Activation of KNCQ1/KCNE1 Channel by Classic PKC is Impaired in Long QT Syndrome Type 1

被引：0
|
作者：
O-Uchi, Jin [1 ]
Lopes, Coeli M. B. [1 ]
机构：
[1] Univ Rochester, Sch Med & Dent, Rochester, NY USA
来源：
BIOPHYSICAL JOURNAL | 2011年 / 100卷 / 03期
关键词：
D O I：
暂无
中图分类号：
Q6 [生物物理学];
学科分类号：
071011 ;
摘要：
引用
收藏
页码：197 / 198
页数：2
相关论文
共 50 条
  • [1] The role of abnormal trafficking of KCNE1 in long QT syndrome 5
    Harmer, S. C.
    Tinker, A.
    BIOCHEMICAL SOCIETY TRANSACTIONS, 2007, 35 : 1074 - 1076
  • [2] Congenital Hyperinsulinism and Long QT Syndrome Attributable to a Variant in KCNE1
    Sigal, Winifred
    Boodhansingh, Kara E.
    Ganguly, Arupa
    Mitteer, Lauren M.
    Stanley, Charles A.
    De Leon, Diva D.
    HORMONE RESEARCH IN PAEDIATRICS, 2025,
  • [3] Mutations in KCNE1 Promote Cardiac Alternans in Long QT Syndrome Type 5 Rabbits
    Kim, Tae Yun
    Kabakov, Anatoli
    Terentyeva, Radmila
    Terentyev, Dmitry A.
    Lu, YiChun
    Odening, Katja E.
    Varro, Andras
    Bosze, Zsuzsanna
    Koren, Gideon
    Choi, Bum-Rak
    BIOPHYSICAL JOURNAL, 2020, 118 (03) : 102A - 102A
  • [4] A Possible Explanation for the Low Penetrance of Pathogenic KCNE1 Variants in Long QT Syndrome Type 5
    Deri, Szilvia
    Hartai, Teodora
    Virag, Laszlo
    Jost, Norbert
    Labro, Alain J.
    Varro, Andras
    Baczko, Istvan
    Nattel, Stanley
    Ordog, Balazs
    PHARMACEUTICALS, 2022, 15 (12)
  • [5] Genomic structure of three long QT syndrome genes: KVLQT1, HERG and KCNE1
    Splawski, I
    Shen, JX
    Timothy, KW
    Vincent, GM
    Lehmann, MH
    Keating, MT
    CIRCULATION, 1998, 98 (17) : 672 - 672
  • [6] Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1
    Splawski, I
    Shen, JX
    Timothy, KW
    Vincent, GM
    Lehmann, MH
    Keating, MT
    GENOMICS, 1998, 51 (01) : 86 - 97
  • [7] KCNE1 D85N polymorphism - a sex-specific modifier in type 1 long QT syndrome?
    Lahtinen, Annukka M.
    Marjamaa, Annukka
    Swan, Heikki
    Kontula, Kimmo
    BMC MEDICAL GENETICS, 2011, 12
  • [8] A homozygous mutation in KCNE1 causes long-QT syndrome without deafness
    Denjoy, I
    Berthet, M
    Gouas, L
    Simon, F
    Lupoglazoff, JM
    Guicheney, P
    CIRCULATION, 2004, 110 (17) : 501 - 502
  • [9] KCNE1 G38S polymorphism is not the cause of long QT syndrome
    Kanters, Jorgen K.
    Olesen, Morten S.
    Christiansen, Michael
    JOURNAL OF ELECTROCARDIOLOGY, 2016, 49 (02) : 249 - 250
  • [10] Long-QT mutations in KCNE1 modulate the 1713-estradiol response of Kv7.1/KCNE1
    Erlandsdotter, Lisa -Marie
    Giammarino, Lucilla
    Halili, Azemine
    Nikesjo, Johan
    Green, Henrik
    Odening, Katja E.
    Liin, Sara I.
    SCIENCE ADVANCES, 2023, 9 (11)
12345