Hochschulschrift
Molecular characterization of DYT-TOR1A dystonia and TUBB4A-linked diseases
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
Lübeck, Universität zu Lübeck, Dissertation, 2016
- Keyword
-
Hirnkrankheit
Neuropsychiatrie
Nervenkrankheit
- Event
-
Veröffentlichung
- (where)
-
Lübeck
- (who)
-
Zentrale Hochschulbibliothek Lübeck
- (when)
-
2017
- Creator
-
Vulinovic, Franca Oriana
- URN
-
urn:nbn:de:gbv:841-20161215289
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:45 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.
Object type
- Hochschulschrift
Associated
- Vulinovic, Franca Oriana
- Zentrale Hochschulbibliothek Lübeck
Time of origin
- 2017
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Functional and molecular properties of DYT-THAP1 dystonia and DYT-SGCE myoclonus-dystonia using patient-derived striatal medium spiny neurons
Molecular genetic mechanisms surrounding x-linked Dystonia-Parkinsonism
Molecular studies of two genetic movement disorders : PRKRA-linked dystonia and PINK1-linked Parkinson disease
Pathophysiology of early-onset isolated dystonia in a DYT-TOR1A rat model with trauma-induced dystonia-like movements
Disturbed brain energy metabolism in a rodent model of DYT-TOR1A dystonia
Detection of Modified Histones from Oral Mucosa of a Patient with DYT- KMT2B Dystonia
Gene-environment interaction elicits dystonia-like features and impaired translational regulation in a DYT-TOR1A mouse model
Early onset torsion dystonia (Oppenheim's dystonia)
Promise and challenges of dystonia brain banking: establishing a human tissue repository for studies of X-Linked Dystonia-Parkinsonism
Factors influencing reduced penetrance and variable expressivity in X-linked dystonia-parkinsonism
Mechanisms underlying age-related penetrance and expressivity in x-linked Dystonia-Parkinsonism
Dyt sprickt god.
Functional and molecular properties of DYT-THAP1 dystonia and DYT-SGCE myoclonus-dystonia using patient-derived striatal medium spiny neurons
Molecular genetic mechanisms surrounding x-linked Dystonia-Parkinsonism
Molecular studies of two genetic movement disorders : PRKRA-linked dystonia and PINK1-linked Parkinson disease
Pathophysiology of early-onset isolated dystonia in a DYT-TOR1A rat model with trauma-induced dystonia-like movements
Disturbed brain energy metabolism in a rodent model of DYT-TOR1A dystonia
Detection of Modified Histones from Oral Mucosa of a Patient with DYT- KMT2B Dystonia
Gene-environment interaction elicits dystonia-like features and impaired translational regulation in a DYT-TOR1A mouse model
Early onset torsion dystonia (Oppenheim's dystonia)
Promise and challenges of dystonia brain banking: establishing a human tissue repository for studies of X-Linked Dystonia-Parkinsonism
Factors influencing reduced penetrance and variable expressivity in X-linked dystonia-parkinsonism
Mechanisms underlying age-related penetrance and expressivity in x-linked Dystonia-Parkinsonism