Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; Crianças; Miocardiopatia hipertrófica familiar; Diagnóstico genético; Penetrância; Children; Familial hypertrophic cardiomyopathy; Genetic testing; Penetrance;
مقالات ISI کاردیومیوپاتی هیپرتروفیک خانوادگی (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.
CaMKII-mediated phosphorylation of RyR2 plays a crucial role in aberrant Ca2+ release as an arrhythmogenic substrate in cardiac troponin T-related familial hypertrophic cardiomyopathy
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; Familial hypertrophic cardiomyopathy; Ryanodine receptor type 2; Troponin T; Ca2+/calmodulin dependent kinase II;
Whole length myosin binding protein C stabilizes myosin S2 as measured by gravitational force spectroscopy
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; Myosin subfragment-2; Myosin binding protein C; Gravitational force spectroscopy; Molecular simulations; Single molecule assays; In vitro motility assay; S1; Subfragment-1; S2; Subfragment-2; LMM; Light meromyosin; SFS; Simulated force spectroscopy; GFS;
A rare mutation in MYH7 gene occurs with overlapping phenotype
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; 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;
Myofilament calcium de-sensitization and contractile uncoupling prevent pause-triggered ventricular tachycardia in mouse hearts with chronic myocardial infarction
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; DAD; delayed afterdepolarization; EAD; early afterdepolarization; FHC; familial hypertrophic cardiomyopathy; HR; heart rate; IVSd; interventricular septal thickness at end-diastole; IVSs; interventricular septal thickness at end-systole; LVIDd; LV interna
Familial hypertrophic cardiomyopathy: Functional effects of myosin mutation R723G in cardiomyocytes
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; Familial hypertrophic cardiomyopathy; β-Myosin missense mutation R723G; Cardiomyocyte function; Slow skeletal muscle; Myofibrillar disarray; Calcium-sensitivity;
Familial hypertrophic cardiomyopathy related E180G mutation increases flexibility of human cardiac α-tropomyosin
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; AFM; atomic force microscopy; αTm; α-tropomyosin; cTnC; cardiac troponin C subunit; cTnI; cardiac troponin I subunit; cTnT; cardiac troponin T subunit; F-actin; filamentous actin; FHC; familial hypertrophic cardiomyopathy; Lc; contour length; le-e; en
Making genetics not so important: Family work in dealing with familial hypertrophic cardiomyopathy
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; New genetics; Family work; Familial hypertrophic cardiomyopathy; Communication; The Netherlands; Genetic testing;
Long-term rescue of a familial hypertrophic cardiomyopathy caused by a mutation in the thin filament protein, tropomyosin, via modulation of a calcium cycling protein
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; Familial hypertrophic cardiomyopathy; Phospholamban; Cardiac function; Diastolic dysfunction; Interstitial fibrosis; Extracellular signal-regulated kinase
Cross-bridge kinetics in myofibrils containing familial hypertrophic cardiomyopathy R58Q mutation in the regulatory light chain of myosin
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; Familial hypertrophic cardiomyopathy; Autocorrelation function; MuscleFHC, familial hypertrophic cardiomyopathy; RLC, regulatory light chain of myosin; SCD, sudden cardiac death; SMD, single molecule detection; PF, polarization of fluorescence; RP, rhodam
Two novel mutations of the MYBPC3 gene identified in Chinese families with hypertrophic cardiomyopathy
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; Familial hypertrophic cardiomyopathy; Genotype; Mutation; MYBPC3; Phenotype;
Rescue of familial cardiomyopathies by modifications at the level of sarcomere and Ca2+ fluxes
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; SR; sarcoplasmic reticulum; RyR; ryanodine receptor; SERCA; sarcoplasmic reticulum Ca2+ ATPase; ATP; adenosine triphosphate; PLB; phospholamban; HCM; hypertrophic cardiomyopathy; FHC; familial hypertrophic cardiomyopathy; DCM; dilated cardiomyopathy; MYH7
Neonatal gene transfer of Serca2a delays onset of hypertrophic remodeling and improves function in familial hypertrophic cardiomyopathy
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; Familial hypertrophic cardiomyopathy; Serca2; Treatment; Gene therapy
Single molecule kinetics in the familial hypertrophic cardiomyopathy D166V mutant mouse heart
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; FHC; Familial Hypertrophic Cardiomyopathy; RLC; Regulatory Light Chain of Myosin; SCD; Sudden Cardiac Death; SMD; Single Molecule Detection; Ψ; Duty Cycle; Tg-WT; Transgenic Wild Type; Tg-D166V; Transgenic D166V RLC Mutant; Ï; Average fluorescence lifet
Cardiac myosin heavy chain isoform exchange alters the phenotype of cTnT-related cardiomyopathies in mouse hearts
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; Familial Hypertrophic Cardiomyopathy; Cardiac Troponin T; Myosin heavy chain Isoforms; Ca2+ kinetics; Contractile performance; Cardiac relaxation;
Malignant and benign mutations in familial cardiomyopathies: Insights into mutations linked to complex cardiovascular phenotypes
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; 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;
The role of Akt/GSK-3β signaling in familial hypertrophic cardiomyopathy
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; Familial hypertrophic cardiomyopathy; Troponin T; Akt; Glycogen synthase kinase-3β (GSK-3β); Cardiomyopathy
Shifts in the myosin heavy chain isozymes in the mouse heart result in increased energy efficiency
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; CK; creatine kinase; COX; cytochrome C oxidase; CS; citrate synthase; |ÎGâ¼Â ATP|; free energy of ATP hydrolysis; DevP; developed pressure; â dP/dt; minimum value of the first derivative of LV pressure; + dP/dt; maximum value of the first derivative
Independent FHC-related cardiac troponin T mutations exhibit specific alterations in myocellular contractility and calcium kinetics
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; Cardiac Troponin T; Familial Hypertrophic Cardiomyopathy; Calcium; Sarcomeric Mechanics; SERCA2a; Sudden Cardiac Death
Utilidad del Doppler pulsado tisular en la detección precoz de anormalidades diastólicas en familiares de primer grado de pacientes con miocardiopatÃa hipertrófica familiar
Keywords: کاردیومیوپاتی هیپرتروفیک خانوادگی; MiocardiopatÃa hipertrófica familiar; Doppler pulsado tisular; VentrÃculo derecho; Familial hypertrophic cardiomyopathy; Doppler tissue imaging; Right ventricle; CIV; contracción isovolumétrica; DPT; Doppler pulsado tisular; MHF; miocardiopatÃa hipe