Pathophysiology of α-synuclein spreading along the nigrostriatal dopaminergic pathway and its age-dependency
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
München, Ludwig-Maximilians-Universität, Dissertation, 2020
- Schlagwort
-
Nervendegeneration
Tiermodell
Parkinson-Krankheit
- Ereignis
-
Veröffentlichung
- (wo)
-
München
- (wer)
-
Universitätsbibliothek der Ludwig-Maximilians-Universität
- (wann)
-
2020
- Urheber
- Beteiligte Personen und Organisationen
-
Michalakis, Stylianos
- DOI
-
10.5282/edoc.26933
- URN
-
urn:nbn:de:bvb:19-269339
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:33 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Sun, Fanfan
- Michalakis, Stylianos
- Universitätsbibliothek der Ludwig-Maximilians-Universität
Entstanden
- 2020
Ähnliche Objekte (12)
Overexpression-Induced α-Synuclein Brain Spreading
α-Synuclein fibril-specific nanobody reduces prion-like α-synuclein spreading in mice
α-synuclein in the pathophysiology of Alzheimer’s disease
Caudo‐rostral brain spreading of α‐synuclein through vagal connections
Defined α-synuclein prion-like molecular assemblies spreading in cell culture
Brain iron enrichment attenuates α‐synuclein spreading after injection of preformed fibrils
The HSP110/HSP70 disaggregation system generates spreading‐competent toxic α‐synuclein species
![Investigation of in vivo dopaminergic neuronal response to proteasome inhibition and mutant α-synuclein [alpha-synuclein] overexpression](/assets/placeholder/searchResultMediaNoDigitisedMedia.png)
Investigation of in vivo dopaminergic neuronal response to proteasome inhibition and mutant α-synuclein [alpha-synuclein] overexpression
Unilateral intranigral administration of β-sitosterol β-D-glucoside triggers pathological α-synuclein spreading and bilateral nigrostriatal dopaminergic neurodegeneration in the rat
Alpha-synuclein spreading in M83 mice brain revealed by detection of pathological α-synuclein by enhanced ELISA
Retina-to-brain spreading of α-synuclein after intravitreal injection of preformed fibrils
27-Hydroxycholesterol increases α-synuclein protein levels through proteasomal inhibition in human dopaminergic neurons
Overexpression-Induced α-Synuclein Brain Spreading
α-Synuclein fibril-specific nanobody reduces prion-like α-synuclein spreading in mice
α-synuclein in the pathophysiology of Alzheimer’s disease
Caudo‐rostral brain spreading of α‐synuclein through vagal connections
Defined α-synuclein prion-like molecular assemblies spreading in cell culture
Brain iron enrichment attenuates α‐synuclein spreading after injection of preformed fibrils
The HSP110/HSP70 disaggregation system generates spreading‐competent toxic α‐synuclein species
Investigation of in vivo dopaminergic neuronal response to proteasome inhibition and mutant α-synuclein [alpha-synuclein] overexpression
Unilateral intranigral administration of β-sitosterol β-D-glucoside triggers pathological α-synuclein spreading and bilateral nigrostriatal dopaminergic neurodegeneration in the rat
Alpha-synuclein spreading in M83 mice brain revealed by detection of pathological α-synuclein by enhanced ELISA
Retina-to-brain spreading of α-synuclein after intravitreal injection of preformed fibrils
27-Hydroxycholesterol increases α-synuclein protein levels through proteasomal inhibition in human dopaminergic neurons
Overexpression-Induced α-Synuclein Brain Spreading
α-Synuclein fibril-specific nanobody reduces prion-like α-synuclein spreading in mice
α-synuclein in the pathophysiology of Alzheimer’s disease
Caudo‐rostral brain spreading of α‐synuclein through vagal connections
Defined α-synuclein prion-like molecular assemblies spreading in cell culture
Brain iron enrichment attenuates α‐synuclein spreading after injection of preformed fibrils
The HSP110/HSP70 disaggregation system generates spreading‐competent toxic α‐synuclein species
Investigation of in vivo dopaminergic neuronal response to proteasome inhibition and mutant α-synuclein [alpha-synuclein] overexpression
Unilateral intranigral administration of β-sitosterol β-D-glucoside triggers pathological α-synuclein spreading and bilateral nigrostriatal dopaminergic neurodegeneration in the rat
Alpha-synuclein spreading in M83 mice brain revealed by detection of pathological α-synuclein by enhanced ELISA
Retina-to-brain spreading of α-synuclein after intravitreal injection of preformed fibrils