-
1
-
-
0029186061
-
Dystrophin, its gene, and the dystrophinopathies
-
Roberts, R.G. (1995) Dystrophin, its gene, and the dystrophinopathies. Adv. Genet. 33, 177-231.
-
(1995)
Adv. Genet.
, vol.33
, pp. 177-231
-
-
Roberts, R.G.1
-
2
-
-
0029873627
-
Clinical and histopathological features of abnormalities of the dystrophin-based membrane cytoskeleton
-
Hoffman, E.P. (1996) Clinical and histopathological features of abnormalities of the dystrophin-based membrane cytoskeleton. Brain Path. 6, 49-61.
-
(1996)
Brain Path.
, vol.6
, pp. 49-61
-
-
Hoffman, E.P.1
-
3
-
-
0027470203
-
The structural and functional diversity of dystrophin
-
Ahn, A.H. and Kunkel, L.M. (1993) The structural and functional diversity of dystrophin. Nature Genet. 3, 283-291.
-
(1993)
Nature Genet.
, vol.3
, pp. 283-291
-
-
Ahn, A.H.1
Kunkel, L.M.2
-
4
-
-
0028047235
-
Dystrophin-glycoprotein complex: Its role in the pathogenesis of muscular dystrophies
-
Matsumura, K. and Campbell, K.P. (1994) Dystrophin-glycoprotein complex: its role in the pathogenesis of muscular dystrophies. Muscle Nerve 17, 2-15.
-
(1994)
Muscle Nerve
, vol.17
, pp. 2-15
-
-
Matsumura, K.1
Campbell, K.P.2
-
5
-
-
0027980295
-
Increasing complexity of the dystrophin-associated protein complex
-
Tinsley, J.T., Blake, D.J., Zuellig, R.A. and Davies, K.E. (1994) Increasing complexity of the dystrophin-associated protein complex. Proc. Natl. Acad. Sci. USA 91, 8307-8313.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 8307-8313
-
-
Tinsley, J.T.1
Blake, D.J.2
Zuellig, R.A.3
Davies, K.E.4
-
6
-
-
0025815479
-
Membrane organization of the dystrophin-glycoprotein complex
-
Ervasti, J.M. and Campbell, K.P. (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
-
7
-
-
0028914964
-
Three muscular dystrophies: Loss of cytoskeleton extracellular matrix linkage
-
Campbell, K.P. (1995) Three muscular dystrophies: loss of cytoskeleton extracellular matrix linkage. Cell 80, 675-679.
-
(1995)
Cell
, vol.80
, pp. 675-679
-
-
Campbell, K.P.1
-
8
-
-
0030219026
-
The genetic basis of neuromuscular disorders
-
Nawrotzki, R., Blake, D.J. and Davies, K.E. (1996) The genetic basis of neuromuscular disorders. Trends Genet. 12, 294-298.
-
(1996)
Trends Genet.
, vol.12
, pp. 294-298
-
-
Nawrotzki, R.1
Blake, D.J.2
Davies, K.E.3
-
9
-
-
0026328022
-
Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice
-
Ohlendieck, K. and Campbell, K.P. (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
-
10
-
-
0027481238
-
Duchenne muscular dystrophy: Deficiency of dystrophin-associated proteins in the sarcolemma
-
Ohlendieck, K., Matsumura, K., Ionasescu, V.V., Towbin, J.A., Bosch, E.P., Weinstein, S.L., Sernett, S.W. and Campbell, K.P. (1993) Duchenne muscular dystrophy: deficiency of dystrophin-associated proteins in the sarcolemma. Neurology 43, 795-800.
-
(1993)
Neurology
, vol.43
, pp. 795-800
-
-
Ohlendieck, K.1
Matsumura, K.2
Ionasescu, V.V.3
Towbin, J.A.4
Bosch, E.P.5
Weinstein, S.L.6
Sernett, S.W.7
Campbell, K.P.8
-
11
-
-
0028146869
-
Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy
-
Roberds, S.L., Letureq, F., Allamand, V., Piccolo, F., Jeanpierre, M., Anderson, R.D., Lim, L.E., Lee, J.C., Tomé, F.M.S., Romero, N.B., Fardeau, M., Beckmann, J.S., Kaplan, J.-C and Campbell, K.P. (1994) Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy. Cell 78, 625-633.
