1887
Volume 2015, Issue 2
  • ISSN: 2305-7823
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2015-07-04
2019-08-20
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References

  1. [1]. Grimm   W., , Maisch   B. . Sudden cardiac death in dilated cardiomyopathy – therapeutic options. . Herz.   2002; ;27: 8 : 750– 759 .
    [Google Scholar]
  2. [2]. Grunig   E., , Tasman   JA., , Kucherer   H., , Franz   W., , Kubler   W., , Katus   HA. . Frequency and phenotypes of familial dilated cardiomyopathy. . Journal of the American College of Cardiology.   1998; ;31: 1 : 186– 194 .
    [Google Scholar]
  3. [3]. Yacoub   MH. . Decade in review–cardiomyopathies: Cardiomyopathy on the move. . Nature reviews Cardiology.   2014; ;11: 11 : 628– 629 .
    [Google Scholar]
  4. [4]. Shaw   T., , Elliott   P., , McKenna   WJ. . Dilated cardiomyopathy: a genetically heterogeneous disease. . Lancet.   2002; ;360: 9334 : 654– 655 .
    [Google Scholar]
  5. [5]. Haghighi   K., , Schmidt   AG., , Hoit   BD., , Brittsan   AG., , Yatani   A., , Lester   JW., , Zhai   J., , Kimura   Y., , Dorn   GW., , MacLennan   DH., , Kranias   EG. . Superinhibition of sarcoplasmic reticulum function by phospholamban induces cardiac contractile failure. . The Journal of biological chemistry . 2001; ;276: 26 : 24145– 24152 .
    [Google Scholar]
  6. [6]. Schmidt   AG., , Zhai   J., , Carr   AN., , Gerst   MJ., , Lorenz   JN., , Pollesello   P., , Annila   A., , Hoit   BD., , Kranias   EG. . Structural and functional implications of the phospholamban hinge domain: impaired SR Ca2 uptake as a primary cause of heart failure. . Cardiovascular research.   2002; ;56: 2 : 248– 259 .
    [Google Scholar]
  7. [7]. Janse   MJ. . Electrophysiological changes in heart failure and their relationship to arrhythmogenesis. . Cardiovascular research.   2004; ;61: 2 : 208– 217 .
    [Google Scholar]
  8. [8]. Pogwizd   SM., , Bers   DM. . Cellular basis of triggered arrhythmias in heart failure. . Trends in cardiovascular medicine.   2004; ;14: 2 : 61– 66 .
    [Google Scholar]
  9. [9]. Haghighi   K., , Kolokathis   F., , Pater   L., , Lynch   RA., , Asahi   M., , Gramolini   AO., , Fan   GC., , Tsiapras   D., , Hahn   HS., , Adamopoulos   S., , Liggett   SB., , Dorn   GW., , MacLennan   DH., , Kremastinos   DT., , Kranias   EG. . Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human. . The Journal of clinical investigation.   2003; ;111: 6 : 869– 876 .
    [Google Scholar]
  10. [10]. Arvanitis   DA., , Sanoudou   D., , Kolokathis   F., , Vafiadaki   E., , Papalouka   V., , Kontrogianni-Konstantopoulos   A., , Theodorakis   GN., , Paraskevaidis   IA., , Adamopoulos   S., , Dorn   GW., , Kremastinos   DT., , Kranias   EG. . The Ser96Ala variant in histidine-rich calcium-binding protein is associated with life-threatening ventricular arrhythmias in idiopathic dilated cardiomyopathy. . European heart journal.   2008; ;29: 20 : 2514– 2525 .
    [Google Scholar]
  11. [11]. Lopes   LR., , Syrris   P., , Guttmann   OP., , O'Mahony   C., , Tang   HC., , Dalageorgou   C., , Jenkins   S., , Hubank   M., , Monserrat   L., , McKenna   WJ., , Plagnol   V., , Elliott   PM. . Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy. . Heart.   2015; ;101: 4 : 294– 301 .
    [Google Scholar]
  12. [12]. Brittsan   AG., , Kranias   EG. . Phospholamban and cardiac contractile function. . Journal of molecular and cellular cardiology.   2000; ;32: 12 : 2131– 2139 .
    [Google Scholar]
  13. [13]. MacLennan   DH., , Kranias   EG. . Phospholamban: a crucial regulator of cardiac contractility. . Nature reviews Molecular cell biology.   2003; ;4: 7 : 566– 577 .
    [Google Scholar]
  14. [14]. Landstrom   AP., , Adekola   BA., , Bos   JM., , Ommen   SR., , Ackerman   MJ. . PLN-encoded phospholamban mutation in a large cohort of hypertrophic cardiomyopathy cases: summary of the literature and implications for genetic testing. . American heart journal.   2011; ;161: 1 : 165– 171 .
    [Google Scholar]
  15. [15]. Roberts   R., , Sigwart   U. . New concepts in hypertrophic cardiomyopathies, part I. . Circulation.   2001; ;104: 17 : 2113– 2116 .
    [Google Scholar]
  16. [16]. Osterziel   KJ., , Perrot   A. . Dilated cardiomyopathy: more genes means more phenotypes. . European heart journal.   2005; ;26: 8 : 751– 754 .
    [Google Scholar]
  17. [17]. Zipes   DP., , Wellens   HJ. . Sudden cardiac death. . Circulation.   1998; ;98: 21 : 2334– 2351 .
    [Google Scholar]
  18. [18]. Bai   Y., , Jones   PP., , Guo   J., , Zhong   X., , Clark   RB., , Zhou   Q., , Wang   R., , Vallmitjana   A., , Benitez   R., , Hove-Madsen   L., , Semeniuk   L., , Guo   A., , Song   LS., , Duff   HJ., , Chen   SR. . Phospholamban knockout breaks arrhythmogenic Ca(2)() waves and suppresses catecholaminergic polymorphic ventricular tachycardia in mice. . Circulation research.   2013; ;113: 5 : 517– 526 .
