-
1
-
-
0023614188
-
Dystrophin: the protein product of the Duchenne muscular dystrophy locus
-
Hoffman, E.P., Brown, R.H. and Kunkel, L.M. (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, R.H.2
Kunkel, L.M.3
-
2
-
-
0023718395
-
Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface
-
Bonilla, E., Samitt, C.E., Miranda, A.F., Hays, A.P., Salviati, G., DiMauro, S., Kunkel, L.M., Hoffman, E.P. and Rowland, L.P. (1988) Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface. Cell, 54, 447-452.
-
(1988)
Cell
, vol.54
, pp. 447-452
-
-
Bonilla, E.1
Samitt, C.E.2
Miranda, A.F.3
Hays, A.P.4
Salviati, G.5
DiMauro, S.6
Kunkel, L.M.7
Hoffman, E.P.8
Rowland, L.P.9
-
3
-
-
0024600620
-
Association of dystrophin and an integral membrane glycoprotein
-
Campbell, K.P. and Kahl, S.D. (1989) Association of dystrophin and an integral membrane glycoprotein. Nature, 338, 259-262.
-
(1989)
Nature
, vol.338
, pp. 259-262
-
-
Campbell, K.P.1
Kahl, S.D.2
-
4
-
-
0026543686
-
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix
-
Ibraghimov-Beskrovnaya, O., Ervasti, J.M., Leveille, C.J., Slaughter, C.A., Sernett, S.W. and Campbell, K.P. (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
-
5
-
-
0027275643
-
A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin
-
Ervasti, J.M. and Campbell, K.P. (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
-
6
-
-
0025242185
-
Glycoprotein complex anchoring dystrophin to sarcolemma
-
Yoshida, M. and Ozawa, E. (1990) Glycoprotein complex anchoring dystrophin to sarcolemma. J. Biochem., 108, 748-752.
-
(1990)
J. Biochem
, vol.108
, pp. 748-752
-
-
Yoshida, M.1
Ozawa, E.2
-
7
-
-
0027460658
-
Dystrophin protects the sarcolemma from stresses developed during muscle contraction
-
Petrof, B.J., Shrager, J.B., Stedman, H.H., Kelly, A.M. and Sweeney, H.L. (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
-
8
-
-
0025662048
-
Dystrophindeficient mdx muscle fibers are preferentially vulnerable to necrosis induced by experimental lengthening contractions
-
Weller, B., Karpati, G. and Carpenter, S. (1990) Dystrophindeficient mdx muscle fibers are preferentially vulnerable to necrosis induced by experimental lengthening contractions. J. Neurol. Sci., 100, 9-13.
-
(1990)
J. Neurol. Sci
, vol.100
, pp. 9-13
-
-
Weller, B.1
Karpati, G.2
Carpenter, S.3
-
9
-
-
0026621049
-
Primary structure of dystrophinrelated protein
-
Tinsley, J.M., Blake, D.J., Roche, A., Fairbrother, U., Riss, J., Byth, B.C., Knight, A.E., Kendrick-Jones, J., Suthers, G.K., Love, D.R., et al. (1992) Primary structure of dystrophinrelated 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
-
10
-
-
0026354979
-
Skeletal myoblasts utilize a novel beta 1-series integrin and not alpha 6 beta 1 for binding to the E8 and T8 fragments of laminin
-
von der Mark, H., Durr, J., Sonnenberg, A., von der Mark, K., Deutzmann, R. and Goodman, S.L. (1991) Skeletal myoblasts utilize a novel beta 1-series integrin and not alpha 6 beta 1 for binding to the E8 and T8 fragments of laminin. J. Biol. Chem., 266, 23593-23601.
-
(1991)
J. Biol. Chem
, vol.266
, pp. 23593-23601
-
-
von der Mark, H.1
Durr, J.2
Sonnenberg, A.3
von der Mark, K.4
Deutzmann, R.5
Goodman, S.L.6
-
11
-
-
0026591586
-
H36-alpha 7 is a novel integrin alpha chain that is developmentally regulated during skeletal myogenesis
-
Song, W.K., Wang, W., Foster, R.F., Bielser, D.A. and Kaufman, S.J. (1992) H36-alpha 7 is a novel integrin alpha chain that is developmentally regulated during skeletal myogenesis. J. Cell Biol., 117, 643-657.
