-
1
-
-
0024815139
-
Dystrophin in skeletal muscle. II. Immunoreactivity in patients with Xp21 muscular dystrophy
-
Nicholson L.V., Davison K., Johnson M.A., et al. Dystrophin in skeletal muscle. II. Immunoreactivity in patients with Xp21 muscular dystrophy. J Neurol Sci 1989, 94:137-146.
-
(1989)
J Neurol Sci
, vol.94
, pp. 137-146
-
-
Nicholson, L.V.1
Davison, K.2
Johnson, M.A.3
-
2
-
-
0024844340
-
Localization and characterization of dystrophin in muscle biopsy specimens from Duchenne muscular dystrophy and various neuromuscular disorders
-
Uchino M., Araki S., Miike T., Teramoto H., Nakamura T., Yasutake T. Localization and characterization of dystrophin in muscle biopsy specimens from Duchenne muscular dystrophy and various neuromuscular disorders. Muscle Nerve 1989, 12:1009-1016.
-
(1989)
Muscle Nerve
, vol.12
, pp. 1009-1016
-
-
Uchino, M.1
Araki, S.2
Miike, T.3
Teramoto, H.4
Nakamura, T.5
Yasutake, T.6
-
3
-
-
0023718118
-
An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus
-
Monaco A.P., Bertelson C.J., Liechti-Gallati S., Moser H., Kunkel L.M. An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus. Genomics 1988, 2:90-95.
-
(1988)
Genomics
, vol.2
, pp. 90-95
-
-
Monaco, A.P.1
Bertelson, C.J.2
Liechti-Gallati, S.3
Moser, H.4
Kunkel, L.M.5
-
4
-
-
0024466501
-
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion
-
Koenig M., Beggs A.H., Moyer M., et al. The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. Am J Hum Genet 1989, 45:498-506.
-
(1989)
Am J Hum Genet
, vol.45
, pp. 498-506
-
-
Koenig, M.1
Beggs, A.H.2
Moyer, M.3
-
5
-
-
0037160782
-
The muscular dystrophies
-
Emery A.E. The muscular dystrophies. Lancet 2002, 359:687-695.
-
(2002)
Lancet
, vol.359
, pp. 687-695
-
-
Emery, A.E.1
-
6
-
-
0036227796
-
Muscular dystrophy into the new millennium
-
Emery A.E. Muscular dystrophy into the new millennium. Neuromuscul Disord 2002, 12:343-349.
-
(2002)
Neuromuscul Disord
, vol.12
, pp. 343-349
-
-
Emery, A.E.1
-
7
-
-
0037447517
-
Therapeutic antisense-induced exon skipping in cultured muscle cells from six different DMD patients
-
Aartsma-Rus A., Janson A.A., Kaman W.E., et al. Therapeutic antisense-induced exon skipping in cultured muscle cells from six different DMD patients. Hum Mol Genet 2003, 12:907-914.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 907-914
-
-
Aartsma-Rus, A.1
Janson, A.A.2
Kaman, W.E.3
-
8
-
-
0035878539
-
Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells
-
van Deutekom J.C., Bremmer-Bout M., Janson A.A., et al. Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells. Hum Mol Genet 2001, 10:1547-1554.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1547-1554
-
-
van Deutekom, J.C.1
Bremmer-Bout, M.2
Janson, A.A.3
-
9
-
-
34248511708
-
Antisense oligonucleotide-induced exon skipping across the human dystrophin gene transcript
-
Wilton S.D., Fall A.M., Harding P.L., McClorey G., Coleman C., Fletcher S. Antisense oligonucleotide-induced exon skipping across the human dystrophin gene transcript. Mol Ther 2007, 15:1288-1296.
-
(2007)
Mol Ther
, vol.15
, pp. 1288-1296
-
-
Wilton, S.D.1
Fall, A.M.2
Harding, P.L.3
McClorey, G.4
Coleman, C.5
Fletcher, S.6
-
10
-
-
0029810520
-
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size?
-
Fanin M., Freda M.P., Vitiello L., Danieli G.A., Pegoraro E., Angelini C. Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size?. Muscle Nerve 1996, 19:1154-1160.
