-
1
-
-
0025998134
-
Population frequencies of inherited neuromuscular diseases: A world survey
-
Emery AE. Population frequencies of inherited neuromuscular diseases: a world survey. Neuromuscul Disord 1991; 1:19-29.
-
(1991)
Neuromuscul Disord
, vol.1
, pp. 19-29
-
-
Emery, A.E.1
-
2
-
-
70350046640
-
Prevalence of Duchenne/Becker muscular dystrophy among males aged 5-24 years - Four states, 2007
-
Romitti P, Puzhankara S, Mathews K, et al. Prevalence of Duchenne/Becker muscular dystrophy among males aged 5-24 years - four states, 2007. MMWR Morb Mortal Wkly Rep 2009; 58:1119-1122.
-
(2009)
MMWR Morb Mortal Wkly Rep
, vol.58
, pp. 1119-1122
-
-
Romitti, P.1
Puzhankara, S.2
Mathews, K.3
-
3
-
-
41749096186
-
Glucocorticoid corticosteroids for Duchenne muscular dystrophy
-
Manzur AY, Kuntzer T, Pike M, et al. Glucocorticoid corticosteroids for Duchenne muscular dystrophy. Cochrane Database Syst Rev 2008; CD003725.
-
(2008)
Cochrane Database Syst Rev
, pp. CD003725
-
-
Manzur, A.Y.1
Kuntzer, T.2
Pike, M.3
-
4
-
-
19244363787
-
Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation
-
McNally EM, Passos-Bueno MR, Bonnemann CG, et al. Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation. Am J Hum Genet 1996; 59:1040-1047.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 1040-1047
-
-
McNally, E.M.1
Passos-Bueno, M.R.2
Bonnemann, C.G.3
-
5
-
-
79959250326
-
Latent TGF-beta structure and activation
-
Shi M, Zhu J, Wang R, et al. Latent TGF-beta structure and activation. Nature 2011; 474:343-349.
-
(2011)
Nature
, vol.474
, pp. 343-349
-
-
Shi, M.1
Zhu, J.2
Wang, R.3
-
6
-
-
3242802874
-
TGF-beta-induced SMAD signaling and gene regulation: Consequences for extracellular matrix remodeling and wound healing
-
Schiller M, Javelaud D, Mauviel A. TGF-beta-induced SMAD signaling and gene regulation: consequences for extracellular matrix remodeling and wound healing. J Dermatol Sci 2004; 35:83-92.
-
(2004)
J Dermatol Sci
, vol.35
, pp. 83-92
-
-
Schiller, M.1
Javelaud, D.2
Mauviel, A.3
-
7
-
-
0037204990
-
Signal transduction by the TGF-beta superfamily
-
Attisano L, Wrana JL. Signal transduction by the TGF-beta superfamily. Science 2002; 296:1646-1647.
-
(2002)
Science
, vol.296
, pp. 1646-1647
-
-
Attisano, L.1
Wrana, J.L.2
-
8
-
-
39049121312
-
How the Smads regulate transcription
-
Ross S, Hill CS. How the Smads regulate transcription. Int J Biochem Cell Biol 2008; 40:383-408.
-
(2008)
Int J Biochem Cell Biol
, vol.40
, pp. 383-408
-
-
Ross, S.1
Hill, C.S.2
-
9
-
-
0033104505
-
TGF-beta induces fibronectin synthesis through a c-Jun N-terminal kinase-dependent, Smad4-independent pathway
-
Hocevar BA, Brown TL, Howe PH. TGF-beta induces fibronectin synthesis through a c-Jun N-terminal kinase-dependent, Smad4-independent pathway. EMBO J 1999; 18:1345-1356.
