Myofibrillar instability exacerbated by acute exercise in filaminopathy.
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U. Schlötzer-Schrehardt | W. Linke | M. Vorgerd | J. Schuld | Z. Orfanos | R. Kley | K. Marcus | A. Unger | S. von Hörsten | R. Schröder | A. Maerkens | F. Chevessier | Lucie M Wolf | P. V. D. van der Ven | Anne-Christine Plank | D. Fürst | Lucie Wolf
[1] W. Rottbauer,et al. The toxic effect of R350P mutant desmin in striated muscle of man and mouse , 2014, Acta Neuropathologica.
[2] X. Puente,et al. Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy , 2014, Nature Communications.
[3] O. Riess,et al. Automated phenotyping and advanced data mining exemplified in rats transgenic for Huntington's disease , 2014, Journal of Neuroscience Methods.
[4] W. Rottbauer,et al. Aciculin interacts with filamin C and Xin and is essential for myofibril assembly, remodeling and maintenance , 2014, Journal of Cell Science.
[5] M. Wilmanns,et al. Identification of Xin-repeat proteins as novel ligands of the SH3 domains of nebulin and nebulette and analysis of their interaction during myofibril formation and remodeling , 2013, Molecular biology of the cell.
[6] P. Saftig,et al. Cellular Mechanotransduction Relies on Tension-Induced and Chaperone-Assisted Autophagy , 2013, Current Biology.
[7] Christian Stephan,et al. A Combined Laser Microdissection and Mass Spectrometry Approach Reveals New Disease Relevant Proteins Accumulating in Aggregates of Filaminopathy Patients* , 2012, Molecular & Cellular Proteomics.
[8] R. Bryson-Richardson,et al. Characterization and investigation of zebrafish models of filamin-related myofibrillar myopathy. , 2012, Human molecular genetics.
[9] I. Ferrer,et al. Pathophysiology of protein aggregation and extended phenotyping in filaminopathy. , 2012, Brain : a journal of neurology.
[10] Hanns Lochmüller,et al. Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency , 2011, Neurology.
[11] K. Reymann,et al. Selective Hippocampal Neurodegeneration in Transgenic Mice Expressing Small Amounts of Truncated Aβ Is Induced by Pyroglutamate–Aβ Formation , 2011, The Journal of Neuroscience.
[12] J. Armstrong,et al. Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathy , 2011, Neuromuscular Disorders.
[13] Robert H. Brown,et al. Mutations in the N-terminal actin-binding domain of filamin C cause a distal myopathy. , 2011, American journal of human genetics.
[14] E. Kordeli,et al. Novel interactions of ankyrins-G at the costameres: the muscle-specific Obscurin/Titin-Binding-related Domain (OTBD) binds plectin and filamin C. , 2011, Experimental cell research.
[15] R. Kley,et al. The sarcomeric Z-disc component myopodin is a multiadapter protein that interacts with filamin and alpha-actinin. , 2010, European journal of cell biology.
[16] Wei Zhang,et al. 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 , 2010, Neuromuscular Disorders.
[17] M. Hoch,et al. Chaperone-Assisted Selective Autophagy Is Essential for Muscle Maintenance , 2010, Current Biology.
[18] B. Schoser,et al. Myofibrillar Myopathies: A Clinical and Myopathological Guide , 2009, Brain pathology.
[19] I. Ferrer,et al. In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy , 2009, European Journal of Human Genetics.
[20] K. Claeys,et al. Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study , 2009, Acta Neuropathologica.
[21] D. Selcen. Myofibrillar myopathies , 2008, Current opinion in neurology.
[22] A. Saltiel,et al. Identification of CAP as a costameric protein that interacts with filamin C. , 2007, Molecular biology of the cell.
[23] C. Heyer,et al. Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients. , 2007, Brain : a journal of neurology.
[24] M. Vorgerd,et al. The pathomechanism of filaminopathy: altered biochemical properties explain the cellular phenotype of a protein aggregation myopathy. , 2007, Human molecular genetics.
[25] O. Carpén,et al. Myotilin – a prominent marker of myofibrillar remodelling , 2007, Neuromuscular Disorders.
[26] L. Kunkel,et al. Loss of FilaminC (FLNc) Results in Severe Defects in Myogenesis and Myotube Structure , 2006, Molecular and Cellular Biology.
[27] T. Holak,et al. Filamins: promiscuous organizers of the cytoskeleton. , 2006, Trends in biochemical sciences.
[28] S. Robertson,et al. Mutations in two regions of FLNB result in atelosteogenesis I and III , 2006, Human mutation.
[29] S. Robertson,et al. A molecular and clinical study of Larsen syndrome caused by mutations in FLNB , 2006, Journal of Medical Genetics.
[30] A. Sonnenberg,et al. The Z-disc proteins myotilin and FATZ-1 interact with each other and are connected to the sarcolemma via muscle-specific filamins , 2005, Journal of Cell Science.
[31] Hanns Lochmüller,et al. A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy. , 2005, American journal of human genetics.
[32] Ana Maria Cuervo,et al. Protein degradation and aging , 2005, Experimental Gerontology.