-
(1996)
Muscle Nerve
, vol.19
, pp. 1154-1160
-
-
Fanin, M.1
Freda, M.P.2
Vitiello, L.3
Danieli, G.A.4
Pegoraro, E.5
Angelini, C.6
-
11
-
-
84890805770
-
Eteplirsen for the treatment of Duchenne muscular dystrophy
-
Mendell J.R., Rodino-Klapac L.R., Sahenk Z., et al. Eteplirsen for the treatment of Duchenne muscular dystrophy. Ann Neurol 2013, 74:637-647.
-
(2013)
Ann Neurol
, vol.74
, pp. 637-647
-
-
Mendell, J.R.1
Rodino-Klapac, L.R.2
Sahenk, Z.3
-
12
-
-
0027200405
-
Functional significance of dystrophin positive fibres in Duchenne muscular dystrophy
-
Nicholson L.V., Johnson M.A., Bushby K.M., Gardner-Medwin D. Functional significance of dystrophin positive fibres in Duchenne muscular dystrophy. Arch Dis Child 1993, 68:632-636.
-
(1993)
Arch Dis Child
, vol.68
, pp. 632-636
-
-
Nicholson, L.V.1
Johnson, M.A.2
Bushby, K.M.3
Gardner-Medwin, D.4
-
13
-
-
0026641794
-
Dystrophin in frameshift deletion patients with Becker muscular dystrophy
-
Gangopadhyay S.B., Sherratt T.G., Heckmatt J.Z., et al. Dystrophin in frameshift deletion patients with Becker muscular dystrophy. Am J Hum Genet 1992, 51:562-570.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 562-570
-
-
Gangopadhyay, S.B.1
Sherratt, T.G.2
Heckmatt, J.Z.3
-
14
-
-
0024447280
-
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy
-
Hodgson S., Hart K., Abbs S., et al. Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy. J Med Genet 1989, 26:682-693.
-
(1989)
J Med Genet
, vol.26
, pp. 682-693
-
-
Hodgson, S.1
Hart, K.2
Abbs, S.3
-
15
-
-
0026018070
-
Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients
-
Chelly J., Gilgenkrantz H., Hugnot J.P., et al. Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients. J Clin Invest 1991, 88:1161-1166.
-
(1991)
J Clin Invest
, vol.88
, pp. 1161-1166
-
-
Chelly, J.1
Gilgenkrantz, H.2
Hugnot, J.P.3
-
16
-
-
0025647598
-
Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies
-
Chelly J., Gilgenkrantz H., Lambert M., et al. Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies. Cell 1990, 63:1239-1248.
-
(1990)
Cell
, vol.63
, pp. 1239-1248
-
-
Chelly, J.1
Gilgenkrantz, H.2
Lambert, M.3
-
17
-
-
78650885049
-
Physiological characterization of muscle strength with variable levels of dystrophin restoration in mdx mice following local antisense therapy
-
Sharp P.S., Bye A.J.H., Wells D.J. Physiological characterization of muscle strength with variable levels of dystrophin restoration in mdx mice following local antisense therapy. Mol Ther 2011, 19:165-171.
-
(2011)
Mol Ther
, vol.19
, pp. 165-171
-
-
Sharp, P.S.1
Bye, A.J.H.2
Wells, D.J.3
-
18
-
-
0029122522
-
Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy
-
Wells D.J., Wells K.E., Asante E.A., et al. Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy. Hum Mol Genet 1995, 4:1245-1250.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1245-1250
-
-
Wells, D.J.1
Wells, K.E.2
Asante, E.A.3
-
19
-
-
84874199731
-
Melanocytes - a novel tool to study mitochondrial dysfunction in Duchenne muscular dystrophy
-
Pellegrini C., Zulian A., Gualandi F., et al. Melanocytes - a novel tool to study mitochondrial dysfunction in Duchenne muscular dystrophy. J Cell Physiol 2013, 228:1323-1331.