-
(1992)
J. Cell Biol
, vol.117
, pp. 643-657
-
-
Song, W.K.1
Wang, W.2
Foster, R.F.3
Bielser, D.A.4
Kaufman, S.J.5
-
12
-
-
0027424701
-
The utrophin and dystrophin genes share similarities in genomic structure
-
Pearce, M., Blake, D.J., Tinsley, J.M., Byth, B.C., Campbell, L., Monaco, A.P. and Davies, K.E. (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
-
13
-
-
0026621608
-
Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle
-
Matsumura, K., Ervasti, J.M., Ohlendieck, K., Kahl, S.D. and Campbell, K.P. (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
-
14
-
-
0031451562
-
Sarcospan: the 25kDa transmembrane component of the dystrophin-glycoprotein complex
-
Crosbie, R.H., Heighway, J., Venzke, D.P., Lee, J.C. and Campbell, K.P. (1997) Sarcospan: the 25kDa transmembrane component of the dystrophin-glycoprotein complex. J. Biol. Chem., 272, 31221-31224.
-
(1997)
J. Biol. Chem
, vol.272
, pp. 31221-31224
-
-
Crosbie, R.H.1
Heighway, J.2
Venzke, D.P.3
Lee, J.C.4
Campbell, K.P.5
-
15
-
-
0033526085
-
Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex
-
Crosbie, R.H., Lebakken, C.S., Holt, K.H., Venzke, D.P., Straub, V., Lee, J.C., Grady, R.M., Chamberlain, J.S., Sanes, J.R. and Campbell, K.P. (1999) Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex. J. Cell Biol., 145, 153-165.
-
(1999)
J. Cell Biol
, vol.145
, pp. 153-165
-
-
Crosbie, R.H.1
Lebakken, C.S.2
Holt, K.H.3
Venzke, D.P.4
Straub, V.5
Lee, J.C.6
Grady, R.M.7
Chamberlain, J.S.8
Sanes, J.R.9
Campbell, K.P.10
-
16
-
-
84867116406
-
Dystrophin and utrophin expression require sarcospan: loss of alpha7 integrin exacerbates a newly discovered muscle phenotype in sarcospannull mice
-
Marshall, J.L., Chou, E., Oh, J., Kwok, A., Burkin, D.J. and Crosbie-Watson, R.H. (2012) Dystrophin and utrophin expression require sarcospan: loss of alpha7 integrin exacerbates a newly discovered muscle phenotype in sarcospannull 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
-
17
-
-
84926488415
-
Sarcospan integration into laminin-binding adhesion complexes that ameliorate muscular dystrophy requires utrophin and alpha7 integrin
-
Marshall, J.L., Oh, J., Chou, E., Lee, J.A., Holmberg, J., Burkin, D.J. and Crosbie-Watson, R.H. (2015) Sarcospan integration into laminin-binding adhesion complexes that ameliorate muscular dystrophy requires utrophin and alpha7 integrin. Hum. Mol. Genet., 24, 2011-2022.
-
(2015)
Hum. Mol. Genet
, vol.24
, pp. 2011-2022
-
-
Marshall, J.L.1
Oh, J.2
Chou, E.3
Lee, J.A.4
Holmberg, J.5
Burkin, D.J.6
Crosbie-Watson, R.H.7
-
18
-
-
56149099711
-
Sarcospan reduces dystrophic pathology: stabilization of the utrophinglycoprotein complex
-
Peter, A.K., Marshall, J.L. and Crosbie, R.H. (2008) Sarcospan reduces dystrophic pathology: stabilization of the utrophinglycoprotein 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
-
19
-
-
84863758958
-
Sarcospan-dependent Akt activation is required for utrophin expression and muscle regeneration
-
Marshall, J.L., Holmberg, J., Chou, E., Ocampo, A.C., Oh, J., Lee, J., Peter, A.K., Martin, P.T. and Crosbie-Watson, R.H. (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
Lee, J.6
Peter, A.K.7
Martin, P.T.8
Crosbie-Watson, R.H.9
-
20
-
-
84882617523
-
The potential of sarcospan in adhesion complex replacement therapeutics for the treatment of muscular dystrophy
-
