-
1
-
-
79751531393
-
Heart disease and stroke statistics: 2011 update: A report from the American Heart Association
-
Roger VL, Go AS, Lloyd-Jones DM, Adams RJ, Berry JD, Brown TM, Carnethon MR, Dai S, de Simone G, Ford ES, Fox CS, Fullerton HJ, Gillespie C, Greenlund KJ, Hailpern SM, Heit JA, Ho PM, Howard VJ, Kissela BM, Kittner SJ, Lackland DT, Lichtman JH, Lisabeth LD, Makuc DM, Marcus GM, Marelli A, Matchar DB, McDermott MM, Meigs JB, Moy CS, Mozaffarian D, Mussolino ME, Nichol G, Paynter NP, Rosamond WD, Sorlie PD, Stafford RS, Turan TN, Turner MB, Wong ND, Wylie-Rosett J. Heart disease and stroke statistics: 2011 update: a report from the American Heart Association. Circulation. 2011;123: 459-463.
-
(2011)
Circulation
, vol.123
, pp. 459-463
-
-
Roger, V.L.1
Go, A.S.2
Lloyd-Jones, D.M.3
Adams, R.J.4
Berry, J.D.5
Brown, T.M.6
Carnethon, M.R.7
Dai, S.8
De Simone, G.9
Ford, E.S.10
Fox, C.S.11
Fullerton, H.J.12
Gillespie, C.13
Greenlund, K.J.14
Hailpern, S.M.15
Heit, J.A.16
Ho, P.M.17
Howard, V.J.18
Kissela, B.M.19
Kittner, S.J.20
Lackland, D.T.21
Lichtman, J.H.22
Lisabeth, L.D.23
Makuc, D.M.24
Marcus, G.M.25
Marelli, A.26
Matchar, D.B.27
McDermott, M.M.28
Meigs, J.B.29
Moy, C.S.30
Mozaffarian, D.31
Mussolino, M.E.32
Nichol, G.33
Paynter, N.P.34
Rosamond, W.D.35
Sorlie, P.D.36
Stafford, R.S.37
Turan, T.N.38
Turner, M.B.39
Wong, N.D.40
Wylie-Rosett, J.41
more..
-
2
-
-
77952966596
-
Harnessing molecular genetics for the diagnosis and management of hypertrophic cardiomyopathy
-
Wang L, Seidman JG, Seidman CE. Harnessing molecular genetics for the diagnosis and management of hypertrophic cardiomyopathy. Ann Intern Med. 2010;152:513-520.
-
(2010)
Ann Intern Med
, vol.152
, pp. 513-520
-
-
Wang, L.1
Seidman, J.G.2
Seidman, C.E.3
-
3
-
-
0036787237
-
Molecular mechanisms of inherited cardiomyopathies
-
Fatkin D, Graham RM. Molecular mechanisms of inherited cardiomyopathies. Physiol Rev. 2002;82:945-980.
-
(2002)
Physiol Rev
, vol.82
, pp. 945-980
-
-
Fatkin, D.1
Graham, R.M.2
-
4
-
-
77952158022
-
The genetics of dilated cardiomyopathy
-
Dellefave L, McNally EM. The genetics of dilated cardiomyopathy. Curr Opin Cardiol. 2010;25:198-204.
-
(2010)
Curr Opin Cardiol
, vol.25
, pp. 198-204
-
-
Dellefave, L.1
McNally, E.M.2
-
5
-
-
77949718853
-
Hypertrophic cardiomyopathy: From genetics to treatment
-
Marian AJ. Hypertrophic cardiomyopathy: from genetics to treatment. Eur J Clin Invest. 2010;40:360-369.
