-
1
-
-
0002273549
-
-
Karpati, G., Hilton-Jones, D. and Griggs, R.C. (eds), Cambridge University Press, Cambridge
-
Hoffman, E.P. (2001) In Karpati, G., Hilton-Jones, D. and Griggs, R.C. (eds), Disorders of Voluntary Muscle. Cambridge University Press, Cambridge, pp. 385-432.
-
(2001)
Disorders of Voluntary Muscle
, pp. 385-432
-
-
Hoffman, E.P.1
-
2
-
-
0036087342
-
Function and genetics of dystrophin and dystrophin-related proteins in muscle
-
Blake, D.J., Weir, A., Newey, S.E. and Davies, K.E. (2002) Function and genetics of dystrophin and dystrophin-related proteins in muscle. Physiol. Rev., 82, 291-329.
-
(2002)
Physiol. Rev.
, vol.82
, pp. 291-329
-
-
Blake, D.J.1
Weir, A.2
Newey, S.E.3
Davies, K.E.4
-
3
-
-
0033122032
-
Adeno-associated virus-mediated gene delivery
-
Snyder, R.O. (1999) Adeno-associated virus-mediated gene delivery. J. Gene Med., 1, 166-175.
-
(1999)
J. Gene Med.
, vol.1
, pp. 166-175
-
-
Snyder, R.O.1
-
4
-
-
0034610364
-
Adeno-associated virus vector carrying human minidystrophin genes effectively ameliorates muscular dystrophy in mdx mouse model
-
Wang, B., Li, J. and Xiao, X. (2000) Adeno-associated virus vector carrying human minidystrophin genes effectively ameliorates muscular dystrophy in mdx mouse model. Proc. Natl Acad. Sci. USA, 97, 13714-13719.
-
(2000)
Proc. Natl Acad. Sci. USA
, vol.97
, pp. 13714-13719
-
-
Wang, B.1
Li, J.2
Xiao, X.3
-
5
-
-
0036385643
-
Adeno-associated virus vector-mediated minidystrophin gene therapy improves dystrophic muscle contractile function in mdx mice
-
Watchko, J., O'Day, T., Wang, B., Zhou, L., Tang, Y., Li, J. and Xiao, X. (2002) Adeno-associated virus vector-mediated minidystrophin gene therapy improves dystrophic muscle contractile function in mdx mice. Hum. Gene Ther., 13, 1451-1460.
-
(2002)
Hum. Gene Ther.
, vol.13
, pp. 1451-1460
-
-
Watchko, J.1
O'Day, T.2
Wang, B.3
Zhou, L.4
Tang, Y.5
Li, J.6
Xiao, X.7
-
6
-
-
0036537529
-
Adeno-associated virus vector gene transfer and sarcolemmal expression of a 144 kDa micro-dystrophin effectively restores the dystrophin- associated protein complex and inhibits myofibre degeneration in nude/mdx mice
-
Fabb, S.A., Wells, D.J., Serpente, P. and Dickson, G. (2002) Adeno-associated virus vector gene transfer and sarcolemmal expression of a 144 kDa micro-dystrophin effectively restores the dystrophin- associated protein complex and inhibits myofibre degeneration in nude/mdx mice. Hum. Mol. Genet., 11, 733-741.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 733-741
-
-
Fabb, S.A.1
Wells, D.J.2
Serpente, P.3
Dickson, G.4
-
7
-
-
0036127393
-
Modular flexibility of dystrophin: Implications for gene therapy of Duchenne muscular dystrophy
-
Harper, S.Q., Hauser, M.A., DelloRusso, C., Duan, D., Crawford, R.W., Phelps, S.F., Harper, H.A., Robinson, A.S., Engelhardt, J.F.,, Brooks, S.V. and Chamberlain, J.S. (2002) Modular flexibility of dystrophin: implications for gene therapy of Duchenne muscular dystrophy. Nat. Med., 8, 253-261.
-
(2002)
Nat. Med.
, vol.8
, pp. 253-261
-
-
Harper, S.Q.1
Hauser, M.A.2
DelloRusso, C.3
Duan, D.4
Crawford, R.W.5
Phelps, S.F.6
Harper, H.A.7
Robinson, A.S.8
Engelhardt, J.F.9
Brooks, S.V.10
Chamberlain, J.S.11
-
8
-
-
0027362435
-
Long-term correction of mouse dystrophic degeneration by adenovirus- mediated transfer of a minidystrophin gene
-
Vincent, N., Ragot, T., Gilgenkrantz, H., Couton, D., Chafey, P., Gregoire, A., Briand, P., Kaplan, J.C., Kahn, A. and Perricaudet, M. (1993) Long-term correction of mouse dystrophic degeneration by adenovirus- mediated transfer of a minidystrophin gene. Nat. Genet., 5, 130-134.
