-
1
-
-
17344363640
-
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
-
Bashir R, Britton S, Strachan T, Keers S, Vafiadaki E, Lako M, Richard I, Marchand S, Bourg N, Argov Z, Sadeh M, Mahjneh I, Marconi G, Passos-Bueno MR, Moreira ES, Zatz M, Beckmann JS, Bushby K (1998) A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B. Nat Genet 20:37-42
-
(1998)
Nat Genet
, vol.20
, pp. 37-42
-
-
Bashir, R.1
Britton, S.2
Strachan, T.3
Keers, S.4
Vafiadaki, E.5
Lako, M.6
Richard, I.7
Marchand, S.8
Bourg, N.9
Argov, Z.10
Sadeh, M.11
Mahjneh, I.12
Marconi, G.13
Passos-Bueno, M.R.14
Moreira, E.S.15
Zatz, M.16
Beckmann, J.S.17
Bushby, K.18
-
2
-
-
17344365600
-
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
-
Liu J, Aoki M, Illa I, Wu C, Fardeau M, Angelini C, Serrano C, Urtizberea JA, Hentati F, Hamida MB, Bohlega S, Culper EJ, Amato AA, Bossie K, Oeltjen J, Bejaoui K, McKenna-Yasek D, Hosler BA, Schurr E, Arahata K, de Jong PJ, Brown RH Jr (1998) Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy. Nat Genet 20:31-36
-
(1998)
Nat Genet
, vol.20
, pp. 31-36
-
-
Liu, J.1
Aoki, M.2
Illa, I.3
Wu, C.4
Fardeau, M.5
Angelini, C.6
Serrano, C.7
Urtizberea, J.A.8
Hentati, F.9
Hamida, M.B.10
Bohlega, S.11
Culper, E.J.12
Amato, A.A.13
Bossie, K.14
Oeltjen, J.15
Bejaoui, K.16
McKenna-Yasek, D.17
Hosler, B.A.18
Schurr, E.19
Arahata, K.20
De Jong, P.J.21
Brown Jr., R.H.22
more..
-
3
-
-
0035943022
-
Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy
-
Aoki M, Liu J, Richard I, Bashir R, Britton S, Keers SM, Oeltjen J, Brown HE, Marchand S, Bourg N, Beley C, McKenna-Yasek D, Arahata K, Bohlega S, Cupler E, Illa I, Majneh I, Barohn RJ, Urtizberea JA, Fardeau M, Amato A, Angelini C, Bushby K, Beckmann JS, Brown RH Jr (2001) Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy. Neurology 57:271-278
-
(2001)
Neurology
, vol.57
, pp. 271-278
-
-
Aoki, M.1
Liu, J.2
Richard, I.3
Bashir, R.4
Britton, S.5
Keers, S.M.6
Oeltjen, J.7
Brown, H.E.8
Marchand, S.9
Bourg, N.10
Beley, C.11
McKenna-Yasek, D.12
Arahata, K.13
Bohlega, S.14
Cupler, E.15
Illa, I.16
Majneh, I.17
Barohn, R.J.18
Urtizberea, J.A.19
Fardeau, M.20
Amato, A.21
Angelini, C.22
Bushby, K.23
Beckmann, J.S.24
Brown Jr., R.H.25
more..