-
(2010)
Eur J Clin Invest
, vol.40
, pp. 360-369
-
-
Marian, A.J.1
-
6
-
-
0037184992
-
The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy
-
DOI 10.1016/S0092-8674(02)01226-6
-
Knoll R, Hoshijima M, Hoffman HM, Person V, Lorenzen-Schmidt I, Bang ML, Hayashi T, Shiga N, Yasukawa H, Schaper W, McKenna W, Yokoyama M, Schork NJ, Omens JH, McCulloch AD, Kimura A, Gregorio CC, Poller W, Schaper J, Schultheiss HP, Chien KR. The cardiac mechanical stretch sensor machinery involves a z disc complex that is defective in a subset of human dilated cardiomyopathy. Cell. 2002;111:943-955. (Pubitemid 36044687)
-
(2002)
Cell
, vol.111
, Issue.7
, pp. 943-955
-
-
Knoll, R.1
Hoshijima, M.2
Hoffman, H.M.3
Person, V.4
Lorenzen-Schmidt, I.5
Bang, M.-L.6
Hayashi, T.7
Shiga, N.8
Yasukawa, H.9
Schaper, W.10
McKenna, W.11
Yokoyama, M.12
Schork, N.J.13
Omens, J.H.14
McCulloch, A.D.15
Kimura, A.16
Gregorio, C.C.17
Poller, W.18
Schaper, J.19
Schultheiss, H.P.20
Chien, K.R.21
more..
-
7
-
-
34147182155
-
Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy
-
DOI 10.1161/01.RES.0000263008.66799.aa
-
Osio A, Tan L, Chen SN, Lombardi R, Nagueh SF, Shete S, Roberts R, Willerson JT, Marian AJ. Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy. Circ Res. 2007;100:766-768. (Pubitemid 46555681)
-
(2007)
Circulation Research
, vol.100
, Issue.6
, pp. 766-768
-
-
Osio, A.1
Tan, L.2
Chen, S.N.3
Lombardi, R.4
Nagueh, S.F.5
Shete, S.6
Roberts, R.7
Willerson, J.T.8
Marian, A.J.9
-
8
-
-
43249119946
-
MURC, a muscle-restricted coiled-coil protein that modulates the Rho/ROCK pathway, induces cardiac dysfunction and conduction disturbance
-
DOI 10.1128/MCB.02186-07
-
Ogata T, Ueyama T, Isodono K, Tagawa M, Takehara N, Kawashima T, Harada K, Takahashi T, Shioi T, Matsubara H, Oh H. MURC, a musclerestricted coiled-coil protein that modulates the Rho/ROCK pathway, induces cardiac dysfunction and conduction disturbance. Mol Cell Biol. 2008;28:3424-3436. (Pubitemid 351657104)
-
(2008)
Molecular and Cellular Biology
, vol.28
, Issue.10
, pp. 3424-3436
-
-
Ogata, T.1
Ueyama, T.2
Isodono, K.3
Tagawa, M.4
Takehara, N.5
Kawashima, T.6
Harada, K.7
Takahashi, T.8
Shioi, T.9
Matsubara, H.10
Oh, H.11
-
9
-
-
55949135301
-
MURC, a muscle-restricted coiled-coil protein, is involved in the regulation of skeletal myogenesis
-
DOI 10.1152/ajpcell.00188.2008
-
Tagawa M, Ueyama T, Ogata T, Takehara N, Nakajima N, Isodono K, Asada S, Takahashi T, Matsubara H, Oh H. MURC, a muscle-restricted coiled-coil protein, is involved in the regulation of skeletal myogenesis. Am J Physiol Cell Physiol. 2008;295:C490-C498. (Pubitemid 352755772)
-
(2008)
American Journal of Physiology - Cell Physiology
, vol.295
, Issue.2
-
-
Tagawa, M.1
Ueyama, T.2
Ogata, T.3
Takehara, N.4
Nakajima, N.5
Isodono, K.6
Asada, S.7
Takahashi, T.8
Matsubara, H.9
Oh, H.10
-
10
-
-
67649583182
-
MURC/cavin-4 and cavin family members form tissue-specific caveolar complexes
-
Bastiani M, Liu L, Hill MM, Jedrychowski MP, Nixon SJ, Lo HP, Abankwa D, Luetterforst R, Fernandez-Rojo M, Breen MR, Gygi SP, Vinten J, Walser PJ, North KN, Hancock JF, Pilch PF, Parton RG. MURC/cavin-4 and cavin family members form tissue-specific caveolar complexes. J Cell Biol. 2009;185:1259-1273.