Marshall, J.L., Kwok, Y., McMorran, B.J., Baum, L.G. and Crosbie-Watson, R.H. (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
-
21
-
-
0031775820
-
Skeletal muscle-specific expression of a utrophin transgene rescues utrophin-dystrophin deficient mice
-
Rafael, J.A., Tinsley, J.M., Potter, A.C., Deconinck, A.E. and Davies, K.E. (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
-
22
-
-
0031727771
-
Expression of full-length utrophin prevents muscular dystrophy in mdx mice
-
Tinsley, J., Deconinck, N., Fisher, R., Kahn, D., Phelps, S., Gillis, J.M. and Davies, K. (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
Gillis, J.M.6
Davies, K.7
-
23
-
-
0033587139
-
Adenovirus-mediated utrophin gene transfer mitigates the dystrophic phenotype of mdx mouse muscles
-
Gilbert, R., Nalbantoglu, J., Petrof, B.J., Ebihara, S., Guibinga, G.H., Tinsley, J.M., Kamen, A., Massie, B., Davies, K.E. and 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
-
24
-
-
0034805152
-
Non-toxic ubiquitous over-expression of utrophin in the mdx mouse
-
Fisher, R., Tinsley, J.M., Phelps, S.R., Squire, S.E., Townsend, E.R., Martin, J.E. and Davies, K.E. (2001) Non-toxic ubiquitous over-expression of utrophin in the mdx mouse. Neuromuscul. Disord., 11, 713-721.
-
(2001)
Neuromuscul. Disord
, vol.11
, pp. 713-721
-
-
Fisher, R.1
Tinsley, J.M.2
Phelps, S.R.3
Squire, S.E.4
Townsend, E.R.5
Martin, J.E.6
Davies, K.E.7
-
25
-
-
11144231268
-
Transgenic expression of [alpha] 7[beta]1 integrin maintains muscle integrity, increases regenerative capacity, promotes hypertrophy, and reduces cardiomyopathy in dystrophic mice
-
Burkin, D.J., Wallace, G.Q., Milner, D.J., Chaney, E.J., Mulligan, J.A. and Kaufman, S.J. (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
-
26
-
-
84991523758
-
Sarcospan Regulates Cardiac Isoproterenol Response and Prevents Duchenne Muscular Dystrophy-Associated Cardiomyopathy
-
Parvatiyar, M.S., Marshall, J.L., Nguyen, R.T., Jordan, M.C., Richardson, V.A., Roos, K.P. and Crosbie-Watson, R.H. (2015) Sarcospan Regulates Cardiac Isoproterenol Response and Prevents Duchenne Muscular Dystrophy-Associated Cardiomyopathy. J. Am. Heart Assoc., 4: e002481.
-
(2015)
J. Am. Heart Assoc
, vol.4
-
-
Parvatiyar, M.S.1
Marshall, J.L.2
Nguyen, R.T.3
Jordan, M.C.4
Richardson, V.A.5
Roos, K.P.6
Crosbie-Watson, R.H.7
-
27
-
-
34247500517
-
Disrupted mechanical stability of the dystrophin-glycoprotein complex causes severe muscular dystrophy in sarcospan transgenic mice
-
Peter, A.K., Miller, G. and Crosbie, R.H. (2007) Disrupted mechanical stability of the dystrophin-glycoprotein complex causes severe muscular dystrophy in sarcospan transgenic mice. J. Cell Sci., 120, 996-1008.
-
(2007)
J. Cell Sci
, vol.120
, pp. 996-1008
-
-
Peter, A.K.1
Miller, G.2
Crosbie, R.H.3
-
28
-
-
0030783172
-
Animal models for muscular dystrophy show different patterns of sarcolemmal disruption
-
Straub, V., Rafael, J.A., Chamberlain, J.S. and Campbell, K.P. (1997) Animal models for muscular dystrophy show different patterns of sarcolemmal disruption. J. Cell Biol., 139, 375-385.
-
(1997)
J. Cell Biol
, vol.139
, pp. 375-385
-
-
Straub, V.1
Rafael, J.A.2
Chamberlain, J.S.3
Campbell, K.P.4
-
29
-
-
0029149471
-
Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy
-
Brenman, J.E., Chao, D.S., Xia, H., Aldape, K. and Bredt, D.S. (1995) Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy. Cell, 82, 743-752.
