-
1
-
-
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. et al. 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).
-
(1987)
Cell
, vol.50
, pp. 509-517
-
-
Koenig, M.1
-
2
-
-
0023614188
-
Dystrophin: The protein product of Duchenne muscular dystrophy locus
-
Hoffman, E.P., Brown, R.H.J. & Kunkel, L.N. Dystrophin: the protein product of Duchenne muscular dystrophy locus. Cell 51, 919-928 (1987).
-
(1987)
Cell
, vol.51
, pp. 919-928
-
-
Hoffman, E.P.1
Brown, R.H.J.2
Kunkel, L.N.3
-
3
-
-
0024815723
-
Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications
-
Dunnen, J. et al. Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications. Am. J. Hum. Genet. 45, 835-847 (1989).
-
(1989)
Am. J. Hum. Genet.
, vol.45
, pp. 835-847
-
-
Dunnen, J.1
-
4
-
-
0024466501
-
The molecular basis for Duchenne versus Becker muscular dystrophy: Correlation of severity with type of deletion
-
Koenig, M. et al. The molecular basis for Duchenne versus Becker muscular dystrophy: Correlation of severity with type of deletion. Am. J. Hum. Genet. 45, 498-506 (1989).
-
(1989)
Am. J. Hum. Genet.
, vol.45
, pp. 498-506
-
-
Koenig, M.1
-
5
-
-
0028845066
-
Dystrophin-glycoprotein complex: Molecular organization and critical roles in skeletal muscle
-
Sunada, Y. & Campbell, K. Dystrophin-glycoprotein complex: Molecular organization and critical roles in skeletal muscle. Curr. Opin. Neural. 8, 379-384 (1995).
-
(1995)
Curr. Opin. Neural.
, vol.8
, pp. 379-384
-
-
Sunada, Y.1
Campbell, K.2
-
6
-
-
0029089582
-
Dystrophin-associated proteins in muscular dystrophy
-
Ozawa, E. et al. Dystrophin-associated proteins in muscular dystrophy. Hum. Mol. Genet. 4, 1711-1716 (1995).
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1711-1716
-
-
Ozawa, E.1
-
7
-
-
0026672412
-
Recent developments in the biology of dystrophin and related molecules
-
Karpati, G. Recent developments in the biology of dystrophin and related molecules. Curr. Opin. Neurol. Neurosurg. 5, 615-621 (1992).
-
(1992)
Curr. Opin. Neurol. Neurosurg.
, vol.5
, pp. 615-621
-
-
Karpati, G.1
-
8
-
-
0027269957
-
Myoblast transfer in Duchenne muscular dystrophy
-
Karpati, G. et al. Myoblast transfer in Duchenne muscular dystrophy. Ann. Neural. 34, 8-17 (1993).
-
(1993)
Ann. Neural.
, vol.34
, pp. 8-17
-
-
Karpati, G.1
-
9
-
-
0027420682
-
The potential for gene therapy in neuromuscular diseases
-
Karpati, G. & Ascadi, G. The potential for gene therapy in neuromuscular diseases. Muscle Nerve 16, 1141-1153 (1993).
-
(1993)
Muscle Nerve
, vol.16
, pp. 1141-1153
-
-
Karpati, G.1
Ascadi, G.2
-
10
-
-
0029906168
-
Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene
-
Tinsley, J.M. et al. Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene. Nature 384, 349-353 (1996).
-
(1996)
Nature
, vol.384
, pp. 349-353
-
-
Tinsley, J.M.1
-
11
-
-
0029921129
-
Utrophin: A structural and functional comparison to dystrophin
-
Blake, D.J., Tinsley, J.M. & Davies, K.E. Utrophin: A structural and functional comparison to dystrophin. Brain Pathol. 6, 37-47 (1996).
-
(1996)
Brain Pathol.
, vol.6
, pp. 37-47
-
-
Blake, D.J.1
Tinsley, J.M.2
Davies, K.E.3
-
12
-
-
0027461720
-
Localization and quantitation of the chromosome 6-encoded dystrophin-related protein in normal and pathological human muscle
-
Karpati, G. et al. Localization and quantitation of the chromosome 6-encoded dystrophin-related protein in normal and pathological human muscle. J. Neuropathol. Exp. Neural. 52, 119-128 (1993).
-
(1993)
J. Neuropathol. Exp. Neural.
, vol.52
, pp. 119-128
-
-
Karpati, G.1
-
13
-
-
0026621608
-
Association of dystrophin-related protein with dystrophin associated proteins in mdx mouse muscle
-
Matsumara, K., Ervasti, J., Ohlendieck, K., Kahl, S. & Campbell, K. Association of dystrophin-related protein with dystrophin associated proteins in mdx mouse muscle. Nature 60, 588-591 (1992).
-
(1992)
Nature
, vol.60
, pp. 588-591
-
-
Matsumara, K.1
Ervasti, J.2
Ohlendieck, K.3
Kahl, S.4
Campbell, K.5
-
14
-
-
0027358450
-
Reciprocal expression of dystrophin and utrophin in muscles of Duchenne muscular dystrophy patients, female DMD carriers and control subjects
-
Mizumo, Y., Nonaka, I., Hirai, S. & Ozawa, E. 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).
-
(1993)
J. Neurol. Sci.
, vol.119
, pp. 43-52
-
-
Mizumo, Y.1
Nonaka, I.2
Hirai, S.3
Ozawa, E.4
-
15
-
-
0027362435
-
Long-term correction of mouse dystrophic degeneration by adenovirus-mediated transfer of a minidystrophin gene
-
Vincent, N. et al. Long-term correction of mouse dystrophic degeneration by adenovirus-mediated transfer of a minidystrophin gene. Nature Genet. 5, 130-134 (1993).
-
(1993)
Nature Genet.
, vol.5
, pp. 130-134
-
-
Vincent, N.1
-
16
-
-
0029741231
-
Transient immunosuppression by FK506 permits a sustained high-level dystrophin expression after adenovirus-mediated dystrophin minigene transfer to skeletal muscles of adult dystrophic (mdx) mice
-
Lochmüller, H. et al. Transient immunosuppression by FK506 permits a sustained high-level dystrophin expression after adenovirus-mediated dystrophin minigene transfer to skeletal muscles of adult dystrophic (mdx) mice. Gene Ther. 3, 706-716 (1996).
-
(1996)
Gene Ther.
, vol.3
, pp. 706-716
-
-
Lochmüller, H.1
-
17
-
-
0029857641
-
In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes
-
Clemens, P.R. et al. In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes. Gene Ther. 3, 965-972 (1996).
-
(1996)
Gene Ther.
, vol.3
, pp. 965-972
-
-
Clemens, P.R.1
-
18
-
-
0027186053
-
Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity
-
Cox, G.A. et al. Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity. Nature 364, 725-729 (1993).
-
(1993)
Nature
, vol.364
, pp. 725-729
-
-
Cox, G.A.1
|