-
1
-
-
84859181514
-
Evidence-based path to newborn screening for Duchenne muscular dystrophy
-
Mendell JR, Shilling C, Leslie ND, Flanigan KM, al-Dahhak R, et al. (2012) Evidence-based path to newborn screening for Duchenne muscular dystrophy. Ann Neurol 71: 304-313.
-
(2012)
Ann Neurol
, vol.71
, pp. 304-313
-
-
Mendell, J.R.1
Shilling, C.2
Leslie, N.D.3
Flanigan, K.M.4
Al-Dahhak, R.5
-
2
-
-
0023614188
-
Dystrophin: the protein product of the Duchenne muscular dystrophy locus
-
Hoffman EP, Brown RH Jr, 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
-
3
-
-
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, et al. (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
-
4
-
-
24644501292
-
Molecular extensibility of mini-dystrophins and a dystrophin rod construct
-
Bhasin N, Law R, Liao G, Safer D, Ellmer J, et al. (2005) Molecular extensibility of mini-dystrophins and a dystrophin rod construct. J Mol Biol 352: 795-806.
-
(2005)
J Mol Biol
, vol.352
, pp. 795-806
-
-
Bhasin, N.1
Law, R.2
Liao, G.3
Safer, D.4
Ellmer, J.5
-
5
-
-
77955095972
-
A biophysical map of the dystrophin rod
-
Mirza A, Sagathevan M, Sahni N, Choi L, Menhart N, (2010) A biophysical map of the dystrophin rod. Biochim Biophys Acta 1804: 1796-1809.
-
(2010)
Biochim Biophys Acta
, vol.1804
, pp. 1796-1809
-
-
Mirza, A.1
Sagathevan, M.2
Sahni, N.3
Choi, L.4
Menhart, N.5
-
6
-
-
77953108170
-
Disease-causing missense mutations in actin binding domain 1 of dystrophin induce thermodynamic instability and protein aggregation
-
Henderson DM, Lee A, Ervasti JM, (2010) Disease-causing missense mutations in actin binding domain 1 of dystrophin induce thermodynamic instability and protein aggregation. Proc Natl Acad Sci U S A 107: 9632-9637.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 9632-9637
-
-
Henderson, D.M.1
Lee, A.2
Ervasti, J.M.3
-
7
-
-
38949130017
-
Biology of the striated muscle dystrophin-glycoprotein complex
-
Ervasti JM, Sonnemann KJ, (2008) Biology of the striated muscle dystrophin-glycoprotein complex. Int Rev Cytol 265: 191-225.
-
(2008)
Int Rev Cytol
, vol.265
, pp. 191-225
-
-
Ervasti, J.M.1
Sonnemann, K.J.2
-
8
-
-
0025815479
-
Membrane organization of the dystrophin-glycoprotein complex
-
Ervasti JM, Campbell KP, (1991) Membrane organization of the dystrophin-glycoprotein complex. Cell 66: 1121-1131.
-
(1991)
Cell
, vol.66
, pp. 1121-1131
-
-
Ervasti, J.M.1
Campbell, K.P.2
-
9
-
-
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
-
10
-
-
0025272250
-
Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle
-
Ervasti JM, Ohlendieck K, Kahl SD, Gaver MG, Campbell KP, (1990) Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle. Nature 345: 315-319.
-
(1990)
Nature
, vol.345
, pp. 315-319
-
-
Ervasti, J.M.1
Ohlendieck, K.2
Kahl, S.D.3
Gaver, M.G.4
Campbell, K.P.5
-
11
-
-
33846271135
-
Dystrophin, its interactions with other proteins, and implications for muscular dystrophy
-
Ervasti JM, (2007) Dystrophin, its interactions with other proteins, and implications for muscular dystrophy. Biochim Biophys Acta 1772: 108-117.
-
(2007)
Biochim Biophys Acta
, vol.1772
, pp. 108-117
-
-
Ervasti, J.M.1
-
12
-
-
57049122968
-
Sarcolemma-localized nNOS is required to maintain activity after mild exercise
-
Kobayashi YM, Rader EP, Crawford RW, Iyengar NK, Thedens DR, et al. (2008) Sarcolemma-localized nNOS is required to maintain activity after mild exercise. Nature 456: 511-515.
-
(2008)
Nature
, vol.456
, pp. 511-515
-
-
Kobayashi, Y.M.1
Rader, E.P.2
Crawford, R.W.3
Iyengar, N.K.4
Thedens, D.R.5
-
13
-
-
0033175570
-
Role for alpha-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies
-
Grady RM, Grange RW, Lau KS, Maimone MM, Nichol MC, et al. (1999) Role for alpha-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies. Nat Cell Biol 1: 215-220.
-
(1999)
Nat Cell Biol
, vol.1
, pp. 215-220
-
-
Grady, R.M.1
Grange, R.W.2
Lau, K.S.3
Maimone, M.M.4
Nichol, M.C.5
-
14
-
-
0031906615
-
Rapid recovery following contraction-induced injury to in situ skeletal muscles in mdx mice
-
Brooks SV, (1998) Rapid recovery following contraction-induced injury to in situ skeletal muscles in mdx mice. J Muscle Res Cell Motil 19: 179-187.
-
(1998)
J Muscle Res Cell Motil
, vol.19
, pp. 179-187
-
-
Brooks, S.V.1
-
15
-
-
0035726738
-
Tibialis anterior muscles in mdx mice are highly susceptible to contraction-induced injury
-
Dellorusso C, Crawford RW, Chamberlain JS, Brooks SV, (2001) Tibialis anterior muscles in mdx mice are highly susceptible to contraction-induced injury. J Muscle Res Cell Motil 22: 467-475.
-
(2001)
J Muscle Res Cell Motil
, vol.22
, pp. 467-475
-
-
Dellorusso, C.1
Crawford, R.W.2
Chamberlain, J.S.3
Brooks, S.V.4
-
16
-
-
44249103048
-
Diaphragm muscle strip preparation for evaluation of gene therapies in mdx mice
-
Faulkner JA, Ng R, Davis CS, Li S, Chamberlain JS, (2008) Diaphragm muscle strip preparation for evaluation of gene therapies in mdx mice. Clin Exp Pharmacol Physiol 35: 725-729.
-
(2008)
Clin Exp Pharmacol Physiol
, vol.35
, pp. 725-729
-
-
Faulkner, J.A.1
Ng, R.2
Davis, C.S.3
Li, S.4
Chamberlain, J.S.5
-
17
-
-
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
-
18
-
-
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 U S A 90: 3710-3714.
-
(1993)
Proc Natl Acad Sci U S A
, 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
-
19
-
-
58749101371
-
The value of mammalian models for duchenne muscular dystrophy in developing therapeutic strategies
-
Banks GB, Chamberlain JS, (2008) The value of mammalian models for duchenne muscular dystrophy in developing therapeutic strategies. Curr Top Dev Biol 84: 431-453.
