-
1
-
-
0029864693
-
Report of the 1995 World Health Organisation/International Society and Federation of Cardiology Task Force on the definition and classification of cardiomyo-pathies
-
Richardson P, McKenna W, Bristow M, Maish B, Mautner B, O'Connell J et al. Report of the 1995 World Health Organisation/International Society and Federation of Cardiology Task Force on the definition and classification of cardiomyo-pathies. Circulation 1996;93:841-842.
-
Circulation
, vol.1996
, Issue.93
, pp. 841-842
-
-
Richardson, P.1
McKenna, W.2
Bristow, M.3
Maish, B.4
Mautner, B.5
O'connell, J.6
-
2
-
-
38349086961
-
Classification of the cardiomyopathies: A position statement from the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases
-
Elliott P, Andersson B, Arbustini E, Bilinska Z, Cecchi F, Charron P et al. Classification of the cardiomyopathies: a position statement from the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases. Eur Heart J 2008;29:270-276.
-
(2008)
Eur Heart J
, vol.29
, pp. 270-276
-
-
Elliott, P.1
Andersson, B.2
Arbustini, E.3
Bilinska, Z.4
Cecchi, F.5
Charron, P.6
-
3
-
-
0029083650
-
Prevalence of hypertrophic cardiomyopathy in a general population of young adults: Echocar-diographic analysis of 4111 subjects in the CARDIA study
-
Maron BJ, Gardin JM, Flack JM, Gidding SS, Kurosaki TT, Bild DE. Prevalence of hypertrophic cardiomyopathy in a general population of young adults: echocar-diographic analysis of 4111 subjects in the CARDIA study. 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
-
4
-
-
0032170493
-
Diagnostic value of electrocardiography and echocardiography for familial hyper-trophic cardiomyopathy in genotyped children
-
Charron P, Dubourg O, Desnos M, Bouhour JB, Isnard R, Hagège A et al. Diagnostic value of electrocardiography and echocardiography for familial hyper-trophic cardiomyopathy in genotyped children. Eur Heart J 1998;19:1377-1382.
-
(1998)
Eur Heart J
, vol.19
, pp. 1377-1382
-
-
Charron, P.1
Dubourg, O.2
Desnos, M.3
Bouhour, J.B.4
Isnard, R.5
Hagège, A.6
-
5
-
-
67349207405
-
Familial hypertrophic cardiomyopathy: Basic concepts and future molecular diagnostics
-
Rodriguez JE, McCudden CR, Willis MS. Familial hypertrophic cardiomyopathy: basic concepts and future molecular diagnostics. Clin Biochem 2009;42:755-765.
-
(2009)
Clin Biochem
, vol.42
, pp. 755-765
-
-
Rodriguez, J.E.1
McCudden, C.R.2
Willis, M.S.3
-
6
-
-
18644374087
-
Genetic testing and genetic counselling in hypertrophic cardiomyopathy: The French experience
-
Charron P, Heron D, Gargiulo M, Richard P, Dubourg O, Desnos M et al. Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience. J Med Genet 2002;39:741-746.
-
(2002)
J Med Genet
, vol.39
, pp. 741-746
-
-
Charron, P.1
Heron, D.2
Gargiulo, M.3
Richard, P.4
Dubourg, O.5
Desnos, M.6
-
7
-
-
61849140724
-
Hyper-trophic cardiomyopathy: Current understanding and treatment objectives
-
Soor GS, Luk A, Ahn E, Abraham JR, Woo A, Ralph-Edwards A et al. Hyper-trophic cardiomyopathy: current understanding and treatment objectives. J Clin Pathol 2009;62:226-235.
-
(2009)
J Clin Pathol
, vol.62
, pp. 226-235
-
-
Soor, G.S.1
Luk, A.2
Ahn, E.3
Abraham, J.R.4
Woo, A.5
Ralph-Edwards, A.6
-
8
-
-
70449192269
-
Asymetrical hypertrophy of the heart in young adults
-
Teare D. Asymetrical 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
-
9
-
-
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
-
10
-
-
34547188258
-
Implantable cardioverter-defibrillators and prevention of sudden cardiac death in hyper-trophic cardiomyopathy
-
Maron BJ, Spirito P, Shen WK, Haas TS, Formisano F, Link MS et al. Implantable cardioverter-defibrillators and prevention of sudden cardiac death in hyper-trophic cardiomyopathy. JAMA 2007;298:405-412.
-
(2007)
JAMA
, vol.298
, pp. 405-412
-
-
Maron, B.J.1
Spirito, P.2
Shen, W.K.3
Haas, T.S.4
Formisano, F.5
Link, M.S.6
-
11
-
-
0034660438
-
Magnitude of left ventricular hypertrophy and risk of sudden death in hypertrophic cardiomyopa-thy
-
Spirito P, Bellone P, Harris KM, Bernabo P, Bruzzi P, Maron BJ. Magnitude of left ventricular hypertrophy and risk of sudden death in hypertrophic cardiomyopa-thy. N Engl J Med 2000;342:1778-1785.
-
(2000)
N Engl J Med
, vol.342
, pp. 1778-1785
-
-
Spirito, P.1
Bellone, P.2
Harris, K.M.3
Bernabo, P.4
Bruzzi, P.5
Maron, B.J.6
-
12
-
-
2942530660
-
Hypertrophic cardiomyopathy
-
Elliott P, McKenna WJ. Hypertrophic cardiomyopathy. Lancet 2004;363: 1881-1891.
-
(2004)
Lancet
, vol.363
, pp. 1881-1891
-
-
Elliott, P.1
McKenna, W.J.2
-
13
-
-
26844513376
-
Dilated-hypokinetic evolution of hypertrophic cardiomyopathy: Prevalence, incidence, risk factors, and prognostic implications in pediatric and adult patients
-
Biagini E, Coccolo F, Ferlito M, Perugini E, Rocchi G, Bacchi-Reggiani L et al. Dilated-hypokinetic evolution of hypertrophic cardiomyopathy: prevalence, incidence, risk factors, and prognostic implications in pediatric and adult patients. J Am Coll Cardiol 2005;46:1543-1550.
