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Kate E O'Driscoll

Researcher at University of Nevada, Reno

Publications -  18
Citations -  881

Kate E O'Driscoll is an academic researcher from University of Nevada, Reno. The author has contributed to research in topics: Interstitial cell of Cajal & ANO1. The author has an hindex of 12, co-authored 18 publications receiving 795 citations.

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Journal ArticleDOI

Expression of anoctamin 1/TMEM16A by interstitial cells of Cajal is fundamental for slow wave activity in gastrointestinal muscles

TL;DR: The fundamental role of ANO1 is demonstrated in the generation of slow waves in GI ICC, which failed to develop by birth in mice homozygous for a null allele of Tmem16a and did not develop subsequent to birth in organ culture, as in wildtype and heterozygous muscles.
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Regulation of calcium-activated chloride channels in smooth muscle cells: a complex picture is emerging

TL;DR: This review provides a summary of recent findings demonstrating the regulation of native ClCa channels in vascular smooth muscle cells by calmodulin-dependent protein kinase II and calcineurin and how their fine tuning by these enzymes may influence vascular tone.
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Muscarinic activation of Ca2+‐activated Cl− current in interstitial cells of Cajal

TL;DR: Interstitial cells of Cajal are tightly associated with excitatory and inhibitory motor neurons in the gastrointestinal tract and these cells are also connected electrically to smooth muscle cells, suggesting that ICC participate in responses to neurotransmitters released from neurons that drive motility and help move nutrients and wastes through the gut.
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Intracellular Ca2+ release from endoplasmic reticulum regulates slow wave currents and pacemaker activity of interstitial cells of Cajal

TL;DR: The hypothesis that the Ca(2+) responsible for the stochastic activation of ANO1 channels during spontaneous transient inward currents (STICs) and synchronized activation of Anoctamin 1 (ANO1) channels during slow wave currents comes from intracellular Ca( 2+) stores is investigated.
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Expression, localization, and functional properties of Bestrophin 3 channel isolated from mouse heart

TL;DR: The functional and mutational studies examining the biophysical properties of mBest3 indicate that it functions as a pore-forming chloride channel that is activated by physiological levels of calcium.