-
1
-
-
0031800293
-
Modification of splicing in the dystrophin gene in cultured Mdx muscle cells by antisense oligoribonucleotides
-
Dunckley MG, Manoharan M, Villiet P, Eperon IC, Dickson G: Modification of splicing in the dystrophin gene in cultured Mdx muscle cells by antisense oligoribonucleotides. Hum. Mol. Genet. 7, 1083-1090 (1998).
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1083-1090
-
-
Dunckley, M.G.1
Manoharan, M.2
Villiet, P.3
Eperon, I.C.4
Dickson, G.5
-
2
-
-
0028819352
-
Modulation of in vitro splicing of the upstream intron by modifying an intra-exon sequence which is deleted from the dystrophin gene in clystrophin Kobe
-
Takeshima Y, Nishio, H, Sakamoto H, Nakamura H, Matsuo M: Modulation of in vitro splicing of the upstream intron by modifying an intra-exon sequence which is deleted from the dystrophin gene in clystrophin Kobe. J. Clin. Invest. 95, 515-520 (1995).
-
(1995)
J. Clin. Invest.
, vol.95
, pp. 515-520
-
-
Takeshima, Y.1
Nishio, H.2
Sakamoto, H.3
Nakamura, H.4
Matsuo, M.5
-
3
-
-
0035878539
-
Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells
-
van Deutekorn JC, Bremmer-Bout M, Janson AA et al.: Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells. Hum. Mol. Genet. 10, 1547-1554 (2001).
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1547-1554
-
-
van Deutekorn, J.C.1
Bremmer-Bout, M.2
Janson, A.A.3
-
4
-
-
0036823504
-
Targeted exon skipping as a potential gene correction therapy for Duchenne muscular dystrophy
-
Aartsma-Rus A, Bremmer-Bout M, Janson AA et al.: Targeted exon skipping as a potential gene correction therapy for Duchenne muscular dystrophy. Neuromuscul. Disord. 12 (Suppl. 1), S71-S77 (2002).
-
(2002)
Neuromuscul. Disord.
, vol.12
, Issue.SUPPL. 1
-
-
Aartsma-Rus, A.1
Bremmer-Bout, M.2
Janson, A.A.3
-
5
-
-
0037447517
-
Therapeutic antisense-induced exon skipping in cultured muscle cells from six different DMD patients
-
Aartsma-Rus A, Janson AA, Kaman WE et al.: Therapeutic antisense-induced exon skipping in cultured muscle cells from six different DMD patients. Hum. Mol. Genet. 12, 907-914 (2003).
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 907-914
-
-
Aartsma-Rus, A.1
Janson, A.A.2
Kaman, W.E.3
-
6
-
-
0347003516
-
Antisense-induced multiexon skipping for Duchenne muscular dystrophy makes more sense
-
Aartsma-Rus A, Janson AA, Kaman WE et al.: Antisense-induced multiexon skipping for Duchenne muscular dystrophy makes more sense. Am. J. Hum. Genet. 74, 83-92 (2004).
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 83-92
-
-
Aartsma-Rus, A.1
Janson, A.A.2
Kaman, W.E.3
-
7
-
-
0035793047
-
Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouse
-
Mann CJ, Honeyman K, Cheng AJ et al.: Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouse. Proc. Natl Acad. Sci. USA 98, 42-47 (2001).
-
(2001)
Proc. Natl Acad. Sci. USA
, vol.98
, pp. 42-47
-
-
Mann, C.J.1
Honeyman, K.2
Cheng, A.J.3
-
8
-
-
0042536463
-
Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse
-
Lu QL, Mann CJ, Lou F et al.: Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse. Nature Med. 9, 1009-1014 (2003).
-
(2003)
Nature Med.
, vol.9
, pp. 1009-1014
-
-
Lu, Q.L.1
Mann, C.J.2
Lou, F.3
-
9
-
-
11844256373
-
Systemic delivery of antisense oligoribonucleotide restores dystrophin expression in bodywide skeletal muscles
-
Lu QL, Rabinowitz A, Chen YC et al: Systemic delivery of antisense oligoribonucleotide restores dystrophin expression in bodywide skeletal muscles. Proc. Natl Acad. Sci. USA 102, 198-203 (2005).
-
(2005)
Proc. Natl Acad. Sci. USA
, vol.102
, pp. 198-203
-
-
Lu, Q.L.1
Rabinowitz, A.2
Chen, Y.C.3
-
10
-
-
32844460899
-
Dystrophin expression in the mdx mouse after localised and systemic administration of a morpholino antisense oligonucleotide
-
Fletcher S, Honeyman K, Fall AM et al.: Dystrophin expression in the mdx mouse after localised and systemic administration of a morpholino antisense oligonucleotide. J. Gene Med. 8, 207-216 (2006).
