Keywords: AM; Atrial cardiomyocyte; AP; Action potential; APA; Action potential amplitude; APD; Action potential duration; CICR; Ca2+-induced Ca2+ release; CK; Creatine kinase; CM; Cardiomyocyte; cTNI; Troponin I, cardiac type; cTnT; Cardiac troponin T; CÂ ÃÂ 40;
مقالات ISI (ترجمه نشده)
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Keywords: AUC; area under the curve; DHPLC; denaturing high-performance liquid chromatography; Dx; diagnosis; HCM; hypertrophic cardiomyopathy; Hx; history; ICD; implantable cardioverter defibrillator; LVOT; left ventricular outflow tract; MLVWT; maximum left ventr
Keywords: nsSNP; non-synonymous single nucleotide polymorphism; MyH7; myosin heavy chain 7; SVM; support vector machine; MyH7; Ebstein's anomaly; Hypertrophic cardiomyopathy; SNP analysis; Amyloid propensity; Bayes theorem;
Paradoxical development of polymyositis-like autoimmunity through augmented expression of autoimmune regulator (AIRE)
Keywords: Medullary thymic epithelial cell (mTEC); AIRE; Muscle; Tolerance; Ab; antibody; APC; antigen-presenting cell; BM; bone marrow; Crp; C-reactive protein; cTEC; cortical thymic epithelial cell; DC; dendritic cell; EpCAM; epithelial cell adhesion molecule 1;
Osteoglycin post-transcriptional regulation by miR-155 induces cellular architecture changes in H9c2 cardiomyoblasts
Keywords: miRNAs; microRNAs; Ogn; osteoglycin/mimecan; 3â²UTR; 3â² untranslated region; HF; heart failure; Socs1; suppressor of cytokine signaling 1; FoxO3a; Forkhead box O3a; ECM; extracellular matrix; GM; growth medium; RIN; RNA integrity number; PBS; Phosphate
A novel MYH7 founder mutation causing Laing distal myopathy in Southern Spain
Keywords: MYH7; Founder mutation; Distal myopathy; Muscle MRI; Genetic linkage analysis;
Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy
Keywords: Exome; Dilated; Cardiomyopathy; Digenic; MYH7; TNNT2;
A comparative study of mutation screening of sarcomeric genes (MYBPC3, MYH7, TNNT2) using single gene approach versus targeted gene panel next generation sequencing in a cohort of HCM patients in Egypt
Keywords: NGS; next generation sequencing; HCM; hypertrophic cardiomyopathy; MYBPC3; myosin binding protein C; MYH7; myosin heavy chain 7; TNNT2; cardiac troponin T2; MYF; Magdi Yacoub Heart Foundation; BA; bibliotheca alexandrina; Genetics; Hypertrophic cardiomyop
(Re-)programming of subtype specific cardiomyocytes
Keywords: ADSC; adipose tissue-derived mesenchymal stem cell; Alcam; activated leukocyte cell adhesion molecule; AMI; acute myocardial infarction; ANF; natriuretic factor; AP; action potential; ASC; adult stem cell; AV; atrioventricular; AVB; atrioventricular bundl
In situ reprogramming to transdifferentiate fibroblasts into cardiomyocytes using adenoviral vectors: Implications for clinical myocardial regeneration
Keywords: in situ cardiac reprogramming; adenoviral vector; gene therapy; Ad; adenoviral/adenovirus; AdGMT; cocktail of adenovirus vectors expressing Gata4, Mef2c, or Tbx5; AdNull; adenoviral vector that does not encode a transgene; cTnT; cardiac troponin T; EF; ej
Laing distal myopathy with a novel mutation in exon 34 of the MYH7 gene
Keywords: MYH7; Laing myopathy; Distal myopathy; CMT; MRI;
Muscle-specific microRNAs in skeletal muscle development
