Related references
Note: Only part of the references are listed.Filamin C variants are associated with a distinctive clinical and immunohistochemical arrhythmogenic cardiomyopathy phenotype
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EMBO JOURNAL (2007)
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HUMAN MOLECULAR GENETICS (2007)
Filamin B deficiency in mice results in skeletal malformations and impaired microvascular development
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Mutations in the gene encoding filamin A as a cause for familial cardiac valvular dystrophy
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Filamin A (FLNA) is required for cell-cell contact in vascular development and cardiac morphogenesis
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Expression of distinct classes of titin isoforms in striated and smooth muscles by alternative splicing, and their conserved interaction with filamins
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JOURNAL OF MOLECULAR BIOLOGY (2006)
Loss of FilaminC (FLNc) results in severe defects in myogenesis and myotube structure
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MOLECULAR AND CELLULAR BIOLOGY (2006)
Unusual splicing events result in distinct Xin isoforms that associate differentially with filamin c and Mena/VASP
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The ubiquitin-specific protease USP25 interacts with three sarcomeric proteins
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Calpain 1-gamma filamin interaction in muscle cells: A possible in situ regulation by PKC-alpha (vol 37, pg 404, 2006)
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INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2006)
Ca2+ and calmodulin regulate the binding of filamin A to actin filaments
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JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
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M Vorgerd et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
An alliance between Ras GTPase-activating protein, filamin C, and Ras GTPase-activating protein SH3 domain-binding protein regulates myocyte growth
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JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
G protein-coupled receptor kinase regulates dopamine D3 receptor signaling by modulating the stability of a receptor-filamin-β-arrestin complex -: A case of autoreceptor regulation
KM Kim et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Mutations in ZASP define a novel form of muscular dystrophy in humans
D Selcen et al.
ANNALS OF NEUROLOGY (2005)
Evidence for myofibril remodeling as opposed to myofibril damage in human muscles with DOMS: an ultrastructural and immunoelectron microscopic study
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HISTOCHEMISTRY AND CELL BIOLOGY (2004)
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BIOCHEMICAL JOURNAL (2004)
Filamin C interacts with the muscular dystrophy KY protein and is abnormally distributed in mouse KY deficient muscle fibres
J Beatham et al.
HUMAN MOLECULAR GENETICS (2004)
Calpain 3 cleaves filamin C and regulates its ability to interact with γ- and δ-sarcoglycans
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MUSCLE & NERVE (2003)
The F-actin cross-linking and focal adhesion protein filamin A is a ligand and in vivo substrate for protein kinase Cα
U Tigges et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
New N-RAP-binding partners α-actinin, filamin and Krp1 detected by yeast two-hybrid screening:: implications for myofibril assembly
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JOURNAL OF CELL SCIENCE (2003)
The mode of myofibril remodelling in human skeletal muscle affected by DOMS induced by eccentric contractions
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Migfilin and Mig-2 link focal adhesions to filamin and the actin cytoskeleton and function in cell shape modulation
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JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
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HUMAN MOLECULAR GENETICS (2002)
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JOURNAL OF CELL SCIENCE (2002)
Calsarcin-3, a novel skeletal muscle-specific member of the calsarcin family, interacts with multiple Z-disc proteins
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Different splice variants of filamin-B affect myogenesis, subcellular distribution, and determine binding to integrin β subunits
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JOURNAL OF CELL BIOLOGY (2002)
The SH2-containing inositol polyphosphate 5-phosphatase, SHIP-2, binds filamin and regulates submembraneous actin
JM Dyson et al.
JOURNAL OF CELL BIOLOGY (2001)
Myozenin:: An α-actinin- and γ-filamin-binding protein of skeletal muscle Z lines
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
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NATURE REVIEWS MOLECULAR CELL BIOLOGY (2001)
FATZ, a filamin-, actinin-, and telethonin-binding protein of the Z-disc of skeletal muscle
G Faulkner et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Genomic structure and fine mapping of the two human filamin gene paralogues FLNB and FLNC and comparative analysis of the filamin gene family
C Chakarova et al.
HUMAN GENETICS (2000)
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PFM van der Ven et al.
JOURNAL OF CELL BIOLOGY (2000)
Filamin 2 (FLN2): A muscle-specific sarcoglycan interacting protein
TG Thompson et al.
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Myotilin is mutated in limb girdle muscular dystrophy 1A
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