The Mutant HTT mRNA-Protein Interactome : Implications in RNA Toxicity in Huntington’s Disease
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Dissertation, 2017
- Keyword
-
Messenger RNA
Brain
Mass spectrometry
Carrier proteins
- Event
-
Veröffentlichung
- (where)
-
Bonn
- (who)
-
Universitäts- und Landesbibliothek Bonn
- (when)
-
2017
- Creator
- URN
-
urn:nbn:de:hbz:5n-48859
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:02 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
- Schilling, Judith
- Universitäts- und Landesbibliothek Bonn
Time of origin
- 2017
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microRNA-128a dysregulation in transgenic Huntington’s disease monkeys
Widespread alterations in microRNA biogenesis in human Huntington’s disease putamen
Soluble mutant huntingtin drives early human pathogenesis in Huntington’s disease
Altered m6A RNA methylation contributes to hippocampal memory deficits in Huntington’s disease mice
Mechanisms of aberrant HTT splicing and its implications on RNA homeostasis in Huntington’s disease
Identify Huntington’s disease associated genes based on restricted Boltzmann machine with RNA-seq data
Single-nucleus RNA-seq identifies Huntington disease astrocyte states
Huntington
Nucleolar stress controls mutant Huntington toxicity and monitors Huntington’s disease progression
HAP40 modulates mutant Huntingtin aggregation and toxicity in Huntington’s disease mice
RNAi mechanisms in Huntington’s disease therapy: siRNA versus shRNA
Analysis of mutant huntingtin aggregation and toxicity in Drosophila models of Huntington’s disease
microRNA-128a dysregulation in transgenic Huntington’s disease monkeys
Widespread alterations in microRNA biogenesis in human Huntington’s disease putamen
Soluble mutant huntingtin drives early human pathogenesis in Huntington’s disease
Altered m6A RNA methylation contributes to hippocampal memory deficits in Huntington’s disease mice
Mechanisms of aberrant HTT splicing and its implications on RNA homeostasis in Huntington’s disease
Identify Huntington’s disease associated genes based on restricted Boltzmann machine with RNA-seq data
Single-nucleus RNA-seq identifies Huntington disease astrocyte states