-
3
-
-
0002639380
-
Recherches sur la paralysie musculaire pseudohypertrophique ou paralysie myo-sclerosique
-
Duchenne GBA (1868) Recherches sur la paralysie musculaire pseudohypertrophique ou paralysie myo-sclerosique. Arch Gen Med 11:5-528
-
(1868)
Arch Gen Med
, vol.11
, pp. 5-528
-
-
Duchenne, G.B.A.1
-
4
-
-
0016688758
-
Neuromuscular disorders in childhood. Old dogmas, new concepts
-
Dubowitz V (1975) Neuromuscular disorders in childhood. Old dogmas, new concepts. Arch Dis Child 50:335-346
-
(1975)
Arch Dis Child
, vol.50
, pp. 335-346
-
-
Dubowitz, V.1
-
7
-
-
0026795393
-
Extraocular muscles are spared in advanced Duchenne dystrophy
-
Kaminski HJ, al Hakim M, Leigh RJ, Katirji MB, Ruff RL (1992) Extraocular muscles are spared in advanced Duchenne dystrophy. Ann Neurol 32:586-588
-
(1992)
Ann Neurol
, vol.32
, pp. 586-588
-
-
Kaminski, H.J.1
Al Hakim, M.2
Leigh, R.J.3
Katirji, M.B.4
Ruff, R.L.5
-
8
-
-
0029143830
-
Absence of extraocular muscle pathology in Duchenne's muscular dystrophy: Role for calcium homeostasis in extraocular muscle sparing
-
Khurana TS, Prendergast RA, Alameddine HS, Tome FM, Fardeau M, Arahata K, Sugita H, Kunkel LM (1995) Absence of extraocular muscle pathology in Duchenne's muscular dystrophy: role for calcium homeostasis in extraocular muscle sparing. J Exp Med 182:467-475
-
(1995)
J Exp Med
, vol.182
, pp. 467-475
-
-
Khurana, T.S.1
Prendergast, R.A.2
Alameddine, H.S.3
Tome, F.M.4
Fardeau, M.5
Arahata, K.6
Sugita, H.7
Kunkel, L.M.8
-
10
-
-
0022444372
-
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy
-
Kunkel LM et al. (1986) Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy. Nature 322:73-77
-
(1986)
Nature
, vol.322
, pp. 73-77
-
-
Kunkel, L.M.1
-
11
-
-
0022496289
-
Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene
-
Monaco AP, Neve RL, Colletti-Feener C, Bertelson CJ, Kurnit DM, Kunkel LM (1986) Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene. Nature 323:646-650
-
(1986)
Nature
, vol.323
, pp. 646-650
-
-
Monaco, A.P.1
Neve, R.L.2
Colletti-Feener, C.3
Bertelson, C.J.4
Kurnit, D.M.5
Kunkel, L.M.6
-
12
-
-
0023614271
-
Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
-
Koenig M, Hoffman EP, Bertelson CJ, Monaco AP, Feener C, Kunkel LM (1987) Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 50:509-517
-
(1987)
Cell
, vol.50
, pp. 509-517
-
-
Koenig, M.1
Hoffman, E.P.2
Bertelson, C.J.3
Monaco, A.P.4
Feener, C.5
Kunkel, L.M.6
-
13
-
-
0023614188
-
Dystrophin: The protein product of the Duchenne muscular dystrophy locus
-
Hoffman EP, Brown RHJr, Kunkel LM (1987) Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 51:919-928
-
(1987)
Cell
, vol.51
, pp. 919-928
-
-
Hoffman, E.P.1
Brown Jr., R.H.2
Kunkel, L.M.3
-
14
-
-
0026535028
-
A yeast artificial chromosome contig containing the complete Duchenne muscular dystrophy gene
-
Monaco AP, Walker AP, Millwood I, Larin Z, Lehrach H (1992) A yeast artificial chromosome contig containing the complete Duchenne muscular dystrophy gene. Genomics 12:465-473
-
(1992)
Genomics
, vol.12
, pp. 465-473
-
-
Monaco, A.P.1
Walker, A.P.2
Millwood, I.3
Larin, Z.4
Lehrach, H.5
-
15
-
-
0026608273
-
Construction of a 2.6-Mb contig in yeast artificial chromosomes spanning the human dystrophin gene using an STS-based approach
-
Coffey AJ, Roberts RG, Green ED, Cole CG, Butler R, Anand R, Giannelli F, Bentley DR (1992) Construction of a 2.6-Mb contig in yeast artificial chromosomes spanning the human dystrophin gene using an STS-based approach. Genomics 12:474-484
-
(1992)
Genomics
, vol.12
, pp. 474-484
-
-
Coffey, A.J.1
Roberts, R.G.2
Green, E.D.3
Cole, C.G.4
Butler, R.5
Anand, R.6
Giannelli, F.7
Bentley, D.R.8
-
16
-
-
0023904860
-
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein
-
Koenig M, Monaco AP, Kunkel LM (1988) The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein. Cell 53:219-226
-
(1988)
Cell
, vol.53
, pp. 219-226
-
-
Koenig, M.1
Monaco, A.P.2
Kunkel, L.M.3
-
18
-
-
0023942674
-
Expression of the murine Duchenne muscular dystrophy gene in muscle and brain
-
Chamberlain JS, Pearlman JA, Muzny DM, Gibbs RA, Ranier JE, Caskey CT, Reeves AA (1988) Expression of the murine Duchenne muscular dystrophy gene in muscle and brain. Science 239:1416-1418
-
(1988)
Science
, vol.239
, pp. 1416-1418
-
-
Chamberlain, J.S.1
Pearlman, J.A.2
Muzny, D.M.3
Gibbs, R.A.4
Ranier, J.E.5
Caskey, C.T.6
Reeves, A.A.7
-
19
-
-
0023906398
-
Expression of the putative Duchenne muscular dystrophy gene in differentiated myogenic cell cultures and in the brain
-
Nudel U, Robzyk K, Yaffe D (1988) Expression of the putative Duchenne muscular dystrophy gene in differentiated myogenic cell cultures and in the brain. Nature 331:635-638
-
(1988)
Nature
, vol.331
, pp. 635-638
-
-
Nudel, U.1
Robzyk, K.2
Yaffe, D.3
-
20
-
-
0024300196
-
Immunoelectron microscopic localization of dystrophin in myofibres
-
Watkins SC, Hoffman EP, Slayter HS, Kunkel LM (1988) Immunoelectron microscopic localization of dystrophin in myofibres. Nature 333:863-866
-
(1988)
Nature
, vol.333
, pp. 863-866
-
-
Watkins, S.C.1
Hoffman, E.P.2
Slayter, H.S.3
Kunkel, L.M.4
-
21
-
-
0023877613
-
Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide
-
Arahata K, Ishiura S, Ishiguro T, Tsukahara T, Suhara Y, Eguchi C, Ishihara T, Nonaka I, Ozawa E, Sugita H (1988) Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide. Nature 333:861-863
-
(1988)
Nature
, vol.333
, pp. 861-863
-
-
Arahata, K.1
Ishiura, S.2
Ishiguro, T.3
Tsukahara, T.4
Suhara, Y.5
Eguchi, C.6
Ishihara, T.7
Nonaka, I.8
Ozawa, E.9
Sugita, H.10
-
22
-
-
0023925292
-
The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle
-
Zubrzycka-Gaarn EE, Bulman DE, Karpati G, Burghes AH, Belfall B, Klamut HJ, Talbot J, Hodges RS, Ray PN, Worton RG (1988) The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle. Nature 333:466-469
-
(1988)
Nature
, vol.333
, pp. 466-469
-
-
Zubrzycka-Gaarn, E.E.1
Bulman, D.E.2
Karpati, G.3
Burghes, A.H.4
Belfall, B.5
Klamut, H.J.6
Talbot, J.7
Hodges, R.S.8
Ray, P.N.9
Worton, R.G.10
-
23
-
-
0025368276
-
Immunocytochemical study of dystrophin at the myotendinous junction
-
Samitt CE, Bonilla E (1990) Immunocytochemical study of dystrophin at the myotendinous junction. Muscle Nerve 13:493-500
-
(1990)
Muscle Nerve
, vol.13
, pp. 493-500
-
-
Samitt, C.E.1
Bonilla, E.2
-
24
-
-
0025931224
-
The subcellular distribution of dystrophin in mouse skeletal, cardiac, and smooth muscle
-
Byers TJ, Kunkel LM, Watkins SC (1991) The subcellular distribution of dystrophin in mouse skeletal, cardiac, and smooth muscle. J Cell Biol 115:411-421
-
(1991)
J Cell Biol
, vol.115
, pp. 411-421
-
-
Byers, T.J.1
Kunkel, L.M.2
Watkins, S.C.3
-
25
-
-
0025750804
-
Localization of dystrophin relative to acetylcholine receptor domains in electric tissue and adult and cultured skeletal muscle
-
Sealock R, Butler MH, Kramarcy NR, Gao KX, Murnane AA, Douville K, Froehner SC (1991) Localization of dystrophin relative to acetylcholine receptor domains in electric tissue and adult and cultured skeletal muscle. J Cell Biol 113:1133-1144
-
(1991)
J Cell Biol
, vol.113
, pp. 1133-1144
-
-
Sealock, R.1
Butler, M.H.2
Kramarcy, N.R.3
Gao, K.X.4
Murnane, A.A.5
Douville, K.6
Froehner, S.C.7
-
26
-
-
0023718118
-
An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus
-
Monaco AP, Bertelson CJ, Liechti-Gallati S, Moser H, Kunkel LM (1988) An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus. Genomics 2:90-95
-
(1988)
Genomics
, vol.2
, pp. 90-95
-
-
Monaco, A.P.1
Bertelson, C.J.2
Liechti-Gallati, S.3
Moser, H.4
Kunkel, L.M.5
-
27
-
-
0028247187
-
Half the dystrophin gene is apparently enough for a mild clinical course: Confirmation of its potential use for gene therapy
-
Passos-Bueno MR, Vainzof M, Marie SK, Zatz M (1994) Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapy. Hum Mol Genet 3:919-922
-
(1994)
Hum Mol Genet
, vol.3
, pp. 919-922
-
-
Passos-Bueno, M.R.1
Vainzof, M.2
Marie, S.K.3
Zatz, M.4
-
28
-
-
0025159208
-
Very mild muscular dystrophy associated with the deletion of 46% of dystrophin
-
England SB, Nicholson LV, Johnson MA, Forrest SM, Love DR, Zubrzycka-Gaarn EE, Bulman DE, Harris JB, Davies KE (1990) Very mild muscular dystrophy associated with the deletion of 46% of dystrophin. Nature 343:180-182
-
(1990)
Nature
, vol.343
, pp. 180-182
-
-
England, S.B.1
Nicholson, L.V.2
Johnson, M.A.3
Forrest, S.M.4
Love, D.R.5
Zubrzycka-Gaarn, E.E.6
Bulman, D.E.7
Harris, J.B.8
Davies, K.E.9
-
29
-
-
0027174251
-
Direct retroviral-mediated transfer of a dystrophin minigene into mdx mouse muscle in vivo
-
Dunckley MG, Wells DJ, Walsh FS, Dickson G (1993) Direct retroviral-mediated transfer of a dystrophin minigene into mdx mouse muscle in vivo. Hum Mol Genet 2:717-723
-
(1993)
Hum Mol Genet
, vol.2
, pp. 717-723
-
-
Dunckley, M.G.1
Wells, D.J.2
Walsh, F.S.3
Dickson, G.4
-
30
-
-
0027408847
-
Efficient adenovirus-mediated transfer of a human minidystrophin gene to skeletal muscle of mdx mice
-
Ragot T, Vincent N, Chafey P, Vigne E, Gilgenkrantz H, Couton D, Cartaud J, Briand P, Kaplan JC, Perricaudet M (1993) Efficient adenovirus-mediated transfer of a human minidystrophin gene to skeletal muscle of mdx mice. Nature 361:647-650
-
(1993)
Nature
, vol.361
, pp. 647-650
-
-
Ragot, T.1
Vincent, N.2
Chafey, P.3
Vigne, E.4
Gilgenkrantz, H.5
Couton, D.6
Cartaud, J.7
Briand, P.8
Kaplan, J.C.9
Perricaudet, M.10
-
31
-
-
0027483791
-
Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype
-
Vainzof M, Passos-Bueno MR, Takata RI, Pavanello RC, Zatz M (1993) Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype. J Neurol Sci 119:38-42
-
(1993)
J Neurol Sci
, vol.119
, pp. 38-42
-
-
Vainzof, M.1
Passos-Bueno, M.R.2
Takata, R.I.3
Pavanello, R.C.4
Zatz, M.5
-
32
-
-
0035168526
-
Long mutant dystrophins and variable phenotypes: Evasion of nonsense-mediated decay?
