Role of single nucleotide polymorphisms (SNPs) in common migraine
نویسندگان
چکیده
منابع مشابه
Novel Single Nucleotide Polymorphisms (SNPs) in Intron 2 and Exon 3 Regions of Leptin Gene in Sumba Ongole Cattle
The bovine leptin (LEP) gene was widely used as a candidate gene for molecular selection to improve productivity traits of cattle. This study was carried out to identify single nucleotide polymorphisms (SNPs) in the LEP gene of Sumba Ongole (SO, Bos indicus) cows using sequencing method. A total of 31 animals were used in this study for analyses. Research showed that total of 16 SNPs w...
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UNLABELLED SNPNB is a user-friendly and platform-independent application for analyzing Single Nucleotide Polymorphism NeighBoring sequence context and nucleotide bias patterns, and subsequently evaluating the effective SNP size for the bias patterns observed from the whole data. It was implemented by Java and Perl. SNPNB can efficiently handle genome-wide or chromosome-wide SNP data analysis in...
متن کاملanalysis of single nucleotide polymorphisms ( SNPs ) in In silico human
Lymphedema is abnormal accumulation of interstitial fluid, due to Introduction inefficient uptake and reduced flow, leading to swelling and disability, mostly in the extremities. Hereditary lymphedema usually occurs as an autosomal dominant trait with allelic heterogeneity. We identified single Methods: nucleotide polymorphisms (SNPs) in the FOXC2 gene using dbSNP, analyzed their effect on the ...
متن کاملAssociation of two Common Single Nucleotide Polymorphisms (SNPs +45T/G and +276G/T) of ADIPOQ Gene with Coronary Artery Disease in Type 2 Diabetic Patients
Background: Adiponectin, an adipocyte-secreted hormone, is known to have anti-atherogenic, anti-inflammatory, and anti-diabetic properties. In the present study, the association between two common single nucleotide polymorphisms (SNPs) (+45T/G and +276G/T) of ADIOPQ gene and coronary artery disease (CAD) was assessed in the subjects with type 2 diabetes (T2DM). Methods: Genotypes of two SNPs we...
متن کاملanalysis of single nucleotide polymorphisms In silico ( SNPs ) in human
Lymphedema is an abnormal accumulation of interstitial fluid, Introduction due to inefficient uptake and reduced flow, leading to swelling and disability, mostly in the extremities. Hereditary lymphedema usually occurs as an autosomal dominant trait with allelic heterogeneity. : We identified single nucleotide polymorphisms (SNPs) in the FOXC2 Methods gene using dbSNP, analyzed their effect on ...
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ژورنال
عنوان ژورنال: The Egyptian Journal of Neurology, Psychiatry and Neurosurgery
سال: 2019
ISSN: 1687-8329
DOI: 10.1186/s41983-019-0093-8