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Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome. , Adams DS ., J Physiol. June 15, 2016; 594 (12): 3245-70.
β2-Adrenergic ion-channel coupled receptors as conformational motion detectors. , Caro LN., PLoS One. March 9, 2011; 6 (3): e18226.
The N-terminal transmembrane domain (TMD0) and a cytosolic linker (L0) of sulphonylurea receptor define the unique intrinsic gating of KATP channels. , Fang K., J Physiol. October 15, 2006; 576 (Pt 2): 379-89.
Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features. , Proks P., Proc Natl Acad Sci U S A. December 14, 2004; 101 (50): 17539-44.
Identification and pharmacological correction of a membrane trafficking defect associated with a mutation in the sulfonylurea receptor causing familial hyperinsulinism. , Partridge CJ., J Biol Chem. September 21, 2001; 276 (38): 35947-52.
A new ER trafficking signal regulates the subunit stoichiometry of plasma membrane K(ATP) channels. , Zerangue N., Neuron. March 1, 1999; 22 (3): 537-48.
MgATP activates the beta cell KATP channel by interaction with its SUR1 subunit. , Gribble FM., Proc Natl Acad Sci U S A. June 9, 1998; 95 (12): 7185-90.