-
Kerr TP, Sewry CA, Robb SA, Roberts RG (2001) Long mutant dystrophins and variable phenotypes: evasion of nonsense-mediated decay? Hum Genet 109:402-407
-
(2001)
Hum Genet
, vol.109
, pp. 402-407
-
-
Kerr, T.P.1
Sewry, C.A.2
Robb, S.A.3
Roberts, R.G.4
-
33
-
-
0024299114
-
alpha-Actinins and the DMD protein contain spectrin-like repeats
-
Davison MD, Critchley DR (1988) alpha-Actinins and the DMD protein contain spectrin-like repeats. Cell 52:159-160
-
(1988)
Cell
, vol.52
, pp. 159-160
-
-
Davison, M.D.1
Critchley, D.R.2
-
35
-
-
0025217703
-
Detailed analysis of the repeat domain of dystrophin reveals four potential hinge segments that may confer flexibility
-
Koenig M, Kunkel LM (1990) Detailed analysis of the repeat domain of dystrophin reveals four potential hinge segments that may confer flexibility. J Biol Chem 265:4560-4566
-
(1990)
J Biol Chem
, vol.265
, pp. 4560-4566
-
-
Koenig, M.1
Kunkel, L.M.2
-
36
-
-
0029915066
-
Towards prediction of cognate complexes between the WW domain and proline-rich ligands
-
Einbond A, Sudol M (1996) Towards prediction of cognate complexes between the WW domain and proline-rich ligands. FEBS Lett 384:1-8
-
(1996)
FEBS Lett
, vol.384
, pp. 1-8
-
-
Einbond, A.1
Sudol, M.2
-
37
-
-
0030034593
-
ZZ and TAZ: New putative zinc fingers in dystrophin and other proteins
-
Ponting CP, Blake DJ, Davies KE, Kendrick-Jones J, Winder SJ (1996) ZZ and TAZ: new putative zinc fingers in dystrophin and other proteins. Trends Biochem Sci 21:11-13
-
(1996)
Trends Biochem Sci
, vol.21
, pp. 11-13
-
-
Ponting, C.P.1
Blake, D.J.2
Davies, K.E.3
Kendrick-Jones, J.4
Winder, S.J.5
-
38
-
-
0017316634
-
Mitochondrial calcium overload: A general mechanism for cell-necrosis in muscle diseases
-
Wrogemann K, Pena SD (1976) Mitochondrial calcium overload: a general mechanism for cell-necrosis in muscle diseases. Lancet I:672-674
-
(1976)
Lancet
, vol.1
, pp. 672-674
-
-
Wrogemann, K.1
Pena, S.D.2
-
39
-
-
0028047235
-
Dystrophin-glycoprotein complex: Its role in the molecular pathogenesis of muscular dystrophies
-
Matsumura K, Campbell KP (1994) Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies. Muscle Nerve 17:2-15
-
(1994)
Muscle Nerve
, vol.17
, pp. 2-15
-
-
Matsumura, K.1
Campbell, K.P.2
-
40
-
-
0028914964
-
Three muscular dystrophies: Loss of cytoskeleton-extracellular matrix linkage
-
Campbell KP (1995) Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage. Cell 80:675-679
-
(1995)
Cell
, vol.80
, pp. 675-679
-
-
Campbell, K.P.1
-
41
-
-
0036591684
-
Muscular dystrophies involving the dystrophin-glycoprotein complex: An overview of current mouse models
-
Durbeej M, Campbell KP (2002) Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models. Curr Opin Genet Dev 12:349-361
-
(2002)
Curr Opin Genet Dev
, vol.12
, pp. 349-361
-
-
Durbeej, M.1
Campbell, K.P.2
-
42
-
-
0030909575
-
Muscular dystrophies and the dystrophin-glycoprotein complex
-
Straub V, Campbell KP (1997) Muscular dystrophies and the dystrophin-glycoprotein complex. Curr Opin Neurol 10:168-175
-
(1997)
Curr Opin Neurol
, vol.10
, pp. 168-175
-
-
Straub, V.1
Campbell, K.P.2
-
44
-
-
0029089582
-
Dystrophin-associated proteins in muscular dystrophy
-
Ozawa E, Yoshida M, Suzuki A, Mizuno Y, Hagiwara Y, Noguchi S (1995) Dystrophin-associated proteins in muscular dystrophy. Hum Mol Genet 4:1711-1716
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1711-1716
-
-
Ozawa, E.1
Yoshida, M.2
Suzuki, A.3
Mizuno, Y.4
Hagiwara, Y.5
Noguchi, S.6
-
45
-
-
0026543686
-
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix
-
Ibraghimov-Beskrovnaya O, Ervasti JM, Leveille CJ, Slaughter CA, Sernett SW, Campbell KP (1992) Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix. Nature 355:696-702
-
(1992)
Nature
, vol.355
, pp. 696-702
-
-
Ibraghimov-Beskrovnaya, O.1
Ervasti, J.M.2
Leveille, C.J.3
Slaughter, C.A.4
Sernett, S.W.5
Campbell, K.P.6
-
46
-
-
0026695175
-
Glycoprotein-binding site of dystrophin is confined to the cysteine-rich domain and the first half of the carboxy-terminal domain
-
Suzuki A, Yoshida M, Yamamoto H, Ozawa E (1992) Glycoprotein-binding site of dystrophin is confined to the cysteine-rich domain and the first half of the carboxy-terminal domain. FEBS Lett 308:154-160
-
(1992)
FEBS Lett
, vol.308
, pp. 154-160
-
-
Suzuki, A.1
Yoshida, M.2
Yamamoto, H.3
Ozawa, E.4
-
47
-
-
0028206868
-
Molecular organization at the glycoprotein-complex-binding site of dystrophin. Three dystrophin-associated proteins bind directly to the carboxy-terminal portion of dystrophin
-
Suzuki A, Yoshida M, Hayashi K, Mizuno Y, Hagiwara Y, Ozawa E (1994) Molecular organization at the glycoprotein-complex-binding site of dystrophin. Three dystrophin-associated proteins bind directly to the carboxy-terminal portion of dystrophin. Eur J Biochem 220:283-292
-
(1994)
Eur J Biochem
, vol.220
, pp. 283-292
-
-
Suzuki, A.1
Yoshida, M.2
Hayashi, K.3
Mizuno, Y.4
Hagiwara, Y.5
Ozawa, E.6
-
48
-
-
0027275643
-
A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin
-
Ervasti JM, Campbell KP (1993) A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin. J Cell Biol 122:809-823
-
(1993)
J Cell Biol
, vol.122
, pp. 809-823
-
-
Ervasti, J.M.1
Campbell, K.P.2
-
49
-
-
0028044626
-
Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin
-
Matsumura K, Burghes AH, Mora M, Tome FM, Morandi L, Cornello F, Leturcq F, Jeanpierre M, Kaplan JC, Reinert P (1994) Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin. J Clin Invest 93:99-105
-
(1994)
J Clin Invest
, vol.93
, pp. 99-105
-
-
Matsumura, K.1
Burghes, A.H.2
Mora, M.3
Tome, F.M.4
Morandi, L.5
Cornello, F.6
Leturcq, F.7
Jeanpierre, M.8
Kaplan, J.C.9
Reinert, P.10
-
50
-
-
0024538824
-
An autosomal transcript in skeletal muscle with homology to dystrophin
-
Love DR, Hill DF, Dickson G, Spurr NK, Byth BC, Marsden RF, Walsh FS, Edwards YH, Davies KE (1989) An autosomal transcript in skeletal muscle with homology to dystrophin. Nature 339:55-58
-
(1989)
Nature
, vol.339
, pp. 55-58
-
-
Love, D.R.1
Hill, D.F.2
Dickson, G.3
Spurr, N.K.4
Byth, B.C.5
Marsden, R.F.6
Walsh, F.S.7
Edwards, Y.H.8
Davies, K.E.9
-
51
-
-
0025167294
-
Identification of a chromosome 6-encoded dystrophin-related protein
-
Khurana TS, Hoffman EP, Kunkel LM (1990) Identification of a chromosome 6-encoded dystrophin-related protein. J Biol Chem 265:16717-16720
-
(1990)
J Biol Chem
, vol.265
, pp. 16717-16720
-
-
Khurana, T.S.1
Hoffman, E.P.2
Kunkel, L.M.3
-
52
-
-
0026621049
-
Primary structure of dystrophin-related protein
-
Tinsley JM, Blake DJ, Roche A, Fairbrother U, Riss J, Byth BC, Knight AE, Kendrick-Jones J, Suthers GK, Love DR (1992) Primary structure of dystrophin-related protein. Nature 360:591-593
-
(1992)
Nature
, vol.360
, pp. 591-593
-
-
Tinsley, J.M.1
Blake, D.J.2
Roche, A.3
Fairbrother, U.4
Riss, J.5
Byth, B.C.6
Knight, A.E.7
Kendrick-Jones, J.8
Suthers, G.K.9
Love, D.R.10
-
53
-
-
0030006540
-
Characterization of DRP2, a novel human dystrophin homologue
-
Roberts RG, Freeman TC, Kendall E, Vetrie DL, Dixon AK, Shaw-Smith C, Bone Q, Bobrow M (1996) Characterization of DRP2, a novel human dystrophin homologue. Nat Genet 13:223-226
-
(1996)
Nat Genet
, vol.13
, pp. 223-226
-
-
Roberts, R.G.1
Freeman, T.C.2
Kendall, E.3
Vetrie, D.L.4
Dixon, A.K.5
Shaw-Smith, C.6
Bone, Q.7
Bobrow, M.8
-
54
-
-
23444461928
-
(CA) repeat polymorphism in the chromosome 18 encoded dystrophin-like protein
-
Khurana TS, Engle EC, Bennett RR, Silverman GA, Selig S, Bruns GA, Kunkel LM (1994) (CA) repeat polymorphism in the chromosome 18 encoded dystrophin-like protein. Hum Mol Genet 3:841
-
(1994)
Hum Mol Genet
, vol.3
, pp. 841
-
-
Khurana, T.S.1
Engle, E.C.2
Bennett, R.R.3
Silverman, G.A.4
Selig, S.5
Bruns, G.A.6
Kunkel, L.M.7
-
55
-
-
0029937712
-
Cloning and characterization of the human homologue of a dystrophin related phosphoprotein found at the Torpedo electric organ post-synaptic membrane
-
