Results 51 to 60 of about 685,668 (343)

RNA Editing and Drug Discovery for Cancer Therapy

open access: yesThe Scientific World Journal, 2013
RNA editing is vital to provide the RNA and protein complexity to regulate the gene expression. Correct RNA editing maintains the cell function and organism development. Imbalance of the RNA editing machinery may lead to diseases and cancers.
Wei-Hsuan Huang   +5 more
doaj   +1 more source

The Integrative Studies on the Functional A-to-I RNA Editing Events in Human Cancers

open access: yesGenomics, Proteomics & Bioinformatics, 2023
Adenosine-to-inosine (A-to-I) RNA editing, constituting nearly 90% of all RNA editing events in humans, has been reported to contribute to the tumorigenesis in diverse cancers.
Sijia Wu   +4 more
doaj   +1 more source

An RNA editing fingerprint of cancer stem cell reprogramming [PDF]

open access: yes, 2015
BackgroundDeregulation of RNA editing by adenosine deaminases acting on dsRNA (ADARs) has been implicated in the progression of diverse human cancers including hematopoietic malignancies such as chronic myeloid leukemia (CML).
Angela C Court   +8 more
core   +1 more source

Darned in 2013: inclusion of model organisms and linking with Wikipedia [PDF]

open access: yes, 2012
DARNED (DAtabase of RNA EDiting, available at http://darned.ucc.ie) is a centralized repository of reference genome coordinates corresponding to RNA nucleotides having altered templated identities in the process of RNA editing.
Baranov, Pavel V.   +3 more
core   +4 more sources

RDDpred: a condition-specific RNA-editing prediction model from RNA-seq data [PDF]

open access: yes, 2016
This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give ...
Benjamin Hur, Min-su Kim, Sun Kim
core   +2 more sources

Transcriptome analysis identification of A-to-I RNA editing in granulosa cells associated with PCOS

open access: yesFrontiers in Endocrinology, 2023
BackgroundPolycystic ovary syndrome (PCOS) is a complex, multifactor disorder in women of reproductive age worldwide. Although RNA editing may contribute to a variety of diseases, its role in PCOS remains unclear.MethodsA discovery RNA-Seq dataset was ...
Fan-Sheng Kong   +19 more
doaj   +1 more source

Genome-wide identification and functional analysis of Apobec-1-mediated C-to-U RNA editing in mouse small intestine and liver [PDF]

open access: yes, 2014
BackgroundRNA editing encompasses a post-transcriptional process in which the genomically templated sequence is enzymatically altered and introduces a modified base into the edited transcript. Mammalian C-to-U RNA editing represents a distinct subtype of
Billing, Anja M   +11 more
core   +3 more sources

Genome-wide identification of A-to-I RNA editing events provides the functional implications in PDAC

open access: yesFrontiers in Oncology, 2023
IntroductionRNA editing, a wide-acknowledged post-transcriptional mechanism, has been reported to be involved in the occurrence and development of cancer, especially the abnormal alteration of adenosine to inosine.
Yue Mei   +11 more
doaj   +1 more source

Combining Insertion and Deletion in RNA-editing Preserves Regularity [PDF]

open access: yes, 2012
Inspired by RNA-editing as occurs in transcriptional processes in the living cell, we introduce an abstract notion of string adjustment, called guided rewriting. This formalism allows simultaneously inserting and deleting elements.
Bošnački, D.   +2 more
core   +3 more sources

High Level of Conservation of Mitochondrial RNA Editing Sites Among Four Populus Species

open access: yesG3: Genes, Genomes, Genetics, 2019
RNA editing occurs in the endosymbiont organelles of higher plants as C-to-U conversions of defined nucleotides. The availability of large quantities of RNA sequencing data makes it possible to identify RNA editing sites and to quantify their editing ...
Wolfram Georg Brenner   +7 more
doaj   +1 more source

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