involvement in ACTA1 nemaline myopathy

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7 January 2021

Conditional transgene expression mediated by the mouse beta-actin locus

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7 January 2021

A novel nemaline myopathy in the Amish caused by a mutation in troponin T1

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7 January 2021

Isoform specificity in the relationship of actin to dendritic spines.

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7 January 2021

Missense mutations of ACTA1 cause dominant congenital myopathy with cores

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7 January 2021

Arginylation of beta-actin regulates actin cytoskeleton and cell motility

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7 January 2021

Mechanisms of angiogenesis

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7 January 2021

Cell migration during gastrulation

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7 January 2021

Functional specificity of actin isoforms

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7 January 2021

Systematic bioinformatic analysis of expression levels of 17,330 human genes across 9,783 samples from 175 types of healthy and pathological tissues

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7 January 2021

Sequences responsible for intracellular localization of beta-actin messenger RNA also affect cell phenotype

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7 January 2021

beta-Actin messenger RNA localization and protein synthesis augment cell motility

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7 January 2021

Rescue of cardiac alpha-actin-deficient mice by enteric smooth muscle gamma-actin

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7 January 2021

Transgenic overexpression of cardiac actin in the mouse heart suggests coregulation of cardiac, skeletal and vascular actin expression.

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7 January 2021

A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy

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7 January 2021

Actin mutations are one cause of congenital fibre type disproportion

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7 January 2021

The actin cytoskeleton in normal and pathological cell motility

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7 January 2021

Muscle actin isoforms are differentially expressed in human satellite cells isolated from donors of different ages

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7 January 2021

A Rho-dependent signaling pathway operating through myosin localizes beta-actin mRNA in fibroblasts

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7 January 2021

Alpha smooth muscle actin expression in developing and adult human lung

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7 January 2021

Identification and order of sequential mutations in beta-actin genes isolated from increasingly tumorigenic human fibroblast strains

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7 January 2021

Novel ACTG1 mutation causing autosomal dominant non-syndromic hearing impairment in a Chinese family.

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7 January 2021

A novel role for non-muscle gamma-actin in skeletal muscle sarcomere assembly

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7 January 2021

Hypertrophie cardiomyopathy: A discussion of nomenclature

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7 January 2021

Modulation of thin filament activation by breakdown or isoform switching of thin filament proteins: physiological and pathological implications

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7 January 2021

Molecular analysis of smooth muscle development in the mouse

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7 January 2021

A comprehensive analysis of the developmental and tissue-specific expression of the isoactin multigene family in the rat

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7 January 2021

A fetal skeletal muscle actin mRNA in the mouse and its identity with cardiac actin mRNA.

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7 January 2021

Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy

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7 January 2021

Clinical and genetic characteristics of alpha cardiac actin gene mutations in hypertrophic cardiomyopathy.

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7 January 2021

The cardiac isoform of α-actin in regenerating and atrophic skeletal muscle, myopathies and rhabdomyomatous tumors: an immunohistochemical study using monoclonal antibodies

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7 January 2021

Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor

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7 January 2021

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy

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7 January 2021

Nemaline myopathy caused by absence of alpha-skeletal muscle actin

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7 January 2021

A heterozygous mutation of beta-actin associated with neutrophil dysfunction and recurrent infection

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7 January 2021

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

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7 January 2021

Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy

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7 January 2021

Regulation of differentiation of vascular smooth muscle cells

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7 January 2021

ZBP2 facilitates binding of ZBP1 to beta-actin mRNA during transcription

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7 January 2021

Molecular control of neuronal migration

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7 January 2021

Structural and dynamic states of actin in the erythrocyte

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7 January 2021

Genomics, the cytoskeleton and motility.

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7 January 2021

Skeletal muscle-specific ablation of gamma(cyto)-actin does not exacerbate the mdx phenotype

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7 January 2021

A mutation of beta -actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia

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7 January 2021

Rho proteins, mental retardation and the cellular basis of cognition

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7 January 2021

A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.

