| scholarly article | Q13442814 |
| P356 | DOI | 10.4161/CHAN.25003 |
| P953 | full work available online at | http://www.tandfonline.com/doi/pdf/10.4161/chan.25003 |
| https://doi.org/10.4161/chan.25003 | ||
| https://europepmc.org/articles/PMC3989359 | ||
| https://europepmc.org/articles/PMC3989359?pdf=render | ||
| https://www.tandfonline.com/doi/pdf/10.4161/chan.25003?needAccess=true | ||
| P932 | PMC publication ID | 3989359 |
| P698 | PubMed publication ID | 23695995 |
| P5875 | ResearchGate publication ID | 236929958 |
| P2093 | author name string | Qing Zhou | |
| Show-Ling Shyng | |||
| Emily B. Pratt | |||
| P2860 | cites work | Regulation of KATP channel activity by diazoxide and MgADP. Distinct functions of the two nucleotide binding folds of the sulfonylurea receptor | Q36436008 |
| Control of Rectification and Gating of Cloned KATP Channels by the Kir6.2 Subunit | Q36445028 | ||
| MgATP activates the beta cell KATP channel by interaction with its SUR1 subunit. | Q36515292 | ||
| ATP activates ATP-sensitive potassium channels composed of mutant sulfonylurea receptor 1 and Kir6.2 with diminished PIP2 sensitivity | Q39430157 | ||
| Sulfonylurea receptor 1 mutations that cause opposite insulin secretion defects with chemical chaperone exposure | Q39893899 | ||
| ATP inhibition of KATP channels: control of nucleotide sensitivity by the N-terminal domain of the Kir6.2 subunit | Q40976849 | ||
| A new ER trafficking signal regulates the subunit stoichiometry of plasma membrane K(ATP) channels | Q41644878 | ||
| Molecular basis for K(ATP) assembly: transmembrane interactions mediate association of a K+ channel with an ABC transporter | Q41734243 | ||
| SUR-dependent modulation of KATP channels by an N-terminal KIR6.2 peptide. Defining intersubunit gating interactions | Q44126962 | ||
| Sulfonylureas correct trafficking defects of ATP-sensitive potassium channels caused by mutations in the sulfonylurea receptor | Q44715007 | ||
| Involvement of the n-terminus of Kir6.2 in coupling to the sulphonylurea receptor | Q48914424 | ||
| The N-terminus of KIR6.2 limits spontaneous bursting and modulates the ATP-inhibition of KATP channels | Q53936555 | ||
| Sulfonylurea receptors set the maximal open probability, ATP sensitivity and plasma membrane density of KATP channels | Q74589534 | ||
| Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor | Q24304448 | ||
| The essential role of the Walker A motifs of SUR1 in K-ATP channel activation by Mg-ADP and diazoxide | Q24532117 | ||
| Crystal Structure of the Eukaryotic Strong Inward-Rectifier K+ Channel Kir2.2 at 3.1 A Resolution | Q27646617 | ||
| Molecular biology of adenosine triphosphate-sensitive potassium channels | Q28141603 | ||
| Sur domains that associate with and gate KATP pores define a novel gatekeeper | Q28203814 | ||
| Truncation of Kir6.2 produces ATP-sensitive K+ channels in the absence of the sulphonylurea receptor | Q28237709 | ||
| KATP channels as molecular sensors of cellular metabolism | Q28303315 | ||
| ATP-sensitive potassium channelopathies: focus on insulin secretion | Q33905803 | ||
| Cloning of the beta cell high-affinity sulfonylurea receptor: a regulator of insulin secretion | Q34308492 | ||
| N-terminal transmembrane domain of SUR1 controls gating of Kir6.2 by modulating channel sensitivity to PIP2 | Q34618893 | ||
| N-terminal transmembrane domain of the SUR controls trafficking and gating of Kir6 channel subunits | Q35208854 | ||
| Engineered interaction between SUR1 and Kir6.2 that enhances ATP sensitivity in KATP channels | Q36130308 | ||
| Congenital hyperinsulinism associated ABCC8 mutations that cause defective trafficking of ATP-sensitive K+ channels: identification and rescue | Q36428374 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 313–317 | |
| P577 | publication date | 2013-05-21 | |
| 2013-07-01 | |||
| P1433 | published in | Channels | Q15764469 |
| P1476 | title | Engineered Kir6.2 mutations that correct the trafficking defect of K(ATP) channels caused by specific SUR1 mutations | |
| Engineered Kir6.2 mutations that correct the trafficking defect of KATPchannels caused by specific SUR1 mutations | |||
| P478 | volume | 7 |
| Q50147769 | Expression, purification, and electrophysiological characterization of a recombinant, fluorescent Kir6.2 in mammalian cells. |
| Q37409971 | Pharmacological rescue of trafficking-impaired ATP-sensitive potassium channels |
| Q35199497 | Structurally distinct ligands rescue biogenesis defects of the KATP channel complex via a converging mechanism |
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