Sadoulet-Puccio HM, Khurana TS, Cohen JB, Kunkel LM (1996) Cloning and characterization of the human homologue of a dystrophin related phosphoprotein found at the Torpedo electric organ post-synaptic membrane. Hum Mol Genet 5:489-496
-
(1996)
Hum Mol Genet
, vol.5
, pp. 489-496
-
-
Sadoulet-Puccio, H.M.1
Khurana, T.S.2
Cohen, J.B.3
Kunkel, L.M.4
-
56
-
-
0029881574
-
Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein
-
Blake DJ, Nawrotzki R, Peters MF, Froehner SC, Davies KE (1996) Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein. J Biol Chem 271:7802-7810
-
(1996)
J Biol Chem
, vol.271
, pp. 7802-7810
-
-
Blake, D.J.1
Nawrotzki, R.2
Peters, M.F.3
Froehner, S.C.4
Davies, K.E.5
-
57
-
-
0031947501
-
Dystrophins in vertebrates and invertebrates
-
Roberts RG, Bobrow M (1998) Dystrophins in vertebrates and invertebrates. Hum Mol Genet 7:589-595
-
(1998)
Hum Mol Genet
, vol.7
, pp. 589-595
-
-
Roberts, R.G.1
Bobrow, M.2
-
58
-
-
0024330387
-
Cross-reactive protein in Duchenne muscle
-
Hoffman EP, Beggs AH, Koenig M, Kunkel LM, Angelini C (1989) Cross-reactive protein in Duchenne muscle. Lancet II:1211-1212
-
(1989)
Lancet
, vol.2
, pp. 1211-1212
-
-
Hoffman, E.P.1
Beggs, A.H.2
Koenig, M.3
Kunkel, L.M.4
Angelini, C.5
-
59
-
-
0024987672
-
Presence of dystrophine-like protein at the neuromuscular junction in Duchenne muscular dystrophy and in "mdx" mutant mice
-
Fardeau M, Tome FM, Collin H, Augier N, Pons F, Leger J, Leger J (1990) Presence of dystrophine-like protein at the neuromuscular junction in Duchenne muscular dystrophy and in "mdx" mutant mice. C R Acad Sci III 311:197-204
-
(1990)
C R Acad Sci III
, vol.311
, pp. 197-204
-
-
Fardeau, M.1
Tome, F.M.2
Collin, H.3
Augier, N.4
Pons, F.5
Leger, J.6
Leger, J.7
-
60
-
-
0025932274
-
Immunolocalization and developmental expression of dystrophin related protein in skeletal muscle
-
Khurana TS, Watkins SC, Chafey P, Chelly J, Tome FM, Fardeau M, Kaplan JC, Kunkel LM (1991) Immunolocalization and developmental expression of dystrophin related protein in skeletal muscle. Neuromuscul Disord 1:185-194
-
(1991)
Neuromuscul Disord
, vol.1
, pp. 185-194
-
-
Khurana, T.S.1
Watkins, S.C.2
Chafey, P.3
Chelly, J.4
Tome, F.M.5
Fardeau, M.6
Kaplan, J.C.7
Kunkel, L.M.8
-
61
-
-
0026355180
-
Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: Presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in proliferating brain cell lines
-
Nguyen TM, Ellis JM, Love DR, Davies KE, Gatter KC, Dickson G, Morris GE (1991) Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in proliferating brain cell lines. J Cell Biol 115:1695-1700
-
(1991)
J Cell Biol
, vol.115
, pp. 1695-1700
-
-
Nguyen, T.M.1
Ellis, J.M.2
Love, D.R.3
Davies, K.E.4
Gatter, K.C.5
Dickson, G.6
Morris, G.E.7
-
62
-
-
0026094250
-
Dystrophin-related protein is localized to neuromuscular junctions of adult skeletal muscle
-
Ohlendieck K, Ervasti JM, Matsumura K, Kahl SD, Leveille CJ, Campbell KP (1991) Dystrophin-related protein is localized to neuromuscular junctions of adult skeletal muscle. Neuron 7:499-508
-
(1991)
Neuron
, vol.7
, pp. 499-508
-
-
Ohlendieck, K.1
Ervasti, J.M.2
Matsumura, K.3
Kahl, S.D.4
Leveille, C.J.5
Campbell, K.P.6
-
63
-
-
0026781882
-
The subcellular distribution of chromosome 6-encoded dystrophin-related protein in the brain
-
Khurana TS, Watkins SC, Kunkel LM (1992) The subcellular distribution of chromosome 6-encoded dystrophin-related protein in the brain. J Cell Biol 119:357-366
-
(1992)
J Cell Biol
, vol.119
, pp. 357-366
-
-
Khurana, T.S.1
Watkins, S.C.2
Kunkel, L.M.3
-
64
-
-
0028837008
-
Calcium/calmodulin-dependent regulation of the NH2-terminal F-actin binding domain of utrophin
-
Winder SJ, Kendrick-Jones J (1995) Calcium/calmodulin-dependent regulation of the NH2-terminal F-actin binding domain of utrophin. FEBS Lett 357:125-128
-
(1995)
FEBS Lett
, vol.357
, pp. 125-128
-
-
Winder, S.J.1
Kendrick-Jones, J.2
-
65
-
-
0032930086
-
Disruption of the utrophin-actin interaction by monoclonal antibodies and prediction of an actin-binding surface of utrophin
-
Morris GE, Nguyen TM, Nguyen TN, Pereboev A, Kendrick-Jones J, Winder SJ (1999) Disruption of the utrophin-actin interaction by monoclonal antibodies and prediction of an actin-binding surface of utrophin. Biochem J 337:119-123
-
(1999)
Biochem J
, vol.337
, pp. 119-123
-
-
Morris, G.E.1
Nguyen, T.M.2
Nguyen, T.N.3
Pereboev, A.4
Kendrick-Jones, J.5
Winder, S.J.6
-
66
-
-
0027424701
-
The utrophin and dystrophin genes share similarities in genomic structure
-
Pearce M, Blake DJ, Tinsley JM, Byth BC, Campbell L, Monaco AP, Davies KE (1993) The utrophin and dystrophin genes share similarities in genomic structure. Hum Mol Genet 2:1765-1772
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1765-1772
-
-
Pearce, M.1
Blake, D.J.2
Tinsley, J.M.3
Byth, B.C.4
Campbell, L.5
Monaco, A.P.6
Davies, K.E.7
-
67
-
-
0029103076
-
Evidence for a utrophin-glycoprotein complex in cultured cell lines and a possible role in cell adhesion
-
James M, Simmons C, Wise CJ, Jones GE, Morris GE (1995) Evidence for a utrophin-glycoprotein complex in cultured cell lines and a possible role in cell adhesion. Biochem Soc Trans 23:398S
-
(1995)
Biochem Soc Trans
, vol.23
-
-
James, M.1
Simmons, C.2
Wise, C.J.3
Jones, G.E.4
Morris, G.E.5
-
68
-
-
0026621608
-
Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle
-
Matsumura K, Ervasti JM, Ohlendieck K, Kahl SD, Campbell KP (1992) Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle. Nature 360:588-591
-
(1992)
Nature
, vol.360
, pp. 588-591
-
-
Matsumura, K.1
Ervasti, J.M.2
Ohlendieck, K.3
Kahl, S.D.4
Campbell, K.P.5
-
69
-
-
0034646942
-
Contribution of the different modules in the utrophin carboxy-terminal region to the formation and regulation of the DAP complex
-
Tommasi d, V, Di Zenzo G, Sudol M, Cesareni G, Dente L (2000) Contribution of the different modules in the utrophin carboxy-terminal region to the formation and regulation of the DAP complex. FEBS Lett 471:229-234
-
(2000)
FEBS Lett
, vol.471
, pp. 229-234
-
-
Tommasi D, V.1
Di Zenzo, G.2
Sudol, M.3
Cesareni, G.4
Dente, L.5
-
70
-
-
0032494120
-
Differential membrane localization and intermolecular associations of alpha-dystrobrevin isoforms in skeletal muscle
-
Peters MF, Sadoulet-Puccio HM, Grady MR, Kramarcy NR, Kunkel LM, Sanes JR, Sealock R, Froehner SC (1998) Differential membrane localization and intermolecular associations of alpha-dystrobrevin isoforms in skeletal muscle. J Cell Biol 142:1269-1278
-
(1998)
J Cell Biol
, vol.142
, pp. 1269-1278
-
-
Peters, M.F.1
Sadoulet-Puccio, H.M.2
Grady, M.R.3
Kramarcy, N.R.4
Kunkel, L.M.5
Sanes, J.R.6
Sealock, R.7
Froehner, S.C.8
-
71
-
-
0028145301
-
Association of utrophin and multiple dystrophin short forms with the mammalian M (r) 58:000 dystrophin-associated protein (syntrophin)
-
Kramarcy NR, Vidal A, Froehner SC, Sealock R (1994) Association of utrophin and multiple dystrophin short forms with the mammalian M (r) 58:000 dystrophin-associated protein (syntrophin). J Biol Chem 269:2870-2876
-
(1994)
J Biol Chem
, vol.269
, pp. 2870-2876
-
-
Kramarcy, N.R.1
Vidal, A.2
Froehner, S.C.3
Sealock, R.4
-
72
-
-
0031467311
-
Beta-dystrobrevin, a new member of the dystrophin family. Identification, cloning, and protein associations
-
Peters MF, O'Brien KF, Sadoulet-Puccio HM, Kunkel LM, Adams ME, Froehner SC (1997) Beta-dystrobrevin, a new member of the dystrophin family. Identification, cloning, and protein associations. J Biol Chem 272:31561-31569
-
(1997)
J Biol Chem
, vol.272
, pp. 31561-31569
-
-
Peters, M.F.1
O'Brien, K.F.2
Sadoulet-Puccio, H.M.3
Kunkel, L.M.4
Adams, M.E.5
Froehner, S.C.6
-
73
-
-
0033837115
-
Assembly of multiple dystrobrevin-containing complexes in the kidney
-
Loh NY, Newey SE, Davies KE, Blake DJ (2000) Assembly of multiple dystrobrevin-containing complexes in the kidney. J Cell Sci 113:2715-2724
-
(2000)
J Cell Sci
, vol.113
, pp. 2715-2724
-
-
Loh, N.Y.1
Newey, S.E.2
