-
3
-
-
0030933063
-
MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure
-
Arber S,Hunter JJ,Ross J,Hongo M,Sansig G,Borg J, et al.MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure.Cell. 1997;88:393-403.
-
(1997)
Cell
, vol.88
, pp. 393-403
-
-
Arber, S.1
Hunter, J.J.2
Ross, J.3
Hongo, M.4
Sansig, G.5
Borg, J.6
-
4
-
-
33745425651
-
The transitional junction: a new functional subcellular domain at the intercalated disc
-
Bennett PM,Maggs AM,Baines AJ,Pinder JC.The transitional junction: a new functional subcellular domain at the intercalated disc.Mol Biol Cell. 2006;17:2091-2100.
-
(2006)
Mol Biol Cell
, vol.17
, pp. 2091-2100
-
-
Bennett, P.M.1
Maggs, A.M.2
Baines, A.J.3
Pinder, J.C.4
-
5
-
-
41149125478
-
Genetic mechanisms controlling cardiovascular development
-
Bentham J,Bhattacharya S.Genetic mechanisms controlling cardiovascular development.Ann N Y Acad Sci. 2008;1123:10-19.
-
(2008)
Ann N Y Acad Sci
, vol.1123
, pp. 10-19
-
-
Bentham, J.1
Bhattacharya, S.2
-
6
-
-
39749191367
-
The developmental genetics of congenital heart disease
-
Bruneau BG.The developmental genetics of congenital heart disease.Nature. 2008;451:943-948.
-
(2008)
Nature
, vol.451
, pp. 943-948
-
-
Bruneau, B.G.1
-
7
-
-
30944435503
-
Sarcomeric protein mutations in dilated cardiomyopathy
-
Chang AN,Potter JD.Sarcomeric protein mutations in dilated cardiomyopathy.Heart Fail Rev. 2005;10:225-235.
-
(2005)
Heart Fail Rev
, vol.10
, pp. 225-235
-
-
Chang, A.N.1
Potter, J.D.2
-
8
-
-
0034648805
-
Genomic circuits and the integrative biology of cardiac diseases
-
Chien KR.Genomic circuits and the integrative biology of cardiac diseases.Nature. 2000;407:227-232.
-
(2000)
Nature
, vol.407
, pp. 227-232
-
-
Chien, K.R.1
-
9
-
-
49649103081
-
The alpha-kinases TRPM6 and TRPM7, but not eef-2 kinase, phosphorylate the assembly domain of myosin IIA, IIB and IIC
-
Clark K,Middelbeek J,Dorovkov MV,Figdor CG,Ryazanov AG,Lasonder E, et al.The alpha-kinases TRPM6 and TRPM7, but not eef-2 kinase, phosphorylate the assembly domain of myosin IIA, IIB and IIC.FEBS Lett. 2008;582:2993-2997.
-
(2008)
FEBS Lett
, vol.582
, pp. 2993-2997
-
-
Clark, K.1
Middelbeek, J.2
Dorovkov, M.V.3
Figdor, C.G.4
Ryazanov, A.G.5
Lasonder, E.6
-
10
-
-
0034673647
-
Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene
-
Dalakas MC,Park KY,Semino-Mora C,Lee HS,Sivakumar K,Goldfarb LG.Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene.N Engl J Med. 2000;342:770-780.
-
(2000)
N Engl J Med
, vol.342
, pp. 770-780
-
-
Dalakas, M.C.1
Park, K.Y.2
Semino-Mora, C.3
Lee, H.S.4
Sivakumar, K.5
Goldfarb, L.G.6
-
11
-
-
1842536165
-
Alpha-kinases: analysis of the family and comparison with conventional protein kinases
-
Drennan D,Ryazanov AG.Alpha-kinases: analysis of the family and comparison with conventional protein kinases.Prog Biophys Mol Biol. 2004;85:1-32.
-
(2004)
Prog Biophys Mol Biol
, vol.85
, pp. 1-32
-
-
Drennan, D.1
Ryazanov, A.G.2
-
12
-
-
0035858885
-
Alterations at the intercalated disk associated with the absence of muscle LIM protein
-
Ehler E,Horowits R,Zuppinger C,Price RL,Perriard E,Leu M, et al.Alterations at the intercalated disk associated with the absence of muscle LIM protein.J Cell Biol. 2001;153:763-772.
-
(2001)
J Cell Biol
, vol.153
, pp. 763-772
-
-
Ehler, E.1
Horowits, R.2
Zuppinger, C.3
Price, R.L.4
Perriard, E.5
Leu, M.6
-
13
-
-
0037089088
-
Remodeling the intercalated disc leads to cardiomyopathy in mice misexpressing cadherins in the heart
-
Ferreira-Cornwell MC,Luo Y,Narula N,Lenox JM,Lieberman M,Radice GL.Remodeling the intercalated disc leads to cardiomyopathy in mice misexpressing cadherins in the heart.J Cell Sci. 2002;115:1623-1634.
