Impaired adult olfactory bulb neurogenesis in the R6/2 mouse model of Huntington's disease
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2202
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Impaired adult olfactory bulb neurogenesis in the R6/2 mouse model of Huntington's disease ; volume:11 ; number:1 ; day:13 ; month:9 ; year:2010 ; pages:1-11 ; date:12.2010
BMC neuroscience ; 11, Heft 1 (13.9.2010), 1-11, 12.2010
- Urheber
-
Kohl, Zacharias
- Beteiligte Personen und Organisationen
-
Regensburger, Martin
Aigner, Robert
Kandasamy, Mahesh
Winner, Beate
Aigner, Ludwig
Winkler, Jürgen
SpringerLink (Online service)
- DOI
-
10.1186/1471-2202-11-114
- URN
-
urn:nbn:de:1111-201603213866
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:59 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
- Kohl, Zacharias
- Regensburger, Martin
- Aigner, Robert
- Kandasamy, Mahesh
- Winner, Beate
- Aigner, Ludwig
- Winkler, Jürgen
- SpringerLink (Online service)
Ähnliche Objekte (12)
Expression des CEA im ersten Trimenon der Schwangerschaft
Mobile sensorbasierte Ganganalyse zur objektiven Beurteilung motorischer Symptome der Huntington Erkrankung
Reduction in Subventricular Zone-Derived Olfactory Bulb Neurogenesis in a Rat Model of Huntington’s Disease Is Accompanied by Striatal Invasion of Neuroblasts
Distinct neuroinflammatory pattern in multiple system atrophy
Generation and characterization of human oligodendroglia as cellular model for Multiple System Atrophy
Compensatory mechanisms and therapeutic approaches in neuronal protein aggregation disorders
Modeling neurodevelopment and cortical dysfunction in SPG11-linked hereditary spastic paraplegia using human induced pluripotent stem cells
Das gastrointestinale Mikrobiom beim idiopathischen Parkinson-Syndrom: Zentrale Rolle von Kovariaten
The autophagy-lysosomal pathway in aggregation, release, and toxicity of alpha-synuclein
G3 Hedonic olfaction in huntington’s disease
MAdCAM-1 and alpha-Synuclein as endogenous regulators of immune responses and tissue susceptibility in neuroinflammation
Oligodendroglia and Myelin in Neurodegenerative Diseases: More Than Just Bystanders?
Expression des CEA im ersten Trimenon der Schwangerschaft
Mobile sensorbasierte Ganganalyse zur objektiven Beurteilung motorischer Symptome der Huntington Erkrankung
Reduction in Subventricular Zone-Derived Olfactory Bulb Neurogenesis in a Rat Model of Huntington’s Disease Is Accompanied by Striatal Invasion of Neuroblasts
Distinct neuroinflammatory pattern in multiple system atrophy
Generation and characterization of human oligodendroglia as cellular model for Multiple System Atrophy
Compensatory mechanisms and therapeutic approaches in neuronal protein aggregation disorders
Modeling neurodevelopment and cortical dysfunction in SPG11-linked hereditary spastic paraplegia using human induced pluripotent stem cells
Das gastrointestinale Mikrobiom beim idiopathischen Parkinson-Syndrom: Zentrale Rolle von Kovariaten
The autophagy-lysosomal pathway in aggregation, release, and toxicity of alpha-synuclein
G3 Hedonic olfaction in huntington’s disease
MAdCAM-1 and alpha-Synuclein as endogenous regulators of immune responses and tissue susceptibility in neuroinflammation
Oligodendroglia and Myelin in Neurodegenerative Diseases: More Than Just Bystanders?
Expression des CEA im ersten Trimenon der Schwangerschaft
Mobile sensorbasierte Ganganalyse zur objektiven Beurteilung motorischer Symptome der Huntington Erkrankung
Reduction in Subventricular Zone-Derived Olfactory Bulb Neurogenesis in a Rat Model of Huntington’s Disease Is Accompanied by Striatal Invasion of Neuroblasts
Distinct neuroinflammatory pattern in multiple system atrophy
Generation and characterization of human oligodendroglia as cellular model for Multiple System Atrophy
Compensatory mechanisms and therapeutic approaches in neuronal protein aggregation disorders
Modeling neurodevelopment and cortical dysfunction in SPG11-linked hereditary spastic paraplegia using human induced pluripotent stem cells
Das gastrointestinale Mikrobiom beim idiopathischen Parkinson-Syndrom: Zentrale Rolle von Kovariaten
The autophagy-lysosomal pathway in aggregation, release, and toxicity of alpha-synuclein
G3 Hedonic olfaction in huntington’s disease
MAdCAM-1 and alpha-Synuclein as endogenous regulators of immune responses and tissue susceptibility in neuroinflammation