Davies, K.E.3
Blake, D.J.4
-
74
-
-
0031712378
-
The therapeutic reactivation of fetal haemoglobin
-
Olivieri NF, Weatherall DJ (1998) The therapeutic reactivation of fetal haemoglobin. Hum Mol Genet 7:1655-1658
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1655-1658
-
-
Olivieri, N.F.1
Weatherall, D.J.2
-
75
-
-
0029906168
-
Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene
-
Tinsley JM, Potter AC, Phelps SR, Fisher R, Trickett JI, Davies KE (1996) Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene. Nature 384:349-353
-
(1996)
Nature
, vol.384
, pp. 349-353
-
-
Tinsley, J.M.1
Potter, A.C.2
Phelps, S.R.3
Fisher, R.4
Trickett, J.I.5
Davies, K.E.6
-
76
-
-
0033587139
-
Adenovirus-mediated utrophin gene transfer mitigates the dystrophic phenotype of mdx mouse muscles
-
Gilbert R, Nalbantoglu J, Petrof BJ, Ebihara S, Guibinga GH, Tinsley JM, Kamen A, Massie B, Davies KE, Karpati G (1999) Adenovirus-mediated utrophin gene transfer mitigates the dystrophic phenotype of mdx mouse muscles. Hum Gene Ther 10:1299-1310
-
(1999)
Hum Gene Ther
, vol.10
, pp. 1299-1310
-
-
Gilbert, R.1
Nalbantoglu, J.2
Petrof, B.J.3
Ebihara, S.4
Guibinga, G.H.5
Tinsley, J.M.6
Kamen, A.7
Massie, B.8
Davies, K.E.9
Karpati, G.10
-
77
-
-
0033758449
-
Animal models for muscular dystrophy: Valuable tools for the development of therapies
-
Allamand V, Campbell KP (2000) Animal models for muscular dystrophy: valuable tools for the development of therapies. Hum Mol Genet 9:2459-2467
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2459-2467
-
-
Allamand, V.1
Campbell, K.P.2
-
78
-
-
0026419948
-
The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy
-
Stedman HH, Sweeney HL, Shrager JB, Maguire HC, Panettieri RA, Petrof B, Narusawa M, Leferovich JM, Sladky JT, Kelly AM (1991) The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy. Nature 352:536-539
-
(1991)
Nature
, vol.352
, pp. 536-539
-
-
Stedman, H.H.1
Sweeney, H.L.2
Shrager, J.B.3
Maguire, H.C.4
Panettieri, R.A.5
Petrof, B.6
Narusawa, M.7
Leferovich, J.M.8
Sladky, J.T.9
Kelly, A.M.10
-
79
-
-
0026546263
-
Contractile properties and susceptibility to exercise-induced damage of normal and mdx mouse tibialis anterior muscle
-
Colch
-
Sacco P, Jones DA, Dick JR, Vrbova G (1992) Contractile properties and susceptibility to exercise-induced damage of normal and mdx mouse tibialis anterior muscle. Clin Sci (Colch) 82:227-236
-
(1992)
Clin Sci
, vol.82
, pp. 227-236
-
-
Sacco, P.1
Jones, D.A.2
Dick, J.R.3
Vrbova, G.4
-
80
-
-
0027248618
-
Increased susceptibility of EDL muscles from mdx mice to damage induced by contractions with stretch
-
Moens P, Baatsen PH, Marechal G (1993) Increased susceptibility of EDL muscles from mdx mice to damage induced by contractions with stretch. J Muscle Res Cell Motil 14:446-451
-
(1993)
J Muscle Res Cell Motil
, vol.14
, pp. 446-451
-
-
Moens, P.1
Baatsen, P.H.2
Marechal, G.3
-
81
-
-
0027460658
-
Dystrophin protects the sarcolemma from stresses developed during muscle contraction
-
Petrof BJ, Shrager JB, Stedman HH, Kelly AM, Sweeney HL (1993) Dystrophin protects the sarcolemma from stresses developed during muscle contraction. Proc Natl Acad Sci USA 90:3710-3714
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 3710-3714
-
-
Petrof, B.J.1
Shrager, J.B.2
Stedman, H.H.3
Kelly, A.M.4
Sweeney, H.L.5
-
82
-
-
0024346882
-
Feline muscular dystrophy with dystrophin deficiency
-
Carpenter JL, Hoffman EP, Romanul FC, Kunkel LM, Rosales RK, Ma NS, Dasbach JJ, Rae JF, Moore FM, McAfee MB (1989) Feline muscular dystrophy with dystrophin deficiency. Am J Pathol 135:909-919
-
(1989)
Am J Pathol
, vol.135
, pp. 909-919
-
-
Carpenter, J.L.1
Hoffman, E.P.2
Romanul, F.C.3
Kunkel, L.M.4
Rosales, R.K.5
Ma, N.S.6
Dasbach, J.J.7
Rae, J.F.8
Moore, F.M.9
McAfee, M.B.10
-
83
-
-
0023883621
-
The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs
-
Cooper BJ, Winand NJ, Stedman H, Valentine BA, Hoffman EP, Kunkel LM, Scott MO, Fischbeck KH, Kornegay JN, Avery RJ (1988) The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs. Nature 334:154-156
-
(1988)
Nature
, vol.334
, pp. 154-156
-
-
Cooper, B.J.1
Winand, N.J.2
Stedman, H.3
Valentine, B.A.4
Hoffman, E.P.5
Kunkel, L.M.6
Scott, M.O.7
Fischbeck, K.H.8
Kornegay, J.N.9
Avery, R.J.10
-
84
-
-
0032966013
-
Molecular analysis of a spontaneous dystrophin 'knockout' dog
-
Schatzberg SJ, Olby NJ, Breen M, Anderson LV, Langford CF, Dickens HF, Wilton SD, Zeiss CJ, Binns MM, Kornegay JN, Morris GE, Sharp NJ (1999) Molecular analysis of a spontaneous dystrophin 'knockout' dog. Neuromuscul Disord 9:289-295
-
(1999)
Neuromuscul Disord
, vol.9
, pp. 289-295
-
-
Schatzberg, S.J.1
Olby, N.J.2
Breen, M.3
Anderson, L.V.4
Langford, C.F.5
Dickens, H.F.6
Wilton, S.D.7
Zeiss, C.J.8
Binns, M.M.9
Kornegay, J.N.10
Morris, G.E.11
Sharp, N.J.12
-
85
-
-
0032424943
-
The physiological evaluation of gene therapies of dystrophin-deficient muscles
-
Gillis JM, Deconinck N (1998) The physiological evaluation of gene therapies of dystrophin-deficient muscles. Adv Exp Med Biol 453:411-416
-
(1998)
Adv Exp Med Biol
, vol.453
, pp. 411-416
-
-
Gillis, J.M.1
Deconinck, N.2
-
86
-
-
0034852658
-
Harnessing the potential of dystrophin-related proteins for ameliorating Duchenne's muscular dystrophy
-
Krag TO, Gyrd-Hansen M, Khurana TS (2001) Harnessing the potential of dystrophin-related proteins for ameliorating Duchenne's muscular dystrophy. Acta Physiol Scand 171:349-358
-
(2001)
Acta Physiol Scand
, vol.171
, pp. 349-358
-
-
Krag, T.O.1
Gyrd-Hansen, M.2
Khurana, T.S.3
-
87
-
-
0038725634
-
Pharmacological strategies for muscular dystrophy
-
Khurana TS, Davies KE (2003) Pharmacological strategies for muscular dystrophy. Nat Rev Drug Discov 2:379-390
-
(2003)
Nat Rev Drug Discov
, vol.2
, pp. 379-390
-
-
Khurana, T.S.1
Davies, K.E.2
-
88
-
-
0036823983
-
Multivariate evaluation of the functional recovery obtained by the overexpression of utrophin in skeletal muscles of the mdx mouse
-
Gillis JM (2002) Multivariate evaluation of the functional recovery obtained by the overexpression of utrophin in skeletal muscles of the mdx mouse. Neuromuscul Disord 12 [Suppl 1]:S90-S94
-
(2002)
Neuromuscul Disord
, vol.12
, Issue.1 SUPPL.
-
-
Gillis, J.M.1
-
89
-
-
0034638834
-
Expression profiling in the muscular dystrophies: Identification of novel aspects of molecular patophysiology
-
Chen YW, Zhao P, Borup R, Hoffman EP (2000) Expression profiling in the muscular dystrophies: identification of novel aspects of molecular patophysiology. J Cell Biol 151:1321-1336
-
(2000)
J Cell Biol
, vol.151
, pp. 1321-1336
-
-
Chen, Y.W.1
Zhao, P.2
Borup, R.3
Hoffman, E.P.4
-
90
-
-
0036721097
-
Global/temporal gene expression in diaphragm and hindlimb muscles of dystrophin-deficient (mdx) mice
-
Rouger K, Le Cuniff M, Steenman M, Potier MC, Gibelin N, Dechesne CA, Leger JJ (2002) Global/temporal gene expression in diaphragm and hindlimb muscles of dystrophin-deficient (mdx) mice. Am J Physiol Cell Physiol 288:C773-C784
-
(2002)
Am J Physiol Cell Physiol
, vol.288
-
-
Rouger, K.1
Le Cuniff, M.2
Steenman, M.3
Potier, M.C.4
Gibelin, N.5
Dechesne, C.A.6
Leger, J.J.7
-
91
-
-
0036823748
-
A web-accessible complete transcriptome of normal human and DMD muscle
-
Bakay M, Zhao P, Chen J, Hoffman EP (2002) A web-accessible complete transcriptome of normal human and DMD muscle. Neuromuscul Disord 12:S125-S141
-
(2002)
Neuromuscul Disord
, vol.12
-
-
Bakay, M.1
Zhao, P.2
Chen, J.3
Hoffman, E.P.4
-
92
-
-
0037069368
-
Gene expression comparison of biopsies from Duchenne muscular dystrophy (DMD) and normal sceletal muscle
-
Haslett JN, Sanoudou D, Kho AT, Bennett RR, Greenberg SA, Kohane IS, Beggs AH, Kunkel LM (2002) Gene expression comparison of biopsies from Duchenne muscular dystrophy (DMD) and normal sceletal muscle. Proc Natl Acad Sci USA 99:15000-15005
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 15000-15005
-
-
Haslett, J.N.1
Sanoudou, D.2
Kho, A.T.3
