The two C-terminal tyrosines stabilize occluded Na/K pump conformations containing Na or K ions

per Vedovato, Natascia, Gadsby, David C.
Publicat 2010

Route, mechanism, and implications of proton import during Na(+)/K(+) exchange by native Na(+)/K(+)-ATPase pumps

per Vedovato, Natascia, Gadsby, David C.
Publicat 2014

The Nucleotide-Binding Sites of SUR1: A Mechanistic Model

per Vedovato, Natascia, Ashcroft, Frances M., Puljung, Michael C.
Publicat a Biophys J (2015)

Neonatal Diabetes and the K(ATP) Channel: From Mutation to Therapy

per Ashcroft, Frances M., Puljung, Michael C., Vedovato, Natascia
Publicat a Trends Endocrinol Metab (2017)

Activation mechanism of ATP-sensitive K(+) channels explored with real-time nucleotide binding

per Puljung, Michael, Vedovato, Natascia, Usher, Samuel, Ashcroft, Frances
Publicat a eLife (2019)

Role of the C‐terminus of SUR in the differential regulation of β‐cell and cardiac K(ATP) channels by MgADP and metabolism

per Vedovato, Natascia, Rorsman, Olof, Hennis, Konstantin, Ashcroft, Frances M., Proks, Peter
Publicat a J Physiol (2018)

Running out of time: the decline of channel activity and nucleotide activation in adenosine triphosphate-sensitive K-channels

per Proks, Peter, Puljung, Michael C., Vedovato, Natascia, Sachse, Gregor, Mulvaney, Rachel, Ashcroft, Frances M.
Publicat a Philos Trans R Soc Lond B Biol Sci (2016)

Correction to ‘Running out of time: the decline of channel activity and nucleotide activation in adenosine triphosphate-sensitive K-channels’

per Proks, Peter, Puljung, Michael C., Vedovato, Natascia, Sachse, Gregor, Mulvaney, Rachel, Ashcroft, Frances M.
Publicat a Philos Trans R Soc Lond B Biol Sci (2016)

Neonatal diabetes caused by a homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensitivity markedly affect diabetes risk

per Vedovato, Natascia, Cliff, Edward, Proks, Peter, Poovazhagi, Varadarajan, Flanagan, Sarah E., Ellard, Sian, Hattersley, Andrew T., Ashcroft, Frances M.
Publicat a Diabetologia (2016)

Hypothermia-induced dystonia and abnormal cerebellar activity in a mouse model with a single disease-mutation in the sodium-potassium pump

per Isaksen, Toke Jost, Kros, Lieke, Vedovato, Natascia, Holm, Thomas Hellesøe, Vitenzon, Ariel, Gadsby, David C., Khodakhah, Kamran, Lykke-Hartmann, Karin
Publicat a PLoS Genet (2017)

Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes

per Babiker, Tarig, Vedovato, Natascia, Patel, Kashyap, Thomas, Nicholas, Finn, Roisin, Männikkö, Roope, Chakera, Ali J., Flanagan, Sarah E., Shepherd, Maggie H., Ellard, Sian, Ashcroft, Frances M., Hattersley, Andrew T.
Publicat a Diabetologia (2016)