-
(1993)
Nat. Genet.
, vol.5
, pp. 130-134
-
-
Vincent, N.1
Ragot, T.2
Gilgenkrantz, H.3
Couton, D.4
Chafey, P.5
Gregoire, A.6
Briand, P.7
Kaplan, J.C.8
Kahn, A.9
Perricaudet, M.10
-
9
-
-
0029918603
-
Functional protection of dystrophic mouse (mdx) muscles after adenovirus-mediated transfer of a dystrophin minigene
-
Deconinck, N., Ragot, T, Marechal, G., Perricaudet, M. and Gillis, J.M. (1996) Functional protection of dystrophic mouse (mdx) muscles after adenovirus-mediated transfer of a dystrophin minigene. Proc. Natl Acad. Sci. USA, 93, 3570-3574.
-
(1996)
Proc. Natl Acad. Sci. USA
, vol.93
, pp. 3570-3574
-
-
Deconinck, N.1
Ragot, T.2
Marechal, G.3
Perricaudet, M.4
Gillis, J.M.5
-
10
-
-
0030066219
-
Dystrophin expression in muscles of mdx mice after adenovirus-mediated in vivo gene transfer
-
Acsadi, G., Lochmuller, H., Jani, A., Huard, J., Massie, B., Prescott, S., Simoneau, M., Petrof, B.J. and Karpati, G. (1996) Dystrophin expression in muscles of mdx mice after adenovirus-mediated in vivo gene transfer. Hum. Gene Ther., 7, 129-140.
-
(1996)
Hum. Gene Ther.
, vol.7
, pp. 129-140
-
-
Acsadi, G.1
Lochmuller, H.2
Jani, A.3
Huard, J.4
Massie, B.5
Prescott, S.6
Simoneau, M.7
Petrof, B.J.8
Karpati, G.9
-
11
-
-
0031907287
-
Adenovirus-mediated dystrophin minigene transfer improves muscle strength in adult dystrophic (MDX) mice
-
Yang, L., Lochmuller, H., Luo, J., Massie, B., Nalbantoglu, J., Karpati, G. and Petrof, B.J. (1998) Adenovirus-mediated dystrophin minigene transfer improves muscle strength in adult dystrophic (MDX) mice. Gene Ther., 5, 369-379.
-
(1998)
Gene Ther.
, vol.5
, pp. 369-379
-
-
Yang, L.1
Lochmuller, H.2
Luo, J.3
Massie, B.4
Nalbantoglu, J.5
Karpati, G.6
Petrof, B.J.7
-
12
-
-
0033587139
-
Adenovirus-mediated utrophin gene transfer mitigates the dystrophic phenotype of mdx mouse muscles
-
Gilbert, R., Nalbantoglu, J., Petrof, B.J., Ebihara, S., Guibinga, G.H., Tinsley, J.M., Kamen, A., Massie, B., Davies, K.E. and Karpati, G. (1999) Adenovirus-mediated utrophin gene transfer mitigates the dystrophic phenotype of mdx mouse muscles. Hum. Gene Ther., 10, 1299-1310.
-
(1999)
Hum. Gene Ther.
, vol.10
, pp. 1299-1310
-
-
Gilbert, R.1
Nalbantoglu, J.2
Petrof, B.J.3
Ebihara, S.4
Guibinga, G.H.5
Tinsley, J.M.6
Kamen, A.7
Massie, B.8
Davies, K.E.9
Karpati, G.10
-
13
-
-
0034622814
-
Differential effects of dystrophin and utrophin gene transfer in immunocompetent muscular dystrophy (mdx) mice
-
Ebihara, S., Guibinga, G.H., Gilbert, R., Nalbantoglu, J., Massie, B., Karpati, G. and Petrof, B.J. (2000) Differential effects of dystrophin and utrophin gene transfer in immunocompetent muscular dystrophy (mdx) mice. Physiol. Genom., 3, 133-144.
-
(2000)
Physiol. Genom.
, vol.3
, pp. 133-144
-
-
Ebihara, S.1
Guibinga, G.H.2
Gilbert, R.3
Nalbantoglu, J.4
Massie, B.5
Karpati, G.6
Petrof, B.J.7
-
14
-
-
0033994291
-
Prevention of the dystrophic phenotype in dystrophin/utrophin-deficient muscle following adenovirus-mediated transfer of a utrophin minigene
-
Wakefield, P.M., Tinsley, J.M., Wood, M.J., Gilbert, R., Karpati, G. and Davies, K.E. (2000) Prevention of the dystrophic phenotype in dystrophin/utrophin-deficient muscle following adenovirus-mediated transfer of a utrophin minigene. Gene Ther., 7, 201-204. F
-
(2000)
Gene Ther.
