نتایج جستجو برای: differential case marking dcm
تعداد نتایج: 1620203 فیلتر نتایج به سال:
PURPOSE Dilated cardiomyopathy (DCM) is a chronic disease characterized by autoimmunity. Th17 cells are a distinct subset from Th1 and Th2 cells and play crucial regulatory functions in inflammatory and autoimmune processes. The current study was designed to investigate the possible involvement of Th17 cells in DCM. METHODS Th17 cells were detected in blood from DCM subjects and healthy blood...
Pregnancy in dilated cardiomyopathy (DCM) has an extremely high risk. However, DCM is usually asymptomatic at a young age. In pregnancy with DCM, it appears progressive and becomes symptomatic. mimicking peripartum (PPCM). We reported case of 23-year-old woman who was 20 weeks pregnant her first child complained chest palpitations severe faintness. These symptoms have happened started during pr...
AIM Mutations in a sarcomeric protein can cause hypertrophic cardiomyopathy (HCM) or dilated cardiomyopathy (DCM), the opposite ends of a spectrum of phenotypic responses of the heart to mutations. We posit the contracting phenotypes could result from differential effects of the mutant proteins on interactions among the sarcomeric proteins. To test the hypothesis, we generated transgenic mice e...
Dilated cardiomyopathy (DCM) is a structural heart disease with strong genetic background. Monogenic forms of DCM are observed in families with mutations located mostly in genes encoding structural and sarcomeric proteins. However, strong evidence suggests that genetic factors also affect the susceptibility to idiopathic DCM. To identify risk alleles for non-familial forms of DCM, we carried ou...
The tasks of a traction engine with suspension elements and additional devices for converting movement (DCM) are considered. object protection, the estimated dynamic state, is solid mass M moment inertia J relative to center gravity. To account material's rheological properties, Boltzmann-Volterra principle used. Mathematical models problem under consideration obtained, which described by syste...
OBJECTIVE Barth Syndrome (BTHS) is an X-linked multisystem disorder (OMIM 302060) usually diagnosed in infancy and characterized by cardiac problems [dilated cardiomyopathy (DCM) ± endocardial fibroelastosis (EFE) ± left ventricular non-compaction (LVNC)], proximal myopathy, feeding problems, growth retardation, neutropenia, organic aciduria and variable respiratory chain abnormalities. We wish...
A New Approach to Ensuring Oral Health Care for People Living With HIV/AIDS: The Dental Case Manager
INTRODUCTION The American Dental Association has identified several barriers to adequate dental care for vulnerable populations, including appropriate case management. The objective of this study was to examine the perceptions, attitudes, and beliefs of dental patients living with HIV/AIDS on the role and value of the dental case manager (DCM) and the effect of DCM services on their oral or ove...
Human dilated cardiomyopathy (DCM) is characterized by congestive heart failure and altered myocardial gene expression. Epigenetic changes, including DNA methylation, are implicated in the development of DCM but have not been studied extensively. Clinical human DCM and nonfailing control left ventricle samples were individually analyzed for DNA methylation and expressional changes. Expression m...
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