-
(1994)
Cell
, vol.78
, pp. 625-633
-
-
Roberds, S.L.1
Letureq, F.2
Allamand, V.3
Piccolo, F.4
Jeanpierre, M.5
Anderson, R.D.6
Lim, L.E.7
Lee, J.C.8
Tomé, F.M.S.9
Romero, N.B.10
Fardeau, M.11
Beckmann, J.S.12
Kaplan, J.-C.13
Campbell, K.P.14
-
12
-
-
0028971219
-
β-sarcoglycan, (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex
-
Bönnemann, C.G., Modi, R., Noguchi, S., Mizuno, Y., Yoshida, M., Gussoni, E., McNally, E.M., Duggan, D.J., Angelini, C., Hoffmann, E.P., Ozawa, E. and Kunkel, L.M. (1995) β-sarcoglycan, (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex. Nature Genet. 11, 266-273.
-
(1995)
Nature Genet.
, vol.11
, pp. 266-273
-
-
Bönnemann, C.G.1
Modi, R.2
Noguchi, S.3
Mizuno, Y.4
Yoshida, M.5
Gussoni, E.6
McNally, E.M.7
Duggan, D.J.8
Angelini, C.9
Hoffmann, E.P.10
Ozawa, E.11
Kunkel, L.M.12
-
13
-
-
0028971221
-
β-sarcoglycan, characterization and rule in limb-girdle muscular dystrophy linked to 4q12
-
Lim, L.E., Duclos, F., Broux, O., Bourg, N., Sunada, Y., Allamand, V., Meyer, J., Richard, I., Moomaw, C., Slaughter, C., Tomé, F.M.S., Fardeau, M., Jackson, C.E., Beckmann J.S. and Campbell, K.P. (1995) β-sarcoglycan, characterization and rule in limb-girdle muscular dystrophy linked to 4q12. Nature Genet. 11, 257-265.
-
(1995)
Nature Genet.
, vol.11
, pp. 257-265
-
-
Lim, L.E.1
Duclos, F.2
Broux, O.3
Bourg, N.4
Sunada, Y.5
Allamand, V.6
Meyer, J.7
Richard, I.8
Moomaw, C.9
Slaughter, C.10
Tomé, F.M.S.11
Fardeau, M.12
Jackson, C.E.13
Beckmann, J.S.14
Campbell, K.P.15
-
14
-
-
0028883973
-
Mutations in the dystrophin-associated protein γsarcogiycan in chromosome 13 muscular dystrophy
-
Noguchi, S., McNally, E.M., Ben Othmane, K., Hagiwara, Y., Mizuno, Y., Yoshida, M., Yamamoto, H., Bsnnemann, C.G., Gussoni, E., Denton, P.H., Hyriakides, T., Middleton, L., Hentati, F., Ben Hamida, M., Nonaka, I., Vance, J.M., Kunkel, L.M. and Ozawa, E. (1995) Mutations in the dystrophin-associated protein γsarcogiycan in chromosome 13 muscular dystrophy. Science 270, 819-822.
-
(1995)
Science
, vol.270
, pp. 819-822
-
-
Noguchi, S.1
McNally, E.M.2
Ben Othmane, K.3
Hagiwara, Y.4
Mizuno, Y.5
Yoshida, M.6
Yamamoto, H.7
Bsnnemann, C.G.8
Gussoni, E.9
Denton, P.H.10
Hyriakides, T.11
Middleton, L.12
Hentati, F.13
Ben Hamida, M.14
Nonaka, I.15
Vance, J.M.16
Kunkel, L.M.17
Ozawa, E.18
-
15
-
-
0029816797
-
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ-sarcoglycan gene
-
Nigro, V., de Sa Moreira, E., Piluso, G., Vainzof, M., Belsito, A., Politano, L., Puca, A.A., Passos Bueno, M.R. and Zatz, M. (1996) Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ-sarcoglycan gene. Nature Genet. 14, 195-198.
-
(1996)
Nature Genet.
, vol.14
, pp. 195-198
-
-
Nigro, V.1
De Sa Moreira, E.2
Piluso, G.3
Vainzof, M.4
Belsito, A.5
Politano, L.6
Puca, A.A.7
Passos Bueno, M.R.8
Zatz, M.9
-
16
-
-
0028905205
-
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A
-
Richard, I., Broux, O., Allamand, V., Fougerousse, F., Chiannilkulchai, N., Bourg, N., Brenguier, L., Devaud, C., Pasturaud, P., Roudaut, C., Hillaire, D., Passos-Bueno, M.-R., Zatz, M., Yischfield, J.A., Fardeau, M., Jackson, C.E., Cohen, D. and Beckmann, J.S. (1995) Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A. Cell 81, 27-40.