-
(2006)
J. Gene Med.
, vol.8
, pp. 207-216
-
-
Fletcher, S.1
Honeyman, K.2
Fall, A.M.3
-
11
-
-
0141760549
-
Enhanced in vivo delivery of antisense oligonucleotides to restore dystrophin expression in adult mdx mouse muscle
-
Wells KE, Fletcher S, Mann CJ, Wilton SD, Wells DJ: Enhanced in vivo delivery of antisense oligonucleotides to restore dystrophin expression in adult mdx mouse muscle. FEBS Lett. 552, 145-149 (2003).
-
(2003)
FEBS Lett.
, vol.552
, pp. 145-149
-
-
Wells, K.E.1
Fletcher, S.2
Mann, C.J.3
Wilton, S.D.4
Wells, D.J.5
-
12
-
-
25644449483
-
Intraperitoneal administration of phosphorothioate antisense oligodeoxynucleotide against splicing enhancer sequence induced exon skipping in dystrophin mRNA expressed in mdx skeletal muscle
-
Takeshima Y, Yagi M, Wada H, Matsuo M: Intraperitoneal administration of phosphorothioate antisense oligodeoxynucleotide against splicing enhancer sequence induced exon skipping in dystrophin mRNA expressed in mdx skeletal muscle. Brain Dev. 27, 488-493 (2005).
-
(2005)
Brain Dev.
, vol.27
, pp. 488-493
-
-
Takeshima, Y.1
Yagi, M.2
Wada, H.3
Matsuo, M.4
-
13
-
-
10044240371
-
Rescue of dystrophic muscle through U7 snRNA-mediated exon skipping
-
Goyenvalle A, Vulin A, Fougerousse F et al.: Rescue of dystrophic muscle through U7 snRNA-mediated exon skipping. Science 306, 1796-1799 (2004).
-
(2004)
Science
, vol.306
, pp. 1796-1799
-
-
Goyenvalle, A.1
Vulin, A.2
Fougerousse, F.3
-
14
-
-
21244476011
-
AAV-mediated gene transfer for treatment of hemophilia
-
Wang L, Herzog RW: AAV-mediated gene transfer for treatment of hemophilia. Curr. Gene Ther. 5, 349-360 (2005).
-
(2005)
Curr. Gene Ther.
, vol.5
, pp. 349-360
-
-
Wang, L.1
Herzog, R.W.2
-
15
-
-
19344369694
-
128th ENMC International Workshop on 'Preclinical optimization and Phase I/II Clinical Trials Using Antisense Oligonucleotides in Duchenne Muscular Dystrophy' 22-24 October 2004, Naarden, The Netherlands
-
Muntoni F, Bushby K, van Ommen G: 128th ENMC International Workshop on 'Preclinical optimization and Phase I/II Clinical Trials Using Antisense Oligonucleotides in Duchenne Muscular Dystrophy' 22-24 October 2004, Naarden, The Netherlands. Neuromuscul. Discord. 15, 450-457 (2005).
-
(2005)
Neuromuscul. Discord.
, vol.15
, pp. 450-457
-
-
Muntoni, F.1
Bushby, K.2
van Ommen, G.3
-
16
-
-
0036303535
-
Phase I trial of BCL-2 antisense oligonucleotide (G3139) administered by continuous intravenous infusion in patients with advanced cancer
-
Morris MJ, Tong WP, Cordon-Cardo C et al.: Phase I trial of BCL-2 antisense oligonucleotide (G3139) administered by continuous intravenous infusion in patients with advanced cancer. Clin. Cancer Res. 8, 679-683 (2002).
-
(2002)
Clin. Cancer Res.
, vol.8
, pp. 679-683
-
-
Morris, M.J.1
Tong, W.P.2
Cordon-Cardo, C.3
-
17
-
-
0034015672
-
Phase I clinical and pharmacokinetic study of bcl-2 antisense oligonucleotide therapy in patients with non-Hodgkin's lymphoma
-
Waters JS, Webb A, Cunningham D et al.: Phase I clinical and pharmacokinetic study of bcl-2 antisense oligonucleotide therapy in patients with non-Hodgkin's lymphoma. J. Clin. Oncol. 18, 1812-1823 (2000).
-
(2000)
J. Clin. Oncol.
, vol.18
, pp. 1812-1823
-
-
Waters, J.S.1
Webb, A.2
Cunningham, D.3
-
18
-
-
2342655229
-
Broadly altered gene expression in blood leukocytes in essential hypertension is absent during treatment
-
Chon H, Gaillard CA, van der Meijden BB et al.: Broadly altered gene expression in blood leukocytes in essential hypertension is absent during treatment. Hypertension 43, 947-951 (2004).