-
(2005)
J Am Coll Cardiol
, vol.46
, pp. 1543-1550
-
-
Biagini, E.1
Coccolo, F.2
Ferlito, M.3
Perugini, E.4
Rocchi, G.5
Bacchi-Reggiani, L.6
-
14
-
-
8544283018
-
Pene-trance of familial hypertrophic cardiomyopathy
-
Charron P, Carrier L, Dubourg O, Tesson F, Desnos M, Richard P et al. Pene-trance of familial hypertrophic cardiomyopathy. Genet Couns 1997;8:107-114.
-
(1997)
Genet Couns
, vol.8
, pp. 107-114
-
-
Charron, P.1
Carrier, L.2
Dubourg, O.3
Tesson, F.4
Desnos, M.5
Richard, P.6
-
15
-
-
0030842476
-
Diagnostic value of electrocardiography and echocardiography for familial hypertrophic car-diomyopathy in a genotyped adult population
-
Charron P, Dubourg O, Desnos M, Isnard R, Hagège A, Millaire A et al. Diagnostic value of electrocardiography and echocardiography for familial hypertrophic car-diomyopathy in a genotyped adult population. Circulation 1997;96:214-219.
-
(1997)
Circulation
, vol.96
, pp. 214-219
-
-
Charron, P.1
Dubourg, O.2
Desnos, M.3
Isnard, R.4
Hagège, A.5
Millaire, A.6
-
16
-
-
0037183373
-
Genetics of familial hypertrophic cardiomyopa-thies and arrhythmias
-
Keller DI, Carrier L, Schwartz K. Genetics of familial hypertrophic cardiomyopa-thies and arrhythmias. Swiss Med Wkly 2002;132:401-407.
-
(2002)
Swiss Med Wkly
, vol.132
, pp. 401-407
-
-
Keller, D.I.1
Carrier, L.2
Schwartz, K.3
-
18
-
-
37549040201
-
Genetic basis of hypertrophic cardiomyopa-thy: From bench to the clinics
-
Alcalai R, Seidman JG, Seidman CE. Genetic basis of hypertrophic cardiomyopa-thy: 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
-
19
-
-
0037630018
-
Hyper-trophic cardiomyopathy: Distribution of disease genes, spectrum of mutations and implications for molecular diagnosis strategy
-
Richard P, Charron P, Carrier L, Ledeuil C, Cheav T, Pichereau C et al. Hyper-trophic cardiomyopathy: distribution of disease genes, spectrum of mutations and implications for molecular diagnosis strategy. Circulation 2003;107: 2227-2232.
-
(2003)
Circulation
, vol.107
, pp. 2227-2232
-
-
Richard, P.1
Charron, P.2
Carrier, L.3
Ledeuil, C.4
Cheav, T.5
Pichereau, C.6
-
20
-
-
0031882122
-
Cardiac myosin binding protein C gene is specifically expressed in heart during murine and human development
-
Fougerousse F, Delezoide AL, Fiszman MY, Schwartz K, Beckmann JS, Carrier L. Cardiac myosin binding protein C gene is specifically expressed in heart during murine and human development. Circ Res 1998;82:130-133.
-
(1998)
Circ Res
, vol.82
, pp. 130-133
-
-
Fougerousse, F.1
Delezoide, A.L.2
Fiszman, M.Y.3
Schwartz, K.4
Beckmann, J.S.5
Carrier, L.6
-
21
-
-
47749102476
-
Cardiac myosin-binding protein C modulates the tuning of the molecular motor in the heart
-
Lecarpentier Y, Vignier N, Oliviero P, Guellich A, Carrier L, Coirault C. Cardiac myosin-binding protein C modulates the tuning of the molecular motor in the heart. Biophys J 2008;95:720-728.
-
(2008)
Biophys J
, vol.95
, pp. 720-728
-
-
Lecarpentier, Y.1
Vignier, N.2
Oliviero, P.3
Guellich, A.4
Carrier, L.5
Coirault, C.6
-
22
-
-
34247519733
-
Cardiac myosin-binding protein C in the heart
-
Carrier L. Cardiac myosin-binding protein C in the heart. Arch Mal Coeur Vaiss 2007;100:238-243.
-
(2007)
Arch Mal Coeur Vaiss
, vol.100
, pp. 238-243
-
-
Carrier, L.1
-
23
-
-
30744440681
-
Length and protein kinase A modulations of myocytes in cardiac myosin binding protein C-deficient mice
-
Cazorla O, Szilagyi S, Vignier N, Salazar G, Kramer E, Vassort G et al. Length and protein kinase A modulations of myocytes in cardiac myosin binding protein C-deficient mice. Cardiovasc Res 2006;69:370-380.
-
(2006)
Cardiovasc Res
, vol.69
, pp. 370-380
-
-
Cazorla, O.1
Szilagyi, S.2
Vignier, N.3
Salazar, G.4
Kramer, E.5
Vassort, G.6
-
24
-
-
37349023159
-
Cardiac myosin-binding protein C is required for complete relaxation in intact myocytes
-
Pohlmann L, Kroger I, Vignier N, Schlossarek S, Kramer E, Coirault C et al. Cardiac myosin-binding protein C is required for complete relaxation in intact myocytes. Circ Res 2007;101:928-938.
-
(2007)
Circ Res
, vol.101
, pp. 928-938
-
-
Pohlmann, L.1
Kroger, I.2
Vignier, N.3
Schlossarek, S.4
Kramer, E.5
Coirault, C.6
-
25
-
-
33847032217
-
Radial displacement of myosin cross-bridges in mouse myocardium due to ablation of myosin binding protein-C
-
Colson BA, Bekyarova T, Fitzsimons DP, Irving TC, Moss RL. Radial displacement of myosin cross-bridges in mouse myocardium due to ablation of myosin binding protein-C. J Mol Biol 2007;367:36-41.
