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- [3] Transmitter release deficits at the neuromuscular synapse of mice with mutations in the Cav2.1 (α1A) subunit of the P/Q-type Ca2+ channel MYASTHENIA GRAVIS AND RELATED DISORDERS: BIOMCHEMICAL BASIS FOR DISEASE OF THE NEUROMUSCULAR JUNCTION, 2003, 998 : 29 - 32
- [5] Dominant-negative effects of human P/Q-type Ca2+ channel mutations associated with episodic ataxia type 2 AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2006, 290 (04): : C1209 - C1220
- [7] Ubiquitin Ligase RNF138 Promotes Episodic Ataxia Type 2-Associated Aberrant Degradation of Human Cav2.1(P/Q-Type) Calcium Channel JOURNAL OF NEUROSCIENCE, 2017, 37 (09): : 2485 - 2503
- [9] Introduction into Cav2.1 of the homologous mutation of Cav1.2 causing the Timothy syndrome questions the role of V421 in the phenotypic definition of P-type Ca2+ channel Pflügers Archiv - European Journal of Physiology, 2008, 457 : 417 - 430
- [10] Introduction into Cav2.1 of the homologous mutation of Cav1.2 causing the Timothy syndrome questions the role of V421 in the phenotypic definition of P-type Ca2+ channel PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2008, 457 (02): : 417 - 430