Plasma Membrane Repair in Health and Disease.

No abstract is available for this paper.

• Publication year

  2016

• Venue

  Current topics in membranes

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/bs.ctm.2015.10.006PMID 26781830PMCID PMC4827257
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Cardioprotection of recombinant human MG53 protein in a porcine model of ischemia and reperfusion injury.

  2015cited by this paper
• MG53-mediated cell membrane repair protects against acute kidney injury

  2015cited by this paper
• Annexin-A5 promotes membrane resealing in human trophoblasts.

  2015cited by this paper
• Poloxomer 188 Has a Deleterious Effect on Dystrophic Skeletal Muscle Function

  2014cited by this paper
• Rapid actin‐cytoskeleton–dependent recruitment of plasma membrane–derived dysferlin at wounds is critical for muscle membrane repair

  2014cited by this paper
• Treatment of acute lung injury by targeting MG53-mediated cell membrane repair

  2014cited by this paper
• Dysferlin and myoferlin regulate transverse tubule formation and glycerol sensitivity.

  2014cited by this paper
• GRAF1 promotes ferlin-dependent myoblast fusion.

  2014cited by this paper
• Dystrophin complex functions as a scaffold for signalling proteins.

  2014cited by this paper
• Annexin A6 modifies muscular dystrophy by mediating sarcolemmal repair

  2014cited by this paper
• EHD1 mediates vesicle trafficking required for normal muscle growth and transverse tubule development.

  2014cited by this paper
• Structure and function of TMEM16 proteins (anoctamins).

  2014cited by this paper
• S100A11 is required for efficient plasma membrane repair and survival of invasive cancer cells

  2014cited by this paper
• Caveolae internalization repairs wounded cells and muscle fibers

  2013cited by this paper
• Calcium-dependent Phospholipid Scramblase Activity of TMEM16 Protein Family Members*

  2013cited by this paper
• Dysferlin interacts with calsequestrin-1, myomesin-2 and dynein in human skeletal muscle.

  2013cited by this paper
• The Phenotype of Dysferlin-Deficient Mice Is Not Rescued by Adeno-Associated Virus–Mediated Transfer of Anoctamin 5

  2013cited by this paper
• Dysferlin stabilizes stress-induced Ca2+ signaling in the transverse tubule membrane

  2013cited by this paper
• Expression of myoferlin in human and murine carcinoma tumors: role in membrane repair, cell proliferation, and tumorigenesis.

  2013cited by this paper
• Differential regulation of EHD3 in human and mammalian heart failure.

  2012cited by this paper
• In vivo imaging of molecular interactions at damaged sarcolemma.

  2012cited by this paper
• The C2A domain in dysferlin is important for association with MG53 (TRIM72)

  2012cited by this paper
• A novel missense mutation in ANO5/TMEM16E is causative for gnathodiaphyseal dyplasia in a large Italian pedigree

  2012cited by this paper
• Lack of Correlation between Outcomes of Membrane Repair Assay and Correction of Dystrophic Changes in Experimental Therapeutic Strategy in Dysferlinopathy

  2012cited by this paper
• Ferlins: Regulators of Vesicle Fusion for Auditory Neurotransmission, Receptor Trafficking and Membrane Repair

  2012cited by this paper
• Recombinant MG53 Protein Modulates Therapeutic Cell Membrane Repair in Treatment of Muscular Dystrophy

  2012cited by this paper
• Enhancing muscle membrane repair by gene delivery of MG53 ameliorates muscular dystrophy and heart failure in δ-Sarcoglycan-deficient hamsters.

  2012cited by this paper
• Sarcolemmal Repair Is a Slow Process and Includes EHD2

  2012cited by this paper
• EHD proteins: key conductors of endocytic transport.

  2011cited by this paper
• Membrane Sealant Poloxamer P188 Protects Against Isoproterenol Induced Cardiomyopathy in Dystrophin Deficient Mice

  2011cited by this paper
• Physiological and histological changes in skeletal muscle following in vivo gene transfer by electroporation

  2011cited by this paper
• Annexin-A5 assembled into two-dimensional arrays promotes cell membrane repair

  2011cited by this paper
• Blebbing confers resistance against cell lysis

  2011cited by this paper
• Skeletal Muscle Differentiation and Fusion Are Regulated by the BAR-containing Rho-GTPase-activating Protein (Rho-GAP), GRAF1*

  2011cited by this paper
• Impaired muscle growth and response to insulin-like growth factor 1 in dysferlin-mediated muscular dystrophy.

  2011cited by this paper
• A new distal myopathy with mutation in anoctamin 5.