-
(2013)
J Cell Physiol
, vol.228
, pp. 1323-1331
-
-
Pellegrini, C.1
Zulian, A.2
Gualandi, F.3
-
20
-
-
84858160046
-
Quantification of dystrophin immunofluorescence in dystrophinopathy muscle specimens
-
Taylor L.E., Kaminoh Y.J., Rodesch C.K., Flanigan K.M. Quantification of dystrophin immunofluorescence in dystrophinopathy muscle specimens. Neuropathol Appl Neurobiol 2012, 38:591-601.
-
(2012)
Neuropathol Appl Neurobiol
, vol.38
, pp. 591-601
-
-
Taylor, L.E.1
Kaminoh, Y.J.2
Rodesch, C.K.3
Flanigan, K.M.4
-
21
-
-
77952372081
-
Immunohistological intensity measurements as a tool to assess sarcolemma-associated protein expression
-
Arechavala-Gomeza V., Kinali M., Feng L., et al. Immunohistological intensity measurements as a tool to assess sarcolemma-associated protein expression. Neuropathol Appl Neurobiol 2010, 36:265-274.
-
(2010)
Neuropathol Appl Neurobiol
, vol.36
, pp. 265-274
-
-
Arechavala-Gomeza, V.1
Kinali, M.2
Feng, L.3
-
22
-
-
83755220617
-
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials
-
Anthony K., Cirak S., Torelli S., et al. Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials. Brain 2011, 134:3547-3559.
-
(2011)
Brain
, vol.134
, pp. 3547-3559
-
-
Anthony, K.1
Cirak, S.2
Torelli, S.3
-
23
-
-
84873895776
-
Distinctive serum miRNA profile in mouse models of striated muscular pathologies
-
Vignier N., Amor F., Fogel P., et al. Distinctive serum miRNA profile in mouse models of striated muscular pathologies. PLoS One 2013, 8:e55281.
-
(2013)
PLoS One
, vol.8
-
-
Vignier, N.1
Amor, F.2
Fogel, P.3
-
24
-
-
79953319448
-
Identification of muscle-specific microRNAs in serum of muscular dystrophy animal models: promising novel blood-based markers for muscular dystrophy
-
Mizuno H., Nakamura A., Aoki Y., et al. Identification of muscle-specific microRNAs in serum of muscular dystrophy animal models: promising novel blood-based markers for muscular dystrophy. PLoS One 2011, 6:e18388.
-
(2011)
PLoS One
, vol.6
-
-
Mizuno, H.1
Nakamura, A.2
Aoki, Y.3
-
25
-
-
79955622637
-
MiRNAs as serum biomarkers for Duchenne muscular dystrophy
-
Cacchiarelli D., Legnini I., Martone J., et al. MiRNAs as serum biomarkers for Duchenne muscular dystrophy. EMBO Mol Med 2011, 3:258-265.
-
(2011)
EMBO Mol Med
, vol.3
, pp. 258-265
-
-
Cacchiarelli, D.1
Legnini, I.2
Martone, J.3
-
26
-
-
84894279286
-
Dystromirs as serum biomarkers for monitoring the disease severity in Duchenne muscular dystrophy
-
Zaharieva I.T., Calissano M., Scoto M., et al. Dystromirs as serum biomarkers for monitoring the disease severity in Duchenne muscular dystrophy. PLoS One 2013, 8:e80263.
-
(2013)
PLoS One
, vol.8
-
-
Zaharieva, I.T.1
Calissano, M.2
Scoto, M.3
-
27
-
-
84934439956
-
Highly multiplexed proteomic platform for biomarker discovery, diagnostics, and therapeutics
-
Mehan M.R., Ostroff R., Wilcox S.K., et al. Highly multiplexed proteomic platform for biomarker discovery, diagnostics, and therapeutics. Adv Exp Med Biol 2013, 735:283-300.
-
(2013)
Adv Exp Med Biol
, vol.735
, pp. 283-300
-
-
Mehan, M.R.1
Ostroff, R.2
Wilcox, S.K.3
-
28
-
-
84880143528
-
Recent advances in capillary electrophoresis-based proteomic techniques for biomarker discovery
-
Wang C., Fang X., Lee C.S. Recent advances in capillary electrophoresis-based proteomic techniques for biomarker discovery. Methods Mol Biol 2013, 984:1-12.