, vol.7
, pp. 201-204
-
-
Wakefield, P.M.1
Tinsley, J.M.2
Wood, M.J.3
Gilbert, R.4
Karpati, G.5
Davies, K.E.6
-
15
-
-
0028328261
-
Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy
-
Yang, Y., Nunes, F.A., Berencsi, K., Furth, E.E., Gonczol, E. and Wilson, J.M. (1994) Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy. Proc. Natl Acad. Sci. USA, 91, 4407-4411.
-
(1994)
Proc. Natl Acad. Sci. USA
, vol.91
, pp. 4407-4411
-
-
Yang, Y.1
Nunes, F.A.2
Berencsi, K.3
Furth, E.E.4
Gonczol, E.5
Wilson, J.M.6
-
16
-
-
0028229147
-
Inactivation of E2a in recombinant adenoviruses improves the prospect for gene therapy in cystic fibrosis
-
Yang, Y., Nunes, F.A., Berencsi, K., Gonczol, E., Engelhardt, J.F. and Wilson, J.M. (1994) Inactivation of E2a in recombinant adenoviruses improves the prospect for gene therapy in cystic fibrosis. Nat. Genet., 7, 362-369.
-
(1994)
Nat. Genet.
, vol.7
, pp. 362-369
-
-
Yang, Y.1
Nunes, F.A.2
Berencsi, K.3
Gonczol, E.4
Engelhardt, J.F.5
Wilson, J.M.6
-
17
-
-
0029966514
-
Recombinant adenovirus deleted of all viral genes for gene therapy of cystic fibrosis
-
Fisher, K.J., Choi, H., Burda, J., Chen, S.J. and Wilson, J.M. (1996) Recombinant adenovirus deleted of all viral genes for gene therapy of cystic fibrosis. Virology, 217, 11-22.
-
(1996)
Virology
, vol.217
, pp. 11-22
-
-
Fisher, K.J.1
Choi, H.2
Burda, J.3
Chen, S.J.4
Wilson, J.M.5
-
18
-
-
0029943155
-
A new adenoviral vector: Replacement of all viral coding sequences with 28 kb of DNA independently expressing both full-length dystrophin and beta-galactosidase
-
Kochanek, S., Clemens, P.R., Mitani, K., Chen, H.H., Chan, S. and Caskey, C.T. (1996) A new adenoviral vector: Replacement of all viral coding sequences with 28 kb of DNA independently expressing both full-length dystrophin and beta-galactosidase. Proc. Natl Acad. Sci. USA, 93, 5731-5736.
-
(1996)
Proc. Natl Acad. Sci. USA
, vol.93
, pp. 5731-5736
-
-
Kochanek, S.1
Clemens, P.R.2
Mitani, K.3
Chen, H.H.4
Chan, S.5
Caskey, C.T.6
-
19
-
-
0030016358
-
Encapsidated adenovirus minichromosomes allow delivery and expression of a 14 kb dystrophin cDNA to muscle cells
-
Kumar-Singh, R. and Chamberlain, J.S. (1996) Encapsidated adenovirus minichromosomes allow delivery and expression of a 14 kb dystrophin cDNA to muscle cells. Hum. Mol. Genet., 5, 913-921.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 913-921
-
-
Kumar-Singh, R.1
Chamberlain, J.S.2
-
20
-
-
0030462599
-
A helper-dependent adenovirus vector system: Removal of helper virus by Cre-mediated excision of the viral packaging signal
-
Parks, R.J., Chen, L., Anton, M., Sankar, U., Rudnicki, M.A. and Graham, F.L. (1996) A helper-dependent adenovirus vector system: removal of helper virus by Cre-mediated excision of the viral packaging signal. Proc. Natl Acad. Sci. USA, 93, 13565-13570.
-
(1996)
Proc. Natl Acad. Sci. USA
, vol.93
, pp. 13565-13570
-
-
Parks, R.J.1
Chen, L.2
Anton, M.3
Sankar, U.4
Rudnicki, M.A.5
Graham, F.L.6
-
21
-
-
13144283616
-
An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene
-
Morsy, M.A., Gu, M., Motzel, S., Zhao, J., Lin, J., Su, Q., Allen, H., Franlin, L., Parks, R.J., Graham, F.L., Kochanek, S., Bett, A.J. and Caskey, C.T. (1998) An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene. Proc. Natl Acad. Sci. USA, 95, 7866-7871.