-
(1995)
Cell
, vol.81
, pp. 27-40
-
-
Richard, I.1
Broux, O.2
Allamand, V.3
Fougerousse, F.4
Chiannilkulchai, N.5
Bourg, N.6
Brenguier, L.7
Devaud, C.8
Pasturaud, P.9
Roudaut, C.10
Hillaire, D.11
Passos-Bueno, M.-R.12
Zatz, M.13
Yischfield, J.A.14
Fardeau, M.15
Jackson, C.E.16
Cohen, D.17
Beckmann, J.S.18
-
17
-
-
0029319426
-
Primary adhanlinopathy: A common cause of autosomal recessive muscular dystrophy of variable phenotype
-
Piccolo, F., Roberds, S.L., Jeanpierre, M., Leturcq, F., Azibi, K., Beldjord, C., Carrié, A., Récan, D., Chaouch, M., Reghis, A., El Kerch, F., Sefiani, A., Voit, T., Merlini, L., Collin, H., Eymard, B., Beckmann, J.S., Romero, N.B., Tomé, F.M.S., Fardeau, M., Campbell, K.P. and Kaplan, J.-C. (1996) Primary adhanlinopathy: a common cause of autosomal recessive muscular dystrophy of variable phenotype. Nature Genet. 10, 243-245.
-
(1996)
Nature Genet.
, vol.10
, pp. 243-245
-
-
Piccolo, F.1
Roberds, S.L.2
Jeanpierre, M.3
Leturcq, F.4
Azibi, K.5
Beldjord, C.6
Carrié, A.7
Récan, D.8
Chaouch, M.9
Reghis, A.10
El Kerch, F.11
Sefiani, A.12
Voit, T.13
Merlini, L.14
Collin, H.15
Eymard, B.16
Beckmann, J.S.17
Romero, N.B.18
Tomé, F.M.S.19
Fardeau, M.20
Campbell, K.P.21
Kaplan, J.-C.22
more..
-
18
-
-
0029906609
-
Advances in the molecular genetics of the limb-girdle type of autosomal recessive progressive muscular dystrophy
-
Beckmann, J.S. and Bushby, K.M.D. (1996) Advances in the molecular genetics of the limb-girdle type of autosomal recessive progressive muscular dystrophy. Curr. Opin. Neurol. 9, 389-393.
-
(1996)
Curr. Opin. Neurol.
, vol.9
, pp. 389-393
-
-
Beckmann, J.S.1
Bushby, K.M.D.2
-
19
-
-
10544234620
-
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies
-
Vainzof, M., Passos-Bueno, M.R., Canovas, M., Moreira, E.S., Pavanello, R.C.M., Marie, S.K., Anderson, L.V.B., Bonneman, C.G., McNally, E.M., Nigro, V., Kunkel, L.M. and Zatz, M. (1996) The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies. Hum. Mol. Genet. 5, 1963-1969.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1963-1969
-
-
Vainzof, M.1
Passos-Bueno, M.R.2
Canovas, M.3
Moreira, E.S.4
Pavanello, R.C.M.5
Marie, S.K.6
Anderson, L.V.B.7
Bonneman, C.G.8
McNally, E.M.9
Nigro, V.10
Kunkel, L.M.11
Zatz, M.12
-
20
-
-
0027375539
-
Two forms of mouse syntrophin, a 58 kDa dystrophin-associated protein, differ in primary structure and tissue distribution
-
Adams, M.E., Butler, M.H., Dwyer, T.M., Peters, M.F., Murnane, A.A. and Froehner. S.C. (1993) Two forms of mouse syntrophin, a 58 kDa dystrophin-associated protein, differ in primary structure and tissue distribution. Neuron 11, 531-540.
