-
1
-
-
0027375539
-
Two forms of mouse syntrophin, a 58 kd dystrophin-associated protein, differ in primary structure and tissue distribution
-
Adams, M.E., M.H. Butler, T.M. Dwyer, M.F. Peters, A.A. Murnane, and S.C. Froehner. 1993. Two forms of mouse syntrophin, a 58 kd 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
-
2
-
-
0027470203
-
The structural and functional diversity of dystrophin
-
Ahn, A.H., and L.M. Kunkel. 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
-
3
-
-
0028947998
-
Syntrophin binds to an alternatively spliced exon of dystrophin
-
Ahn, A.H., and L.M. Kunkel. 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
-
4
-
-
0028917646
-
Association of aciculin with dystrophin and utrophin
-
Belkin, A.M., and K. Burridge. 1995. Association of aciculin with dystrophin and utrophin. J. Biol. Chem. 270:6328-6337.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 6328-6337
-
-
Belkin, A.M.1
Burridge, K.2
-
5
-
-
0026674204
-
An intact cysteine-rich domain is required for dystrophin function
-
Bies, R.D., C.T. Caskey, and R. Fenwick. 1992. An intact cysteine-rich domain is required for dystrophin function. J. Clin. Invest. 90:666-672.
-
(1992)
J. Clin. Invest.
, vol.90
, pp. 666-672
-
-
Bies, R.D.1
Caskey, C.T.2
Fenwick, R.3
-
6
-
-
0029881574
-
Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein
-
Blake, D.J., R. Nawrotzki, M.F. Peters, S.C. Froehner, and K.E. Davies. 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
-
7
-
-
13344277364
-
Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and α1-symrophin mediated by PDZ domains
-
Brenman, J.E., D.S. Chao, S.H. Gee, A.W. McGee, S.E. Craven, D.R. Santillano, Z. Wu, F. Huang, H. Xia, M.F. Peters, et al. 1996. Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and α1-symrophin mediated by PDZ domains. Cell. 84:757-767.
-
(1996)
Cell
, vol.84
, pp. 757-767
-
-
Brenman, J.E.1
Chao, D.S.2
Gee, S.H.3
McGee, A.W.4
Craven, S.E.5
Santillano, D.R.6
Wu, Z.7
Huang, F.8
Xia, H.9
Peters, M.F.10
-
8
-
-
0028971219
-
β-Sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex
-
Bönnemann, C.G., R. Modi, S. Noguchi, Y. Mizuno, M. Yoshida, E. Gussoni, E.M. McNally, D.J. Duggan, C. Angelini, E.P. Hoffman, E. Ozawa, and L.M. Kunkel. 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
Hoffman, E.P.10
Ozawa, E.11
Kunkel, L.M.12
-
9
-
-
34447491275
-
-
Chamberlain, J.S., J.A. Pearlman, D.M. Muzny, A. Civetello, N.J. Farwell, R. Malek, P. Powaser, A.A. Reeves, C. Lee, and C.T. Caskey. 1991. Genbank accession number M68859.
-
(1991)
Genbank Accession Number M68859
-
-
Chamberlain, J.S.1
Pearlman, J.A.2
Muzny, D.M.3
Civetello, A.4
Farwell, N.J.5
Malek, R.6
Powaser, P.7
Reeves, A.A.8
Lee, C.9
Caskey, C.T.10
-
10
-
-
0027186053
-
Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity
-
Cox, G.A., N.M. Cole, K. Matsumura, S.F. Phelps, S.D. Hauschka, K.P. Campbell, J.A. Faulkner, and J.S. Chamberlain. 1993. Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity. Nature (Lond.). 364:725-729.
-
(1993)
Nature (Lond.)
, vol.364
, pp. 725-729
-
-
Cox, G.A.1
Cole, N.M.2
Matsumura, K.3
Phelps, S.F.4
Hauschka, S.D.5
Campbell, K.P.6
Faulkner, J.A.7
Chamberlain, J.S.8
-
11
-
-
0027273835
-
New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin
-
Cox, G.A., S.F. Phelps, V.M. Chapman, and J.S. Chamberlain. 1993. New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin. Nature Genet. 4:87-93.
