-
1
-
-
70449192269
-
Asymmetrical hypertrophy of the heart in young adults
-
Teare D. Asymmetrical hypertrophy of the heart in young adults. Br Heart J 1958; 20: 1-8.
-
(1958)
Br Heart J
, vol.20
, pp. 1-8
-
-
Teare, D.1
-
2
-
-
0029083650
-
Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults
-
Maron BJ, Gardin JM, Flack JM, Gidding SS, Kurosaki TT, Bild DE. Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults. Circulation 1995; 92: 785-789.
-
(1995)
Circulation
, vol.92
, pp. 785-789
-
-
Maron, B.J.1
Gardin, J.M.2
Flack, J.M.3
Gidding, S.S.4
Kurosaki, T.T.5
Bild, D.E.6
-
3
-
-
0018936424
-
Sudden death in young athletes
-
Maron B, Roberts W, McAllister H, Rosing D, Epstein S. Sudden death in young athletes. Circulation 1980; 62: 218-229.
-
(1980)
Circulation
, vol.62
, pp. 218-229
-
-
Maron, B.1
Roberts, W.2
McAllister, H.3
Rosing, D.4
Epstein, S.5
-
4
-
-
0022576463
-
Causes of sudden death in competitive athletes
-
Maron B, Epstein S, Roberts W. Causes of sudden death in competitive athletes. J Am Coll Cardiol 1986; 7: 204-214.
-
(1986)
J Am Coll Cardiol
, vol.7
, pp. 204-214
-
-
Maron, B.1
Epstein, S.2
Roberts, W.3
-
5
-
-
34147201740
-
Genetics of hypertrophic cardiomyopathy: One, two, or more diseases?
-
Bos JM, Ommen SR, Ackerman MJ. Genetics of hypertrophic cardiomyopathy: one, two, or more diseases? Curr Opin Cardiol 2007; 22: 193-199.
-
(2007)
Curr Opin Cardiol
, vol.22
, pp. 193-199
-
-
Bos, J.M.1
Ommen, S.R.2
Ackerman, M.J.3
-
6
-
-
0042734704
-
Sudden death in young athletes
-
Maron BJ. Sudden death in young athletes. N Engl J Med 2003; 349: 1064-1075.
-
(2003)
N Engl J Med
, vol.349
, pp. 1064-1075
-
-
Maron, B.J.1
-
7
-
-
0037070514
-
Hypertrophic cardiomyopathy: A systematic review
-
Maron BJ. Hypertrophic cardiomyopathy: A systematic review. JAMA 2002; 287: 1308-1320.
-
(2002)
JAMA
, vol.287
, pp. 1308-1320
-
-
Maron, B.J.1
-
8
-
-
0035923562
-
Impact of atrial fibrillation on the clinical course of hypertrophic cardiomyopathy
-
Olivotto I, Cecchi F, Casey SA, Dolara A, Traverse JH, Maron BJ. Impact of atrial fibrillation on the clinical course of hypertrophic cardiomyopathy. Circulation 2001; 104: 2517-2524.
-
(2001)
Circulation
, vol.104
, pp. 2517-2524
-
-
Olivotto, I.1
Cecchi, F.2
Casey, S.A.3
Dolara, A.4
Traverse, J.H.5
Maron, B.J.6
-
9
-
-
0020360481
-
The natural history of left ventricular hypertrophy in hypertrophic cardiomyopathy: An electrocardiographic study
-
McKenna WJ, Borggrefe M, England D, Deanfield J, Oakley CM, Goodwin JF. The natural history of left ventricular hypertrophy in hypertrophic cardiomyopathy: an electrocardiographic study. Circulation 1982; 66: 1233-1240.
-
(1982)
Circulation
, vol.66
, pp. 1233-1240
-
-
McKenna, W.J.1
Borggrefe, M.2
England, D.3
Deanfield, J.4
Oakley, C.M.5
Goodwin, J.F.6
-
10
-
-
0023269245
-
Occurrence and significance of progressive left ventricular wall thinning and relative cavity dilatation in hypertrophic cardiomyopathy
-
Spirito P, Maron BJ, Bonow RO, Epstein SE. Occurrence and significance of progressive left ventricular wall thinning and relative cavity dilatation in hypertrophic cardiomyopathy. Am J Cardiol 1987; 60: 123-129.
-
(1987)
Am J Cardiol
, vol.60
, pp. 123-129
-
-
Spirito, P.1
Maron, B.J.2
Bonow, R.O.3
Epstein, S.E.4
-
11
-
-
0024426784
-
Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1
-
Jarcho JA, McKenna W, Pare JA, et al. Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1. N Engl J Med 1989; 321: 1372-1378.
-
(1989)
N Engl J Med
, vol.321
, pp. 1372-1378
-
-
Jarcho, J.A.1
McKenna, W.2
Pare, J.A.3
-
12
-
-
0025040392
-
A molecular basis for familial hypertrophic cardiomyopathy: A beta cardiac myosin heavy chain gene missense mutation
-
Geisterfer-Lowrance AA, Kass S, Tanigawa G, et al. A molecular basis for familial hypertrophic cardiomyopathy: A beta cardiac myosin heavy chain gene missense mutation. Cell 1990; 62: 999-1006.
-
(1990)
Cell
, vol.62
, pp. 999-1006
-
-
Geisterfer-Lowrance, A.A.1
Kass, S.2
Tanigawa, G.3
-
13
-
-
0038125906
-
Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden
-
Morner S, Richard P, Kazzam E, et al. Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden. J Mol Cell Cardiol 2003; 35: 841-849.
-
(2003)
J Mol Cell Cardiol
, vol.35
, pp. 841-849
-
-
Morner, S.1
Richard, P.2
Kazzam, E.3
-
14
-
-
12444270692
-
Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy
-
Erdmann J, Daehmlow S, Wischke S, et al. Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy. Clin Genet 2003; 64: 339-349.
-
(2003)
Clin Genet
, vol.64
, pp. 339-349
-
-
Erdmann, J.1
Daehmlow, S.2
Wischke, S.3
-
15
-
-
20044382630
-
Yield of genetic testing in hypertrophic cardiomyopathy
-
van Driest SL, Ommen SR, Tajik AJ, Gersh BJ, Ackerman MJ. Yield of genetic testing in hypertrophic cardiomyopathy. Mayo Clin Proc 2005; 80: 739-744.