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 7866-7871
-
-
Morsy, M.A.1
Gu, M.2
Motzel, S.3
Zhao, J.4
Lin, J.5
Su, Q.6
Allen, H.7
Franlin, L.8
Parks, R.J.9
Graham, F.L.10
Kochanek, S.11
Bett, A.J.12
Caskey, C.T.13
-
22
-
-
0031916435
-
Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity
-
Schiedner, G., Morral, N., Parks, R.J., Wu, Y., Koopmans, S.C., Langston, C., Graham, F.L., Beaudet, A.L. and Kochanek, S. (1998) Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity. Nat. Genet., 18, 180-183.
-
(1998)
Nat. Genet.
, vol.18
, pp. 180-183
-
-
Schiedner, G.1
Morral, N.2
Parks, R.J.3
Wu, Y.4
Koopmans, S.C.5
Langston, C.6
Graham, F.L.7
Beaudet, A.L.8
Kochanek, S.9
-
23
-
-
0033540620
-
DNA from both high-capacity and first-generation adenoviral vectors remains intact in skeletal muscle
-
Chen, H.H., Mack, L.M., Choi, S.Y., Ontell, M., Kochanek, S. and Clemens, P.R. (1999) DNA from both high-capacity and first-generation adenoviral vectors remains intact in skeletal muscle. Hum. Gene Ther., 10, 365-373.
-
(1999)
Hum. Gene Ther.
, vol.10
, pp. 365-373
-
-
Chen, H.H.1
Mack, L.M.2
Choi, S.Y.3
Ontell, M.4
Kochanek, S.5
Clemens, P.R.6
-
24
-
-
0034630303
-
Prolonged expression and effective readministration of erythropoietin delivered with a fully deleted adenoviral vector
-
Maione, D., Wiznerowicz, M., Delmastro, P., Cortese, R., Ciliberto, G., La Monica, N. and Savino, R. (2000) Prolonged expression and effective readministration of erythropoietin delivered with a fully deleted adenoviral vector. Hum. Gene Ther., 11, 859-868.
-
(2000)
Hum. Gene Ther.
, vol.11
, pp. 859-868
-
-
Maione, D.1
Wiznerowicz, M.2
Delmastro, P.3
Cortese, R.4
Ciliberto, G.5
La Monica, N.6
Savino, R.7
-
25
-
-
0034244414
-
Prolonged transgene expression mediated by a helper-dependent adenoviral vector (hdAd) in the central nervous system
-
Zou, L., Zhou, H., Pastore, L. and Yang, K. (2000) Prolonged transgene expression mediated by a helper-dependent adenoviral vector (hdAd) in the central nervous system. Mol. Ther., 2, 105-113.
-
(2000)
Mol. Ther.
, vol.2
, pp. 105-113
-
-
Zou, L.1
Zhou, H.2
Pastore, L.3
Yang, K.4
-
26
-
-
0029857641
-
In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes
-
Clemens, P.R., Kochanek, S., Sunada, Y., Chan, S., Chen, H.H., Campbell, K.P. and Caskey, C.T. (1996) In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes. Gene Ther., 3, 965-972.
-
(1996)
Gene Ther.
, vol.3
, pp. 965-972
-
-
Clemens, P.R.1
Kochanek, S.2
Sunada, Y.3
Chan, S.4
Chen, H.H.5
Campbell, K.P.6
Caskey, C.T.7
-
27
-
-
0347927259
-
Immune response to full-length dystrophin delivered to Dmd muscle by a high-capacity adenoviral vector
-
Gilchrist, S.C., Ontell, M.P., Kochanek, S. and Clemens, P.R. (2002) Immune response to full-length dystrophin delivered to Dmd muscle by a high-capacity adenoviral vector. Mol. Ther., 6, 359-368.
-
(2002)
Mol. Ther.
, vol.6
, pp. 359-368
-
-
Gilchrist, S.C.1
Ontell, M.P.2
Kochanek, S.3
Clemens, P.R.4
-
28
-
-
0036790998
-
Functional correction of adult mdx mouse muscle using gutted adenoviral vectors expressing full-length dystrophin
-
DelloRusso, C., Scott, J.M., Hartigan-O'Connor, D., Salvatori, G., Barjot, C., Robinson, A.S., Crawford, R.W., Brooks, S.V. and Chamberlain, J.S. (2002) Functional correction of adult mdx mouse muscle using gutted adenoviral vectors expressing full-length dystrophin. Proc. Natl Acad. Sci. USA, 99, 12979-12984.
-
(2002)
Proc. Natl Acad. Sci. USA
, vol.99
, pp. 12979-12984
-
-
DelloRusso, C.1
Scott, J.M.2
Hartigan-O'Connor, D.3
Salvatori, G.4
Barjot, C.5
Robinson, A.S.6
Crawford, R.W.7
Brooks, S.V.8
Chamberlain, J.S.9
-
29
-
-
0034807864
-
Dystrophin expression in muscle following gene transfer with a fully deleted ('gutted') adenovirus is markedly improved by trans-acting adenoviral gene products
-
Gilbert, R., Nalbantoglu, J., Howell, J.M., Davies, L., Fletcher, S., Amalfitano, A., Petrof, B.J., Kamen, A., Massie, B. and Karpati, G. (2001) Dystrophin expression in muscle following gene transfer with a fully deleted ('gutted') adenovirus is markedly improved by trans-acting adenoviral gene products. Hum. Gene Ther., 12, 1741-1755.
