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 *

136 related articles for article (PubMed ID: 35526388)

  • 61. Association of Genetic and Clinical Aspects of Congenital Long QT Syndrome With Life-Threatening Arrhythmias in Japanese Patients.
    Shimizu W; Makimoto H; Yamagata K; Kamakura T; Wada M; Miyamoto K; Inoue-Yamada Y; Okamura H; Ishibashi K; Noda T; Nagase S; Miyazaki A; Sakaguchi H; Shiraishi I; Makiyama T; Ohno S; Itoh H; Watanabe H; Hayashi K; Yamagishi M; Morita H; Yoshinaga M; Aizawa Y; Kusano K; Miyamoto Y; Kamakura S; Yasuda S; Ogawa H; Tanaka T; Sumitomo N; Hagiwara N; Fukuda K; Ogawa S; Aizawa Y; Makita N; Ohe T; Horie M; Aiba T
    JAMA Cardiol; 2019 Mar; 4(3):246-254. PubMed ID: 30758498
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.
    Kapa S; Tester DJ; Salisbury BA; Harris-Kerr C; Pungliya MS; Alders M; Wilde AA; Ackerman MJ
    Circulation; 2009 Nov; 120(18):1752-60. PubMed ID: 19841300
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Patient-Specific and Gene-Corrected Induced Pluripotent Stem Cell-Derived Cardiomyocytes Elucidate Single-Cell Phenotype of Short QT Syndrome.
    Guo F; Sun Y; Wang X; Wang H; Wang J; Gong T; Chen X; Zhang P; Su L; Fu G; Su J; Yang S; Lai R; Jiang C; Liang P
    Circ Res; 2019 Jan; 124(1):66-78. PubMed ID: 30582453
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Digenic heterozygous mutations of KCNH2 and SCN5A induced young and early-onset long QT syndrome and sinoatrial node dysfunction.
    Yang Z; Ma Y; Huang J; Xian J; Huang Y; Wu L; Zhu W; Wang F; Chen L; Lin X; Lin Y
    Ann Noninvasive Electrocardiol; 2022 Jan; 27(1):e12889. PubMed ID: 34755423
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Trafficking defect and proteasomal degradation contribute to the phenotype of a novel KCNH2 long QT syndrome mutation.
    Mihic A; Chauhan VS; Gao X; Oudit GY; Tsushima RG
    PLoS One; 2011 Mar; 6(3):e18273. PubMed ID: 21483829
    [TBL] [Abstract][Full Text] [Related]  

  • 66. A novel life-threatening mutation in long QT2 syndrome.
    Biernacka E; Szperl M; Kosiec A; Roszczynko M; Hoffman P
    Kardiol Pol; 2015; 73(11):1097-100. PubMed ID: 25987402
    [TBL] [Abstract][Full Text] [Related]  

  • 67. An intronic mutation causes long QT syndrome.
    Zhang L; Vincent GM; Baralle M; Baralle FE; Anson BD; Benson DW; Whiting B; Timothy KW; Carlquist J; January CT; Keating MT; Splawski I
    J Am Coll Cardiol; 2004 Sep; 44(6):1283-91. PubMed ID: 15364333
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Modeling long QT syndrome type 2 on-a-chip via in-depth assessment of isogenic gene-edited 3D cardiac tissues.
    Veldhuizen J; Mann HF; Karamanova N; Van Horn WD; Migrino RQ; Brafman D; Nikkhah M
    Sci Adv; 2022 Dec; 8(50):eabq6720. PubMed ID: 36525500
    [TBL] [Abstract][Full Text] [Related]  

  • 69. 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]  

  • 70. Long QT syndrome with mutations in three genes: A rare case.
    Fernandes M; Martins Ribeiro S; Sanfins V; Lourenço A
    Rev Port Cardiol; 2015 May; 34(5):359.e1-5. PubMed ID: 25935074
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Allele-specific RNA interference rescues the long-QT syndrome phenotype in human-induced pluripotency stem cell cardiomyocytes.
    Matsa E; Dixon JE; Medway C; Georgiou O; Patel MJ; Morgan K; Kemp PJ; Staniforth A; Mellor I; Denning C
    Eur Heart J; 2014 Apr; 35(16):1078-87. PubMed ID: 23470493
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Characterization of novel KCNH2 mutations in type 2 long QT syndrome manifesting as seizures.
    Keller DI; Grenier J; Christé G; Dubouloz F; Osswald S; Brink M; Ficker E; Chahine M
    Can J Cardiol; 2009 Aug; 25(8):455-62. PubMed ID: 19668779
    [TBL] [Abstract][Full Text] [Related]  

  • 73. C-terminal HERG (LQT2) mutations disrupt IKr channel regulation through 14-3-3epsilon.
    Choe CU; Schulze-Bahr E; Neu A; Xu J; Zhu ZI; Sauter K; Bähring R; Priori S; Guicheney P; Mönnig G; Neapolitano C; Heidemann J; Clancy CE; Pongs O; Isbrandt D
    Hum Mol Genet; 2006 Oct; 15(19):2888-902. PubMed ID: 16923798
    [TBL] [Abstract][Full Text] [Related]  

  • 74. An Interdomain KCNH2 Mutation Produces an Intermediate Long QT Syndrome.
    Osterbur ML; Zheng R; Marion R; Walsh C; McDonald TV
    Hum Mutat; 2015 Aug; 36(8):764-73. PubMed ID: 25914329
    [TBL] [Abstract][Full Text] [Related]  

  • 75. New onset seizures in a patient with Long QT Syndrome (LQTS2) and a pathogenic carboxyl-terminus frameshift variant of the KCNH2 gene.
    Zarroli K; Querfurth H
    J Clin Neurosci; 2018 Jul; 53():253-255. PubMed ID: 29739726
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects.
    Swan H; Viitasalo M; Piippo K; Laitinen P; Kontula K; Toivonen L
    J Am Coll Cardiol; 1999 Sep; 34(3):823-9. PubMed ID: 10483966
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Position of premature termination codons determines susceptibility of hERG mutations to nonsense-mediated mRNA decay in long QT syndrome.
    Gong Q; Stump MR; Zhou Z
    Gene; 2014 Apr; 539(2):190-7. PubMed ID: 24530480
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Generation of two iPSC lines from long QT syndrome patients carrying SNTA1 variants.
    Jimenez-Tellez N; Vera CD; Yildirim Z; Vicente Guevara J; Zhang T; Wu JC
    Stem Cell Res; 2023 Feb; 66():103003. PubMed ID: 36528013
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Novel characteristics of a trafficking-defective G572R-hERG channel linked to hereditary long QT syndrome.
    Lian J; Huang N; Zhou J; Ge S; Huang X; Huo J; Liu L; Xu W; Zhang S; Yang X; Zhou J; Huang C
    Can J Cardiol; 2010 Oct; 26(8):417-22. PubMed ID: 20931094
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Congenital long QT syndrome with compound mutations in the KCNH2 gene.
    Bando S; Soeki T; Matsuura T; Niki T; Ise T; Yamaguchi K; Taketani Y; Iwase T; Yamada H; Wakatsuki T; Akaike M; Aiba T; Shimizu W; Sata M
    Heart Vessels; 2014 Jul; 29(4):554-9. PubMed ID: 24057343
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.