Keywords: HDAC4; histone deacetylase 4; MEF2; myocyte enhancer factor 2; miRNA; microRNA; MRFs; myogenic regulatory factors; MYF5; myogenic factor 5; MYF6; myogenic factor 6 (herculin); MYH6; myosin, heavy chain 6, cardiac muscle, alpha; MYH7; myosin, heavy chain 7
Fenofibrate unexpectedly induces cardiac hypertrophy in mice lacking MuRF1
Keywords: ANP; atrial natriuretic peptide; apoA-I; apolipoprotein A-I; apoA-II; apolipoprotein A-I; APOH; apolipoprotein H; βMHC; beta-myosin heavy chain; MYH7; myosin heavy chain 7; BNP; brain natriuretic peptide; cJun; Jun proto-oncogene; cMyBP-c; cardiac myosin
Distal myopathy with coexisting heterozygous TIA1 and MYH7 Variants
Keywords: Digenic myopathy; Distal myopathy; Hypertrophic cardiomyopathy; MYH7; TIA1;
miR-208b upregulation interferes with calcium handling in HL-1 atrial myocytes: Implications in human chronic atrial fibrillation
Keywords: CAF; chronic atrial fibrillation; SR; sinus rhythm; miR; microRNA; qRT-PCR; quantitative reverse transcription-polymerase chain reaction; FC; x-fold change; SERCA2; sarcoplasmic reticulum Ca2 + ATPase 2; miR-208a; MYH7; Connexin 43; Ca2Â + remodeling; ICa
A rare mutation in MYH7 gene occurs with overlapping phenotype
Keywords: MYH7; Left ventricular non-compation; Cardiomyopathy; FTD; Laing Distal Myopathy; Overlapping syndrome; ACTA1; actin 1; CPK; creatine phosphokinase; CFTD; Congenital Fiber Type Disproportion; COX; cytochrome C oxidase; DES; desmin; EMG; electromyography;
Homozygous MYH7 R1820W mutation results in recessive myosin storage myopathy: Scapuloperoneal and respiratory weakness with dilated cardiomyopathy
Keywords: Myosin storage myopathy; Dilated cardiomyopathy; MYH7;
A novel MYH7 Leu1453pro mutation resulting in Laing distal myopathy in an Irish family
Keywords: MYH7; Laing distal myopathy; Epilepsy; Brain white matter disease;
Ascribing novel functions to the sarcomeric protein, myosin binding protein H (MyBPH) in cardiac sarcomere contraction
Keywords: MyBPH; myosin binding protein H; cMyBPC; cardiac myosin binding protein C; LVH; left ventricular hypertrophy; HCM; hypertrophic cardiomyopathy; ALP; autophagy-lysosome pathway; AbA; Aureobasidin A; HIS3; imidazoleglycerolphosphate dehydratase; ADE2; phosp
NDRG2 promotes myoblast proliferation and caspase 3/7 activities during differentiation, and attenuates hydrogen peroxide - But not palmitate-induced toxicity
Keywords: NDRG2; N-myc downstream-regulated gene 2; MRFs; myogenic regulatory factors; Cdk; cyclin-dependent kinase; Rb; retinoblastoma; Myf5; myogenic factor 5; MyoD; myogenic differentiation; p27; p27 kip1; p21; p21 waf1/cip1; Akt; thymoma viral proto-oncogene; P
Cardiac myosin-binding protein C (MYBPC3) in cardiac pathophysiology
Keywords: AAV; adeno-associated virus; AON; antisense oligonucleotide; bp; base pair; Ca2+; Â calcium; CaMKII; Ca2+/calmodulin-dependent kinase II; Chr; chromosome; CK2; casein kinase 2; CMH4; hypertrophic cardiomyopathy, locus 4; cMyBP-C; cardiac myosin-binding pr
Exome sequencing identifies Laing distal myopathy MYH7 mutation in a Roma family previously diagnosed with distal neuronopathy
Keywords: MYH7; Distal myopathy; Laing distal myopathy; Whole exome sequencing; Myosinopathies;
Detection of a large duplication mutation in the myosin-binding protein C3 gene in a case of hypertrophic cardiomyopathy