-
(2001)
Hum. Gene Ther.
, vol.12
, pp. 1741-1755
-
-
Gilbert, R.1
Nalbantoglu, J.2
Howell, J.M.3
Davies, L.4
Fletcher, S.5
Amalfitano, A.6
Petrof, B.J.7
Kamen, A.8
Massie, B.9
Karpati, G.10
-
30
-
-
0036799827
-
Improved performance of a fully gutted adenovirus vector containing two full-length dystrophin cDNAs regulated by a strong promoter
-
Gilbert, R., Liu, A., Petrof, B., Nalbantoglu, J. and Karpati, G. (2002) Improved performance of a fully gutted adenovirus vector containing two full-length dystrophin cDNAs regulated by a strong promoter. Mol. Ther., 6, 501-509.
-
(2002)
Mol. Ther.
, vol.6
, pp. 501-509
-
-
Gilbert, R.1
Liu, A.2
Petrof, B.3
Nalbantoglu, J.4
Karpati, G.5
-
31
-
-
0029962474
-
In vivo expression of full-length human dystrophin from adenoviral vectors deleted of all viral genes
-
Haecker, S.E., Stedman, H.H., Balice-Gordon, R.J., Smith, D.B., Greelish, J.P., Mitchell, M.A., Wells, A., Sweeney, H.L. and Wilson, J.M. (1996) In vivo expression of full-length human dystrophin from adenoviral vectors deleted of all viral genes. Hum. Gene Ther., 7, 1907-1914.
-
(1996)
Hum. Gene Ther.
, vol.7
, pp. 1907-1914
-
-
Haecker, S.E.1
Stedman, H.H.2
Balice-Gordon, R.J.3
Smith, D.B.4
Greelish, J.P.5
Mitchell, M.A.6
Wells, A.7
Sweeney, H.L.8
Wilson, J.M.9
-
32
-
-
0033382340
-
Understanding dystrophinopathies: An inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse
-
Gillis, J.M. (1999) Understanding dystrophinopathies: an inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse. J. Muscle Res. Cell Motil., 20, 605-625.
-
(1999)
J. Muscle Res. Cell Motil.
, vol.20
, pp. 605-625
-
-
Gillis, J.M.1
-
33
-
-
0023697916
-
Small-caliber skeletal muscle fibers do not suffer necrosis in mdx mouse dystrophy
-
Karpati, G., Carpenter, S. and Prescott, S. (1988) Small-caliber skeletal muscle 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
-
34
-
-
0026328022
-
Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice
-
Ohlendieck, K., Campbell, K.P. (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
-
35
-
-
0027481238
-
Duchenne muscular dystrophy: Deficiency of dystrophin-associated proteins in the sarcolemma
-
Ohlendieck, K., Matsumura, K., Ionasescu, V.V., Towbin, J.A., Bosch, E.P., Weinstein, S.L., Sernett, S.W. and Campbell, K.P. (1993) Duchenne muscular dystrophy: deficiency of dystrophin-associated proteins in the sarcolemma. Neurology, 43, 795-800.
-
(1993)
Neurology
, vol.43
, pp. 795-800
-
-
Ohlendieck, K.1
Matsumura, K.2
Ionasescu, V.V.3
Towbin, J.A.4
Bosch, E.P.5
Weinstein, S.L.6
Sernett, S.W.7
Campbell, K.P.8
-
36
-
-
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
-
37
-
-
0034689474
-
Immune response to adenovirus-delivered antigens upregulates utrophin and results in mitigation of muscle pathology in mdx mice
-
Yamamoto, K., Yuasa, K., Miyagoe, Y., Hosaka, Y., Tsukita, K., Yamamoto, H., Nabeshima, Y.I. and Takeda, S. (2000) Immune response to adenovirus-delivered antigens upregulates utrophin and results in mitigation of muscle pathology in mdx mice. Hum. Gene Ther., 11, 669-680.
-
(2000)
Hum. Gene Ther.
, vol.11
, pp. 669-680
-
-
Yamamoto, K.1
Yuasa, K.2
Miyagoe, Y.3
Hosaka, Y.4
Tsukita, K.5
Yamamoto, H.6
Nabeshima, Y.I.7
Takeda, S.8
-
38
-
-
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
-
Lochmuller, H., Petrof, B.J., Pari, G., Larochelle, N., Dodelet, V., Wang, Q., Allen, C., Prescott, S., Massie, B., Nalbantoglu, J. and Karpati, G. (1996) 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)
Gene Ther.
