132 related articles for article (PubMed ID: 9893156)
1. In vivo short-term expression of a hypertrophic cardiomyopathy mutation in adult rabbit myocardium: myofibrillar incorporation without early disarray.
Yu Q; Zhao G; Marian AJ
Proc Assoc Am Physicians; 1999; 111(1):45-56. PubMed ID: 9893156
[TBL] [Abstract][Full Text] [Related]
2. Expression of a mutant (Arg92Gln) human cardiac troponin T, known to cause hypertrophic cardiomyopathy, impairs adult cardiac myocyte contractility.
Marian AJ; Zhao G; Seta Y; Roberts R; Yu QT
Circ Res; 1997 Jul; 81(1):76-85. PubMed ID: 9201030
[TBL] [Abstract][Full Text] [Related]
3. Dominant-negative effect of a mutant cardiac troponin T on cardiac structure and function in transgenic mice.
Oberst L; Zhao G; Park JT; Brugada R; Michael LH; Entman ML; Roberts R; Marian AJ
J Clin Invest; 1998 Oct; 102(8):1498-505. PubMed ID: 9788962
[TBL] [Abstract][Full Text] [Related]
4. Expression of a mutation causing hypertrophic cardiomyopathy disrupts sarcomere assembly in adult feline cardiac myocytes.
Marian AJ; Yu QT; Mann DL; Graham FL; Roberts R
Circ Res; 1995 Jul; 77(1):98-106. PubMed ID: 7788887
[TBL] [Abstract][Full Text] [Related]
5. Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defect and the cardiac phenotype of hypertrophic cardiomyopathy.
Tsybouleva N; Zhang L; Chen S; Patel R; Lutucuta S; Nemoto S; DeFreitas G; Entman M; Carabello BA; Roberts R; Marian AJ
Circulation; 2004 Mar; 109(10):1284-91. PubMed ID: 14993121
[TBL] [Abstract][Full Text] [Related]
6. Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca2+ desensitization.
Lu QW; Morimoto S; Harada K; Du CK; Takahashi-Yanaga F; Miwa Y; Sasaguri T; Ohtsuki I
J Mol Cell Cardiol; 2003 Dec; 35(12):1421-7. PubMed ID: 14654368
[TBL] [Abstract][Full Text] [Related]
7. Hypertrophic cardiomyopathy: histopathological features of sudden death in cardiac troponin T disease.
Varnava AM; Elliott PM; Baboonian C; Davison F; Davies MJ; McKenna WJ
Circulation; 2001 Sep; 104(12):1380-4. PubMed ID: 11560853
[TBL] [Abstract][Full Text] [Related]
8. Decreased left ventricular ejection fraction in transgenic mice expressing mutant cardiac troponin T-Q(92), responsible for human hypertrophic cardiomyopathy.
Lim DS; Oberst L; McCluggage M; Youker K; Lacy J; DeMayo F; Entman ML; Roberts R; Michael LH; Marian AJ
J Mol Cell Cardiol; 2000 Mar; 32(3):365-74. PubMed ID: 10731436
[TBL] [Abstract][Full Text] [Related]
9. Identification of a contractile deficit in adult cardiac myocytes expressing hypertrophic cardiomyopathy-associated mutant troponin T proteins.
Rust EM; Albayya FP; Metzger JM
J Clin Invest; 1999 May; 103(10):1459-67. PubMed ID: 10330428
[TBL] [Abstract][Full Text] [Related]
10. Angiotensin II blockade reverses myocardial fibrosis in a transgenic mouse model of human hypertrophic cardiomyopathy.
Lim DS; Lutucuta S; Bachireddy P; Youker K; Evans A; Entman M; Roberts R; Marian AJ
Circulation; 2001 Feb; 103(6):789-91. PubMed ID: 11171784
[TBL] [Abstract][Full Text] [Related]
11. Evolution of expression of cardiac phenotypes over a 4-year period in the beta-myosin heavy chain-Q403 transgenic rabbit model of human hypertrophic cardiomyopathy.
