نتایج جستجو برای: mirna binding site snp

تعداد نتایج: 747797  

2017
Stefano Beretta Carlo Maj Ivan Merelli

MicroRNAs (miRNAs) are small non-coding RNA molecules that have an important role in a wide range of biological processes, since they interact with specific mRNAs affecting the expression of the corresponding proteins. The role of miRNA can be deeply influenced by Single Nucleotide Polymorphisms (SNPs), in particular in their seed sites, since these variations may modify their affinity with par...

Journal: :Cancer research 2013
Xia Pu Jack A Roth Michelle A T Hildebrandt Yuanqing Ye Hua Wei John D Minna Scott M Lippman Xifeng Wu

Given the density of single-nucleotide polymorphisms (SNP) in the human genome and the sensitivity of single-nucleotide changes in microRNA (miRNA) functionality and processing, we asked whether polymorphisms within miRNA processing pathways and binding sites may influence non-small cell lung cancer (NSCLC) patients' prognosis. We genotyped 240 miRNA-related SNPs in 535 patients with stage I an...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه رازی - دانشکده علوم 1393

سرطان معده یکی از مهم ترین انواع سرطان ها و دومین سرطان کشنده پس از سرطان ریه به خصوص در کشورهای آسیای شرقی است. بروز سرطان معده حاصل برهم کنش فاکتورهای محیطی ( وفاکتورهای ژنتیکی است . آلودگی با هلیکوباکترپیلوری به عنوان یک عامل اصلی در نموسرطان شناخته شده است. البته فقط تعداد کمی از افراد مبتلا به این عفونت به سرطان معده مبتلا می شوند و بر این اساس حدس می زنند که فاکتورهای ژنتیکی خود فرد نیز د...

2012
Junhua Luo Qingqing Cai Wei Wang Hui Huang Hong Zeng Wang He Weixi Deng Hao Yu Eddie Chan Chi-fai NG Jian Huang Tianxin Lin

PURPOSE To investigate the biological function of HOXB5 in human bladder cancer and explore whether the HOXB5 3'-UTR SNP (1010A/G), which is located within the microRNA-7 binding site, was correlated with clinical features of bladder cancer. METHODS Expression of HOXB5 in 35 human bladder cancer tissues and 8 cell lines were examined using real-time PCR and immunohistochemistry. Next, we expl...

2011
John C. Castle

Rates of SNPs (single nucleotide polymorphisms) and cross-species genomic sequence conservation reflect intra- and inter-species variation, respectively. Here, I report SNP rates and genomic sequence conservation adjacent to mRNA processing regions and show that, as expected, more SNPs occur in less conserved regions and that functional regions have fewer SNPs. Results are confirmed using both ...

2016
Ah-Reum Lee Jongkeun Park Keum Ji Jung Sun Ha Jee Sungjoo Kim-Yoon

PURPOSE MicroRNAs (miRNAs) are noncoding RNAs that play roles as tumor suppressors or oncogenes by regulating the expression of target genes via binding to seed-match sequences. Polymorphisms in the miRNA-binding site of a target gene can alter miRNA binding and potentially affect the risk of cancer. The objective of this study was to identify single-nucleotide polymorphisms (SNPs) in miRNA-bin...

Introduction: Spermatogenesis is a strictly regulated process in sperm production that is needed for sperm production transcriptional and posttranscriptional regulations. The cytoplasmic polyadenylation element binding (CPEB) protein regulates cytoplasmic polyadenylation of mRNAs in oogenesis and spermatogenesis. The purpose of the present studywas examining the association between rs2303846, ...

Journal: :Molecular carcinogenesis 2015
Qiming Wang Hongliang Liu Huihua Xiong Zhensheng Liu Li-E Wang Ji Qian Ramya Muddasani Victoria Lu Dongfeng Tan Jaffer A Ajani Qingyi Wei

CD133 is one of the most common stem cell markers, and functional single nucleotide polymorphisms (SNPs) of CD133 may modulate its gene functions and thus cancer risk and patient survival. We hypothesized that potentially functional CD133 SNPs are associated with gastric cancer (GC) risk and survival. To test this hypothesis, we conducted a case-control study of 371 GC patients and 313 cancer-f...

2012
Nina Norgren Urban Hellman Bo Göran Ericzon Malin Olsson Ole B. Suhr

BACKGROUND Hereditary transthyretin (TTR) amyloidosis (ATTR) is an autosomal dominant disease characterized by extracellular deposits of amyloid fibrils composed of misfolded TTR. The differences in penetrance and age at onset are vast, both between and within populations, with a generally late onset for Swedish carriers. In a recent study the entire TTR gene including the 3' UTR in Swedish, Fr...

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