-
(2008)
Curr Top Dev Biol
, vol.84
, pp. 431-453
-
-
Banks, G.B.1
Chamberlain, J.S.2
-
20
-
-
0024538824
-
An autosomal transcript in skeletal muscle with homology to dystrophin
-
Love DR, Hill DF, Dickson G, Spurr NK, Byth BC, et al. (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
-
21
-
-
0025932274
-
Immunolocalization and developmental expression of dystrophin related protein in skeletal muscle
-
Khurana TS, Watkins SC, Chafey P, Chelly J, Tome FM, et al. (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
-
22
-
-
0027745279
-
Dystrophin and dystrophin-related protein (utrophin) distribution in normal and dystrophin-deficient skeletal muscles
-
Pons F, Nicholson LV, Robert A, Voit T, Leger JJ, (1993) Dystrophin and dystrophin-related protein (utrophin) distribution in normal and dystrophin-deficient skeletal muscles. Neuromuscul Disord 3: 507-514.
-
(1993)
Neuromuscul Disord
, vol.3
, pp. 507-514
-
-
Pons, F.1
Nicholson, L.V.2
Robert, A.3
Voit, T.4
Leger, J.J.5
-
23
-
-
0030848969
-
Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy
-
Deconinck AE, Rafael JA, Skinner JA, Brown SC, Potter AC, et al. (1997) Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy. Cell 90: 717-727.
-
(1997)
Cell
, vol.90
, pp. 717-727
-
-
Deconinck, A.E.1
Rafael, J.A.2
Skinner, J.A.3
Brown, S.C.4
Potter, A.C.5
-
24
-
-
0030848338
-
Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: a model for Duchenne muscular dystrophy
-
Grady RM, Teng H, Nichol MC, Cunningham JC, Wilkinson RS, et al. (1997) Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: a model for Duchenne muscular dystrophy. Cell 90: 729-738.
-
(1997)
Cell
, vol.90
, pp. 729-738
-
-
Grady, R.M.1
Teng, H.2
Nichol, M.C.3
Cunningham, J.C.4
Wilkinson, R.S.5
-
25
-
-
0028117937
-
Absence of dystrophin and utrophin in a boy with severe muscular dystrophy
-
Chevron MP, Echenne B, Demaille J, (1994) Absence of dystrophin and utrophin in a boy with severe muscular dystrophy. N Engl J Med 331: 1162-1163.
-
(1994)
N Engl J Med
, vol.331
, pp. 1162-1163
-
-
Chevron, M.P.1
Echenne, B.2
Demaille, J.3
-
26
-
-
0031727771
-
Expression of full-length utrophin prevents muscular dystrophy in mdx mice
-
Tinsley J, Deconinck N, Fisher R, Kahn D, Phelps S, et al. (1998) Expression of full-length utrophin prevents muscular dystrophy in mdx mice. Nat Med 4: 1441-1444.
-
(1998)
Nat Med
, vol.4
, pp. 1441-1444
-
-
Tinsley, J.1
Deconinck, N.2
Fisher, R.3
Kahn, D.4
Phelps, S.5
-
27
-
-
0027461720
-
Localization and quantitation of the chromosome 6-encoded dystrophin-related protein in normal and pathological human muscle
-
Karpati G, Carpenter S, Morris GE, Davies KE, Guerin C, et al. (1993) Localization and quantitation of the chromosome 6-encoded dystrophin-related protein in normal and pathological human muscle. J Neuropathol Exp Neurol 52: 119-128.
-
(1993)
J Neuropathol Exp Neurol
, vol.52
, pp. 119-128
-
-
Karpati, G.1
Carpenter, S.2
Morris, G.E.3
Davies, K.E.4
Guerin, C.5
-
28
-
-
0027358450
-
Reciprocal expression of dystrophin and utrophin in muscles of Duchenne muscular dystrophy patients, female DMD-carriers and control subjects
-
Mizuno Y, Nonaka I, Hirai S, Ozawa E, (1993) Reciprocal expression of dystrophin and utrophin in muscles of Duchenne muscular dystrophy patients, female DMD-carriers and control subjects. J Neurol Sci 119: 43-52.
-
(1993)
J Neurol Sci
, vol.119
, pp. 43-52
-
-
Mizuno, Y.1
Nonaka, I.2
Hirai, S.3
Ozawa, E.4
-
29
-
-
33745183090
-
Naturally occurring utrophin correlates with disease severity in Duchenne muscular dystrophy
-
Kleopa KA, Drousiotou A, Mavrikiou E, Ormiston A, Kyriakides T, (2006) Naturally occurring utrophin correlates with disease severity in Duchenne muscular dystrophy. Hum Mol Genet 15: 1623-1628.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 1623-1628
-
-
Kleopa, K.A.1
Drousiotou, A.2
Mavrikiou, E.3
Ormiston, A.4
Kyriakides, T.5
-
30
-
-
0029160868
-
Absence of correlation between utrophin localization and quantity and the clinical severity in Duchenne/Becker dystrophies
-
Vainzof M, Passos-Bueno MR, Man N, Zatz M, (1995) Absence of correlation between utrophin localization and quantity and the clinical severity in Duchenne/Becker dystrophies. Am J Med Genet 58: 305-309.
-
(1995)
Am J Med Genet
, vol.58
, pp. 305-309
-
-
Vainzof, M.1
Passos-Bueno, M.R.2
Man, N.3
Zatz, M.4
-
31
-
-
0030824137
-
The abnormal expression of utrophin in Duchenne and Becker muscular dystrophy is age related
-
Taylor J, Muntoni F, Dubowitz V, Sewry CA, (1997) The abnormal expression of utrophin in Duchenne and Becker muscular dystrophy is age related. Neuropathol Appl Neurobiol 23: 399-405.
-
(1997)
Neuropathol Appl Neurobiol
, vol.23
, pp. 399-405
-
-
Taylor, J.1
Muntoni, F.2
Dubowitz, V.3
Sewry, C.A.4
-
32
-
-
84883713705
-
Anti-dystrophin T cell responses in Duchenne muscular dystrophy: prevalence and a glucocorticoid treatment effect
-
Flanigan KM, Campbell K, Viollet L, Wang W, Gomez AM, et al. (2013) Anti-dystrophin T cell responses in Duchenne muscular dystrophy: prevalence and a glucocorticoid treatment effect. Hum Gene Ther 24: 797-806.
-
(2013)
Hum Gene Ther
, vol.24
, pp. 797-806
-
-
Flanigan, K.M.1
Campbell, K.2
Viollet, L.3
Wang, W.4
Gomez, A.M.5
-
33
-
-
84878016335
-
Therapy for Duchenne muscular dystrophy: renewed optimism from genetic approaches
-
Fairclough RJ, Wood MJ, Davies KE, (2013) Therapy for Duchenne muscular dystrophy: renewed optimism from genetic approaches. Nat Rev Genet 14: 373-378.
-
(2013)
Nat Rev Genet
, vol.14
, pp. 373-378
-
-
Fairclough, R.J.1
Wood, M.J.2
Davies, K.E.3
-
34
-
-
84890054617
-
Human Treg responses allow sustained recombinant adeno-associated virus-mediated transgene expression
-
Mueller C, Chulay JD, Trapnell BC, Humphries M, Carey B, et al. (2013) Human Treg responses allow sustained recombinant adeno-associated virus-mediated transgene expression. J Clin Invest 123: 5310-5318.
