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Global Transcriptome Analysis of RNA Abundance Regulation by ADAR in Lung Adenocarcinoma

open access: yesEBioMedicine, 2018
Despite tremendous advances in targeted therapies against lung adenocarcinoma, the majority of patients do not benefit from personalized treatments. A deeper understanding of potential therapeutic targets is crucial to increase the survival of patients ...
Dvir Aran, Idit Kosti, David P Carbone
exaly   +3 more sources

Adar contributes to genome integrity by regulating R-loop homeostasis in Drosophila [PDF]

open access: yesBMC Biology
Background Adenosine deaminase acting on RNA (Adar) is a critical enzyme involved in post-transcriptional epigenetic regulation through adenosine-to-inosine (A-to-I) RNA editing.
Xuedi Zhang   +8 more
doaj   +2 more sources

Origins and evolution of ADAR‐mediated RNA editing [PDF]

open access: yesIUBMB Life, 2009
AbstractAdenosine deaminases acting on RNA (ADARs) convert adenosines to inosines in double‐stranded RNA in animals. Identification of more ADAR targets and genome sequences of diverse eukaryotes present an opportunity to elucidate the origin and evolution of ADAR‐mediated RNA editing.
Yongfeng Jin
exaly   +3 more sources

Unbiased Identification of trans Regulators of ADAR and A-to-I RNA Editing

open access: yesCell Reports, 2020
Summary: Adenosine-to-inosine RNA editing is catalyzed by adenosine deaminase acting on RNA (ADAR) enzymes that deaminate adenosine to inosine. Although many RNA editing sites are known, few trans regulators have been identified.
Anne L Sapiro, Qin Li, James J Moresco
exaly   +3 more sources

What do editors do? Understanding the physiological functions of A-to-I RNA editing by adenosine deaminase acting on RNAs [PDF]

open access: yesOpen Biology, 2020
Adenosine-to-inosine (A-to-I) editing is a post-transcriptional modification of RNA which changes its sequence, coding potential and secondary structure.
Jacki E. Heraud-Farlow   +1 more
doaj   +1 more source

ADAR, the carcinogenesis mechanisms of ADAR and related clinical applications [PDF]

open access: yesAnnals of Translational Medicine, 2019
Adenosine deaminases acting on RNA (ADARs) catalyze the conversion of adenosine (A) to inosine (I) in double-stranded RNA, which can change the codons after transcription. Abnormal ADAR editing is present in a variety of cancers. However, the study of the biological effects of ADARs in cancer is not very deep.
Yue, Zhang   +3 more
openaire   +2 more sources

The ADAR protein family [PDF]

open access: yesGenome Biology, 2012
Adenosine to inosine (A-to-I) RNA editing is a post-transcriptional process by which adenosines are selectively converted to inosines in double-stranded RNA (dsRNA) substrates. A highly conserved group of enzymes, the adenosine deaminase acting on RNA (ADAR) family, mediates this reaction.
Savva, Yiannis A   +2 more
openaire   +2 more sources

ANALYSIS OF FAST NEUTRON TRANSPORT IN CHLORIDE SALTS USING MONTE CARLO METHOD

open access: yesActa Polytechnica CTU Proceedings, 2020
The aim of this paper is to present results of fast neutron behavior analysis within the chloride salts environment using simulations based on Monte Carlo method (MCNP 6.2).
Ondřej Šťastný   +4 more
doaj   +1 more source

Heterochromatin: On the ADAR Radar? [PDF]

open access: yesCurrent Biology, 2005
Vigilin proteins, the absence of which is known to cause abnormalities in heterochromatin, have been found to bind edited RNAs. Molecular complexes including vigilin comprise proteins involved with RNA editing and with DNA repair, making connections between these processes and RNA-based silencing mechanisms.
Fernandez, H.R.   +3 more
openaire   +2 more sources

Identification of the pathogenic variants in three Chinese families with dyschromatosis symmetrica hereditaria [PDF]

open access: yesJichu yixue yu linchuang, 2023
Objective To analyze the clinical features and to identify the pathogenic variants in three Chinese families with dyschromatosis symmetrica hereditaria (DSH).
YANG Xueting, GUO Kexin, SUN Yang, WANG Rongrong, MA Donglai, ZHANG Xue
doaj   +1 more source

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