-
1
-
-
0023903626
-
Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome
-
Davies, KE, Smith, TJ, Bundey, S, Read, AP, Flint, T, Bell, M et al. (1988). Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome. J Med Genet 25: 9-13.
-
(1988)
J Med Genet
, vol.25
, pp. 9-13
-
-
Davies, K.E.1
Smith, T.J.2
Bundey, S.3
Read, A.P.4
Flint, T.5
Bell, M.6
-
2
-
-
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
-
-
Kp, C.1
-
3
-
-
0027182201
-
Interaction of dystrophin with cytoskeletal proteins: Binding to talin and actin
-
Senter, L, Luise, M, Presotto, C, Betto, R, Teresi, A, Ceoldo, S et al. (1993). Interaction of dystrophin with cytoskeletal proteins: binding to talin and actin. Biochem Biophys Res Commun 192: 899-904.
-
(1993)
Biochem Biophys Res Commun
, vol.192
, pp. 899-904
-
-
Senter, L.1
Luise, M.2
Presotto, C.3
Betto, R.4
Teresi, A.5
Ceoldo, S.6
-
4
-
-
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 and 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
-
5
-
-
0026067790
-
Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma
-
Ohlendieck, K, Ervasti, JM, Snook, JB and Campbell, KP (1991). Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma. J Cell Biol 112: 135-148.
-
(1991)
J Cell Biol
, vol.112
, pp. 135-148
-
-
Ohlendieck, K.1
Ervasti, J.M.2
Snook, J.B.3
Kp, C.4
-
6
-
-
14044272136
-
Dimeric galectin-1 binds with high affnity to alpha2, 3-sialylated and non-sialylated terminal N-acetyllactosamine units on surface-bound extended glycans
-
Leppänen, A, Stowell, S, Blixt, O and Cummings, RD (2005). Dimeric galectin-1 binds with high affnity to alpha2, 3-sialylated and non-sialylated terminal N-acetyllactosamine units on surface-bound extended glycans. J Biol Chem 280: 5549-5562.
-
(2005)
J Biol Chem
, vol.280
, pp. 5549-5562
-
-
Leppänen, A.1
Stowell, S.2
Blixt, O.3
Cummings, R.D.4
-
7
-
-
33749556658
-
Galectin-1: A small protein with major functions
-
Camby, I, Le Mercier, M, Lefranc, F and Kiss, R (2006). Galectin-1: a small protein with major functions. Glycobiology 16: 137R-157R.
-
(2006)
Glycobiology
, vol.16
, pp. 137R-157R
-
-
Camby, I.1
Le Mercier, M.2
Lefranc, F.3
Kiss, R.4
-
8
-
-
84856556856
-
Galectin-1 research in T cell immunity: Past, present and future
-
Cedeno-Laurent, F and Dimitroff, CJ (2012). Galectin-1 research in T cell immunity: past, present and future. Clin Immunol 142: 107-116.
-
(2012)
Clin Immunol
, vol.142
, pp. 107-116
-
-
Cedeno-Laurent, F.1
Dimitroff, C.J.2
-
9
-
-
54549114513
-
Degeneration of dystrophic or injured skeletal muscles induces high expression of Galectin-1
-
Cerri, DG, Rodrigues, LC, Stowell, SR, Araujo, DD, Coelho, MC, Oliveira, SR et al. (2008). Degeneration of dystrophic or injured skeletal muscles induces high expression of Galectin-1. Glycobiology 18: 842-850.
-
(2008)
Glycobiology
, vol.18
, pp. 842-850
-
-
Cerri, D.G.1
Rodrigues, L.C.2
Stowell, S.R.3
Araujo, D.D.4
Coelho, M.C.5
Oliveira, S.R.6
-
10
-
-
33749185593
-
Galectin-1 induces skeletal muscle differentiation in human fetal mesenchymal stem cells and increases muscle regeneration
-
Chan, J, O'Donoghue, K, Gavina, M, Torrente, Y, Kennea, N, Mehmet, H et al. (2006). Galectin-1 induces skeletal muscle differentiation in human fetal mesenchymal stem cells and increases muscle regeneration. Stem Cells 24: 1879-1891.