-
(2005)
Mayo Clin Proc
, vol.80
, pp. 739-744
-
-
van Driest, S.L.1
Ommen, S.R.2
Tajik, A.J.3
Gersh, B.J.4
Ackerman, M.J.5
-
16
-
-
0037630018
-
Hypertrophic cardiomyopathy: Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy
-
Richard P, Charron P, Carrier L, et al. Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation 2003; 107: 2227-2232.
-
(2003)
Circulation
, vol.107
, pp. 2227-2232
-
-
Richard, P.1
Charron, P.2
Carrier, L.3
-
17
-
-
16344385637
-
Sarcomeric genotyping in hypertrophic cardiomyopathy
-
van Driest SL, Ommen SR, Tajik AJ, Gersh BJ, Ackerman MJ. Sarcomeric genotyping in hypertrophic cardiomyopathy. Mayo Clin Proc 2005; 80: 463-469.
-
(2005)
Mayo Clin Proc
, vol.80
, pp. 463-469
-
-
van Driest, S.L.1
Ommen, S.R.2
Tajik, A.J.3
Gersh, B.J.4
Ackerman, M.J.5
-
18
-
-
15844400653
-
Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle
-
Poetter K, Jiang H, Hassanzadeh S, et al. Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle. Nat Genet 1996; 13: 63-69.
-
(1996)
Nat Genet
, vol.13
, pp. 63-69
-
-
Poetter, K.1
Jiang, H.2
Hassanzadeh, S.3
-
19
-
-
0037150221
-
Myosin light chain mutation causes autosomal recessive cardiomyopathy with mid-cavitary hypertrophy and restrictive physiology
-
Olson TM, Karst ML, Whitby FG, Driscoll DJ. Myosin light chain mutation causes autosomal recessive cardiomyopathy with mid-cavitary hypertrophy and restrictive physiology. Circulation 2002; 105: 2337-2340.
-
(2002)
Circulation
, vol.105
, pp. 2337-2340
-
-
Olson, T.M.1
Karst, M.L.2
Whitby, F.G.3
Driscoll, D.J.4
-
20
-
-
0028844204
-
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
-
Watkins H, Conner D, Thierfelder L, et al. Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy. Nat Genet 1995; 11: 434-437.
-
(1995)
Nat Genet
, vol.11
, pp. 434-437
-
-
Watkins, H.1
Conner, D.2
Thierfelder, L.3
-
21
-
-
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: R39-R43.
-
(1999)
J Clin Invest
, vol.103
-
-
Mogensen, J.1
Klausen, I.C.2
Pedersen, A.K.3
-
22
-
-
0028178083
-
Alphatropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere
-
Thierfelder L, Watkins H, MacRae C, et al. Alphatropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere. Cell 1994; 77: 701-712.
-
(1994)
Cell
, vol.77
, pp. 701-712
-
-
Thierfelder, L.1
Watkins, H.2
Macrae, C.3
-
23
-
-
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: 3793-82.
-
(1997)
Nat Genet
, vol.16
, pp. 3782-3793
-
-
Kimura, A.1
Harada, H.2
Park, J.E.3
-
24
-
-
0033610050
-
Structural analysis of the titin gene in hypertrophic cardiomyopathy: Identification of a novel disease gene
-
Satoh M, Takahashi M, Sakamoto T, Hiroe M, Marumo F, Kimura A. Structural analysis of the titin gene in hypertrophic cardiomyopathy: Identification of a novel disease gene. Biochem Biophys Res Comm 1999; 262: 411-417.
-
(1999)
Biochem Biophys Res Comm
, vol.262
, pp. 411-417
-
-
Satoh, M.1
Takahashi, M.2
Sakamoto, T.3
Hiroe, M.4
Marumo, F.5
Kimura, A.6
-
25
-
-
67650091283
-
Cardiac ankyrin repeat protein gene (ANKRD1) mutations in hypertrophic cardiomyopathy
-
Arimura T, Bos JM, Sato A, et al. Cardiac ankyrin repeat protein gene (ANKRD1) mutations in hypertrophic cardiomyopathy. J Am Coll Cardiol 2009; 54: 334-342.
-
(2009)
J Am Coll Cardiol
, vol.54
, pp. 334-342
-
-
Arimura, T.1
Bos, J.M.2
Sato, A.3
-
26
-
-
78650688851
-
Mutation type is not clinically useful in predicting prognosis in hypertrophic cardiomyopathy
-
Landstrom AP, Ackerman MJ. Mutation type is not clinically useful in predicting prognosis in hypertrophic cardiomyopathy. Circulation 2010; 122: 2441-2450.
-
(2010)
Circulation
, vol.122
, pp. 2441-2450
-
-
Landstrom, A.P.1
Ackerman, M.J.2
-
27
-
-
0041663609
-
Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy
-
van Driest SL, Ellsworth EG, Ommen SR, Tajik AJ, Gersh BJ, Ackerman MJ. Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy. Circulation 2003; 108: 445-451.
-
(2003)
Circulation
, vol.108
, pp. 445-451
-
-
van Driest, S.L.1
Ellsworth, E.G.2
Ommen, S.R.3
Tajik, A.J.4
Gersh, B.J.5
Ackerman, M.J.6
-
28
-
-
7044264544
-
Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy
-
van Driest SL, Vasile VC, Ommen SR, et al. Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy. J Am Coll Cardiol 2004; 44: 1903-1910.
-
(2004)
J Am Coll Cardiol
, vol.44
, pp. 1903-1910
-
-
van Driest, S.L.1
Vasile, V.C.2
Ommen, S.R.3
-
29
-
-
33645655544
-
Echocardiographyguided genetic testing in hypertrophic cardiomyopathy: Septal morphological features predict the presence of myofilament mutations
-
Binder J, Ommen SR, Gersh BJ, et al. Echocardiographyguided genetic testing in hypertrophic cardiomyopathy: septal morphological features predict the presence of myofilament mutations. Mayo Clin Proc 2006; 81: 459-467.
-
(2006)
Mayo Clin Proc
, vol.81
, pp. 459-467
-
-
Binder, J.1
Ommen, S.R.2
Gersh, B.J.3
-
30
-
-
0035378612
-
First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy
-
Hoffmann B, Schmidt-Traub H, Perrot A, Osterziel KJ, Geßner R. First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy. Hum Mutat 2001; 17: 524.