-
(1993)
Neuron
, vol.11
, pp. 531-540
-
-
Adams, M.E.1
Butler, M.H.2
Dwyer, T.M.3
Peters, M.F.4
Murnane, A.A.5
Froehner, S.C.6
-
21
-
-
0028219584
-
Cloning of human basic Al, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24
-
Ahn, A.H., Yoshida, M., Anderson, M.S., Feener, C.A., Selig, S., Hagiwara, Y., Ozawa, E. and Kunkel, L.M. (1994) Cloning of human basic Al, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24. Proc. Natl. Acad. Sci. USA 91, 4446-4450.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 4446-4450
-
-
Ahn, A.H.1
Yoshida, M.2
Anderson, M.S.3
Feener, C.A.4
Selig, S.5
Hagiwara, Y.6
Ozawa, E.7
Kunkel, L.M.8
-
22
-
-
0027998866
-
Heterogeneity of the 59 kDa dystrophin-associated protein revealed by cDNA cloning and expression
-
Yang, B., Ibraghimov-Beskrovnaya, O., Moomaw, C.R., Slaughter, C.A. and Campbell. K.P. (1994) Heterogeneity of the 59 kDa dystrophin-associated protein revealed by cDNA cloning and expression. J. Biol. Chem. 269, 6040-6044.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 6040-6044
-
-
Yang, B.1
Ibraghimov-Beskrovnaya, O.2
Moomaw, C.R.3
Slaughter, C.A.4
Campbell, K.P.5
-
23
-
-
0028947998
-
Syntrophin binds to an alternatively spliced exon of dystrophin
-
Ahn, A.H. and Kunkel, L.M. (1995) Syntrophin binds to an alternatively spliced exon of dystrophin. J. Cell Biol. 128, 363-371.
-
(1995)
J. Cell Biol.
, vol.128
, pp. 363-371
-
-
Ahn, A.H.1
Kunkel, L.M.2
-
24
-
-
0028985719
-
Mammalian α1- and β1-syntrophin bind to the alternative splice-prone region of the dystrophin COOH terminus
-
Suzuki, A., Yoshida, M. and Ozawa, E. (1995) Mammalian α1- and β1-syntrophin bind to the alternative splice-prone region of the dystrophin COOH terminus. J. Cell Biol. 128, 373-381.
-
(1995)
J. Cell Biol.
, vol.128
, pp. 373-381
-
-
Suzuki, A.1
Yoshida, M.2
Ozawa, E.3
-
25
-
-
0028806695
-
Direct binding of Torpedo syntrophin to dystrophin and the 87 kDa dystrophin homologue
-
Dwyer, T.M. and Froehner, S.C. (1995) Direct binding of Torpedo syntrophin to dystrophin and the 87 kDa dystrophin homologue. FEBS Lett. 375, 91-94.
-
(1995)
FEBS Lett.
, vol.375
, pp. 91-94
-
-
Dwyer, T.M.1
Froehner, S.C.2
-
26
-
-
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
-
27
-
-
0024445583
-
A novel 87000-Mr protein associated with acetylcholine receptors in Torpedo electric organ and vertebrate skeletal muscle
-
Carr, C., Fischbach, G.D. and Cohen, J.B. (1989) A novel 87000-Mr protein associated with acetylcholine receptors in Torpedo electric organ and vertebrate skeletal muscle. J. Cell Biol. 109, 1753-1764.
-
(1989)
J. Cell Biol.
, vol.109
, pp. 1753-1764
-
-
Carr, C.1
Fischbach, G.D.2
Cohen, J.B.3
-
28
-
-
0026611958
-
Association of the Mr 58,000 postsynaptic protein of electric tissue with Torpedo dystrophin and the Mr 87,000 postsynaptic protein
-
Butler, M.H., Douville, K., Murnane, A.A., Kramarcy, N.R., Cohen, J.B., Sealock, R. and Froehner, S.C. (1992) Association of the Mr 58,000 postsynaptic protein of electric tissue with Torpedo dystrophin and the Mr 87,000 postsynaptic protein. J. Biol. Chem. 267, 6213-6218.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 6213-6218
-
-
Butler, M.H.1
Douville, K.2
Murnane, A.A.3
Kramarcy, N.R.4
Cohen, J.B.5
Sealock, R.6
Froehner, S.C.7
-
29
-
-
0027481757
-
The 87K postsynaptic membrane protein from Torpedo is a protein-tyrosine kinase substrate homologous to dystrophin
-
Wagner, K.R., Cohen, J.B. and Huganir, R.L. (1993) The 87K postsynaptic membrane protein from Torpedo is a protein-tyrosine kinase substrate homologous to dystrophin. Neuron 10, 511-522.