-
(1999)
EMBO J
, vol.18
, pp. 1345-1356
-
-
Hocevar, B.A.1
Brown, T.L.2
Howe, P.H.3
-
10
-
-
84919459069
-
A Wnt-TGFbeta2 axis induces a fibrogenic program in muscle stem cells from dystrophic mice
-
Biressi S, Miyabara EH, Gopinath SD, et al. A Wnt-TGFbeta2 axis induces a fibrogenic program in muscle stem cells from dystrophic mice. Sci Transl Med 2014; 6:267ra176.
-
(2014)
Sci Transl Med
, vol.6
, pp. 267ra176
-
-
Biressi, S.1
Miyabara, E.H.2
Gopinath, S.D.3
-
11
-
-
0036549082
-
Control of connective tissue gene expression by TGF beta: Role of Smad proteins in fibrosis
-
Verrecchia F, Mauviel A. Control of connective tissue gene expression by TGF beta: role of Smad proteins in fibrosis. Curr Rheumatol Rep 2002; 4:143-149.
-
(2002)
Curr Rheumatol Rep
, vol.4
, pp. 143-149
-
-
Verrecchia, F.1
Mauviel, A.2
-
12
-
-
84920677763
-
A phase 1/2a follistatin gene therapy trial for becker muscular dystrophy
-
Mendell JR, Sahenk Z, Malik V, et al. A phase 1/2a follistatin gene therapy trial for becker muscular dystrophy. Mol Ther 2015; 23:192-201.
-
(2015)
Mol Ther
, vol.23
, pp. 192-201
-
-
Mendell, J.R.1
Sahenk, Z.2
Malik, V.3
-
13
-
-
25444505994
-
Early onset of inflammation and later involvement of TGFbeta in Duchenne muscular dystrophy
-
Chen YW, Nagaraju K, Bakay M, et al. Early onset of inflammation and later involvement of TGFbeta in Duchenne muscular dystrophy. Neurology 2005; 65:826-834.
-
(2005)
Neurology
, vol.65
, pp. 826-834
-
-
Chen, Y.W.1
Nagaraju, K.2
Bakay, M.3
-
14
-
-
84867004601
-
TGFbeta signaling: Its role in fibrosis formation and myopathies
-
MacDonald EM, Cohn RD. TGFbeta signaling: its role in fibrosis formation and myopathies. Curr Opin Rheumatol 2012; 24:628-634.
-
(2012)
Curr Opin Rheumatol
, vol.24
, pp. 628-634
-
-
MacDonald, E.M.1
Cohn, R.D.2
-
15
-
-
0029153067
-
Expression of transforming growth factor-beta 1 in dystrophic patient muscles correlates with fibrosis. Pathogenetic role of a fibrogenic cytokine
-
Bernasconi P, Torchiana E, Confalonieri P, et al. Expression of transforming growth factor-beta 1 in dystrophic patient muscles correlates with fibrosis. Pathogenetic role of a fibrogenic cytokine. J Clin Invest 1995; 96:1137-1144.
-
(1995)
J Clin Invest
, vol.96
, pp. 1137-1144
-
-
Bernasconi, P.1
Torchiana, E.2
Confalonieri, P.3
-
16
-
-
84857993316
-
Differential expression of genes involved in the degeneration and regeneration pathways in mouse models for muscular dystrophies
-
Onofre-Oliveira PC, Santos AL, Martins PM, et al. Differential expression of genes involved in the degeneration and regeneration pathways in mouse models for muscular dystrophies. Neuromolecular Med 2012; 14:74-83.
-
(2012)
Neuromolecular Med
, vol.14
, pp. 74-83
-
-
Onofre-Oliveira, P.C.1
Santos, A.L.2
Martins, P.M.3
-
17
-
-
33645672459
-
Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome
-
Habashi JP, Judge DP, Holm TM, et al. Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome. Science 2006; 312:117-121.
