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 *

217 related articles for article (PubMed ID: 35768468)

  • 61. A hERG mutation E1039X produced a synergistic lesion on I
    Wu J; Mizusawa Y; Ohno S; Ding WG; Higaki T; Wang Q; Kohjitani H; Makiyama T; Itoh H; Toyoda F; James AF; Hancox JC; Matsuura H; Horie M
    Sci Rep; 2018 Feb; 8(1):3129. PubMed ID: 29449639
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Functional interactions between KCNE1 C-terminus and the KCNQ1 channel.
    Chen J; Zheng R; Melman YF; McDonald TV
    PLoS One; 2009; 4(4):e5143. PubMed ID: 19340287
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Conformational changes of an ion-channel during gating and emerging electrophysiologic properties: Application of a computational approach to cardiac Kv7.1.
    Nekouzadeh A; Rudy Y
    Prog Biophys Mol Biol; 2016 Jan; 120(1-3):18-27. PubMed ID: 26743208
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Identification and characterisation of a novel KCNQ1 mutation in a family with Romano-Ward syndrome.
    Zehelein J; Thomas D; Khalil M; Wimmer AB; Koenen M; Licka M; Wu K; Kiehn J; Brockmeier K; Kreye VA; Karle CA; Katus HA; Ulmer HE; Schoels W
    Biochim Biophys Acta; 2004 Nov; 1690(3):185-92. PubMed ID: 15511625
    [TBL] [Abstract][Full Text] [Related]  

  • 65. PKA and PKC partially rescue long QT type 1 phenotype by restoring channel-PIP2 interactions.
    Matavel A; Medei E; Lopes CM
    Channels (Austin); 2010; 4(1):3-11. PubMed ID: 19934648
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Sudden death associated with QT interval prolongation and KCNQ1 gene mutation in a family of English Springer Spaniels.
    Ware WA; Reina-Doreste Y; Stern JA; Meurs KM
    J Vet Intern Med; 2015; 29(2):561-8. PubMed ID: 25779927
    [TBL] [Abstract][Full Text] [Related]  

  • 67. 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]  

  • 68. Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome.
    Grunnet M; Behr ER; Calloe K; Hofman-Bang J; Till J; Christiansen M; McKenna WJ; Olesen SP; Schmitt N
    Heart Rhythm; 2005 Nov; 2(11):1238-49. PubMed ID: 16253915
    [TBL] [Abstract][Full Text] [Related]  

  • 69. A founder mutation of the potassium channel KCNQ1 in long QT syndrome: implications for estimation of disease prevalence and molecular diagnostics.
    Piippo K; Swan H; Pasternack M; Chapman H; Paavonen K; Viitasalo M; Toivonen L; Kontula K
    J Am Coll Cardiol; 2001 Feb; 37(2):562-8. PubMed ID: 11216980
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Preparation, functional characterization, and NMR studies of human KCNE1, a voltage-gated potassium channel accessory subunit associated with deafness and long QT syndrome.
    Tian C; Vanoye CG; Kang C; Welch RC; Kim HJ; George AL; Sanders CR
    Biochemistry; 2007 Oct; 46(41):11459-72. PubMed ID: 17892302
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Upregulation of KCNE1 induces QT interval prolongation in patients with chronic heart failure.
    Watanabe E; Yasui K; Kamiya K; Yamaguchi T; Sakuma I; Honjo H; Ozaki Y; Morimoto S; Hishida H; Kodama I
    Circ J; 2007 Apr; 71(4):471-8. PubMed ID: 17384445
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Structural Basis of Human KCNQ1 Modulation and Gating.
    Sun J; MacKinnon R
    Cell; 2020 Jan; 180(2):340-347.e9. PubMed ID: 31883792
    [TBL] [Abstract][Full Text] [Related]  

  • 73. The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.
    Winkel BG; Larsen MK; Berge KE; Leren TP; Nissen PH; Olesen MS; Hollegaard MV; Jespersen T; Yuan L; Nielsen N; Haunsø S; Svendsen JH; Wang Y; Kristensen IB; Jensen HK; Tfelt-Hansen J; Banner J
    J Cardiovasc Electrophysiol; 2012 Oct; 23(10):1092-8. PubMed ID: 22882672
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Do K
    Tsvetkov D; Kaßmann M; Tano JY; Chen L; Schleifenbaum J; Voelkl J; Lang F; Huang Y; Gollasch M
    Br J Pharmacol; 2017 Jan; 174(2):150-162. PubMed ID: 28000293
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Dominant-negative I(Ks) suppression by KCNQ1-deltaF339 potassium channels linked to Romano-Ward syndrome.
    Thomas D; Wimmer AB; Karle CA; Licka M; Alter M; Khalil M; Ulmer HE; Kathöfer S; Kiehn J; Katus HA; Schoels W; Koenen M; Zehelein J
    Cardiovasc Res; 2005 Aug; 67(3):487-97. PubMed ID: 15950200
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Impaired ion channel function related to a common KCNQ1 mutation - implications for risk stratification in long QT syndrome 1.
    Aidery P; Kisselbach J; Schweizer PA; Becker R; Katus HA; Thomas D
    Gene; 2012 Dec; 511(1):26-33. PubMed ID: 23000022
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Mechanisms of KCNQ1 channel dysfunction in long QT syndrome involving voltage sensor domain mutations.
    Huang H; Kuenze G; Smith JA; Taylor KC; Duran AM; Hadziselimovic A; Meiler J; Vanoye CG; George AL; Sanders CR
    Sci Adv; 2018 Mar; 4(3):eaar2631. PubMed ID: 29532034
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Impaired KCNQ1-KCNE1 and phosphatidylinositol-4,5-bisphosphate interaction underlies the long QT syndrome.
    Park KH; Piron J; Dahimene S; Mérot J; Baró I; Escande D; Loussouarn G
    Circ Res; 2005 Apr; 96(7):730-9. PubMed ID: 15746441
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Gating and flickery block differentially affected by rubidium in homomeric KCNQ1 and heteromeric KCNQ1/KCNE1 potassium channels.
    Pusch M; Bertorello L; Conti F
    Biophys J; 2000 Jan; 78(1):211-26. PubMed ID: 10620287
    [TBL] [Abstract][Full Text] [Related]  

  • 80. A hydrophobicity-dependent motif responsible for surface expression of cardiac potassium channel.
    Pan N; Sun J; Lv C; Li H; Ding J
    Cell Signal; 2009 Feb; 21(2):349-55. PubMed ID: 19041715
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.