-
(2007)
J Mol Biol
, vol.367
, pp. 36-41
-
-
Colson, B.A.1
Bekyarova, T.2
Fitzsimons, D.P.3
Irving, T.C.4
Moss, R.L.5
-
26
-
-
0031891357
-
Genotype-phenotype correlations in familial hypertrophic cardiomyopathy: A comparison between mutations in the cardiac protein-C and the b-myosin heavy chain genes
-
Charron P, Dubourg O, Desnos M, Isnard R, Hagège A, Bonne G et al. Genotype-phenotype correlations in familial hypertrophic cardiomyopathy: a comparison between mutations in the cardiac protein-C and the b-myosin heavy chain genes. Eur Heart J 1998;19:139-145.
-
(1998)
Eur Heart J
, vol.19
, pp. 139-145
-
-
Charron, P.1
Dubourg, O.2
Desnos, M.3
Isnard, R.4
Hagège, A.5
Bonne, G.6
-
27
-
-
0032580520
-
Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy
-
Niimura H, Bachinski LL, Sangwatanaroj S, Watkins H, Chudley AE, McKenna W et al. Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy. N Engl J Med 1998;338:1248-1257.
-
(1998)
N Engl J Med
, vol.338
, pp. 1248-1257
-
-
Niimura, H.1
Bachinski, L.L.2
Sangwatanaroj, S.3
Watkins, H.4
Chudley, A.E.5
McKenna, W.6
-
28
-
-
17344372574
-
Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene
-
Yu B, French JA, Carrier L, Jeremy RW, McTaggart DR, Nicholson MR et al. Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene. J Med Genet 1998;35:205-210.
-
(1998)
J Med Genet
, vol.35
, pp. 205-210
-
-
Yu, B.1
French, J.A.2
Carrier, L.3
Jeremy, R.W.4
McTaggart, D.R.5
Nicholson, M.R.6
-
29
-
-
0027138216
-
Familial hypertrophic cardiomyopathy: Microsatellite haplotyping and identification of a hot-spot for mutations in the b-myosin heavy chain gene
-
Dausse E, Komajda M, Dubourg O, Fetler L, Dufour C, Carrier L et al. Familial hypertrophic cardiomyopathy: microsatellite haplotyping and identification of a hot-spot for mutations in the b-myosin heavy chain gene. J Clin Invest 1993;92: 2807-2813.
-
(1993)
J Clin Invest
, vol.92
, pp. 2807-2813
-
-
Dausse, E.1
Komajda, M.2
Dubourg, O.3
Fetler, L.4
Dufour, C.5
Carrier, L.6
-
30
-
-
0031055854
-
Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hyper-trophic cardiomyopathy
-
Carrier L, Bonne G, Bährend E, Yu B, Richard P, Niel F et al. Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hyper-trophic cardiomyopathy. Circ Res 1997;80:427-434.
-
(1997)
Circ Res
, vol.80
, pp. 427-434
-
-
Carrier, L.1
Bonne, G.2
Bährend, E.3
Yu, B.4
Richard, P.5
Niel, F.6
-
31
-
-
0031597427
-
AT1 receptor A/C1166 polymorphism contributes to cardiac hypertrophy in subjects with hypertrophic cardiomyopathy
-
Osterop AP, Kofflard MJ, Sandkuijl LA, ten Cate FJ, Krams R, Schalekamp MA et al. AT1 receptor A/C1166 polymorphism contributes to cardiac hypertrophy in subjects with hypertrophic cardiomyopathy. Hypertension 1998;32:825-830.
-
(1998)
Hypertension
, vol.32
, pp. 825-830
-
-
Osterop, A.P.1
Kofflard, M.J.2
Sandkuijl, L.A.3
Ten Cate, F.J.4
Krams, R.5
Ma Et Al, S.6
-
32
-
-
0035672057
-
Angiotensin II type 2 receptors and cardiac hypertrophy in women with hypertrophic cardiomyopathy
-
Deinum J, van Gool JM, Kofflard MJ, ten Cate FJ, Danser AH. Angiotensin II type 2 receptors and cardiac hypertrophy in women with hypertrophic cardiomyopathy. Hypertension 2001;38:1278-1281.
-
(2001)
Hypertension
, vol.38
, pp. 1278-1281
-
-
Deinum J1
Van Gool, J.M.2
Kofflard, M.J.3
Ten Cate, F.J.4
Danser, A.H.5
-
33
-
-
67650086995
-
A new polymorphism in human calmodulin III promoter is a potential modifier gene for familial hypertrophic cardiomyopathy
-
Friedrich F, Bausero P, Sun Y, Treszl A, Krämer E, Juhr D et al. A new polymorphism in human calmodulin III promoter is a potential modifier gene for familial hypertrophic cardiomyopathy. Eur Heart J 2009;30:1648-1655.
-
(2009)
Eur Heart J
, vol.30
, pp. 1648-1655
-
-
Friedrich, F.1
Bausero, P.2
Sun, Y.3
Treszl, A.4
Krämer, E.5
Juhr, D.6
-
34
-
-
0030976860
-
The in vitro motility activity of b-cardiac myosin depends on the nature of the b-myosin heavy chain gene mutation in hypertrophic cardiomyopathy
-
Cuda G, Fananapazir L, Epstein ND, Sellers JR. The in vitro motility activity of b-cardiac myosin depends on the nature of the b-myosin heavy chain gene mutation in hypertrophic cardiomyopathy. J Muscle Res Cell Motil 1997;18: 275-283.
-
(1997)
J Muscle Res Cell Motil
, vol.18
, pp. 275-283
-
-
Cuda, G.1
Fananapazir, L.2
Epstein, N.D.3
Sellers, J.R.4
-
35
-
-
0031883848
-
A mutant tropomyosin that causes hypertrophic cardiomyopathy is expressed in vivo and associated with an increased calcium sensitivity
-
Bottinelli R, Coviello DA, Redwood CS, Pellegrino MA, Maron BJ, Spirito P et al. A mutant tropomyosin that causes hypertrophic cardiomyopathy is expressed in vivo and associated with an increased calcium sensitivity. Circ Res 1998;82: 106-115.
