-
1
-
-
11244320353
-
The nuclear lamina comes of age
-
Gruenbaum Y, Margalit A, Goldman RD, Shumaker DK, Wilson KL (2005) The nuclear lamina comes of age. Nat Rev Mol Cell Biol 6: 21-31.
-
(2005)
Nat Rev Mol Cell Biol
, vol.6
, pp. 21-31
-
-
Gruenbaum, Y.1
Margalit, A.2
Goldman, R.D.3
Shumaker, D.K.4
Wilson, K.L.5
-
2
-
-
1542317663
-
Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction
-
Lammerding J, Schulze PC, Takahashi T, Kozlov S, Sullivan T, et al. (2004) Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction. J Clin Invest 113: 370-378.
-
(2004)
J Clin Invest
, vol.113
, pp. 370-378
-
-
Lammerding, J.1
Schulze, P.C.2
Takahashi, T.3
Kozlov, S.4
Sullivan, T.5
-
3
-
-
29944445023
-
Coupling of the nucleus and cytoplasm: Role of the LINC complex
-
Crisp M, Liu Q, Roux K, Rattner JB, Shanahan C, et al. (2006) Coupling of the nucleus and cytoplasm: role of the LINC complex. J Cell Biol 172: 41-53.
-
(2006)
J Cell Biol
, vol.172
, pp. 41-53
-
-
Crisp, M.1
Liu, Q.2
Roux, K.3
Rattner, J.B.4
Shanahan, C.5
-
4
-
-
7944232477
-
Decreased mechanical stiffness in LMNA-/- cells is caused by defective nucleocytoskeletal integrity: Implications for the development of laminopathies
-
Broers JL, Peeters EA, Kuijpers HJ, Endert J, Bouten CV, et al. (2004) Decreased mechanical stiffness in LMNA-/- cells is caused by defective nucleocytoskeletal integrity: implications for the development of laminopathies. Hum Mol Genet 13: 2567-2580.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 2567-2580
-
-
Broers, J.L.1
Peeters, E.A.2
Kuijpers, H.J.3
Endert, J.4
Bouten, C.V.5
-
5
-
-
16544362438
-
Structural organization and functions of the nucleus in development, aging, and disease
-
Mounkes L, Stewart CL (2004) Structural organization and functions of the nucleus in development, aging, and disease. Curr Top Dev Biol 61: 191-228.
-
(2004)
Curr Top Dev Biol
, vol.61
, pp. 191-228
-
-
Mounkes, L.1
Stewart, C.L.2
-
6
-
-
85047692354
-
How do mutations in lamins A and C cause disease?
-
Worman HJ, Courvalin JC (2004) How do mutations in lamins A and C cause disease? J Clin Invest 113: 349-351.
-
(2004)
J Clin Invest
, vol.113
, pp. 349-351
-
-
Worman, H.J.1
Courvalin, J.C.2
-
7
-
-
0034536268
-
Mutations in the LMNA gene encoding lamin A/C
-
Genschel J, Schmidt HH (2000) Mutations in the LMNA gene encoding lamin A/C. Hum Mutat 16: 451-459.
-
(2000)
Hum Mutat
, vol.16
, pp. 451-459
-
-
Genschel, J.1
Schmidt, H.H.2
-
8
-
-
0037420074
-
Natural history of dilated cardiomyopathy due to lamin A/C gene mutations
-
Taylor MR, Fain PR, Sinagra G, Robinson ML, Robertson AD, et al. (2003) Natural history of dilated cardiomyopathy due to lamin A/C gene mutations. J Am Coll Cardiol 41: 771-780.
-
(2003)
J Am Coll Cardiol
, vol.41
, pp. 771-780
-
-
Taylor, M.R.1
Fain, P.R.2
Sinagra, G.3
Robinson, M.L.4
Robertson, A.D.5
-
9
-
-
0037183491
-
Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy
-
van der Kooi AJ, Bonne G, Eymard B, Duboc D, Talim B, et al. (2002) Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy. Neurology 59: 620-623.
-
(2002)
Neurology
, vol.59
, pp. 620-623
-
-
van der Kooi, A.J.1
Bonne, G.2
Eymard, B.3
Duboc, D.4
Talim, B.5
-
10
-
-
0042327845
-
Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations
-
Sebillon P, Bouchier C, Bidot LD, Bonne G, Ahamed K, et al. (2003) Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations. J Med Genet 40: 560-567.