-
4
-
-
0033972161
-
Myoferlin, a candidate gene and potential modifier of muscular dystrophy
-
Davis DB, Delmonte AJ, Ly CT, McNally EM (2000) Myoferlin, a candidate gene and potential modifier of muscular dystrophy. Hum Mol Genet 9:217-226
-
(2000)
Hum Mol Genet
, vol.9
, pp. 217-226
-
-
Davis, D.B.1
Delmonte, A.J.2
Ly, C.T.3
McNally, E.M.4
-
5
-
-
0347379869
-
Dysferlin interacts with annexins A1 and A2 and mediates sarcolemmal wound-healing
-
Lennon NJ, Kho A, Bacskai BJ, Perlmutter SL, Hyman BT, Brown RH Jr (2003) Dysferlin interacts with annexins A1 and A2 and mediates sarcolemmal wound-healing. J Biol Chem 278:50466-50473
-
(2003)
J Biol Chem
, vol.278
, pp. 50466-50473
-
-
Lennon, N.J.1
Kho, A.2
Bacskai, B.J.3
Perlmutter, S.L.4
Hyman, B.T.5
Brown Jr., R.H.6
-
6
-
-
0035880516
-
The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle
-
Matsuda C, Hayashi YK, Ogawa M, Aoki M, Murayama K, Nishino I, Nonaka I, Arahata K, Brown RH Jr (2001) The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle. Hum Mol Genet 10:1761-1766
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1761-1766
-
-
Matsuda, C.1
Hayashi, Y.K.2
Ogawa, M.3
Aoki, M.4
Murayama, K.5
Nishino, I.6
Nonaka, I.7
Arahata, K.8
Brown Jr., R.H.9
-
7
-
-
16844373171
-
Dysferlin interacts with affixin (beta-parvin) at the sarcolemma
-
Matsuda C, Kameyama K, Tagawa K, Ogawa M, Suzuki A, Yamaji S, Okamoto H, Nishino I, Hayashi YK (2005) Dysferlin interacts with affixin (beta-parvin) at the sarcolemma. J Neuropathol Exp Neurol 64:334-340
-
(2005)
J Neuropathol Exp Neurol
, vol.64
, pp. 334-340
-
-
Matsuda, C.1
Kameyama, K.2
Tagawa, K.3
Ogawa, M.4
Suzuki, A.5
Yamaji, S.6
Okamoto, H.7
Nishino, I.8
Hayashi, Y.K.9
-
8
-
-
33847406320
-
AHNAK, a novel component of the dysferlin protein complex, redistributes to the cytoplasm with dysferlin during skeletal muscle regeneration
-
Huang Y, Laval SH, van Remoortere A, Baudier J, Benaud C, Anderson LV, Straub V, Deelder A, Frants RR, den Dunnen JT, Bushby K, van der Maarel SM (2007) AHNAK, a novel component of the dysferlin protein complex, redistributes to the cytoplasm with dysferlin during skeletal muscle regeneration. FASEB J 21:732-742
-
(2007)
FASEB J
, vol.21
, pp. 732-742
-
-
Huang, Y.1
Laval, S.H.2
Van Remoortere, A.3
Baudier, J.4
Benaud, C.5
Anderson, L.V.6
Straub, V.7
Deelder, A.8
Frants, R.R.9
Den Dunnen, J.T.10
Bushby, K.11
Van Der Maarel, S.M.12
-
9
-
-
0037738510
-
Defective membrane repair in dysferlin-deficient muscular dystrophy
-
Bansal D, Miyake K, Vogel SS, Groh S, Chen CC, Williamson R, McNeil PL, Campbell KP (2003) Defective membrane repair in dysferlin-deficient muscular dystrophy. Nature 423:168-172
-
(2003)
Nature
, vol.423
, pp. 168-172
-
-
Bansal, D.1
Miyake, K.2
Vogel, S.S.3
Groh, S.4
Chen, C.C.5
Williamson, R.6
McNeil, P.L.7
Campbell, K.P.8
-
10
-
-
5744230326
-
Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency
-