  2010cited by this paper
• Myoferlin regulation by NFAT in muscle injury, regeneration and repair

  2010cited by this paper
• Endocytic Recycling Proteins EHD1 and EHD2 Interact with Fer-1-like-5 (Fer1L5) and Mediate Myoblast Fusion*

  2010cited by this paper
• Dysferlin associates with the developing T‐tubule system in rodent and human skeletal muscle

  2010cited by this paper
• Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies.

  2010cited by this paper
• The endocytic recycling regulator EHD1 is essential for spermatogenesis and male fertility in mice

  2010cited by this paper
• Myoferlin is required for insulin‐like growth factor response and muscle growth

  2010cited by this paper
• Genetic background affects properties of satellite cells and mdx phenotypes.

  2010cited by this paper
• Efficient recovery of dysferlin deficiency by dual adeno-associated vector-mediated gene transfer.

  2010cited by this paper
• Chronic administration of membrane sealant prevents severe cardiac injury and ventricular dilatation in dystrophic dogs.

  2010cited by this paper
• Annexin-A6 presents two modes of association with phospholipid membranes. A combined QCM-D, AFM and cryo-TEM study.

  2009cited by this paper
• Characterization of lipid binding specificities of dysferlin C2 domains reveals novel interactions with phosphoinositides.

  2009cited by this paper
• MG53 nucleates assembly of cell membrane repair machinery

  2009cited by this paper
• Loss of TMEM16A Causes a Defect in Epithelial Ca2+-dependent Chloride Transport*

  2009cited by this paper
• Membrane Repair Defects in Muscular Dystrophy Are Linked to Altered Interaction between MG53, Caveolin-3, and Dysferlin*◆

  2009cited by this paper
• Integration of single and multicellular wound responses.

  2009cited by this paper
• ANO2 is the cilial calcium-activated chloride channel that may mediate olfactory amplification

  2009cited by this paper
• DNA transfection of mammalian skeletal muscles using in vivo electroporation.

  2009cited by this paper
• Genetic manipulation of dysferlin expression in skeletal muscle: novel insights into muscular dystrophy.

  2009cited by this paper
• Annexin A1 Regulates Intestinal Mucosal Injury, Inflammation, and Repair1

  2008cited by this paper
• Mechanisms of EHD/RME‐1 Protein Function in Endocytic Transport

  2008cited by this paper
• The GTPase-Activating Protein GRAF1 Regulates the CLIC/GEEC Endocytic Pathway

  2008cited by this paper
• The Endocytic Recycling Protein EHD2 Interacts with Myoferlin to Regulate Myoblast Fusion*

  2008cited by this paper
• Heterogeneity and timing of translocation and membrane-mediated assembly of different annexins.

  2008cited by this paper
• EHD1 and Eps15 Interact with Phosphatidylinositols via Their Eps15 Homology Domains*

  2007cited by this paper
• Shared as well as distinct roles of EHD proteins revealed by biochemical and functional comparisons in mammalian cells and C. elegans

  2007cited by this paper
• Molecular characterization of GDD1/TMEM16E, the gene product responsible for autosomal dominant gnathodiaphyseal dysplasia.

  2007cited by this paper
• Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes.

  2007cited by this paper
• Recycling to the Plasma Membrane is Delayed in EHD1 Knockout Mice

  2006cited by this paper
• Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse.

  2006cited by this paper
• Requirement for Annexin A1 in Plasma Membrane Repair*

  2006cited by this paper
• Regulation of actin dynamics by annexin 2

  2006cited by this paper
• Annexin A5 polymorphism (−1C→T) and the presence of anti-annexin A5 antibodies in the antiphospholipid syndrome

  2006cited by this paper
• Genetic background influences muscular dystrophy.

  2005cited by this paper
• TRIM/RBCC, a novel class of ‘single protein RING finger’ E3 ubiquitin ligases

  2005cited by this paper
• Molecular cloning and characterization of the murine gnathodiaphyseal dysplasia gene GDD1.

  2005cited by this paper
• An emergency response team for membrane repair

  2005cited by this paper
• Annexins: linking Ca2+ signalling to membrane dynamics

  2005cited by this paper
• Dystrophic heart failure blocked by membrane sealant poloxamer

  2005cited by this paper
• Normal myoblast fusion requires myoferlin

  2005cited by this paper
• Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophies

  2005cited by this paper
• Annexin II regulates fibrin homeostasis and neoangiogenesis in vivo.

  2004cited by this paper
• Annexin 2 Binding to Phosphatidylinositol 4,5-Bisphosphate on Endocytic Vesicles Is Regulated by the Stress Response Pathway*

  2004cited by this paper
• An Annexin 2 Phosphorylation Switch Mediates p11-dependent Translocation of Annexin 2 to the Cell Surface*

  2004cited by this paper
• Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency.

  2004cited by this paper
• [A patient with limb girdle muscular dystrophy type 2B (LGMD2B) manifesting cardiomyopathy].

  2004cited by this paper
• Dysferlin and the plasma membrane repair in muscular dystrophy.