-
(2001)
Hum Mutat
, vol.17
, pp. 524
-
-
Hoffmann, B.1
Schmidt-Traub, H.2
Perrot, A.3
Osterziel, K.J.4
Geßner, R.5
-
31
-
-
28244469709
-
Cardiac troponin C-L29Q, related to hypertrophic cardiomyopathy, hinders the transduction of the protein kinase A dependent phosphorylation signal from cardiac troponin I to C
-
Schmidtmann A, Lindow C, Villard S, et al. Cardiac troponin C-L29Q, related to hypertrophic cardiomyopathy, hinders the transduction of the protein kinase A dependent phosphorylation signal from cardiac troponin I to C. FEBS Journal 2005; 272: 6087-6097.
-
(2005)
FEBS Journal
, vol.272
, pp. 6087-6097
-
-
Schmidtmann, A.1
Lindow, C.2
Villard, S.3
-
32
-
-
37349117667
-
Modulation of cardiac troponin C function by the cardiac-specific N-terminus of troponin I: Influence of PKA phosphorylation and involvement in cardiomyopathies
-
Baryshnikova OK, Li MX, Sykes BD. Modulation of cardiac troponin C function by the cardiac-specific N-terminus of troponin I: Influence of PKA phosphorylation and involvement in cardiomyopathies. J Mol Biol 2008; 375: 735-751.
-
(2008)
J Mol Biol
, vol.375
, pp. 735-751
-
-
Baryshnikova, O.K.1
Li, M.X.2
Sykes, B.D.3
-
33
-
-
43049104563
-
Familial hypertrophic cardiomyopathy-related cardiac troponin C mutation L29Q affects Ca2+ binding and myofilament contractility
-
Liang B, Chung F, Qu Y, et al. Familial hypertrophic cardiomyopathy-related cardiac troponin C mutation L29Q affects Ca2+ binding and myofilament contractility. Physiol Genomics 2008; 33: 257-266.
-
(2008)
Physiol Genomics
, vol.33
, pp. 257-266
-
-
Liang, B.1
Chung, F.2
Qu, Y.3
-
34
-
-
0034059761
-
Regulation of contraction in striated muscle
-
Gordon AM, Homsher E, Regnier M. Regulation of contraction in striated muscle. Physiol Rev 2000; 80: 853-924.
-
(2000)
Physiol Rev
, vol.80
, pp. 853-924
-
-
Gordon, A.M.1
Homsher, E.2
Regnier, M.3
-
35
-
-
48849100715
-
Molecular and functional characterization of novel hypertrophic cardiomyopathy susceptibility mutations in TNNC1-encoded troponin C
-
Landstrom AP, Parvatiyar MS, Pinto JR, et al. Molecular and functional characterization of novel hypertrophic cardiomyopathy susceptibility mutations in TNNC1-encoded troponin C. J Mol Cell Cardiol 2008; 45: 281-288.
-
(2008)
J Mol Cell Cardiol
, vol.45
, pp. 281-288
-
-
Landstrom, A.P.1
Parvatiyar, M.S.2
Pinto, J.R.3
-
36
-
-
43649089498
-
A novel mutant cardiac troponin C disrupts molecular motions critical for calcium binding affinity and cardiomyocyte contractility
-
Lim CC, Yang H, Yang M, et al. A novel mutant cardiac troponin C disrupts molecular motions critical for calcium binding affinity and cardiomyocyte contractility. Biophys J 2008; 94: 3577-3589.
-
(2008)
Biophys J
, vol.94
, pp. 3577-3589
-
-
Lim, C.C.1
Yang, H.2
Yang, M.3
-
37
-
-
70350448975
-
Functional analysis of a unique troponin C mutation, GLY159ASP, that causes familial dilated cardiomyopathy, studied in explanted heart muscle
-
Dyer EC, Jacques AM, Hoskins AC, et al. Functional analysis of a unique troponin C mutation, GLY159ASP, that causes familial dilated cardiomyopathy, studied in explanted heart muscle. Circ Heart Fail 2009; 2: 456-464.
-
(2009)
Circ Heart Fail
, vol.2
, pp. 456-464
-
-
Dyer, E.C.1
Jacques, A.M.2
Hoskins, A.C.3
-
38
-
-
3042718653
-
Molecular and cellular aspects of troponin cardiomyopathies
-
Gomes AV, Potter JD. Molecular and cellular aspects of troponin cardiomyopathies. Ann NY Acad Sci 2004; 1015: 214-224.
-
(2004)
Ann NY Acad Sci
, vol.1015
, pp. 214-224
-
-
Gomes, A.V.1
Potter, J.D.2
-
39
-
-
77951621530
-
Mutations in Troponin that cause HCM, DCM AND RCM: What can we learn about thin filament function?
-
Willott RH, Gomes AV, Chang AN, Parvatiyar MS, Pinto JR, Potter JD. Mutations in Troponin that cause HCM, DCM AND RCM: What can we learn about thin filament function? J Mol Cell Cardiol 2010; 48: 882-892.
-
(2010)
J Mol Cell Cardiol
, vol.48
, pp. 882-892
-
-
Willott, R.H.1
Gomes, A.V.2
Chang, A.N.3
Parvatiyar, M.S.4
Pinto, J.R.5
Potter, J.D.6
-
40
-
-
67650544956
-
A functional and structural study of troponin C mutations related to hypertrophic cardiomyopathy
-
Pinto JR, Parvatiyar MS, Jones MA, Liang J, Ackerman MJ, Potter JD. A functional and structural study of troponin C mutations related to hypertrophic cardiomyopathy. J Biol Chem 2009; 284: 19090-19100.
-
(2009)
J Biol Chem
, vol.284
, pp. 19090-19100
-
-
Pinto, J.R.1
Parvatiyar, M.S.2
Jones, M.A.3
Liang, J.4
Ackerman, M.J.5
Potter, J.D.6
-
41
-
-
77953240679
-
Hypertrophic cardiomyopathylinked mutation D145E drastically alters calcium binding by the C-domain of cardiac troponin C
-
Swindle N, Tikunova SB. Hypertrophic cardiomyopathylinked mutation D145E drastically alters calcium binding by the C-domain of cardiac troponin C. Biochemistry 2010; 49: 4813-4820.
