Different modification pathways for m1A58 incorporation in yeast elongator and initiator tRNAs
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
In: bioRxiv, 2022.12.16.520695, 35 S.
- Classification
-
Biowissenschaften, Biologie
- Event
-
Veröffentlichung
- (where)
-
Frankfurt am Main
- (who)
-
Universitätsbibliothek Johann Christian Senckenberg
- (when)
-
2022
- Creator
- DOI
-
10.1101/2022.12.16.520695
- URN
-
urn:nbn:de:hebis:30:3-731361
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
- 14.08.2025, 10:47 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Yared, Marcel-Joseph
- Yoluç, Yasemin
- Catala, Marjorie
- Tisné, Carine
- Kaiser, Stefanie
- Barraud, Pierre
- Universitätsbibliothek Johann Christian Senckenberg
Time of origin
- 2022
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Histone modification pattern evolution after yeast gene duplication
Initiatoren
A single sequence context cannot satisfy all non-AUG initiator codons in yeast†
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Highly chromophoric fluorescent‐labeled methionyl‐initiator tRNAs applicable in living cells
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Incorporation of pyrrolysine derivatives into proteins and development of bioorthogonal protein modification methods
Structural Modification in Carbon Nanotubes by Boron Incorporation
Incorporation of reporter genes into mitochondrial DNA in budding yeast
Histone modification pattern evolution after yeast gene duplication
Initiatoren
A single sequence context cannot satisfy all non-AUG initiator codons in yeast†
Yeast autonomously replicating sequence (ARS): Identification, function, and modification
Highly chromophoric fluorescent‐labeled methionyl‐initiator tRNAs applicable in living cells
Incorporation of Conjugated Diynes in Perovskites and their Post‐Synthetic Modification
Agitatoren, Initiatoren
Incorporation of bridged nucleic acids into CRISPR RNAs improves Cas9 endonuclease specificity
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