-
(2003)
J Med Genet
, vol.40
, pp. 560-567
-
-
Sebillon, P.1
Bouchier, C.2
Bidot, L.D.3
Bonne, G.4
Ahamed, K.5
-
11
-
-
30444446953
-
Primary prevention of sudden death in patients with lamin A/C gene mutations
-
Meune C, Van Berlo JH, Anselme F, Bonne G, Pinto YM, et al. (2006) Primary prevention of sudden death in patients with lamin A/C gene mutations. N Engl J Med 354: 209-210.
-
(2006)
N Engl J Med
, vol.354
, pp. 209-210
-
-
Meune, C.1
Van Berlo, J.H.2
Anselme, F.3
Bonne, G.4
Pinto, Y.M.5
-
12
-
-
77951581169
-
A novel LMNA mutation (R189W) in familial dilated cardiomyopathy: Evidence for a 'hot spot' region at exon 3: A case report
-
Botto N, Vittorini S, Colombo MG, Biagini A, Paradossi U, et al. (2010) A novel LMNA mutation (R189W) in familial dilated cardiomyopathy: evidence for a 'hot spot' region at exon 3: a case report. Cardiovasc Ultrasound 8: 9.
-
(2010)
Cardiovasc Ultrasound
, vol.8
, pp. 9
-
-
Botto, N.1
Vittorini, S.2
Colombo, M.G.3
Biagini, A.4
Paradossi, U.5
-
13
-
-
52949150857
-
Lamin A/C gene and the heart: How genetics may impact clinical care
-
Mestroni L, Taylor MR (2008) Lamin A/C gene and the heart: how genetics may impact clinical care. J Am Coll Cardiol 52: 1261-1262.
-
(2008)
J Am Coll Cardiol
, vol.52
, pp. 1261-1262
-
-
Mestroni, L.1
Taylor, M.R.2
-
14
-
-
0035153087
-
Lamins in disease: Why do ubiquitously expressed nuclear envelope proteins give rise to tissue-specific disease phenotypes?
-
Hutchison CJ, Alvarez-Reyes M, Vaughan OA (2001) Lamins in disease: why do ubiquitously expressed nuclear envelope proteins give rise to tissue-specific disease phenotypes? J Cell Sci 114: 9-19.
-
(2001)
J Cell Sci
, vol.114
, pp. 9-19
-
-
Hutchison, C.J.1
Alvarez-Reyes, M.2
Vaughan, O.A.3
-
15
-
-
33646486276
-
Mutation Glu82Lys in lamin A/C gene is associated with cardiomyopathy and conduction defect
-
Wang H, Wang J, Zheng W, Wang X, Wang S, et al. (2006) Mutation Glu82Lys in lamin A/C gene is associated with cardiomyopathy and conduction defect. Biochem Biophys Res Commun 344: 17-24.
-
(2006)
Biochem Biophys Res Commun
, vol.344
, pp. 17-24
-
-
Wang, H.1
Wang, J.2
Zheng, W.3
Wang, X.4
Wang, S.5
-
16
-
-
43149117884
-
Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
-
Sagelius H, Rosengardten Y, Hanif M, Erdos MR, Rozell B, et al. (2008) Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease. J Cell Sci 121: 969-978.
-
(2008)
J Cell Sci
, vol.121
, pp. 969-978
-
-
Sagelius, H.1
Rosengardten, Y.2
Hanif, M.3
Erdos, M.R.4
Rozell, B.5
-
17
-
-
19944426537
-
Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies
-
Arimura T, Helbling-Leclerc A, Massart C, Varnous S, Niel F, et al. (2005) Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies. Hum Mol Genet 14: 155-169.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 155-169
-
-
Arimura, T.1
Helbling-Leclerc, A.2
Massart, C.3
Varnous, S.4
Niel, F.5
-
18
-
-
34247137974
-
Genetic variation in the B-type natiuretic peptide pathway affects BNP levels
-
Lanfear DE, Stolker JM, Marsh S, Rich MW, McLeod HL (2007) Genetic variation in the B-type natiuretic peptide pathway affects BNP levels. Cardiovasc Drugs Ther 21: 55-62.