-
(1998)
Circ Res
, vol.82
, pp. 106-115
-
-
Bottinelli, R.1
Coviello, D.A.2
Redwood, C.S.3
Pellegrino, M.A.4
Maron, B.J.5
Spirito, P.6
-
36
-
-
12144286221
-
Human homo-zygous R403W mutant cardiac myosin presents disproportionate enhancement of mechanical and enzymatic properties
-
Keller DI, Coirault C, Rau T, Cheav T, Weyand M, Amann K et al. Human homo-zygous R403W mutant cardiac myosin presents disproportionate enhancement of mechanical and enzymatic properties. J Mol Cell Cardiol 2004;36:355-362.
-
(2004)
J Mol Cell Cardiol
, vol.36
, pp. 355-362
-
-
Keller, D.I.1
Coirault, C.2
Rau, T.3
Cheav, T.4
Weyand, M.5
Amann, K.6
-
37
-
-
0033607481
-
COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytes
-
Flavigny J, Souchet M, Sébillon P, Berrebi-Bertrand I, Hainque B, Mallet A et al. COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytes. J Mol Biol 1999;294:443-456.
-
(1999)
J Mol Biol
, vol.294
, pp. 443-456
-
-
Flavigny, J.1
Souchet, M.2
Sébillon, P.3
Berrebi-Bertrand, I.4
Hainque, B.5
Mallet, A.6
-
38
-
-
0030852878
-
Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization of cardiac transcript and protein
-
Rottbauer W, Gautel M, Zehelein J, Labeit S, Franz WM, Fischer C et al. Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization of cardiac transcript and protein. J Clin Invest 1997;100:475-482.
-
(1997)
J Clin Invest
, vol.100
, pp. 475-482
-
-
Rottbauer, W.1
Gautel, M.2
Zehelein, J.3
Labeit, S.4
Franz, W.M.5
Fischer, C.6
-
39
-
-
0034724252
-
A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetrance
-
Moolman JA, Reith S, Uhl K, Bailey S, Gautel M, Jeschke B et al. A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetrance. Circulation 2000;101:1396-1402.
-
(2000)
Circulation
, vol.101
, pp. 1396-1402
-
-
Moolman, J.A.1
Reith, S.2
Uhl, K.3
Bailey, S.4
Gautel, M.5
Jeschke, B.6
-
40
-
-
64949138383
-
Cardiac myosin-binding protein C mutations and hypertrophic cardiomyopathy: Haploinsufficiency, deranged phosphorylation, and cardiomyocyte dysfunction
-
van Dijk SJ, Dooijes D, Dos Remedios C, Michels M, Lamers JM, Winegrad S et al. Cardiac myosin-binding protein C mutations and hypertrophic cardiomyopathy: haploinsufficiency, deranged phosphorylation, and cardiomyocyte dysfunction. Circulation 2009;119:1473-1483.
-
(2009)
Circulation
, vol.119
, pp. 1473-1483
-
-
Van Dijk, S.J.1
Dooijes, D.2
Dos Remedios, C.3
Michels, M.4
Lamers, J.M.5
Winegrad, S.6
-
41
-
-
0032749319
-
In vivo modeling of myosin binding protein C familial hypertrophic cardiomyopathy
-
Yang Q, Sanbe A, Osinska H, Hewett TE, Klevitsky R, Robbins J. In vivo modeling of myosin binding protein C familial hypertrophic cardiomyopathy. Circ Res 1999; 85:841-847.
-
(1999)
Circ Res
, vol.85
, pp. 841-847
-
-
Yang, Q.1
Sanbe, A.2
Osinska, H.3
Hewett, T.E.4
Klevitsky, R.5
Robbins, J.6
-
42
-
-
37448999729
-
Altered myocardial gene expression reveals possible maladaptive processes in heterozygous and homozygous cardiac myosin-binding protein C knockout mice
-
Eijssen LM, van den Bosch BJ, Vignier N, Lindsey PJ, van den Burg CM, Carrier L et al. Altered myocardial gene expression reveals possible maladaptive processes in heterozygous and homozygous cardiac myosin-binding protein C knockout mice. Genomics 2008;91:52-60.
-
(2008)
Genomics
, vol.91
, pp. 52-60
-
-
Eijssen, L.M.1
Van Den Bosch, B.J.2
Vignier, N.3
Lindsey, P.J.4
Van Den Burg, C.M.5
Carrier, L.6
-
43
-
-
3142570567
-
Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice
-
Carrier L, Knoell R, Vignier N, Keller DI, Bausero P, Prudhon B et al. Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice. Cardiovasc Res 2004;63: 293-304.
-
(2004)
Cardiovasc Res
, vol.63
, pp. 293-304
-
-
Carrier, L.1
Knoell, R.2
Vignier, N.3
Keller, D.I.4
Bausero, P.5
Prudhon, B.6
-
45
-
-
19444368979
-
Nonsense-mediated mRNA decay in mammals
-
Maquat LE. Nonsense-mediated mRNA decay in mammals. J Cell Sci 2005;118: 1773-1776.
-
(2005)
J Cell Sci
, vol.118
, pp. 1773-1776
-
-
Maquat, L.E.1
-
47
-
-
0031840487
-
At least one intron is required for the nonsense-mediated decay of triosephosphate isomerase mRNA: A possible link between nuclear splicing and cytoplasmic translation
-
Zhang J, Sun X, Qian Y, LaDuca JP, Maquat LE. At least one intron is required for the nonsense-mediated decay of triosephosphate isomerase mRNA: a possible link between nuclear splicing and cytoplasmic translation. Mol Cell Biol 1998;18: 5272-5283.
-
(1998)
Mol Cell Biol
, vol.18
, pp. 5272-5283
-
-
Zhang, J.1
Sun, X.2
Qian, Y.3
Laduca, J.P.4
Maquat, L.E.5
-
48
-
-
54849413018
-
Introducing sense into nonsense in treatments of human genetic diseases
-
Linde L, Kerem B. Introducing sense into nonsense in treatments of human genetic diseases. Trends Genet 2008;24:552-563.
