نتایج جستجو برای: genetic association study

تعداد نتایج: 4665124  

2014
Stanislav Kopriva Anna Koprivova Andrea L. Harper Martin Trick Ian Bancroft John Innes

Journal: :International Journal of Legal Medicine 2020

Journal: :physiology and pharmacology 0
zahra abedi kichi department of genetics, faculty of biological sciences, tarbiat modares university, tehran, iran fatemeh khani-habibabadi department of genetics, faculty of biological sciences, tarbiat modares university, tehran, iran mohammadali sahraian ms research center, neuroscience institute, tehran university of medical sciences, tehran, iran rosita doosti ms research center, neuroscience institute, tehran university of medical sciences, tehran, iran mehrdad behmanesh department of genetics, faculty of biological sciences, tarbiat modares university, tehran, iran

introduction: to protect genomes of all organisms from internal and external damages and maintain the genome integrity and the continuity of life, repair system has been developed in all living cells. defects in repair system are responsible for various kinds of disease including cancers and neurodegenerative diseases such as multiple sclerosis (ms). the relationship between various components ...

2016
Xue Li Peige Song Maria Timofeeva Xiangrui Meng Igor Rudan Julian Little Jack Satsangi Harry Campbell Evropi Theodoratou

We provide a comprehensive field synopsis of genetic and epigenetic associations for paediatric Inflammatory Bowel Disease (IBD). A systematic review was performed and included 84 genetic association studies reporting data for 183 polymorphisms in 71 genes. Meta-analyses were conducted for 20 SNPs in 10 genes of paediatric Crohn's disease (CD) and for 8 SNPs in 5 genes of paediatric ulcerative ...

Journal: :the journal of tehran university heart center 0
pier mannucci angelo bianchi bonomi hemophilia and thrombosis centre, università degli studi di milano, milan, ita luca lotta angelo bianchi bonomi hemophilia and thrombosis centre, università degli studi di milano, milan, ita flora peyvandi angelo bianchi bonomi hemophilia and thrombosis centre, università degli studi di milano, milan, ita

myocardial infarction (mi) and its major determinant, coronary artery disease (cad), are complex diseases arising from the interaction between several genetic and environmental factors. until recently, the genetic basis of these diseases was poorly understood. genome-wide genetic association studies have afforded a comprehensive insight into the association between genetic variants and diseases...

2017
Sébastien Robiou-du-Pont Sonia S. Anand Katherine M. Morrison Sarah D. McDonald Stephanie A. Atkinson Koon K. Teo David Meyre

Previous genome wide association studies (GWAS) identified associations of multiple common variants with diastolic and systolic blood pressure traits in adults. However, the contribution of these loci to variations of blood pressure in early life is unclear. We assessed the child and parental contributions of 33 GWAS single-nucleotide polymorphisms (SNPs) for blood pressure in 1,525 participant...

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