Ho M, Post CM, Donahue LR, Lidov HG, Bronson RT, Goolsby H, Watkins SC, Cox GA, Brown RH Jr (2004) Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency. Hum Mol Genet 13:1999-2010
-
(2004)
Hum Mol Genet
, vol.13
, pp. 1999-2010
-
-
Ho, M.1
Post, C.M.2
Donahue, L.R.3
Lidov, H.G.4
Bronson, R.T.5
Goolsby, H.6
Watkins, S.C.7
Cox, G.A.8
Brown Jr., R.H.9
-
11
-
-
27144441053
-
Increased susceptibility to complement attack due to down-regulation of decay-accelerating factor/CD55 in dysferlin-deficient muscular dystrophy
-
Wenzel K, Zabojszcza J, Carl M, Taubert S, Lass A, Harris CL, Ho M, Schulz H, Hummel O, Hubner N, Osterziel KJ, Spuler S (2005) Increased susceptibility to complement attack due to down-regulation of decay-accelerating factor/CD55 in dysferlin-deficient muscular dystrophy. J Immunol 175:6219-6225
-
(2005)
J Immunol
, vol.175
, pp. 6219-6225
-
-
Wenzel, K.1
Zabojszcza, J.2
Carl, M.3
Taubert, S.4
Lass, A.5
Harris, C.L.6
Ho, M.7
Schulz, H.8
Hummel, O.9
Hubner, N.10
Osterziel, K.J.11
Spuler, S.12
-
12
-
-
0032955751
-
Dysferlin is a plasma membrane protein and is expressed early in human development
-
Anderson LV, Davison K, Moss JA, Young C, Cullen MJ, Walsh J, Johnson MA, Bashir R, Britton S, Keers S, Argov Z, Mahjneh I, Fougerousse F, Beckmann JS, Bushby KM (1999) Dysferlin is a plasma membrane protein and is expressed early in human development. Hum Mol Genet 8:855-861
-
(1999)
Hum Mol Genet
, vol.8
, pp. 855-861
-
-
Anderson, L.V.1
Davison, K.2
Moss, J.A.3
Young, C.4
Cullen, M.J.5
Walsh, J.6
Johnson, M.A.7
Bashir, R.8
Britton, S.9
Keers, S.10
Argov, Z.11
Mahjneh, I.12
Fougerousse, F.13
Beckmann, J.S.14
Bushby, K.M.15
-
13
-
-
10744220036
-
Molecular analysis of LGMD-2B and MM patients: Identification of novel DYSF mutations and possible founder effect in the Italian population
-
Cagliani R, Fortunato F, Giorda R, Rodolico C, Bonaglia MC, Sironi M, D'Angelo MG, Prelle A, Locatelli F, Toscano A, Bresolin N, Comi GP (2003) Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian population. Neuromuscul Disord 13:788-795
-
(2003)
Neuromuscul Disord
, vol.13
, pp. 788-795
-
-
Cagliani, R.1
Fortunato, F.2
Giorda, R.3
Rodolico, C.4
Bonaglia, M.C.5
Sironi, M.6
D'Angelo, M.G.7
Prelle, A.8
Locatelli, F.9
Toscano, A.10
Bresolin, N.11
Comi, G.P.12
-
14
-
-
0032850960
-
Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B
-
Bittner RE, Anderson LV, Burkhardt E, Bashir R, Vafiadaki E, Ivanova S, Raffelsberger T, Maerk I, Hoger H, Jung M, Karbasiyan M, Storch M, Lassmann H, Moss JA, Davison K, Harrison R, Bushby KM, Reis A (1999) Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B. Nat Genet 23:141-142
-
(1999)
Nat Genet
, vol.23
, pp. 141-142
-
-
Bittner, R.E.1
Anderson, L.V.2
Burkhardt, E.3
Bashir, R.4
Vafiadaki, E.5
Ivanova, S.6
Raffelsberger, T.7
Maerk, I.8
Hoger, H.9
Jung, M.10
Karbasiyan, M.11
Storch, M.12
Lassmann, H.13
Moss, J.A.14
Davison, K.15
Harrison, R.16
Bushby, K.M.17
Reis, A.18
-
15
-
-
0035809747
-
Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation
-
Vafiadaki E, Reis A, Keers S, Harrison R, Anderson LV, Raffelsberger T, Ivanova S, Hoger H, Bittner RE, Bushby K, Bashir R (2001) Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation. Neuroreport 12:625-629
-
(2001)
Neuroreport
, vol.12
, pp. 625-629
-
-
Vafiadaki, E.1
Reis, A.2
Keers, S.3
Harrison, R.4
Anderson, L.V.5
Raffelsberger, T.6
Ivanova, S.7
Hoger, H.8
Bittner, R.E.9
Bushby, K.10
Bashir, R.11
-
16
-
-
33745314105
-
Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfolding
-
Wenzel K, Carl M, Perrot A, Zabojszcza J, Assadi M, Ebeling M, Geier C, Robinson PN, Kress W, Osterziel KJ, Spuler S (2006) Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfolding. Hum Mutat 27:599-600
-
(2006)
Hum Mutat
, vol.27
, pp. 599-600
-
-
Wenzel, K.1
Carl, M.2
Perrot, A.3
Zabojszcza, J.4
Assadi, M.5
Ebeling, M.6
Geier, C.7
Robinson, P.N.8
Kress, W.9
Osterziel, K.J.10
Spuler, S.11
-
17
-
-
33847046276
-
Painful enlargement of the calf muscles in limb girdle muscular dystrophy type 2B (LGMD2B) with a novel compound heterozygous mutation in DYSF
-
Diers A, Carl M, Stoltenburg-Didinger G, Vorgerd M, Spuler S (2007) Painful enlargement of the calf muscles in limb girdle muscular dystrophy type 2B (LGMD2B) with a novel compound heterozygous mutation in DYSF. Neuromuscul Disord 17:157-162
-
(2007)
Neuromuscul Disord
, vol.17
, pp. 157-162
-
-
Diers, A.1
Carl, M.2
Stoltenburg-Didinger, G.3
Vorgerd, M.4
Spuler, S.5
-
18
-
-
0018231715
-
Recommendations regarding quantitation in M-mode echocardiography: Results of a survey of echocardiographic measurements
-
Sahn DJ, DeMaria A, Kisslo J, Weyman A (1978) Recommendations regarding quantitation in M-mode echocardiography: results of a survey of echocardiographic measurements. Circulation 58:1072-1083
-
(1978)
Circulation
, vol.58
, pp. 1072-1083
-
-
Sahn, D.J.1
Demaria, A.2
Kisslo, J.3
Weyman, A.4
-
19
-
-
0032934453
-
Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy
-
Mestroni L, Maisch B, McKenna WJ, Schwartz K, Charron P, Rocco C, Tesson F, Richter A, Wilke A, Komajda M (1999) Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy. Eur Heart J 20:93-102
-
(1999)
Eur Heart J
, vol.20
, pp. 93-102
-
-
Mestroni, L.1
Maisch, B.2
McKenna, W.J.3
Schwartz, K.4
Charron, P.5
Rocco, C.6
Tesson, F.7
Richter, A.8
Wilke, A.9
Komajda, M.10
-
20
-
-
0033017175
-
The pathogenesis of familial hypertrophic cardiomyopathy: Early and evolving effects from an alpha-cardiac myosin heavy chain missense mutation
-
Georgakopoulos D, Christe ME, Giewat M, Seidman CM, Seidman JG, Kass DA (1999) The pathogenesis of familial hypertrophic cardiomyopathy: early and evolving effects from an alpha-cardiac myosin heavy chain missense mutation. Nat Med 5:327-330
-
(1999)
Nat Med
, vol.5
, pp. 327-330
-
-
Georgakopoulos, D.1
Christe, M.E.2
Giewat, M.3
Seidman, C.M.4
Seidman, J.G.5
Kass, D.A.6
-
21
-
-
0344578043
-