-
(1993)
Neuron
, vol.10
, pp. 511-522
-
-
Wagner, K.R.1
Cohen, J.B.2
Huganir, R.L.3
-
30
-
-
0029881574
-
Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein
-
Blake, D.J., Nawrotzki, R., Peters, M.F., Froehner, S.C. and Davies, K.E. (1996) Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein. J. Biol. Chem. 271, 7802-7810.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 7802-7810
-
-
Blake, D.J.1
Nawrotzki, R.2
Peters, M.F.3
Froehner, S.C.4
Davies, K.E.5
-
31
-
-
0029937712
-
Cloning and characterization of the human homologue of a dystrophin related phosphoprotein found at the Torpedo electric organ post-synaptic membrane
-
Sadoulet-Puccio, H.M., Khurana, T.S., Cohen, J.B. and Kunkel, L.M. (1996) Cloning and characterization of the human homologue of a dystrophin related phosphoprotein found at the Torpedo electric organ post-synaptic membrane. Hum. Mol. Genet. 5, 489-496.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 489-496
-
-
Sadoulet-Puccio, H.M.1
Khurana, T.S.2
Cohen, J.B.3
Kunkel, L.M.4
-
32
-
-
0031081719
-
Genomic organization of the mouse dystrobrevin gene: Comparative analysis with the dystrophin gene
-
Ambrose H.J., Blake, D.J., Nawrotzki, R.A. and Davies, K.E. (1997) Genomic organization of the mouse dystrobrevin gene: Comparative analysis with the dystrophin gene. Genomics 39, 359-369.
-
(1997)
Genomics
, vol.39
, pp. 359-369
-
-
Ambrose, H.J.1
Blake, D.J.2
Nawrotzki, R.A.3
Davies, K.E.4
-
33
-
-
0028980250
-
Dystrophin-associated protein A0 is a homologue of the Torpedo 87K protein
-
Yoshida, M., Yamamoto, H., Noguchi, S., Mizuno, Y., Hagiwara, Y. and Ozawa, E. (1995) Dystrophin-associated protein A0 is a homologue of the Torpedo 87K protein. FEBS Lett. 367, 311-314.
-
(1995)
FEBS Lett.
, vol.367
, pp. 311-314
-
-
Yoshida, M.1
Yamamoto, H.2
Noguchi, S.3
Mizuno, Y.4
Hagiwara, Y.5
Ozawa, E.6
-
34
-
-
10344249872
-
Mutations that disrupt the carboxyl-terminus of γ-sarcoglycan cause muscular dystrophy
-
McNally, E.M., Duggan, D., Gorospe, J.R., Bönnemann, C.G., Fanin, M., Pegoraro, E., Lidov, H.G.W., Noguchi, S., Ozawa, E., Finkel, R.S., Cruse, R.P., Angelini, C., Kunkel L.M. and Hoffman. E.P. (1996) Mutations that disrupt the carboxyl-terminus of γ-sarcoglycan cause muscular dystrophy. Hum. Mol. Genet. 5, 1841-1847.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1841-1847
-
-
McNally, E.M.1
Duggan, D.2
Gorospe, J.R.3
Bönnemann, C.G.4
Fanin, M.5
Pegoraro, E.6
Lidov, H.G.W.7
Noguchi, S.8
Ozawa, E.9
Finkel, R.S.10
Cruse, R.P.11
Angelini, C.12
Kunkel, L.M.13
Hoffman, E.P.14
-
35
-
-
0029149757
-
Interactions between dystrophin-glycoprotein complex
-
Madhavan, R. and Jarrett, H.W. (1995) Interactions between dystrophin-glycoprotein complex. Biochemistry 34, 12204-12209.
-
(1995)
Biochemistry
, vol.34
, pp. 12204-12209
-
-
Madhavan, R.1
Jarrett, H.W.2
-
36
-
-
0028987269
-
Coiled-coil regions in the carboxy-terminal domains of dystrophin and related proteins: Potentials for protein-protein interactions
-
Blake, D.J., Tinsley, J.M., Davies, K.E., Knight, A.E., Winder, S.J. and Kendrick-Jones, J. (1995) Coiled-coil regions in the carboxy-terminal domains of dystrophin and related proteins: potentials for protein-protein interactions. Trends Biochem. Sci. 20, 133-135.
-
(1995)
Trends Biochem. Sci.