-
(2006)
Science
, vol.312
, pp. 117-121
-
-
Habashi, J.P.1
Judge, D.P.2
Holm, T.M.3
-
18
-
-
79955882466
-
Losartan restores skeletal muscle remodeling and protects against disuse atrophy in sarcopenia
-
Burks TN, Andres-Mateos E, Marx R, et al. Losartan restores skeletal muscle remodeling and protects against disuse atrophy in sarcopenia. Sci Transl Med 2011; 3:82ra37.
-
(2011)
Sci Transl Med
, vol.3
, pp. 82ra37
-
-
Burks, T.N.1
Andres-Mateos, E.2
Marx, R.3
-
19
-
-
79959470063
-
Inhibiting TGF-beta activity improves respiratory function in mdx mice
-
Nelson CA, Hunter RB, Quigley LA, et al. Inhibiting TGF-beta activity improves respiratory function in mdx mice. Am J Pathol 2011; 178:2611-2621.
-
(2011)
Am J Pathol
, vol.178
, pp. 2611-2621
-
-
Nelson, C.A.1
Hunter, R.B.2
Quigley, L.A.3
-
20
-
-
84908367208
-
Asynchronous remodeling is a driver of failed regeneration in Duchenne muscular dystrophy
-
Dadgar S, Wang Z, Johnston H, et al. Asynchronous remodeling is a driver of failed regeneration in Duchenne muscular dystrophy. J Cell Biol 2014; 207:139-158.
-
(2014)
J Cell Biol
, vol.207
, pp. 139-158
-
-
Dadgar, S.1
Wang, Z.2
Johnston, H.3
-
21
-
-
84922134591
-
Excess SMAD signaling contributes to heart and muscle dysfunction in muscular dystrophy
-
Goldstein JA, Bogdanovich S, Beiriger A, et al. Excess SMAD signaling contributes to heart and muscle dysfunction in muscular dystrophy. Hum Mol Genet 2014; 23:6722-6731.
-
(2014)
Hum Mol Genet
, vol.23
, pp. 6722-6731
-
-
Goldstein, J.A.1
Bogdanovich, S.2
Beiriger, A.3
-
22
-
-
84929896576
-
Genetic disruption of Smad7 impairs skeletal muscle growth and regeneration
-
Cohen TV, Kollias HD, Liu N, et al. Genetic disruption of Smad7 impairs skeletal muscle growth and regeneration. J Physiol 2015; 593:2479-2497.
-
(2015)
J Physiol
, vol.593
, pp. 2479-2497
-
-
Cohen, T.V.1
Kollias, H.D.2
Liu, N.3
-
23
-
-
84941758541
-
Myofiber-specific inhibition of TGFbeta signaling protects skeletal muscle from injury and dystrophic disease in mice
-
Accornero F, Kanisicak O, Tjondrokoesoemo A, et al. Myofiber-specific inhibition of TGFbeta signaling protects skeletal muscle from injury and dystrophic disease in mice. Hum Mol Genet 2014; 23:6903-6915.
-
(2014)
Hum Mol Genet
, vol.23
, pp. 6903-6915
-
-
Accornero, F.1
Kanisicak, O.2
Tjondrokoesoemo, A.3
-
24
-
-
84922519082
-
Targeting TGF-beta signaling by antisense oligonucleotide-mediated knockdown of TGF-beta type i receptor
-
Kemaladewi DU, Pasteuning S, van der Meulen JW, et al. Targeting TGF-beta signaling by antisense oligonucleotide-mediated knockdown of TGF-beta type I receptor. Mol Ther Nucleic Acids 2014; 3:e156.
-
(2014)
Mol Ther Nucleic Acids
, vol.3
, pp. e156
-
-
Kemaladewi, D.U.1
Pasteuning, S.2
Van Der Meulen, J.W.3
-
25
-
-
48949116144
-
Osteopontin and skeletal muscle myoblasts: Association with muscle regeneration and regulation of myoblast function in vitro
-
Uaesoontrachoon K, Yoo HJ, Tudor EM, et al. Osteopontin and skeletal muscle myoblasts: association with muscle regeneration and regulation of myoblast function in vitro. Int J Biochem Cell Biol 2008; 40:2303-2314.
