Hochschulschrift
Identification of disease modulating compounds in juvenile neuronal ceroid lipofuscinosis (JNCL)
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
Frankfurt am Main, Johann Wolfgang Goethe-Universität, Dissertation, 2016
- Ereignis
-
Veröffentlichung
- (wo)
-
Frankfurt am Main
- (wer)
-
Universitätsbibliothek Johann Christian Senckenberg
- (wann)
-
2016
- Urheber
- Beteiligte Personen und Organisationen
-
Ruonala, Mika
Cotman, Susan
Volknandt, Walter
Dierkes, Paul
- URN
-
urn:nbn:de:hebis:30:3-412999
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:49 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.
Objekttyp
- Hochschulschrift
Beteiligte
- Petcherski, Anton
- Ruonala, Mika
- Cotman, Susan
- Volknandt, Walter
- Dierkes, Paul
- Universitätsbibliothek Johann Christian Senckenberg
Entstanden
- 2016
Ähnliche Objekte (12)
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
Neuronal ceroid lipofuscinosis type 1: a case report
Mutationsspektrum der spätinfantilen und juvenilen neuronalen Ceroid-Lipofuszinosen
Neuronal ceroid lipofuscinosis type 7: 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
Neuronal ceroid lipofuscinosis type 1: a case report
Mutationsspektrum der spätinfantilen und juvenilen neuronalen Ceroid-Lipofuszinosen
Neuronal ceroid lipofuscinosis type 7: 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
Neuronal ceroid lipofuscinosis type 1: a case report
Mutationsspektrum der spätinfantilen und juvenilen neuronalen Ceroid-Lipofuszinosen
Neuronal ceroid lipofuscinosis type 7: a case report
Modeling neuronal ceroid lipofuscinosis in zebrafish by genome engineering