-
(2009)
J Cell Biol
, vol.185
, pp. 1259-1273
-
-
Bastiani, M.1
Liu, L.2
Hill, M.M.3
Jedrychowski, M.P.4
Nixon, S.J.5
Lo, H.P.6
Abankwa, D.7
Luetterforst, R.8
Fernandez-Rojo, M.9
Breen, M.R.10
Gygi, S.P.11
Vinten, J.12
Walser, P.J.13
North, K.N.14
Hancock, J.F.15
Pilch, P.F.16
Parton, R.G.17
-
11
-
-
33646693410
-
Contemporary definitions and classification of the cardiomyopathies: An American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention
-
DOI 10.1161/CIRCULATIONAHA.106.174287, PII 0000301720060411000015
-
Maron BJ, Towbin JA, Thiene G, Antzelevitch C, Corrado D, Arnett D, Moss AJ, Seidman CE, Young JB. Contemporary definitions and classification of the cardiomyopathies: an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention. Circulation. 2006;113:1807-1816. (Pubitemid 43958474)
-
(2006)
Circulation
, vol.113
, Issue.14
, pp. 1807-1816
-
-
Maron, B.J.1
Towbin, J.A.2
Thiene, G.3
Antzelevitch, C.4
Corrado, D.5
Arnett, D.6
Moss, A.J.7
Seidman, C.E.8
Young, J.B.9
-
12
-
-
67650535224
-
Clinical and genetic modifiers of long-term survival in heart failure
-
Cresci S, Kelly RJ, Cappola TP, Diwan A, Dries D, Kardia SL, Dorn GW II. Clinical and genetic modifiers of long-term survival in heart failure. J Am Coll Cardiol. 2009;54:432-444.
-
(2009)
J Am Coll Cardiol
, vol.54
, pp. 432-444
-
-
Cresci, S.1
Kelly, R.J.2
Cappola, T.P.3
Diwan, A.4
Dries, D.5
Kardia, S.L.6
Dorn, I.I.G.W.7
-
13
-
-
0035869223
-
Prediction of deleterious human alleles
-
Sunyaev S, Ramensky V, Koch I, Lathe W III, Kondrashov AS, Bork P. Prediction of deleterious human alleles. Hum Mol Genet. 2001;10: 591-597. (Pubitemid 32229363)
-
(2001)
Human Molecular Genetics
, vol.10
, Issue.6
, pp. 591-597
-
-
Sunyaev, S.1
Ramensky, V.2
Koch, I.3
Lathe III, W.4
Kondrashov, A.S.5
Bork, P.6
-
14
-
-
37549040201
-
Genetic basis of hypertrophic cardiomyopathy: From bench to the clinics
-
Alcalai R, Seidman JG, Seidman CE. Genetic basis of hypertrophic cardiomyopathy: from bench to the clinics. J Cardiovasc Electrophysiol. 2008;19:104-110.
-
(2008)
J Cardiovasc Electrophysiol
, vol.19
, pp. 104-110
-
-
Alcalai, R.1
Seidman, J.G.2
Seidman, C.E.3
-
15
-
-
33947531466
-
Reviews of translational medicine and genomics in cardiovascular disease: new disease taxonomy and therapeutic implications. cardiomyopathies: Therapeutics based on molecular phenotype
-
DOI 10.1016/j.jacc.2006.10.073, PII S0735109707001301
-
Ashrafian H, Watkins H. Reviews of translational medicine and genomics in cardiovascular disease: new disease taxonomy and therapeutic implications cardiomyopathies: therapeutics based on molecular phenotype. J Am Coll Cardiol. 2007;49:1251-1264. (Pubitemid 46470069)
-
(2007)
Journal of the American College of Cardiology
, vol.49
, Issue.12
, pp. 1251-1264
-
-
Ashrafian, H.1
Watkins, H.2
-
16
-
-
66149101609
-
Genetic fate mapping identifies second heart field progenitor cells as a source of adipocytes in arrhythmogenic right ventricular cardiomyopathy
-
Lombardi R, Dong J, Rodriguez G, Bell A, Leung TK, Schwartz RJ, Willerson JT, Brugada R, Marian AJ. Genetic fate mapping identifies second heart field progenitor cells as a source of adipocytes in arrhythmogenic right ventricular cardiomyopathy. Circ Res. 2009;104: 1076-1084.
