نتایج جستجو برای: lincrna

تعداد نتایج: 344  

2017
Elizabeth D Au Rosario Fernandez-Godino Tadeusz J Kaczynksi Maria E Sousa Michael H Farkas

Long intervening non-coding RNAs (lincRNAs) are increasingly being implicated as important factors in many aspects of cellular development, function, and disease, but remain poorly understood. In this study, we examine the human retinal pigment epithelium (RPE) lincRNA transcriptome using RNA-Seq data generated from human fetal RPE (fRPE), RPE derived from human induced pluripotent stem cells (...

2017
Muhammad G. Kibriya Farzana Jasmine Faruque Parvez Maria Argos Shantanu Roy Rachelle Paul-Brutus Tariqul Islam Alauddin Ahmed Muhammad Rakibuz-Zaman Justin Shinkle Vesna Slavkovich Joseph H. Graziano Habibul Ahsan

BACKGROUND Exposure to arsenic in drinking water is a global health problem and arsenic-induced skin lesions are hallmark of chronic arsenic toxicity. We and others have reported germline genetic variations as risk factors for such skin lesions. The role of copy number variation (CNV) in the germline DNA in this regard is unknown. METHODS From a large prospectively followed-up cohort, exposed...

2014
Jianqin Li Bin Wu Jiang Xu Chang Liu

Ganoderma lucidum is a white-rot fungus best-known for its medicinal activities. We have previously sequenced its genome and annotated the protein coding genes. However, long non-coding RNAs in G. lucidum genome have not been analyzed. In this study, we have identified and characterized long intergenic non-coding RNAs (lincRNA) in G. lucidum systematically. We developed a computational pipeline...

2014
Samreen Falak Sebastian Schafer Amelie Baud Oliver Hummel Herbert Schulz Dominique Gauguier Norbert Hubner Mary Osborne-Pellegrin

The inbred Brown Norway (BN) rat develops spontaneous ruptures of the internal elastic lamina (RIEL) of the abdominal aorta (AA) and iliac arteries. Prior studies with crosses of the BN/Orl RJ (susceptible) and LOU/M (resistant) showed the presence of a significant QTL on chromosome 5 and the production of congenic rats proved the involvement of this locus. In this study, we further dissected t...

2018
Harshavardhan Janga Marina Aznaourova Fabian Boldt Katrin Damm Arnold Grünweller Leon N Schulte

CRISPR/Cas9-based approaches have greatly facilitated targeted genomic deletions. Contrary to coding genes however, which can be functionally knocked out by frame-shift mutagenesis, non-coding RNA (ncRNA) gene knockouts have remained challenging. Here we present a universal ncRNA knockout approach guided by epigenetic hallmarks, which enables robust gene silencing even in provisionally annotate...

2015
Yanghua He Yi Ding Fei Zhan Huanmin Zhang Bo Han Gangqing Hu Keji Zhao Ning Yang Ying Yu Li Mao Jiuzhou Song

Long intergenic non-coding RNAs (lincRNAs) associated with a number of cancers and other diseases have been identified in mammals, but they are still formidable to be comprehensively identified and characterized. Marek's disease (MD) is a T cell lymphoma of chickens induced by Marek's disease virus (MDV). Here, we used a MD chicken model to develop a precise pipeline for identifying lincRNAs an...

Journal: :The EMBO journal 2013
Leina Lu Kun Sun Xiaona Chen Yu Zhao Lijun Wang Liang Zhou Hao Sun Huating Wang

Skeletal muscle differentiation is orchestrated by a network of transcription factors, epigenetic regulators, and non-coding RNAs. The transcription factor Yin Yang 1 (YY1) silences multiple target genes in myoblasts (MBs) by recruiting Ezh2 (Enhancer of Zeste Homologue2). To elucidate genome-wide YY1 binding in MBs, we performed chromatin immunoprecipitation (ChIP)-seq and found 1820 specific ...

Journal: :Genome research 2017
Xiang Yu James W Davenport Karen A Urtishak Marie L Carillo Sager J Gosai Christos P Kolaris Jo Ann W Byl Eric F Rappaport Neil Osheroff Brian D Gregory Carolyn A Felix

Type II topoisomerases orchestrate proper DNA topology, and they are the targets of anti-cancer drugs that cause treatment-related leukemias with balanced translocations. Here, we develop a high-throughput sequencing technology to define TOP2 cleavage sites at single-base precision, and use the technology to characterize TOP2A cleavage genome-wide in the human K562 leukemia cell line. We find t...

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