-
(2002)
J Cell Sci
, vol.115
, pp. 1623-1634
-
-
Ferreira-Cornwell, M.C.1
Luo, Y.2
Narula, N.3
Lenox, J.M.4
Lieberman, M.5
Radice, G.L.6
-
14
-
-
0034999263
-
Progression from hypertrophic to dilated cardiomyopathy in mice that express a mutant myosin transgene
-
Freeman K,Colon-Rivera C,Olsson MC,Moore RL,Weinberger HD,Grupp IL, et al.Progression from hypertrophic to dilated cardiomyopathy in mice that express a mutant myosin transgene.Am J Physiol Heart Circ Physiol. 2001;280:H151-H159.
-
(2001)
Am J Physiol Heart Circ Physiol
, vol.280
-
-
Freeman, K.1
Colon-Rivera, C.2
Olsson, M.C.3
Moore, R.L.4
Weinberger, H.D.5
Grupp, I.L.6
-
15
-
-
53549114498
-
Large-scale gene trapping in C57BL/6N mouse embryonic stem cells
-
Hansen GM,Markesich DC,Burnett MB,Zhu Q,Dionne KM,Richter LJ, et al.Large-scale gene trapping in C57BL/6N mouse embryonic stem cells.Genome Res. 2008;18:1670-1679.
-
(2008)
Genome Res
, vol.18
, pp. 1670-1679
-
-
Hansen, G.M.1
Markesich, D.C.2
Burnett, M.B.3
Zhu, Q.4
Dionne, K.M.5
Richter, L.J.6
-
16
-
-
0035929580
-
A novel myocyte-specific gene Midori promotes the differentiation of P19CL6 cells into cardiomyocytes
-
Hosoda T,Monzen K,Hiroi Y,Oka T,Takimoto E,Yazaki Y, et al.A novel myocyte-specific gene Midori promotes the differentiation of P19CL6 cells into cardiomyocytes.J Biol Chem. 2001;276:35978-35989.
-
(2001)
J Biol Chem
, vol.276
, pp. 35978-35989
-
-
Hosoda, T.1
Monzen, K.2
Hiroi, Y.3
Oka, T.4
Takimoto, E.5
Yazaki, Y.6
-
17
-
-
26244448543
-
Cardiac manifestations in the mouse model of mucopolysaccharidosis I
-
Jordan MC,Zheng Y,Ryazantsev S,Rozengurt N,Roos KP,Neufeld EF.Cardiac manifestations in the mouse model of mucopolysaccharidosis I.Mol Genet Metab. 2005;86:233-243.
-
(2005)
Mol Genet Metab
, vol.86
, pp. 233-243
-
-
Jordan, M.C.1
Zheng, Y.2
Ryazantsev, S.3
Rozengurt, N.4
Roos, K.P.5
Neufeld, E.F.6
-
18
-
-
0034619996
-
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy
-
Kamisago M,Sharma SD,DePalma SR,Solomon S,Sharma P,McDonough B, et al.Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.N Engl J Med. 2000;343:1688-1696.
-
(2000)
N Engl J Med
, vol.343
, pp. 1688-1696
-
-
Kamisago, M.1
Sharma, S.D.2
DePalma, S.R.3
Solomon, S.4
Sharma, P.5
McDonough, B.6
-
19
-
-
53149121986
-
Molecular etiology and pathogenesis of hereditary cardiomyopathy
-
Kimura A.Molecular etiology and pathogenesis of hereditary cardiomyopathy.Circ J. 2008;72 (suppl A): A38-A48.
-
(2008)
Circ J
, vol.72
, Issue.SUPPL. A
-
-
Kimura, A.1
-
20
-
-
2342621479
-
The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma
-
Lapidos KA,Kakkar R,McNally EM.The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma.Circ Res. 2004;94:1023-1031.
-
(2004)
Circ Res
, vol.94
, pp. 1023-1031
-
-
Lapidos, K.A.1
Kakkar, R.2
McNally, E.M.3
-
21
-
-
0033520037
-
Desmin mutation responsible for idiopathic dilated cardiomyopathy
-
Li D,Tapscoft T,Gonzalez O,Burch PE,Quinones MA,Zoghbi WA, et al.Desmin mutation responsible for idiopathic dilated cardiomyopathy.Circulation. 1999;100:461-464.
