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Titlebook: Cardiovascular Disease, Volume 1; Genetics Qing K. Wang Book 2007 Humana Press 2007 Chromosom.bioinformatics.cardiovascular.gene therapy.ge

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Paradigmatic Lessons from Nuclear Driplinesr disease, such as coronary artery disease and myocardial infarction, variance component analysis holds some unique advantages. This analysis approach is versatile, affording the user the ability to incorporate the interplay between risk factors, genetic susceptibility, the effect of environmental f
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General survey of photopion nuclear physics, genetic basis for these traits and to characterize their functional consequences, mouse models are widely used, not only because of their genetic and physiological similarity to humans, but also because an extraordinary variety of genetic resources enable rigorous functional studies. Chromosome sub
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Marcela Raices,Maximiliano A. D’Angeloght result from the interactions of multiple genetic and environmental factors, none of which can cause disease solely by themselves. To reveal the genetic bases of MI, we performed a large-scale, case-control association study using 92,788 gene-based single-nucleotide polymorphism (SNP) markers. We
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Nuclear Physics and Its Applicationsarrhythmogenic disorders such as long QT syndrome (LQTS), catecholaminergic polymorphic ventricular tachycardia (CPVT), Andersen-Tawil syndrome, Brugada Syndrome, and Timothy syndrome. In addition, the genetic basis for cardiomyopathic processes vulnerable to sudden arrhythmic death—hypertrophic car
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Radioactivity – The Physics and Biology). The matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometrically based technique represents a new promising approach to SNP analysis. We have developed a new MALDI-TOF-based mini-sequencing assay, termed “VSET,” for genotyping of SNPs. In this assay, specific frag
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Qing K. WangIncludes supplementary material:
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Methods in Molecular Medicinehttp://image.papertrans.cn/c/image/221921.jpg
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