-
(2013)
J Clin Invest
, vol.123
, pp. 5310-5318
-
-
Mueller, C.1
Chulay, J.D.2
Trapnell, B.C.3
Humphries, M.4
Carey, B.5
-
35
-
-
79551667507
-
Biglycan recruits utrophin to the sarcolemma and counters dystrophic pathology in mdx mice
-
Amenta AR, Yilmaz A, Bogdanovich S, McKechnie BA, Abedi M, et al. (2011) Biglycan recruits utrophin to the sarcolemma and counters dystrophic pathology in mdx mice. Proc Natl Acad Sci U S A 108: 762-767.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 762-767
-
-
Amenta, A.R.1
Yilmaz, A.2
Bogdanovich, S.3
McKechnie, B.A.4
Abedi, M.5
-
36
-
-
0026460270
-
The dystrophin-related protein, utrophin, is expressed on the sarcolemma of regenerating human skeletal muscle fibres in dystrophies and inflammatory myopathies
-
Helliwell TR, Man NT, Morris GE, Davies KE, (1992) The dystrophin-related protein, utrophin, is expressed on the sarcolemma of regenerating human skeletal muscle fibres in dystrophies and inflammatory myopathies. Neuromuscul Disord 2: 177-184.
-
(1992)
Neuromuscul Disord
, vol.2
, pp. 177-184
-
-
Helliwell, T.R.1
Man, N.T.2
Morris, G.E.3
Davies, K.E.4
-
37
-
-
0345118164
-
A-utrophin up-regulation in mdx skeletal muscle is independent of regeneration
-
Weir AP, Morgan JE, Davies KE, (2004) A-utrophin up-regulation in mdx skeletal muscle is independent of regeneration. Neuromuscul Disord 14: 19-23.
-
(2004)
Neuromuscul Disord
, vol.14
, pp. 19-23
-
-
Weir, A.P.1
Morgan, J.E.2
Davies, K.E.3
-
38
-
-
84897064754
-
The therapeutic potential of skeletal muscle plasticity in Duchenne muscular dystrophy: phenotypic modifiers as pharmacologic targets
-
Ljubicic V, Burt M, Jasmin BJ, (2013) The therapeutic potential of skeletal muscle plasticity in Duchenne muscular dystrophy: phenotypic modifiers as pharmacologic targets. FASEB J 28: 548-568.
-
(2013)
FASEB J
, vol.28
, pp. 548-568
-
-
Ljubicic, V.1
Burt, M.2
Jasmin, B.J.3
-
39
-
-
84882617523
-
The potential of sarcospan in adhesion complex replacement therapeutics for the treatment of muscular dystrophy
-
Marshall JL, Kwok Y, McMorran BJ, Baum LG, Crosbie-Watson RH, (2013) The potential of sarcospan in adhesion complex replacement therapeutics for the treatment of muscular dystrophy. FEBS J 280: 4210-4229.
-
(2013)
FEBS J
, vol.280
, pp. 4210-4229
-
-
Marshall, J.L.1
Kwok, Y.2
McMorran, B.J.3
Baum, L.G.4
Crosbie-Watson, R.H.5
-
40
-
-
57049168054
-
Molecular and cellular adaptations to chronic myotendinous strain injury in mdx mice expressing a truncated dystrophin
-
Banks GB, Combs AC, Chamberlain JR, Chamberlain JS, (2008) Molecular and cellular adaptations to chronic myotendinous strain injury in mdx mice expressing a truncated dystrophin. Hum Mol Genet 17: 3975-3986.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 3975-3986
-
-
Banks, G.B.1
Combs, A.C.2
Chamberlain, J.R.3
Chamberlain, J.S.4
-
41
-
-
77953228905
-
The polyproline site in hinge 2 influences the functional capacity of truncated dystrophins
-
Banks GB, Judge LM, Allen JM, Chamberlain JS, (2010) The polyproline site in hinge 2 influences the functional capacity of truncated dystrophins. PLoS Genet 6: e1000958.
-
(2010)
PLoS Genet
, vol.6
-
-
Banks, G.B.1
Judge, L.M.2
Allen, J.M.3
Chamberlain, J.S.4
-
42
-
-
0011497688
-
Immunological characterization of the subunit of the 100 A filaments from muscle cells
-
Lazarides E, Hubbard BD, (1976) Immunological characterization of the subunit of the 100 A filaments from muscle cells. Proc Natl Acad Sci U S A 73: 4344-4348.
-
(1976)
Proc Natl Acad Sci U S A
, vol.73
, pp. 4344-4348
-
-
Lazarides, E.1
Hubbard, B.D.2
-
43
-
-
0017814974
-
Specificity of desmin to avian and mammalian muscle cells
-
Lazarides E, Balzer DR Jr, (1978) Specificity of desmin to avian and mammalian muscle cells. Cell 14: 429-438.
-
(1978)
Cell
, vol.14
, pp. 429-438
-
-
Lazarides, E.1
Balzer Jr., D.R.2
-
44
-
-
0030879081
-
Desmin is essential for the tensile strength and integrity of myofibrils but not for myogenic commitment, differentiation, and fusion of skeletal muscle
-
Li Z, Mericskay M, Agbulut O, Butler-Browne G, Carlsson L, et al. (1997) Desmin is essential for the tensile strength and integrity of myofibrils but not for myogenic commitment, differentiation, and fusion of skeletal muscle. J Cell Biol 139: 129-144.
-
(1997)
J Cell Biol
, vol.139
, pp. 129-144
-
-
Li, Z.1
Mericskay, M.2
Agbulut, O.3
Butler-Browne, G.4
Carlsson, L.5
-
45
-
-
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
-
46
-
-
0038190993
-
Costameres: the Achilles' heel of Herculean muscle
-
Ervasti JM, (2003) Costameres: the Achilles' heel of Herculean muscle. J Biol Chem 278: 13591-13594.
-
(2003)
J Biol Chem
, vol.278
, pp. 13591-13594
-
-
Ervasti, J.M.1
-
47
-
-
0036320665
-
Sarcolemmal organization in skeletal muscle lacking desmin: evidence for cytokeratins associated with the membrane skeleton at costameres
-
O'Neill A, Williams MW, Resneck WG, Milner DJ, Capetanaki Y, et al. (2002) Sarcolemmal organization in skeletal muscle lacking desmin: evidence for cytokeratins associated with the membrane skeleton at costameres. Mol Biol Cell 13: 2347-2359.
-
(2002)
Mol Biol Cell
, vol.13
, pp. 2347-2359
-
-
O'Neill, A.1
Williams, M.W.2
Resneck, W.G.3
Milner, D.J.4
Capetanaki, Y.5
-
48
-
-
0029893923
-
Cardiovascular lesions and skeletal myopathy in mice lacking desmin
-
Li Z, Colucci-Guyon E, Pincon-Raymond M, Mericskay M, Pournin S, et al. (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
-
49
-
-
11244256463
-
Dystrophin- and MLP-deficient mouse hearts: marked differences in morphology and function, but similar accumulation of cytoskeletal proteins
-
Wilding JR, Schneider JE, Sang AE, Davies KE, Neubauer S, et al. (2005) Dystrophin- and MLP-deficient mouse hearts: marked differences in morphology and function, but similar accumulation of cytoskeletal proteins. FASEB J 19: 79-81.
-
(2005)
FASEB J
, vol.19
, pp. 79-81
-
-
Wilding, J.R.1
Schneider, J.E.2
Sang, A.E.3
Davies, K.E.4
Neubauer, S.5
-
50
-
-
77953292369
-
Proteomic profiling of naturally protected extraocular muscles from the dystrophin-deficient mdx mouse
-
Lewis C, Ohlendieck K, (2010) Proteomic profiling of naturally protected extraocular muscles from the dystrophin-deficient mdx mouse. Biochem Biophys Res Commun 396: 1024-1029.