-
(2004)
Hypertension
, vol.43
, pp. 947-951
-
-
Chon, H.1
Gaillard, C.A.2
van der Meijden, B.B.3
-
19
-
-
23444456921
-
Gene expression profile in the muscles of patients with inflammatory myopathies: Effect of therapy with IVIg and biological validation of clinically relevant genes
-
Raju R, Dalakas MC: Gene expression profile in the muscles of patients with inflammatory myopathies: effect of therapy with IVIg and biological validation of clinically relevant genes. Brain 128, 1887-1896 (2005).
-
(2005)
Brain
, vol.128
, pp. 1887-1896
-
-
Raju, R.1
Dalakas, M.C.2
-
20
-
-
25444520238
-
Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiting
-
Turk R, Sterrenburg E, de Meijer EJ et al.: Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiting. BMC Genomics 6, 98 (2005).
-
(2005)
BMC Genomics
, vol.6
, pp. 98
-
-
Turk, R.1
Sterrenburg, E.2
de Meijer, E.J.3
-
21
-
-
0013181060
-
Improved antisense oligonucleotide induced exon skipping in the mdx mouse model of muscular dystrophy
-
Mann CJ, Honeyman K, McClorey G, Fletcher S, Wilton SD: Improved antisense oligonucleotide induced exon skipping in the mdx mouse model of muscular dystrophy. J. Gene Med 4, 644-654 (2002).
-
(2002)
J. Gene Med
, vol.4
, pp. 644-654
-
-
Mann, C.J.1
Honeyman, K.2
McClorey, G.3
Fletcher, S.4
Wilton, S.D.5
-
22
-
-
29244458622
-
Noninvasive monitoring of therapeutic gene transfer in animal models of muscular dystrophies
-
Bartoli M, Poupiot J, Goyenvalle A et al: Noninvasive monitoring of therapeutic gene transfer in animal models of muscular dystrophies. Gene Ther. 13, 20-28 (2006).
-
(2006)
Gene Ther.
, vol.13
, pp. 20-28
-
-
Bartoli, M.1
Poupiot, J.2
Goyenvalle, A.3
-
23
-
-
4344693568
-
Targeted exon skipping in transgenic hDMD mice: A model for direct preclinical screening of human-specific antisense oitgonucleotides
-
Bremmer-Bout M, Aartsma-Rus A, de Meijer EJ et al: Targeted exon skipping in transgenic hDMD mice: a model for direct preclinical screening of human-specific antisense oitgonucleotides. Mol. Ther. 10, 232-240 (2004).
-
(2004)
Mol. Ther.
, vol.10
, pp. 232-240
-
-
Bremmer-Bout, M.1
Aartsma-Rus, A.2
de Meijer, E.J.3
-
25
-
-
2942550697
-
GOTree Machine (GOTM: A web-based platform for interpreting sets of interesting genes using Gene Ontology hierarchies
-
Zhang B, Schmoyer D, Kirov S, Snoddy J: GOTree Machine (GOTM: a web-based platform for interpreting sets of interesting genes using Gene Ontology hierarchies. BMC Bioinformatics 5, l6 (2004).
-
(2004)
BMC Bioinformatics
, vol.5
-
-
Zhang, B.1
Schmoyer, D.2
Kirov, S.3
Snoddy, J.4
-
26
-
-
30744443289
-
Common pathological mechanisms in mouse models for muscular dystrophies
-
Turk R, Sterrenburg E, van der Wees CG et al.: Common pathological mechanisms in mouse models for muscular dystrophies. FASEB J. 20, 127-129 (2006).
-
(2006)
FASEB J.
, vol.20
, pp. 127-129
-
-
Turk, R.1
Sterrenburg, E.2
van der Wees, C.G.3
-
27
-
-
27644532724
-
Decorin and biglycan expression is differentially altered in several muscular dystrophies
-
Zanotti S, Negri T, Cappelletti C et al.: Decorin and biglycan expression is differentially altered in several muscular dystrophies. Brain 128, 2546-2555 (2005).
-
(2005)
Brain
, vol.128
, pp. 2546-2555
-
-
Zanotti, S.1
Negri, T.2
Cappelletti, C.3
-
28
-
-
0035861219
-
MUSEAP, a novel reporter gene for the study of long-term gene expression in immunocompetent mice
-
Wang M, Orsini C, Casanova D et al.: MUSEAP, a novel reporter gene for the study of long-term gene expression in immunocompetent mice. Gene 279,99-108 (2001).