, vol.3
, pp. 706-716
-
-
Lochmuller, H.1
Petrof, B.J.2
Pari, G.3
Larochelle, N.4
Dodelet, V.5
Wang, Q.6
Allen, C.7
Prescott, S.8
Massie, B.9
Nalbantoglu, J.10
Karpati, G.11
-
39
-
-
0031902429
-
Combinatorial blockade of calcineurin and CD28 signaling facilitates primary and secondary therapeutic gene transfer by adenovirus vectors in dystrophic (mdx) mouse muscles
-
Guibinga, G.H., Lochmuller, H., Massie, B., Nalbantoglu, J., Karpati, G. and Petrof, B.J. (1998) Combinatorial blockade of calcineurin and CD28 signaling facilitates primary and secondary therapeutic gene transfer by adenovirus vectors in dystrophic (mdx) mouse muscles. J. Virol., 72, 4601-4609.
-
(1998)
J. Virol.
, vol.72
, pp. 4601-4609
-
-
Guibinga, G.H.1
Lochmuller, H.2
Massie, B.3
Nalbantoglu, J.4
Karpati, G.5
Petrof, B.J.6
-
40
-
-
0032530110
-
Cellular immune response to adenoviral vector infected cells does not require de novo viral gene expression: Implications for gene therapy
-
Kafri, T., Morgan, D., Krahl, T., Sarvetnick, N., Sherman, L. and Verma, I. (1998) Cellular immune response to adenoviral vector infected cells does not require de novo viral gene expression: implications for gene therapy. Proc. Natl Acad. Sci. USA, 95, 11377-11382.
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 11377-11382
-
-
Kafri, T.1
Morgan, D.2
Krahl, T.3
Sarvetnick, N.4
Sherman, L.5
Verma, I.6
-
41
-
-
0029936764
-
Immune responses to transgene-encoded proteins limit the stability of gene expression after injection of replication-defective adenovirus vectors
-
Tripathy, S.K., Black, H.B., Goldwasser, E. and Leiden, J.M. (1996) Immune responses to transgene-encoded proteins limit the stability of gene expression after injection of replication-defective adenovirus vectors. Nat. Med., 2, 545-550.
-
(1996)
Nat. Med.
, vol.2
, pp. 545-550
-
-
Tripathy, S.K.1
Black, H.B.2
Goldwasser, E.3
Leiden, J.M.4
-
42
-
-
0029825458
-
Immunology of gene therapy with adenoviral vectors in mouse skeletal muscle
-
Yang, Y., Haecker, S.E., Su, Q. and Wilson, J.M. (1996) Immunology of gene therapy with adenoviral vectors in mouse skeletal muscle. Hum. Mol. Genet., 5, 1703-1712.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1703-1712
-
-
Yang, Y.1
Haecker, S.E.2
Su, Q.3
Wilson, J.M.4
-
43
-
-
0031049699
-
Persistence in muscle of an adenoviral vector that lacks all viral genes
-
Chen, H.H., Mack, L.M., Kelly, R., Ontell, M., Kochanek, S. and Clemens, P.R. (1997) Persistence in muscle of an adenoviral vector that lacks all viral genes. Proc. Natl Acad. Sci. USA, 94, 1645-1650.
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 1645-1650
-
-
Chen, H.H.1
Mack, L.M.2
Kelly, R.3
Ontell, M.4
Kochanek, S.5
Clemens, P.R.6
-
44
-
-
0035667634
-
Immune evasion by muscle-specific gene expression in dystrophic muscle
-
Hartigan-O'Connor, D., Kirk, C.J., Crawford, R., Mule, J.J. and Chamberlain, J.S. (2001) Immune evasion by muscle-specific gene expression in dystrophic muscle. Mol. Ther., 4, 525-533.
-
(2001)
Mol. Ther.
, vol.4
, pp. 525-533
-
-
Hartigan-O'Connor, D.1
Kirk, C.J.2
Crawford, R.3
Mule, J.J.4
Chamberlain, J.S.5
-
45
-
-
0031958992
-
Interferons impair early transgene expression by adenovirus-mediated gene transfer in muscle cells
-
Acsadi, G., O'Hagan, D., Lochmuller, H., Prescott, S., Larochelle, N., Nallantoglu, J., Jani, A. and Karpati, G. (1998) Interferons impair early transgene expression by adenovirus-mediated gene transfer in muscle cells. J. Mol. Med., 76, 442-450.
