Pin1 promotes human CaV2.1 channel polyubiquitination by RNF138: pathophysiological implication for episodic ataxia type 2
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
-
Pin1 promotes human CaV2.1 channel polyubiquitination by RNF138: pathophysiological implication for episodic ataxia type 2 ; volume:22 ; number:1 ; day:28 ; month:11 ; year:2024 ; pages:1-26 ; date:12.2024
Cell communication and signaling ; 22, Heft 1 (28.11.2024), 1-26, 12.2024
- Creator
-
Fu, Ssu-Ju
Cheng, Kai-Min
Hsiao, Cheng-Tsung
Fang, Ya-Ching
Jeng, Chung-Jiuan
Tang, Chih-Yung
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s12964-024-01960-9
- URN
-
urn:nbn:de:101:1-2502132144495.901274022862
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:36 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.
Associated
- Fu, Ssu-Ju
- Cheng, Kai-Min
- Hsiao, Cheng-Tsung
- Fang, Ya-Ching
- Jeng, Chung-Jiuan
- Tang, Chih-Yung
- SpringerLink (Online service)
Other Objects (12)
Pathophysiological changes in the hippocampus in a murine model of episodic ataxia type 6
Episodic Vestibulocerebellar Ataxia Associated with a CACNA1G Missense Variant
Apo state pore opening as functional basis of increased EAAT anion channel activity in episodic ataxia 6
Pathophysiological Implication of Vitamin D in Diabetic Kidney Disease
Deferiprone targets aconitase: Implication for Friedreich's ataxia treatment
A Chinese boy with episodic ataxia and low CSF glucose
Episodic ataxia and severe infantile phenotype in spinocerebellar ataxia type 14: expansion of the phenotype and novel mutations
Episodic ataxia type 2 with a novel missense variant (Leu602Arg) in CACNA1A
Episodic Ataxia Type 1: Natural History and Effect on Quality of Life
A point mutation associated with episodic ataxia 6 increases glutamate transporter anion currents
Correction to: Episodic Ataxia Type 1: Natural History and Effect on Quality of Life
Pathophysiological properties of CLIC3 chloride channel in human gastric cancer cells
Pathophysiological changes in the hippocampus in a murine model of episodic ataxia type 6
Episodic Vestibulocerebellar Ataxia Associated with a CACNA1G Missense Variant
Apo state pore opening as functional basis of increased EAAT anion channel activity in episodic ataxia 6
Pathophysiological Implication of Vitamin D in Diabetic Kidney Disease
Deferiprone targets aconitase: Implication for Friedreich's ataxia treatment
A Chinese boy with episodic ataxia and low CSF glucose
Episodic ataxia and severe infantile phenotype in spinocerebellar ataxia type 14: expansion of the phenotype and novel mutations
Episodic ataxia type 2 with a novel missense variant (Leu602Arg) in CACNA1A
Episodic Ataxia Type 1: Natural History and Effect on Quality of Life
A point mutation associated with episodic ataxia 6 increases glutamate transporter anion currents
Correction to: Episodic Ataxia Type 1: Natural History and Effect on Quality of Life
Pathophysiological properties of CLIC3 chloride channel in human gastric cancer cells
Pathophysiological changes in the hippocampus in a murine model of episodic ataxia type 6
Episodic Vestibulocerebellar Ataxia Associated with a CACNA1G Missense Variant
Apo state pore opening as functional basis of increased EAAT anion channel activity in episodic ataxia 6
Pathophysiological Implication of Vitamin D in Diabetic Kidney Disease
Deferiprone targets aconitase: Implication for Friedreich's ataxia treatment
A Chinese boy with episodic ataxia and low CSF glucose
Episodic ataxia and severe infantile phenotype in spinocerebellar ataxia type 14: expansion of the phenotype and novel mutations
Episodic ataxia type 2 with a novel missense variant (Leu602Arg) in CACNA1A
Episodic Ataxia Type 1: Natural History and Effect on Quality of Life
A point mutation associated with episodic ataxia 6 increases glutamate transporter anion currents
Correction to: Episodic Ataxia Type 1: Natural History and Effect on Quality of Life