Filamin C plays an essential role in the maintenance of the structural integrity of cardiac and skeletal muscles, revealed by the medaka mutant zacro. (Q48220223)

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scientific article published on 14 October 2011

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English	Filamin C plays an essential role in the maintenance of the structural integrity of cardiac and skeletal muscles, revealed by the medaka mutant zacro.	scientific article published on 14 October 2011

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15 January 2020

Filamin C plays an essential role in the maintenance of the structural integrity of cardiac and skeletal muscles, revealed by the medaka mutant zacro (English)

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Hiroaki Mitsuhashi

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Sumio Isogai

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Takahiro Nakata

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Atsushi Kawakami

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Ikuya Nonaka

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Satoru Noguchi

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Yukiko K Hayashi

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Developmental Biology

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Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide

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Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo

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Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

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Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

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Delta-sarcoglycan is necessary for early heart and muscle development in zebrafish

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Cytoprotection against mechanical forces delivered through beta 1 integrins requires induction of filamin A.

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Loss of FilaminC (FLNc) results in severe defects in myogenesis and myotube structure

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Mutations in the N-terminal actin-binding domain of filamin C cause a distal myopathy

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Costameres: the Achilles' heel of Herculean muscle

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FATZ, a filamin-, actinin-, and telethonin-binding protein of the Z-disc of skeletal muscle

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The many faces of filamin: a versatile molecular scaffold for cell motility and signalling

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The Z-disc proteins myotilin and FATZ-1 interact with each other and are connected to the sarcolemma via muscle-specific filamins

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The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathies

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7 January 2021

Delta-sarcoglycan is required for early zebrafish muscle organization

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7 January 2021

Modeling human muscle disease in zebrafish

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Mutations in the integrin alpha7 gene cause congenital myopathy

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Dystrophin: the protein product of the Duchenne muscular dystrophy locus

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Temporal and spatial patterns of gene expression for the hatching enzyme in the teleost embryo, Oryzias latipes.

1 reference

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Analysis of the origin and development of hatching gland cells by transplantation of the embryonic shield in the fish, Oryzias latipes.

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Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency.

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A recessive lethal mutation, tb, that bends the midbrain region of the neural tube in the early embryo of the medaka.

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Stages of normal development in the medaka Oryzias latipes

1 reference

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7 January 2021

Cell death and mechanoprotection by filamin a in connective tissues after challenge by applied tensile forces

1 reference

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7 January 2021

Large-scale isolation of ESTs from medaka embryos and its application to medaka developmental genetics.

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7 January 2021

Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients

1 reference

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7 January 2021

Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis

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β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

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7 January 2021

The sarcomeric Z-disc component myopodin is a multiadapter protein that interacts with filamin and alpha-actinin

1 reference

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7 January 2021

Filamin binds to the cytoplasmic domain of the beta1-integrin. Identification of amino acids responsible for this interaction

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The pathomechanism of filaminopathy: altered biochemical properties explain the cellular phenotype of a protein aggregation myopathy

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A novel heterozygous deletion-insertion mutation (2695-2712 del/GTTTGT ins) in exon 18 of the filamin C gene causes filaminopathy in a large Chinese family.

1 reference

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Integrins: redundant or important players in skeletal muscle?

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Absence of integrin alpha 7 causes a novel form of muscular dystrophy

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Selective defect of sarcoglycan complex in severe childhood autosomal recessive muscular dystrophy muscle

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Cytoplasmic gamma actin as a Z-disc protein

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Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

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Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

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Chicken gizzard filamin, retina filamin and cgABP260 are respectively, smooth muscle-, non-muscle- and pan-muscle-type isoforms: distribution and localization in muscles.

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Zebrafish integrin-linked kinase is required in skeletal muscles for strengthening the integrin-ECM adhesion complex

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Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

1 reference

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Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans.

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7 January 2021

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

1 reference

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Immunocytochemical study of dystrophin at the myotendinous junction

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Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients

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In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy

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Zebrafish orthologs of human muscular dystrophy genes

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Filamins as integrators of cell mechanics and signalling

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Zebrafish models of collagen VI-related myopathies

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Spatial and temporal expression of the beta1D integrin during mouse development

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1 reference

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Indications for a novel muscular dystrophy pathway. gamma-filamin, the muscle-specific filamin isoform, interacts with myotilin

1 reference

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A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy.

1 reference

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Sex-Linked Inheritance of the lf Locus in the Medaka Fish (Oryzias latipes).

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Immunoelectron microscopic localization of dystrophin in myofibres

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