-
(2008)
Trends Genet
, vol.24
, pp. 552-563
-
-
Linde, L.1
Kerem, B.2
-
49
-
-
39849085883
-
Incomplete nonsense-mediated decay of mutant lamin A/C mRNA provokes dilated cardio-myopathy and ventricular tachycardia
-
Geiger SK, Bar H, Ehlermann P, Walde S, Rutschow D, Zeller R et al. Incomplete nonsense-mediated decay of mutant lamin A/C mRNA provokes dilated cardio-myopathy and ventricular tachycardia. J Mol Med 2008;86:281-289.
-
(2008)
J Mol Med
, vol.86
, pp. 281-289
-
-
Geiger, S.K.1
Bar, H.2
Ehlermann, P.3
Walde, S.4
Rutschow, D.5
Zeller, R.6
-
50
-
-
33751255699
-
Proteasome-mediated degradation of integral inner nuclear membrane protein emerin in fibroblasts lacking A-type lamins
-
Muchir A, Massart C, van Engelen BG, Lammens M, Bonne G, Worman HJ. Proteasome-mediated degradation of integral inner nuclear membrane protein emerin in fibroblasts lacking A-type lamins. Biochem Biophys Res Commun 2006; 351:1011-1017.
-
(2006)
Biochem Biophys Res Commun
, vol.351
, pp. 1011-1017
-
-
Muchir, A.1
Massart, C.2
Van Engelen, B.G.3
Lammens, M.4
Bonne, G.5
Worman, H.J.6
-
51
-
-
34347332362
-
Nonsense mutations in hERG cause a decrease in mutant mRNA transcripts by nonsense-mediated mRNA decay in human long-QT syndrome
-
Gong Q, Zhang L, Vincent GM, Horne BD, Zhou Z. Nonsense mutations in hERG cause a decrease in mutant mRNA transcripts by nonsense-mediated mRNA decay in human long-QT syndrome. Circulation 2007;116:17-24.
-
(2007)
Circulation
, vol.116
, pp. 17-24
-
-
Gong, Q.1
Zhang, L.2
Vincent, G.M.3
Horne, B.D.4
Zhou, Z.5
-
52
-
-
68249092692
-
Nonsense-mediated mRNA decay and ubiquitin-proteasome system regulate cMyBP-C mutant levels in cardiomyopathic mice
-
Vignier N, Schlossarek S, Fraysse B, Mearini G, Kraemer E, Pointu H et al. Nonsense-mediated mRNA decay and ubiquitin-proteasome system regulate cMyBP-C mutant levels in cardiomyopathic mice. Circ Res 2009;105:239-248.
-
(2009)
Circ Res
, vol.105
, pp. 239-248
-
-
Vignier, N.1
Schlossarek, S.2
Fraysse, B.3
Mearini, G.4
Kraemer, E.5
Pointu, H.6
-
53
-
-
33646523185
-
The ubiquitin-proteasome system: Focus on the heart
-
Zolk O, Schenke C, Sarikas A. The ubiquitin-proteasome system: focus on the heart. Cardiovasc Res 2006;70:410-421.
-
(2006)
Cardiovasc Res
, vol.70
, pp. 410-421
-
-
Zolk, O.1
Schenke, C.2
Sarikas, A.3
-
55
-
-
33644859083
-
The ubiquitin proteolytic system: From a vague idea, through basic mechanisms, and onto human diseases and drug targeting
-
PII 0000611420060124100003
-
Ciechanover A. The ubiquitin proteolytic system: from a vague idea through basic mechanisms, and onto human diseases and drug targeting. Neurology 2006;66: S7-S19. (Pubitemid 43739979)
-
(2006)
Neurology
, vol.66
, Issue.2 SUPPL. 1
-
-
Ciechanover, A.1
-
56
-
-
72949098600
-
Proteasome inhibitors and cardiac cell growth
-
Hedhli N, Depre C. Proteasome inhibitors and cardiac cell growth. Cardiovasc Res 2010;85:321-329.
-
Cardiovasc Res
, vol.2010
, Issue.85
, pp. 321-329
-
-
Hedhli, N.1
Depre, C.2
-
57
-
-
14844338880
-
Impairment of the ubiquitin-proteasome system by truncated cardiac myosin binding protein C mutants
-
Sarikas A, Carrier L, Schenke C, Doll D, Flavigny J, Lindenberg KS et al. Impairment of the ubiquitin-proteasome system by truncated cardiac myosin binding protein C mutants. Cardiovasc Res 2005;66:33-44.
-
(2005)
Cardiovasc Res
, vol.66
, pp. 33-44
-
-
Sarikas, A.1
Carrier, L.2
Schenke, C.3
Doll, D.4
Flavigny, J.5
Lindenberg, K.S.6
-
58
-
-
72949105996
-
Atrogin-1 and MuRF1 regulate cardiac MyBP-C levels via different mechanisms
-
Mearini G, Gedicke G, Schlossarek S, Witt CC, Krämer E, Cao P et al. Atrogin-1 and MuRF1 regulate cardiac MyBP-C levels via different mechanisms. Cardiovasc Res 2010;85:357-366.
-
Cardiovasc Res
, vol.2010
, Issue.85
, pp. 357-366
-
-
Mearini, G.1
Gedicke, G.2
Schlossarek, S.3
Witt, C.C.4
Krämer, E.5
Cao, P.6
-
59
-
-
0242458978
-
Biomo-lecular interactions between human recombinant b-MyHC and cMyBP-Cs implicated in familial hypertrophic cardiomyopathy
-
Flavigny J, Robert P, Camelin J, Schwartz K, Carrier L, Berebbi-Bertrand I. Biomo-lecular interactions between human recombinant b-MyHC and cMyBP-Cs implicated in familial hypertrophic cardiomyopathy. Cardiovasc Res 2003;60:388-396.