-
(2006)
Stem Cells
, vol.24
, pp. 1879-1891
-
-
Chan, J.1
O'Donoghue, K.2
Gavina, M.3
Torrente, Y.4
Kennea, N.5
Mehmet, H.6
-
11
-
-
0037081723
-
The effect of galectin-1 on the differentiation of fbroblasts and myoblasts in vitro
-
Goldring, K, Jones, GE, Thiagarajah, R and Watt, DJ (2002). The effect of galectin-1 on the differentiation of fbroblasts and myoblasts in vitro. J Cell Sci 115(Pt 2): 355-366.
-
(2002)
J Cell Sci
, vol.115
, pp. 355-366
-
-
Goldring, K.1
Jones, G.E.2
Thiagarajah, R.3
Watt, D.J.4
-
12
-
-
0036133365
-
The muscle-specifc marker desmin is expressed in a proportion of human dermal fbroblasts after their exposure to galectin-1
-
Goldring, K, Jones, GE, Sewry, CA and Watt, DJ (2002). The muscle-specifc marker desmin is expressed in a proportion of human dermal fbroblasts after their exposure to galectin-1. Neuromuscul Disord 12: 183-186.
-
(2002)
Neuromuscul Disord
, vol.12
, pp. 183-186
-
-
Goldring, K.1
Jones, G.E.2
Sewry, C.A.3
Watt, D.J.4
-
13
-
-
34247354630
-
Lack of galectin-1 results in defects in myoblast fusion and muscle regeneration
-
Georgiadis, V, Stewart, HJ, Pollard, HJ, Tavsanoglu, Y, Prasad, R, Horwood, J et al. (2007). Lack of galectin-1 results in defects in myoblast fusion and muscle regeneration. Dev Dyn 236: 1014-1024.
-
(2007)
Dev Dyn
, vol.236
, pp. 1014-1024
-
-
Georgiadis, V.1
Stewart, H.J.2
Pollard, H.J.3
Tavsanoglu, Y.4
Prasad, R.5
Horwood, J.6
-
14
-
-
0028053242
-
Selective modulation of the interaction of alpha 7 beta 1 integrin with fbronectin and laminin by L-14 lectin during skeletal muscle differentiation
-
Gu, M, Wang, W, Song, WK, Cooper, DN and Kaufman, SJ (1994). Selective modulation of the interaction of alpha 7 beta 1 integrin with fbronectin and laminin by L-14 lectin during skeletal muscle differentiation. J Cell Sci 107 (Pt 1): 175-181.
-
(1994)
J Cell Sci
, vol.107
, pp. 175-181
-
-
Gu, M.1
Wang, W.2
Song, W.K.3
Cooper, D.N.4
Kaufman, S.J.5
-
15
-
-
79955722544
-
Mechanical stimuli on C2C12 myoblasts affect myoblast differentiation, focal adhesion kinase phosphorylation and galectin-1 expression: A proteomic approach
-
Grossi, A, Lametsch, R, Karlsson, AH and Lawson, MA (2011). Mechanical stimuli on C2C12 myoblasts affect myoblast differentiation, focal adhesion kinase phosphorylation and galectin-1 expression: a proteomic approach. Cell Biol Int 35: 579-586.
-
(2011)
Cell Biol Int
, vol.35
, pp. 579-586
-
-
Grossi, A.1
Lametsch, R.2
Karlsson, A.H.3
Ma, L.4
-
16
-
-
84883055833
-
The 6-minute walk test and other endpoints in Duchenne muscular dystrophy: Longitudinal natural history observations over 48 weeks from a multicenter study
-
McDonald, CM, Henricson, EK, Abresch, RT, Florence, JM, Eagle, M, Gappmaier, E et al.; PTC124-GD-007-DMD Study Group. (2013). The 6-minute walk test and other endpoints in Duchenne muscular dystrophy: longitudinal natural history observations over 48 weeks from a multicenter study. Muscle Nerve 48: 343-356.
-
(2013)
Muscle Nerve
, vol.48
, pp. 343-356
-
-
McDonald, C.M.1
Henricson, E.K.2
Abresch, R.T.3
Florence, J.M.4
Eagle, M.5
Gappmaier, E.6
-
17
-
-
7044272470
-
Progression of kyphosis in mdx mice
-
Laws, N and Hoey, A (2004). Progression of kyphosis in mdx mice. J Appl Physiol (1985) 97: 1970-1977.
