-
1
-
-
0021358756
-
Duchenne muscular dystrophy: Pathogenic aspects and genetic prevention
-
Moser, H. 1984. Duchenne muscular dystrophy: pathogenic aspects and genetic prevention. Hum. Genet. 66:17-40.
-
(1984)
Hum. Genet.
, vol.66
, pp. 17-40
-
-
Moser, H.1
-
2
-
-
0023904860
-
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein
-
Koenig, M., Monaco, A.P., and Kunkel, L.M. 1988. The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein. Cell. 53:219-228.
-
(1988)
Cell.
, vol.53
, pp. 219-228
-
-
Koenig, M.1
Monaco, A.P.2
Kunkel, L.M.3
-
3
-
-
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. 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
-
4
-
-
0025971262
-
Molecular diagnostics of Duchenne/Becker dystrophy: New additions to a rapidly expanding literature
-
Hoffman, E.P. 1991. Molecular diagnostics of Duchenne/Becker dystrophy: new additions to a rapidly expanding literature. J. Neurol. Sci. 101:129-132.
-
(1991)
J. Neurol. Sci.
, vol.101
, pp. 129-132
-
-
Hoffman, E.P.1
-
5
-
-
0029073192
-
Spectrum of small mutations in the dystrophin coding region
-
Prior, T. W., et al. 1995. Spectrum of small mutations in the dystrophin coding region. Am. J. Hum. Genet. 57:22-33.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 22-33
-
-
Prior, T.W.1
-
6
-
-
0024353559
-
The molecular basis of muscular dystrophy in the mdx mouse: A point mutation
-
Sicinski, P. et al. 1989. The molecular basis of muscular dystrophy in the mdx mouse: a point mutation. Science. 244:1578-1580.
-
(1989)
Science
, vol.244
, pp. 1578-1580
-
-
Sicinski, P.1
-
7
-
-
0023697916
-
Small-caliber skeletal fibers do not suffer necrosis in mdx mouse dystrophy
-
Karpati, G., Carpenter, S., and Prescott, S. 1988. Small-caliber skeletal fibers do not suffer necrosis in mdx mouse dystrophy. Muscle Nerve. 11:795-803.
-
(1988)
Muscle Nerve
, vol.11
, pp. 795-803
-
-
Karpati, G.1
Carpenter, S.2
Prescott, S.3
-
8
-
-
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
-
9
-
-
0026419948
-
The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy
-
Stedman, H.H., et al. 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
-
10
-
-
0018379922
-
Phenotypic suppression of nonsense mutants in yeast by aminoglycoside antibiotics
-
Palmer, E., Wilhelm, J.M., and Sherman, F. 1979. Phenotypic suppression of nonsense mutants in yeast by aminoglycoside antibiotics. Nature. 277:148-150.
-
(1979)
Nature
, vol.277
, pp. 148-150
-
-
Palmer, E.1
Wilhelm, J.M.2
Sherman, F.3
-
11
-
-
0018344962
-
Phenotypic suppression and misreading in Saccharomyces cerevisiae
-
Singh, A., Ursic, D.,and Davies, J. 1979. Phenotypic suppression and misreading in Saccharomyces cerevisiae. Nature. 277:146-148.
-
(1979)
Nature
, vol.277
, pp. 146-148
-
-
Singh, A.1
Ursic, D.2
Davies, J.3
-
12
-
-
0030702773
-
Suppression of a CFTR premature stop mutation in a bronchial epithelial cell line
-
Bedwell, D.M., et al. 1997. Suppression of a CFTR premature stop mutation in a bronchial epithelial cell line. Nat. Med. 3:1280-1284.
-
(1997)
Nat. Med.
, vol.3
, pp. 1280-1284
-
-
Bedwell, D.M.1
-
13
-
-
0029994529
-
Aminoglycoside antibiotics restore CFTR function by overcoming premature stop codons
-
Howard, M., Frizzell, R.A., and Bedwell, D.M. 1996. Aminoglycoside antibiotics restore CFTR function by overcoming premature stop codons. Nat. Med. 2:467-469.
-
(1996)
Nat. Med.
, vol.2
, pp. 467-469
-
-
Howard, M.1
Frizzell, R.A.2
Bedwell, D.M.3
-
14
-
-
0030634743
-
Skeletal muscle cultures
-
H.L. Sweeney and C. Emerson, editors. Academic Press. San Diego, CA.
-
Neville, C., Rosenthal, N., McGrew, M., Bogdanova, N., and Hauschka, S. 1998. Skeletal muscle cultures. In Methods in all biology. Volume 52. H.L. Sweeney and C. Emerson, editors. Academic Press. San Diego, CA. 85-116.
-
(1998)
Methods in All Biology
, vol.52
, pp. 85-116
-
-
Neville, C.1
Rosenthal, N.2
McGrew, M.3
Bogdanova, N.4
Hauschka, S.5
-
15
-
-
0030631017
-
Structure-function analysis of cytoskeletal/contractile proteins in avian myotubes
-
H.L. Sweeney and C. Emerson, editors. Academic Press. San Diego, CA.