-
(1993)
Nature Genet.
, vol.4
, pp. 87-93
-
-
Cox, G.A.1
Phelps, S.F.2
Chapman, V.M.3
Chamberlain, J.S.4
-
12
-
-
0028134623
-
Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy
-
Cox, G.A., Y. Sunada, K.P. Campbell, and J.S. Chamberlain. 1994. Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy. Nature Genet. 8:333-339.
-
(1994)
Nature Genet.
, vol.8
, pp. 333-339
-
-
Cox, G.A.1
Sunada, Y.2
Campbell, K.P.3
Chamberlain, J.S.4
-
13
-
-
0025159208
-
Very mild muscular dystrophy associated with the deletion of 46% of dystrophin
-
England, S.B., L.V. Nicholson, M.A. Johnson, S.M. Forrest, D.R. Love, E.E. Zubrzycka-Gaarn, D.E. Bulman, J.B. Harris, and K.E. Davies. 1990. Very mild muscular dystrophy associated with the deletion of 46% of dystrophin. Nature (Lond.). 343:180-182.
-
(1990)
Nature (Lond.)
, vol.343
, pp. 180-182
-
-
England, S.B.1
Nicholson, L.V.2
Johnson, M.A.3
Forrest, S.M.4
Love, D.R.5
Zubrzycka-Gaarn, E.E.6
Bulman, D.E.7
Harris, J.B.8
Davies, K.E.9
-
14
-
-
0027275643
-
A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin
-
Ervasti, J.M., and K.P. Campbell. 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
-
16
-
-
0025272250
-
Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle
-
Ervasti, J.M., K. Ohlendieck, S.D. Kahl, M.G. Gaver, and K.P. Campbell. 1990. Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle. Nature (Lond.). 345:315-319.
-
(1990)
Nature (Lond.)
, vol.345
, pp. 315-319
-
-
Ervasti, J.M.1
Ohlendieck, K.2
Kahl, S.D.3
Gaver, M.G.4
Campbell, K.P.5
-
17
-
-
0028051872
-
Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice
-
Greenberg, D.S., Y. Sunada, K.P. Campbell, D. Yaffe, and U. Nudel. 1994. Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice. Nature Genet. 8:340-344.
-
(1994)
Nature Genet.
, vol.8
, pp. 340-344
-
-
Greenberg, D.S.1
Sunada, Y.2
Campbell, K.P.3
Yaffe, D.4
Nudel, U.5
-
18
-
-
0026587401
-
A truncated dystrophin lacking the C-terminal domains is localized at the muscle membrane
-
Helliwell, T.R., J.M. Ellis, R.C. Mountford, R.E. Appleton, and G.E. Morris. 1992. A truncated dystrophin lacking the C-terminal domains is localized at the muscle membrane. Am. J. Hum. Genet. 50:508-514.
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 508-514
-
-
Helliwell, T.R.1
Ellis, J.M.2
Mountford, R.C.3
Appleton, R.E.4
Morris, G.E.5
-
19
-
-
0026049619
-
Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of Duchenne muscular dystrophy
-
Hoffman, E.P., C.A. Garcia, J.S. Chamberlain, C. Angelini, J.R. Lupski, and R. Fenwick. 1991. Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of Duchenne muscular dystrophy. Ann. Neurol. 30:605-610.
-
(1991)
Ann. Neurol.
, vol.30
, pp. 605-610
-
-
Hoffman, E.P.1
Garcia, C.A.2
Chamberlain, J.S.3
Angelini, C.4
Lupski, J.R.5
Fenwick, R.6
-
21
-
-
0026543686
-
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix
-
Ibraghimov-Beskrovnaya, O., J.M. Ervasti, C.J. Leveille, C.A. Slaughter, S.W. Sernett, and K.P. Campbell. 1992. Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix. Nature (Lond.). 355:696-702.
-
(1992)
Nature (Lond.)