-
(2004)
J Appl Physiol (1985)
, vol.97
, pp. 1970-1977
-
-
Laws, N.1
Hoey, A.2
-
18
-
-
33846827008
-
Scoliosis in patients with Duchenne muscular dystrophy
-
Karol, LA (2007). Scoliosis in patients with Duchenne muscular dystrophy. J Bone Joint Surg Am 89 Suppl 1: 155-162.
-
(2007)
J Bone Joint Surg Am
, vol.89
, pp. 155-162
-
-
Karol, L.A.1
-
19
-
-
77958085251
-
Suppression of renal fbrosis by galectin-1 in high glucose-treated renal epithelial cells
-
Okano, K, Tsuruta, Y, Yamashita, T, Takano, M, Echida, Y and Nitta, K (2010). Suppression of renal fbrosis by galectin-1 in high glucose-treated renal epithelial cells. Exp Cell Res 316: 3282-3291.
-
(2010)
Exp Cell Res
, vol.316
, pp. 3282-3291
-
-
Okano, K.1
Tsuruta, Y.2
Yamashita, T.3
Takano, M.4
Echida, Y.5
Nitta, K.6
-
20
-
-
84904392467
-
Induction of galectin-1 by TGF-β1 accelerates fbrosis through enhancing nuclear retention of Smad2
-
Lim, MJ, Ahn, J, Yi, JY, Kim, MH, Son, AR, Lee, SL et al. (2014). Induction of galectin-1 by TGF-β1 accelerates fbrosis through enhancing nuclear retention of Smad2. Exp Cell Res 326: 125-135.
-
(2014)
Exp Cell Res
, vol.326
, pp. 125-135
-
-
Lim, M.J.1
Ahn, J.2
Yi, J.Y.3
Kim, M.H.4
Son, A.R.5
Lee, S.L.6
-
21
-
-
79955618736
-
Current status of pharmaceutical and genetic therapeutic approaches to treat DMD
-
Pichavant, C, Aartsma-Rus, A, Clemens, PR, Davies, KE, Dickson, G, Takeda, S et al. (2011). Current status of pharmaceutical and genetic therapeutic approaches to treat DMD. Mol Ther 19: 830-840.
-
(2011)
Mol Ther
, vol.19
, pp. 830-840
-
-
Pichavant, C.1
Aartsma-Rus, A.2
Clemens, P.R.3
Davies, K.E.4
Dickson, G.5
Takeda, S.6
-
22
-
-
77956322846
-
Change in natural history of Duchenne muscular dystrophy with long-term corticosteroid treatment: Implications for management
-
Moxley, RT 3rd, Pandya, S, Ciafaloni, E, Fox, DJ and Campbell, K (2010). Change in natural history of Duchenne muscular dystrophy with long-term corticosteroid treatment: implications for management. J Child Neurol 25: 1116-1129.
-
(2010)
J Child Neurol
, vol.25
, pp. 1116-1129
-
-
Moxley, R.T.1
Pandya, S.2
Ciafaloni, E.3
Fox, D.J.4
Campbell, K.5
-
23
-
-
84901065506
-
Molecular and cell-based therapies for muscle degenerations: A road under construction
-
Berardi, E, Annibali, D, Cassano, M, Crippa, S and Sampaolesi, M (2014). Molecular and cell-based therapies for muscle degenerations: a road under construction. Front Physiol 5: 119.
-
(2014)
Front Physiol
, vol.5
, pp. 119
-
-
Berardi, E.1
Annibali, D.2
Cassano, M.3
Crippa, S.4
Sampaolesi, M.5
-
24
-
-
0036823498
-
Pharmacological control of cellular calcium handling in dystrophic skeletal muscle
-
Ruegg, UT, Nicolas-Métral, V, Challet, C, Bernard-Hélary, K, Dorchies, OM, Wagner, S et al. (2002). Pharmacological control of cellular calcium handling in dystrophic skeletal muscle. Neuromuscul Disord 12 Suppl 1: S155-S161.
-
(2002)
Neuromuscul Disord
, vol.12
, pp. S155-S161
-
-
Ruegg, U.T.1
Nicolas-Métral, V.2
Challet, C.3
Bernard-Hélary, K.4
Dorchies, O.M.5
Wagner, S.6
-
25
-
-
84886411393
-
Muscular dystrophies and other genetic myopathies
-
Shieh, PB (2013). Muscular dystrophies and other genetic myopathies. Neurol Clin 31: 1009-1029.
