Fast method for skeletal tissue gene expression analysis
نویسندگان
چکیده
منابع مشابه
Cloning, structural analysis, and expression of the human fast twitch skeletal muscle troponin C gene.
The gene encoding human fast skeletal muscle troponin C (TnC) was cloned, mapped, and sequenced. The locations of intron positions in this gene were compared to those in the related genes for mouse slow skeletal TnC and vertebrate and nonvertebrate calmodulins. We detected strikingly similar purine-rich DNA sequences on the coding strand in the basal promoter of the genes for fast and slow trop...
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BACKGROUND Although high throughput technologies for gene profiling are reliable tools, sample/tissue heterogeneity limits their outcomes when applied to identify molecular markers. Indeed, inter-sample differences in cell composition contribute to scatter the data, preventing detection of small but relevant changes in gene expression level. To date, attempts to circumvent this difficulty were ...
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Muscle has an intrinsic ability to change its mass and phenotype in response to activity. This process involves quantitative and qualitative changes
متن کاملGene expression in skeletal muscle.
Muscle has an intrinsic ability to change its mass and phenotype in response to activity. This process involves quantitative and qualitative changes in gene expression, including that of the myosin heavy chain isogenes that encode different types of molecular motors. This, and the differential expression of metabolic genes, results in altered fatigue resistance and power output. The regulation ...
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The element-free Galerkin method is employed for two-dimensional analysis of steady-state heat transfer. The unknown response of the system, i.e. temperature is approximated using the moving least squares technique. Numerical integration of governing simultaneous system of equations is performed by Gauss quadrature and new modified nodal integration techniques. Numerical examples and tests have...
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ژورنال
عنوان ژورنال: Biomedical Reports
سال: 2016
ISSN: 2049-9434,2049-9442
DOI: 10.3892/br.2016.699