-
(2010)
Biochem Biophys Res Commun
, vol.396
, pp. 1024-1029
-
-
Lewis, C.1
Ohlendieck, K.2
-
51
-
-
34347374860
-
Dystrophin-deficient mdx mice display a reduced life span and are susceptible to spontaneous rhabdomyosarcoma
-
Chamberlain JS, Metzger J, Reyes M, Townsend D, Faulkner JA, (2007) Dystrophin-deficient mdx mice display a reduced life span and are susceptible to spontaneous rhabdomyosarcoma. FASEB J 21: 2195-2204.
-
(2007)
FASEB J
, vol.21
, pp. 2195-2204
-
-
Chamberlain, J.S.1
Metzger, J.2
Reyes, M.3
Townsend, D.4
Faulkner, J.A.5
-
52
-
-
79955130118
-
Physiology, structure, and susceptibility to injury of skeletal muscle in mice lacking keratin 19-based and desmin-based intermediate filaments
-
Lovering RM, O'Neill A, Muriel JM, Prosser BL, Strong J, et al. (2011) Physiology, structure, and susceptibility to injury of skeletal muscle in mice lacking keratin 19-based and desmin-based intermediate filaments. Am J Physiol Cell Physiol 300: C803-813.
-
(2011)
Am J Physiol Cell Physiol
, vol.300
-
-
Lovering, R.M.1
O'Neill, A.2
Muriel, J.M.3
Prosser, B.L.4
Strong, J.5
-
53
-
-
50549098032
-
Microutrophin delivery through rAAV6 increases lifespan and improves muscle function in dystrophic dystrophin/utrophin-deficient mice
-
Odom GL, Gregorevic P, Allen JM, Finn E, Chamberlain JS, (2008) Microutrophin delivery through rAAV6 increases lifespan and improves muscle function in dystrophic dystrophin/utrophin-deficient mice. Mol Ther 16: 1539-1545.
-
(2008)
Mol Ther
, vol.16
, pp. 1539-1545
-
-
Odom, G.L.1
Gregorevic, P.2
Allen, J.M.3
Finn, E.4
Chamberlain, J.S.5
-
54
-
-
0025880785
-
Dystrophin-related protein in the fetal and denervated skeletal muscles of normal and mdx mice
-
Takemitsu M, Ishiura S, Koga R, Kamakura K, Arahata K, et al. (1991) Dystrophin-related protein in the fetal and denervated skeletal muscles of normal and mdx mice. Biochem Biophys Res Commun 180: 1179-1186.
-
(1991)
Biochem Biophys Res Commun
, vol.180
, pp. 1179-1186
-
-
Takemitsu, M.1
Ishiura, S.2
Koga, R.3
Kamakura, K.4
Arahata, K.5
-
55
-
-
26944467581
-
A and B utrophin in human muscle and sarcolemmal A-utrophin associated with tumours
-
Sewry CA, Nowak KJ, Ehmsen JT, Davies KE, (2005) A and B utrophin in human muscle and sarcolemmal A-utrophin associated with tumours. Neuromuscul Disord 15: 779-785.
-
(2005)
Neuromuscul Disord
, vol.15
, pp. 779-785
-
-
Sewry, C.A.1
Nowak, K.J.2
Ehmsen, J.T.3
Davies, K.E.4
-
56
-
-
0028066835
-
An E box in the desmin promoter cooperates with the E box and MEF-2 sites of a distal enhancer to direct muscle-specific transcription
-
Li H, Capetanaki Y, (1994) An E box in the desmin promoter cooperates with the E box and MEF-2 sites of a distal enhancer to direct muscle-specific transcription. EMBO J 13: 3580-3589.
-
(1994)
EMBO J
, vol.13
, pp. 3580-3589
-
-
Li, H.1
Capetanaki, Y.2
-
57
-
-
0029558009
-
Cytoskeletal control of myogenesis: a desmin null mutation blocks the myogenic pathway during embryonic stem cell differentiation
-
Weitzer G, Milner DJ, Kim JU, Bradley A, Capetanaki Y, (1995) Cytoskeletal control of myogenesis: a desmin null mutation blocks the myogenic pathway during embryonic stem cell differentiation. Dev Biol 172: 422-439.
-
(1995)
Dev Biol
, vol.172
, pp. 422-439
-
-
Weitzer, G.1
Milner, D.J.2
Kim, J.U.3
Bradley, A.4
Capetanaki, Y.5
-
58
-
-
0030966537
-
Desmin in muscle formation and maintenance: knockouts and consequences
-
Capetanaki Y, Milner DJ, Weitzer G, (1997) Desmin in muscle formation and maintenance: knockouts and consequences. Cell Struct Funct 22: 103-116.
-
(1997)
Cell Struct Funct
, vol.22
, pp. 103-116
-
-
Capetanaki, Y.1
Milner, D.J.2
Weitzer, G.3
-
59
-
-
0034952084
-
Lack of desmin results in abortive muscle regeneration and modifications in synaptic structure
-
Agbulut O, Li Z, Perie S, Ludosky MA, Paulin D, et al. (2001) Lack of desmin results in abortive muscle regeneration and modifications in synaptic structure. Cell Motil Cytoskeleton 49: 51-66.
-
(2001)
Cell Motil Cytoskeleton
, vol.49
, pp. 51-66
-
-
Agbulut, O.1
Li, Z.2
Perie, S.3
Ludosky, M.A.4
Paulin, D.5
-
60
-
-
44149113780
-
Myofiber integrity depends on desmin network targeting to Z-disks and costameres via distinct plectin isoforms
-
Konieczny P, Fuchs P, Reipert S, Kunz WS, Zeold A, et al. (2008) Myofiber integrity depends on desmin network targeting to Z-disks and costameres via distinct plectin isoforms. J Cell Biol 181: 667-681.
-
(2008)
J Cell Biol
, vol.181
, pp. 667-681
-
-
Konieczny, P.1
Fuchs, P.2
Reipert, S.3
Kunz, W.S.4
Zeold, A.5
-
61
-
-
0026328022
-
Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice
-
Ohlendieck K, Campbell KP, (1991) Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice. J Cell Biol 115: 1685-1694.
-
(1991)
J Cell Biol
, vol.115
, pp. 1685-1694
-
-
Ohlendieck, K.1
Campbell, K.P.2
-
62
-
-
84883818628
-
Skeletal muscle programming and re-programming
-
Fong AP, Tapscott SJ, (2013) Skeletal muscle programming and re-programming. Curr Opin Genet Dev 23: 568-573.
-
(2013)
Curr Opin Genet Dev
, vol.23
, pp. 568-573
-
-
Fong, A.P.1
Tapscott, S.J.2
-
63
-
-
33749557894
-
MyoD inhibits Fstl1 and Utrn expression by inducing transcription of miR-206
-
Rosenberg MI, Georges SA, Asawachaicharn A, Analau E, Tapscott SJ, (2006) MyoD inhibits Fstl1 and Utrn expression by inducing transcription of miR-206. J Cell Biol 175: 77-85.
