Tissue distribution of 5-hydroxymethylcytosine and search for active demethylation intermediatesChemical discrimination between dC and 5MedC via their hydroxylamine adductsReversible bond formation enables the replication and amplification of a crosslinking salen complex as an orthogonal base pair"Post-it" type connected DNA created with a reversible covalent cross-linkThe discovery of 5-formylcytosine in embryonic stem cell DNA.Structural biology of DNA photolyases and cryptochromes.Structure and function of noncanonical nucleobases.Formation and Direct Repair of UV-induced Dimeric DNA Pyrimidine Lesions.Quantitative LC-MS Provides No Evidence for m6 dA or m4 dC in the Genome of Mouse Embryonic Stem Cells and Tissues.5-Formylcytosine Could Be a Semipermanent Base in Specific Genome Sites.The CDK5 repressor CDK5RAP1 is a methylthiotransferase acting on nuclear and mitochondrial RNAIsotope-based analysis of modified tRNA nucleosides correlates modification density with translational efficiencyQuantification of the sixth DNA base hydroxymethylcytosine in the brain.Tet oxidizes thymine to 5-hydroxymethyluracil in mouse embryonic stem cell DNA.5-Formylcytosine to cytosine conversion by C-C bond cleavage in vivo.Non-canonical bases in the genome: The regulatory information layer in DNA.5-Formyl- and 5-Carboxydeoxycytidines Do Not Cause Accumulation of Harmful Repair Intermediates in Stem Cells.Dynamic readers for 5-(hydroxy)methylcytosine and its oxidized derivatives.Low values of 5-hydroxymethylcytosine (5hmC), the "sixth base," are associated with anaplasia in human brain tumors.Parallel isotope-based quantification of modified tRNA nucleosides.ALKBH5-induced demethylation of mono- and dimethylated adenosineTET3 Is Recruited by REST for Context-Specific Hydroxymethylation and Induction of Gene ExpressionMechanism and Stem-Cell Activity of 5-Carboxycytosine Decarboxylation Determined by Isotope TracingSystems-Based Analysis of Modified tRNA BasesSynthesis of Threefold Glycosylated Proteins using Click Chemistry and Genetically Encoded Unnatural Amino AcidsIsotope-dilution mass spectrometry for exact quantification of noncanonical DNA nucleosides
P50
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P50
description
Austrian pharmacologist
@en
Austrian pharmacologist
@en-ca
Austrian pharmacologist
@en-gb
cógaseolaí Ostarach
@ga
farmacolojiste osteraices
@lfn
farmacoloog uit Oostenrijk
@nl
farmacólogo austríaco
@es
österreichischer Mediziner und Hochschullehrer
@de
österreichischer Mediziner und Hochschullehrer
@de-at
عالم صيدلية نمساوي
@ar
name
Markus Müller
@ast
Markus Müller
@bar
Markus Müller
@ca
Markus Müller
@da
Markus Müller
@de
Markus Müller
@de-at
Markus Müller
@en
Markus Müller
@es
Markus Müller
@fr
Markus Müller
@ga
type
label
Markus Müller
@ast
Markus Müller
@bar
Markus Müller
@ca
Markus Müller
@da
Markus Müller
@de
Markus Müller
@de-at
Markus Müller
@en
Markus Müller
@es
Markus Müller
@fr
Markus Müller
@ga
altLabel
Univ.-Prof. Dr. Markus Müller
@bar
Univ.-Prof. Dr. Markus Müller
@de
Univ.-Prof. Dr. Markus Müller
@de-at
Univ.-Prof. Dr. Markus Müller
@en
Univ.-Prof. Dr. Markus Müller
@fr
Univ.-Prof. Dr. Markus Müller
@it
Univ.-Prof. Dr. Markus Müller
@nl
Univ.-Prof. Dr. Markus Müller
@no
Univ.-Prof. Dr. Markus Müller
@pl
prefLabel
Markus Müller
@ast
Markus Müller
@bar
Markus Müller
@ca
Markus Müller
@da
Markus Müller
@de
Markus Müller
@de-at
Markus Müller
@en
Markus Müller
@es
Markus Müller
@fr
Markus Müller
@ga
P214
P227
P244
P269
P21
P214
P227
P244
no2011064716
P269
P27
P31
P373
Markus Müller (physician)
P496
0000-0002-3579-3317
P569
1967-08-23T00:00:00Z
P734
P735
P7859
lccn-no2011064716