Nagueh SF; Chen S; Patel R; Tsybouleva N; Lutucuta S; Kopelen HA; Zoghbi WA; Quiñones MA; Roberts R; Marian AJ
J Mol Cell Cardiol; 2004 May; 36(5):663-73. PubMed ID: 15135661
[TBL] [Abstract][Full Text] [Related]
12. Transgenic rat hearts expressing a human cardiac troponin T deletion reveal diastolic dysfunction and ventricular arrhythmias.
Frey N; Franz WM; Gloeckner K; Degenhardt M; Müller M; Müller O; Merz H; Katus HA
Cardiovasc Res; 2000 Aug; 47(2):254-64. PubMed ID: 10946062
[TBL] [Abstract][Full Text] [Related]
13. Induction and reversal of cardiac phenotype of human hypertrophic cardiomyopathy mutation cardiac troponin T-Q92 in switch on-switch off bigenic mice.
Lutucuta S; Tsybouleva N; Ishiyama M; Defreitas G; Wei L; Carabello B; Marian AJ
J Am Coll Cardiol; 2004 Dec; 44(11):2221-30. PubMed ID: 15582321
[TBL] [Abstract][Full Text] [Related]
14. Point mutations in human beta cardiac myosin heavy chain have differential effects on sarcomeric structure and assembly: an ATP binding site change disrupts both thick and thin filaments, whereas hypertrophic cardiomyopathy mutations display normal assembly.
Becker KD; Gottshall KR; Hickey R; Perriard JC; Chien KR
J Cell Biol; 1997 Apr; 137(1):131-40. PubMed ID: 9105042
[TBL] [Abstract][Full Text] [Related]
15. Phenotypic variation of familial hypertrophic cardiomyopathy caused by the Phe(110)-->Ile mutation in cardiac troponin T.
Lin T; Ichihara S; Yamada Y; Nagasaka T; Ishihara H; Nakashima N; Yokota M
Cardiology; 2000; 93(3):155-62. PubMed ID: 10965086
[TBL] [Abstract][Full Text] [Related]
16. The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy.
Ahmad F; Banerjee SK; Lage ML; Huang XN; Smith SH; Saba S; Rager J; Conner DA; Janczewski AM; Tobita K; Tinney JP; Moskowitz IP; Perez-Atayde AR; Keller BB; Mathier MA; Shroff SG; Seidman CE; Seidman JG
PLoS One; 2008 Jul; 3(7):e2642. PubMed ID: 18612386
[TBL] [Abstract][Full Text] [Related]
17. Pathogenesis associated with a restrictive cardiomyopathy mutant in cardiac troponin T is due to reduced protein stability and greatly increased myofilament Ca2+ sensitivity.
Parvatiyar MS; Pinto JR
Biochim Biophys Acta; 2015 Feb; 1850(2):365-72. PubMed ID: 25450489
[TBL] [Abstract][Full Text] [Related]
18. Mutation location of HCM-causing troponin T mutations defines the degree of myofilament dysfunction in human cardiomyocytes.
Schuldt M; Johnston JR; He H; Huurman R; Pei J; Harakalova M; Poggesi C; Michels M; Kuster DWD; Pinto JR; van der Velden J
J Mol Cell Cardiol; 2021 Jan; 150():77-90. PubMed ID: 33148509
[TBL] [Abstract][Full Text] [Related]
19. Human cardiomyopathy mutations induce myocyte hyperplasia and activate hypertrophic pathways during cardiogenesis in zebrafish.
Becker JR; Deo RC; Werdich AA; Panàkovà D; Coy S; MacRae CA
Dis Model Mech; 2011 May; 4(3):400-10. PubMed ID: 21245263
[TBL] [Abstract][Full Text] [Related]
20. A transgenic rabbit model for human hypertrophic cardiomyopathy.
Marian AJ; Wu Y; Lim DS; McCluggage M; Youker K; Yu QT; Brugada R; DeMayo F; Quinones M; Roberts R
J Clin Invest; 1999 Dec; 104(12):1683-92. PubMed ID: 10606622
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]