-
(2003)
Cardiovasc Res
, vol.60
, pp. 388-396
-
-
Flavigny, J.1
Robert, P.2
Camelin, J.3
Schwartz, K.4
Carrier, L.5
Berebbi-Bertrand, I.6
-
60
-
-
56649089678
-
Ubiquitin-proteasome system impairment caused by a missense cardiac myosin-binding protein C mutation and associated with cardiac dysfunction in hyper-trophic cardiomyopathy
-
Bahrudin U, Morisaki H, Morisaki T, Ninomiya H, Higaki K, Nanba E et al. Ubiquitin-proteasome system impairment caused by a missense cardiac myosin-binding protein C mutation and associated with cardiac dysfunction in hyper-trophic cardiomyopathy. J Mol Biol 2008;384:896-907.
-
(2008)
J Mol Biol
, vol.384
, pp. 896-907
-
-
Bahrudin, U.1
Morisaki, H.2
Morisaki, T.3
Ninomiya, H.4
Higaki, K.5
Nanba, E.6
-
61
-
-
0023918541
-
Storage of phosphorylated desmin in a familial myopathy
-
Rappaport L, Contard F, Samuel JL, Delcayre C, Marotte F, Tome F et al. Storage of phosphorylated desmin in a familial myopathy. FEBS Lett 1988;231:421-425.
-
(1988)
FEBS Lett
, vol.231
, pp. 421-425
-
-
Rappaport, L.1
Contard, F.2
Samuel, J.L.3
Delcayre, C.4
Marotte, F.5
Tome, F.6
-
62
-
-
17344361902
-
A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopa-thy
-
Vicart P, Caron A, Guicheney P, Li Z, Prevost MC, Faure A et al. A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopa-thy. Nat Genet 1998;20:92-95.
-
(1998)
Nat Genet
, vol.20
, pp. 92-95
-
-
Vicart, P.1
Caron, A.2
Guicheney, P.3
Li, Z.4
Prevost, M.C.5
Faure, A.6
-
63
-
-
0035816115
-
Expression of R120G-alphaB-crystallin causes aberrant desmin and alphaB-crystallin aggregation and cardiomyopathy in mice
-
Wang X, Osinska H, Klevitsky R, Gerdes AM, Nieman M, Lorenz J et al. Expression of R120G-alphaB-crystallin causes aberrant desmin and alphaB-crystallin aggregation and cardiomyopathy in mice. Circ Res 2001;89:84-91.
-
(2001)
Circ Res
, vol.89
, pp. 84-91
-
-
Wang, X.1
Osinska, H.2
Klevitsky, R.3
Gerdes, A.M.4
Nieman, M.5
Lorenz, J.6
-
64
-
-
26444486021
-
Reversal of amyloid-induced heart disease in desmin-related cardiomyopathy
-
Sanbe A, Osinska H, Villa C, Gulick J, Klevitsky R, Glabe CG et al. Reversal of amyloid-induced heart disease in desmin-related cardiomyopathy. Proc Natl Acad Sci USA 2005;102:13592-13597.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 13592-13597
-
-
Sanbe, A.1
Osinska, H.2
Villa, C.3
Gulick, J.4
Klevitsky, R.5
Glabe, C.G.6
-
65
-
-
27944450427
-
Intrasarcoplasmic amyloidosis impairs proteolytic function of proteasomes in cardiomyocytes by compromising substrate uptake
-
Chen Q, Liu JB, Horak KM, Zheng H, Kumarapeli AR, Li J et al. Intrasarcoplasmic amyloidosis impairs proteolytic function of proteasomes in cardiomyocytes by compromising substrate uptake. Circ Res 2005;97:1018-1026.
-
(2005)
Circ Res
, vol.97
, pp. 1018-1026
-
-
Chen, Q.1
Liu, J.B.2
Horak, K.M.3
Zheng, H.4
Kumarapeli, A.R.5
Li, J.6
-
66
-
-
33644883329
-
Impairment of the ubiquitin-proteasome system in desminopathy mouse hearts
-
Liu J, Chen Q, Huang W, Horak KM, Zheng H, Mestril R et al. Impairment of the ubiquitin-proteasome system in desminopathy mouse hearts. FASEB J 2006;20: 362-364.
-
(2006)
FASEB J
, vol.20
, pp. 362-364
-
-
Liu, J.1
Chen, Q.2
Huang, W.3
Horak, K.M.4
Zheng, H.5
Mestril, R.6
-
67
-
-
33645055949
-
Aberrant protein aggregation is essential for a mutant desmin to impair the proteolytic function of the ubiquitin-proteasome system in cardiomyocytes
-
Liu J, Tang M, Mestril R, Wang X. Aberrant protein aggregation is essential for a mutant desmin to impair the proteolytic function of the ubiquitin-proteasome system in cardiomyocytes. J Mol Cell Cardiol 2006;40:451-454.
-
(2006)
J Mol Cell Cardiol
, vol.40
, pp. 451-454
-
-
Liu, J.1
Tang, M.2
Mestril, R.3
Wang, X.4
-
68
-
-
70349359488
-
Adrenergic stress unmasks exaggerated septal hypertrophy and proteasome impairment in heterozygous cMyBP-C mutant mice. (Abstract)
-
Schuermann F, Schlossarek S, Mearini G, Geertz B, Vignier N, Eschenhagen T et al. Adrenergic stress unmasks exaggerated septal hypertrophy and proteasome impairment in heterozygous cMyBP-C mutant mice. (Abstract). Circulation 2008; 118:S521-S521.
-
(2008)
Circulation
, vol.118
-
-
Schuermann, F.1
Schlossarek, S.2
Mearini, G.3
Geertz, B.4
Vignier, N.5
Eschenhagen, T.6
-
69
-
-
30544446127
-
Depression of proteasome activities during the progression of cardiac dysfunction in pressure-overloaded heart of mice
-
Tsukamoto O, Minamino T, Okada K, Shintani Y, Takashima S, Kato H et al. Depression of proteasome activities during the progression of cardiac dysfunction in pressure-overloaded heart of mice. Biochem Biophys Res Commun 2006;340: 1125-1133.
