نتایج جستجو برای: alu pcr

تعداد نتایج: 177312  

2014
Lily Bazak Erez Y. Levanon Eli Eisenberg

A-to-I RNA editing is apparently the most abundant post-transcriptional modification in primates. Virtually all editing sites reside within the repetitive Alu SINEs. Alu sequences are the dominant repeats in the human genome and thus are likely to pair with neighboring reversely oriented repeats and form double-stranded RNA structures that are bound by ADAR enzymes. Editing levels vary consider...

Journal: :Molecular biology and evolution 1989
I L Gonzalez R Petersen J E Sylvester

A 2,700-bp segment of human ribosomal DNA (rDNA) spacer upstream of the rRNA promoter contains a set of four Alu elements, two in the direction of rRNA transcription and two in the opposite orientation. We report and compare the sequences of these Alu elements found in three rDNA clones and seek to determine the origin of the cluster, either from a single insertion followed by duplications or f...

2011
John A. Moran Randall J. Olson

Geographic atrophy (GA), an untreatable advanced form of age-related macular degeneration, results from retinal pigmented epithelium (RPE) cell degeneration. Here we show that the microRNA (miRNA)processing enzyme DICER1 is reduced in the RPE of humans with GA, and that conditional ablation of Dicer1, but not seven other miRNA-processing enzymes, induces RPE degeneration in mice. DICER1 knockdo...

2012
Bradley J. Wagstaff Dale J. Hedges Rebecca S. Derbes Rebeca Campos Sanchez Francesca Chiaromonte Kateryna D. Makova Astrid M. Roy-Engel

Alu elements are trans-mobilized by the autonomous non-LTR retroelement, LINE-1 (L1). Alu-induced insertion mutagenesis contributes to about 0.1% human genetic disease and is responsible for the majority of the documented instances of human retroelement insertion-induced disease. Here we introduce a SINE recovery method that provides a complementary approach for comprehensive analysis of the im...

Journal: :Genome research 2017
Mireia Jordà Anna Díez-Villanueva Izaskun Mallona Berta Martín Sergi Lois Víctor Barrera Manel Esteller Tanya Vavouri Miguel A Peinado

Cancer cells exhibit multiple epigenetic changes with prominent local DNA hypermethylation and widespread hypomethylation affecting large chromosomal domains. Epigenome studies often disregard the study of repeat elements owing to technical complexity and their undefined role in genome regulation. We have developed NSUMA (Next-generation Sequencing of UnMethylated Alu), a cost-effective approac...

2014
Abdul Kareem E Kavitha

Reversible logic is one of the emerging technologies having promising applications in quantum computing. This project will deal with the design of a 16 bit reversible Arithmetic Logic Unit (ALU) with 15 operations is presented by making use of Double Peres gate, Fredkin gate, Toffolli gate, DKG gate and NOT gate. A new VLSI architecture for ALU using reversible logic gates is proposed. ALU is o...

Journal: :Genome research 2004
Dale J Hedges Pauline A Callinan Richard Cordaux Jinchuan Xing Erin Barnes Mark A Batzer

Alu elements are primate-specific members of the SINE (short interspersed element) retroposon family, which comprise approximately 10% of the human genome. Here we report the first chromosomal-level comparison examining the Alu retroposition dynamics following the divergence of humans and chimpanzees. We find a twofold increase in Alu insertions in humans in comparison to the common chimpanzee ...

Journal: :E3S web of conferences 2021

Myocardial infarction (MI) is a multifactorial coronary artery disease influenced by environmental and genetic factors. Being one of the leading causes morbidity mortality in developed countries, it becoming national health concern developing countries such as Morocco. In present work, we aim to study association between 4 Alu polymorphisms (ACE, FXIII-B, TPA-25 APOA1) genes risk MI Moroccan po...

Journal: :Genome research 1996
R Deka P P Majumder M D Shriver D N Stivers Y Zhong L M Yu R Barrantes S J Yin T Miki J Hundrieser C H Bunker S T McGarvey S Sakallah R E Ferrell R Chakraborty

We have analyzed the CTG repeat length and the neighboring Alu insertion/deletion (+/-) polymorphism in DNA samples from 16 ethnically and geographically diverse human populations to understand the evolutionary dynamics of the myotonic dystrophy-associated CTG repeat. Our results show that the CTG repeat length is variable in human populations. Although the (CTG)5 repeat is the most common alle...

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