-
1
-
-
0034976642
-
The molecular generic basis for hypertrophic cardiomyopathy
-
Marian AJ, Roberts R. The molecular generic basis for hypertrophic cardiomyopathy. J Mol Cell Cardiol 2001;33(4): 655-70
-
(2001)
J. Mol. Cell Cardiol.
, vol.4
, Issue.33
, pp. 655-670
-
-
Marian, A.J.1
Roberts, R.2
-
2
-
-
0030765610
-
Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy
-
Kimura A, Harada H, Park JE, et al. Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy. Nat Genet 1997; 16(4): 379-82
-
(1997)
Nat. Genet.
, vol.16
, Issue.4
, pp. 379-382
-
-
Kimura, A.1
Harada, H.2
Park, J.E.3
-
3
-
-
0033847945
-
Deletion in the cardiac troponin I gene in a family from northern Sweden with hypertrophic cardiomyopathy
-
Morner S, Richard P, Kazzam E, Hainque B, Schwartz K, Waldenstrom A. Deletion in the cardiac troponin I gene in a family from northern Sweden with hypertrophic cardiomyopathy. J Mol Cell Cardiol 2000; 32(3): 521-5
-
(2000)
J. Mol. Cell Cardiol.
, vol.32
, Issue.3
, pp. 521-525
-
-
Morner, S.1
Richard, P.2
Kazzam, E.3
Hainque, B.4
Schwartz, K.5
Waldenstrom, A.6
-
4
-
-
0037192339
-
Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly
-
Niimura H, Patton KK, McKenna WJ, et al. Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly. Circulation 2002; 105(4): 446-51
-
(2002)
Circulation
, vol.105
, Issue.4
, pp. 446-451
-
-
Niimura, H.1
Patton, K.K.2
McKenna, W.J.3
-
5
-
-
18744433901
-
Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy
-
Mogensen J, Klausen IC, Pedersen AK, et al. Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy. J Clin Invest 1999; 103 (10): 39-43
-
(1999)
J. Clin. Invest.
, vol.103
, Issue.10
, pp. 39-43
-
-
Mogensen, J.1
Klausen, I.C.2
Pedersen, A.K.3
-
6
-
-
25544447700
-
Protocols for molecular biology of cardiovascular system
-
Beijing: Beijing Medical University and Union Medical Colleges Press
-
Hui RT, Zhou XL. Protocols for molecular biology of cardiovascular system. Beijing: Beijing Medical University and Union Medical Colleges Press 1998:22-5
-
(1998)
, pp. 22-25
-
-
Hui, R.T.1
Zhou, X.L.2
-
7
-
-
0034698086
-
Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy
-
Elliott K, Watkins H, Redwood CS. Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy. J Biol Chem 2000; 275(29): 22069-74
-
(2000)
J. Biol. Chem.
, vol.275
, Issue.29
, pp. 22069-22074
-
-
Elliott, K.1
Watkins, H.2
Redwood, C.S.3
-
8
-
-
0035695803
-
Functional consequences of the mutations in human cardiac troponin I gene found in familial hypertrophic cardiomyopathy
-
Takahashi-Yanaga F, Morimoto S, Harada K, et al. Functional consequences of the mutations in human cardiac troponin I gene found in familial hypertrophic cardiomyopathy. J Mol Cell Cardiol 2001; 33(12): 2095-107
-
(2001)
J. Mol. Cell Cardiol.
, vol.33
, Issue.12
, pp. 2095-2107
-
-
Takahashi-Yanaga, F.1
Morimoto, S.2
Harada, K.3
-
9
-
-
0037023758
-
Functional analysis of a troponin I (R145G) mutation associated with familial hypertrophic cardiomyopathy
-
Lang R, Gomes AV, Zhao J, Housmans PR, Miller T, Potter JD. Functional analysis of a troponin I (R145G) mutation associated with familial hypertrophic cardiomyopathy. J Biol Chem 2002; 277(14): 11670-8
-
(2002)
J. Biol. Chem.
, vol.277
, Issue.14
, pp. 11670-11678
-
-
Lang, R.1
Gomes, A.V.2
Zhao, J.3
Housmans, P.R.4
Miller, T.5
Potter, J.D.6
-
10
-
-
0037144655
-
Myofilament calcium sensitivity and cardiac disease: Insights from troponin I isoforms and mutants
-
Westfall MV, Borton AR, Albayya FP, Metzger JM. Myofilament calcium sensitivity and cardiac disease: insights from troponin I isoforms and mutants. Circ Res 2002; 91(6): 525-31
-
(2002)
Circ. Res.
, vol.91
, Issue.6
, pp. 525-531
-
-
Westfall, M.V.1
Borton, A.R.2
Albayya, F.P.3
Metzger, J.M.4
-
11
-
-
0036499710
-
Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility
-
Burton D, Abdulrazzak H, Knott A, et al. Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility. Biochem J 2002; 362(Pt 2): 443-51
-
(2002)
Biochem. J.
, vol.362
, Issue.PART 2
, pp. 443-451
-
-
Burton, D.1
Abdulrazzak, H.2
Knott, A.3
-
12
-
-
0034721807
-
Transgenic modeling of a cardiac troponin I mutation linked to familial hypertrophic cardiomyopathy
-
James J, Zhang Y, Osinska H, et al. Transgenic modeling of a cardiac troponin I mutation linked to familial hypertrophic cardiomyopathy. Circ Res 2000; 87: 805-11
-
(2000)
Circ. Res.
, vol.87
, pp. 805-811
-
-
James, J.1
Zhang, Y.2
Osinska, H.3
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