-
(2006)
J Cell Biol
, vol.175
, pp. 77-85
-
-
Rosenberg, M.I.1
Georges, S.A.2
Asawachaicharn, A.3
Analau, E.4
Tapscott, S.J.5
-
64
-
-
84455172952
-
Translational regulation of utrophin by miRNAs
-
Basu U, Lozynska O, Moorwood C, Patel G, Wilton SD, et al. (2011) Translational regulation of utrophin by miRNAs. PLoS One 6: e29376.
-
(2011)
PLoS One
, vol.6
-
-
Basu, U.1
Lozynska, O.2
Moorwood, C.3
Patel, G.4
Wilton, S.D.5
-
65
-
-
0033200108
-
Expression of the utrophin gene during myogenic differentiation
-
Gramolini AO, Jasmin BJ, (1999) Expression of the utrophin gene during myogenic differentiation. Nucleic Acids Res 27: 3603-3609.
-
(1999)
Nucleic Acids Res
, vol.27
, pp. 3603-3609
-
-
Gramolini, A.O.1
Jasmin, B.J.2
-
66
-
-
2142816651
-
Structural and functional roles of desmin in mouse skeletal muscle during passive deformation
-
Shah SB, Davis J, Weisleder N, Kostavassili I, McCulloch AD, et al. (2004) Structural and functional roles of desmin in mouse skeletal muscle during passive deformation. Biophys J 86: 2993-3008.
-
(2004)
Biophys J
, vol.86
, pp. 2993-3008
-
-
Shah, S.B.1
Davis, J.2
Weisleder, N.3
Kostavassili, I.4
McCulloch, A.D.5
-
67
-
-
35148891642
-
Cognitive outcome following brain injury and treatment with an inhibitor of Nogo-A in association with an attenuated downregulation of hippocampal growth-associated protein-43 expression
-
Marklund N, Bareyre FM, Royo NC, Thompson HJ, Mir AK, et al. (2007) Cognitive outcome following brain injury and treatment with an inhibitor of Nogo-A in association with an attenuated downregulation of hippocampal growth-associated protein-43 expression. J Neurosurg 107: 844-853.
-
(2007)
J Neurosurg
, vol.107
, pp. 844-853
-
-
Marklund, N.1
Bareyre, F.M.2
Royo, N.C.3
Thompson, H.J.4
Mir, A.K.5
-
68
-
-
2442548917
-
Modifications of chromatin structure and gene expression following induced alterations of cellular shape
-
Vergani L, Grattarola M, Nicolini C, (2004) Modifications of chromatin structure and gene expression following induced alterations of cellular shape. Int J Biochem Cell Biol 36: 1447-1461.
-
(2004)
Int J Biochem Cell Biol
, vol.36
, pp. 1447-1461
-
-
Vergani, L.1
Grattarola, M.2
Nicolini, C.3
-
69
-
-
0030953763
-
Geometric control of cell life and death
-
Chen CS, Mrksich M, Huang S, Whitesides GM, Ingber DE, (1997) Geometric control of cell life and death. Science 276: 1425-1428.
-
(1997)
Science
, vol.276
, pp. 1425-1428
-
-
Chen, C.S.1
Mrksich, M.2
Huang, S.3
Whitesides, G.M.4
Ingber, D.E.5
-
70
-
-
11144355499
-
Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice
-
Nikolova V, Leimena C, McMahon AC, Tan JC, Chandar S, et al. (2004) Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice. J Clin Invest 113: 357-369.
-
(2004)
J Clin Invest
, vol.113
, pp. 357-369
-
-
Nikolova, V.1
Leimena, C.2
McMahon, A.C.3
Tan, J.C.4
Chandar, S.5
-
71
-
-
79952361967
-
Plectin interacts with the rod domain of type III intermediate filament proteins desmin and vimentin
-
Favre B, Schneider Y, Lingasamy P, Bouameur JE, Begre N, et al. (2011) Plectin interacts with the rod domain of type III intermediate filament proteins desmin and vimentin. Eur J Cell Biol 90: 390-400.
-
(2011)
Eur J Cell Biol
, vol.90
, pp. 390-400
-
-
Favre, B.1
Schneider, Y.2
Lingasamy, P.3
Bouameur, J.E.4
Begre, N.5
-
72
-
-
60549111399
-
Muscular integrity-a matter of interlinking distinct structures via plectin
-
Konieczny P, Wiche G, (2008) Muscular integrity-a matter of interlinking distinct structures via plectin. Adv Exp Med Biol 642: 165-175.
-
(2008)
Adv Exp Med Biol
, vol.642
, pp. 165-175
-
-
Konieczny, P.1
Wiche, G.2
-
73
-
-
0034789719
-
Increased expression of utrophin in a slow vs. a fast muscle involves posttranscriptional events
-
Gramolini AO, Belanger G, Thompson JM, Chakkalakal JV, Jasmin BJ, (2001) Increased expression of utrophin in a slow vs. a fast muscle involves posttranscriptional events. Am J Physiol Cell Physiol 281: C1300-1309.
-
(2001)
Am J Physiol Cell Physiol
, vol.281
-
-
Gramolini, A.O.1
Belanger, G.2
Thompson, J.M.3
Chakkalakal, J.V.4
Jasmin, B.J.5
-
74
-
-
25444500449
-
Calcineurin-NFAT signaling, together with GABP and peroxisome PGC-1{alpha}, drives utrophin gene expression at the neuromuscular junction
-
Angus LM, Chakkalakal JV, Mejat A, Eibl JK, Belanger G, et al. (2005) Calcineurin-NFAT signaling, together with GABP and peroxisome PGC-1{alpha}, drives utrophin gene expression at the neuromuscular junction. Am J Physiol Cell Physiol 289: C908-917.
-
(2005)
Am J Physiol Cell Physiol
, vol.289
-
-
Angus, L.M.1
Chakkalakal, J.V.2
Mejat, A.3
Eibl, J.K.4
Belanger, G.5
-
75
-
-
84879418084
-
Rescue of dystrophic skeletal muscle by PGC-1alpha involves restored expression of dystrophin-associated protein complex components and satellite cell signaling
-
Hollinger K, Gardan-Salmon D, Santana C, Rice D, Snella E, et al. (2013) Rescue of dystrophic skeletal muscle by PGC-1alpha involves restored expression of dystrophin-associated protein complex components and satellite cell signaling. Am J Physiol Regul Integr Comp Physiol 305: R13-23.
-
(2013)
Am J Physiol Regul Integr Comp Physiol
, vol.305
-
-
Hollinger, K.1
Gardan-Salmon, D.2
Santana, C.3
Rice, D.4
Snella, E.5
-
76
-
-
84855685417
-
Rescue of dystrophic skeletal muscle by PGC-1alpha involves a fast to slow fiber type shift in the mdx mouse
-
Selsby JT, Morine KJ, Pendrak K, Barton ER, Sweeney HL, (2012) Rescue of dystrophic skeletal muscle by PGC-1alpha involves a fast to slow fiber type shift in the mdx mouse. PLoS One 7: e30063.
-
(2012)
PLoS One
, vol.7
-
-
Selsby, J.T.1
Morine, K.J.2
Pendrak, K.3
Barton, E.R.4
Sweeney, H.L.5
-
77
-
-
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, et al. (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 U S A 100: 7791-7796.
