Defining a Unifying Mechanism for Select Cardiomyopathy-Linked Variants of Desmoplakin

被引：0
|
作者：
Ackermann, Maegen
Manring, Heather
Ng, Ronald
Albertelli, Taylor
Bobbili, Prameela Jyothi
Stevens, Tyler
Jacoby, Daniel
Janssen, Paul
Kilic, Ahmet
Wright, Nathan
Wright, Nathan
Qyang, Y.
Campbell, S.
机构：
来源：
CIRCULATION RESEARCH | 2018年 / 123卷
关键词：
D O I：
10.1161/res.123.suppl_1.375
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
A375
引用
收藏
页数：2
相关论文
共 50 条
  • [21] Comparable Calcium Handling and Contractility in Human IPSC Cardiomyocyte Models of Three Different Hypertrophic Cardiomyopathy-Linked Mutations
    Kim, Kyungsoo
    Wang, Lili
    Sequeira, Vasco
    Wu, Joseph C.
    Knollmann, Bjorn C.
    BIOPHYSICAL JOURNAL, 2018, 114 (03) : 619A - 619A
  • [22] Hair and cutaneous phenotypes linked to Arrhythmogenic Cardiomyopathy caused by Desmoplakin haploinsufficiency: an additional disease marker
    Castelletti, S.
    Maruthappu, T.
    Posafalvi, A.
    Syrris, P.
    O'Toole, E. A.
    Green, K. J.
    Tinker, A.
    McKenna, W. J.
    Kelsell, D. P.
    EUROPEAN HEART JOURNAL, 2018, 39 : 1206 - 1206
  • [23] Myosin Regulatory Light Chain Phosphorylation Rescues Cardiac Dysfunction Caused by Familial Hypertrophic Cardiomyopathy-Linked Mutations
    Muthu, Priya
    Kazmierczak, Katarzyna
    Huang, Wenrui
    Rojas, Ana I.
    Szczesna-Cordary, Danuta
    BIOPHYSICAL JOURNAL, 2012, 102 (03) : 557A - 557A
  • [24] HCM and DCM cardiomyopathy-linked α-tropomyosin mutations influence off-state stability and crossbridge interaction on thin filaments
    Farman, Gerrie P.
    Rynkiewicz, Michael J.
    Orzechowski, Marek
    Lehman, William
    Moore, Jeffrey R.
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2018, 647 : 84 - 92
  • [25] The structural and functional effects of the familial hypertrophic cardiomyopathy-linked cardiac troponin C mutation, L29Q
    Robertson, Ian M.
    Sevrieva, Ivanka
    Li, Monica X.
    Irving, Malcolm
    Sun, Yin-Biao
    Sykes, Brian D.
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2015, 87 : 257 - 269
  • [26] Identification of dilated cardiomyopathy-linked key genes by bioinformatics methods and evaluating the impact of tannic acid and monosodium glutamate in rats
    Karadas, Habibe
    Tosun, Hilal
    Ceylan, Hamid
    BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, 2024,
  • [27] MYOCARDITIS PRESENTATION OF ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY LINKED TO DESMOPLAKIN C.3526DELG GENE MUTATION
    Reddy, Krishna Theja
    Syeda, Humera
    Bains, Nainjot
    Karimi, Afshin
    Ho, Andrew
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2021, 77 (18) : 2224 - 2224
  • [28] Impact of familial hypertrophic cardiomyopathy-linked mutations in the NH2 terminus of the RLC on β-myosin cross-bridge mechanics
    Farman, Gerrie P.
    Muthu, Priya
    Kazmierczak, Katarzyna
    Szczesna-Cordary, Danuta
    Moore, Jeffrey R.
    JOURNAL OF APPLIED PHYSIOLOGY, 2014, 117 (12) : 1471 - 1477
  • [29] Cardiomyopathy-Linked Mutation K15N in Tropomyosin Alters Calcium-Dependent Regulation of Reconstituted Cardiac Thin Filaments
    Ly, Thu N.
    Schlecht, William
    Colpan, Mert
    Dong, Wen-Ji
    Kostyukova, Alla S.
    BIOPHYSICAL JOURNAL, 2018, 114 (03) : 141A - 141A
  • [30] Ca2+-sensitizing effect of familial hypertrophic cardiomyopathy-linked troponin T mutation reduces contractile reserve of mouse heart
    Sirenko, SG
    Potter, JD
    Knollmann, BC
    CIRCULATION, 2004, 110 (17) : 108 - 108
12345