-
1
-
-
77953546004
-
Congenital muscular dystrophies: toward molecular therapeutic interventions
-
Collins J, Bonnemann CG, (2010) Congenital muscular dystrophies: toward molecular therapeutic interventions. Curr Neurol Neurosci Rep 10: 83-91.
-
(2010)
Curr Neurol Neurosci Rep
, vol.10
, pp. 83-91
-
-
Collins, J.1
Bonnemann, C.G.2
-
2
-
-
0028232215
-
Congenital muscular dystrophy with merosin deficiency
-
Tome FM, Evangelista T, Leclerc A, Sunada Y, Manole E, et al. (1994) Congenital muscular dystrophy with merosin deficiency. C R Acad Sci III 317: 351-357.
-
(1994)
C R Acad Sci III
, vol.317
, pp. 351-357
-
-
Tome, F.M.1
Evangelista, T.2
Leclerc, A.3
Sunada, Y.4
Manole, E.5
-
3
-
-
4444234437
-
The congenital muscular dystrophies in 2004: a century of exciting progress
-
Muntoni F, Voit T, (2004) The congenital muscular dystrophies in 2004: a century of exciting progress. Neuromuscul Disord 14: 635-649.
-
(2004)
Neuromuscul Disord
, vol.14
, pp. 635-649
-
-
Muntoni, F.1
Voit, T.2
-
4
-
-
0035030357
-
Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophy
-
Hayashi YK, Tezak Z, Momoi T, Nonaka I, Garcia CA, et al. (2001) Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophy. Neuromuscul Disord 11: 350-359.
-
(2001)
Neuromuscul Disord
, vol.11
, pp. 350-359
-
-
Hayashi, Y.K.1
Tezak, Z.2
Momoi, T.3
Nonaka, I.4
Garcia, C.A.5
-
5
-
-
0032528845
-
Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models
-
Kuang W, Xu H, Vachon PH, Liu L, Loechel F, et al. (1998) Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models. J Clin Invest 102: 844-852.
-
(1998)
J Clin Invest
, vol.102
, pp. 844-852
-
-
Kuang, W.1
Xu, H.2
Vachon, P.H.3
Liu, L.4
Loechel, F.5
-
6
-
-
0028135436
-
Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene
-
Xu H, Wu XR, Wewer UM, Engvall E, (1994) Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene. Nat Genet 8: 297-302.
-
(1994)
Nat Genet
, vol.8
, pp. 297-302
-
-
Xu, H.1
Wu, X.R.2
Wewer, U.M.3
Engvall, E.4
-
7
-
-
0030610896
-
Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy
-
Miyagoe Y, Hanaoka K, Nonaka I, Hayasaka M, Nabeshima Y, et al. (1997) Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy. FEBS Lett 415: 33-39.
-
(1997)
FEBS Lett
, vol.415
, pp. 33-39
-
-
Miyagoe, Y.1
Hanaoka, K.2
Nonaka, I.3
Hayasaka, M.4
Nabeshima, Y.5
-
8
-
-
85047693919
-
Inhibition of apoptosis improves outcome in a model of congenital muscular dystrophy
-
Girgenrath M, Dominov JA, Kostek CA, Miller JB, (2004) Inhibition of apoptosis improves outcome in a model of congenital muscular dystrophy. J Clin Invest 114: 1635-1639.
-
(2004)
J Clin Invest
, vol.114
, pp. 1635-1639
-
-
Girgenrath, M.1
Dominov, J.A.2
Kostek, C.A.3
Miller, J.B.4
-
9
-
-
17744385764
-
Muscle-specific BCL2 expression ameliorates muscle disease in laminin {alpha}2-deficient, but not in dystrophin-deficient, mice
-
Dominov JA, Kravetz AJ, Ardelt M, Kostek CA, Beermann ML, et al. (2005) Muscle-specific BCL2 expression ameliorates muscle disease in laminin {alpha}2-deficient, but not in dystrophin-deficient, mice. Hum Mol Genet 14: 1029-1040.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 1029-1040
-
-
Dominov, J.A.1
Kravetz, A.J.2
Ardelt, M.3
Kostek, C.A.4
Beermann, M.L.5
-
10
-
-
73349085584
-
Omigapil ameliorates the pathology of muscle dystrophy caused by laminin-alpha2 deficiency
-
Erb M, Meinen S, Barzaghi P, Sumanovski LT, Courdier-Fruh I, et al. (2009) Omigapil ameliorates the pathology of muscle dystrophy caused by laminin-alpha2 deficiency. J Pharmacol Exp Ther 331: 787-795.
-
(2009)
J Pharmacol Exp Ther
, vol.331
, pp. 787-795
-
-
Erb, M.1
Meinen, S.2
Barzaghi, P.3
Sumanovski, L.T.4
Courdier-Fruh, I.5
-
11
-
-
0035223401
-
An orally active anti-apoptotic molecule (CGP 3466B) preserves mitochondria and enhances survival in an animal model of motoneuron disease
-
Sagot Y, Toni N, Perrelet D, Lurot S, King B, et al. (2000) An orally active anti-apoptotic molecule (CGP 3466B) preserves mitochondria and enhances survival in an animal model of motoneuron disease. Br J Pharmacol 131: 721-728.