-
(1995)
Cell
, vol.82
, pp. 743-752
-
-
Brenman, J.E.1
Chao, D.S.2
Xia, H.3
Aldape, K.4
Bredt, D.S.5
-
30
-
-
57049122968
-
Sarcolemma-localized nNOS is required to maintain activity after mild exercise
-
Kobayashi, Y.M., Rader, E.P., Crawford, R.W., Iyengar, N.K., Thedens, D.R., Faulkner, J.A., Parikh, S.V., Weiss, R.M., Chamberlain, J.S., Moore, S.A., 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
Faulkner, J.A.6
Parikh, S.V.7
Weiss, R.M.8
Chamberlain, J.S.9
Moore, S.A.10
-
31
-
-
0034610326
-
Functional muscle ischemia in neuronal nitric oxide synthase-deficient skeletal muscle of children with Duchenne muscular dystrophy
-
Sander, M., Chavoshan, B., Harris, S.A., Iannaccone, S.T., Stull, J.T., Thomas, G.D. and Victor, R.G. (2000) Functional muscle ischemia in neuronal nitric oxide synthase-deficient skeletal muscle of children with Duchenne muscular dystrophy. Proc. Natl Acad. Sci. U S A, 97, 13818-13823.
-
(2000)
Proc. Natl Acad. Sci. U S A
, vol.97
, pp. 13818-13823
-
-
Sander, M.1
Chavoshan, B.2
Harris, S.A.3
Iannaccone, S.T.4
Stull, J.T.5
Thomas, G.D.6
Victor, R.G.7
-
32
-
-
0026419948
-
The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy
-
Stedman, H.H., Sweeney, H.L., Shrager, J.B., Maguire, H.C., Panettieri, R.A., Petrof, B., Narusawa, M., Leferovich, J.M., Sladky, J.T. and Kelly, A.M. (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
-
33
-
-
42649127369
-
Mdx respiratory impairment following fibrosis of the diaphragm
-
Ishizaki, M., Suga, T., Kimura, E., Shiota, T., Kawano, R., Uchida, Y., Uchino, K., Yamashita, S., Maeda, Y.,. and Uchino, M. (2008) Mdx respiratory impairment following fibrosis of the diaphragm. Neuromuscul. Disord., 18, 342-348.
-
(2008)
Neuromuscul. Disord
, vol.18
, pp. 342-348
-
-
Ishizaki, M.1
Suga, T.2
Kimura, E.3
Shiota, T.4
Kawano, R.5
Uchida, Y.6
Uchino, K.7
Yamashita, S.8
Maeda, Y.9
Uchino, M.10
-
34
-
-
84946771407
-
Reengineering a transmembrane protein to treat muscular dystrophy using exon skipping
-
Gao, Q.Q., Wyatt, E., Goldstein, J.A., LoPresti, P., Castillo, L.M., Gazda, A., Petrossian, N., Earley, J.U., Hadhazy, M., Barefield, D.Y., et al. (2015) Reengineering a transmembrane protein to treat muscular dystrophy using exon skipping. J. Clin. Invest., 125, 4186-4195.
-
(2015)
J. Clin. Invest
, vol.125
, pp. 4186-4195
-
-
Gao, Q.Q.1
Wyatt, E.2
Goldstein, J.A.3
LoPresti, P.4
Castillo, L.M.5
Gazda, A.6
Petrossian, N.7
Earley, J.U.8
Hadhazy, M.9
Barefield, D.Y.10
-
35
-
-
0035164890
-
Lung function in children with Duchenne's muscular dystrophy
-
Tangsrud, S., Petersen, I.L., Lodrup Carlsen, K.C. and Carlsen, K.H. (2001) Lung function in children with Duchenne's muscular dystrophy. Respir. Med., 95, 898-903.
-
(2001)
Respir. Med
, vol.95
, pp. 898-903
-
-
Tangsrud, S.1
Petersen, I.L.2
Lodrup Carlsen, K.C.3
Carlsen, K.H.4
-
36
-
-
84969248261
-
Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype
-
Capote, J., Kramerova, I., Martinez, L., Vetrone, S., Barton, E.R., Sweeney, H.L., Miceli, M.C. and Spencer, M.J. (2016) Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype. J. Cell Biol., 213, 275-288.
