Keywords: دیسفرلین; Membrane integrity; Membrane repair; Muscular dystrophy; Heart failure; Dysferlin; TRIM72/MG53; Dystrophin;
مقالات ISI دیسفرلین (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: دیسفرلین; LGMD; limb girdle muscular dystrophy; CK; creatine kinase levels; MG53; mitsugumin 53; Cx; connexins; TRPV2; transient receptor potential vanilloid type 2; STB; syncytiotrophoblasts; Muscular dystrophies; Dysferlin; Dysferlinopathies; Membrane repair; Ves
Keywords: دیسفرلین; Duchenne muscular dystrophy; Dystrophin; Sarcoglycan; limb-girdle muscular dystrophy; Dysferlin; Dystroglycan;
Keywords: دیسفرلین; Limb-girdle muscular dystrophy; Calpain 3; Dysferlin; Sarcoglycan; Fukutin-related protein; Anoctamin 5; Lamin A/C;
Keywords: دیسفرلین; CALQ1; calsequestrin-1; Cav-3; caveolin-3; DHPR; dihydropyridine receptor; DMD; Duchenne muscular dystrophy; DYNC1LI2; cytoplasmic dynein 1 light intermediate chain 2; FLIM-FRET; fluorescence lifetime imaging-fluorescence resonance energy transfer; FS
Trypanosoma cruzi modulates gene expression of plasma membrane repair-related proteins
Keywords: دیسفرلین; Trypanosoma cruzi; Membrane repair; Dysferlin; Acid sphingomyelinase; Transcriptional factor EB; Gene expression; Host interaction;
Gene co-expression network analysis of dysferlinopathy: Altered cellular processes and functional prediction of TOR1AIP1, a novel muscular dystrophy gene
Keywords: دیسفرلین; Muscle dystrophy; Co-expression; TOR1AIP1; Dysferlin;
Enzymatic cleavage of myoferlin releases a dual C2-domain module linked to ERK signalling
Keywords: دیسفرلین; DOCs; double C2-like-domain-containing proteins; SLPs; synaptotagmin-like proteins; ERK; extracellular-signal-regulated kinase; pERK; phosphorylated ERK; MAPK; mitogen-activated protein kinase; DYSF; dysferlin; MYOF; myoferlin; OTOF; otoferlin; CAPN1; cal
Limb-Girdle Muscular Dystrophy 2B and Miyoshi Presentations of Dysferlinopathy
Keywords: دیسفرلین; Limb girdle muscular dystrophy 2B; Miyoshi myopathy; Dysferlin; Caveolin; Calpain;
Dysferlin mutations and mitochondrial dysfunction
Keywords: دیسفرلین; Dysferlin; Mitochondria; LGMD2B; Immunofluorescence; Histochemistry; Cytochrome c oxidase deficiency;
Regeneration in bipinnaria larvae of the bat star Patiria miniata induces rapid and broad new gene expression
Keywords: دیسفرلین; Vasa; SRAP; Dysferlin; Vitellogenin; Transcription; Repair; Patterning
Dysferlinopathy in Iran: Clinical and genetic report
Keywords: دیسفرلین; Limb girdle muscular dystrophy; Dysferlin; Dysferlinopathy; Iran; Epidemiology; Mutation; Miyoshi disease;
Inhibition of inflammation with celastrol fails to improve muscle function in dysferlin-deficient A/J mice
Keywords: دیسفرلین; Muscular dystrophy; Skeletal muscle; Dysferlin; Celastrol; NF-κB; Inflammation;
Achilles Tendon Lengthening for Equinus Foot with Miyoshi Myopathy: A Case Report
Keywords: دیسفرلین; 4ankle equinus; dysferlin; gastrosoleus equinus; muscular dystrophy; surgery; triceps surae
Anoctamin 5 muscular dystrophy associated with a silent p.Leu115Leu mutation resulting in exon skipping
Keywords: دیسفرلین; Anoctamin 5; Dysferlin; Mutation; Silent mutation; Exon skipping;
Dysferlin is essential for endocytosis in the sea star oocyte
Keywords: دیسفرلین; Dysferlin; Sea star; Plasma membrane; Oocytes; Endocytosis; Gastrulation;
6th Dysferlin Conference, 3-6 April 2013, Arlington, Virginia, USA
Keywords: دیسفرلین; Dysferlin; Muscular dystrophy; Limb girdle muscular dystrophy; LGMD;
AHNAK: The giant jack of all trades
Keywords: دیسفرلین; AHNAK; L-type calcium channel; Dysferlin; Cardiac/skeletal muscle; Cancer; Metastasis;
DYSF mutation analysis in a group of Chinese patients with dysferlinopathy
Keywords: دیسفرلین; Dysferlin; Limb-girdle muscular dystrophy (LGMD); Miyoshi myopathy (MM); Distal myopathy with anterior tibial onste (DMAT); Mutation;
Cloning, expression, and preliminary characterization of the dysferlin tegument protein in Schistosoma japonicum
Keywords: دیسفرلین; Schistosoma japonicum; Dysferlin; Plasma membrane repair;
Muscular dystrophy in dysferlin-deficient mouse models
Keywords: دیسفرلین; Dysferlin; Muscular dystrophy; Mouse models
GREG cells, a dysferlin-deficient myogenic mouse cell line
Keywords: دیسفرلین; Dysferlin; Myoblast; Myotube; Resealing
Dystrophin and dysferlin double mutant mice: a novel model for rhabdomyosarcoma
Keywords: دیسفرلین; Muscular dystrophy; dystrophin; dysferlin; rhabdomyosarcoma; cytogenetics
Absence of T and B lymphocytes modulates dystrophic features in dysferlin deficient animal model