-
(2003)
Proc Natl Acad Sci U S A
, 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
-
78
-
-
1242353110
-
Stimulation of calcineurin signaling attenuates the dystrophic pathology in mdx mice
-
Chakkalakal JV, Harrison MA, Carbonetto S, Chin E, Michel RN, et al. (2004) Stimulation of calcineurin signaling attenuates the dystrophic pathology in mdx mice. Hum Mol Genet 13: 379-388.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 379-388
-
-
Chakkalakal, J.V.1
Harrison, M.A.2
Carbonetto, S.3
Chin, E.4
Michel, R.N.5
-
79
-
-
10044237735
-
Glucocorticoid treatment alleviates dystrophic myofiber pathology by activation of the calcineurin/NF-AT pathway
-
St-Pierre SJ, Chakkalakal JV, Kolodziejczyk SM, Knudson JC, Jasmin BJ, et al. (2004) Glucocorticoid treatment alleviates dystrophic myofiber pathology by activation of the calcineurin/NF-AT pathway. FASEB J 18: 1937-1939.
-
(2004)
FASEB J
, vol.18
, pp. 1937-1939
-
-
St-Pierre, S.J.1
Chakkalakal, J.V.2
Kolodziejczyk, S.M.3
Knudson, J.C.4
Jasmin, B.J.5
-
80
-
-
34547645404
-
Calcineurin-A alpha activation enhances the structure and function of regenerating muscles after myotoxic injury
-
Stupka N, Schertzer JD, Bassel-Duby R, Olson EN, Lynch GS, (2007) Calcineurin-A alpha activation enhances the structure and function of regenerating muscles after myotoxic injury. Am J Physiol Regul Integr Comp Physiol 293: R686-694.
-
(2007)
Am J Physiol Regul Integr Comp Physiol
, vol.293
-
-
Stupka, N.1
Schertzer, J.D.2
Bassel-Duby, R.3
Olson, E.N.4
Lynch, G.S.5
-
81
-
-
36148950932
-
Ca2+/calmodulin-based signalling in the regulation of the muscle fibre phenotype and its therapeutic potential via modulation of utrophin A and myostatin expression
-
Michel RN, Chin ER, Chakkalakal JV, Eibl JK, Jasmin BJ, (2007) Ca2+/calmodulin-based signalling in the regulation of the muscle fibre phenotype and its therapeutic potential via modulation of utrophin A and myostatin expression. Appl Physiol Nutr Metab 32: 921-929.
-
(2007)
Appl Physiol Nutr Metab
, vol.32
, pp. 921-929
-
-
Michel, R.N.1
Chin, E.R.2
Chakkalakal, J.V.3
Eibl, J.K.4
Jasmin, B.J.5
-
82
-
-
80051692198
-
Chronic AMPK activation evokes the slow, oxidative myogenic program and triggers beneficial adaptations in mdx mouse skeletal muscle
-
Ljubicic V, Miura P, Burt M, Boudreault L, Khogali S, et al. (2011) Chronic AMPK activation evokes the slow, oxidative myogenic program and triggers beneficial adaptations in mdx mouse skeletal muscle. Hum Mol Genet 20: 3478-3493.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 3478-3493
-
-
Ljubicic, V.1
Miura, P.2
Burt, M.3
Boudreault, L.4
Khogali, S.5
-
83
-
-
70449388874
-
Pharmacological activation of PPARbeta/delta stimulates utrophin A expression in skeletal muscle fibers and restores sarcolemmal integrity in mature mdx mice
-
Miura P, Chakkalakal JV, Boudreault L, Belanger G, Hebert RL, et al. (2009) Pharmacological activation of PPARbeta/delta stimulates utrophin A expression in skeletal muscle fibers and restores sarcolemmal integrity in mature mdx mice. Hum Mol Genet 18: 4640-4649.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 4640-4649
-
-
Miura, P.1
Chakkalakal, J.V.2
Boudreault, L.3
Belanger, G.4
Hebert, R.L.5
-
84
-
-
48649086140
-
IRES-mediated translation of utrophin A is enhanced by glucocorticoid treatment in skeletal muscle cells
-
Miura P, Andrews M, Holcik M, Jasmin BJ, (2008) IRES-mediated translation of utrophin A is enhanced by glucocorticoid treatment in skeletal muscle cells. PLoS One 3: e2309.
-
(2008)
PLoS One
, vol.3
-
-
Miura, P.1
Andrews, M.2
Holcik, M.3
Jasmin, B.J.4
-
85
-
-
84861843663
-
Skeletal muscle fibrosis develops in response to desmin deletion
-
Meyer GA, Lieber RL, (2012) Skeletal muscle fibrosis develops in response to desmin deletion. Am J Physiol Cell Physiol 302: C1609-1620.
-
(2012)
Am J Physiol Cell Physiol
, vol.302
-
-
Meyer, G.A.1
Lieber, R.L.2
-
86
-
-
84878634729
-
Role of the cytoskeleton in muscle transcriptional responses to altered use
-
Meyer GA, Schenk S, Lieber RL, (2013) Role of the cytoskeleton in muscle transcriptional responses to altered use. Physiol Genomics 45: 321-331.
-
(2013)
Physiol Genomics
, vol.45
, pp. 321-331
-
-
Meyer, G.A.1
Schenk, S.2
Lieber, R.L.3
-
87
-
-
0021015222
-
Expression of intermediate filament-associated proteins paranemin and synemin in chicken development
-
Price MG, Lazarides E, (1983) Expression of intermediate filament-associated proteins paranemin and synemin in chicken development. J Cell Biol 97: 1860-1874.
-
(1983)
J Cell Biol
, vol.97
, pp. 1860-1874
-
-
Price, M.G.1
Lazarides, E.2
-
88
-
-
0032878518
-
Molecular characteristics and interactions of the intermediate filament protein synemin. Interactions with alpha-actinin may anchor synemin-containing heterofilaments
-
Bellin RM, Sernett SW, Becker B, Ip W, Huiatt TW, et al. (1999) Molecular characteristics and interactions of the intermediate filament protein synemin. Interactions with alpha-actinin may anchor synemin-containing heterofilaments. J Biol Chem 274: 29493-29499.
-
(1999)
J Biol Chem
, vol.274
, pp. 29493-29499
-
-
Bellin, R.M.1
Sernett, S.W.2
Becker, B.3
Ip, W.4
Huiatt, T.W.5
-
89
-
-
33845315905
-
The intermediate filament protein, synemin, is an AKAP in the heart
-
Russell MA, Lund LM, Haber R, McKeegan K, Cianciola N, et al. (2006) The intermediate filament protein, synemin, is an AKAP in the heart. Arch Biochem Biophys 456: 204-215.
-
(2006)
Arch Biochem Biophys
, vol.456
, pp. 204-215
-
-
Russell, M.A.1
Lund, L.M.2
Haber, R.3
McKeegan, K.4
Cianciola, N.5
-
90
-
-
77950823179
-
Modulation of ryanodine receptor Ca2+ channels (Review)
-
Ozawa T, (2010) Modulation of ryanodine receptor Ca2+ channels (Review). Mol Med Rep 3: 199-204.
-
(2010)
Mol Med Rep
, vol.3
, pp. 199-204
-
-
Ozawa, T.1
-
91
-
-
26044448082
-
Phosphorylation of ryanodine receptors
-
Danila CI, Hamilton SL, (2004) Phosphorylation of ryanodine receptors. Biol Res 37: 521-525.