-
(2013)
Neurol Clin
, vol.31
, pp. 1009-1029
-
-
Shieh, P.B.1
-
26
-
-
0029906168
-
Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene
-
Tinsley, JM, Potter, AC, Phelps, SR, Fisher, R, Trickett, JI and 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
-
27
-
-
79551667507
-
Biglycan recruits utrophin to the sarcolemma and counters dystrophic pathology in mdx mice
-
Amenta, AR, Yilmaz, A, Bogdanovich, S, McKechnie, BA, Abedi, M, Khurana, TS et al. (2011). Biglycan recruits utrophin to the sarcolemma and counters dystrophic pathology in mdx mice. Proc Natl Acad Sci USA 108: 762-767.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 762-767
-
-
Amenta, A.R.1
Yilmaz, A.2
Bogdanovich, S.3
McKechnie, B.A.4
Abedi, M.5
Khurana, T.S.6
-
28
-
-
11144231268
-
Transgenic expression of {alpha}7{beta}1 integrin maintains muscle integrity, increases regenerative capacity, promotes hypertrophy, and reduces cardiomyopathy in dystrophic mice
-
Burkin, DJ, Wallace, GQ, Milner, DJ, Chaney, EJ, Mulligan, JA and Kaufman, SJ (2005). Transgenic expression of {alpha}7{beta}1 integrin maintains muscle integrity, increases regenerative capacity, promotes hypertrophy, and reduces cardiomyopathy in dystrophic mice. Am J Pathol 166: 253-263.
-
(2005)
Am J Pathol
, vol.166
, pp. 253-263
-
-
Burkin, D.J.1
Wallace, G.Q.2
Milner, D.J.3
Chaney, E.J.4
Mulligan, J.A.5
Kaufman, S.J.6
-
29
-
-
84862907349
-
Recombinant MG53 protein modulates therapeutic cell membrane repair in treatment of muscular dystrophy
-
Weisleder, N, Takizawa, N, Lin, P, Wang, X, Cao, C, Zhang, Y et al. (2012). Recombinant MG53 protein modulates therapeutic cell membrane repair in treatment of muscular dystrophy. Sci Transl Med 4: 139ra85.
-
(2012)
Sci Transl Med
, vol.4
, pp. 139ra85
-
-
Weisleder, N.1
Takizawa, N.2
Lin, P.3
Wang, X.4
Cao, C.5
Zhang, Y.6
-
30
-
-
66349121942
-
Functional substitution by TAT-utrophin in dystrophin-defcient mice
-
Sonnemann, KJ, Heun-Johnson, H, Turner, AJ, Baltgalvis, KA, Lowe, DA and Ervasti, JM (2009). Functional substitution by TAT-utrophin in dystrophin-defcient mice. PLoS Med 6: e1000083.
-
(2009)
PLoS Med
, vol.6
, pp. e1000083
-
-
Sonnemann, K.J.1
Heun-Johnson, H.2
Turner, A.J.3
Baltgalvis, K.A.4
Lowe, D.A.5
Ervasti, J.M.6
-
31
-
-
33845666156
-
Biglycan regulates the expression and sarcolemmal localization of dystrobrevin, syntrophin, and nNOS
-
Mercado, ML, Amenta, AR, Hagiwara, H, Rafi, MS, Lechner, BE, Owens, RT 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
Rafi, M.S.4
Lechner, B.E.5
Owens, R.T.6
-
32
-
-
84863164982
-
Biglycan is an extracellular MuSK binding protein important for synapse stability
-
Amenta, AR, Creely, HE, Mercado, ML, Hagiwara, H, McKechnie, BA, Lechner, BE et al. (2012). Biglycan is an extracellular MuSK binding protein important for synapse stability. J Neurosci 32: 2324-2334.
