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Thesis

Molecular pharmacology of native and exogenous vascular ion channels

Abstract:

Vascular Ca2+-activated chloride channels (CaCCs), are a class of ligand- and voltage-gated channels that couple agonist binding and inositol triphosphate (IP3) signalling to depolarisation of the cell membrane and smooth muscle contraction. The elucidation of the precise physiological role and the pharmacological profile of this channel has been accelerated by the recent discovery of the gene (TMEM16A) coding for these channels. Based on the rationale that depolarising me...

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Division:
MSD
Department:
Pharmacology
Role:
Author

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Role:
Supervisor
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Funding agency for:
Ta, C
Type of award:
DPhil
Level of award:
Doctoral
Awarding institution:
University of Oxford
UUID:
uuid:798b4303-12d5-40b2-a850-0a68a03865a1
Deposit date:
2017-04-09

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