-
(2013)
Methods Mol Biol
, vol.984
, pp. 1-12
-
-
Wang, C.1
Fang, X.2
Lee, C.S.3
-
29
-
-
84871556673
-
Challenges in biomarker discovery: combining expert insights with statistical analysis of complex Omics data
-
McDermott J.E., Wang J., Mitchell H., et al. Challenges in biomarker discovery: combining expert insights with statistical analysis of complex Omics data. Exp Opin Med Diagn 2013, 7:37-51.
-
(2013)
Exp Opin Med Diagn
, vol.7
, pp. 37-51
-
-
McDermott, J.E.1
Wang, J.2
Mitchell, H.3
-
30
-
-
84877944128
-
Metabolomics analysis for biomarker discovery: advances and challenges
-
Monteiro M.S., Carvalho M., Bastos M.L., Guedes de Pinho P. Metabolomics analysis for biomarker discovery: advances and challenges. Curr Med Chem 2013, 20:257-271.
-
(2013)
Curr Med Chem
, vol.20
, pp. 257-271
-
-
Monteiro, M.S.1
Carvalho, M.2
Bastos, M.L.3
Guedes de Pinho, P.4
-
31
-
-
84868217697
-
Systems biology approach for new target and biomarker identification
-
Wang I.M., Stone D.J., Nickle D., Loboda A., Puig O., Roberts C. Systems biology approach for new target and biomarker identification. Curr Top Microbiol Immunol 2013, 363:169-199.
-
(2013)
Curr Top Microbiol Immunol
, vol.363
, pp. 169-199
-
-
Wang, I.M.1
Stone, D.J.2
Nickle, D.3
Loboda, A.4
Puig, O.5
Roberts, C.6
-
33
-
-
79960898220
-
Serum matrix metalloproteinase-9 (MMP-9) as a biomarker for monitoring disease progression in Duchenne muscular dystrophy (DMD)
-
Nadarajah V.D., van Putten M., Chaouch A., et al. Serum matrix metalloproteinase-9 (MMP-9) as a biomarker for monitoring disease progression in Duchenne muscular dystrophy (DMD). Neuromuscul Disord 2011, 21:569-578.
-
(2011)
Neuromuscul Disord
, vol.21
, pp. 569-578
-
-
Nadarajah, V.D.1
van Putten, M.2
Chaouch, A.3
-
34
-
-
84866175449
-
Metabolic profile of dystrophic mdx mouse muscles analyzed with in vitro magnetic resonance spectroscopy (MRS)
-
Martins-Bach A.B., Bloise A.C., Vainzof M., Rahnamaye Rabbani S. Metabolic profile of dystrophic mdx mouse muscles analyzed with in vitro magnetic resonance spectroscopy (MRS). Magn Reson Imaging 2012, 30:1167-1176.
-
(2012)
Magn Reson Imaging
, vol.30
, pp. 1167-1176
-
-
Martins-Bach, A.B.1
Bloise, A.C.2
Vainzof, M.3
Rahnamaye Rabbani, S.4
-
35
-
-
62149084519
-
Muscle metabolism in Duchenne muscular dystrophy assessed by in vivo proton magnetic resonance spectroscopy
-
Hsieh T.J., Jaw T.S., Chuang H.Y., Jong Y.J., Liu G.C., Li C.W. Muscle metabolism in Duchenne muscular dystrophy assessed by in vivo proton magnetic resonance spectroscopy. J Comput Assist Tomogr 2009, 33:150-154.
-
(2009)
J Comput Assist Tomogr
, vol.33
, pp. 150-154
-
-
Hsieh, T.J.1
Jaw, T.S.2
Chuang, H.Y.3
Jong, Y.J.4
Liu, G.C.5
Li, C.W.6
-
36
-
-
84868383391
-
Targeted exon skipping to address "leaky" mutations in the dystrophin gene
-
Fletcher S., Adkin C.F., Meloni P., et al. Targeted exon skipping to address "leaky" mutations in the dystrophin gene. Mol Ther Nucleic Acids 2012, 1:e48.
-
(2012)
Mol Ther Nucleic Acids
, vol.1
-
-
Fletcher, S.1
Adkin, C.F.2
Meloni, P.3
|