Age-related left ventricular function in the mouse: Analysis based on in vivo pressure-volume relationships
-
Yang B, Larson DF, Watson R (1999) Age-related left ventricular function in the mouse: analysis based on in vivo pressure-volume relationships. Am J Physiol 277:H1906-H1913
-
(1999)
Am J Physiol
, vol.277
-
-
Yang, B.1
Larson, D.F.2
Watson, R.3
-
22
-
-
12344280017
-
Summaries of Affymetrix GeneChip probe level data
-
Irizarry RA, Bolstad BM, Collin F, Cope LM, Hobbs B, Speed TP (2003) Summaries of Affymetrix GeneChip probe level data. Nucleic Acids Res 31:e15
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 15
-
-
Irizarry, R.A.1
Bolstad, B.M.2
Collin, F.3
Cope, L.M.4
Hobbs, B.5
Speed, T.P.6
-
23
-
-
0142179210
-
Local-pooled-error test for identifying differentially expressed genes with a small number of replicated microarrays
-
Jain N, Thatte J, Braciale T, Ley K, O'Connell M, Lee JK (2003) Local-pooled-error test for identifying differentially expressed genes with a small number of replicated microarrays. Bioinformatics 19:1945-1951
-
(2003)
Bioinformatics
, vol.19
, pp. 1945-1951
-
-
Jain, N.1
Thatte, J.2
Braciale, T.3
Ley, K.4
O'Connell, M.5
Lee, J.K.6
-
24
-
-
0042424602
-
Statistical significance for genomewide studies
-
Storey JD, Tibshirani R (2003) Statistical significance for genomewide studies. Proc Natl Acad Sci U S A 100:9440-9445
-
(2003)
Proc Natl Acad Sci U S a
, vol.100
, pp. 9440-9445
-
-
Storey, J.D.1
Tibshirani, R.2
-
26
-
-
0027399391
-
An improved strategy and a useful housekeeping gene for RNA analysis from formalin-fixed, paraffin-embedded tissues by PCR
-
Finke J, Fritzen R, Ternes P, Lange W, Dolken G (1993) An improved strategy and a useful housekeeping gene for RNA analysis from formalin-fixed, paraffin-embedded tissues by PCR. Biotechniques 14:448-453
-
(1993)
Biotechniques
, vol.14
, pp. 448-453
-
-
Finke, J.1
Fritzen, R.2
Ternes, P.3
Lange, W.4
Dolken, G.5
-
27
-
-
0033009836
-
Rat porphobilinogen deaminase gene: A pseudogene-free internal standard for laser-assisted cell picking
-
Fink L, Stahl U, Ermert L, Kummer W, Seeger W, Bohle RM (1999) Rat porphobilinogen deaminase gene: a pseudogene-free internal standard for laser-assisted cell picking. Biotechniques 26:510-516
-
(1999)
Biotechniques
, vol.26
, pp. 510-516
-
-
Fink, L.1
Stahl, U.2
Ermert, L.3
Kummer, W.4
Seeger, W.5
Bohle, R.M.6
-
28
-
-
0035710746
-
Analysis of relative gene expression data using real-time quantitative PCR and the 2(-delta delta C(T)) method
-
Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2(-delta delta C(T)) method. Methods 25:402-408
-
(2001)
Methods
, vol.25
, pp. 402-408
-
-
Livak, K.J.1
Schmittgen, T.D.2
-
29
-
-
1242320058
-
At the crossroads of myocardial signaling: The role of Z-discs in intracellular signaling and cardiac function
-
Pyle WG, Solaro RJ (2004) At the crossroads of myocardial signaling: the role of Z-discs in intracellular signaling and cardiac function. Circ Res 94:296-305