-
(2008)
Int J Biochem Cell Biol
, vol.40
, pp. 2303-2314
-
-
Uaesoontrachoon, K.1
Yoo, H.J.2
Tudor, E.M.3
-
26
-
-
0034740591
-
TGFbeta and BMP-2 activation of the OPN promoter: Roles of smad- and hox-binding elements
-
Hullinger TG, Pan Q, Viswanathan HL, et al. TGFbeta and BMP-2 activation of the OPN promoter: roles of smad- and hox-binding elements. Exp Cell Res 2001; 262:69-74.
-
(2001)
Exp Cell Res
, vol.262
, pp. 69-74
-
-
Hullinger, T.G.1
Pan, Q.2
Viswanathan, H.L.3
-
27
-
-
84866240116
-
TGFBR2 but not SPP1 genotype modulates osteopontin expression in Duchenne muscular dystrophy muscle
-
Piva L, Gavassini BF, Bello L, et al. TGFBR2 but not SPP1 genotype modulates osteopontin expression in Duchenne muscular dystrophy muscle. J Pathol 2012; 228:251-259.
-
(2012)
J Pathol
, vol.228
, pp. 251-259
-
-
Piva, L.1
Gavassini, B.F.2
Bello, L.3
-
28
-
-
67650739257
-
A genetic polymorphism in transforming growth factor beta receptor-2 is associated with serum osteopontin
-
Biros E, Clancy P, Norman PE, et al. A genetic polymorphism in transforming growth factor beta receptor-2 is associated with serum osteopontin. Int J Immunogenet 2009; 36:241-244.
-
(2009)
Int J Immunogenet
, vol.36
, pp. 241-244
-
-
Biros, E.1
Clancy, P.2
Norman, P.E.3
-
29
-
-
67651005390
-
Osteopontin promotes fibrosis in dystrophic mouse muscle by modulating immune cell subsets and intramuscular TGF-beta
-
Vetrone SA, Montecino-Rodriguez E, Kudryashova E, et al. Osteopontin promotes fibrosis in dystrophic mouse muscle by modulating immune cell subsets and intramuscular TGF-beta. J Clin Invest 2009; 119:1583-1594.
-
(2009)
J Clin Invest
, vol.119
, pp. 1583-1594
-
-
Vetrone, S.A.1
Montecino-Rodriguez, E.2
Kudryashova, E.3
-
30
-
-
78751634526
-
SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy
-
Pegoraro E, Hoffman EP, Piva L, et al. SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy. Neurology 2011; 76:219-226.
-
(2011)
Neurology
, vol.76
, pp. 219-226
-
-
Pegoraro, E.1
Hoffman, E.P.2
Piva, L.3
-
31
-
-
15244354176
-
Polymorphisms in the osteopontin promoter affect its transcriptional activity
-
Giacopelli F, Marciano R, Pistorio A, et al. Polymorphisms in the osteopontin promoter affect its transcriptional activity. Physiol Genomics 2004; 20: 87-96.
-
(2004)
Physiol Genomics
, vol.20
, pp. 87-96
-
-
Giacopelli, F.1
Marciano, R.2
Pistorio, A.3
-
32
-
-
84925643643
-
Genetic modifiers of ambulation in the cooperative international Neuromuscular research group Duchenne natural history study
-
Bello L, Kesari A, Gordish-Dressman H, et al. Genetic modifiers of ambulation in the cooperative international Neuromuscular research group Duchenne natural history study. Ann Neurol 2015; 77:684-696.
-
(2015)
Ann Neurol
, vol.77
, pp. 684-696
-
-
Bello, L.1
Kesari, A.2
Gordish-Dressman, H.3
-
33
-
-
84866252725
-
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy
-
Bello L, Piva L, Barp A, et al. Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy. Neurology 2012; 79:159-162.
