- Alternative title
-
Mechanismus und Funktion der mitochondrialen m3C-tRNA Methyltransferase METTL8
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
Regensburg, Universität Regensburg, Dissertation, 2022
- Keyword
-
Transfer RNA
- Event
-
Veröffentlichung
- (where)
-
Regensburg
- (who)
-
Universitätsbibliothek Regensburg
- (when)
-
2022
- Creator
-
Schöller, Eva Maria
- Contributor
-
Meister, Gunter
Sprangers, Remco
- URN
-
urn:nbn:de:bvb:355-epub-515974
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:32 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
- Schöller, Eva Maria
- Meister, Gunter
- Sprangers, Remco
- Universitätsbibliothek Regensburg
Time of origin
- 2022
Other Objects (12)
Expanded tRNA methyltransferase family member TRMT9B regulates synaptic growth and function
The RNA methyltransferase METTL8 installs m3C32 in mitochondrial tRNAsThr/Ser(UCN) to optimise tRNA structure and mitochondrial translation
The loss of Kti11's cytosolic tRNA modification function affects mitochondrial homeostasis
A novel splice variant of Elp3/Kat9 regulates mitochondrial tRNA modification and function
Structural basis for human mitochondrial tRNA maturation
Human mitochondrial leucyl tRNA synthetase can suppress non cognate pathogenic mt‐ tRNA mutations
The tRNA methyltransferase Dnmt2 is required for accurate polypeptide synthesis during haematopoiesis
CO2-sensitive tRNA modification associated with human mitochondrial disease
Structure and mechanism of a methyltransferase ribozyme
The isolated carboxy‐terminal domain of human mitochondrial leucyl‐ tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells
A dual role of human tRNA methyltransferase hTrmt13 in regulating translation and transcription
Mitochondrial RNA processing in absence of tRNA punctuations in octocorals
Expanded tRNA methyltransferase family member TRMT9B regulates synaptic growth and function
The RNA methyltransferase METTL8 installs m3C32 in mitochondrial tRNAsThr/Ser(UCN) to optimise tRNA structure and mitochondrial translation
The loss of Kti11's cytosolic tRNA modification function affects mitochondrial homeostasis
A novel splice variant of Elp3/Kat9 regulates mitochondrial tRNA modification and function
Structural basis for human mitochondrial tRNA maturation
Human mitochondrial leucyl tRNA synthetase can suppress non cognate pathogenic mt‐ tRNA mutations
The tRNA methyltransferase Dnmt2 is required for accurate polypeptide synthesis during haematopoiesis
CO2-sensitive tRNA modification associated with human mitochondrial disease
Structure and mechanism of a methyltransferase ribozyme
The isolated carboxy‐terminal domain of human mitochondrial leucyl‐ tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells
A dual role of human tRNA methyltransferase hTrmt13 in regulating translation and transcription
Mitochondrial RNA processing in absence of tRNA punctuations in octocorals
Expanded tRNA methyltransferase family member TRMT9B regulates synaptic growth and function
The RNA methyltransferase METTL8 installs m3C32 in mitochondrial tRNAsThr/Ser(UCN) to optimise tRNA structure and mitochondrial translation
The loss of Kti11's cytosolic tRNA modification function affects mitochondrial homeostasis
A novel splice variant of Elp3/Kat9 regulates mitochondrial tRNA modification and function
Structural basis for human mitochondrial tRNA maturation
Human mitochondrial leucyl tRNA synthetase can suppress non cognate pathogenic mt‐ tRNA mutations
The tRNA methyltransferase Dnmt2 is required for accurate polypeptide synthesis during haematopoiesis
CO2-sensitive tRNA modification associated with human mitochondrial disease
Structure and mechanism of a methyltransferase ribozyme
The isolated carboxy‐terminal domain of human mitochondrial leucyl‐ tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells
A dual role of human tRNA methyltransferase hTrmt13 in regulating translation and transcription