-
(2009)
Circ Res
, vol.104
, pp. 1076-1084
-
-
Lombardi, R.1
Dong, J.2
Rodriguez, G.3
Bell, A.4
Leung, T.K.5
Schwartz, R.J.6
Willerson, J.T.7
Brugada, R.8
Marian, A.J.9
-
17
-
-
0042164600
-
Inhibitory cardiac transcription factor, SRF-N, is generated by caspase 3 cleavage in human heart failure and attenuated by ventricular unloading
-
DOI 10.1161/01.CIR.0000084502.02147.83
-
Chang J, Wei L, Otani T, Youker KA, Entman ML, Schwartz RJ. Inhibitory cardiac transcription factor, srf-n, is generated by caspase 3 cleavage in human heart failure and attenuated by ventricular unloading. Circulation. 2003;108:407-413. (Pubitemid 36935532)
-
(2003)
Circulation
, vol.108
, Issue.4
, pp. 407-413
-
-
Chang, J.1
Wei, L.2
Otani, T.3
Youker, K.A.4
Entman, M.L.5
Schwartz, R.J.6
-
18
-
-
0032694585
-
Cardiac-specific overexpression of RhoA results in sinus and atrioventricular nodal dysfunction and contractile failure
-
Sah VP, Minamisawa S, Tam SP, Wu TH, Dorn GW, Ross J, Chien KR, Brown JH. Cardiac-specific overexpression of RhoA results in sinus and atrioventricular nodal dysfunction and contractile failure. J Clin Invest. 1999;103:1627-1634. (Pubitemid 29534356)
-
(1999)
Journal of Clinical Investigation
, vol.103
, Issue.12
, pp. 1627-1634
-
-
Sah, V.P.1
Minamisawa, S.2
Tam, S.P.3
Wu, T.H.4
Dorn II, G.W.5
Ross Jr., J.6
Chien, K.R.7
Brown, J.H.8
-
19
-
-
4644288506
-
Disruption of rho signaling results in progressive atrioventricular conduction defects while ventricular function remains preserved
-
Wei L, Taffet GE, Khoury DS, Bo J, Li Y, Yatani A, Delaughter MC, Klevitsky R, Hewett TE, Robbins J, Michael LH, Schneider MD, Entman ML, Schwartz RJ. Disruption of rho signaling results in progressive atrioventricular conduction defects while ventricular function remains preserved. FASEB J. 2004;18:857-859.
-
(2004)
FASEB J
, vol.18
, pp. 857-859
-
-
Wei, L.1
Taffet, G.E.2
Khoury, D.S.3
Bo, J.4
Li, Y.5
Yatani, A.6
Delaughter, M.C.7
Klevitsky, R.8
Hewett, T.E.9
Robbins, J.10
Michael, L.H.11
Schneider, M.D.12
Entman, M.L.13
Schwartz, R.J.14
-
20
-
-
0031920515
-
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy
-
DOI 10.1038/ng0498-365
-
Minetti C, Sotgia F, Bruno C, Scartezzini P, Broda P, Bado M, Masetti E, Mazzocco M, Egeo A, Donati MA, Volonte D, Galbiati F, Cordone G, Bricarelli FD, Lisanti MP, Zara F. Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy. Nat Genet. 1998; 18:365-368. (Pubitemid 28158166)
-
(1998)
Nature Genetics
, vol.18
, Issue.4
, pp. 365-368
-
-
Minetti, C.1
Sotgia, F.2
Bruno, C.3
Scartezzini, P.4
Broda, P.5
Bado, M.6
Masetti, E.7
Mazzocco, M.8
Egeo, A.9
Donati, M.A.10
Volonte, D.11
Galbiati, F.12
Cordone, G.13
Bricarelli, F.D.14
Lisanti, M.P.15
Zara, F.16
-
21
-
-
10744220034
-
Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathy
-
DOI 10.1016/j.bbrc.2003.11.101
-
Hayashi T, Arimura T, Ueda K, Shibata H, Hohda S, Takahashi M, Hori H, Koga Y, Oka N, Imaizumi T. Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathy. Biochem Biophys Res Commun. 2004;313:178-184. (Pubitemid 37524041)
-
(2004)
Biochemical and Biophysical Research Communications
, vol.313
, Issue.1
, pp. 178-184
-
-
Hayashi, T.1
Arimura, T.2
Ueda, K.3
Shibata, H.4
Hohda, S.5
Takahashi, M.6
Hori, H.7
Koga, Y.8
Oka, N.9
Imaizumi, T.10
Yasunami, M.11
Kimura, A.12
-
22
-
-
0034988861
-
Mutations in cis can confound genotype-phenotype correlations in hypertrophic cardiomyopathy
-
Blair E, Price SJ, Baty CJ, Ostman-Smith I, Watkins H. Mutations in cis can confound genotype-phenotype correlations in hypertrophic cardiomyopathy. J Med Genet. 2001;38:385-388.
