-
9
-
-
0034264444
-
Cytosine methylation confers instability on the cardiac troponin T gene in hypertrophic cardiomyopathy
-
(2000)
J. Med. Genet.
, vol.37
-
-
D'Cruz, L.G.1
Baboonian, C.2
Phillimore, H.E.3
Taylor, R.4
Elliott, P.M.5
Vamava, A.6
Davison, F.7
McKenna, W.J.8
Carter, N.D.9
-
11
-
-
8044244822
-
Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy
-
(1996)
Circulation
, vol.94
, pp. 3069-3073
-
-
Forissier, J.F.1
Carrier, L.2
Farza, H.3
Bonne, G.4
Bercovici, J.5
Richard, P.6
Hainque, B.7
Townsend, P.J.8
Yacoub, M.H.9
Faure, S.10
Dubourg, O.11
Millaire, A.12
Hagege, A.A.13
Desnos, M.14
Komajda, M.15
Schwartz, K.16
-
31
-
-
0035971216
-
Inotropic stimulation induces cardiac dysfunction in transgenic mice expressing a troponin T (179N) mutation linked to familial hypertrophic cardiomyopathy
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 10039-10048
-
-
Knollmann, B.C.1
Blatt, S.A.2
Horton, K.3
De Freitas, F.4
Miller, T.5
Bell, M.6
Housmans, P.R.7
Weissman, N.J.8
Morad, M.9
Potter, J.D.10
-
33
-
-
0014949207
-
Cleavage of structural proteins during the assembly of the head of bacteriophage T4
-
(1970)
Nature
, vol.227
, pp. 680-685
-
-
Laemmli, U.K.1
-
34
-
-
0033844586
-
Decreased left ventricular ejection fraction in transgenic mice expressing mutant cardiac troponin T-Q(92), responsible for human hypertrophic cardiomyopathy
-
(2000)
J. Mol. Cell. Cardiol.
, vol.32
, pp. 365-374
-
-
Lim, D.S.1
Oberst, L.2
McCluggage, M.3
Youker, K.4
Lacy, J.5
DeMayo, F.6
Entman, M.L.7
Roberts, R.8
Michael, L.H.9
Marian, A.J.10
-
38
-
-
0035830841
-
Abnormal contractile function in transgenic mice expressing an FHC-linked troponin T (179N) mutation
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 3743-3755
-
-
Miller, T.1
Szczesna, D.2
Housmans, P.R.3
Zhao, J.4
De Freitas, F.5
Gomes, A.V.6
Culbreath, L.7
McCue, J.8
Wang, Y.9
Xu, Y.10
Kerrick, W.G.11
Potter, J.D.12
-
44
-
-
0032532087
-
Dominant-negative effect of a mutant cardiac troponin T on cardiac structure and function in transgenic mice
-
(1998)
J. Clin. Invest.
, vol.102
, pp. 1498-1505
-
-
Oberst, L.1
Zhao, G.2
Park, J.T.3
Brugada, R.4
Michael, L.H.5
Entman, M.L.6
Roberts, R.7
Marian, A.J.8
-
47
-
-
0027989325
-
A modified micro-Bradford procedure for elimination of interference from sodium dodecyl sulfate, other detergents, and lipids
-
(1994)
Anal. Biochem.
, vol.220
, pp. 424-426
-
-
Pande, S.V.1
Murthy, M.S.2
-
54
-
-
0034625768
-
Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein
-
(2000)
Circ. Res.
, vol.86
, pp. 1146-1152
-
-
Redwood, C.1
Lohmann, K.2
Bing, W.3
Esposito, G.M.4
Elliott, K.5
Abdulrazzak, H.6
Knott, A.7
Purcell, I.8
Marston, S.9
Watkins, H.10
-
55
-
-
0023180728
-
Alpha-tropomyosin gene organization. Alternative splicing of duplicated isotype-specific exons accounts for the production of smooth and striated muscle isoforms
-
(1987)
J. Biol. Chem.
, vol.262
, pp. 4755-4765
-
-
Ruiz-Opazo, N.1
Nadal-Ginard, B.2
-
62
-
-
0032716486
-
Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy
-
(1999)
J. Clin. Invest.
, vol.104
, pp. 469-481
-
-
Tardiff, J.C.1
Hewett, T.E.2
Palmer, B.M.3
Olsson, C.4
Factor, S.M.5
Moore, R.L.6
Robbins, J.7
Leinwand, L.A.8
-
63
-
-
0028178083
-
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere
-
(1994)
Cell
, vol.77
, pp. 701-712
-
-
Thierfelder, L.1
Watkins, H.2
MacRae, C.3
Lamas, R.4
McKenna, W.5
Vosberg, H.P.6
Seidman, J.G.7
Seidman, C.E.8
-
66
-
-
0028902929
-
Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy
-
(1995)
N. Engl. J. Med.
, vol.332
, pp. 1058-1064
-
-
Watkins, H.1
McKenna, W.J.2
Thierfelder, L.3
Suk, H.J.4
Anan, R.5
O'Donoghue, A.6
Spirito, P.7
Matsumori, A.8
Moravec, C.S.9
Seidman, J.G.10
Seidman, C.E.11
-
69
-
-
0033605422
-
2+ sensitization and potentiation of the maximum level of myofibrillar ATPase activity caused by mutations of troponin T found in familial hypertrophic cardiomyopathy
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 8806-8812
-
-
Yanaga, F.1
Morimoto, S.2
Ohtsuki, I.3
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