-
(2010)
Biochemistry
, vol.49
, pp. 4813-4820
-
-
Swindle, N.1
Tikunova, S.B.2
-
42
-
-
79956056921
-
Novel frameshift mutation in troponin C (TNNC1) associated with hypertrophic cardiomyopathy and sudden death
-
Chung W, Kitner C, Maron B. Novel frameshift mutation in troponin C (TNNC1) associated with hypertrophic cardiomyopathy and sudden death. Cardiol Young 2011; 21 93: 345-348.
-
(2011)
Cardiol Young
, vol.21
, Issue.93
, pp. 345-348
-
-
Chung, W.1
Kitner, C.2
Maron, B.3
-
43
-
-
67649854428
-
Diagnostic, prognostic, and therapeutic implications of genetic testing for hypertrophic cardiomyopathy
-
Bos JM, Towbin JA, Ackerman MJ. Diagnostic, prognostic, and therapeutic implications of genetic testing for hypertrophic cardiomyopathy. J Am Coll Cardiol 2009; 54: 201-211.
-
(2009)
J Am Coll Cardiol
, vol.54
, pp. 201-211
-
-
Bos, J.M.1
Towbin, J.A.2
Ackerman, M.J.3
-
45
-
-
0037049977
-
Cardiac excitation-contraction coupling
-
Bers DM. Cardiac excitation-contraction coupling. Nature 2002; 415: 198-205.
-
(2002)
Nature
, vol.415
, pp. 198-205
-
-
Bers, D.M.1
-
46
-
-
17944398302
-
Calcium-induced release of calcium from the cardiac sarcoplasmic reticulum
-
Fabiato A. Calcium-induced release of calcium from the cardiac sarcoplasmic reticulum. Am J Physiol Cell Physiol 1983; 245: C1-C14.
-
(1983)
Am J Physiol Cell Physiol
, vol.245
-
-
Fabiato, A.1
-
47
-
-
0035966862
-
Ca2+ signaling between single L-type Ca2+ channels and ryanodine receptors in heart cells
-
Wang S-Q, Song L-S, Lakatta EG, Cheng H. Ca2+ signaling between single L-type Ca2+ channels and ryanodine receptors in heart cells. Nature 2001; 410: 592-596.
-
(2001)
Nature
, vol.410
, pp. 592-596
-
-
Wang, S.-Q.1
Song, L.-S.2
Lakatta, E.G.3
Cheng, H.4
-
48
-
-
0032949168
-
Local control models of cardiac excitation-contraction coupling
-
Stern MD, Song L-S, Cheng H, et al. Local control models of cardiac excitation-contraction coupling. J Gen Physiol 1999; 113: 469-489.
-
(1999)
J Gen Physiol
, vol.113
, pp. 469-489
-
-
Stern, M.D.1
Song, L.-S.2
Cheng, H.3
-
49
-
-
0022921924
-
Sequence analysis of phospholamban. Identification of phosphorylation sites and two major structural domains
-
Simmerman HK, Collins JH, Theibert JL, Wegener AD, Jones LR. Sequence analysis of phospholamban. Identification of phosphorylation sites and two major structural domains. J Biol Chem 1986; 261: 1333341.
-
(1986)
J Biol Chem
, vol.261
, pp. 1333341
-
-
Simmerman, H.K.1
Collins, J.H.2
Theibert, J.L.3
Wegener, A.D.4
Jones, L.R.5
-
50
-
-
0022931531
-
The nature of the modulation of Ca2+ transport as studied by reconstitution of cardiac sarcoplasmic reticulum
-
Inui M, Chamberlain BK, Saito A, Fleischer S. The nature of the modulation of Ca2+ transport as studied by reconstitution of cardiac sarcoplasmic reticulum. J Biol Chem 1986; 261: 1794-1800.
-
(1986)
J Biol Chem
, vol.261
, pp. 1794-1800
-
-
Inui, M.1
Chamberlain, B.K.2
Saito, A.3
Fleischer, S.4
-
51
-
-
78650272451
-
PLN-encoded phospholamban mutation in a large cohort of hypertrophic cardiomyopathy cases: Summary of the literature and implications for genetic testing
-
Landstrom A, Adekola B, Bos J, Ommen S, Ackerman M. PLN-encoded phospholamban mutation in a large cohort of hypertrophic cardiomyopathy cases: Summary of the literature and implications for genetic testing. Am Heart J 2011; 161: 165-171.
-
(2011)
Am Heart J
, vol.161
, pp. 165-171
-
-
Landstrom, A.1
Adekola, B.2
Bos, J.3
Ommen, S.4
Ackerman, M.5
-
52
-
-
0344406208
-
Mutation of the phospholamban promoter associated with hypertrophic cardiomyopathy
-
Minamisawa S, Sato Y, Tatsuguchi Y, et al. Mutation of the phospholamban promoter associated with hypertrophic cardiomyopathy. Biochem. Biophys Res Commun 2003; 304: 1-4.
-
(2003)
Biochem. Biophys Res Commun
, vol.304
, pp. 1-4
-
-
Minamisawa, S.1
Sato, Y.2
Tatsuguchi, Y.3
-
53
-
-
33846095295
-
Mutational screening of phospholamban gene in hypertrophic and idiopathic dilated cardiomyopathy and functional study of the PLN - 42 C>G mutation
-
Medin M, Hermida-Prieto M, Monserrat L, et al. Mutational screening of phospholamban gene in hypertrophic and idiopathic dilated cardiomyopathy and functional study of the PLN - 42 C>G mutation. Eur J Heart Fail 2007; 9: 37-43.
-
(2007)
Eur J Heart Fail
, vol.9
, pp. 37-43
-
-
Medin, M.1
Hermida-Prieto, M.2
Monserrat, L.3
-
54
-
-
85047687537
-
Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human
-
Haghighi K, Kolokathis F, Pater L, et al. Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human. J Clin Invest 2003; 111: 869-876.
-
(2003)
J Clin Invest
, vol.111
, pp. 869-876
-
-
Haghighi, K.1
Kolokathis, F.2
Pater, L.3
-
55
-
-
34548118345
-
Genetic screening of calcium regulation genes in familial hypertrophic cardiomyopathy
-
Chiu C, Tebo M, Ingles J, et al. Genetic screening of calcium regulation genes in familial hypertrophic cardiomyopathy. J Mol Cell Cardiol 2007; 43: 337-343.