-
(2007)
Cardiovasc Drugs Ther
, vol.21
, pp. 55-62
-
-
Lanfear, D.E.1
Stolker, J.M.2
Marsh, S.3
Rich, M.W.4
McLeod, H.L.5
-
19
-
-
12144288228
-
Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defect and the cardiac phenotype of hypertrophic cardiomyopathy
-
Tsybouleva N, Zhang L, Chen S, Patel R, Lutucuta S, et al. (2004) Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defect and the cardiac phenotype of hypertrophic cardiomyopathy. Circulation 109: 1284-1291.
-
(2004)
Circulation
, vol.109
, pp. 1284-1291
-
-
Tsybouleva, N.1
Zhang, L.2
Chen, S.3
Patel, R.4
Lutucuta, S.5
-
20
-
-
12944329901
-
Cardiac fibrosis in mice lacking brain natriuretic peptide
-
Tamura N, Ogawa Y, Chusho H, Nakamura K, Nakao K, et al. (2000) Cardiac fibrosis in mice lacking brain natriuretic peptide. Proc Natl Acad Sci U S A 97: 4239-4244.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 4239-4244
-
-
Tamura, N.1
Ogawa, Y.2
Chusho, H.3
Nakamura, K.4
Nakao, K.5
-
21
-
-
58849125703
-
Genotype-phenotype correlations in ACTA1 mutations that cause congenital myopathies
-
Feng JJ, Marston S (2009) Genotype-phenotype correlations in ACTA1 mutations that cause congenital myopathies. Neuromuscul Disord 19: 6-16.
-
(2009)
Neuromuscul Disord
, vol.19
, pp. 6-16
-
-
Feng, J.J.1
Marston, S.2
-
22
-
-
33748292887
-
The relationship between myocardial extracellular matrix remodeling and ventricular function
-
Brower GL, Gardner JD, Forman MF, Murray DB, Voloshenyuk T, et al. (2006) The relationship between myocardial extracellular matrix remodeling and ventricular function. Eur J Cardiothorac Surg 30: 604-610.
-
(2006)
Eur J Cardiothorac Surg
, vol.30
, pp. 604-610
-
-
Brower, G.L.1
Gardner, J.D.2
Forman, M.F.3
Murray, D.B.4
Voloshenyuk, T.5
-
23
-
-
0141653901
-
Ventricular remodeling after infarction and the extracellular collagen matrix: When is enough enough?
-
Jugdutt BI (2003) Ventricular remodeling after infarction and the extracellular collagen matrix: when is enough enough? Circulation 108: 1395-1403.
-
(2003)
Circulation
, vol.108
, pp. 1395-1403
-
-
Jugdutt, B.I.1
-
24
-
-
33747893889
-
Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy
-
Wang Y, Herron AJ, Worman HJ (2006) Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy. Hum Mol Genet 15: 2479-2489.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 2479-2489
-
-
Wang, Y.1
Herron, A.J.2
Worman, H.J.3
-
25
-
-
26444595257
-
Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in mice
-
Mounkes LC, Kozlov SV, Rottman JN, Stewart CL (2005) Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in mice. Hum Mol Genet 14: 2167-2180.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 2167-2180
-
-
Mounkes, L.C.1
Kozlov, S.V.2
Rottman, J.N.3
Stewart, C.L.4
-
26
-
-
0031686054
-
Nuclear lamins: Their structure, assembly, and interactions
-
Stuurman N, Heins S, Aebi U (1998) Nuclear lamins: their structure, assembly, and interactions. J Struct Biol 122: 42-66.
-
(1998)
J Struct Biol
, vol.122
, pp. 42-66
-
-
Stuurman, N.1
Heins, S.2
Aebi, U.3
-
27
-
-
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, et al. (2000) Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene. N Engl J Med 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
-
28
-
-
0036347096
-
Life at the edge: The nuclear envelope and human disease
-
Burke B, Stewart CL (2002) Life at the edge: the nuclear envelope and human disease. Nat Rev Mol Cell Biol 3: 575-585.
-
(2002)
Nat Rev Mol Cell Biol
, vol.3
, pp. 575-585
-
-
Burke, B.1
Stewart, C.L.2
-
29
-
-
0036843975
-
Lamins: Building blocks or regulators of gene expression?