-
(2001)
Gene
, vol.279
, pp. 99-108
-
-
Wang, M.1
Orsini, C.2
Casanova, D.3
-
29
-
-
0036823748
-
A web-accessible complete transcriptome of normal human and DMD muscle
-
Bakay M, Zhao P, Chen J, Hoffman EP: A web-accessible complete transcriptome of normal human and DMD muscle. Neuromuscul. Disord. 12(Suppl. 1), S125-Sl4l (2002).
-
(2002)
Neuromuscul. Disord.
, vol.12
, Issue.SUPPL. 1
-
-
Bakay, M.1
Zhao, P.2
Chen, J.3
Hoffman, E.P.4
-
30
-
-
0037069368
-
Gene expression comparison of biopsies from Duchenne muscular dystrophy (DMD) and normal skeletal muscle
-
Haslett JN, Sanoudou D, Kho AT et al.: Gene expression comparison of biopsies from Duchenne muscular dystrophy (DMD) and normal skeletal muscle. Proc. Natl Acad. Sci. USA 99, 15000-15005 (2002).
-
(2002)
Proc. Natl Acad. Sci. USA
, vol.99
, pp. 15000-15005
-
-
Haslett, J.N.1
Sanoudou, D.2
Kho, A.T.3
-
31
-
-
0036471858
-
A chronic inflammatory response dominates the skeletal muscle molecular signature In dystrophin-deficient mdx mice
-
Porter JD, Khanna S, Kaminski HJ et al.: A chronic inflammatory response dominates the skeletal muscle molecular signature In dystrophin-deficient mdx mice. Hum. Mol. Genet. 11, 263-272 (2002).
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 263-272
-
-
Porter, J.D.1
Khanna, S.2
Kaminski, H.J.3
-
32
-
-
0035016040
-
The expression of intermediate filament protein nestin as related to vimentin and desmin in regenerating skeletal muscle
-
Vaittinen S, Lukka R, Sahlgren C et al.: The expression of intermediate filament protein nestin as related to vimentin and desmin in regenerating skeletal muscle. J. Neuropathol. Exp. Neurol. 60, 588-597 (2001).
-
(2001)
J. Neuropathol. Exp. Neurol.
, vol.60
, pp. 588-597
-
-
Vaittinen, S.1
Lukka, R.2
Sahlgren, C.3
-
33
-
-
0028568024
-
The expression of vimentin in satellite cells of regenerating skeletal muscle in vivo
-
Vater R, Cullen MJ, Harris JB: The expression of vimentin in satellite cells of regenerating skeletal muscle in vivo. Histocbem. J. 26, 916-928 (1994).
-
(1994)
Histocbem. J.
, vol.26
, pp. 916-928
-
-
Vater, R.1
Cullen, M.J.2
Harris, J.B.3
-
34
-
-
2642576049
-
Toxicogenomics of subchronic hexachlorobenzene exposure in Brown Norway rats
-
Ezendam J, Staedtler F, Pennings J et al.: Toxicogenomics of subchronic hexachlorobenzene exposure in Brown Norway rats. Environ. Health Perspect. 112, 782-791 (2004).
-
(2004)
Environ. Health Perspect.
, vol.112
, pp. 782-791
-
-
Ezendam, J.1
Staedtler, F.2
Pennings, J.3
-
35
-
-
11144355440
-
Applications of microarrays with toxicologically relevant genes (tox genes) for the evaluation of chemical toxicants in Sprague Dawley rats in vivo and human hepatocytes in vitro
-
Kier LD, Neft R, Tang L et al.: Applications of microarrays with toxicologically relevant genes (tox genes) for the evaluation of chemical toxicants in Sprague Dawley rats in vivo and human hepatocytes in vitro. Mutat. Res. 549, 101-113 (2004).
-
(2004)
Mutat. Res.
, vol.549
, pp. 101-113
-
-
Kier, L.D.1
Neft, R.2
Tang, L.3
-
36
-
-
17944383948
-
Identifying toxic mechanisms using DNA microarrays: Evidence that an experimental inhibitor of cell adhesion molecule expression signals through the aryl hydrocarbon nuclear receptor
-
Waring JF, Gum R, Morfitt D et al.: Identifying toxic mechanisms using DNA microarrays: evidence that an experimental inhibitor of cell adhesion molecule expression signals through the aryl hydrocarbon nuclear receptor. Toxicology 181-182, 537-550 (2002).
-
(2002)
Toxicology
, vol.181-182
, pp. 537-550
-
-
Waring, J.F.1
Gum, R.2
Morfitt, D.3
|