-
(2007)
J Mol Cell Cardiol
, vol.43
, pp. 337-343
-
-
Chiu, C.1
Tebo, M.2
Ingles, J.3
-
56
-
-
37849031506
-
Immuno-proteomic approach to excitation-contraction coupling in skeletal and cardiac muscle: Molecular insights revealed by the mitsugumins
-
Weisleder N, Takeshima H, Ma J. Immuno-proteomic approach to excitation-contraction coupling in skeletal and cardiac muscle: Molecular insights revealed by the mitsugumins. Cell Calcium 2008; 43: 1-8.
-
(2008)
Cell Calcium
, vol.43
, pp. 1-8
-
-
Weisleder, N.1
Takeshima, H.2
Ma, J.3
-
57
-
-
66349127484
-
Molecular evolution of the junctophilin gene family
-
Garbino A, van Oort RJ, Dixit SS, Landstrom AP, Ackerman MJ, Wehrens XHT. Molecular evolution of the junctophilin gene family. Physiol Genomics 2009; 37: 175-186.
-
(2009)
Physiol Genomics
, vol.37
, pp. 175-186
-
-
Garbino, A.1
van Oort, R.J.2
Dixit, S.S.3
Landstrom, A.P.4
Ackerman, M.J.5
Wehrens, X.H.T.6
-
59
-
-
0033636778
-
Junctophilins: A novel family of junctional membrane complex proteins
-
Takeshima H, Komazaki S, Nishi M, Iino M, Kangawa K. Junctophilins: a novel family of junctional membrane complex proteins. Mol Cell 2000; 6: 11-22.
-
(2000)
Mol Cell
, vol.6
, pp. 11-22
-
-
Takeshima, H.1
Komazaki, S.2
Nishi, M.3
Iino, M.4
Kangawa, K.5
-
61
-
-
8444237010
-
Junctophilin type 2 is associated with caveolin-3 and is down-regulated in the hypertrophic and dilated cardiomyopathies
-
Minamisawa S, Oshikawa J, Takeshima H, et al. Junctophilin type 2 is associated with caveolin-3 and is down-regulated in the hypertrophic and dilated cardiomyopathies. Biochem Biophys Res Commun. 2004; 325:852-856.
-
(2004)
Biochem Biophys Res Commun
, vol.325
, pp. 852-856
-
-
Minamisawa, S.1
Oshikawa, J.2
Takeshima, H.3
-
62
-
-
33846990914
-
Intermolecular failure of L-type Ca2 channel and ryanodine receptor signaling in hypertrophy
-
Xu M, Zhou P, Xu S-M, et al. Intermolecular failure of L-type Ca2 channel and ryanodine receptor signaling in hypertrophy. PLoS Biology 2007; 5: e21.
-
(2007)
PLoS Biology
, vol.5
-
-
Xu, M.1
Zhou, P.2
Xu, S.-M.3
-
63
-
-
77956230883
-
T-tubule remodeling during transition from hypertrophy to heart failure
-
Wei S, Guo A, Chen B, et al. T-tubule remodeling during transition from hypertrophy to heart failure. Circ Res 2010; 107: 520-531.
-
(2010)
Circ Res
, vol.107
, pp. 520-531
-
-
Wei, S.1
Guo, A.2
Chen, B.3
-
64
-
-
79955930209
-
Junctophilin-2 expression silencing causes cardiocyte hypertrophy and abnormal intracellular calcium-handling
-
Landstrom A, Kellen C, Dixit S, et al. Junctophilin-2 expression silencing causes cardiocyte hypertrophy and abnormal intracellular calcium-handling. Circ Heart Fail. 2011; 4(2): 214-223.
-
(2011)
Circ Heart Fail
, vol.4
, Issue.2
, pp. 214-223
-
-
Landstrom, A.1
Kellen, C.2
Dixit, S.3
-
65
-
-
79952739100
-
Disrupted junctional membrane complexes and hyperactive ryanodine receptors after acute junctophilin knockdown in mice / clinical perspective
-
van Oort RJ, Garbino A, Wang W, et al. Disrupted junctional membrane complexes and hyperactive ryanodine receptors after acute junctophilin knockdown in mice / clinical perspective. Circulation 2011; 123: 979-988.
-
(2011)
Circulation
, vol.123
, pp. 979-988
-
-
van Oort, R.J.1
Garbino, A.2
Wang, W.3
-
66
-
-
34249724562
-
Mutations in JPH2-encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humans
-
Landstrom AP, Weisleder N, Batalden KB, et al. Mutations in JPH2-encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humans. J Mol Cell Cardiol. 2007; 42: 1026-1035.
-
(2007)
J Mol Cell Cardiol
, vol.42
, pp. 1026-1035
-
-
Landstrom, A.P.1
Weisleder, N.2
Batalden, K.B.3
-
67
-
-
42449101304
-
TRPC3-interacting triadic proteins in skeletal muscle
-
Woo JS, Kim DH, Allen PD, Lee EH. TRPC3-interacting triadic proteins in skeletal muscle. Biochem J 2008; 411: 399-405.
-
(2008)
Biochem J
, vol.411
, pp. 399-405
-
-
Woo, J.S.1
Kim, D.H.2
Allen, P.D.3
Lee, E.H.4
-
68
-
-
67650234246
-
Glutamate at position 227 of junctophilin-2 is involved in binding to TRPC3
-
Woo J, Hwang J, Ko J, Kim D, Ma J, Lee E. Glutamate at position 227 of junctophilin-2 is involved in binding to TRPC3. Mol Cell Biochem 2009; 328(1-2): 25-32.
-
(2009)
Mol Cell Biochem
, vol.328
, Issue.1-2
, pp. 25-32
-
-
Woo, J.1
Hwang, J.2
Ko, J.3
Kim, D.4
Ma, J.5
Lee, E.6
-
69
-
-
33744524661
-
Functional coupling between TRPC3 and RyR1 regulates the expressions of key triadic proteins
-
Lee EH, Cherednichenko G, Pessah IN, Allen PD. Functional coupling between TRPC3 and RyR1 regulates the expressions of key triadic proteins. J Biol Chem 2006; 281: 10042-10048.
-
(2006)
J Biol Chem
, vol.281
, pp. 10042-10048
-
-
Lee, E.H.1
Cherednichenko, G.2
Pessah, I.N.3
Allen, P.D.4
-
70
-
-
77950902596
-
S165F mutation of junctophilin 2 affects Ca2+ signalling in skeletal muscle
-
Woo JS, Hwang JH, Ko JK, et al. S165F mutation of junctophilin 2 affects Ca2+ signalling in skeletal muscle. Biochem J 2010; 427: 125-134.