, vol.20
, pp. 133-135
-
-
Blake, D.J.1
Tinsley, J.M.2
Davies, K.E.3
Knight, A.E.4
Winder, S.J.5
Kendrick-Jones, J.6
-
37
-
-
0028137134
-
Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform
-
Rafael, J.A., Sunada, Y., Cole, N.M., Campbell, K.P., Faulkner, J.A. and Chamberlain, J.S. (1994) Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform. Hum. Mol. Genet. 3, 1725-1733.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1725-1733
-
-
Rafael, J.A.1
Sunada, Y.2
Cole, N.M.3
Campbell, K.P.4
Faulkner, J.A.5
Chamberlain, J.S.6
-
38
-
-
0029959354
-
Forced expression of dystrophin deletion constructs reveals structure-function correlations
-
Rafael, J.A., Cox, G.A., Corrado, K., Jung, D., Campbell, K.P. and Chamberlain, J.S. (1996) Forced expression of dystrophin deletion constructs reveals structure-function correlations. J. Cell Biol. 134, 93-102.
-
(1996)
J. Cell Biol.
, vol.134
, pp. 93-102
-
-
Rafael, J.A.1
Cox, G.A.2
Corrado, K.3
Jung, D.4
Campbell, K.P.5
Chamberlain, J.S.6
-
39
-
-
0029835575
-
Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophy
-
Chao, D.S., Gorospe, J.R.M., Brenman, J.E., Rafael, J.A., Peters, M.F., Froehner, S.C., Hoffmann, E.P., Chamberlain, J.S. and Bredt, D.S. (1996) Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophy. J. Exp. Med. 184, 609-618.
-
(1996)
J. Exp. Med.
, vol.184
, pp. 609-618
-
-
Chao, D.S.1
Gorospe, J.R.M.2
Brenman, J.E.3
Rafael, J.A.4
Peters, M.F.5
Froehner, S.C.6
Hoffmann, E.P.7
Chamberlain, J.S.8
Bredt, D.S.9
-
40
-
-
8044254229
-
Neural nitric oxide synthase and dystrophin-deficient muscular dystrophy
-
Chang, W.J., Iannaccone, S.T., Lau, K.S., Masters, B.S.S., McCabe, T.J., McMillan, K., Padre, R.C., Spencer, M.J., Tidball, J.G. and Stull, J.T. (1996) Neural nitric oxide synthase and dystrophin-deficient muscular dystrophy. Proc. Natl. Acad. Sci. USA 93, 9142-9147.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 9142-9147
-
-
Chang, W.J.1
Iannaccone, S.T.2
Lau, K.S.3
Masters, B.S.S.4
McCabe, T.J.5
McMillan, K.6
Padre, R.C.7
Spencer, M.J.8
Tidball, J.G.9
Stull, J.T.10
-
41
-
-
0029013328
-
The expression of dystrophin-associated glycoproteins during skeletal muscle degeneration and regeneration: An immunofluorescence study
-
Vater, R., Harris, J.B., Anderson, L.V.B., Roberds, S.L., Campbell, K.P. and Cullen, M.J. (1995) The expression of dystrophin-associated glycoproteins during skeletal muscle degeneration and regeneration: an immunofluorescence study. J. Neuropathol. Exp. Neurol. 54, 557-569.
-
(1995)
J. Neuropathol. Exp. Neurol.
, vol.54
, pp. 557-569
-
-
Vater, R.1
Harris, J.B.2
Anderson, L.V.B.3
Roberds, S.L.4
Campbell, K.P.5
Cullen, M.J.6
-
42
-
-
0027203989
-
Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, immunochemical, and histopathological data. Part I. Trends across the clinical groups
-
Nicholson, L.V.B., Johnson, M.A., Bushby, K.M.D., Gardner-Mervin, D., Curtis, A., Ginjaar, I.B., den Dunnen, J.T., Welch, J.L., Butler, T.J., Bakker, E., van Ommen, G.-J.B. and Harris, J.B. (1993) Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, immunochemical, and histopathological data. Part I. Trends across the clinical groups. J. Med. Genet. 30, 728-736.
-
(1993)
J. Med. Genet.
, vol.30
, pp. 728-736
-
-
Nicholson, L.V.B.1
Johnson, M.A.2
Bushby, K.M.D.3
Gardner-Mervin, D.4
Curtis, A.5
Ginjaar, I.B.6
Den Dunnen, J.T.7
Welch, J.L.8
Butler, T.J.9
Bakker, E.10
Van Ommen, G.-J.B.11
Harris, J.B.12
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