These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 37031592)

  • 41. Dynamic subunit stoichiometry confers a progressive continuum of pharmacological sensitivity by KCNQ potassium channels.
    Yu H; Lin Z; Mattmann ME; Zou B; Terrenoire C; Zhang H; Wu M; McManus OB; Kass RS; Lindsley CW; Hopkins CR; Li M
    Proc Natl Acad Sci U S A; 2013 May; 110(21):8732-7. PubMed ID: 23650380
    [TBL] [Abstract][Full Text] [Related]  

  • 42. The role of abnormal trafficking of KCNE1 in long QT syndrome 5.
    Harmer SC; Tinker A
    Biochem Soc Trans; 2007 Nov; 35(Pt 5):1074-6. PubMed ID: 17956282
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Identification of specific pore residues mediating KCNQ1 inactivation. A novel mechanism for long QT syndrome.
    Seebohm G; Scherer CR; Busch AE; Lerche C
    J Biol Chem; 2001 Apr; 276(17):13600-5. PubMed ID: 11278406
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Mutation analysis of potassium channel genes KCNQ1 and KCNH2 in patients with long QT syndrome.
    Liu W; Hu D; Li C; Li P; Li Y; Li Z; Li L; Qin X; Dong W; Qi Y; Chen S; Wang Q
    Chin Med J (Engl); 2003 Sep; 116(9):1333-5. PubMed ID: 14527360
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Biophysical properties of mutant KCNQ1 S277L channels linked to hereditary long QT syndrome with phenotypic variability.
    Aidery P; Kisselbach J; Schweizer PA; Becker R; Katus HA; Thomas D
    Biochim Biophys Acta; 2011 Apr; 1812(4):488-94. PubMed ID: 21241800
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Characterization of an LQT5-related mutation in KCNE1, Y81C: implications for a role of KCNE1 cytoplasmic domain in IKs channel function.
    Wu DM; Lai LP; Zhang M; Wang HL; Jiang M; Liu XS; Tseng GN
    Heart Rhythm; 2006 Sep; 3(9):1031-40. PubMed ID: 16945797
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Rb+ efflux through functional activation of cardiac KCNQ1/minK channels by the benzodiazepine R-L3 (L-364,373).
    Jow F; Tseng E; Maddox T; Shen R; Kowal D; Dunlop J; Mekonnen B; Wang K
    Assay Drug Dev Technol; 2006 Aug; 4(4):443-50. PubMed ID: 16945016
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Functional phenotype variations of two novel K
    Hammami Bomholtz S; Refaat M; Buur Steffensen A; David JP; Espinosa K; Nussbaum R; Wojciak J; Hjorth Bentzen B; Scheinman M; Schmitt N
    Pacing Clin Electrophysiol; 2020 Feb; 43(2):210-216. PubMed ID: 31899541
    [TBL] [Abstract][Full Text] [Related]  

  • 49. The N-terminal juxtamembranous domain of KCNQ1 is critical for channel surface expression: implications in the Romano-Ward LQT1 syndrome.
    Dahimène S; Alcoléa S; Naud P; Jourdon P; Escande D; Brasseur R; Thomas A; Baró I; Mérot J
    Circ Res; 2006 Nov; 99(10):1076-83. PubMed ID: 17053194
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Characterization of a novel mutant KCNQ1 channel subunit lacking a large part of the C-terminal domain.
    Kimoto K; Kinoshita K; Yokoyama T; Hata Y; Komatsu T; Tsushima E; Nishide K; Yamaguchi Y; Mizumaki K; Tabata T; Inoue H; Nishida N; Fukurotani K
    Biochem Biophys Res Commun; 2013 Oct; 440(2):283-8. PubMed ID: 24070608
    [TBL] [Abstract][Full Text] [Related]  

  • 51. KCNQ1 channels voltage dependence through a voltage-dependent binding of the S4-S5 linker to the pore domain.
    Choveau FS; Rodriguez N; Abderemane Ali F; Labro AJ; Rose T; Dahimène S; Boudin H; Le Hénaff C; Escande D; Snyders DJ; Charpentier F; Mérot J; Baró I; Loussouarn G
    J Biol Chem; 2011 Jan; 286(1):707-16. PubMed ID: 20940310
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Hexachlorophene is a potent KCNQ1/KCNE1 potassium channel activator which rescues LQTs mutants.
    Zheng Y; Zhu X; Zhou P; Lan X; Xu H; Li M; Gao Z
    PLoS One; 2012; 7(12):e51820. PubMed ID: 23251633
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Phosphatidylinositol-4,5-bisphosphate is required for KCNQ1/KCNE1 channel function but not anterograde trafficking.
    Royal AA; Tinker A; Harmer SC
    PLoS One; 2017; 12(10):e0186293. PubMed ID: 29020060
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Characterization and subcellular localization of KCNQ1 with a heterozygous mutation in the C terminus.
    Yamashita F; Horie M; Kubota T; Yoshida H; Yumoto Y; Kobori A; Ninomiya T; Kono Y; Haruna T; Tsuji K; Washizuka T; Takano M; Otani H; Sasayama S; Aizawa Y
    J Mol Cell Cardiol; 2001 Feb; 33(2):197-207. PubMed ID: 11162126
    [TBL] [Abstract][Full Text] [Related]  

  • 55. KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
    Liu W; Yang J; Hu D; Kang C; Li C; Zhang S; Li P; Chen Z; Qin X; Ying K; Li Y; Li Y; Li Z; Cheng X; Li L; Qi Y; Chen S; Wang Q
    Hum Mutat; 2002 Dec; 20(6):475-6. PubMed ID: 12442276
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Interaction between the cardiac rapidly (IKr) and slowly (IKs) activating delayed rectifier potassium channels revealed by low K+-induced hERG endocytic degradation.
    Guo J; Wang T; Yang T; Xu J; Li W; Fridman MD; Fisher JT; Zhang S
    J Biol Chem; 2011 Oct; 286(40):34664-74. PubMed ID: 21844197
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Gating-related molecular motions in the extracellular domain of the IKs channel: implications for IKs channelopathy.
    Wang YH; Jiang M; Xu XL; Hsu KL; Zhang M; Tseng GN
    J Membr Biol; 2011 Feb; 239(3):137-56. PubMed ID: 21152909
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Upgraded molecular models of the human KCNQ1 potassium channel.
    Kuenze G; Duran AM; Woods H; Brewer KR; McDonald EF; Vanoye CG; George AL; Sanders CR; Meiler J
    PLoS One; 2019; 14(9):e0220415. PubMed ID: 31518351
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Ginsenoside Rg3 activates human KCNQ1 K+ channel currents through interacting with the K318 and V319 residues: a role of KCNE1 subunit.
    Choi SH; Shin TJ; Lee BH; Chu DH; Choe H; Pyo MK; Hwang SH; Kim BR; Lee SM; Lee JH; Kim DH; Kim HC; Rhim HW; Nah SY
    Eur J Pharmacol; 2010 Jul; 637(1-3):138-47. PubMed ID: 20399767
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Structural Modelling of KCNQ1 and KCNH2 Double Mutant Proteins, Identified in Two Severe Long QT Syndrome Cases, Reveals New Insights into Cardiac Channelopathies.
    Agudelo WA; Gil-Quiñones SR; Fonseca A; Arenas A; Castro L; Sierra-Díaz DC; Patarroyo MA; Laissue P; Suárez CF; Cabrera R
    Int J Mol Sci; 2021 Nov; 22(23):. PubMed ID: 34884666
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.