-
(2004)
Circ Res
, vol.94
, pp. 296-305
-
-
Pyle, W.G.1
Solaro, R.J.2
-
30
-
-
0030933063
-
MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure
-
Arber S, Hunter JJ, Ross J Jr, Hongo M, Sansig G, Borg J, Perriard JC, Chien KR, Caroni P (1997) MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure. Cell 88:393-403
-
(1997)
Cell
, vol.88
, pp. 393-403
-
-
Arber, S.1
Hunter, J.J.2
Ross Jr., J.3
Hongo, M.4
Sansig, G.5
Borg, J.6
Perriard, J.C.7
Chien, K.R.8
Caroni, P.9
-
31
-
-
0037470052
-
Characterization and in vivo functional analysis of splice variants of cypher
-
Huang C, Zhou Q, Liang P, Hollander MS, Sheikh F, Li X, Greaser M, Shelton GD, Evans S, Chen J (2003) Characterization and in vivo functional analysis of splice variants of cypher. J Biol Chem 278:7360-7365
-
(2003)
J Biol Chem
, vol.278
, pp. 7360-7365
-
-
Huang, C.1
Zhou, Q.2
Liang, P.3
Hollander, M.S.4
Sheikh, F.5
Li, X.6
Greaser, M.7
Shelton, G.D.8
Evans, S.9
Chen, J.10
-
32
-
-
0035033212
-
Adult mice deficient in actinin-associated LIM-domain protein reveal a developmental pathway for right ventricular cardiomyopathy
-
Pashmforoush M, Pomies P, Peterson KL, Kubalak S, Ross J Jr, Hefti A, Aebi U, Beckerle MC, Chien KR (2001) Adult mice deficient in actinin-associated LIM-domain protein reveal a developmental pathway for right ventricular cardiomyopathy. Nat Med 7:591-597
-
(2001)
Nat Med
, vol.7
, pp. 591-597
-
-
Pashmforoush, M.1
Pomies, P.2
Peterson, K.L.3
Kubalak, S.4
Ross Jr., J.5
Hefti, A.6
Aebi, U.7
Beckerle, M.C.8
Chien, K.R.9
-
33
-
-
0037453074
-
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy
-
Geier C, Perrot A, Ozcelik C, Binner P, Counsell D, Hoffmann K, Pilz B, Martiniak Y, Gehmlich K, van der Ven PF, Furst DO, Vornwald A, von Hodenberg E, Nurnberg P, Scheffold T, Dietz R, Osterziel KJ (2003) Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy. Circulation 107:1390-1395
-
(2003)
Circulation
, vol.107
, pp. 1390-1395
-
-
Geier, C.1
Perrot, A.2
Ozcelik, C.3
Binner, P.4
Counsell, D.5
Hoffmann, K.6
Pilz, B.7
Martiniak, Y.8
Gehmlich, K.9
Van Der Ven, P.F.10
Furst, D.O.11
Vornwald, A.12
Von Hodenberg, E.13
Nurnberg, P.14
Scheffold, T.15
Dietz, R.16
Osterziel, K.J.17
-
34
-
-
9644281144
-
Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy
-
Hayashi T, Arimura T, Itoh-Satoh M, Ueda K, Hohda S, Inagaki N, Takahashi M, Hori H, Yasunami M, Nishi H, Koga Y, Nakamura H, Matsuzaki M, Choi BY, Bae SW, You CW, Han KH, Park JE, Knoll R, Hoshijima M, Chien KR, Kimura A (2004) Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy. J Am Coll Cardiol 44:2192-2201
-
(2004)
J Am Coll Cardiol
, vol.44
, pp. 2192-2201
-
-
Hayashi, T.1
Arimura, T.2
Itoh-Satoh, M.3
Ueda, K.4
Hohda, S.5
Inagaki, N.6
Takahashi, M.7
Hori, H.8
Yasunami, M.9
Nishi, H.10
Koga, Y.11
Nakamura, H.12
Matsuzaki, M.13
Choi, B.Y.14
Bae, S.W.15
You, C.W.16
Han, K.H.17
Park, J.E.18
Knoll, R.19
Hoshijima, M.20
Chien, K.R.21
Kimura, A.22
more..