Bennett, R.R.4
Greenberg, S.A.5
Kohane, I.S.6
Beggs, A.H.7
Kunkel, L.M.8
-
93
-
-
0037444212
-
cDNA microarray analysis of individual Duchenne muscular dystrophy patients
-
Noguchi S, Tsukahara T, Fujita M, Kurokawa R, Tachikawa M, Toda T, Tsujimoto A, Arahata K, Nishino I (2003) cDNA microarray analysis of individual Duchenne muscular dystrophy patients. Hum Mol Genet 12:595-600
-
(2003)
Hum Mol Genet
, vol.12
, pp. 595-600
-
-
Noguchi, S.1
Tsukahara, T.2
Fujita, M.3
Kurokawa, R.4
Tachikawa, M.5
Toda, T.6
Tsujimoto, A.7
Arahata, K.8
Nishino, I.9
-
94
-
-
0024540879
-
Conversion of mdx myofibres from dystrophin-negative to positive by injection of normal myoblasts
-
Partridge TA, Morgan JE, Coulton GR, Hoffman EP, Kunkel LM (1989) Conversion of mdx myofibres from dystrophin-negative to positive by injection of normal myoblasts. Nature 337:176-179
-
(1989)
Nature
, vol.337
, pp. 176-179
-
-
Partridge, T.A.1
Morgan, J.E.2
Coulton, G.R.3
Hoffman, E.P.4
Kunkel, L.M.5
-
95
-
-
0026560260
-
Normal dystrophin transcripts detected in Duchenne muscular dystrophy patients after myoblast transplantation
-
Gussoni E, Pavlath GK, Lanctot AM, Sharma KR, Miller RG, Steinman L, Blau HM (1992) Normal dystrophin transcripts detected in Duchenne muscular dystrophy patients after myoblast transplantation. Nature 356:435-438
-
(1992)
Nature
, vol.356
, pp. 435-438
-
-
Gussoni, E.1
Pavlath, G.K.2
Lanctot, A.M.3
Sharma, K.R.4
Miller, R.G.5
Steinman, L.6
Blau, H.M.7
-
96
-
-
8244228688
-
Myoblast implantation in Duchenne muscular dystrophy: The San Francisco study
-
Miller RG, Sharma KR, Pavlath GK, Gussoni E, Mynhier M, Lanctot AM, Greco CM, Steinman L, Blau HM (1997) Myoblast implantation in Duchenne muscular dystrophy: the San Francisco study. Muscle Nerve 20:469-478
-
(1997)
Muscle Nerve
, vol.20
, pp. 469-478
-
-
Miller, R.G.1
Sharma, K.R.2
Pavlath, G.K.3
Gussoni, E.4
Mynhier, M.5
Lanctot, A.M.6
Greco, C.M.7
Steinman, L.8
Blau, H.M.9
-
97
-
-
0031722886
-
Pilot study of myoblast transfer in the treatment of Becker muscular dystrophy
-
Neumeyer AM, Cros D, McKenna-Yasek D, Zawadzka A, Hoffman EP, Pegoraro E, Hunter RG, Munsat TL, Brown RH Jr (1998) Pilot study of myoblast transfer in the treatment of Becker muscular dystrophy. Neurology 51:589-592
-
(1998)
Neurology
, vol.51
, pp. 589-592
-
-
Neumeyer, A.M.1
Cros, D.2
McKenna-Yasek, D.3
Zawadzka, A.4
Hoffman, E.P.5
Pegoraro, E.6
Hunter, R.G.7
Munsat, T.L.8
Brown Jr., R.H.9
-
98
-
-
0027166930
-
Results of a triple blind clinical study of myoblast transplantations without immunosuppressive treatment in young boys with Duchenne muscular dystrophy
-
Tremblay JP, Malouin F, Roy R, Huard J, Bouchard JP, Satoh A, Richards CL (1993) Results of a triple blind clinical study of myoblast transplantations without immunosuppressive treatment in young boys with Duchenne muscular dystrophy. Cell Transplant 2:99-112
-
(1993)
Cell Transplant
, vol.2
, pp. 99-112
-
-
Tremblay, J.P.1
Malouin, F.2
Roy, R.3
Huard, J.4
Bouchard, J.P.5
Satoh, A.6
Richards, C.L.7
-
99
-
-
0028954859
-
The childhood muscular dystrophies: Diseases sharing a common pathogenesis of membrane instability
-
Mendell JR, Sahenk Z, Prior TW (1995) The childhood muscular dystrophies: diseases sharing a common pathogenesis of membrane instability. J Child Neurol 10:150-159
-
(1995)
J Child Neurol
, vol.10
, pp. 150-159
-
-
Mendell, J.R.1
Sahenk, Z.2
Prior, T.W.3
-
100
-
-
0032080573
-
Dystrophin acts as a transplantation rejection antigen in dystrophin-deficient mice: Implication for gene therapy
-
Ohtsuka Y, Udaka K, Yamashiro Y, Yagita H, Okumura K (1998) Dystrophin acts as a transplantation rejection antigen in dystrophin-deficient mice: implication for gene therapy. J Immunol 160:4635-4640
-
(1998)
J Immunol
, vol.160
, pp. 4635-4640
-
-
Ohtsuka, Y.1
Udaka, K.2
Yamashiro, Y.3
Yagita, H.4
Okumura, K.5
-
101
-
-
0030865245
-
The fate of individual myoblasts after transplantation into muscles of DMD patients
-
Gussoni E, Blau HM, Kunkel LM (1997) The fate of individual myoblasts after transplantation into muscles of DMD patients. Nat Med 3:970-977
-
(1997)
Nat Med
, vol.3
, pp. 970-977
-
-
Gussoni, E.1
Blau, H.M.2
Kunkel, L.M.3
-
102
-
-
0037113042
-
The role of CD34 expression and cellular fusion in the regeneration capacity of myogenic progenitor cells
-
Jankowski RJ, Deasy BM, Cao B, Gates C, Huard J (2002) The role of CD34 expression and cellular fusion in the regeneration capacity of myogenic progenitor cells. J Cell Sci 115:4361-4374
-
(2002)
J Cell Sci
, vol.115
, pp. 4361-4374
-
-
Jankowski, R.J.1
Deasy, B.M.2
Cao, B.3
Gates, C.4
Huard, J.5
-
103
-
-
0032489651
-
Muscle regeneration by bone marrow-derived myogenic progenitors
-
Ferrari G, Cusella-De Angelis G, Coletta M, Paolucci E, Stornaiuolo A, Cossu G, Mavilio F (1998) Muscle regeneration by bone marrow-derived myogenic progenitors. Science 279:1528-1530
-
(1998)
Science
, vol.279
, pp. 1528-1530
-
-
Ferrari, G.1
Cusella-De Angelis, G.2
Coletta, M.3
Paolucci, E.4
Stornaiuolo, A.5
Cossu, G.6
Mavilio, F.7
-
104
-
-
0033598374
-
Dystrophin expression in the mdx mouse restored by stem cell transplantation
-
Gussoni E, Soneoka Y, Strickland CD, Buzney EA, Khan MK, Flint AF, Kunkel LM, Mulligan RC (1999) Dystrophin expression in the mdx mouse restored by stem cell transplantation. Nature 401:390-394
-
(1999)
Nature
, vol.401
, pp. 390-394
-
-
Gussoni, E.1
Soneoka, Y.2
Strickland, C.D.3
Buzney, E.A.4
Khan, M.K.5
Flint, A.F.6
Kunkel, L.M.7
Mulligan, R.C.8
-
105
-
-
2042538384
-
Recruitment of bone-marrow-derived cells by skeletal and cardiac muscle in adult dystrophic mdx mice
-
Berl
-
Bittner RE, Schofer C, Weipoltshammer K, Ivanova S, Streubel B, Hauser E, Freilinger M, Hoger H, Elbe-Burger A, Wachtler F (1999) Recruitment of bone-marrow-derived cells by skeletal and cardiac muscle in adult dystrophic mdx mice. Anat Embryol (Berl) 199:391-396
-
(1999)
Anat Embryol
, vol.199
, pp. 391-396
-
-
Bittner, R.E.1
Schofer, C.2
Weipoltshammer, K.3
Ivanova, S.4
Streubel, B.5
Hauser, E.6
Freilinger, M.7
Hoger, H.8
Elbe-Burger, A.9
Wachtler, F.10
-
106
-
-
0036736786
-
Long-term persistence of donor nuclei in a Duchenne muscular dystrophy patient receiving bone marrow transplantation
-
Gussoni E, Bennett RR, Muskiewicz KR, Meyerrose T, Nolta JA, Gilgoff I, Stein J, Chan YM, Lidov HG, Bonnemann CG, Von Moers A, Morris GE, Den Dunnen JT, Chamberlain JS, Kunkel LM, Weinberg K (2002) Long-term persistence of donor nuclei in a Duchenne muscular dystrophy patient receiving bone marrow transplantation. J Clin Invest 110:807-814
-
(2002)
J Clin Invest
, vol.110
, pp. 807-814
-
-
Gussoni, E.1
Bennett, R.R.2
Muskiewicz, K.R.3
Meyerrose, T.4
Nolta, J.A.5
Gilgoff, I.6
Stein, J.7
Chan, Y.M.8
Lidov, H.G.9
Bonnemann, C.G.10
Von Moers, A.11
Morris, G.E.12
Den Dunnen, J.T.13
Chamberlain, J.S.14
Kunkel, L.M.15
Weinberg, K.16
-
107
-
-
0033917878
-
Myogenic stem cells for the therapy of primary myopathies: Wishful thinking or therapeutic perspective?
-
Cossu G, Mavilio F (2000) Myogenic stem cells for the therapy of primary myopathies: wishful thinking or therapeutic perspective? J Clin Invest 105:1669-1674
-
(2000)
J Clin Invest
, vol.105
, pp. 1669-1674
-
-
Cossu, G.1
Mavilio, F.2
-
108
-
-
0029906168
-
Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene
-
Tinsley JM, Potter AC, Phelps SR, Fisher R, Trickett JI, Davies KE (1996) Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene. Nature 384:349-353
-
(1996)
Nature
, vol.384
, pp. 349-353
-
-
Tinsley, J.M.1
Potter, A.C.2
Phelps, S.R.3
Fisher, R.4
Trickett, J.I.5
Davies, K.E.6
-
109
-
-
0036823755
-
Gene transfer studies in animals: What do they really tell us about the prospects for gene therapy in DMD?
-
Wells D, Wells K (2002) Gene transfer studies in animals: what do they really tell us about the prospects for gene therapy in DMD? Neuromuscul Disord 12 [Suppl]:S11
-
(2002)
Neuromuscul Disord
, vol.12
, Issue.SUPPL.
