Dolphin, Annette C
University College London
3 papers on CoChatORCID 0000-0003-4626-4856
Most cited papers
- Verified
Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension
Azizan, E. A. B., Poulsen, H., Tuluc, P., Zhou, J., Clausen, M. V., Lieb, A., Maniero, C., Garg, S., Bochukova, E. G., Zhao, W., et al. (2013) · Nature Genetics
Hormonal Regulation and HypertensionAdrenal and Paraganglionic Tumors
Cited by 544
- Verified
Ducky Mouse Phenotype of Epilepsy and Ataxia Is Associated with Mutations in the Cacna2d2 Gene and Decreased Calcium Channel Current in Cerebellar Purkinje Cells
Barclay, J., Balaguero, N., Mione, M., Ackerman, S. L., Letts, V. A., Brodbeck, J., Canti, C., Meir, A., Page, K. M., Kusumi, K., et al. (2001) · The Journal of Neuroscience
Ion channel regulation and functionEpilepsy research and treatment
Cited by 326
- Verified
The involvement of multiple calcium channel sub-types in glutamate release from cerebellar granule cells and its modulation by GABAB receptor activation
Huston, E., Cullen, G. P., Burley, J. R., & Dolphin, A. C. (1995) · Neuroscience
Neuroscience and Neuropharmacology ResearchIon channel regulation and function
Cited by 60
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