-
(2000)
Br J Pharmacol
, vol.131
, pp. 721-728
-
-
Sagot, Y.1
Toni, N.2
Perrelet, D.3
Lurot, S.4
King, B.5
-
12
-
-
33750719088
-
TCH346 as a neuroprotective drug in Parkinson's disease: a double-blind, randomised, controlled trial
-
Olanow CW, Schapira AH, LeWitt PA, Kieburtz K, Sauer D, et al. (2006) TCH346 as a neuroprotective drug in Parkinson's disease: a double-blind, randomised, controlled trial. Lancet Neurol 5: 1013-1020.
-
(2006)
Lancet Neurol
, vol.5
, pp. 1013-1020
-
-
Olanow, C.W.1
Schapira, A.H.2
LeWitt, P.A.3
Kieburtz, K.4
Sauer, D.5
-
13
-
-
34548119851
-
Phase II/III randomized trial of TCH346 in patients with ALS
-
Miller R, Bradley W, Cudkowicz M, Hubble J, Meininger V, et al. (2007) Phase II/III randomized trial of TCH346 in patients with ALS. Neurology 69: 776-784.
-
(2007)
Neurology
, vol.69
, pp. 776-784
-
-
Miller, R.1
Bradley, W.2
Cudkowicz, M.3
Hubble, J.4
Meininger, V.5
-
14
-
-
65949114863
-
Preclinical drug trials in the mdx mouse: assessment of reliable and sensitive outcome measures
-
Spurney CF, Gordish-Dressman H, Guerron AD, Sali A, Pandey GS, et al. (2009) Preclinical drug trials in the mdx mouse: assessment of reliable and sensitive outcome measures. Muscle Nerve 39: 591-602.
-
(2009)
Muscle Nerve
, vol.39
, pp. 591-602
-
-
Spurney, C.F.1
Gordish-Dressman, H.2
Guerron, A.D.3
Sali, A.4
Pandey, G.S.5
-
15
-
-
0011261078
-
Conditional up-regulation of MHC class I in skeletal muscle leads to self-sustaining autoimmune myositis and myositis-specific autoantibodies
-
Nagaraju K, Raben N, Loeffler L, Parker T, Rochon PJ, et al. (2000) Conditional up-regulation of MHC class I in skeletal muscle leads to self-sustaining autoimmune myositis and myositis-specific autoantibodies. Proc Natl Acad Sci U S A 97: 9209-9214.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 9209-9214
-
-
Nagaraju, K.1
Raben, N.2
Loeffler, L.3
Parker, T.4
Rochon, P.J.5
-
16
-
-
14444274334
-
Targeted disruption of the acid alpha-glucosidase gene in mice causes an illness with critical features of both infantile and adult human glycogen storage disease type II
-
Raben N, Nagaraju K, Lee E, Kessler P, Byrne B, et al. (1998) Targeted disruption of the acid alpha-glucosidase gene in mice causes an illness with critical features of both infantile and adult human glycogen storage disease type II. J Biol Chem 273: 19086-19092.
-
(1998)
J Biol Chem
, vol.273
, pp. 19086-19092
-
-
Raben, N.1
Nagaraju, K.2
Lee, E.3
Kessler, P.4
Byrne, B.5
-
17
-
-
0034212319
-
Modulation of disease severity in mice with targeted disruption of the acid alpha-glucosidase gene
-
Raben N, Nagaraju K, Lee E, Plotz P, (2000) Modulation of disease severity in mice with targeted disruption of the acid alpha-glucosidase gene. Neuromuscul Disord 10: 283-291.
-
(2000)
Neuromuscul Disord
, vol.10
, pp. 283-291
-
-
Raben, N.1
Nagaraju, K.2
Lee, E.3
Plotz, P.4
-
18
-
-
79951479823
-
Losartan decreases cardiac muscle fibrosis and improves cardiac function in dystrophin-deficient mdx mice
-
Spurney CF, Sali A, Guerron AD, Iantorno M, Yu Q, et al. (2011) Losartan decreases cardiac muscle fibrosis and improves cardiac function in dystrophin-deficient mdx mice. J Cardiovasc Pharmacol Ther 16: 87-95.
-
(2011)
J Cardiovasc Pharmacol Ther
, vol.16
, pp. 87-95
-
-
Spurney, C.F.1
Sali, A.2
Guerron, A.D.3
Iantorno, M.4
Yu, Q.5
-
19
-
-
0034523131
-
Neurorescuing effects of the GAPDH ligand CGP 3466B
-
Waldmeier PC, Boulton AA, Cools AR, Kato AC, Tatton WG (2000) Neurorescuing effects of the GAPDH ligand CGP 3466B. J Neural Transm Suppl: 197-214.
-
(2000)
J Neural Transm Suppl
, pp. 197-214
-
-
Waldmeier, P.C.1
Boulton, A.A.2
Cools, A.R.3
Kato, A.C.4
Tatton, W.G.5
|