[33] Ana Maria Cuervo,et al. Autophagy and Aging: The Importance of Maintaining "Clean" Cells , 2005, Autophagy.
[34] S. Robertson. Filamin A: phenotypic diversity. , 2005, Current opinion in genetics & development.
[35] C. Walsh,et al. The many faces of filamin: A versatile molecular scaffold for cell motility and signalling , 2004, Nature Cell Biology.
[36] I. Marty,et al. Tubular aggregates are from whole sarcoplasmic reticulum origin: alterations in calcium binding protein expression in mouse skeletal muscle during aging , 2004, Neuromuscular Disorders.
[37] L. Thornell,et al. Evidence for myofibril remodeling as opposed to myofibril damage in human muscles with DOMS: an ultrastructural and immunoelectron microscopic study , 2004, Histochemistry and Cell Biology.
[38] R. Demir,et al. Localization of vascular endothelial growth factor in the zona pellucida of developing ovarian follicles in the rat: a possible role in destiny of follicles , 2003, Histochemistry and Cell Biology.
[39] L. Thornell,et al. The mode of myofibril remodelling in human skeletal muscle affected by DOMS induced by eccentric contractions , 2003, Histochemistry and Cell Biology.
[40] Walter Stöcklein,et al. The limits of promiscuity: isoform-specific dimerization of filamins. , 2003, Biochemistry.
[41] L. Thornell,et al. Desmin and actin alterations in human muscles affected by delayed onset muscle soreness: a high resolution immunocytochemical study , 2002, Histochemistry and Cell Biology.
[42] E. Olson,et al. Calsarcin-3, a Novel Skeletal Muscle-specific Member of the Calsarcin Family, Interacts with Multiple Z-disc Proteins* , 2002, The Journal of Biological Chemistry.
[43] G. Kirfel,et al. The biological role of the Alzheimer amyloid precursor protein in epithelial cells , 2002, Histochemistry and Cell Biology.
[44] U. Proske,et al. Muscle damage from eccentric exercise: mechanism, mechanical signs, adaptation and clinical applications , 2001, The Journal of physiology.
[45] A. Sonnenberg,et al. Structural and functional aspects of filamins. , 2001, Biochimica et biophysica acta.
[46] L. Kunkel,et al. Myozenin: An α-actinin- and γ-filamin-binding protein of skeletal muscle Z lines , 2001 .
[47] J. Hartwig,et al. Filamins as integrators of cell mechanics and signalling , 2001, Nature Reviews Molecular Cell Biology.
[48] G. Lanfranchi,et al. FATZ, a Filamin-, Actinin-, and Telethonin-binding Protein of the Z-disc of Skeletal Muscle* , 2000, The Journal of Biological Chemistry.
[49] G. Butler-Browne,et al. Age-related appearance of tubular aggregates in the skeletal muscle of almost all male inbred mice , 2000, Histochemistry and Cell Biology.
[50] D. McDonald,et al. Shear stress-induced upregulation of connexin 43 expression in endothelial cells on upstream surfaces of rat cardiac valves , 2000, Histochemistry and Cell Biology.
[51] S. Kempa,et al. Indications for a Novel Muscular Dystrophy Pathway , 2000, Journal of Cell Biology.
[52] Simon C Watkins,et al. Filamin 2 (FLN2): A Muscle-specific Sarcoglycan Interacting Protein , 2000 .
[53] M. Tarnopolsky,et al. Changes in human skeletal muscle ultrastructure and force production after acute resistance exercise. , 1995, Journal of applied physiology.
[54] R. Armstrong,et al. Lesions in the rat soleus muscle following eccentrically biased exercise. , 1988, The American journal of anatomy.
[55] J. Fridén. Muscle Soreness After Exercise: Implications of Morphological Changes , 1984, International journal of sports medicine.
[56] K. R. Mills,et al. Ultrastructural changes after concentric and eccentric contractions of human muscle , 1983, Journal of the Neurological Sciences.
[57] M. Sjöström,et al. Myofibrillar Damage Following Intense Eccentric Exercise in Man , 1983, International journal of sports medicine.
[58] M. Sjöström,et al. A morphological study of delayed muscle soreness , 1981, Experientia.
[59] H. Meltzer,et al. Incidence of Z band streaming and myofibrillar disruptions in skeletal muscle from healthy young people , 1976, Neurology.
[60] M. Vorgerd,et al. Filamin C-related myopathies: pathology and mechanisms , 2012, Acta Neuropathologica.
[61] I. Nonaka,et al. Filamin C plays an essential role in the maintenance of the structural integrity of cardiac and skeletal muscles, revealed by the medaka mutant zacro. , 2012, Developmental biology.
[62] R. Fitts,et al. Five myofibrillar lesion types in eccentrically challenged, unloaded rat adductor longus muscle—a test model , 1999, The Anatomical record.
[63] Rappold,et al. Human Molecular Genetics , 1996, Nature Medicine.
[64] R. Armstrong,et al. Eccentric exercise-induced injury to rat skeletal muscle. , 1983, Journal of applied physiology: respiratory, environmental and exercise physiology.