-
(2016)
J. Cell Biol
, vol.213
, pp. 275-288
-
-
Capote, J.1
Kramerova, I.2
Martinez, L.3
Vetrone, S.4
Barton, E.R.5
Sweeney, H.L.6
Miceli, M.C.7
Spencer, M.J.8
-
37
-
-
0033982722
-
Sarcospan-deficient mice maintain normal muscle function
-
Lebakken, C.S., Venzke, D.P., Hrstka, R.F., Consolino, C.M., Faulkner, J.A., Williamson, R.A. and Campbell, K.P. (2000) Sarcospan-deficient mice maintain normal muscle function. Mol. Cell. Biol., 20, 1669-1677.
-
(2000)
Mol. Cell. Biol
, vol.20
, pp. 1669-1677
-
-
Lebakken, C.S.1
Venzke, D.P.2
Hrstka, R.F.3
Consolino, C.M.4
Faulkner, J.A.5
Williamson, R.A.6
Campbell, K.P.7
-
38
-
-
84873460035
-
Isometric and eccentric force generation assessment of skeletal muscles isolated from murine models of muscular dystrophies
-
Moorwood, C., Liu, M., Tian, Z. and Barton, E.R. (2013) Isometric and eccentric force generation assessment of skeletal muscles isolated from murine models of muscular dystrophies. J. Vis. Exp., e50036.
-
(2013)
J. Vis. Exp
-
-
Moorwood, C.1
Liu, M.2
Tian, Z.3
Barton, E.R.4
-
39
-
-
84855998142
-
Endpoint measures in the mdx mouse relevant for muscular dystrophy pre-clinical studies
-
Kobayashi, Y.M., Rader, E.P., Crawford, R.W. and Campbell, K.P. (2012) Endpoint measures in the mdx mouse relevant for muscular dystrophy pre-clinical studies. Neuromuscul. Disord., 22, 34-42.
-
(2012)
Neuromuscul. Disord
, vol.22
, pp. 34-42
-
-
Kobayashi, Y.M.1
Rader, E.P.2
Crawford, R.W.3
Campbell, K.P.4
-
40
-
-
0041430538
-
Ventilatory dysfunction in mdx mice: impact of tumor necrosis factor-alpha deletion
-
Gosselin, L.E., Barkley, J.E., Spencer, M.J., McCormick, K.M. and Farkas, G.A. (2003) Ventilatory dysfunction in mdx mice: impact of tumor necrosis factor-alpha deletion. Muscle Nerve, 28, 336-343.
-
(2003)
Muscle Nerve
, vol.28
, pp. 336-343
-
-
Gosselin, L.E.1
Barkley, J.E.2
Spencer, M.J.3
McCormick, K.M.4
Farkas, G.A.5
-
41
-
-
84940121801
-
Respiratory Control in the mdx Mouse Model of Duchenne Muscular Dystrophy
-
Burns, D.P., Edge, D., O'Malley, D. and O'Halloran, K.D. (2015) Respiratory Control in the mdx Mouse Model of Duchenne Muscular Dystrophy. Adv. Exp. Med. Biol., 860, 239-244.
-
(2015)
Adv. Exp. Med. Biol
, vol.860
, pp. 239-244
-
-
Burns, D.P.1
Edge, D.2
O'Malley, D.3
O'Halloran, K.D.4
-
42
-
-
84899120609
-
Exon-skipping therapy: a roadblock, detour, or bump in the road?
-
Hoffman, E.P. and McNally, E.M. (2014) Exon-skipping therapy: a roadblock, detour, or bump in the road?. Sci. Transl. Med., 6, 230fs214.
-
(2014)
Sci. Transl. Med
, vol.6
-
-
Hoffman, E.P.1
McNally, E.M.2
-
43
-
-
0034683567
-
Assembly of the dystrophin-associated protein complex does not require the dystrophin COOH-terminal domain
-
Crawford, G.E., Faulkner, J.A., Crosbie, R.H., Campbell, K.P., Froehner, S.C. and Chamberlain, J.S. (2000) Assembly of the dystrophin-associated protein complex does not require the dystrophin COOH-terminal domain. J. Cell Biol., 150, 1399-1410.
-
(2000)
J. Cell Biol
, vol.150
, pp. 1399-1410
-
-
Crawford, G.E.1
Faulkner, J.A.2
Crosbie, R.H.3
Campbell, K.P.4
Froehner, S.C.5
Chamberlain, J.S.6
|