-
35
-
-
0032751526
-
The absence of desmin leads to cardiomyocyte hypertrophy and cardiac dilation with compromised systolic function
-
Milner DJ, Taffet GE, Wang X, Pham T, Tamura T, Hartley C, Gerdes AM, Capetanaki Y (1999) The absence of desmin leads to cardiomyocyte hypertrophy and cardiac dilation with compromised systolic function. J Mol Cell Cardiol 31:2063-2076
-
(1999)
J Mol Cell Cardiol
, vol.31
, pp. 2063-2076
-
-
Milner, D.J.1
Taffet, G.E.2
Wang, X.3
Pham, T.4
Tamura, T.5
Hartley, C.6
Gerdes, A.M.7
Capetanaki, Y.8
-
36
-
-
0037188943
-
Actin capping protein: An essential element in protein kinase signaling to the myofilaments
-
Pyle WG, Hart MC, Cooper JA, Sumandea MP, de Tombe PP, Solaro RJ (2002) Actin capping protein: an essential element in protein kinase signaling to the myofilaments. Circ Res 90:1299-1306
-
(2002)
Circ Res
, vol.90
, pp. 1299-1306
-
-
Pyle, W.G.1
Hart, M.C.2
Cooper, J.A.3
Sumandea, M.P.4
De Tombe, P.P.5
Solaro, R.J.6
-
37
-
-
0028073676
-
Muscle LIM protein, a novel essential regulator of myogenesis, promotes myogenic differentiation
-
Arber S, Halder G, Caroni P (1994) Muscle LIM protein, a novel essential regulator of myogenesis, promotes myogenic differentiation. Cell 79:221-231
-
(1994)
Cell
, vol.79
, pp. 221-231
-
-
Arber, S.1
Halder, G.2
Caroni, P.3
-
38
-
-
0037184992
-
The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy
-
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 (2002) The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy. Cell 111:943-955
-
(2002)
Cell
, vol.111
, 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..
-
39
-
-
13444311551
-
Attenuation of cardiac remodeling after myocardial infarction by muscle LIM protein-calcineurin signaling at the sarcomeric Z-disc
-
Heineke J, Ruetten H, Willenbockel C, Gross SC, Naguib M, Schaefer A, Kempf T, Hilfiker-Kleiner D, Caroni P, Kraft T, Kaiser RA, Molkentin JD, Drexler H, Wollert KC (2005) Attenuation of cardiac remodeling after myocardial infarction by muscle LIM protein-calcineurin signaling at the sarcomeric Z-disc. Proc Natl Acad Sci U S A 102:1655-1660
-
(2005)
Proc Natl Acad Sci U S a
, vol.102
, pp. 1655-1660
-
-
Heineke, J.1
Ruetten, H.2
Willenbockel, C.3
Gross, S.C.4
Naguib, M.5
Schaefer, A.6
Kempf, T.7
Hilfiker-Kleiner, D.8
Caroni, P.9
Kraft, T.10
Kaiser, R.A.11
Molkentin, J.D.12
Drexler, H.13
Wollert, K.C.14
-
40
-
-
0033538565
-
Cypher, a striated muscle-restricted PDZ and LIM domain-containing protein, binds to alpha-actinin-2 and protein kinase C
-
Zhou Q, Ruiz-Lozano P, Martone ME, Chen J (1999) Cypher, a striated muscle-restricted PDZ and LIM domain-containing protein, binds to alpha-actinin-2 and protein kinase C. J Biol Chem 274:19807-19813
-
(1999)
J Biol Chem
, vol.274
, pp. 19807-19813
-
-
Zhou, Q.1
Ruiz-Lozano, P.2
Martone, M.E.3
Chen, J.4
-
41
-
-
0034616654
-
ENH, containing PDZ and LIM domains, heart/skeletal muscle-specific protein, associates with cytoskeletal proteins through the PDZ domain
-
Nakagawa N, Hoshijima M, Oyasu M, Saito N, Tanizawa K, Kuroda S (2000) ENH, containing PDZ and LIM domains, heart/skeletal muscle-specific protein, associates with cytoskeletal proteins through the PDZ domain. Biochem Biophys Res Commun 272:505-512
