The miRNA Targetome of Coronary Artery Disease is Perturbed by Functional Polymorphisms Identified and Prioritized by in-depth Bioinformatics Analyses Exploiting Genome-wide Association Studies

The miRNA Targetome of Coronary Artery Disease is Perturbed by Functional Polymorphisms Identified and Prioritized by in-depth Bioinformatics Analyses Exploiting Genome-wide Association Studies


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دانشگاه علوم پزشکی تبریز
دانشگاه علوم پزشکی تبریز

نویسندگان: میلاد بسطامی , زیبا نریمان صالح فام

کلمات کلیدی: 1000 genomes project; coronary artery disease; genome wide association study; miRNA; single nucleotide polymorphism

نشریه: 12516 , 1 , 594 , 2016

اطلاعات کلی مقاله
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نویسنده ثبت کننده مقاله میلاد بسطامی
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه دانشکده پزشکی
کد مقاله 58759
عنوان فارسی مقاله The miRNA Targetome of Coronary Artery Disease is Perturbed by Functional Polymorphisms Identified and Prioritized by in-depth Bioinformatics Analyses Exploiting Genome-wide Association Studies
عنوان لاتین مقاله The miRNA Targetome of Coronary Artery Disease is Perturbed by Functional Polymorphisms Identified and Prioritized by in-depth Bioinformatics Analyses Exploiting Genome-wide Association Studies
ناشر 7
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ خیر
عنوان نشریه (خارج از لیست فوق)
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح یک – ISI - Web of Science
آدرس لینک مقاله/ همایش در شبکه اینترنت http://www.sciencedirect.com/science/article/pii/S0378111916307004

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In recent years, genome-wide association studies (GWAS) have made great progress in elucidating the genetic influence on complex traits. An overwhelming number of GWAS signals resides in regulatory elements, therefore most post-GWAS studies focused only on transcriptional regulatory variants. However, recent findings have expanded the spectrum of trait/disease-associated regulatory variants beyond transcriptional level and highlighted the importance of post-transcriptional variants like those in miRNA targetome. The present work integrated genome-wide association data of coronary artery disease (CAD) with population-specific linkage disequilibrium structures from 1000 Genomes Project to map disease associations to miRNA targetome. Moreover, we performed a variety of functional prediction analyses to prioritize disease-associated variants (DAVs) influencing miRNA targetome and in-silico analyses to get insights into their functional significance. In conclusion, although the role of miRNA targetome variations in the development of CAD still has to be fully elucidated, we provided a systematic bioinformatics approach to the miRNA targetome variations in CAD. The results of this study will be valuable for researchers interested in the identification of CAD GWAS signals that may implicate polymorphic miRNA targeting.

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نویسنده نفر چندم مقاله
میلاد بسطامیاول
زیبا نریمان صالح فامدوم

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1-s2.0-S0378111916307004-main.pdf1395/06/251677098دانلود