-
(2010)
Biochem J
, vol.427
, pp. 125-134
-
-
Woo, J.S.1
Hwang, J.H.2
Ko, J.K.3
-
71
-
-
34249664521
-
Mutation of junctophilin type 2 associated with hypertrophic cardiomyopathy
-
Matsushita Y, Furukawa T, Kasanuki H, et al. Mutation of junctophilin type 2 associated with hypertrophic cardiomyopathy. J Hum Genet 2007; 52: 543-548.
-
(2007)
J Hum Genet
, vol.52
, pp. 543-548
-
-
Matsushita, Y.1
Furukawa, T.2
Kasanuki, H.3
-
72
-
-
0035969990
-
Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia
-
Laitinen PJ, Brown KM, Piippo K, et al. Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia. Circulation. 2001; 103(4): 485-490.
-
(2001)
Circulation
, vol.103
, Issue.4
, pp. 485-490
-
-
Laitinen, P.J.1
Brown, K.M.2
Piippo, K.3
-
73
-
-
0035895322
-
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
-
Priori SG, Napolitano C, Tiso N, et al. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia. Circulation 2001; 103: 196-200.
-
(2001)
Circulation
, vol.103
, pp. 196-200
-
-
Priori, S.G.1
Napolitano, C.2
Tiso, N.3
-
74
-
-
34147146134
-
A mechanism for sudden infant death syndrome (SIDS): Stress-induced leak via ryanodine receptors
-
Tester DJ, Dura M, Carturan E, et al. A mechanism for sudden infant death syndrome (SIDS): Stress-induced leak via ryanodine receptors. Heart Rhythm 2007; 4: 733-739.
-
(2007)
Heart Rhythm
, vol.4
, pp. 733-739
-
-
Tester, D.J.1
Dura, M.2
Carturan, E.3
-
75
-
-
0035253502
-
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)
-
Tiso N, Stephan DA, Nava A, et al. Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2). Hum Mol Genet 2001; 10: 189-194.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 189-194
-
-
Tiso, N.1
Stephan, D.A.2
Nava, A.3
-
76
-
-
56449087586
-
Abstract 915: A novel missense mutation in cardiac ryanodine receptor gene as a possible cause of hypertrophic cardiomyopathy: Evidence from familial analysis
-
Fujino N, Ino H, Hayashi K, et al. Abstract 915: A novel missense mutation in cardiac ryanodine receptor gene as a possible cause of hypertrophic cardiomyopathy: Evidence from familial analysis. Circulation 2006; 114: 2, 165.
-
(2006)
Circulation
, vol.114
, Issue.2
, pp. 165
-
-
Fujino, N.1
Ino, H.2
Hayashi, K.3
-
77
-
-
71849090068
-
The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either ctecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: A comprehensive open reading frame mutational analysis
-
Medeiros-Domingo A, Bhuiyan ZA, Tester DJ, et al. The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either ctecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: A comprehensive open reading frame mutational analysis. J Am Coll Cardiol 2009; 54: 2065-2074.
-
(2009)
J Am Coll Cardiol
, vol.54
, pp. 2065-2074
-
-
Medeiros-Domingo, A.1
Bhuiyan, Z.A.2
Tester, D.J.3
-
78
-
-
77649218547
-
Mutations in alphaactinin-2 cause hypertrophic cardiomyopathy: A genomewide analysis
-
Chiu C, Bagnall RD, Ingles J, et al. Mutations in alphaactinin-2 cause hypertrophic cardiomyopathy: A genomewide analysis. J Am Coll Cardiol 2010; 55: 1127-1135.
-
(2010)
J Am Coll Cardiol
, vol.55
, pp. 1127-1135
-
-
Chiu, C.1
Bagnall, R.D.2
Ingles, J.3
-
79
-
-
0035858868
-
Phosphorylationdependent regulation of ryanodine receptors
-
Marx SO, Reiken S, Hisamatsu Y, et al. Phosphorylationdependent regulation of ryanodine receptors. J Cell Biol 2001; 153: 699-708.
-
(2001)
J Cell Biol
, vol.153
, pp. 699-708
-
-
Marx, S.O.1
Reiken, S.2
Hisamatsu, Y.3
-
80
-
-
0028940654
-
Rapid adaptation of cardiac ryanodine receptors: Modulation by Mg2+ and phosphorylation
-
Valdivia HH, Kaplan JH, Ellis-Davies GC, Lederer WJ. Rapid adaptation of cardiac ryanodine receptors: modulation by Mg2+ and phosphorylation. Science 1995; 267: 1997-2000.
-
(1995)
Science
, vol.267
, pp. 1997-2000
-
-
Valdivia, H.H.1
Kaplan, J.H.2
Ellis-Davies, G.C.3
Lederer, W.J.4
-
81
-
-
0034640113
-
PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor): Defective regulation in failing hearts
-
Marx SO, Reiken S, Hisamatsu Y, et al. PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor): defective regulation in failing hearts. Cell 2000; 101: 365-376.
-
(2000)
Cell
, vol.101
, pp. 365-376
-
-
Marx, S.O.1
Reiken, S.2
Hisamatsu, Y.3
-
82
-
-
0141831981
-
Sarcoplasmic reticulum Ca2+ and heart failure: Roles of diastolic leak and Ca2+ transport
-
Bers DM, Eisner DA, Valdivia HH. Sarcoplasmic reticulum Ca2+ and heart failure: Roles of diastolic leak and Ca2+ transport. Circ Res 2003; 93: 487-490.
-
(2003)
Circ Res
, vol.93
, pp. 487-490
-
-
Bers, D.M.1
Eisner, D.A.2
Valdivia, H.H.3
-
83
-
-
0029934608
-
Effects of rapamycin on ryanodine receptor/Ca2+-release channels from cardiac muscle
-
Kaftan E, Marks AR, Ehrlich BE. Effects of rapamycin on ryanodine receptor/Ca2+-release channels from cardiac muscle. Circ Res 1996; 78: 990-997.