-
(2000)
Biochem Biophys Res Commun
, vol.272
, pp. 505-512
-
-
Nakagawa, N.1
Hoshijima, M.2
Oyasu, M.3
Saito, N.4
Tanizawa, K.5
Kuroda, S.6
-
42
-
-
0029893923
-
Cardiovascular lesions and skeletal myopathy in mice lacking desmin
-
Li Z, Colucci-Guyon E, Pincon-Raymond M, Mericskay M, Pournin S, Paulin D, Babinet C (1996) Cardiovascular lesions and skeletal myopathy in mice lacking desmin. Dev Biol 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
Babinet, C.7
-
43
-
-
0029738727
-
Disruption of muscle architecture and myocardial degeneration in mice lacking desmin
-
Milner DJ, Weitzer G, Tran D, Bradley A, Capetanaki Y (1996) Disruption of muscle architecture and myocardial degeneration in mice lacking desmin. J Cell Biol 134:1255-1270
-
(1996)
J Cell Biol
, vol.134
, pp. 1255-1270
-
-
Milner, D.J.1
Weitzer, G.2
Tran, D.3
Bradley, A.4
Capetanaki, Y.5
-
44
-
-
0036872241
-
Desmin cytoskeleton: A potential regulator of muscle mitochondrial behavior and function
-
Capetanaki Y (2002) Desmin cytoskeleton: a potential regulator of muscle mitochondrial behavior and function. Trends Cardiovasc Med 12:339-348
-
(2002)
Trends Cardiovasc Med
, vol.12
, pp. 339-348
-
-
Capetanaki, Y.1
-
45
-
-
20844453758
-
Requirement of nuclear factor-kappaB in angiotensin II- and isoproterenol-induced cardiac hypertrophy in vivo
-
Freund C, Schmidt-Ullrich R, Baurand A, Dunger S, Schneider W, Loser P, El Jamali A, Dietz R, Scheidereit C, Bergmann MW (2005) Requirement of nuclear factor-kappaB in angiotensin II- and isoproterenol-induced cardiac hypertrophy in vivo. Circulation 111:2319-2325
-
(2005)
Circulation
, vol.111
, pp. 2319-2325
-
-
Freund, C.1
Schmidt-Ullrich, R.2
Baurand, A.3
Dunger, S.4
Schneider, W.5
Loser, P.6
El Jamali, A.7
Dietz, R.8
Scheidereit, C.9
Bergmann, M.W.10
-
46
-
-
33751234251
-
Airway epithelial repair, regeneration, and remodeling after injury in chronic obstructive pulmonary disease
-
Puchelle E, Zahm JM, Tournier JM, Coraux C (2006) Airway epithelial repair, regeneration, and remodeling after injury in chronic obstructive pulmonary disease. Proc Am Thorac Soc 3:726-733
-
(2006)
Proc Am Thorac Soc
, vol.3
, pp. 726-733
-
-
Puchelle, E.1
Zahm, J.M.2
Tournier, J.M.3
Coraux, C.4
-
47
-
-
25644456042
-
Cellular and molecular mechanisms of the epithelial repair in IBD
-
Suppl 1
-
Okamoto R, Watanabe M (2005) Cellular and molecular mechanisms of the epithelial repair in IBD. Dig Dis Sci 50(Suppl 1):S34-S38
-
(2005)
Dig Dis Sci
, vol.50
-
-
Okamoto, R.1
Watanabe, M.2
-
48
-
-
3242801462
-
A patient with limb girdle muscular dystrophy type 2B (LGMD2B) manifesting cardiomyopathy
-
Kuru S, Yasuma F, Wakayama T, Kimura S, Konagaya M, Aoki M, Tanabe M, Takahashi T (2004) A patient with limb girdle muscular dystrophy type 2B (LGMD2B) manifesting cardiomyopathy. Rinsho Shinkeigaku 44:375-378
-
(2004)
Rinsho Shinkeigaku
, vol.44
, pp. 375-378
-
-
Kuru, S.1
Yasuma, F.2
Wakayama, T.3
Kimura, S.4
Konagaya, M.5
Aoki, M.6
Tanabe, M.7
Takahashi, T.8
|