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7 January 2021

A method for rapidly screening functionality of actin mutants and tagged actins

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7 January 2021

Expression of actin mutants to study their roles in cardiomyopathy

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7 January 2021

Sequential activation of alpha-actin genes during avian cardiogenesis: vascular smooth muscle alpha-actin gene transcripts mark the onset of cardiomyocyte differentiation

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7 January 2021

The dystrophin complex forms a mechanically strong link between the sarcolemma and costameric actin

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7 January 2021

Clinical and genetic heterogeneity in nemaline myopathy--a disease of skeletal muscle thin filaments

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7 January 2021

Skeletal muscle repair in a mouse model of nemaline myopathy

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7 January 2021

Cellular distribution of smooth muscle actins during mammalian embryogenesis: expression of the alpha-vascular but not the gamma-enteric isoform in differentiating striated myocytes

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7 January 2021

A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathy

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7 January 2021

Impaired vascular contractility and blood pressure homeostasis in the smooth muscle alpha-actin null mouse

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7 January 2021

Gene switching in myogenesis: differential expression of the chicken actin multigene family

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7 January 2021

Restricted beta-galactosidase expression of a hygromycin-lacZ gene targeted to the beta-actin locus and embryonic lethality of beta-actin mutant mice.

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7 January 2021

The physiological significance of beta -actin mRNA localization in determining cell polarity and directional motility

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7 January 2021

Strong and ubiquitous expression of transgenes targeted into the beta-actin locus by Cre/lox cassette replacement.

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7 January 2021

Cytoplasmic gamma-actin is not required for skeletal muscle development but its absence leads to a progressive myopathy

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7 January 2021

Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1).

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7 January 2021

Transient production of alpha-smooth muscle actin by skeletal myoblasts during differentiation in culture and following intramuscular implantation

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7 January 2021

Distal transgene insertion affects CpG island maintenance during differentiation.

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7 January 2021

α-Actin isoform distribution in normal and failing human heart: a morphological, morphometric, and biochemical study

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7 January 2021

Urogenital tract expression of enhanced green fluorescent protein in transgenic mice driven by a smooth muscle gamma-actin promoter

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7 January 2021

Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy

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7 January 2021

Deficient polymerization in vitro of a point-mutated beta-actin expressed in a transformed human fibroblast cell line

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7 January 2021

Quantitative changes in cytoskeletal beta- and gamma-actin mRNAs and apparent absence of sarcomeric actin gene transcripts in early mouse embryos

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7 January 2021

Activity-Dependent Trafficking and Dynamic Localization of Zipcode Binding Protein 1 and β-Actin mRNA in Dendrites and Spines of Hippocampal Neurons

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7 January 2021

Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy.

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7 January 2021

A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)

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7 January 2021

alpha-Skeletal muscle actin mutants causing different congenital myopathies induce similar cytoskeletal defects in cell line cultures

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7 January 2021

At least six different actins are expressed in a higher mammal: an analysis based on the amino acid sequence of the amino-terminal tryptic peptide

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7 January 2021

Chordate muscle actins differ distinctly from invertebrate muscle actins. The evolution of the different vertebrate muscle actins

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7 January 2021

Dominant negative effect of cytoplasmic actin isoproteins on cardiomyocyte cytoarchitecture and function

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7 January 2021

138th ENMC Workshop: nemaline myopathy, 20-22 May 2005, Naarden, The Netherlands

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7 January 2021

Interaction of thymosin beta 4 with muscle and platelet actin: implications for actin sequestration in resting platelets

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7 January 2021

Identification and distribution of actin in spermatogenic cells and spermatozoa of the rabbit

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7 January 2021

Nebulin regulates thin filament length, contractility, and Z-disk structure in vivo

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7 January 2021

Alpha-smooth muscle actin is transiently expressed in embryonic rat cardiac and skeletal muscles

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7 January 2021

Neurotrophin-induced transport of a beta-actin mRNP complex increases beta-actin levels and stimulates growth cone motility.

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7 January 2021

Macrophage colony-stimulating factor expression in retrovirally transduced cells is dependent upon both the adherence status of the target cells and its 5' flanking untranslated region.

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7 January 2021

Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).

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7 January 2021

Identifiers

DOI

10.1002/CM.20350

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20 August 2017

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