-
(1996)
Circ Res
, vol.78
, pp. 990-997
-
-
Kaftan, E.1
Marks, A.R.2
Ehrlich, B.E.3
-
84
-
-
3042763171
-
Ca2+/calmodulin-dependent protein kinase II phosphorylation regulates the cardiac ryanodine receptor
-
Wehrens XHT, Lehnart SE, Reiken SR, Marks AR. Ca2+/calmodulin-dependent protein kinase II phosphorylation regulates the cardiac ryanodine receptor. Circ Res 2004; 94: e61-e70.
-
(2004)
Circ Res
, vol.94
-
-
Wehrens, X.H.T.1
Lehnart, S.E.2
Reiken, S.R.3
Marks, A.R.4
-
85
-
-
0023372321
-
The structure of calsequestrin in triads of vertebrate skeletal muscle: A deep-etch study
-
Franzini-Armstrong C, Kenney LJ, Varriano-Marston E. The structure of calsequestrin in triads of vertebrate skeletal muscle: a deep-etch study. J Cell Biol 1987; 105: 49-56.
-
(1987)
J Cell Biol
, vol.105
, pp. 49-56
-
-
Franzini-Armstrong, C.1
Kenney, L.J.2
Varriano-Marston, E.3
-
86
-
-
0032038691
-
Regulation of Ca2+ signaling in transgenic mouse cardiac myocytes overexpressing calsequestrin
-
Jones LR, Suzuki YJ, Wang W, et al. Regulation of Ca2+ signaling in transgenic mouse cardiac myocytes overexpressing calsequestrin. J Clin Invest 1998; 101: 1385-1393.
-
(1998)
J Clin Invest
, vol.101
, pp. 1385-1393
-
-
Jones, L.R.1
Suzuki, Y.J.2
Wang, W.3
-
87
-
-
0032561337
-
Cardiac-specific overexpression of mouse cardiac calsequestrin is associated with depressed cardiovascular function and hypertrophy in transgenic mice
-
Sato Y, Ferguson DG, Sako H, et al. Cardiac-specific overexpression of mouse cardiac calsequestrin is associated with depressed cardiovascular function and hypertrophy in transgenic mice. J Biol Chem 1998; 273: 28470-28477.
-
(1998)
J Biol Chem
, vol.273
, pp. 28470-28477
-
-
Sato, Y.1
Ferguson, D.G.2
Sako, H.3
-
88
-
-
0037131020
-
Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia
-
Postma AV, Denjoy I, Hoorntje TM, et al. Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia. Circ Res 2002; 91: e21-e26.
-
(2002)
Circ Res
, vol.91
-
-
Postma, A.V.1
Denjoy, I.2
Hoorntje, T.M.3
-
89
-
-
33748512585
-
Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia
-
di Barletta MR, Viatchenko-Karpinski S, Nori A, et al. Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia. Circulation 2006; 114: 1012-1019.
-
(2006)
Circulation
, vol.114
, pp. 1012-1019
-
-
di Barletta, M.R.1
Viatchenko-Karpinski, S.2
Nori, A.3
-
90
-
-
0035802110
-
Functional specialization of calreticulin domains
-
Nakamura K, Zuppini A, Arnaudeau S, et al. Functional specialization of calreticulin domains. J. Cell Biol. 2001; 154: 961-972.
-
(2001)
J. Cell Biol
, vol.154
, pp. 961-972
-
-
Nakamura, K.1
Zuppini, A.2
Arnaudeau, S.3
-
91
-
-
0028870646
-
Calcium-dependent translocation of sorcin to membranes: Functional relevance in contractile tissue
-
Meyers MB, Zamparelli C, Verzili D, Dicker AP, Blanck TJJ, Chiancone E. Calcium-dependent translocation of sorcin to membranes: functional relevance in contractile tissue. FEBS Lett 1995; 357: 230-234.
-
(1995)
FEBS Lett
, vol.357
, pp. 230-234
-
-
Meyers, M.B.1
Zamparelli, C.2
Verzili, D.3
Dicker, A.P.4
Blanck, T.J.J.5
Chiancone, E.6
-
92
-
-
0141817953
-
Sorcin inhibits calcium release and modulates excitationcontraction coupling in the heart
-
Farrell E, Antaramian A, Rueda A, Gomez A, Valdivia H. Sorcin inhibits calcium release and modulates excitationcontraction coupling in the heart. J Biol Chem 2003; 278: 34660-34666.
-
(2003)
J Biol Chem
, vol.278
, pp. 34660-34666
-
-
Farrell, E.1
Antaramian, A.2
Rueda, A.3
Gomez, A.4
Valdivia, H.5
-
93
-
-
0032563129
-
Sorcin associates with the pore-forming subunit of voltage-dependent L-type Ca2+ channels
-
Meyers M, Puri T, Chien A, et al. Sorcin associates with the pore-forming subunit of voltage-dependent L-type Ca2+ channels. J Biol Chem 1998; 30: 18930-18935.
-
(1998)
J Biol Chem
, vol.30
, pp. 18930-18935
-
-
Meyers, M.1
Puri, T.2
Chien, A.3
-
94
-
-
0030875726
-
Modulation of cardiac ryanodine receptors by sorcin
-
Lokuta A, Meyers M, Sander P, Fishman G, Valdivia H. Modulation of cardiac ryanodine receptors by sorcin. J Biol Chem 1997; 272: 25333-25338.
-
(1997)
J Biol Chem
, vol.272
, pp. 25333-25338
-
-
Lokuta, A.1
Meyers, M.2
Sander, P.3
Fishman, G.4
Valdivia, H.5
-
95
-
-
4244126128
-
Abstract - A naturally-occurring sorcin missense mutation (F112L) is associated with hypertrophic cardiomyopathy, hypertension, and impaired modulation of cardiac ryanodine receptor
-
Mohiddin S, Antaramian A, Farrell E, et al. Abstract - A naturally-occurring sorcin missense mutation (F112L) is associated with hypertrophic cardiomyopathy, hypertension, and impaired modulation of cardiac ryanodine receptor. Circulation 2002; 106: 2, 319.
-
(2002)
Circulation
, vol.106
, Issue.2
, pp. 319
-
-
Mohiddin, S.1
Antaramian, A.2
Farrell, E.3
-
96
-
-
0033018816
-
Reliable identification of large numbers of candidate SNPs from public EST data
-
Buetow KH, Edmonson MN, Cassidy AB. Reliable identification of large numbers of candidate SNPs from public EST data. Nat Genet 1999; 21: 323-325.