-
Sweeney, H.L., and Feng, H. 1998. Structure-function analysis of cytoskeletal/contractile proteins in avian myotubes. In Methods in cell biology. Volume 52. H.L. Sweeney and C. Emerson, editors. Academic Press. San Diego, CA. 275-282.
-
(1998)
Methods in Cell Biology
, vol.52
, pp. 275-282
-
-
Sweeney, H.L.1
Feng, H.2
-
16
-
-
0028906702
-
Antibiotic therapeutics in laboratory animals
-
Morris, T.H. 1995. Antibiotic therapeutics in laboratory animals. Lab. Anim. 29:16-36.
-
(1995)
Lab. Anim.
, vol.29
, pp. 16-36
-
-
Morris, T.H.1
-
17
-
-
0031013486
-
Aminoglycoside nephrotoxicity
-
Swan, S.K. 1997. Aminoglycoside nephrotoxicity. Semin. Nepbrol. 17:27-33.
-
(1997)
Semin. Nepbrol.
, vol.17
, pp. 27-33
-
-
Swan, S.K.1
-
18
-
-
0032416479
-
Viral-mediated expression of insulin-like growth factor I blocks the aging-related loss of skeletal muscle function
-
Barton-Davis, E.R., Shoturma, D.I., Musaro, A., Rosenthal, N., and Sweeney, H.L. 1998. Viral-mediated expression of insulin-like growth factor I blocks the aging-related loss of skeletal muscle function. Proc. Natl. Acad. Sci. USA. 95:15603-15607.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 15603-15607
-
-
Barton-Davis, E.R.1
Shoturma, D.I.2
Musaro, A.3
Rosenthal, N.4
Sweeney, H.L.5
-
19
-
-
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
-
20
-
-
0023614188
-
Dystrophin: The protein product of the Duchenne muscular dystrophy locus
-
Hoffman, E.P., Brown, R.H., Jr., 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., Jr.2
Kunkel, L.M.3
-
21
-
-
10344249872
-
Mutations that disrupt the carboxyl-terminus of γ-sarcoglycan cause muscular dystrophy
-
McNally, E.M., et al. 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
-
22
-
-
0028137134
-
Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform
-
Rafael, J.A., et al. 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
-
23
-
-
0030068133
-
Variable efficacy of radical scavengers and iron chelators to attenuate gentamicin ototoxicity in guinea pig in vivo
-
Song, B., and Schacht, J. 1996. Variable efficacy of radical scavengers and iron chelators to attenuate gentamicin ototoxicity in guinea pig in vivo. Hear. Res. 94:87-93.
-
(1996)
Hear. Res.
, vol.94
, pp. 87-93
-
-
Song, B.1
Schacht, J.2
-
24
-
-
0021888924
-
2,3-dihydroxybenzoic acid
-
Pearce, R.A., Finley, R.J., Mustard, R.A., and Duff, J.H. 1985. 2,3-dihydroxybenzoic acid. Arch. Surg. 120:937-940.
-
(1985)
Arch. Surg.
, vol.120
, pp. 937-940
-
-
Pearce, R.A.1
Finley, R.J.2
Mustard, R.A.3
Duff, J.H.4
-
25
-
-
0029997857
-
Progress towards gene therapy for Duchenne muscular dystrophy
-
Hauser, M.A., and Chamberlain, J.S. 1996. Progress towards gene therapy for Duchenne muscular dystrophy. J. Endocrinol. 149:373-378.
-
(1996)
J. Endocrinol.
, vol.149
, pp. 373-378
-
-
Hauser, M.A.1
Chamberlain, J.S.2
-
26
-
-
0027420682
-
The potential for gene therapy in Duchenne muscular dystrophy and other genetic muscle diseases
-
Karpati, G., and Ascadi, G. 1993. The potential for gene therapy in Duchenne muscular dystrophy and other genetic muscle diseases. Muscle Nerve. 16:1141-1153.
-
(1993)
Muscle Nerve
, vol.16
, pp. 1141-1153
-
-
Karpati, G.1
Ascadi, G.2
-
27
-
-
0030763563
-
Improved adenoviral vectors for gene therapy of Duchenne muscular dystrophy
-
Hauser, M.A., Amalfitano, A., Kumar-Singh, R., Hauschka, S.D., and Chamberlain, J.S. 1997. Improved adenoviral vectors for gene therapy of Duchenne muscular dystrophy. Neuromuscul. Disord. 7:277-283.
-
(1997)
Neuromuscul. Disord.
, vol.7
, pp. 277-283
-
-
Hauser, M.A.1
Amalfitano, A.2
Kumar-Singh, R.3
Hauschka, S.D.4
Chamberlain, J.S.5
-
28
-
-
0029122523
-
Expression of full-length and truncated dystrophin mini-genes in transgeinc mdx mice
-
Phelps, S.F., et al. 1995. Expression of full-length and truncated dystrophin mini-genes in transgeinc mdx mice. Hum. Mol. Genet. 4:1251-1258.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1251-1258
-
-
Phelps, S.F.1
-
29
-
-
0031900882
-
Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: From Southern blot to protein truncation test
-
Tuffery, S. et al. 1998. Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation test. Hum. Genet. 102:334-342.
-
(1998)
Hum. Genet.
, vol.102
, pp. 334-342
-
-
Tuffery, S.1
|