Absence of dysferlin alters myogenin expression and delays human muscle differentiation "in vitro". - Wikidata - awgldk - TriplyDB

Absence of dysferlin alters myogenin expression and delays human muscle differentiation "in vitro".

Absence of dysferlin alters myogenin expression and delays human muscle differentiation "in vitro".

http://www.wikidata.org/entity/Q52021000

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Fam65b is important for formation of the HDAC6-dysferlin protein complex during myogenic cell differentiation Crystal structures of the human Dysferlin inner DysF domain Focal adhesion kinase signaling regulates the expression of caveolin 3 and beta1 integrin, genes essential for normal myoblast fusion.Bone marrow transplantation in dysferlin-deficient mice results in a mild functional improvement.Dysferlin regulates cell membrane repair by facilitating injury-triggered acid sphingomyelinase secretion.Dysferlin interacts with histone deacetylase 6 and increases alpha-tubulin acetylation Myogenesis in dysferlin-deficient myoblasts is inhibited by an intrinsic inflammatory response.Proteasomal inhibition restores biological function of mis-sense mutated dysferlin in patient-derived muscle cells.Dysferlin-deficient immortalized human myoblasts and myotubes as a useful tool to study dysferlinopathy.New aspects on patients affected by dysferlin deficient muscular dystrophy Genetic ablation of complement C3 attenuates muscle pathology in dysferlin-deficient mice While dysferlin and myoferlin are coexpressed in the human placenta, only dysferlin expression is responsive to trophoblast fusion in model systems.Upregulated IL-1β in dysferlin-deficient muscle attenuates regeneration by blunting the response to pro-inflammatory macrophages Dysferlin and muscle membrane repair.1α,25(OH)(2)-Vitamin D3 increases dysferlin expression in vitro and in a human clinical trial.Membrane fusion in muscle development and repair.Sp1 transcription factor interaction with accumulated prelamin a impairs adipose lineage differentiation in human mesenchymal stem cells: essential role of sp1 in the integrity of lipid vesicles.Attenuated muscle regeneration is a key factor in dysferlin-deficient muscular dystrophy.Placental dysferlin expression is reduced in severe preeclampsia.Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy.Exon 32 Skipping of Dysferlin Rescues Membrane Repair in Patients' Cells Translational research and therapeutic perspectives in dysferlinopathies.Ferlin proteins in myoblast fusion and muscle growth.Molecular diagnosis of muscular dystrophies, focused on limb girdle muscular dystrophies.Dexamethasone induces dysferlin in myoblasts and enhances their myogenic differentiation.Dysferlin overexpression in skeletal muscle produces a progressive myopathy.Altered RIG-I/DDX58-mediated innate immunity in dermatomyositis.Full-length dysferlin expression driven by engineered human dystrophic blood derived CD133+ stem cells.Impaired muscle growth and response to insulin-like growth factor 1 in dysferlin-mediated muscular dystrophy.Reverse engineering gene network identifies new dysferlin-interacting proteins.Dysferlin aggregation in limb-girdle muscular dystrophy type 2B/Miyoshi Myopathy necessitates mutational screen for diagnosis [corrected].The increase of pericyte population in human neuromuscular disorders supports their role in muscle regeneration in vivo.Treatment with Recombinant Human MG53 Protein Increases Membrane Integrity in a Mouse Model of Limb Girdle Muscular Dystrophy 2B.Myoblast fusion confusion: the resolution begins.The susceptibility to experimental autoimmune encephalomyelitis is not related to dysferlin-deficiency.Genetic and epigenetic determinants of low dysferlin expression in monocytes.Role of thrombospondin 1 in macrophage inflammation in dysferlin myopathy.Serum exosomes can restore cellular function in vitro and be used for diagnosis in dysferlinopathy.Landscape of alternative splicing in Capra_hircus

P2860

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P2860

Absence of dysferlin alters myogenin expression and delays human muscle differentiation "in vitro".

http://www.wikidata.org/entity/Q52021000

description

2006 nî lūn-bûn

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Absence of dysferlin alters my ...... le differentiation "in vitro".

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Absence of dysferlin alters my ...... le differentiation "in vitro".

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Absence of dysferlin alters my ...... le differentiation "in vitro".

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P2093

Carolina de la Torre

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Isabel Illa

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Mario Soriano

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Noemí de Luna

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Raúl Dominguez-Perles

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Ricardo Rojas-García

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P2860

Calcium-sensitive phospholipid binding properties of normal and mutant ferlin C2 domains

The basic helix-loop-helix transcription factors myogenin and Id2 mediate specific induction of caveolin-3 gene expression during embryonic development

Defective membrane repair in dysferlin-deficient muscular dystrophy

Dysferlin interacts with annexins A1 and A2 and mediates sarcolemmal wound-healing

The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B

Inactivation of the myogenic bHLH gene MRF4 results in up-regulation of myogenin and rib anomalies

Muscle deficiency and neonatal death in mice with a targeted mutation in the myogenin gene

C2-domains, structure and function of a universal Ca2+-binding domain

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17092-17098

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10.1074/JBC.M601885200

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25

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281

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José M García-Verdugo

Eduard Gallardo

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2006-04-11T00:00:00Z

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16608842

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