    [Google Scholar]
  19. [19]. Foell   JD., , Balijepalli   RC., , Delisle   BP., , Yunker   AM., , Robia   SL., , Walker   JW., , McEnery   MW., , January   CT., , Kamp   TJ. . Molecular heterogeneity of calcium channel beta-subunits in canine and human heart: evidence for differential subcellular localization. . Physiological genomics.   2004; ;17: 2 : 183– 200 .
    [Google Scholar]
  20. [20]. Lao   QZ., , Kobrinsky   E., , Harry   JB., , Ravindran   A., , Soldatov   NM. . New Determinant for the CaVbeta2 subunit modulation of the CaV1.2 calcium channel. . The Journal of biological chemistry . 2008; ;283: 23 : 15577– 15588 .
    [Google Scholar]
  21. [21]. Antzelevitch   C., , Pollevick   GD., , Cordeiro   JM., , Casis   O., , Sanguinetti   MC., , Aizawa   Y., , Guerchicoff   A., , Pfeiffer   R., , Oliva   A., , Wollnik   B., , Gelber   P., , Bonaros   EP Jr., , Burashnikov   E., , Wu   Y., , Sargent   JD., , Schickel   S., , Oberheiden   R., , Bhatia   A., , Hsu   LF., , Haïssaguerre   M., , Schimpf   R. . Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death. . Circulation.   2007; ;115: 4 : 442– 449 .
    [Google Scholar]
  22. [22]. Burashnikov   E., , Pfeiffer   R., , Barajas-Martinez   H., , Delpon   E., , Hu   D., , Desai   M., , Borggrefe   M., , Häissaguerre   M., , Kanter   R., , Pollevick   GD., , Guerchicoff   A., , Laiño   R., , Marieb   M., , Nademanee   K., , Nam   GB., , Robles   R., , Schimpf   R., , Stapleton   DD., , Viskin   S., , Winters   S., , Wolpert   C. . Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death. . Heart rhythm: the official journal of the Heart Rhythm Society.   2010; ;7: 12 : 1872– 1882 .
    [Google Scholar]
  23. [23]. Molina-Navarro   MM., , Rosello-Lleti   E., , Ortega   A., , Tarazon   E., , Otero   M., , Martinez-Dolz   L., , Lago   F., , González-Juanatey   JR., , España   F., , García-Pavía   P., , Montero   JA., , Portolés   M., , Rivera   M. . Differential gene expression of cardiac ion channels in human dilated cardiomyopathy. . PloS one.   2013; ;8: 12 : e79792 .
    [Google Scholar]
  24. [24]. Brandmayr   J., , Poomvanicha   M., , Domes   K., , Ding   J., , Blaich   A., , Wegener   JW., , Moosmang   S., , Hofmann   F. . Deletion of the C-terminal phosphorylation sites in the cardiac beta-subunit does not affect the basic beta-adrenergic response of the heart and the Ca(v)1.2 channel. . The Journal of biological chemistry . 2012; ;287: 27 : 22584– 22592 .
    [Google Scholar]
  25. [25]. Opatowsky   Y., , Chen   CC., , Campbell   KP., , Hirsch   JA. . Structural analysis of the voltage-dependent calcium channel beta subunit functional core and its complex with the alpha 1 interaction domain. . Neuron.   2004; ;42: 3 : 387– 399 .
    [Google Scholar]
  26. [26]. Carboni   N., , Marrosu   G., , Porcu   M., , Mateddu   A., , Solla   E., , Cocco   E., , Maioli   MA., , Oppo   V., , Piras   R., , Marrosu   MG. . Dilated cardiomyopathy with conduction defects in a patient with partial merosin deficiency due to mutations in the laminin-alpha2-chain gene: a chance association or a novel phenotype?.   Muscle & nerve.   2011; ;44: 5 : 826– 828 .
    [Google Scholar]
  27. [27]. Hohenester   E., , Tisi   D., , Talts   JF., , Timpl   R. . The crystal structure of a laminin G-like module reveals the molecular basis of alpha-dystroglycan binding to laminins, perlecan, and agrin. . Molecular cell.   1999; ;4: 5 : 783– 792 .
    [Google Scholar]
  28. [28]. Marshall   JD., , Hinman   EG., , Collin   GB., , Beck   S., , Cerqueira   R., , Maffei   P., , Milan   G., , Zhang   W., , Wilson   DI., , Hearn   T., , Tavares   P., , Vettor   R., , Veronese   C., , Martin   M., , So   WV., , Nishina   PM., , Naggert   JK. . Spectrum of ALMS1 variants and evaluation of genotype-phenotype correlations in Alstrom syndrome. . Human mutation.   2007; ;28: 11 : 1114– 1123 .
    [Google Scholar]
  29. [29]. Czosek   RJ., , Goldenberg   P., , Miller   EM., , Spicer   R., , Towbin   JA., , Ware   SM. . Cardiac electrical system involvement in Alström syndrome: uncommon causes of dilated cardiomyopathies. . Cardiogenetics.   2012; ;2: e2 : 6– 10 .
    [Google Scholar]
  30. [30]. Li   G., , Vega   R., , Nelms   K., , Gekakis   N., , Goodnow   C., , McNamara   P., , Wu   H., , Hong   NA., , Glynne   R. . A role for Alstrom syndrome protein, alms1, in kidney ciliogenesis and cellular quiescence. . PLoS genetics.   2007; ;3: 1 : e8 .
    [Google Scholar]
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