-
Hutchison CJ (2002) Lamins: building blocks or regulators of gene expression? Nat Rev Mol Cell Biol 3: 848-858.
-
(2002)
Nat Rev Mol Cell Biol
, vol.3
, pp. 848-858
-
-
Hutchison, C.J.1
-
30
-
-
11144355499
-
Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice
-
Nikolova V, Leimena C, McMahon AC, Tan JC, Chandar S, et al. (2004) Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice. J Clin Invest 113: 357-369.
-
(2004)
J Clin Invest
, vol.113
, pp. 357-369
-
-
Nikolova, V.1
Leimena, C.2
McMahon, A.C.3
Tan, J.C.4
Chandar, S.5
-
31
-
-
39149083716
-
Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease
-
Wolf CM, Wang L, Alcalai R, Pizard A, Burgon PG, et al. (2008) Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease. J Mol Cell Cardiol 44: 293-303.
-
(2008)
J Mol Cell Cardiol
, vol.44
, pp. 293-303
-
-
Wolf, C.M.1
Wang, L.2
Alcalai, R.3
Pizard, A.4
Burgon, P.G.5
-
32
-
-
65549136073
-
Is the FAS/FAS-L pathway a promising target for treating inflammatory heart disease?
-
Henriques-Pons A, de Oliveira GM (2009) Is the FAS/FAS-L pathway a promising target for treating inflammatory heart disease? J Cardiovasc Pharmacol 53: 94-99.
-
(2009)
J Cardiovasc Pharmacol
, vol.53
, pp. 94-99
-
-
Henriques-Pons, A.1
de Oliveira, G.M.2
-
33
-
-
0034646172
-
The cardiac FAS (APO-1/CD95) Receptor/FAS ligand system: Relation to diastolic wall stress in volume-overload hypertrophy in vivo and activation of the transcription factor AP-1 in cardiac myocytes
-
Wollert KC, Heineke J, Westermann J, Lüdde M, Fiedler B, et al. (2000) The cardiac FAS (APO-1/CD95) Receptor/FAS ligand system: relation to diastolic wall stress in volume-overload hypertrophy in vivo and activation of the transcription factor AP-1 in cardiac myocytes. Circulation 101: 1172-1178.
-
(2000)
Circulation
, vol.101
, pp. 1172-1178
-
-
Wollert, K.C.1
Heineke, J.2
Westermann, J.3
Lüdde, M.4
Fiedler, B.5
-
34
-
-
0036273957
-
Hypoxia predisposes neonatal rat ventricular myocytes to apoptosis induced by activation of the FAS (CD95/Apo-1) receptor: FAS activation and apoptosis in hypoxic myocytes
-
Yaniv G, Shilkrut M, Lotan R, Berke G, Larisch S, et al. (2002) Hypoxia predisposes neonatal rat ventricular myocytes to apoptosis induced by activation of the FAS (CD95/Apo-1) receptor: FAS activation and apoptosis in hypoxic myocytes. Cardiovasc Res 54: 611-623.
-
(2002)
Cardiovasc Res
, vol.54
, pp. 611-623
-
-
Yaniv, G.1
Shilkrut, M.2
Lotan, R.3
Berke, G.4
Larisch, S.5
-
35
-
-
24344437772
-
The 1,4,5- inositol trisphosphate pathway is a key component in FAS-mediated hypertrophy in neonatal rat ventricular myocytes
-
Barac YD, Zeevi-Levin N, Yaniv G, Reiter I, Milman F, et al. (2005) The 1,4,5- inositol trisphosphate pathway is a key component in FAS-mediated hypertrophy in neonatal rat ventricular myocytes. Cardiovasc Res 68: 75-86.
-
(2005)
Cardiovasc Res
, vol.68
, pp. 75-86
-
-
Barac, Y.D.1
Zeevi-Levin, N.2
Yaniv, G.3
Reiter, I.4
Milman, F.5
-
36
-
-
35648998932
-
Cardiac FAS receptor-dependent apoptotic pathway in obese Zucker rats
-
Lee SD, Tzang BS, Kuo WW, Lin YM, Yang AL, et al. (2007) Cardiac FAS receptor-dependent apoptotic pathway in obese Zucker rats. Obesity (Silver Spring) 15: 2407-2415.