-
(1998)
J. Mol. Med.
, vol.76
, pp. 442-450
-
-
Acsadi, G.1
O'Hagan, D.2
Lochmuller, H.3
Prescott, S.4
Larochelle, N.5
Nallantoglu, J.6
Jani, A.7
Karpati, G.8
-
46
-
-
0031581174
-
Promoter attenuation in gene therapy: Interferon-gamma and tumor necrosis factor-alpha inhibit transgene expression
-
Qin, L., Ding, Y., Pahud, D.R., Chang, E., Imperiale, M.J. and Bromberg, J. S. (1997) Promoter attenuation in gene therapy: interferon-gamma and tumor necrosis factor-alpha inhibit transgene expression. Hum. Gene Ther., 8, 2019-2029.
-
(1997)
Hum. Gene Ther.
, vol.8
, pp. 2019-2029
-
-
Qin, L.1
Ding, Y.2
Pahud, D.R.3
Chang, E.4
Imperiale, M.J.5
Bromberg, J.S.6
-
47
-
-
0032080573
-
Dystrophin acts as a transplantation rejection antigen in dystrophin-deficient mice: Implication for gene therapy
-
Ohtsuka, Y., Udaka, K., Yamashiro, Y., Yagita, H. and Okumura, K. (1998) Dystrophin acts as a transplantation rejection antigen in dystrophin-deficient mice: implication for gene therapy. J. Immunol., 160, 4635-4640.
-
(1998)
J. Immunol.
, vol.160
, pp. 4635-4640
-
-
Ohtsuka, Y.1
Udaka, K.2
Yamashiro, Y.3
Yagita, H.4
Okumura, K.5
-
48
-
-
0033623151
-
Immune responses to dystrophin: Implications for gene therapy of Duchenne muscular dystrophy
-
Ferrer, A., Wells, K.E. and Wells, D.J. (2000) Immune responses to dystrophin: implications for gene therapy of Duchenne muscular dystrophy. Gene Ther., 7, 1439-1446.
-
(2000)
Gene Ther.
, vol.7
, pp. 1439-1446
-
-
Ferrer, A.1
Wells, K.E.2
Wells, D.J.3
-
49
-
-
0026355180
-
Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: Presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in proliferating brain cell lines
-
Nguyen, T.M., Ellis, J.M., Love, D.R., Davies, K.E., Gatter, K.C., Dickson, G. and Morris, G.E. (1991) Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in proliferating brain cell lines. J. Cell Biol., 115, 1695-1700.
-
(1991)
J. Cell Biol.
, vol.115
, pp. 1695-1700
-
-
Nguyen, T.M.1
Ellis, J.M.2
Love, D.R.3
Davies, K.E.4
Gatter, K.C.5
Dickson, G.6
Morris, G.E.7
-
50
-
-
0029906168
-
Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene
-
Tinsley, J.M., Potter, A.C., Phelps, S.R., Fisher, R., Trickett, J.I. and Davies, K.E. (1996) Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene. Nature, 384, 349-353.
-
(1996)
Nature
, vol.384
, pp. 349-353
-
-
Tinsley, J.M.1
Potter, A.C.2
Phelps, S.R.3
Fisher, R.4
Trickett, J.I.5
Davies, K.E.6
-
51
-
-
0031727771
-
Expression of full-length utrophin prevents muscular dystrophy in mdx mice
-
Tinsley, J., Deconinck, N., Fisher, R., Kahn, D., Phelps, S., Gillis, J.M. and Davies, K. (1998) Expression of full-length utrophin prevents muscular dystrophy in mdx mice. Nat. Med., 4, 1441-1444.
-
(1998)
Nat. Med.
, vol.4
, pp. 1441-1444
-
-
Tinsley, J.1
Deconinck, N.2
Fisher, R.3
Kahn, D.4
Phelps, S.5
Gillis, J.M.6
Davies, K.7
-
52
-
-
0035915778
-
Muscle-specific promoters may be necessary for adeno-associated virus- mediated gene transfer in the treatment of muscular dystrophies
-
Cordier, L., Gao, G.R, Hack, A.A., McNally, E.M., Wilson, J.M., Chirmule, N. and Sweeney, H.L. (2001) Muscle-specific promoters may be necessary for adeno-associated virus- mediated gene transfer in the treatment of muscular dystrophies. Hum. Gene Ther., 12, 205-215.
-
(2001)
Hum. Gene Ther.
, vol.12
, pp. 205-215
-
-
Cordier, L.1
Gao, G.R.2
Hack, A.A.3
McNally, E.M.4
Wilson, J.M.5
Chirmule, N.6
Sweeney, H.L.7
-
53
-
-
0035494438
-
A nitric oxide synthase transgene ameliorates muscular dystrophy in mdx mice
-
Wehling, M., Spencer, M.J. and Tidball, J.G. (2001) A nitric oxide synthase transgene ameliorates muscular dystrophy in mdx mice. J. Cell Biol., 155, 123-131.