-
(2001)
J Med Genet
, vol.38
, pp. 385-388
-
-
Blair, E.1
Price, S.J.2
Baty, C.J.3
Ostman-Smith, I.4
Watkins, H.5
-
23
-
-
7044264544
-
Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy
-
DOI 10.1016/j.jacc.2004.07.045, PII S0735109704016146
-
Van Driest SL, Vasile VC, Ommen SR, Will ML, Tajik AJ, Gersh BJ, Ackerman MJ. Myosin binding protein c mutations and compound heterozygosity in hypertrophic cardiomyopathy. J Am Coll Cardiol. 2004; 44:1903-1910. (Pubitemid 39424094)
-
(2004)
Journal of the American College of Cardiology
, vol.44
, Issue.9
, pp. 1903-1910
-
-
Van Driest, S.L.1
Vasile, V.C.2
Ommen, S.R.3
Will, M.L.4
Tajik, A.J.5
Gersh, B.J.6
Ackerman, M.J.7
-
24
-
-
0037423552
-
Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system
-
DOI 10.1161/01.RES.0000052672.97759.36
-
Bezzina CR, Rook MB, Groenewegen WA, Herfst LJ, van der Wal AC, Lam J, Jongsma HJ, Wilde AA, Mannens MM. Compound heterozygosity for mutations (w156x and r225w) in scn5a associated with severe cardiac conduction disturbances and degenerative changes in the conduction system. Circ Res. 2003;92:159-168. (Pubitemid 36254272)
-
(2003)
Circulation Research
, vol.92
, Issue.2
, pp. 159-168
-
-
Bezzina, C.R.1
Rook, M.B.2
Groenewegen, W.A.3
Herfst, L.J.4
Van Der Wal, A.C.5
Lam, J.6
Jongsma, H.J.7
Wilde, A.A.M.8
Mannens, M.M.A.M.9
-
25
-
-
0031922826
-
A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutated β-myosin heavy chain genes
-
DOI 10.1007/s004390050695
-
Jeschke B, Uhl K, Weist B, Schroder D, Meitinger T, Dohlemann C, Vosberg HP. A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutated beta-myosin heavy chain genes. Hum Genet. 1998;102:299-304. (Pubitemid 28185218)
-
(1998)
Human Genetics
, vol.102
, Issue.3
, pp. 299-304
-
-
Jeschke, B.1
Uhl, K.2
Weist, B.3
Schroder, D.4
Meitinger, T.5
Dohlemann, C.6
Vosberg, H.-P.7
-
26
-
-
77449112270
-
Nature's genetic gradients and the clinical phenotype
-
Marian AJ. Nature's genetic gradients and the clinical phenotype. Circ Cardiovasc Genet. 2009;2:537-539.
-
(2009)
Circ Cardiovasc Genet
, vol.2
, pp. 537-539
-
-
Marian, A.J.1
|