Vascular K(ATP) channels: dephosphorylation and deactivation

Por Tammaro, Paolo
Publicado em 2009

The Kir6.2-F333I mutation differentially modulates K(ATP) channels composed of SUR1 or SUR2 subunits

Por Tammaro, Paolo, Ashcroft, Frances
Publicado em 2007

Keeping the heart going: a new role for K(ATP) channels

Por Tammaro, Paolo, Ashcroft, Frances M
Publicado em 2006

A mutation in the ATP-binding site of the Kir6.2 subunit of the K(ATP) channel alters coupling with the SUR2A subunit

Por Tammaro, Paolo, Ashcroft, Frances M
Publicado em 2007

A cytosolic factor that inhibits K(ATP) channels expressed in Xenopus oocytes by impairing Mg-nucleotide activation by SUR1

Por Tammaro, Paolo, Ashcroft, Frances M
Publicado em 2009

TMEM16A/Anoctamin 1 protein mediates calcium-activated chloride currents in pulmonary arterial smooth muscle cells

Por Manoury, Boris, Tamuleviciute, Aiste, Tammaro, Paolo
Publicado em 2010

Functional effects of naturally occurring KCNJ11 mutations causing neonatal diabetes on cloned cardiac K(ATP) channels

Por Tammaro, Paolo, Proks, Peter, Ashcroft, Frances M
Publicado em 2006

Putative pore-loops of TMEM16/anoctamin channels affect channel density in cell membranes

Por Adomaviciene, Aiste, Smith, Keith J, Garnett, Hannah, Tammaro, Paolo
Publicado em 2013

Pharmacological evidence for a key role of voltage-gated K(+) channels in the function of rat aortic smooth muscle cells

Por Tammaro, Paolo, Smith, Amy L, Hutchings, Simon R, Smirnov, Sergey V
Publicado em 2004

Kir6.2 mutations causing neonatal diabetes provide new insights into Kir6.2–SUR1 interactions

Por Tammaro, Paolo, Girard, Christophe, Molnes, Janne, Njølstad, Pål R, Ashcroft, Frances M
Publicado em 2005

Electrophysiologically distinct smooth muscle cell subtypes in rat conduit and resistance pulmonary arteries

Por Smirnov, Sergey V, Beck, Richard, Tammaro, Paolo, Ishii, Tetsuro, Aaronson, Philip I
Publicado em 2002

Mechanism of allosteric activation of TMEM16A/ANO1 channels by a commonly used chloride channel blocker

Por Ta, Chau M, Adomaviciene, Aiste, Rorsman, Nils J G, Garnett, Hannah, Tammaro, Paolo
Publicado no Br J Pharmacol (2016)

Disease-causing mutations associated with four bestrophinopathies exhibit disparate effects on the localization, but not the oligomerization, of Bestrophin-1

Por Johnson, Adiv A., Lee, Yong-Suk, Chadburn, Andrew J., Tammaro, Paolo, Manson, Forbes D., Marmorstein, Lihua Y., Marmorstein, Alan D.
Publicado em 2014

Autosomal Dominant Hypercalciuria in a Mouse Model Due to a Mutation of the Epithelial Calcium Channel, TRPV5

Por Loh, Nellie Y., Bentley, Liz, Dimke, Henrik, Verkaart, Sjoerd, Tammaro, Paolo, Gorvin, Caroline M., Stechman, Michael J., Ahmad, Bushra N., Hannan, Fadil M., Piret, Sian E., Evans, Holly, Bellantuono, Ilaria, Hough, Tertius A., Fraser, William D., Hoenderop, Joost G. J., Ashcroft, Frances M., Brown, Steve D. M., Bindels, René J. M., Cox, Roger D., Thakker, Rajesh V.
Publicado em 2013