-
(2012)
J Neurosci
, vol.32
, pp. 2324-2334
-
-
Amenta, A.R.1
Creely, H.E.2
Mercado, M.L.3
Hagiwara, H.4
McKechnie, B.A.5
Lechner, B.E.6
-
33
-
-
66049117408
-
Laminin-111 protein therapy prevents muscle disease in the mdx mouse model for Duchenne muscular dystrophy
-
Rooney, JE, Gurpur, PB and Burkin, DJ (2009). Laminin-111 protein therapy prevents muscle disease in the mdx mouse model for Duchenne muscular dystrophy. Proc Natl Acad Sci USA 106: 7991-7996.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 7991-7996
-
-
Rooney, J.E.1
Gurpur, P.B.2
Burkin, D.J.3
-
34
-
-
84867116406
-
Dystrophin and utrophin expression require sarcospan: Loss of α7 integrin exacerbates a newly discovered muscle phenotype in sarcospan-null mice
-
Marshall, JL, Chou, E, Oh, J, Kwok, A, Burkin, DJ and Crosbie-Watson, RH (2012). Dystrophin and utrophin expression require sarcospan: loss of α7 integrin exacerbates a newly discovered muscle phenotype in sarcospan-null mice. Hum Mol Genet 21: 4378-4393.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 4378-4393
-
-
Marshall, J.L.1
Chou, E.2
Oh, J.3
Kwok, A.4
Burkin, D.J.5
Crosbie-Watson, R.H.6
-
35
-
-
78651227209
-
Mesenchymal stem cell-mediated T cell suppression occurs through secreted galectins
-
Sioud, M, Mobergslien, A, Boudabous, A and Fløisand, Y (2011). Mesenchymal stem cell-mediated T cell suppression occurs through secreted galectins. Int J Oncol 38: 385-390.
-
(2011)
Int J Oncol
, vol.38
, pp. 385-390
-
-
Sioud, M.1
Mobergslien, A.2
Boudabous, A.3
Fløisand, Y.4
-
36
-
-
84883766237
-
Pharmacological prospects in the treatment of Duchenne muscular dystrophy
-
Ruegg, UT (2013). Pharmacological prospects in the treatment of Duchenne muscular dystrophy. Curr Opin Neurol 26: 577-584.
-
(2013)
Curr Opin Neurol
, vol.26
, pp. 577-584
-
-
Ruegg, U.T.1
-
37
-
-
84883050768
-
The 6-minute walk test and other clinical endpoints in duchenne muscular dystrophy: Reliability, concurrent validity, and minimal clinically important differences from a multicenter study
-
McDonald, CM, Henricson, EK, Abresch, RT, Florence, J, Eagle, M, Gappmaier, E et al.; PTC124-GD-007-DMD Study Group. (2013). The 6-minute walk test and other clinical endpoints in duchenne muscular dystrophy: reliability, concurrent validity, and minimal clinically important differences from a multicenter study. Muscle Nerve 48: 357-368.
-
(2013)
Muscle Nerve
, vol.48
, pp. 357-368
-
-
McDonald, C.M.1
Henricson, E.K.2
Abresch, R.T.3
Florence, J.4
Eagle, M.5
Gappmaier, E.6
-
38
-
-
84879902003
-
The 6-minute walk test and person-reported outcomes in boys with duchenne muscular dystrophy and typically developing controls: Longitudinal comparisons and clinically-meaningful changes over one year
-
Henricson, E, Abresch, R, Han, JJ, Nicorici, A, Goude Keller, E, de Bie, E et al. (2013). The 6-minute walk test and person-reported outcomes in boys with duchenne muscular dystrophy and typically developing controls: longitudinal comparisons and clinically-meaningful changes over one year. PLoS Curr 5:.
-
(2013)
PLoS Curr
, vol.5
-
-
Henricson, E.1
Abresch, R.2
Han, J.J.3
Nicorici, A.4
Goude Keller, E.5
De Bie, E.6
-
39
-
-
0024600393
-
Duchenne muscular dystrophy: Patterns of clinical progression and effects of supportive therapy
-
Brooke, MH, Fenichel, GM, Griggs, RC, Mendell, JR, Moxley, R, Florence, J et al. (1989). Duchenne muscular dystrophy: patterns of clinical progression and effects of supportive therapy. Neurology 39: 475-481.
