Hochschulschrift
Identification of disease modulating compounds in juvenile neuronal ceroid lipofuscinosis (JNCL)
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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Frankfurt am Main, Johann Wolfgang Goethe-Universität, Dissertation, 2016
- Event
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Veröffentlichung
- (where)
-
Frankfurt am Main
- (who)
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Universitätsbibliothek Johann Christian Senckenberg
- (when)
-
2016
- Creator
- Contributor
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Ruonala, Mika
Cotman, Susan
Volknandt, Walter
Dierkes, Paul
- URN
-
urn:nbn:de:hebis:30:3-412999
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:49 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
- Petcherski, Anton
- Ruonala, Mika
- Cotman, Susan
- Volknandt, Walter
- Dierkes, Paul
- Universitätsbibliothek Johann Christian Senckenberg
Time of origin
- 2016
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Juvenile neuronal ceroid lipofuscinosis : toponomics approach to identifying new drug targets
Retinal degeneration and immunomodulation in juvenile Neuronal Ceroid Lipofuscinosis (jNCL) mice
Glial cells are functionally impaired in juvenile neuronal ceroid lipofuscinosis and detrimental to neurons
Defective synaptic transmission causes disease signs in a mouse model of juvenile neuronal ceroid lipofuscinosis
Defective synaptic transmission causes disease signs in a mouse model of Juvenile Neuronal Ceroid Lipofuscinosis
Synapse alterations precede neuronal damage and storage pathology in a human cerebral organoid model of CLN3-juvenile neuronal ceroid lipofuscinosis
Modeling juvenile neuronal ceroid lipofuscinosis by genome editing in human induced pluripotent stem cells and cerebral organoids
Mutationsspektrum der spätinfantilen und juvenilen neuronalen Ceroid-Lipofuszinosen
Neuronal ceroid lipofuscinosis type 7: a case report
Neuronal ceroid lipofuscinosis type 1: a case report
Modeling neuronal ceroid lipofuscinosis in zebrafish by genome engineering
Moving towards effective therapeutic strategies for Neuronal Ceroid Lipofuscinosis
Juvenile neuronal ceroid lipofuscinosis : toponomics approach to identifying new drug targets
Retinal degeneration and immunomodulation in juvenile Neuronal Ceroid Lipofuscinosis (jNCL) mice
Glial cells are functionally impaired in juvenile neuronal ceroid lipofuscinosis and detrimental to neurons
Defective synaptic transmission causes disease signs in a mouse model of juvenile neuronal ceroid lipofuscinosis
Defective synaptic transmission causes disease signs in a mouse model of Juvenile Neuronal Ceroid Lipofuscinosis
Synapse alterations precede neuronal damage and storage pathology in a human cerebral organoid model of CLN3-juvenile neuronal ceroid lipofuscinosis
Modeling juvenile neuronal ceroid lipofuscinosis by genome editing in human induced pluripotent stem cells and cerebral organoids
Mutationsspektrum der spätinfantilen und juvenilen neuronalen Ceroid-Lipofuszinosen
Neuronal ceroid lipofuscinosis type 7: a case report
Neuronal ceroid lipofuscinosis type 1: a case report
Modeling neuronal ceroid lipofuscinosis in zebrafish by genome engineering