, 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
-
22
-
-
18544402590
-
Absence of γ-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12
-
Jung, D., F. Leturcq, Y. Sunada, F. Duclos, F.M.S. Tomé, C. Moomaw, L. Merlini, K. Azibi, M. Chaouch, C. Slaughter, M. Fardeau, J-C. Kaplan, and K. P. Campbell. 1996. Absence of γ-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12. FEBS Lett. 381:15-20.
-
(1996)
FEBS Lett.
, vol.381
, pp. 15-20
-
-
Jung, D.1
Leturcq, F.2
Sunada, Y.3
Duclos, F.4
Tomé, F.M.S.5
Moomaw, C.6
Merlini, L.7
Azibi, K.8
Chaouch, M.9
Slaughter, C.10
Fardeau, M.11
Kaplan, J.-C.12
Campbell, K.P.13
-
23
-
-
0028805790
-
Identification and characterization of the dystrophin anchoring site on β-dystroglycan
-
Jung, D., B. Yang, J. Meyer, J.S. Chamberlain, and K.P. Campbell. 1995. Identification and characterization of the dystrophin anchoring site on β-dystroglycan. J. Biol. Chem. 270:27305-27310.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 27305-27310
-
-
Jung, D.1
Yang, B.2
Meyer, J.3
Chamberlain, J.S.4
Campbell, K.P.5
-
24
-
-
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., E.P. Hoffman, C.J. Bertelson, A.P. Monaco, C. Feener, and L.M. Kunkel. 1987. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell. 50:509-517.
-
(1987)
Cell
, vol.50
, pp. 509-517
-
-
Koenig, M.1
Hoffman, E.P.2
Bertelson, C.J.3
Monaco, A.P.4
Feener, C.5
Kunkel, L.M.6
-
25
-
-
0025217703
-
Detailed analysis of the repeat domain of dystrophin reveals four potential hinge segments that may confer flexibility
-
Koenig, M., and L.M. Kunkel. 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
-
26
-
-
0025969678
-
Expression of recombinant dystrophin and its localization to the cell membrane
-
Lee, C.C., J.A. Pearlman, J.S. Chamberlain, and C.T. Caskey. 1991. Expression of recombinant dystrophin and its localization to the cell membrane. Nature (Lond.). 349:334-336.
-
(1991)
Nature (Lond.)
, vol.349
, pp. 334-336
-
-
Lee, C.C.1
Pearlman, J.A.2
Chamberlain, J.S.3
Caskey, C.T.4
-
27
-
-
0028971221
-
β-Sarcoglycan: Characterization and role in limb-girdle muscular dystrophy linked to 4q12
-
Lira, L.E., F. Duclos, O. Broux, N. Bourg, Y. Sunada, V. Allamand, J. Meyer, I. Z. Richard, C. Moomaw, C. Slaughter, et al. 1995. β-Sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12. Nature Genet. 11:257-265.
-
(1995)
Nature Genet.
, vol.11
, pp. 257-265
-
-
Lira, L.E.1
Duclos, F.2
Broux, O.3
Bourg, N.4
Sunada, Y.5
Allamand, V.6
Meyer, J.7
Richard, I.Z.8
Moomaw, C.9
Slaughter, C.10
-
28
-
-
0029164775
-
Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophin
-
Ljunggren, A., D. Duggan, E. McNally, K.B. Boylan, C.H. Gama, L.M. Kunkel, and E.P. Hoffman. 1995. Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophin. Ann. Neurol. 38:367-372.
-
(1995)
Ann. Neurol.
, vol.38
, pp. 367-372
-
-
Ljunggren, A.1
Duggan, D.2
McNally, E.3
Boylan, K.B.4
Gama, C.H.5
Kunkel, L.M.6
Hoffman, E.P.7
-
29
-
-
0027176661
-
Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin
-
Matsumura, K., F.M.S. Tomé, V. Ionasescu, J.M. Ervasti, R.D. Anderson, N.B. Romero, D. Simon, D. Récan, J.-C. Kaplan, M. Fardeau, and K.P. Campbell. 1993. Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin. J. Clin. Invest. 92:866-871.