-
(2006)
Biochem Biophys Res Commun
, vol.340
, pp. 1125-1133
-
-
Tsukamoto, O.1
Minamino, T.2
Okada, K.3
Shintani, Y.4
Takashima, S.5
Kato, H.6
-
70
-
-
33344473389
-
Atrophy, hypertrophy, and hypoxemia induce transcriptional regulators of the ubiquitin proteasome system in the rat heart
-
Razeghi P, Baskin KK, Sharma S, Young ME, Stepkowski S, Essop MF et al. Atrophy, hypertrophy, and hypoxemia induce transcriptional regulators of the ubiquitin proteasome system in the rat heart. Biochem Biophys Res Commun 2006;342: 361-364.
-
(2006)
Biochem Biophys Res Commun
, vol.342
, pp. 361-364
-
-
Razeghi, P.1
Baskin, K.K.2
Sharma, S.3
Young, M.E.4
Stepkowski, S.5
Essop, M.F.6
-
71
-
-
33748581280
-
Enhanced ubiquitination of cytoskeletal proteins in pressure overloaded myocardium is accompanied by changes in specific E3 ligases
-
Balasubramanian S, Mani S, Shiraishi H, Johnston RK, Yamane K, Willey CD et al. Enhanced ubiquitination of cytoskeletal proteins in pressure overloaded myocardium is accompanied by changes in specific E3 ligases. J Mol Cell Cardiol 2006;41: 669-679.
-
(2006)
J Mol Cell Cardiol
, vol.41
, pp. 669-679
-
-
Balasubramanian, S.1
Mani, S.2
Shiraishi, H.3
Johnston, R.K.4
Yamane, K.5
Willey, C.D.6
-
72
-
-
72949113180
-
Alterations of the ubiquitin-proteasome system in cardiomyopathic cMyBP-C mice. (Abstract)
-
Sultan K, Schlossarek S, Englmann D, Vignier N, Eschenhagen T, Carrier L. Alterations of the ubiquitin-proteasome system in cardiomyopathic cMyBP-C mice. (Abstract). J Mol Cell Cardiol 2007;42:S167.
-
(2007)
J Mol Cell Cardiol
, vol.42
-
-
Sultan, K.1
Schlossarek, S.2
Englmann, D.3
Vignier, N.4
Eschenhagen, T.5
Carrier, L.6
-
73
-
-
0037328263
-
Hyperubiquitination of proteins in dilated cardiomyopathy
-
Weekes J, Morrison K, Mullen A, Wait R, Barton P, Dunn MJ. Hyperubiquitination of proteins in dilated cardiomyopathy. Proteomics 2003;3:208-216.
-
(2003)
Proteomics
, vol.3
, pp. 208-216
-
-
Weekes, J.1
Morrison, K.2
Mullen, A.3
Wait, R.4
Barton, P.5
Dunn, M.J.6
-
74
-
-
48749126678
-
Elevated p53 expression is associated with dysregulation of the ubiquitin-proteasome system in dilated cardiomyopathy
-
Birks EJ, Latif N, Enesa K, Folkvang T, Luong le A, Sarathchandra P et al. Elevated p53 expression is associated with dysregulation of the ubiquitin-proteasome system in dilated cardiomyopathy. Cardiovasc Res 2008;79:472-480.
-
(2008)
Cardiovasc Res
, vol.79
, pp. 472-480
-
-
Birks, E.J.1
Latif, N.2
Enesa, K.3
Folkvang, T.4
Luong Le, A.5
Sarathchandra, P.6
-
75
-
-
38849202469
-
Proteasome activation during cardiac hypertrophy by the chaperone H11 Kinase/Hsp22
-
Hedhli N, Wang L, Wang Q, Rashed E, Tian Y, Sui X et al. Proteasome activation during cardiac hypertrophy by the chaperone H11 Kinase/Hsp22. Cardiovasc Res 2008;77:497-505.
-
(2008)
Cardiovasc Res
, vol.77
, pp. 497-505
-
-
Hedhli, N.1
Wang, L.2
Wang, Q.3
Rashed, E.4
Tian, Y.5
Sui, X.6
-
76
-
-
33750356583
-
Nonsense-mediated mRNA decay: Target genes and functional diversification of effectors
-
Rehwinkel J, Raes J, Izaurralde E. Nonsense-mediated mRNA decay: target genes and functional diversification of effectors. Trends Biochem Sci 2006;31: 639-646.
-
(2006)
Trends Biochem Sci
, vol.31
, pp. 639-646
-
-
Rehwinkel, J.1
Raes, J.2
Izaurralde, E.3
-
77
-
-
33746889124
-
Specific inhibition of nonsense-mediated mRNA decay components, SMG-1 or Upf1, rescues the phenotype of Ullrich disease fibroblasts
-
Usuki F, Yamashita A, Kashima I, Higuchi I, Osame M, Ohno S. Specific inhibition of nonsense-mediated mRNA decay components, SMG-1 or Upf1, rescues the phenotype of Ullrich disease fibroblasts. Mol Ther 2006;14:351-360.
-
(2006)
Mol Ther
, vol.14
, pp. 351-360
-
-
Usuki, F.1
Yamashita, A.2
Kashima, I.3
Higuchi, I.4
Osame, M.5
Ohno, S.6
-
78
-
-
7444230353
-
Pharmacologic therapy for stop mutations: How much CFTR activity is enough?
-
Kerem E. Pharmacologic therapy for stop mutations: how much CFTR activity is enough? Curr Opin Pulm Med 2004;10:547-552.
-
(2004)
Curr Opin Pulm Med
, vol.10
, pp. 547-552
-
-
Kerem, E.1
-
79
-
-
0043092426
-
Gentamicin administration in Duchenne patients with premature stop codon Preliminary results
-
Politano L, Nigro G, Nigro V, Piluso G, Papparella S, Paciello O et al. Gentamicin administration in Duchenne patients with premature stop codon. Preliminary results. Acta Myol 2003;22:15-21.
-
(2003)
Acta Myol
, vol.22
, pp. 15-21
-
-
Politano, L.1
Nigro, G.2
Nigro, V.3
Piluso, G.4
Papparella, S.5
Paciello, O.6
-
81
-
-
13544261687
-
Genetic factors in aminoglycoside toxicity
-
Fischel-Ghodsian N. Genetic factors in aminoglycoside toxicity. Pharmacogenomics 2005;6:27-36.