-
(1989)
Neurology
, vol.39
, pp. 475-481
-
-
Brooke, M.H.1
Fenichel, G.M.2
Griggs, R.C.3
Mendell, J.R.4
Moxley, R.5
Florence, J.6
-
40
-
-
76549130473
-
Diagnosis and management of Duchenne muscular dystrophy, part 2: Implementation of multidisciplinary care
-
Bushby, K, Finkel, R, Birnkrant, DJ, Case, LE, Clemens, PR, Cripe, L et al.; DMD Care Considerations Working Group. (2010). Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care. Lancet Neurol 9: 177-189.
-
(2010)
Lancet Neurol
, vol.9
, pp. 177-189
-
-
Bushby, K.1
Finkel, R.2
Birnkrant, D.J.3
Case, L.E.4
Clemens, P.R.5
Cripe, L.6
-
41
-
-
72149108443
-
Diagnosis and management of Duchenne muscular dystrophy, part 1: Diagnosis, and pharmacological and psychosocial management
-
Bushby, K, Finkel, R, Birnkrant, DJ, Case, LE, Clemens, PR, Cripe, L et al.; DMD Care Considerations Working Group. (2010). Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management. Lancet Neurol 9: 77-93.
-
(2010)
Lancet Neurol
, vol.9
, pp. 77-93
-
-
Bushby, K.1
Finkel, R.2
Birnkrant, D.J.3
Case, L.E.4
Clemens, P.R.5
Cripe, L.6
-
42
-
-
65649112428
-
NO more muscle fatigue
-
Heydemann, A and McNally, E (2009). NO more muscle fatigue. J Clin Invest 119: 448-450.
-
(2009)
J Clin Invest
, vol.119
, pp. 448-450
-
-
Heydemann, A.1
McNally, E.2
-
43
-
-
84869992582
-
Fatigue in muscular dystrophies
-
Angelini, C and Tasca, E (2012). Fatigue in muscular dystrophies. Neuromuscul Disord 22 Suppl 3: S214-S220.
-
(2012)
Neuromuscul Disord
, vol.22
, pp. S214-S220
-
-
Angelini, C.1
Tasca, E.2
-
44
-
-
0036517197
-
Duchenne muscular dystrophy
-
Sussman, M (2002). Duchenne muscular dystrophy. J Am Acad Orthop Surg 10: 138-151.
-
(2002)
J Am Acad Orthop Surg
, vol.10
, pp. 138-151
-
-
Sussman, M.1
-
45
-
-
84877294642
-
Effects of prednisolone on the dystrophin-associated proteins in the blood-brain barrier and skeletal muscle of dystrophic mdx mice
-
Tamma, R, Annese, T, Capogrosso, RF, Cozzoli, A, Benagiano, V, Sblendorio, V et al. (2013). Effects of prednisolone on the dystrophin-associated proteins in the blood-brain barrier and skeletal muscle of dystrophic mdx mice. Lab Invest 93: 592-610.
-
(2013)
Lab Invest
, vol.93
, pp. 592-610
-
-
Tamma, R.1
Annese, T.2
Capogrosso, R.F.3
Cozzoli, A.4
Benagiano, V.5
Sblendorio, V.6
-
46
-
-
84900332737
-
Galectin-1 in early acute myocardial infarction
-
Al-Salam, S and Hashmi, S (2014). Galectin-1 in early acute myocardial infarction. PLoS One 9: e86994.
-
(2014)
PLoS One
, vol.9
, pp. e86994
-
-
Al-Salam, S.1
Hashmi, S.2
-
47
-
-
84883870224
-
Levels of α7 integrin and laminin-α2 are increased following prednisone treatment in the mdx mouse and GRMD dog models of Duchenne muscular dystrophy
-
Wuebbles, RD, Sarathy, A, Kornegay, JN and Burkin, DJ (2013). Levels of α7 integrin and laminin-α2 are increased following prednisone treatment in the mdx mouse and GRMD dog models of Duchenne muscular dystrophy. Dis Model Mech 6: 1175-1184.
-
(2013)
Dis Model Mech
, vol.6
, pp. 1175-1184
-
-
Wuebbles, R.D.1
Sarathy, A.2
Kornegay, J.N.3
Burkin, D.J.4
-
48
-
-
0029827468
-
The mdx-amplifcation-resistant mutation system assay, a simple and rapid polymerase chain reaction-based detection of the mdx allele
-
Amalftano, A and Chamberlain, JS (1996). The mdx-amplifcation-resistant mutation system assay, a simple and rapid polymerase chain reaction-based detection of the mdx allele. Muscle Nerve 19: 1549-1553.