-
(1999)
Circulation
, vol.100
, pp. 461-464
-
-
Li, D.1
Tapscoft, T.2
Gonzalez, O.3
Burch, P.E.4
Quinones, M.A.5
Zoghbi, W.A.6
-
22
-
-
0029893923
-
Cardiovascular lesions and skeletal myopathy in mice lacking desmin
-
Li Z,Colucci-Guyon E,Pincon-Raymond M,Mericskay M,Pournin S,Paulin D, et al.Cardiovascular lesions and skeletal myopathy in mice lacking desmin.Dev Biol. 1996;175:362-366.
-
(1996)
Dev Biol
, vol.175
, pp. 362-366
-
-
Li, Z.1
Colucci-Guyon, E.2
Pincon-Raymond, M.3
Mericskay, M.4
Pournin, S.5
Paulin, D.6
-
23
-
-
0030911475
-
Control of mouse cardiac morphogenesis and myogenesis by transcription factor MEF2C
-
Lin Q,Schwarz J,Bucana C,Olson EN.Control of mouse cardiac morphogenesis and myogenesis by transcription factor MEF2C.Science. 1997;276:1404-1407.
-
(1997)
Science
, vol.276
, pp. 1404-1407
-
-
Lin, Q.1
Schwarz, J.2
Bucana, C.3
Olson, E.N.4
-
24
-
-
0033621141
-
Mechanisms and models in heart failure: a combinatorial approach
-
Mann DL.Mechanisms and models in heart failure: a combinatorial approach.Circulation. 1999;100:999-1008.
-
(1999)
Circulation
, vol.100
, pp. 999-1008
-
-
Mann, D.L.1
-
25
-
-
0037070514
-
Hypertrophic cardiomyopathy: a systematic review
-
Maron BJ.Hypertrophic cardiomyopathy: a systematic review.J Am Med Assoc. 2002;287:1308-1320.
-
(2002)
J Am Med Assoc
, vol.287
, pp. 1308-1320
-
-
Maron, B.J.1
-
26
-
-
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
-
27
-
-
0026319459
-
The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy
-
Michels VV,Moll PP,Miller FA,Tajik AJ,Chu JS,Driscoll DJ, et al.The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy.N Engl J Med. 1992;326:77-82.
-
(1992)
N Engl J Med
, vol.326
, pp. 77-82
-
-
Michels, V.V.1
Moll, P.P.2
Miller, F.A.3
Tajik, A.J.4
Chu, J.S.5
Driscoll, D.J.6
-
28
-
-
42949149810
-
Shared genetic causes of cardiac hypertrophy in children and adults
-
Morita H,Rehm HL,Menesses A,McDonough B,Roberts AE,Kucherlapati R, et al.Shared genetic causes of cardiac hypertrophy in children and adults.N Engl J Med. 2008;358:1899-1908.
-
(2008)
N Engl J Med
, vol.358
, pp. 1899-1908
-
-
Morita, H.1
Rehm, H.L.2
Menesses, A.3
McDonough, B.4
Roberts, A.E.5
Kucherlapati, R.6
-
30
-
-
0037192309
-
Metavinculin mutations alter actin interaction in dilated cardiomyopathy
-
Olson TM,Illenberger S,Kishimoto NY,Huttelmaier S,Keating MT,Jockusch BM.Metavinculin mutations alter actin interaction in dilated cardiomyopathy.Circulation. 2002;105:431-437.
-
(2002)
Circulation
, vol.105
, pp. 431-437
-
-
Olson, T.M.1
Illenberger, S.2
Kishimoto, N.Y.3
Huttelmaier, S.4
Keating, M.T.5
Jockusch, B.M.6
-
32
-
-
0031042948
-
Developmental defects in mouse embryos lacking N-cadherin
-
Radice GL,Rayburn H,Matsunami H,Knudsen KA,Takeichi M,Hynes RO.Developmental defects in mouse embryos lacking N-cadherin.Dev Biol. 1997;181:64-78.
-
(1997)
Dev Biol
, vol.181
, pp. 64-78
-
-
Radice, G.L.1
Rayburn, H.2
Matsunami, H.3
Knudsen, K.A.4
Takeichi, M.5
Hynes, R.O.6
-
33
-
-
0029864693
-
Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies
-
Richardson P,McKenna W,Bristow M,Maisch B,Mautner B,O'Connell J, et al.Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.Circulation. 1996;93:841-842.
-
(1996)
Circulation
, vol.93
, pp. 841-842
-
-
Richardson, P.1
McKenna, W.2
Bristow, M.3
Maisch, B.4
Mautner, B.5
O'Connell, J.6
-
34
-
-
2842589822
-
N-cadherin involvement in cardiac myocyte interaction and myofibrillogenesis
-
Soler AP,Knudsen KA.N-cadherin involvement in cardiac myocyte interaction and myofibrillogenesis.Dev Biol. 1994;162:9-17.