-
(2005)
Pharmacogenomics
, vol.6
, pp. 27-36
-
-
Fischel-Ghodsian, N.1
-
82
-
-
33947529670
-
Safety, tolerability, and pharmacokinetics of PTC124, a nonaminoglycoside nonsense mutation suppressor, following single-and multiple-dose administration to healthy male and female adult volunteers
-
Hirawat S, Welch EM, Elfring GL, Northcutt VJ, Paushkin S, Hwang S et al. Safety, tolerability, and pharmacokinetics of PTC124, a nonaminoglycoside nonsense mutation suppressor, following single-and multiple-dose administration to healthy male and female adult volunteers. J Clin Pharmacol 2007;47:430-444.
-
(2007)
J Clin Pharmacol
, vol.47
, pp. 430-444
-
-
Hirawat, S.1
Welch, E.M.2
Elfring, G.L.3
Northcutt, V.J.4
Paushkin, S.5
Hwang, S.6
-
83
-
-
34347330301
-
Modulating the expression of disease genes with RNA-based therapy
-
Wood M, Yin H, McClorey G. Modulating the expression of disease genes with RNA-based therapy. PLoS Genet 2007;3:e109.
-
(2007)
PLoS Genet
, vol.3
-
-
Wood, M.1
Yin, H.2
McClorey, G.3
-
84
-
-
38549105011
-
Suppression of cardiomyocyte hypertrophy by inhibition of the ubiquitin-proteasome system
-
Meiners S, Dreger H, Fechner M, Bieler S, Rother W, Gunther C et al. Suppression of cardiomyocyte hypertrophy by inhibition of the ubiquitin-proteasome system. Hypertension 2008;51:302-308.
-
(2008)
Hypertension
, vol.51
, pp. 302-308
-
-
Meiners, S.1
Dreger, H.2
Fechner, M.3
Bieler, S.4
Rother, W.5
Gunther, C.6
-
85
-
-
39149097822
-
Protea-some inhibition promotes regression of left ventricular hypertrophy
-
Stansfield WE, Tang RH, Moss NC, Baldwin AS, Willis MS, Selzman CH. Protea-some inhibition promotes regression of left ventricular hypertrophy. Am J Physiol Heart Circ Physiol 2008;294:H645-H650.
-
(2008)
Am J Physiol Heart Circ Physiol
, vol.294
-
-
Stansfield, W.E.1
Tang, R.H.2
Moss, N.C.3
Baldwin, A.S.4
Willis, M.S.5
Selzman, C.H.6
-
86
-
-
57049121279
-
Proteasome inhibition decreases cardiac remodeling after initiation of pressure overload
-
Hedhli N, Lizano P, Hong C, Fritzky LF, Dhar SK, Liu H et al. Proteasome inhibition decreases cardiac remodeling after initiation of pressure overload. Am J Physiol Heart Circ Physiol 2008;295:H1385-H1393.
-
(2008)
Am J Physiol Heart Circ Physiol
, vol.295
-
-
Hedhli, N.1
Lizano, P.2
Hong, C.3
Fritzky, L.F.4
Dhar, S.K.5
Liu, H.6
-
87
-
-
56649108096
-
Acute severe cardiac failure in a myeloma patient due to proteasome inhibitor bortezomib
-
Hacihanefioglu A, Tarkun P, Gonullu E. Acute severe cardiac failure in a myeloma patient due to proteasome inhibitor bortezomib. Int J Hematol 2008;88:219-222.
-
(2008)
Int J Hematol
, vol.88
, pp. 219-222
-
-
Hacihanefioglu, A.1
Tarkun, P.2
Gonullu, E.3
-
88
-
-
34447123834
-
Unexpected cardiotoxicity in haematological bortezomib treated patients
-
Orciuolo E, Buda G, Cecconi N, Galimberti S, Versari D, Cervetti G et al. Unexpected cardiotoxicity in haematological bortezomib treated patients. Br J Haema-tol 2007;138:396-397.
-
(2007)
Br J Haema-tol
, vol.138
, pp. 396-397
-
-
Orciuolo, E.1
Buda, G.2
Cecconi, N.3
Galimberti, S.4
Versari, D.5
Cervetti, G.6
-
89
-
-
33744909144
-
Severe reversible cardiac failure after bortezomib treatment combined with chemotherapy in a non-small cell lung cancer patient: A case report
-
Voortman J, Giaccone G. Severe reversible cardiac failure after bortezomib treatment combined with chemotherapy in a non-small cell lung cancer patient: a case report. BMC Cancer 2006;6:129.
-
(2006)
BMC Cancer
, vol.6
, pp. 129
-
-
Voortman, J.1
Giaccone, G.2
-
90
-
-
62749139577
-
Inhibiting Hdm2and ubiquitin-activating enzyme: Targeting the ubiquitin conjugating system in cancer
-
Weissman AM, Yang Y, Kitagaki J, Sasiela CA, Beutler JA, O'Keefe BR. Inhibiting Hdm2 and ubiquitin-activating enzyme: targeting the ubiquitin conjugating system in cancer. Ernst Schering Found Symp Proc 2008;171-190.
-
(2008)
Ernst Schering Found Symp Proc
, pp. 171-190
-
-
Weissman, A.M.1
Yang, Y.2
Kitagaki, J.3
Sasiela, C.A.4
Beutler, J.A.5
O'keefe, B.R.6
-
92
-
-
0141760313
-
Pro-teasome inhibitor (MG-132) treatment of mdx mice rescues the expression and membrane localization of dystrophin and dystrophin-associated proteins
-
Bonuccelli G, Sotgia F, Schubert W, Park DS, Frank PG, Woodman SE et al. Pro-teasome inhibitor (MG-132) treatment of mdx mice rescues the expression and membrane localization of dystrophin and dystrophin-associated proteins. Am J Pathol 2003;163:1663-1675.
-
(2003)
Am J Pathol
, vol.163
, pp. 1663-1675
-
-
Bonuccelli, G.1
Sotgia, F.2
Schubert, W.3
Park, D.S.4
Frank, P.G.5
Woodman, S.E.6
|