-
(1999)
Nat Genet
, vol.21
, pp. 323-325
-
-
Buetow, K.H.1
Edmonson, M.N.2
Cassidy, A.B.3
-
97
-
-
17344391629
-
HGBASE: A database of SNPs and other variations in and around human genes
-
Brookes AJ, Lehvaslaiho H, Siegfried M, et al. HGBASE: a database of SNPs and other variations in and around human genes. Nucl Acids Res 2000; 28: 356-360.
-
(2000)
Nucl Acids Res
, vol.28
, pp. 356-360
-
-
Brookes, A.J.1
Lehvaslaiho, H.2
Siegfried, M.3
-
98
-
-
33846816468
-
Expression of a sorcin missense mutation in the heart modulates excitationcontraction coupling
-
Collis LP, Meyers MB, Zhang J, et al. Expression of a sorcin missense mutation in the heart modulates excitationcontraction coupling. FASEB J 2007; 21: 475-487.
-
(2007)
FASEB J
, vol.21
, pp. 475-487
-
-
Collis, L.P.1
Meyers, M.B.2
Zhang, J.3
-
100
-
-
38049177758
-
Molecular basis for the impaired function of the natural F112L sorcin mutant: X-ray crystal structure, calcium affinity, and interaction with annexin VII and the ryanodine receptor
-
Franceschini S, Ilari A, Verzili D, et al. Molecular basis for the impaired function of the natural F112L sorcin mutant: X-ray crystal structure, calcium affinity, and interaction with annexin VII and the ryanodine receptor. FASEB J 2008; 22: 295-306.
-
(2008)
FASEB J
, vol.22
, pp. 295-306
-
-
Franceschini, S.1
Ilari, A.2
Verzili, D.3
-
101
-
-
0036702526
-
Calcium, calmodulin, and calciumcalmodulin kinase II: Heartbeat to heartbeat and beyond
-
Maier LS, Bers DM. Calcium, calmodulin, and calciumcalmodulin kinase II: heartbeat to heartbeat and beyond. J Mol Cell Cardiol 2002; 34: 919-939.
-
(2002)
J Mol Cell Cardiol
, vol.34
, pp. 919-939
-
-
Maier, L.S.1
Bers, D.M.2
-
102
-
-
3242744450
-
Role of Ca2+/calmodulin-dependent protein kinase II in cardiac hypertrophy and heart failure
-
Zhang T, Brown JH. Role of Ca2+/calmodulin-dependent protein kinase II in cardiac hypertrophy and heart failure. Cardiovasc Res 2004; 63: 476-486.
-
(2004)
Cardiovasc Res
, vol.63
, pp. 476-486
-
-
Zhang, T.1
Brown, J.H.2
-
103
-
-
84889006323
-
Does contractile Ca2+ control calcineurin-NFAT signaling and pathological hypertrophy in cardiac myocytes?
-
Houser S, Molkentin J. Does contractile Ca2+ control calcineurin-NFAT signaling and pathological hypertrophy in cardiac myocytes? Sci Signal 2008; 1: pe31.
-
(2008)
Sci Signal
, vol.1
-
-
Houser, S.1
Molkentin, J.2
-
104
-
-
19244386873
-
CaM kinase signaling induces cardiac hypertrophy and activates the MEF2 transcription factor in vivo
-
Passier R, Zeng H, Frey N, et al. CaM kinase signaling induces cardiac hypertrophy and activates the MEF2 transcription factor in vivo. J Clin Invest 2000; 105: 1395-1406.
-
(2000)
J Clin Invest
, vol.105
, pp. 1395-1406
-
-
Passier, R.1
Zeng, H.2
Frey, N.3
-
105
-
-
34147093584
-
Nuclear calcium/calmodulin-dependent protein kinase II{delta} preferentially transmits signals to histone deacetylase 4 in cardiac cells
-
Little GH, Bai Y, Williams T, Poizat C. Nuclear calcium/calmodulin-dependent protein kinase II{delta} preferentially transmits signals to histone deacetylase 4 in cardiac cells. J Biol Chem 2007; 282: 7219-7231.
-
(2007)
J Biol Chem
, vol.282
, pp. 7219-7231
-
-
Little, G.H.1
Bai, Y.2
Williams, T.3
Poizat, C.4
-
106
-
-
0037162697
-
Class II histone deacetylases act as signal-responsive repressors of cardiac hypertrophy
-
Zhang CL, McKinsey TA, Chang S, Antos CL, Hill JA, Olson EN. Class II histone deacetylases act as signal-responsive repressors of cardiac hypertrophy. Cell 2002; 110: 479-488.
-
(2002)
Cell
, vol.110
, pp. 479-488
-
-
Zhang, C.L.1
McKinsey, T.A.2
Chang, S.3
Antos, C.L.4
Hill, J.A.5
Olson, E.N.6
-
107
-
-
0032540267
-
A calcineurindependent transcriptional pathway for cardiac hypertrophy
-
Molkentin JD, Lu J-R, Antos CL, et al. A calcineurindependent transcriptional pathway for cardiac hypertrophy. Cell 1998; 93: 215-228.
-
(1998)
Cell
, vol.93
, pp. 215-228
-
-
Molkentin, J.D.1
Lu, J.-R.2
Antos, C.L.3
-
108
-
-
52049114958
-
NFATc2 is a necessary mediator of calcineurin-dependent cardiac hypertrophy and heart failure
-
Bourajjaj M, Armand A-S, da Costa Martins PA, et al. NFATc2 is a necessary mediator of calcineurin-dependent cardiac hypertrophy and heart failure. J Biol Chem 2008; 283: 22295-22303.
-
(2008)
J Biol Chem
, vol.283
, pp. 22295-22303
-
-
Bourajjaj, M.1
Armand, A.-S.2
da Costa, M.P.A.3
-
109
-
-
70549084819
-
GWAS or Gee Whiz, PSAS or Pshaw: Elucidating the biologic and clinical significance of genetic variation in cardiovascular disease
-
Landstrom AP, Ackerman MJ. GWAS or Gee Whiz, PSAS or Pshaw: Elucidating the biologic and clinical significance of genetic variation in cardiovascular disease. Heart Rhythm 2009; 6: 1751-1753.
-
(2009)
Heart Rhythm
, vol.6
, pp. 1751-1753
-
-
Landstrom, A.P.1
Ackerman, M.J.2
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