-
-
Wells, D.1
Wells, K.2
-
110
-
-
0034610364
-
Adeno-associated virus vector carrying human minidystrophin genes effectively ameliorates muscular dystrophy in mdx mouse model
-
Wang B, Li J, Xiao X (2000) Adeno-associated virus vector carrying human minidystrophin genes effectively ameliorates muscular dystrophy in mdx mouse model. Proc Natl Acad Sci USA 97:13714-13719
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 13714-13719
-
-
Wang, B.1
Li, J.2
Xiao, X.3
-
111
-
-
0036127393
-
Modular flexibility of dystrophin: Implications for gene therapy of Duchenne muscular dystrophy
-
Harper SQ, Hauser MA, DelloRusso C, Duan D, Crawford RW, Phelps SF, Harper HA, Robinson AS, Engelhardt JF, Brooks SV, Chamberlain JS (2002) Modular flexibility of dystrophin: implications for gene therapy of Duchenne muscular dystrophy. Nat Med 8:253-261
-
(2002)
Nat Med
, vol.8
, pp. 253-261
-
-
Harper, S.Q.1
Hauser, M.A.2
DelloRusso, C.3
Duan, D.4
Crawford, R.W.5
Phelps, S.F.6
Harper, H.A.7
Robinson, A.S.8
Engelhardt, J.F.9
Brooks, S.V.10
Chamberlain, J.S.11
-
112
-
-
0034622814
-
Differential effects of dystrophin and utrophin gene transfer in immunocompetent muscular dystrophy (mdx) mice
-
Ebihara S, Guibinga GH, Gilbert R, Nalbantoglu J, Massie B, Karpati G, Petrof BJ (2000) Differential effects of dystrophin and utrophin gene transfer in immunocompetent muscular dystrophy (mdx) mice. Physiol Genomics 3:133-144
-
(2000)
Physiol Genomics
, vol.3
, pp. 133-144
-
-
Ebihara, S.1
Guibinga, G.H.2
Gilbert, R.3
Nalbantoglu, J.4
Massie, B.5
Karpati, G.6
Petrof, B.J.7
-
113
-
-
0027070497
-
Expression of naked plasmids by cultured myotubes and entry of plasmids into T tubules and caveolae of mammalian skeletal muscle
-
Wolff JA, Dowty ME, Jiao S, Repetto G, Berg RK, Ludtke JJ, Williams P, Slautterback DB (1992) Expression of naked plasmids by cultured myotubes and entry of plasmids into T tubules and caveolae of mammalian skeletal muscle. J Cell Sci 103:1249-1259
-
(1992)
J Cell Sci
, vol.103
, pp. 1249-1259
-
-
Wolff, J.A.1
Dowty, M.E.2
Jiao, S.3
Repetto, G.4
Berg, R.K.5
Ludtke, J.J.6
Williams, P.7
Slautterback, D.B.8
-
114
-
-
0030774806
-
High expression of naked plasmid DNA in muscles of young rodents
-
Danko I, Williams P, Herweijer H, Zhang G, Latendresse JS, Bock I, Wolff JA (1997) High expression of naked plasmid DNA in muscles of young rodents. Hum Mol Genet 6:1435-1443
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1435-1443
-
-
Danko, I.1
Williams, P.2
Herweijer, H.3
Zhang, G.4
Latendresse, J.S.5
Bock, I.6
Wolff, J.A.7
-
115
-
-
0025887093
-
Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs
-
Acsadi G, Dickson G, Love DR, Jani A, Walsh FS, Gurusinghe A, Wolff JA, Davies KE (1991) Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs. Nature 352:815-818
-
(1991)
Nature
, vol.352
, pp. 815-818
-
-
Acsadi, G.1
Dickson, G.2
Love, D.R.3
Jani, A.4
Walsh, F.S.5
Gurusinghe, A.6
Wolff, J.A.7
Davies, K.E.8
-
116
-
-
0036823752
-
Current protocol of a research phase I clinical trial of full-length dystrophin plasmid DNA in Duchenne/Becker muscular dystrophies. I. Rationale
-
Thioudellet C, Blot S, Squiban P, Fardeau M, Braun S (2002) Current protocol of a research phase I clinical trial of full-length dystrophin plasmid DNA in Duchenne/Becker muscular dystrophies. I. Rationale. Neuromuscul Disord 12 [Suppl 1]:S49-S51
-
(2002)
Neuromuscul Disord
, vol.12
, Issue.1 SUPPL.
-
-
Thioudellet, C.1
Blot, S.2
Squiban, P.3
Fardeau, M.4
Braun, S.5
-
117
-
-
0036824011
-
Current protocol of a research phase I clinical trial of full-length dystrophin plasmid DNA in Duchenne/Becker muscular dystrophies. II. Clinical protocol
-
Romero NB, Benveniste O, Payan C, Braun S, Squiban P, Herson S, Fardeau M (2002) Current protocol of a research phase I clinical trial of full-length dystrophin plasmid DNA in Duchenne/Becker muscular dystrophies. II. Clinical protocol Neuromuscul Disord 12 [Suppl 1]:S45-S48
-
(2002)
Neuromuscul Disord
, vol.12
, Issue.1 SUPPL.
-
-
Romero, N.B.1
Benveniste, O.2
Payan, C.3
Braun, S.4
Squiban, P.5
Herson, S.6
Fardeau, M.7
-
118
-
-
0034624974
-
Rescue of dystrophin expression in mdx mouse muscle by RNA/DNA oligonucleotides
-
Rando TA, Disatnik MH, Zhou LZ (2000) Rescue of dystrophin expression in mdx mouse muscle by RNA/DNA oligonucleotides. Proc Natl Acad Sci USA 97:5363-5368
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 5363-5368
-
-
Rando, T.A.1
Disatnik, M.H.2
Zhou, L.Z.3
-
119
-
-
0034086776
-
In vivo targeted repair of a point mutation in the canine dystrophin gene by a chimeric RNA/DNA oligonucleotide
-
Bartlett RJ, Stockinger S, Denis MM, Bartlett WT, Inverardi L, Le TT, Thi MN, Morris GE, Bogan DJ, Metcalf-Bogan J, Kornegay JN (2000) In vivo targeted repair of a point mutation in the canine dystrophin gene by a chimeric RNA/DNA oligonucleotide. Nat Biotechnol 18:615-622
-
(2000)
Nat Biotechnol
, vol.18
, pp. 615-622
-
-
Bartlett, R.J.1
Stockinger, S.2
Denis, M.M.3
Bartlett, W.T.4
Inverardi, L.5
Le, T.T.6
Thi, M.N.7
Morris, G.E.8
Bogan, D.J.9
Metcalf-Bogan, J.10
Kornegay, J.N.11
-
120
-
-
0031800293
-
Modification of splicing in the dystrophin gene in cultured Mdx muscle cells by antisense oligoribonucleotides
-
Dunckley MG, Manoharan M, Villiet P, Eperon IC, Dickson G (1998) Modification of splicing in the dystrophin gene in cultured Mdx muscle cells by antisense oligoribonucleotides. Hum Mol Genet 7:1083-1090
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1083-1090
-
-
Dunckley, M.G.1
Manoharan, M.2
Villiet, P.3
Eperon, I.C.4
Dickson, G.5
-
121
-
-
0033044501
-
Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides
-
Wilton SD, Lloyd F, Carville K, Fletcher S, Honeyman K, Agrawal S, Kole R (1999) Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides. Neuromuscul Disord 9:330-338
-
(1999)
Neuromuscul Disord
, vol.9
, pp. 330-338
-
-
Wilton, S.D.1
Lloyd, F.2
Carville, K.3
Fletcher, S.4
Honeyman, K.5
Agrawal, S.6
Kole, R.7
-
122
-
-
0035793047
-
Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouse
-
Mann CJ, Honeyman K, Cheng AJ, Ly T, Lloyd F, Fletcher S, Morgan JE, Partridge TA, Wilton SD (2001) Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouse. Proc Natl Acad Sci USA 98:42-47
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 42-47
-
-
Mann, C.J.1
Honeyman, K.2
Cheng, A.J.3
Ly, T.4
Lloyd, F.5
Fletcher, S.6
Morgan, J.E.7
Partridge, T.A.8
Wilton, S.D.9
-
123
-
-
0035878539
-
Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells
-
Deutekom JC van, Bremmer-Bout M, Janson AA, Ginjaar IB, Baas F, Den Dunnen JT, van Ommen GJ (2001) Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells. Hum Mol Genet 10:1547-1554
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1547-1554
-
-
Van Deutekom, J.C.1
Bremmer-Bout, M.2
Janson, A.A.3
Ginjaar, I.B.4
Baas, F.5
Den Dunnen, J.T.6
Van Ommen, G.J.7
-
124
-
-
0042536463
-
Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse
-
Lu QL, Mann CJ, Lou F, Bou-Gharios G, Morris GE, Xue SA, Fletcher S, Partridge TA, Wilton SD (2003) Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse. Nat Med 9:1009-1014
-
(2003)
Nat Med
, vol.9
, pp. 1009-1014
-
-
Lu, Q.L.1
Mann, C.J.2
Lou, F.3
Bou-Gharios, G.4
Morris, G.E.5
Xue, S.A.6
Fletcher, S.7
Partridge, T.A.8
Wilton, S.D.9
-
125
-
-
0035894583
-
Gentamicin in pharmacogenetic approach to treatment of cystic fibrosis
-
Hamilton JW (2001) Gentamicin in pharmacogenetic approach to treatment of cystic fibrosis. Lancet 358:2014-2016
-
(2001)
Lancet
, vol.358
, pp. 2014-2016
-
-
Hamilton, J.W.1
-
126
-
-
0034073736
-
A pilot study of the effect of gentamicin on nasal potential difference measurements in cystic fibrosis patients carrying stop mutations
-
Wilschanski M, Famini C, Blau H, Rivlin J, Augarten A, Avital A, Kerem B, Kerem E (2000) A pilot study of the effect of gentamicin on nasal potential difference measurements in cystic fibrosis patients carrying stop mutations. Am J Respir Crit Care Med 161:860-865
-
(2000)
Am J Respir Crit Care Med
, vol.161
, pp. 860-865
-
-
Wilschanski, M.1
Famini, C.2
Blau, H.3
Rivlin, J.4
Augarten, A.5
Avital, A.6
Kerem, B.7
Kerem, E.8
-
127
-
-
0032720705
-
Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx mice
-
Barton-Davis ER, Cordier L, Shoturma DI, Leland SE, Sweeney HL (1999) Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx mice. J Clin Invest 104:375-381
-
(1999)
J Clin Invest
, vol.104
, pp. 375-381
-
-
Barton-Davis, E.R.1
Cordier, L.2
Shoturma, D.I.3
Leland, S.E.4
Sweeney, H.L.5
-
128
-
-
0034982292
-
Gentamicin treatment of Duchenne and Becker muscular dystrophy due to nonsense mutations
-
Wagner KR, Hamed S, Hadley DW, Gropman AL, Burstein AH, Escolar DM, Hoffman EP, Fischbeck KH (2001) Gentamicin treatment of Duchenne and Becker muscular dystrophy due to nonsense mutations. Ann Neurol 49:706-711
-
(2001)
Ann Neurol
, vol.49
, pp. 706-711
-
-
Wagner, K.R.1
Hamed, S.2
Hadley, D.W.3
Gropman, A.L.4
Burstein, A.H.5
Escolar, D.M.6
Hoffman, E.P.7
Fischbeck, K.H.8
-
129
-
-
0037408464
-
Gentamicin fails to increase dystrophin expression in dystrophin-deficient muscle
-
Dunant P, Walter MC, Karpati G, Lochmuller H (2003) Gentamicin fails to increase dystrophin expression in dystrophin-deficient muscle. Muscle Nerve 27:624-627
-
(2003)
Muscle Nerve
, vol.27
, pp. 624-627
-
-
Dunant, P.1
Walter, M.C.2
Karpati, G.3