-
(2004)
Biol Res
, vol.37
, pp. 521-525
-
-
Danila, C.I.1
Hamilton, S.L.2
-
92
-
-
77958048278
-
Molecular mechanism of calcium channel regulation in the fight-or-flight response
-
Fuller MD, Emrick MA, Sadilek M, Scheuer T, Catterall WA, (2010) Molecular mechanism of calcium channel regulation in the fight-or-flight response. Sci Signal 3: ra70.
-
(2010)
Sci Signal
, vol.3
-
-
Fuller, M.D.1
Emrick, M.A.2
Sadilek, M.3
Scheuer, T.4
Catterall, W.A.5
-
93
-
-
33144470004
-
Cardiac-specific overexpression of sarcolipin in phospholamban null mice impairs myocyte function that is restored by phosphorylation
-
Gramolini AO, Trivieri MG, Oudit GY, Kislinger T, Li W, et al. (2006) Cardiac-specific overexpression of sarcolipin in phospholamban null mice impairs myocyte function that is restored by phosphorylation. Proc Natl Acad Sci U S A 103: 2446-2451.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 2446-2451
-
-
Gramolini, A.O.1
Trivieri, M.G.2
Oudit, G.Y.3
Kislinger, T.4
Li, W.5
-
94
-
-
56149099711
-
Sarcospan reduces dystrophic pathology: stabilization of the utrophin-glycoprotein complex
-
Peter AK, Marshall JL, Crosbie RH, (2008) Sarcospan reduces dystrophic pathology: stabilization of the utrophin-glycoprotein complex. J Cell Biol 183: 419-427.
-
(2008)
J Cell Biol
, vol.183
, pp. 419-427
-
-
Peter, A.K.1
Marshall, J.L.2
Crosbie, R.H.3
-
95
-
-
84863758958
-
Sarcospan-dependent Akt activation is required for utrophin expression and muscle regeneration
-
Marshall JL, Holmberg J, Chou E, Ocampo AC, Oh J, et al. (2012) Sarcospan-dependent Akt activation is required for utrophin expression and muscle regeneration. J Cell Biol 197: 1009-1027.
-
(2012)
J Cell Biol
, vol.197
, pp. 1009-1027
-
-
Marshall, J.L.1
Holmberg, J.2
Chou, E.3
Ocampo, A.C.4
Oh, J.5
-
96
-
-
0037117602
-
Overexpression of the cytotoxic T cell GalNAc transferase in skeletal muscle inhibits muscular dystrophy in mdx mice
-
Nguyen HH, Jayasinha V, Xia B, Hoyte K, Martin PT, (2002) Overexpression of the cytotoxic T cell GalNAc transferase in skeletal muscle inhibits muscular dystrophy in mdx mice. Proc Natl Acad Sci U S A 99: 5616-5621.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 5616-5621
-
-
Nguyen, H.H.1
Jayasinha, V.2
Xia, B.3
Hoyte, K.4
Martin, P.T.5
-
97
-
-
65649133138
-
RhoA leads to up-regulation and relocalization of utrophin in muscle fibers
-
Gauthier-Rouviere C, Bonet-Kerrache A, (2009) RhoA leads to up-regulation and relocalization of utrophin in muscle fibers. Biochem Biophys Res Commun 384: 322-328.
-
(2009)
Biochem Biophys Res Commun
, vol.384
, pp. 322-328
-
-
Gauthier-Rouviere, C.1
Bonet-Kerrache, A.2
-
98
-
-
80052601574
-
A novel role of vimentin filaments: binding and stabilization of collagen mRNAs
-
Challa AA, Stefanovic B, (2011) A novel role of vimentin filaments: binding and stabilization of collagen mRNAs. Mol Cell Biol 31: 3773-3789.
-
(2011)
Mol Cell Biol
, vol.31
, pp. 3773-3789
-
-
Challa, A.A.1
Stefanovic, B.2
-
99
-
-
84875699165
-
A cell-based high-throughput screening assay for posttranscriptional utrophin upregulation
-
Moorwood C, Soni N, Patel G, Wilton SD, Khurana TS, (2013) A cell-based high-throughput screening assay for posttranscriptional utrophin upregulation. J Biomol Screen 18: 400-406.
-
(2013)
J Biomol Screen
, vol.18
, pp. 400-406
-
-
Moorwood, C.1
Soni, N.2
Patel, G.3
Wilton, S.D.4
Khurana, T.S.5
-
100
-
-
39449128867
-
Modulation of utrophin A mRNA stability in fast versus slow muscles via an AU-rich element and calcineurin signaling
-
Chakkalakal JV, Miura P, Belanger G, Michel RN, Jasmin BJ, (2008) Modulation of utrophin A mRNA stability in fast versus slow muscles via an AU-rich element and calcineurin signaling. Nucleic Acids Res 36: 826-838.
-
(2008)
Nucleic Acids Res
, vol.36
, pp. 826-838
-
-
Chakkalakal, J.V.1
Miura, P.2
Belanger, G.3
Michel, R.N.4
Jasmin, B.J.5
-
101
-
-
34249697100
-
Muscle intermediate filaments and their links to membranes and membranous organelles
-
Capetanaki Y, Bloch RJ, Kouloumenta A, Mavroidis M, Psarras S, (2007) Muscle intermediate filaments and their links to membranes and membranous organelles. Exp Cell Res 313: 2063-2076.
-
(2007)
Exp Cell Res
, vol.313
, pp. 2063-2076
-
-
Capetanaki, Y.1
Bloch, R.J.2
Kouloumenta, A.3
Mavroidis, M.4
Psarras, S.5
-
102
-
-
0041854263
-
Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)
-
Li W, Zhang Q, Oiso N, Novak EK, Gautam R, et al. (2003) Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1). Nat Genet 35: 84-89.
-
(2003)
Nat Genet
, vol.35
, pp. 84-89
-
-
Li, W.1
Zhang, Q.2
Oiso, N.3
Novak, E.K.4
Gautam, R.5
-
103
-
-
0031775820
-
Skeletal muscle-specific expression of a utrophin transgene rescues utrophin-dystrophin deficient mice
-
Rafael JA, Tinsley JM, Potter AC, Deconinck AE, Davies KE, (1998) Skeletal muscle-specific expression of a utrophin transgene rescues utrophin-dystrophin deficient mice. Nat Genet 19: 79-82.
-
(1998)
Nat Genet
, vol.19
, pp. 79-82
-
-
Rafael, J.A.1
Tinsley, J.M.2
Potter, A.C.3
Deconinck, A.E.4
Davies, K.E.5
-
104
-
-
66349121942
-
Functional substitution by TAT-utrophin in dystrophin-deficient mice
-
Sonnemann KJ, Heun-Johnson H, Turner AJ, Baltgalvis KA, Lowe DA, et al. (2009) Functional substitution by TAT-utrophin in dystrophin-deficient mice. PLoS Med 6: e1000083.
-
(2009)
PLoS Med
, vol.6
-
-
Sonnemann, K.J.1
Heun-Johnson, H.2
Turner, A.J.3
Baltgalvis, K.A.4
Lowe, D.A.5
-
105
-
-
33845666156
-
Biglycan regulates the expression and sarcolemmal localization of dystrobrevin, syntrophin, and nNOS
-
Mercado ML, Amenta AR, Hagiwara H, Rafii MS, Lechner BE, et al. (2006) Biglycan regulates the expression and sarcolemmal localization of dystrobrevin, syntrophin, and nNOS. FASEB J 20: 1724-1726.