-
(2007)
Obesity (Silver Spring)
, vol.15
, pp. 2407-2415
-
-
Lee, S.D.1
Tzang, B.S.2
Kuo, W.W.3
Lin, Y.M.4
Yang, A.L.5
-
37
-
-
40049084481
-
Role of apoptosis in pressure-overload cardiomyopathy
-
Anselmi A, Gaudino M, Baldi A, Vetrovec GW, Bussani R, et al. (2008) Role of apoptosis in pressure-overload cardiomyopathy. J Cardiovasc Med (Hagerstown) 9: 227-232.
-
(2008)
J Cardiovasc Med (Hagerstown)
, vol.9
, pp. 227-232
-
-
Anselmi, A.1
Gaudino, M.2
Baldi, A.3
Vetrovec, G.W.4
Bussani, R.5
-
39
-
-
0035834279
-
Molecular steps of death receptor and mitochondrial pathways of apoptosis
-
Gupta S (2001) Molecular steps of death receptor and mitochondrial pathways of apoptosis. Life Sci 69: 2957-2964.
-
(2001)
Life Sci
, vol.69
, pp. 2957-2964
-
-
Gupta, S.1
-
40
-
-
0033529281
-
Apoptosis in heart failure: Release of cytochrome c from mitochondria and activation of caspase-3 in human cardiomyopathy
-
Narula J, Pandey P, Arbustini E, Haider N, Narula N, et al. (1999) Apoptosis in heart failure: release of cytochrome c from mitochondria and activation of caspase-3 in human cardiomyopathy. Proc Natl Acad Sci U S A 96: 8144-8149.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 8144-8149
-
-
Narula, J.1
Pandey, P.2
Arbustini, E.3
Haider, N.4
Narula, N.5
-
41
-
-
0029845123
-
Medical therapy can improve the biological properties of the chronically failing heart. A new era in the treatment of heart failure
-
Eichhorn EJ, Bristow MR (1996) Medical therapy can improve the biological properties of the chronically failing heart. A new era in the treatment of heart failure. Circulation 94: 2285-2296.
-
(1996)
Circulation
, vol.94
, pp. 2285-2296
-
-
Eichhorn, E.J.1
Bristow, M.R.2
-
42
-
-
0028908119
-
The cellular basis of dilated cardiomyopathy in humans
-
Beltrami CA, Finato N, Rocco M, Feruglio GA, Puricelli C, et al. (1995) The cellular basis of dilated cardiomyopathy in humans. J Mol Cell Cardiol 27: 291-305.
-
(1995)
J Mol Cell Cardiol
, vol.27
, pp. 291-305
-
-
Beltrami, C.A.1
Finato, N.2
Rocco, M.3
Feruglio, G.A.4
Puricelli, C.5
-
43
-
-
76149084859
-
Role of A-type lamins in signaling, transcription, and chromatin organization
-
Andrés V, González JM (2009) Role of A-type lamins in signaling, transcription, and chromatin organization. J Cell Biol 187: 945-957.
-
(2009)
J Cell Biol
, vol.187
, pp. 945-957
-
-
Andrés, V.1
González, J.M.2
-
44
-
-
46349112116
-
The changes of the cardiac structure and function in cTnTR141W transgenic mice
-
Juan F, Wei D, Xiongzhi Q, Ran D, Chunmei M, et al. (2008) The changes of the cardiac structure and function in cTnTR141W transgenic mice. Int J Cardiol 128: 83-90.
-
(2008)
Int J Cardiol
, vol.128
, pp. 83-90
-
-
Juan, F.1
Wei, D.2
Xiongzhi, Q.3
Ran, D.4
Chunmei, M.5
-
45
-
-
0242693150
-
Temporal changes in ventricular function assessed echocardiographically in conscious and anesthetized mice
-
Rottman JN, Ni G, Khoo M, Wang Z, Zhang W, et al. (2003) Temporal changes in ventricular function assessed echocardiographically in conscious and anesthetized mice. J Am Soc Echocardiogr 16: 1150-1157.
-
(2003)
J Am Soc Echocardiogr
, vol.16
, pp. 1150-1157
-
-
Rottman, J.N.1
Ni, G.2
Khoo, M.3
Wang, Z.4
Zhang, W.5
|