-
(1994)
Dev Biol
, vol.162
, pp. 9-17
-
-
Soler, A.P.1
Knudsen, K.A.2
-
35
-
-
0031214113
-
Null mutation in the desmin gene gives rise to a cardiomyopathy
-
Thornell L,Carlsson L,Li Z,Mericskay M,Paulin D.Null mutation in the desmin gene gives rise to a cardiomyopathy.J Mol Cell Cardiol. 1997;29:2107-2124.
-
(1997)
J Mol Cell Cardiol
, vol.29
, pp. 2107-2124
-
-
Thornell, L.1
Carlsson, L.2
Li, Z.3
Mericskay, M.4
Paulin, D.5
-
36
-
-
33750121615
-
Incidence, causes, and outcomes of dilated cardiomyopathy in children
-
Towbin JA,Lowe AM,Colan SD,Sleeper LA,Orav EJ,Clunie S, et al.Incidence, causes, and outcomes of dilated cardiomyopathy in children.J Am Med Assoc. 2006;296:1867-1876.
-
(2006)
J Am Med Assoc
, vol.296
, pp. 1867-1876
-
-
Towbin, J.A.1
Lowe, A.M.2
Colan, S.D.3
Sleeper, L.A.4
Orav, E.J.5
Clunie, S.6
-
37
-
-
33748035384
-
MEF2 activates a genetic program promoting chamber dilation and contractile dysfunction in calcineurin-induced heart failure
-
Van Oort RJ,van Rooij E,Bourajjaj M,Schimmel J,Jansen MA,van der Nagel R, et al.MEF2 activates a genetic program promoting chamber dilation and contractile dysfunction in calcineurin-induced heart failure.Circulation. 2006;114:298-308.
-
(2006)
Circulation
, vol.114
, pp. 298-308
-
-
van Oort, R.J.1
van Rooij, E.2
Bourajjaj, M.3
Schimmel, J.4
Jansen, M.A.5
van der Nagel, R.6
-
38
-
-
32044458438
-
Identification of a metavinculin missense mutation, R975W, associated with both hypertrophic and dilated cardiomyopathy
-
Vasile VC,Will ML,Ommen SR,Edwards WD,Olson TM,Ackerman MJ.Identification of a metavinculin missense mutation, R975W, associated with both hypertrophic and dilated cardiomyopathy.Mol Genet Metab. 2006;87:169-174.
-
(2006)
Mol Genet Metab
, vol.87
, pp. 169-174
-
-
Vasile, V.C.1
Will, M.L.2
Ommen, S.R.3
Edwards, W.D.4
Olson, T.M.5
Ackerman, M.J.6
-
39
-
-
0029558009
-
Cytoskeletal control of myogenesis: a desmin null mutation blocks the myogenic pathway during embryonic stem cell differentiation
-
Weitzer G,Milner DJ,Kim JU,Bradley A,Capetanaki Y.Cytoskeletal control of myogenesis: a desmin null mutation blocks the myogenic pathway during embryonic stem cell differentiation.Dev Biol. 1995;172:422-439.
-
(1995)
Dev Biol
, vol.172
, pp. 422-439
-
-
Weitzer, G.1
Milner, D.J.2
Kim, J.U.3
Bradley, A.4
Capetanaki, Y.5
-
40
-
-
33746816978
-
Altered energy transfer from mitochondria to sarcoplasmic reticulum after cytoarchitectural perturbations in mice hearts
-
Wilding JR,Joubert F,de Araujo C,Fortin D,Novotova M,Veksler V, et al.Altered energy transfer from mitochondria to sarcoplasmic reticulum after cytoarchitectural perturbations in mice hearts.J Physiol. 2006;575:191-200.
-
(2006)
J Physiol
, vol.575
, pp. 191-200
-
-
Wilding, J.R.1
Joubert, F.2
de Araujo, C.3
Fortin, D.4
Novotova, M.5
Veksler, V.6
-
41
-
-
10744226663
-
Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention
-
Zambrowicz BP,Abuin A,Ramirez-Solis R,Richter LJ,Piggott J,Beltrandelrio H, et al.Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention.Proc Natl Acad Sci U S A. 2003;100:14109-14114.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 14109-14114
-
-
Zambrowicz, B.P.1
Abuin, A.2
Ramirez-Solis, R.3
Richter, L.J.4
Piggott, J.5
Beltrandelrio, H.6
-
42
-
-
0032499252
-
Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells
-
Zambrowicz BP,Friedrich GA,Buxton EC,Lilleberg SL,Person C,Sands AT.Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells.Nature. 1998;392:608-611.
-
(1998)
Nature
, vol.392
, pp. 608-611
-
-
Zambrowicz, B.P.1
Friedrich, G.A.2
Buxton, E.C.3
Lilleberg, S.L.4
Person, C.5
Sands, A.T.6
|