-
(1993)
J. Clin. Invest.
, vol.92
, pp. 866-871
-
-
Matsumura, K.1
Tomé, F.M.S.2
Ionasescu, V.3
Ervasti, J.M.4
Anderson, R.D.5
Romero, N.B.6
Simon, D.7
Récan, D.8
Kaplan, J.-C.9
Fardeau, M.10
Campbell, K.P.11
-
30
-
-
0024499182
-
Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasia
-
McCabe, E.R., J. Towbin, J. Chamberlain, L. Baumbach, J. Witkowski, G.J. van Ommen, M. Koenig, L.M. Kunkel, and W.K. Seltzer. 1989. Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasia. J. Clin. Invest. 83:95-99.
-
(1989)
J. Clin. Invest.
, vol.83
, pp. 95-99
-
-
McCabe, E.R.1
Towbin, J.2
Chamberlain, J.3
Baumbach, L.4
Witkowski, J.5
Van Ommen, G.J.6
Koenig, M.7
Kunkel, L.M.8
Seltzer, W.K.9
-
31
-
-
0024988383
-
In vitro polyadenylation is stimulated by the presence of an upstream intron
-
Niwa, M., S.D. Rose, and S.M. Berget. 1990. In vitro polyadenylation is stimulated by the presence of an upstream intron. Genes Dev. 4:1552-1559.
-
(1990)
Genes Dev.
, vol.4
, pp. 1552-1559
-
-
Niwa, M.1
Rose, S.D.2
Berget, S.M.3
-
32
-
-
0028883973
-
Mutations in the dystrophin-associaled protein gamma-sarcoglycan in chromosome 13 muscular dystrophy
-
Noguchi, S., E.M. McNally, K. Ben Othmane, Y. Hagiwara, Y. Mizuno, M. Yoshida, H. Yamamoto, C.G. Bönnemann, E. Gussoni, P.H. Denton, et al. 1995. Mutations in the dystrophin-associaled protein gamma-sarcoglycan in chromosome 13 muscular dystrophy. Science (Wash. DC). 270: 819-822.
-
(1995)
Science (Wash. DC)
, 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
Bönnemann, C.G.8
Gussoni, E.9
Denton, P.H.10
-
33
-
-
0026328022
-
Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice
-
Ohlendieck, K., and K.P. Campbell. 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
-
34
-
-
0026067790
-
Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma
-
Ohlendieck, K., J.M. Ervasti, J.B. Snook, and K.P. Campbell. 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
Campbell, K.P.4
-
35
-
-
0028077885
-
Troponin T is capable of binding dystrophin via a leucine zipper
-
Pearlman, J.A., P.A. Powaser, S.J. Elledge, and C.T. Caskey. 1994. Troponin T is capable of binding dystrophin via a leucine zipper. FEBS Lett. 354:183-186.
-
(1994)
FEBS Lett.
, vol.354
, pp. 183-186
-
-
Pearlman, J.A.1
Powaser, P.A.2
Elledge, S.J.3
Caskey, C.T.4
-
36
-
-
0027935193
-
β2-syntrophin: Localization at the neuromuscular junction in skeletal muscle
-
Peters, M.F., N.R. Kramarcy, R. Sealock, and S.C. Froehner. 1994. β2-syntrophin: localization at the neuromuscular junction in skeletal muscle. NeuroReport. 5:1577-1580.
-
(1994)
NeuroReport
, vol.5
, pp. 1577-1580
-
-
Peters, M.F.1
Kramarcy, N.R.2
Sealock, R.3
Froehner, S.C.4
-
37
-
-
0029122523
-
Expression of full-length and truncated dystrophin mini-genes in transgenic mdx mice
-
Phelps, S.F., M.A. Hauser, N.M. Cole, J.A. Rafael, R.T. Hinkle, J.A. Faulkner, and J.S. Chamberlain. 1995. Expression of full-length and truncated dystrophin mini-genes in transgenic mdx mice. Hum. Mol. Genet. 4: 1251-1258.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1251-1258
-
-
Phelps, S.F.1
Hauser, M.A.2
Cole, N.M.3
Rafael, J.A.4
Hinkle, R.T.5
Faulkner, J.A.6
Chamberlain, J.S.7
-
38
-
-
0030034593
-
ZZ and TAZ: New putative zinc fingers in dystrophin and other proteins
-
Ponting, C.P., D.J. Blake, K.E. Davies, J. Kendrick-Jones, and S.J. Winder. 1996. ZZ and TAZ: new putative zinc fingers in dystrophin and other proteins. Trends Biochem. Sci. 21:11-13.