-
(2012)
Neurology
, vol.79
, pp. 159-162
-
-
Bello, L.1
Piva, L.2
Barp, A.3
-
34
-
-
84942104192
-
Validation of genetic modifiers for Duchenne muscular dystrophy: A multicentre study assessing SPP1 and LTBP4 variants
-
[Epub ahead of print]
-
van den Bergen JC, Hiller M, Bohringer S, et al. Validation of genetic modifiers for Duchenne muscular dystrophy: a multicentre study assessing SPP1 and LTBP4 variants. J Neurol Neurosurg Psychiatry 2014. [Epub ahead of print]. doi: 10.1136/jnnp-2014-308409.
-
(2014)
J Neurol Neurosurg Psychiatry
-
-
Van Den Bergen, J.C.1
Hiller, M.2
Bohringer, S.3
-
35
-
-
84878390222
-
LTBP4 genotype predicts age of ambulatory loss in Duchenne muscular dystrophy
-
Flanigan KM, Ceco E, Lamar KM, et al. LTBP4 genotype predicts age of ambulatory loss in Duchenne muscular dystrophy. Ann Neurol 2013; 73: 481-488.
-
(2013)
Ann Neurol
, vol.73
, pp. 481-488
-
-
Flanigan, K.M.1
Ceco, E.2
Lamar, K.M.3
-
36
-
-
30744443289
-
Common pathological mechanisms in mouse models for muscular dystrophies
-
Turk R, Sterrenburg E, van der Wees CG, et al. Common pathological mechanisms in mouse models for muscular dystrophies. Faseb j 2006; 20:127-129.
-
(2006)
Faseb J
, vol.20
, pp. 127-129
-
-
Turk, R.1
Sterrenburg, E.2
Van Der Wees, C.G.3
-
37
-
-
0033840527
-
Specific sequence motif of 8-Cys repeats of TGFbeta binding proteins, LTBPs, creates a hydrophobic interaction surface for binding of small latent TGF-beta
-
Saharinen J, Keski-Oja J. Specific sequence motif of 8-Cys repeats of TGFbeta binding proteins, LTBPs, creates a hydrophobic interaction surface for binding of small latent TGF-beta. Mol Biol Cell 2000; 11:2691-2704.
-
(2000)
Mol Biol Cell
, vol.11
, pp. 2691-2704
-
-
Saharinen, J.1
Keski-Oja, J.2
-
38
-
-
84936765397
-
Latent transforming growth factor binding protein 4 regulates transforming growth factor beta receptor stability
-
Su CT, Huang JW, Chiang CK, et al. Latent transforming growth factor binding protein 4 regulates transforming growth factor beta receptor stability. Hum Mol Genet 2015; 14:4024-4036.
-
(2015)
Hum Mol Genet
, vol.14
, pp. 4024-4036
-
-
Su, C.T.1
Huang, J.W.2
Chiang, C.K.3
-
39
-
-
84855525455
-
LTBPs, more than just an escort service
-
Todorovic V, Rifkin DB. LTBPs, more than just an escort service. J Cell Biochem 2012; 113:410-418.
-
(2012)
J Cell Biochem
, vol.113
, pp. 410-418
-
-
Todorovic, V.1
Rifkin, D.B.2
-
40
-
-
72849135317
-
Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice
-
Heydemann A, Ceco E, Lim JE, et al. Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice. J Clin Invest 2009; 119:3703-3712.
-
(2009)
J Clin Invest
, vol.119
, pp. 3703-3712
-
-
Heydemann, A.1
Ceco, E.2
Lim, J.E.3
-
41
-
-
84908426315
-
Targeting latent TGFbeta release in muscular dystrophy
-
Ceco E, Bogdanovich S, Gardner B, et al. Targeting latent TGFbeta release in muscular dystrophy. Sci Transl Med 2014; 6:259ra144.