  2004cited by this paper
• Dysferlin Interacts with Annexins A1 and A2 and Mediates Sarcolemmal Wound-healing*

  2003cited by this paper
• Defective membrane repair in dysferlin-deficient muscular dystrophy

  2003cited by this paper
• Impaired membrane resealing and autoimmune myositis in synaptotagmin VII–deficient mice

  2003cited by this paper
• Dysferlin expression in tubular aggregates: their possible relationship to endoplasmic reticulum stress

  2003cited by this paper
• Amphiphysin 2 (Bin1) and T-Tubule Biogenesis in Muscle

  2002cited by this paper
• Direct observation of poloxamer 188 insertion into lipid monolayers.

  2002cited by this paper
• Annexins: from structure to function.

  2002cited by this paper
• Calcium-sensitive Phospholipid Binding Properties of Normal and Mutant Ferlin C2 Domains*

  2002cited by this paper
• Plasma membrane repair is mediated by Ca(2+)-regulated exocytosis of lysosomes.

  2001cited by this paper
• Amphiphilic, tri‐block copolymers provide potent, membrane‐targeted neuroprotection

  2001cited by this paper
• Phosphorylation mutants elucidate the mechanism of annexin IV-mediated membrane aggregation.

  2001cited by this paper
• EHD2, EHD3, and EHD4 encode novel members of a highly conserved family of EH domain-containing proteins.

  2000cited by this paper
• Differential requirement for individual sarcoglycans and dystrophin in the assembly and function of the dystrophin-glycoprotein complex.

  2000cited by this paper
• Intracellular accumulation and reduced sarcolemmal expression of dysferlin in limb–girdle muscular dystrophies

  2000cited by this paper
• Immunological Development and Cardiovascular Function Are Normal in Annexin VI Null Mutant Mice

  1999cited by this paper
• Wound-induced assembly and closure of an actomyosin purse string in Xenopus oocytes.

  1999cited by this paper
• Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B

  1999cited by this paper
• A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B

  1998cited by this paper

• Determinantes de elevación de troponina T cardiaca de alta sensibilidad posterior al cierre percutáneo de una comunicación interauricular

  2025cites this paper
• Phosphoinositides in membrane remodeling during infections and cellular stresses.

  2025cites this paper
• Dysferlin and the Regulation of Ca2+ Release in Skeletal Muscle

  2025cites this paper
• The Role of Skeletal Muscle in Amyotrophic Lateral Sclerosis: State of the Art 2025

  2025cites this paper
• MG53 Protein-Mediated biomimetic nanotherapeutics for the treatment of acute myocardial infarction by driving the impaired plasma membrane resealing

  2024cites this paper
• Prkd1 regulates the formation and repair of plasma membrane disruptions (PMD) in osteocytes.

  2024cites this paper
• Nanodysferlins support membrane repair and binding to TRIM72/MG53 but do not localize to t-tubules or stabilize Ca2+ signaling

  2024cites this paper
• MG53/TRIM72: multi-organ repair protein and beyond

  2024cites this paper
• Syntaxin 4-enhanced plasma membrane repair isindependent of dysferlin in skeletal muscle.

  2024cites this paper
• Muscle regeneration and muscle stem cells in metabolic disease.

  2024cites this paper
• Critical role of PCYT2 in muscle health and aging

  2023cites this paper
• Influence of DUX4 Expression in Facioscapulohumeral Muscular Dystrophy and Possible Treatments

  2023cites this paper
• Annexin A6 mediates calcium-dependent exosome secretion during plasma membrane repair

  2023cites this paper
• PCYT2-regulated lipid biosynthesis is critical to muscle health and ageing

  2023cites this paper
• Enteropathogenic E. coli infection co-elicits lysosomal exocytosis and lytic host cell death

  2023cites this paper
• Regenerating Myofibers after an Acute Muscle Injury: What Do We Really Know about Them?

  2023cites this paper
• Muscle is a stage, and cells and factors are merely players.

  2022cites this paper
• A conserved annexin A6–mediated membrane repair mechanism in muscle, heart, and nerve

  2022cites this paper
• Elevated Ca2+ at the triad junction underlies dysregulation of Ca2+ signaling in dysferlin-null skeletal muscle

  2022cites this paper
• Deficient Sarcolemma Repair in ALS: A Novel Mechanism with Therapeutic Potential

  2022cites this paper
• usEP Effects on the Endoplasmic Reticulum (ER)

  2021cites this paper
• Valor Prognóstico de Níveis Elevados de Troponina I Isolados em Pacientes sem Síndrome Coronariana Aguda Admitidos no Serviço de Emergência

  2021cites this paper
• Histopathology of Duchenne muscular dystrophy in correlation with changes in proteomic biomarkers.