-
(1996)
Trends Biochem. Sci.
, vol.21
, pp. 11-13
-
-
Ponting, C.P.1
Blake, D.J.2
Davies, K.E.3
Kendrick-Jones, J.4
Winder, S.J.5
-
39
-
-
0028137134
-
Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform
-
Rafael, J.A., Y. Sunada, N.M. Cole, K.P. Campbell, J.A. Faulkner, and J.S. Chamberlain. 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
-
40
-
-
0027361264
-
Primary structure and muscle-specific expression of the 50-kDa dystrophin-associated glycoprotein (adhalin)
-
Roberds, S.L., R.D. Anderson, O. Ibraghimov-Beskrovnaya, and K.P. Campbell. 1993. Primary structure and muscle-specific expression of the 50-kDa dystrophin-associated glycoprotein (adhalin). J Biol Chem. 268: 23739-23742.
-
(1993)
J Biol Chem
, vol.268
, pp. 23739-23742
-
-
Roberds, S.L.1
Anderson, R.D.2
Ibraghimov-Beskrovnaya, O.3
Campbell, K.P.4
-
41
-
-
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., M. Yoshida, K. Hayashi, Y. Mizuno, Y. Hagiwara, and E. Ozawa. 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
-
42
-
-
0028985719
-
Mammalian α1- and β1-syntrophin bind to the alternative splice-prone region of the dystrophin COOH terminus
-
Suzuki, A., M. Yoshida, and E. Ozawa. 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
-
43
-
-
0029122522
-
Expression of human full-length and minidystrophin in transgenic mdx mice: Implications for gene therapy of Duchenne muscular dystrophy
-
Wells, D.J., K.E. Wells, E.A. Asante, G. Turner, Y. Sunada, K.P. Campbell, F.S. Walsh, and G. Dickson. 1995. Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy. Hum. Mol. Genet. 4:1245-1250.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1245-1250
-
-
Wells, D.J.1
Wells, K.E.2
Asante, E.A.3
Turner, G.4
Sunada, Y.5
Campbell, K.P.6
Walsh, F.S.7
Dickson, G.8
-
44
-
-
0028833771
-
Frameshift deletions of exons 3-7 and revertant fibers in Duchenne muscular dystrophy: Mechanisms of dystrophin production
-
Winnard, A.V., J.R. Mendell, T.W. Prior, J. Florence, and A.H.M. Burghes. 1995. Frameshift deletions of exons 3-7 and revertant fibers in Duchenne muscular dystrophy: mechanisms of dystrophin production. Am. J. Hum. Genet. 56:158-166.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 158-166
-
-
Winnard, A.V.1
Mendell, J.R.2
Prior, T.W.3
Florence, J.4
Burghes, A.H.M.5
-
45
-
-
0028986593
-
Identification of α1-syntrophin binding to syntrophin triplet, dystrophin, and utrophin
-
Yang, B., D. Jung, J.A. Rafael, J. S. Chamberlain, and K.P. Campbell. 1995. Identification of α1-syntrophin binding to syntrophin triplet, dystrophin, and utrophin. J. Biol. Chem. 270:4975-1978.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 4975-11978
-
-
Yang, B.1
Jung, D.2
Rafael, J.A.3
Chamberlain, J.S.4
Campbell, K.P.5
-
46
-
-
0028980250
-
Dystrophin-associated protein AU is a homologue of the Torpedo 87K protein
-
Yoshida, M., H. Yamamoto, S. Noguchi, Y. Mizuno, Y. Hagiwara, and E. Ozawa. 1995. Dystrophin-associated protein AU 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
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