BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 25223803)

  • 1. Insights in KIR2.1 channel structure and function by an evolutionary approach; cloning and functional characterization of the first reptilian inward rectifier channel KIR2.1, derived from the California kingsnake (Lampropeltis getula californiae).
    Houtman MJ; Korte SM; Ji Y; Kok B; Vos MA; Stary-Weinzinger A; van der Heyden MA
    Biochem Biophys Res Commun; 2014 Oct; 452(4):992-7. PubMed ID: 25223803
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular characterization of an inward rectifier channel (IKir) found in avian vestibular hair cells: cloning and expression of pKir2.1.
    Correia MJ; Wood TG; Prusak D; Weng T; Rennie KJ; Wang HQ
    Physiol Genomics; 2004 Oct; 19(2):155-69. PubMed ID: 15316115
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification and functional characterisation of a novel KCNJ2 mutation, Val302del, causing Andersen-Tawil syndrome.
    Ördög B; Hategan L; Kovács M; Seprényi G; Kohajda Z; Nagy I; Hegedűs Z; Környei L; Jost N; Katona M; Szekeres M; Forster T; Papp JG; Varró A; Sepp R
    Can J Physiol Pharmacol; 2015 Jul; 93(7):569-75. PubMed ID: 26103554
    [TBL] [Abstract][Full Text] [Related]  

  • 4. PA-6 inhibits inward rectifier currents carried by V93I and D172N gain-of-function K
    Ji Y; Veldhuis MG; Zandvoort J; Romunde FL; Houtman MJC; Duran K; van Haaften G; Zangerl-Plessl EM; Takanari H; Stary-Weinzinger A; van der Heyden MAG
    J Biomed Sci; 2017 Jul; 24(1):44. PubMed ID: 28711067
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotype.
    Limberg MM; Zumhagen S; Netter MF; Coffey AJ; Grace A; Rogers J; Böckelmann D; Rinné S; Stallmeyer B; Decher N; Schulze-Bahr E
    Basic Res Cardiol; 2013 May; 108(3):353. PubMed ID: 23644778
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Contribution of cytosolic cysteine residues to the gating properties of the Kir2.1 inward rectifier.
    Garneau L; Klein H; Parent L; Sauvé R
    Biophys J; 2003 Jun; 84(6):3717-29. PubMed ID: 12770878
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cytoplasmic domain structures of Kir2.1 and Kir3.1 show sites for modulating gating and rectification.
    Pegan S; Arrabit C; Zhou W; Kwiatkowski W; Collins A; Slesinger PA; Choe S
    Nat Neurosci; 2005 Mar; 8(3):279-87. PubMed ID: 15723059
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Tamoxifen inhibits inward rectifier K+ 2.x family of inward rectifier channels by interfering with phosphatidylinositol 4,5-bisphosphate-channel interactions.
    Ponce-Balbuena D; López-Izquierdo A; Ferrer T; Rodríguez-Menchaca AA; Aréchiga-Figueroa IA; Sánchez-Chapula JA
    J Pharmacol Exp Ther; 2009 Nov; 331(2):563-73. PubMed ID: 19654266
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Stretch-induced alterations of human Kir2.1 channel currents.
    He Y; Xiao J; Yang Y; Zhou Q; Zhang Z; Pan Q; Liu Y; Chen Y
    Biochem Biophys Res Commun; 2006 Dec; 351(2):462-7. PubMed ID: 17067550
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Low-affinity spermine block mediating outward currents through Kir2.1 and Kir2.2 inward rectifier potassium channels.
    Ishihara K; Yan DH
    J Physiol; 2007 Sep; 583(Pt 3):891-908. PubMed ID: 17640933
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Two Kir2.1 channel populations with different sensitivities to Mg(2+) and polyamine block: a model for the cardiac strong inward rectifier K(+) channel.
    Yan DH; Ishihara K
    J Physiol; 2005 Mar; 563(Pt 3):725-44. PubMed ID: 15618275
    [TBL] [Abstract][Full Text] [Related]  

  • 12. T75M-KCNJ2 mutation causing Andersen-Tawil syndrome enhances inward rectification by changing Mg2+ sensitivity.
    Tani Y; Miura D; Kurokawa J; Nakamura K; Ouchida M; Shimizu K; Ohe T; Furukawa T
    J Mol Cell Cardiol; 2007 Aug; 43(2):187-96. PubMed ID: 17582433
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Kir2.x inward rectifier potassium channels are differentially regulated by adrenergic alpha1A receptors.
    Zitron E; Günth M; Scherer D; Kiesecker C; Kulzer M; Bloehs R; Scholz EP; Thomas D; Weidenhammer C; Kathöfer S; Bauer A; Katus HA; Karle CA
    J Mol Cell Cardiol; 2008 Jan; 44(1):84-94. PubMed ID: 18035370
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Flecainide increases Kir2.1 currents by interacting with cysteine 311, decreasing the polyamine-induced rectification.
    Caballero R; Dolz-Gaitón P; Gómez R; Amorós I; Barana A; González de la Fuente M; Osuna L; Duarte J; López-Izquierdo A; Moraleda I; Gálvez E; Sánchez-Chapula JA; Tamargo J; Delpón E
    Proc Natl Acad Sci U S A; 2010 Aug; 107(35):15631-6. PubMed ID: 20713726
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Trafficking-competent and trafficking-defective KCNJ2 mutations in Andersen syndrome.
    Ballester LY; Benson DW; Wong B; Law IH; Mathews KD; Vanoye CG; George AL
    Hum Mutat; 2006 Apr; 27(4):388. PubMed ID: 16541386
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Inward rectifier potassium current (I K1) and Kir2 composition of the zebrafish (Danio rerio) heart.
    Hassinen M; Haverinen J; Hardy ME; Shiels HA; Vornanen M
    Pflugers Arch; 2015 Dec; 467(12):2437-46. PubMed ID: 25991088
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel inwardly rectifying K+ channel, Kir2.5, is upregulated under chronic cold stress in fish cardiac myocytes.
    Hassinen M; Paajanen V; Vornanen M
    J Exp Biol; 2008 Jul; 211(Pt 13):2162-71. PubMed ID: 18552306
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome.
    Preisig-Müller R; Schlichthörl G; Goerge T; Heinen S; Brüggemann A; Rajan S; Derst C; Veh RW; Daut J
    Proc Natl Acad Sci U S A; 2002 May; 99(11):7774-9. PubMed ID: 12032359
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currents.
    Hattori T; Makiyama T; Akao M; Ehara E; Ohno S; Iguchi M; Nishio Y; Sasaki K; Itoh H; Yokode M; Kita T; Horie M; Kimura T
    Cardiovasc Res; 2012 Mar; 93(4):666-73. PubMed ID: 22155372
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Kir2.1 and K2P1 channels reconstitute two levels of resting membrane potential in cardiomyocytes.
    Zuo D; Chen K; Zhou M; Liu Z; Chen H
    J Physiol; 2017 Aug; 595(15):5129-5142. PubMed ID: 28543529
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.