-
(2006)
FASEB J
, vol.20
, pp. 1724-1726
-
-
Mercado, M.L.1
Amenta, A.R.2
Hagiwara, H.3
Rafii, M.S.4
Lechner, B.E.5
-
106
-
-
77953550591
-
Sarcolemmal nNOS anchoring reveals a qualitative difference between dystrophin and utrophin
-
Li D, Bareja A, Judge L, Yue Y, Lai Y, et al. (2010) Sarcolemmal nNOS anchoring reveals a qualitative difference between dystrophin and utrophin. J Cell Sci 123: 2008-2013.
-
(2010)
J Cell Sci
, vol.123
, pp. 2008-2013
-
-
Li, D.1
Bareja, A.2
Judge, L.3
Yue, Y.4
Lai, Y.5
-
107
-
-
0025159208
-
Very mild muscular dystrophy associated with the deletion of 46% of dystrophin
-
England SB, Nicholson LV, Johnson MA, Forrest SM, Love DR, et al. (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
-
108
-
-
0036560492
-
Syntrophins and dystrobrevins: defining the dystrophin scaffold at synapses
-
Albrecht DE, Froehner SC, (2002) Syntrophins and dystrobrevins: defining the dystrophin scaffold at synapses. Neurosignals 11: 123-129.
-
(2002)
Neurosignals
, vol.11
, pp. 123-129
-
-
Albrecht, D.E.1
Froehner, S.C.2
-
109
-
-
0035494421
-
In vivo requirement of the alpha-syntrophin PDZ domain for the sarcolemmal localization of nNOS and aquaporin-4
-
Adams ME, Mueller HA, Froehner SC, (2001) In vivo requirement of the alpha-syntrophin PDZ domain for the sarcolemmal localization of nNOS and aquaporin-4. J Cell Biol 155: 113-122.
-
(2001)
J Cell Biol
, vol.155
, pp. 113-122
-
-
Adams, M.E.1
Mueller, H.A.2
Froehner, S.C.3
-
110
-
-
84856402915
-
Influences of desmin and keratin 19 on passive biomechanical properties of mouse skeletal muscle
-
Shah SB, Love JM, O'Neill A, Lovering RM, Bloch RJ, (2012) Influences of desmin and keratin 19 on passive biomechanical properties of mouse skeletal muscle. J Biomed Biotechnol 2012: 704061.
-
(2012)
J Biomed Biotechnol
, vol.2012
, pp. 704061
-
-
Shah, S.B.1
Love, J.M.2
O'Neill, A.3
Lovering, R.M.4
Bloch, R.J.5
-
111
-
-
84862961772
-
The paradox of muscle hypertrophy in muscular dystrophy
-
xii
-
Kornegay JN, Childers MK, Bogan DJ, Bogan JR, Nghiem P, et al. (2012) The paradox of muscle hypertrophy in muscular dystrophy. Phys Med Rehabil Clin N Am 23: 149-172, xii.
-
(2012)
Phys Med Rehabil Clin N Am
, vol.23
, pp. 149-172
-
-
Kornegay, J.N.1
Childers, M.K.2
Bogan, D.J.3
Bogan, J.R.4
Nghiem, P.5
-
112
-
-
77955158006
-
Sequencing protocols to genotype mdx, mdx(4cv), and mdx(5cv) mice
-
Banks GB, Combs AC, Chamberlain JS, (2010) Sequencing protocols to genotype mdx, mdx(4cv), and mdx(5cv) mice. Muscle Nerve 42: 268-270.
-
(2010)
Muscle Nerve
, vol.42
, pp. 268-270
-
-
Banks, G.B.1
Combs, A.C.2
Chamberlain, J.S.3
-
113
-
-
33745894322
-
rAAV6-microdystrophin preserves muscle function and extends lifespan in severely dystrophic mice
-
Gregorevic P, Allen JM, Minami E, Blankinship MJ, Haraguchi M, et al. (2006) rAAV6-microdystrophin preserves muscle function and extends lifespan in severely dystrophic mice. Nat Med 12: 787-789.
-
(2006)
Nat Med
, vol.12
, pp. 787-789
-
-
Gregorevic, P.1
Allen, J.M.2
Minami, E.3
Blankinship, M.J.4
Haraguchi, M.5
-
114
-
-
62749156048
-
Truncated dystrophins can influence neuromuscular synapse structure
-
Banks GB, Chamberlain JS, Froehner SC, (2009) Truncated dystrophins can influence neuromuscular synapse structure. Mol Cell Neurosci 40: 433-441.
-
(2009)
Mol Cell Neurosci
, vol.40
, pp. 433-441
-
-
Banks, G.B.1
Chamberlain, J.S.2
Froehner, S.C.3
-
115
-
-
37749028738
-
Fluorophore-labeled myosin-specific antibodies simplify muscle-fiber phenotyping
-
Gregorevic P, Meznarich NA, Blankinship MJ, Crawford RW, Chamberlain JS, (2008) Fluorophore-labeled myosin-specific antibodies simplify muscle-fiber phenotyping. Muscle Nerve 37: 104-106.
-
(2008)
Muscle Nerve
, vol.37
, pp. 104-106
-
-
Gregorevic, P.1
Meznarich, N.A.2
Blankinship, M.J.3
Crawford, R.W.4
Chamberlain, J.S.5
-
116
-
-
34548419653
-
Functional capacity of dystrophins carrying deletions in the N-terminal actin-binding domain
-
Banks GB, Gregorevic P, Allen JM, Finn EE, Chamberlain JS, (2007) Functional capacity of dystrophins carrying deletions in the N-terminal actin-binding domain. Hum Mol Genet 16: 2105-2113.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 2105-2113
-
-
Banks, G.B.1
Gregorevic, P.2
Allen, J.M.3
Finn, E.E.4
Chamberlain, J.S.5
-
117
-
-
33645782024
-
Cytoplasmic gamma-actin contributes to a compensatory remodeling response in dystrophin-deficient muscle
-
Hanft LM, Rybakova IN, Patel JR, Rafael-Fortney JA, Ervasti JM, (2006) Cytoplasmic gamma-actin contributes to a compensatory remodeling response in dystrophin-deficient muscle. Proc Natl Acad Sci U S A 103: 5385-5390.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 5385-5390
-
-
Hanft, L.M.1
Rybakova, I.N.2
Patel, J.R.3
Rafael-Fortney, J.A.4
Ervasti, J.M.5
-
118
-
-
67650556403
-
Validation of housekeeping genes for quantitative real-time PCR in in-vivo and in-vitro models of cerebral ischaemia
-
Gubern C, Hurtado O, Rodriguez R, Morales JR, Romera VG, et al. (2009) Validation of housekeeping genes for quantitative real-time PCR in in-vivo and in-vitro models of cerebral ischaemia. BMC Mol Biol 10: 57.
-
(2009)
BMC Mol Biol
, vol.10
, pp. 57
-
-
Gubern, C.1
Hurtado, O.2
Rodriguez, R.3
Morales, J.R.4
Romera, V.G.5
|