-
(2001)
J. Cell Biol.
, vol.155
, pp. 123-131
-
-
Wehling, M.1
Spencer, M.J.2
Tidball, J.G.3
-
54
-
-
0036471858
-
A chronic inflammatory response dominates the skeletal muscle molecular signature in dystrophin-deficient mdx mice
-
Porter, J.D., Khanna, S., Kaminski, H.J., Rao, J.S., Merriam, A.P., Richmonds, C.R., Leahy, P., Li, J., Goo, W. and Andrade, F.H. (2002) A chronic inflammatory response dominates the skeletal muscle molecular signature in dystrophin-deficient mdx mice. Hum. Mol. Genet., 11, 263-272.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 263-272
-
-
Porter, J.D.1
Khanna, S.2
Kaminski, H.J.3
Rao, J.S.4
Merriam, A.P.5
Richmonds, C.R.6
Leahy, P.7
Li, J.8
Goo, W.9
Andrade, F.H.10
-
55
-
-
0032488509
-
Efficient utrophin expression following adenovirus gene transfer in dystrophic muscle
-
Gilbert, R., Nalbantoglu, J., Tinsley, J.M., Massie, B., Davies, K.E. and Karpati, G. (1998) Efficient utrophin expression following adenovirus gene transfer in dystrophic muscle. Biochem. Biophys. Res. Commun., 242, 244-247.
-
(1998)
Biochem. Biophys. Res. Commun.
, vol.242
, pp. 244-247
-
-
Gilbert, R.1
Nalbantoglu, J.2
Tinsley, J.M.3
Massie, B.4
Davies, K.E.5
Karpati, G.6
-
56
-
-
0030723508
-
Expression of truncated utrophin leads to major functional improvements in dystrophin-deficient muscles of mice
-
Deconinck, N., Tinsley, J., De Backer, F., Fisher, R., Kahn, D., Phelps, S., Davies, K. and Gillis, J.M. (1997) Expression of truncated utrophin leads to major functional improvements in dystrophin-deficient muscles of mice. Nat. Med., 3, 1216-1221.
-
(1997)
Nat. Med.
, vol.3
, pp. 1216-1221
-
-
Deconinck, N.1
Tinsley, J.2
De Backer, F.3
Fisher, R.4
Kahn, D.5
Phelps, S.6
Davies, K.7
Gillis, J.M.8
-
57
-
-
0027186053
-
Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity
-
Cox, G.A., Cole, N.M., Matsumura, K., Phelps, S.F., Hauschka, S.D., Campbell, K.P., Faulkner, J.A. and Chamberlain, J.S. (1993) Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity. Nature, 364, 725-729.
-
(1993)
Nature
, 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
-
58
-
-
0025884056
-
Efficient selection for high-expression transfectants with a novel eukaryotic vector
-
Niwa, H., Yamamura, K. and Miyazaki, J. (1991) Efficient selection for high-expression transfectants with a novel eukaryotic vector. Gene, 108, 193-199.
-
(1991)
Gene
, vol.108
, pp. 193-199
-
-
Niwa, H.1
Yamamura, K.2
Miyazaki, J.3
-
59
-
-
0029836780
-
Evaluation of the concentration and bioactivity of adenovirus vectors for gene therapy
-
Mittereder, N., March, K.L. and Trapnell, B.C. (1996) Evaluation of the concentration and bioactivity of adenovirus vectors for gene therapy. J. Virol., 70, 7498-7509.
-
(1996)
J. Virol.
, vol.70
, pp. 7498-7509
-
-
Mittereder, N.1
March, K.L.2
Trapnell, B.C.3
-
60
-
-
0030855528
-
Sensitivity and reproducibility in adenoviral infectious titer determination
-
Nyberg-Hoffman, C., Shabram, P., Li, W., Giroux, D. and Aguilar-Cordova, E. (1997) Sensitivity and reproducibility in adenoviral infectious titer determination. Nat. Med., 3, 808-811.
-
(1997)
Nat. Med.
, vol.3
, pp. 808-811
-
-
Nyberg-Hoffman, C.1
Shabram, P.2
Li, W.3
Giroux, D.4
Aguilar-Cordova, E.5
-
61
-
-
0002025785
-
-
Murray, E. (ed.), Humana Press, Clifton, NJ
-
Graham, F., Prevec, L. (1991) In Murray, E. (ed.), Gene Transfer and Expression Protocols. Humana Press, Clifton, NJ, pp. 109-114.
-
(1991)
Gene Transfer and Expression Protocols
, pp. 109-114
-
-
Graham, F.1
Prevec, L.2
|