Lochmuller, H.4
-
130
-
-
0021319355
-
The influence of aminoglycoside antibiotics on the in vitro function of rat liver ribosomes
-
Loveless MO, Kohlhepp SJ, Gilbert DN (1984) The influence of aminoglycoside antibiotics on the in vitro function of rat liver ribosomes. J Lab Clin Med 103:294-303
-
(1984)
J Lab Clin Med
, vol.103
, pp. 294-303
-
-
Loveless, M.O.1
Kohlhepp, S.J.2
Gilbert, D.N.3
-
131
-
-
0032538956
-
Structural origins of gentamicin antibiotic action
-
Yoshizawa S, Fourmy D, Puglisi JD (1998) Structural origins of gentamicin antibiotic action. EMBO J 17:6437-6448
-
(1998)
EMBO J
, vol.17
, pp. 6437-6448
-
-
Yoshizawa, S.1
Fourmy, D.2
Puglisi, J.D.3
-
132
-
-
0033382340
-
Understanding dystrophinopathies: An inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse
-
Gillis JM (1999) Understanding dystrophinopathies: an inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse. J Muscle Res Cell Motil 20:605-625
-
(1999)
J Muscle Res Cell Motil
, vol.20
, pp. 605-625
-
-
Gillis, J.M.1
-
133
-
-
0036359149
-
Expression profiling reveals metabolic and structural components of extraocular muscles
-
Fischer MD, Gorospe JR, Felder E, Bogdanovich S, Pedrosa-Domellof F, Ahima RS, Rubinstein NA, Hoffman EP, Khurana TS (2002) Expression profiling reveals metabolic and structural components of extraocular muscles. Physiol Genomics 9:71-84
-
(2002)
Physiol Genomics
, vol.9
, pp. 71-84
-
-
Fischer, M.D.1
Gorospe, J.R.2
Felder, E.3
Bogdanovich, S.4
Pedrosa-Domellof, F.5
Ahima, R.S.6
Rubinstein, N.A.7
Hoffman, E.P.8
Khurana, T.S.9
-
134
-
-
0027415027
-
Regulation of membrane-mediated chronic muscle degeneration in dystrophic hamsters by calcium-channel blockers: Diltiazem, nifedipine and verapamil
-
Johnson PL, Bhattacharya SK (1993) Regulation of membrane-mediated chronic muscle degeneration in dystrophic hamsters by calcium-channel blockers: diltiazem, nifedipine and verapamil. J Neurol Sci 115:76-90
-
(1993)
J Neurol Sci
, vol.115
, pp. 76-90
-
-
Johnson, P.L.1
Bhattacharya, S.K.2
-
135
-
-
0033982278
-
Delay of muscle degeneration and necrosis in mdx mice by calpain inhibition
-
Badalamente MA, Stracher A (2000) Delay of muscle degeneration and necrosis in mdx mice by calpain inhibition. Muscle Nerve 23:106-111
-
(2000)
Muscle Nerve
, vol.23
, pp. 106-111
-
-
Badalamente, M.A.1
Stracher, A.2
-
136
-
-
0036798005
-
Overexpression of a calpastatin transgene in mdx muscle reduces dystrophic pathology
-
Spencer MJ, Mellgren RL (2002) Overexpression of a calpastatin transgene in mdx muscle reduces dystrophic pathology. Hum Mol Genet 11:2645-2655
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2645-2655
-
-
Spencer, M.J.1
Mellgren, R.L.2
-
137
-
-
0021176654
-
Monoclonal antibody analysis of mononuclear cells in myopathies. I. Quantitation of subsets according to diagnosis and sites of accumulation and demonstration and counts of muscle fibers invaded by T cells
-
Arahata K, Engel AG (1984) Monoclonal antibody analysis of mononuclear cells in myopathies. I. Quantitation of subsets according to diagnosis and sites of accumulation and demonstration and counts of muscle fibers invaded by T cells. Ann Neurol 16:193-208
-
(1984)
Ann Neurol
, vol.16
, pp. 193-208
-
-
Arahata, K.1
Engel, A.G.2
-
138
-
-
0023949590
-
Monoclonal antibody analysis of mononuclear cells in myopathies. IV. Cell-mediated cytotoxicity and muscle fiber necrosis
-
Arahata K, Engel AG (1988) Monoclonal antibody analysis of mononuclear cells in myopathies. IV. Cell-mediated cytotoxicity and muscle fiber necrosis. Ann Neurol 23:168-173
-
(1988)
Ann Neurol
, vol.23
, pp. 168-173
-
-
Arahata, K.1
Engel, A.G.2
-
139
-
-
0013819875
-
On the effect of corticoid administration on creatine phosphokinase in progressive muscular dystrophy
-
Barthelmai W (1965) On the effect of corticoid administration on creatine phosphokinase in progressive muscular dystrophy. Verh Dtsch Ges Inn Med 71:624-626
-
(1965)
Verh Dtsch Ges Inn Med
, vol.71
, pp. 624-626
-
-
Barthelmai, W.1
-
140
-
-
0016287539
-
Prednisone in Duchenne muscular dystrophy
-
Drachman DB, Toyka KV, Myer E (1974) Prednisone in Duchenne muscular dystrophy. Lancet II:1409-1412
-
(1974)
Lancet
, vol.2
, pp. 1409-1412
-
-
Drachman, D.B.1
Toyka, K.V.2
Myer, E.3
-
141
-
-
0027499704
-
Duchenne dystrophy: Randomized, controlled trial of prednisone (18 months) and azathioprine (12 months)
-
Griggs RC, Moxley RT III, Mendell JR, Fenichel GM, Brooke MH, Pestronk A, Miller JP, Cwik VA, Pandya S, Robison J (1993) Duchenne dystrophy: randomized, controlled trial of prednisone (18 months) and azathioprine (12 months). Neurology 43:520-527
-
(1993)
Neurology
, vol.43
, pp. 520-527
-
-
Griggs, R.C.1
Moxley III, R.T.2
Mendell, J.R.3
Fenichel, G.M.4
Brooke, M.H.5
Pestronk, A.6
Miller, J.P.7
Cwik, V.A.8
Pandya, S.9
Robison, J.10
-
142
-
-
0028280495
-
Deflazacort in Duchenne dystrophy: Study of long-term effect
-
Angelini C, Pegoraro E, Turella E, Intino MT, Pini A, Costa C (1994) Deflazacort in Duchenne dystrophy: study of long-term effect. Muscle Nerve 17:386-391
-
(1994)
Muscle Nerve
, vol.17
, pp. 386-391
-
-
Angelini, C.1
Pegoraro, E.2
Turella, E.3
Intino, M.T.4
Pini, A.5
Costa, C.6
-
143
-
-
0035122405
-
Helper (CD4 (+)) and cytotoxic (CD8 (+)) T cells promote the pathology of dystrophin-deficient muscle
-
Spencer MJ, Montecino-Rodriguez E, Dorshkind K, Tidball JG (2001) Helper (CD4 (+)) and cytotoxic (CD8 (+)) T cells promote the pathology of dystrophin-deficient muscle. Clin Immunol 98:235-243
-
(2001)
Clin Immunol
, vol.98
, pp. 235-243
-
-
Spencer, M.J.1
Montecino-Rodriguez, E.2
Dorshkind, K.3
Tidball, J.G.4
-
145
-
-
0036917316
-
Sizing up muscular dystrophy
-
Zammit PS, Partridge TA (2002) Sizing up muscular dystrophy. Nat Med 8:1355-1356
-
(2002)
Nat Med
, vol.8
, pp. 1355-1356
-
-
Zammit, P.S.1
Partridge, T.A.2
-
146
-
-
0036544519
-
Muscle-specific expression of insulin-like growth factor I counters muscle decline in mdx mice
-
Barton ER, Morris L, Musaro A, Rosenthal N, Sweeney HL (2002) Muscle-specific expression of insulin-like growth factor I counters muscle decline in mdx mice. J Cell Biol 157:137-148
-
(2002)
J Cell Biol
, vol.157
, pp. 137-148
-
-
Barton, E.R.1
Morris, L.2
Musaro, A.3
Rosenthal, N.4
Sweeney, H.L.5
-
147
-
-
0035067333
-
IGF-I treatment improves the functional properties of fast- And slow-twitch skeletal muscles from dystrophic mice
-
Lynch GS, Cuffe SA, Plant DR, Gregorevic P (2001) IGF-I treatment improves the functional properties of fast-and slow-twitch skeletal muscles from dystrophic mice. Neuromuscul Disord 11:260-268
-
(2001)
Neuromuscul Disord
, vol.11
, pp. 260-268
-
-
Lynch, G.S.1
Cuffe, S.A.2
Plant, D.R.3
Gregorevic, P.4
-
148
-
-
0031010050
-
Regulation of skeletal muscle mass in mice by a new TGF-beta superfamily member
-
McPherron AC, Lawler AM, Lee SJ (1997) Regulation of skeletal muscle mass in mice by a new TGF-beta superfamily member. Nature 387:83-90
-
(1997)
Nature
, vol.387
, pp. 83-90
-
-
McPherron, A.C.1
Lawler, A.M.2
Lee, S.J.3
-
149
-
-
16944364045
-
A deletion in the bovine myostatin gene causes the double-muscled phenotype in cattle
-
Grobet L, Martin LJ, Poncelet D, Pirottin D, Brouwers B, Riquet J, Schoeberlein A, Dunner S, Menissier F, Massabanda J, Fries R, Hanset R, Georges M (1997) A deletion in the bovine myostatin gene causes the double-muscled phenotype in cattle. Nat Genet 17:71-74
-
(1997)
Nat Genet
, vol.17
, pp. 71-74
-
-
Grobet, L.1
Martin, L.J.2
Poncelet, D.3
Pirottin, D.4
Brouwers, B.5
Riquet, J.6
Schoeberlein, A.7
Dunner, S.8
Menissier, F.9
Massabanda, J.10
Fries, R.11
Hanset, R.12
Georges, M.13
-
150
-
-
0034716993
-
Dominant negative myostatin produces hypertrophy without hyperplasia in muscle
-
Zhu X, Hadhazy M, Wehling M, Tidball JG, McNally EM (2000) Dominant negative myostatin produces hypertrophy without hyperplasia in muscle. FEBS Lett 474:71-75
-
(2000)
FEBS Lett
, vol.474
, pp. 71-75
-
-
Zhu, X.1
Hadhazy, M.2
Wehling, M.3
Tidball, J.G.4
McNally, E.M.5
-
151
-
-
0035979253
-
Regulation of myostatin activity and muscle growth
-
Lee SJ, McPherron AC (2001) Regulation of myostatin activity and muscle growth. Proc Natl Acad Sci USA 98:9306-9311
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 9306-9311
-
-
Lee, S.J.1
McPherron, A.C.2
-
152
-
-
0034792235
-
Expression of myostatin pro domain results in muscular transgenic mice
-
Yang J, Ratovitski T, Brady JP, Solomon MB, Wells KD, Wall RJ (2001) Expression of myostatin pro domain results in muscular transgenic mice. Mol Reprod Dev 60:351-361
-
(2001)
Mol Reprod Dev
, vol.60
, pp. 351-361
-
-
Yang, J.1
Ratovitski, T.2
Brady, J.P.3
Solomon, M.B.4
Wells, K.D.5
Wall, R.J.6
-
153
-
-
0036296159
-
A missense mutant myostatin causes hyperplasia without hypertrophy in the mouse muscle
-
Nishi M, Yasue A, Nishimatu S, Nohno T, Yamaoka T, Itakura M, Moriyama K, Ohuchi H, Noji S (2002) A missense mutant myostatin causes hyperplasia without hypertrophy in the mouse muscle. Biochem Biophys Res Commun 293:247-251
-
(2002)
Biochem Biophys Res Commun
, vol.293
, pp. 247-251
-
-
Nishi, M.1
Yasue, A.2
Nishimatu, S.3
Nohno, T.4
Yamaoka, T.5
Itakura, M.6
Moriyama, K.7
Ohuchi, H.8
Noji, S.9
-
154
-
-
0036200822
-
Suppression of body fat accumulation in myostatin-deficient mice
-
McPherron AC, Lee SJ (2002) Suppression of body fat accumulation in myostatin-deficient mice. J Clin Invest 109:595-601