  2021cites this paper
• ANO5 ensures trafficking of annexins in wounded myofibers

  2021cites this paper
• PCYT2 controls muscle health and muscle aging

  2021cites this paper
• The Role of POPDC Proteins in Cardiac Pacemaking and Conduction

  2021cites this paper
• Effects of usEPs on Plasma Membranes—Pores, Channels, and Repair

  2021cites this paper
• Trauma, a Matter of the Heart—Molecular Mechanism of Post-Traumatic Cardiac Dysfunction

  2021cites this paper
• Molecular and cellular basis of genetically inherited skeletal muscle disorders

  2021cites this paper
• Repairing plasma membrane damage in regulated necrotic cell death

  2021cites this paper
• Plasma membrane disruption (PMD) formation and repair in mechanosensitive tissues.

  2021cites this paper
• Sarcolemma wounding activates dynamin‐dependent endocytosis in striated muscle

  2020cites this paper
• Introducing a mammalian nerve-muscle preparation ideal for physiology and microscopy, the transverse auricular muscle in the ear of the mouse.

  2020cites this paper
• Defective Trafficking of Annexins to the Site of Injury in ANO5-Knockout Muscle Fibers

  2020cites this paper
• The effects of a 50 km ultramarathon race on high sensitivity cardiac troponin I and NT-proBNP in highly trained athletes.

  2020cites this paper
• Early evaluation of myocardial injury by means of high-sensitivity methods for cardiac troponins after strenuous and prolonged exercise.

  2020cites this paper
• Annexin A2 Mediates Dysferlin Accumulation and Muscle Cell Membrane Repair

  2020cites this paper
• Ischemia reperfusion injury provokes adverse left ventricular remodeling in dysferlin-deficient hearts through a pathway that involves TIRAP dependent signaling

  2020cites this paper
• Cardiotoxic effects and myocardial injury: the search for a more precise definition of drug cardiotoxicity

  2020cites this paper
• Knockdown of the E3 Ubiquitin ligase UBR5 and its role in skeletal muscle anabolism

  2020cites this paper
• Multi-Cellular Functions of MG53 in Muscle Calcium Signaling and Regeneration

  2020cites this paper
• High-throughput Measurement of Plasma Membrane Resealing Efficiency in Mammalian Cells.

  2019cites this paper
• Multisite Intracellular Recordings by MEA.

  2019cites this paper
• POPDC proteins and cardiac function.

  2019cites this paper
• News about non-secretory exocytosis: mechanisms, properties, and functions

  2019cites this paper
• Recombinant annexin A6 promotes membrane repair and protects against muscle injury.

  2019cites this paper
• Cardiomyocyte damage control in heart failure and the role of the sarcolemma

  2019cites this paper
• Structural and signaling role of lipids in plasma membrane repair.

  2019cites this paper
• Phosphoinositides in the control of lysosome function and homeostasis.

  2019cites this paper
• Differential physiological roles for BIN1 isoforms in skeletal muscle development, function and regeneration

  2018cites this paper
• Intracellular Delivery by Membrane Disruption: Mechanisms, Strategies, and Concepts.

  2018cites this paper
• Mechanism by which dysferlin promotes repair of exercise‐induced skeletal muscie injury in rats

  2018cites this paper
• Massive surface membrane expansion without involvement of classical exocytic mechanisms

  2018cites this paper
• Possible mechanisms behind cardiac troponin elevations

  2018cites this paper
• Membrane Repair Mechanisms against Permeabilization by Pore-Forming Toxins

  2018cites this paper
• Untangling the complexity of limb‐girdle muscular dystrophies

  2018cites this paper
• Cell Membrane Repair Assay Using a Two-photon Laser Microscope.

  2018cites this paper
• Myoferlin regulates epithelial cancer cell plasticity and migration through autocrine TGF-β1 signaling

  2018cites this paper
• How is cardiac troponin released from injured myocardium?

  2018cites this paper
• Annexins: Ca2+ Effectors Determining Membrane Trafficking in the Late Endocytic Compartment.

  2017cites this paper
• Annexin A6 in the liver: From the endocytic compartment to cellular physiology.

  2017cites this paper
• High-Throughput Microplate-Based Assay to Monitor Plasma Membrane Wounding and Repair

  2017cites this paper
• Annexin A2 links poor myofiber repair with inflammation and adipogenic replacement of the injured muscle

  2017cites this paper
• Mitochondrial redox signaling enables repair of injured skeletal muscle cells

  2017cites this paper
• Novel domain architectures and functional determinants in atypical annexins revealed by phylogenomic analysis

  2017cites this paper
• CFTR-mediated anion secretion across intestinal epithelium-like Caco-2 monolayer under PTH stimulation is dependent on intermediate conductance K+ channels.

  2017cites this paper
• Zinc in Wound Healing Modulation

  2017cites this paper