-
(1996)
Muscle Nerve
, vol.19
, pp. 1549-1553
-
-
Amalftano, A.1
Chamberlain, J.S.2
-
49
-
-
33748085730
-
Passive mechanical properties of maturing extensor digitorum longus are not affected by lack of dystrophin
-
Wolff, AV, Niday, AK, Voelker, KA, Call, JA, Evans, NP, Granata, KP et al. (2006). Passive mechanical properties of maturing extensor digitorum longus are not affected by lack of dystrophin. Muscle Nerve 34: 304-312.
-
(2006)
Muscle Nerve
, vol.34
, pp. 304-312
-
-
Wolff, A.V.1
Niday, A.K.2
Voelker, K.A.3
Call, J.A.4
Evans, N.P.5
Granata, K.P.6
-
50
-
-
33745493594
-
Severe muscular dystrophy in mice that lack dystrophin and alpha7 integrin
-
Rooney, JE, Welser, JV, Dechert, MA, Flintoff-Dye, NL, Kaufman, SJ and Burkin, DJ (2006). Severe muscular dystrophy in mice that lack dystrophin and alpha7 integrin. J Cell Sci 119(Pt 11): 2185-2195.
-
(2006)
J Cell Sci
, vol.119
, pp. 2185-2195
-
-
Rooney, J.E.1
Welser, J.V.2
Dechert, M.A.3
Flintoff-Dye, N.L.4
Kaufman, S.J.5
Burkin, D.J.6
-
51
-
-
58249110400
-
Laminin-111 restores regenerative capacity in a mouse model for alpha7 integrin congenital myopathy
-
Rooney, JE, Gurpur, PB, Yablonka-Reuveni, Z and Burkin, DJ (2009). Laminin-111 restores regenerative capacity in a mouse model for alpha7 integrin congenital myopathy. Am J Pathol 174: 256-264.
-
(2009)
Am J Pathol
, vol.174
, pp. 256-264
-
-
Rooney, J.E.1
Gurpur, P.B.2
Yablonka-Reuveni, Z.3
Burkin, D.J.4
-
52
-
-
0027787640
-
Expression of alpha 7 integrin cytoplasmic domains during skeletal muscle development: Alternate forms, conformational change, and homologies with serine/threonine kinases and tyrosine phosphatases
-
Song, WK, Wang, W, Sato, H, Bielser, DA and Kaufman, SJ (1993). Expression of alpha 7 integrin cytoplasmic domains during skeletal muscle development: alternate forms, conformational change, and homologies with serine/threonine kinases and tyrosine phosphatases. J Cell Sci 106 (Pt 4): 1139-1152.
-
(1993)
J Cell Sci
, vol.106
, pp. 1139-1152
-
-
Song, W.K.1
Wang, W.2
Sato, H.3
Bielser, D.A.4
Kaufman, S.J.5
-
53
-
-
84859075862
-
Laminin-111 protein therapy reduces muscle pathology and improves viability of a mouse model of merosin-defcient congenital muscular dystrophy
-
Rooney, JE, Knapp, JR, Hodges, BL, Wuebbles, RD and Burkin, DJ (2012) Laminin-111 protein therapy reduces muscle pathology and improves viability of a mouse model of merosin-defcient congenital muscular dystrophy. Am J Pathol 180: 1593-1602.
-
(2012)
Am J Pathol
, vol.180
, pp. 1593-1602
-
-
Rooney, J.E.1
Knapp, J.R.2
Hodges, B.L.3
Wuebbles, R.D.4
Burkin, D.J.5
-
54
-
-
84926430427
-
Toll-like receptor 4 ablation in mdx mice reveals innate immunity as a therapeutic target in Duchenne muscular dystrophy
-
Giordano, C, Mojumdar, K, Liang, F, Lemaire, C, Li, T, Richardson, J et al. (2015). Toll-like receptor 4 ablation in mdx mice reveals innate immunity as a therapeutic target in Duchenne muscular dystrophy. Hum Mol Genet 24: 2147-2162.
-
(2015)
Hum Mol Genet
, vol.24
, pp. 2147-2162
-
-
Giordano, C.1
Mojumdar, K.2
Liang, F.3
Lemaire, C.4
Li, T.5
Richardson, J.6
|