-
(2014)
Sci Transl Med
, vol.6
, pp. 259ra144
-
-
Ceco, E.1
Bogdanovich, S.2
Gardner, B.3
-
42
-
-
78651360166
-
Distinct genetic regions modify specific muscle groups in muscular dystrophy
-
Swaggart KA, Heydemann A, Palmer AA, et al. Distinct genetic regions modify specific muscle groups in muscular dystrophy. Physiol Genomics 2011; 43:24-31.
-
(2011)
Physiol Genomics
, vol.43
, pp. 24-31
-
-
Swaggart, K.A.1
Heydemann, A.2
Palmer, A.A.3
-
43
-
-
84899083880
-
Annexin A6 modifies muscular dystrophy by mediating sarcolemmal repair
-
Swaggart KA, Demonbreun AR, Vo AH, et al. Annexin A6 modifies muscular dystrophy by mediating sarcolemmal repair. Proc Natl Acad Sci U S A 2014; 111:6004-6009.
-
(2014)
Proc Natl Acad Sci U S A
, vol.111
, pp. 6004-6009
-
-
Swaggart, K.A.1
Demonbreun, A.R.2
Vo, A.H.3
-
45
-
-
20344369564
-
Annexins: Linking Ca2+ signalling to membrane dynamics
-
Gerke V, Creutz CE, Moss SE. Annexins: linking Ca2+ signalling to membrane dynamics. Nat Rev Mol Cell Biol 2005; 6:449-461.
-
(2005)
Nat Rev Mol Cell Biol
, vol.6
, pp. 449-461
-
-
Gerke, V.1
Creutz, C.E.2
Moss, S.E.3
-
46
-
-
84924431318
-
Annexin-A5 promotes membrane resealing in human trophoblasts
-
[Epub ahead of print]
-
Carmeille R, Degrelle SA, Plawinski L, et al. Annexin-A5 promotes membrane resealing in human trophoblasts. Biochim Biophys Acta 2015; doi:10.1016/ j.bbamcr.2014.12.038. [Epub ahead of print]
-
(2015)
Biochim Biophys Acta
-
-
Carmeille, R.1
Degrelle, S.A.2
Plawinski, L.3
-
47
-
-
0347379869
-
Dysferlin interacts with annexins A1 and A2 and mediates sarcolemmal wound-healing
-
Lennon NJ, Kho A, Bacskai BJ, et al. Dysferlin interacts with annexins A1 and A2 and mediates sarcolemmal wound-healing. J Biol Chem 2003; 278: 50466-50473.
-
(2003)
J Biol Chem
, vol.278
, pp. 50466-50473
-
-
Lennon, N.J.1
Kho, A.2
Bacskai, B.J.3
-
48
-
-
33746701373
-
Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophies
-
Cagliani R, Magri F, Toscano A, et al. Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophies. Hum Mutat 2005; 26:283.
-
(2005)
Hum Mutat
, vol.26
, pp. 283
-
-
Cagliani, R.1
Magri, F.2
Toscano, A.3
-
49
-
-
84858198502
-
In vivo imaging of molecular interactions at damaged sarcolemma
-
Roostalu U, Strahle U. In vivo imaging of molecular interactions at damaged sarcolemma. Dev Cell 2012; 22:515-529.
-
(2012)
Dev Cell
, vol.22
, pp. 515-529
-
-
Roostalu, U.1
Strahle, U.2
-
50
-
-
84922213768
-
Circulating annexin A2 as a biomarker in gastric cancer patients: Correlation with clinical variables
-
Tas F, Tilgen Yasasever C, Karabulut S, et al. Circulating annexin A2 as a biomarker in gastric cancer patients: correlation with clinical variables. Biomed Pharmacother 2015; 69:237-241.
-
(2015)
Biomed Pharmacother
, vol.69
, pp. 237-241
-
-
Tas, F.1
Tilgen Yasasever, C.2
Karabulut, S.3
|