Keywords: bp; base pair; DNA; deoxyribonucleic acid; dNTP; deoxynucleotide; EDTA; ethylenediaminetetraacetic acid; HCM; hypertrophic cardiomyopathy; Hg; mercury; LMM; light meromyosin domain; LV; left ventricle; LVEDD; left ventricular end-diastolic diameter; MYB
MicroRNA-214 provokes cardiac hypertrophy via repression of EZH2
Keywords: EZH2; enhancer of zeste homolog 2; PRC2; polycomb repressor complex 2; miR-214; microRNA-214; UTR; untranslated region; Six1; sine oculis homeobox homolog 1; Lenti-miR-214; lentivirus-miR-214; Lenti-spg; lentivirus-miR-214 sponge; Acta1; actin alpha 1; My
A novel MYH7 mutation with prominent paraspinal and proximal muscle involvement
Keywords: Laing distal myopathy; MYH7; Exome; MRI; Korean;
New phenotype and pathology features in MYH7-related distal myopathy
Keywords: MYH7; Slow-β myosin; Laing distal myopathy; Cytoplasmic body;
Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy
Keywords: Dilated cardiomyopathy; Molecular diagnosis; LMNA; MYH7; TNNT2; RBM20
A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy
Keywords: MYH7; Congenital fiber type disproportion; Myosin storage myopathy; Mutation;
Malignant and benign mutations in familial cardiomyopathies: Insights into mutations linked to complex cardiovascular phenotypes
Keywords: ACTA; α-skeletal actin gene; ACTC; cardiac actin gene; ACTN2; α-actinin 2; ANKRD1; ankyrin repeat protein gene; βMHC; beta myosin heavy chain; CSRP3; muscle LIM protein gene; DCM; dilated cardiomyopathy; FHC; familial hypertrophic cardiomyopathy; HCM;
Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutation
Keywords: Myosin storage myopathy; Cardiomyopathy; Pathology; MYH7; Myosin heavy chain; Left ventricular non compaction
A PCR-based integrated protocol for the structural analysis of the 13th exon of the human β-myosin heavy chain gene (MYH7): Development of a diagnostic tool for HCM disease
Keywords: Arginine403 (R403); β-myosin heavy chain; Hypertrophic cardiomyopathy (HCM); MYH7; Polymerase chain reaction (PCR)
Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation
Keywords: MYH7; Distal myopathy; Val606Met; Cardiomyopathy
MYH7 gene mutation in myosin storage myopathy and scapulo-peroneal myopathy
Keywords: Myosin storage myopathy; Scapulo-peroneal myopathy; MYH7; Slow myosin
Long-term cultured human myotubes decrease contractile gene expression and regulate apoptosis-related genes
Keywords: IGFBP2; Insulin-like growth factor-binding protein 2; HSPA2; antiapoptotic gene heat-shock 70-kd protein 2; WSL-1; tumor necrosis factor receptor superfamily, member 25; TNNI1; slow-twitch troponin I; MYL1; myosin light chain 1; MYH2; myosin heavy chain 2
Yield of Genetic Testing in Hypertrophic Cardiomyopathy
Keywords: DHPLC; denaturing high-performance liquid chromatography; HCM; hypertrophic cardiomyopathy; ICD; implantable cardioverter-defibrillator; LVWT; left ventricular wall thickness; MYBPC3; myosin binding protein C; MYH7; myosin heavy chain; SCD; sudden cardiac
Sarcomeric Genotyping in Hypertrophic Cardiomyopathy
Keywords: ACTC; actin; HCM; hypertrophic cardiomyopathy; LVWT; left ventricular wall thickness; MYBPC3; myosin binding protein C; MYH7; myosin heavy chain; MYL2; regulatory myosin light chain; MYL3; essential myosin light chain; TNNI3; troponin I; TNNT2; troponin T