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Human ABH3 structure and key residues for oxidative demethylation to reverse DNA/RNA damageMammalian ALKBH8 possesses tRNA methyltransferase activity required for the biogenesis of multiple wobble uridine modifications implicated in translational decodingALKBH5 is a mammalian RNA demethylase that impacts RNA metabolism and mouse fertilityHuman AlkB homolog 1 is a mitochondrial protein that demethylates 3-methylcytosine in DNA and RNAALKBH8-mediated formation of a novel diastereomeric pair of wobble nucleosides in mammalian tRNARepair deficient mice reveal mABH2 as the primary oxidative demethylase for repairing 1meA and 3meC lesions in DNAIdentification of a novel, widespread, and functionally important PCNA-binding motifA majority of m6A residues are in the last exons, allowing the potential for 3' UTR regulationGenome-wide profiling of DNA 5-hydroxymethylcytosine during rat Sertoli cell maturation.m6A mRNA modifications are deposited in nascent pre-mRNA and are not required for splicing but do specify cytoplasmic turnover.The human base excision repair enzyme SMUG1 directly interacts with DKC1 and contributes to RNA quality control.Protozoan ALKBH8 oxygenases display both DNA repair and tRNA modification activities.Roles of Trm9- and ALKBH8-like proteins in the formation of modified wobble uridines in Arabidopsis tRNA.UNG-initiated base excision repair is the major repair route for 5-fluorouracil in DNA, but 5-fluorouracil cytotoxicity depends mainly on RNA incorporation.The DNA dioxygenase ALKBH2 protects Arabidopsis thaliana against methylation damage.Biochemical reconstitution of TET1-TDG-BER-dependent active DNA demethylation reveals a highly coordinated mechanismRNA base damage and repair.AlkB demethylases flip out in different ways.Proteome alterations associated with transformation of multiple myeloma to secondary plasma cell leukemia.A robust, sensitive assay for genomic uracil determination by LC/MS/MS reveals lower levels than previously reported.A novel method for the efficient and selective identification of 5-hydroxymethylcytosine in genomic DNA.Changes of 5-hydroxymethylcytosine distribution during myeloid and lymphoid differentiation of CD34+ cells.Insights into the mechanisms of ifosfamide encephalopathy: drug metabolites have agonistic effects on alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)/kainate receptors and induce cellular acidification in mouse cortical neurons.Synergistic Actions of Ogg1 and Mutyh DNA Glycosylases Modulate Anxiety-like Behavior in Mice.A ubiquitin-dependent signalling axis specific for ALKBH-mediated DNA dealkylation repair.Methylation damage to RNA induced in vivo in Escherichia coli is repaired by endogenous AlkB as part of the adaptive response.Variability of coumarin 7- and 3-hydroxylation in a Jordanian population is suggestive of a functional polymorphism in cytochrome P450 CYP2A6The DNA modification N6-methyl-2'-deoxyadenosine (m6dA) drives activity-induced gene expression and is required for fear extinctionRecessive Truncating Mutations in ALKBH8 Cause Intellectual Disability and Severe Impairment of Wobble Uridine Modification
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description
hulumtuese
@sq
researcher
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wetenschapper
@nl
հետազոտող
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name
Cathrine B Vågbø
@ast
Cathrine B Vågbø
@en
Cathrine B Vågbø
@es
Cathrine B Vågbø
@nl
Cathrine B Vågbø
@sl
type
label
Cathrine B Vågbø
@ast
Cathrine B Vågbø
@en
Cathrine B Vågbø
@es
Cathrine B Vågbø
@nl
Cathrine B Vågbø
@sl
prefLabel
Cathrine B Vågbø
@ast
Cathrine B Vågbø
@en
Cathrine B Vågbø
@es
Cathrine B Vågbø
@nl
Cathrine B Vågbø
@sl
P1053
N-3226-2017
P106
P21
P31
P3829
P496
0000-0003-3959-7409