-
(2002)
J Clin Invest
, vol.109
, pp. 595-601
-
-
McPherron, A.C.1
Lee, S.J.2
-
155
-
-
0034883063
-
GDF-8 propeptide binds to GDF-8 and antagonizes biological activity by inhibiting GDF-8 receptor binding
-
Thies RS, Chen T, Davies MV, Tomkinson KN, Pearson AA, Shakey QA, Wolfman NM (2001) GDF-8 propeptide binds to GDF-8 and antagonizes biological activity by inhibiting GDF-8 receptor binding. Growth Factors 18:251-259
-
(2001)
Growth Factors
, vol.18
, pp. 251-259
-
-
Thies, R.S.1
Chen, T.2
Davies, M.V.3
Tomkinson, K.N.4
Pearson, A.A.5
Shakey, Q.A.6
Wolfman, N.M.7
-
156
-
-
0034704106
-
Myostatin, a negative regulator of muscle growth, functions by inhibiting myoblast proliferation
-
Thomas M, Langley B, Berry C, Sharma M, Kirk S, Bass J, Kambadur R (2000) Myostatin, a negative regulator of muscle growth, functions by inhibiting myoblast proliferation. J Biol Chem 275:40235-40243
-
(2000)
J Biol Chem
, vol.275
, pp. 40235-40243
-
-
Thomas, M.1
Langley, B.2
Berry, C.3
Sharma, M.4
Kirk, S.5
Bass, J.6
Kambadur, R.7
-
159
-
-
0037191752
-
Functional improvement of dystrophic muscle by myostatin blockade
-
Bogdanovich S, Krag TO, Barton ER, Morris LD, Whittemore LA, Ahima RS, Khurana TS (2002) Functional improvement of dystrophic muscle by myostatin blockade. Nature 420:418-421
-
(2002)
Nature
, vol.420
, pp. 418-421
-
-
Bogdanovich, S.1
Krag, T.O.2
Barton, E.R.3
Morris, L.D.4
Whittemore, L.A.5
Ahima, R.S.6
Khurana, T.S.7
-
160
-
-
0036895736
-
Loss of myostatin attenuates severity of muscular dystrophy in mdx mice
-
Wagner KR, McPherron AC, Winik N, Lee SJ (2002) Loss of myostatin attenuates severity of muscular dystrophy in mdx mice. Ann Neurol 52:832-836
-
(2002)
Ann Neurol
, vol.52
, pp. 832-836
-
-
Wagner, K.R.1
McPherron, A.C.2
Winik, N.3
Lee, S.J.4
-
161
-
-
0033001067
-
Discordant expression of utrophin and its transcript in human and mouse skeletal muscles
-
Gramolini AO, Karpati G, Jasmin BJ (1999) Discordant expression of utrophin and its transcript in human and mouse skeletal muscles. J Neuropathol Exp Neurol 58:235-244
-
(1999)
J Neuropathol Exp Neurol
, vol.58
, pp. 235-244
-
-
Gramolini, A.O.1
Karpati, G.2
Jasmin, B.J.3
-
162
-
-
0033427671
-
Nitric oxide and 1-arginine cause an accumulation of utrophin at the sarcolemma: A possible compensation for dystrophin loss in Duchenne muscular dystrophy
-
Chaubourt E, Fossier P, Baux G, Leprince C, Israel M, De La Porte S (1999) Nitric oxide and 1-arginine cause an accumulation of utrophin at the sarcolemma: a possible compensation for dystrophin loss in Duchenne muscular dystrophy. Neurobiol Dis 6:499-507
-
(1999)
Neurobiol Dis
, vol.6
, pp. 499-507
-
-
Chaubourt, E.1
Fossier, P.2
Baux, G.3
Leprince, C.4
Israel, M.5
De La Porte, S.6
-
163
-
-
0029003446
-
G-utrophin, the autosomal homologue of dystrophin Dp116, is expressed in sensory ganglia and brain
-
Blake DJ, Schofield JN, Zuellig RA, Gorecki DC, Phelps SR, Barnard EA, Edwards YH, Davies KE (1995) G-utrophin, the autosomal homologue of dystrophin Dp116, is expressed in sensory ganglia and brain. Proc Natl Acad Sci USA 92:3697-3701
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 3697-3701
-
-
Blake, D.J.1
Schofield, J.N.2
Zuellig, R.A.3
Gorecki, D.C.4
Phelps, S.R.5
Barnard, E.A.6
Edwards, Y.H.7
Davies, K.E.8
-
164
-
-
0032770342
-
Up71 and up140, two novel transcripts of utrophin that are homologues of short forms of dystrophin
-
Wilson J, Putt W, Jimenez C, Edwards YH (1999) Up71 and up140, two novel transcripts of utrophin that are homologues of short forms of dystrophin. Hum Mol Genet 8:1271-1278
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1271-1278
-
-
Wilson, J.1
Putt, W.2
Jimenez, C.3
Edwards, Y.H.4
-
165
-
-
0028910291
-
Full-length and short forms of utrophin, the dystrophin-related protein
-
Nguyen TM, Helliwell TR, Simmons C, Winder SJ, Kendrick-Jones J, Davies KE, Morris GE (1995) Full-length and short forms of utrophin, the dystrophin-related protein. FEBS Lett 358:262-266
-
(1995)
FEBS Lett
, vol.358
, pp. 262-266
-
-
Nguyen, T.M.1
Helliwell, T.R.2
Simmons, C.3
Winder, S.J.4
Kendrick-Jones, J.5
Davies, K.E.6
Morris, G.E.7
-
166
-
-
0033066109
-
Characterization of dystrophin and utrophin diversity in the mouse
-
Lumeng CN, Phelps SF, Rafael JA, Cox GA, Hutchinson TL, Begy CR, Adkins E, Wiltshire R, Chamberlain JS (1999) Characterization of dystrophin and utrophin diversity in the mouse. Hum Mol Genet 8:593-599
-
(1999)
Hum Mol Genet
, vol.8
, pp. 593-599
-
-
Lumeng, C.N.1
Phelps, S.F.2
Rafael, J.A.3
Cox, G.A.4
Hutchinson, T.L.5
Begy, C.R.6
Adkins, E.7
Wiltshire, R.8
Chamberlain, J.S.9
-
168
-
-
0033598694
-
A second promoter provides an alternative target for therapeutic up-regulation of utrophin in Duchenne muscular dystrophy
-
Burton EA, Tinsley JM, Holzfeind PJ, Rodrigues NR, Davies KE (1999) A second promoter provides an alternative target for therapeutic up-regulation of utrophin in Duchenne muscular dystrophy. Proc Natl Acad Sci USA 96:14025-14030
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 14025-14030
-
-
Burton, E.A.1
Tinsley, J.M.2
Holzfeind, P.J.3
Rodrigues, N.R.4
Davies, K.E.5
-
169
-
-
0034603148
-
Utrophin transcription is activated by an intronic enhancer
-
Galvagni F, Oliviero S (2000) Utrophin transcription is activated by an intronic enhancer. J Biol Chem 275:3168-3172
-
(2000)
J Biol Chem
, vol.275
, pp. 3168-3172
-
-
Galvagni, F.1
Oliviero, S.2
-
170
-
-
0037160098
-
A- and B-utrophin have different expression patterns and are differentially up-regulated in mdx muscle
-
Weir AP, Burton EA, Harrod G, Davies KE (2002) A-and B-utrophin have different expression patterns and are differentially up-regulated in mdx muscle. J Biol Chem 277:45285-45290
-
(2002)
J Biol Chem
, vol.277
, pp. 45285-45290
-
-
Weir, A.P.1
Burton, E.A.2
Harrod, G.3
Davies, K.E.4
-
171
-
-
0033057369
-
Induction of utrophin gene expression by heregulin in skeletal muscle cells: Role of the N-box motif and GA binding protein
-
Gramolini AO, Angus LM, Schaeffer L, Burton EA, Tinsley JM, Davies KE, Changeux JP, Jasmin BJ (1999) Induction of utrophin gene expression by heregulin in skeletal muscle cells: role of the N-box motif and GA binding protein. Proc Natl Acad Sci USA 96:3223-3227
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 3223-3227
-
-
Gramolini, A.O.1
Angus, L.M.2
Schaeffer, L.3
Burton, E.A.4
Tinsley, J.M.5
Davies, K.E.6
Changeux, J.P.7
Jasmin, B.J.8
-
172
-
-
0032978374
-
Activation of utrophin promoter by heregulin via the ets-related transcription factor complex GA-binding protein alpha/beta
-
Khurana TS, Rosmarin AG, Shang J, Krag TO, Das S, Gammeltoft S (1999) Activation of utrophin promoter by heregulin via the ets-related transcription factor complex GA-binding protein alpha/beta. Mol Biol Cell 10:2075-2086
-
(1999)
Mol Biol Cell
, vol.10
, pp. 2075-2086
-
-
Khurana, T.S.1
Rosmarin, A.G.2
Shang, J.3
Krag, T.O.4
Das, S.5
Gammeltoft, S.6
-
173
-
-
0035584042
-
The role of basal and myogenic factors in the transcriptional activation of utrophin promoter A: Implications for therapeutic up-regulation in Duchenne muscular dystrophy
-
Perkins KJ, Burton EA, Davies KE (2001) The role of basal and myogenic factors in the transcriptional activation of utrophin promoter A: implications for therapeutic up-regulation in Duchenne muscular dystrophy. Nucleic Acids Res 29:4843-4850
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 4843-4850
-
-
Perkins, K.J.1
Burton, E.A.2
Davies, K.E.3
-
174
-
-
0035830950
-
Sp1 and Sp3 physically interact and co-operate with GABP for the activation of the utrophin promoter
-
Galvagni F, Capo S, Oliviero S (2001) Sp1 and Sp3 physically interact and co-operate with GABP for the activation of the utrophin promoter. J Mol Biol 306:985-996
-
(2001)
J Mol Biol
, vol.306
, pp. 985-996
-
-
Galvagni, F.1
Capo, S.2
Oliviero, S.3
-
175
-
-
0037093783
-
Sp1 and the ets-related transcription factor complex GABP alpha/beta functionally cooperate to activate the utrophin promoter
-
Gyrd-Hansen M, Krag TO, Rosmarin AG, Khurana TS (2002) Sp1 and the ets-related transcription factor complex GABP alpha/beta functionally cooperate to activate the utrophin promoter. J Neurol Sci 197:27-35
-
(2002)
J Neurol Sci
, vol.197
, pp. 27-35
-
-
Gyrd-Hansen, M.1
Krag, T.O.2
Rosmarin, A.G.3
Khurana, T.S.4
-
176
-
-
0037596624
-
Expression of utrophin a mRNA correlates with the oxidative capacity of skeletal muscle fiber types and is regulated by calcineurin/NFAT signaling
-
Chakkalakal JV, Stocksley MA, Harrison MA, Angus LM, Deschenes-Furry J, St Pierre S, Megeney LA, Chin ER, Michel RN, Jasmin BJ (2003) Expression of utrophin A mRNA correlates with the oxidative capacity of skeletal muscle fiber types and is regulated by calcineurin/NFAT signaling. Proc Natl Acad Sci USA 100:7791-7796
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 7791-7796
-
-
Chakkalakal, J.V.1
Stocksley, M.A.2
Harrison, M.A.3
Angus, L.M.4
Deschenes-Furry, J.5
St Pierre, S.6
Megeney, L.A.7
Chin, E.R.8
Michel, R.N.9
Jasmin, B.J.10
-
177
-
-
0036133504
-
Therapeutic possibilities in muscular dystrophy: The hope versus hype
-
Dubowitz V (2002) Therapeutic possibilities in muscular dystrophy: the hope versus hype. Neuromuscul Disord 12:116
-
(2002)
Neuromuscul Disord
, vol.12
, pp. 116
-
-
Dubowitz, V.1
|