Keywords: دیسفرلین; Dysferlin; Lymphocytes; Scid/A/J mice
Characterization of zebrafish dysferlin by morpholino knockdown
Keywords: دیسفرلین; Dysferlin; Zebrafish; Morpholino;
Proteomic identification of dysferlin-interacting protein complexes in human vascular endothelium
Keywords: دیسفرلین; Dysferlin; Vascular endothelium; Vesicle trafficking; Protein cargo;
Evaluation of commercial dysferlin antibodies on canine, mouse and human skeletal muscle
Keywords: دیسفرلین; Dysferlin; Muscular dystrophy; Immunostaining
The distribution and characterization of skeletal muscle lesions in dysferlin-deficient SJL and A/J mice
Keywords: دیسفرلین; A/J mouse; Dysferlin; ER stress; Macrophages; SJL mouse; XBP1
Dexamethasone induces dysferlin in myoblasts and enhances their myogenic differentiation
Keywords: دیسفرلین; Dysferlinopathy; Limb-girdle muscular dystrophy type 2B; Miyoshi myopathy; Glucocorticoid; Myotube; C2C12; Myoblast differentiation; Dysferlin; Dexamethasone
A new phenotype of dysferlinopathy with congenital onset
Keywords: دیسفرلین; Dysferlin; Congenital muscular dystrophy; LGMD2B
Placental Dysferlin Expression is Reduced in Severe Preeclampsia
Keywords: دیسفرلین; Dysferlin; Myoferlin; Preeclampsia; Placenta
Therapeutic Possibilities in the Autosomal Recessive Limb-Girdle Muscular Dystrophies
Keywords: دیسفرلین; Limb-girdle muscular dystrophy; sarcoglycan; calpain 3; dysferlin; dystroglycan;
Solution Structure of the Inner DysF Domain of Myoferlin and Implications for Limb Girdle Muscular Dystrophy Type 2B
Keywords: دیسفرلین; LGMD, limb girdle muscular dystrophy; PDB, Protein Data Bank; HSQC, heteronuclear single quantum coherence; NOE, nuclear Overhauser enhancement; TSR, thrombospondin repeat; NOESY, nuclear Overhauser enhancement spectroscopymuscular dystrophy; dysferlin; m
Limb–girdle muscular dystrophy: Diagnostic evaluation, frequency and clues to pathogenesis
Keywords: دیسفرلین; Limb–girdle muscular dystrophy; Dysferlin
Dysferlinopathy in the Jews of the Caucasus: A frequent mutation in the dysferlin gene
Keywords: دیسفرلین; Dysferlin; LGMD2B; Muscular dystrophy; Founder effect
Painful enlargement of the calf muscles in limb girdle muscular dystrophy type 2B (LGMD2B) with a novel compound heterozygous mutation in DYSF
Keywords: دیسفرلین; Dysferlin; Limb girdle muscular dystrophy type 2B; Non-sense mediated RNA decay;
Dysferlin expression in monocytes: A source of mRNA for mutation analysis
Keywords: دیسفرلین; Peripheral blood monocytes; cDNA; Dysferlin; Dysferlinopathy; Western blot
A third of LGMD2A biopsies have normal calpain 3 proteolytic activity as determined by an in vitro assay
Keywords: دیسفرلین; LGMD2A; Calpain 3 proteolytic activity; Diagnosis; Dysferlin
In silico functional and structural characterisation of ferlin proteins by mapping disease-causing mutations and evolutionary information onto three-dimensional models of their C2 domains
Keywords: دیسفرلین; C2 domain; Dysferlin; Muscular dystrophy; Otoferlin; Evolutionary analysis; Structural modelling
Molecular and cellular basis of calpainopathy (limb girdle muscular dystrophy type 2A)
Keywords: دیسفرلین; Calpain; Dystrophy; Muscle; Dysferlin; Titin
Dysferlin mutation in a Chinese pedigree with Miyoshi myopathy
Keywords: دیسفرلین; Dysferlin; Miyoshi myopathy; Linkage analysis; Western blot; Molecular defect
Loss of Podocyte Dysferlin Expression Is Associated With Minimal Change Nephropathy
Keywords: دیسفرلین; Dysferlin; podocyte; minimal change nephropathy;
Muscle protein analysis in the detection of heterozygotes for recessive limb girdle muscular dystrophy type 2B and 2E
Keywords: دیسفرلین; Dysferlin; Heterozygote diagnosis; LGMD; Limb girdle muscular dystrophy; Sarcoglycan
Mutation impact on dysferlin inferred from database analysis and computer-based structural predictions
Keywords: دیسفرلین; Dysferlin; Limb-girdle muscular dystrophy; Miyoshi myopathy; Mutation analysis; Computer based structural predictions
Expression profiling with progression of dystrophic change in dysferlin-deficient mice (SJL)
Keywords: دیسفرلین; cDNA; complementary deoxyribonucleic acid; cRNA; complementary ribonucleic acid; CARP; cardiac ankyrin repeated protein; Cspg2; chondroitin sulfate proteoglycan 2; Cxcl; CXC chemokine ligand; EAE; experimental allergic encephalomyelitis; GTP; guanosine 5â
The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient mice
Keywords: دیسفرلین; Dysferlin; Muscular dystrophy; Expression profile;