-
1
-
-
18244375299
-
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C
-
10.1093/hmg/10.25.2851, 11741828
-
Brockington M, Yuva Y, Prandini P, Brown SC, Torelli S, Benson MA, Herrmann R, Anderson LV, Bashir R, Burgunder JM, et al. Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. Hum Mol Genet 2001, 10:2851-2859. 10.1093/hmg/10.25.2851, 11741828.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2851-2859
-
-
Brockington, M.1
Yuva, Y.2
Prandini, P.3
Brown, S.C.4
Torelli, S.5
Benson, M.A.6
Herrmann, R.7
Anderson, L.V.8
Bashir, R.9
Burgunder, J.M.10
-
2
-
-
0035212037
-
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan
-
10.1086/324412, 1235559, 11592034
-
Brockington M, Blake DJ, Prandini P, Brown SC, Torelli S, Benson MA, Ponting CP, Estournet B, Romero NB, Mercuri E, et al. Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan. Am J Hum Genet 2001, 69:1198-1209. 10.1086/324412, 1235559, 11592034.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1198-1209
-
-
Brockington, M.1
Blake, D.J.2
Prandini, P.3
Brown, S.C.4
Torelli, S.5
Benson, M.A.6
Ponting, C.P.7
Estournet, B.8
Romero, N.B.9
Mercuri, E.10
-
3
-
-
0026543686
-
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix
-
Ibraghimov-Beskrovnaya O, Ervasti JM, Leveille CJ, Slaughter CA, Sernett SW, Campbell KP. Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix. Nature 1992, 20;355:696-702.
-
(1992)
Nature
, vol.20
, Issue.355
, pp. 696-702
-
-
Ibraghimov-Beskrovnaya, O.1
Ervasti, J.M.2
Leveille, C.J.3
Slaughter, C.A.4
Sernett, S.W.5
Campbell, K.P.6
-
4
-
-
12744279620
-
Fukutin-related protein mutations that cause congenital muscular dystrophy result in ER-retention of the mutant protein in cultured cells
-
Esapa CT, McIlhinney RA, Blake DJ. Fukutin-related protein mutations that cause congenital muscular dystrophy result in ER-retention of the mutant protein in cultured cells. Hum Mol Genet 2005, 14:295-305.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 295-305
-
-
Esapa, C.T.1
McIlhinney, R.A.2
Blake, D.J.3
-
5
-
-
28244500576
-
Sub-cellular localisation of fukutin related protein in different cell lines and in the muscle of patients with MDC1C and LGMD2I
-
10.1016/j.nmd.2005.09.004, 16288869
-
Torelli S, Brown SC, Brockington M, Dolatshad NF, Jimenez C, Skordis L, Feng LH, Merlini L, Jones DH, Romero N, et al. Sub-cellular localisation of fukutin related protein in different cell lines and in the muscle of patients with MDC1C and LGMD2I. Neuromuscul Disord 2005, 15:836-843. 10.1016/j.nmd.2005.09.004, 16288869.
-
(2005)
Neuromuscul Disord
, vol.15
, pp. 836-843
-
-
Torelli, S.1
Brown, S.C.2
Brockington, M.3
Dolatshad, N.F.4
Jimenez, C.5
Skordis, L.6
Feng, L.H.7
Merlini, L.8
Jones, D.H.9
Romero, N.10
-
6
-
-
33646353390
-
High prevalence and phenotype-genotype correlations of limb girdle muscular dystrophy type 2I in Denmark
-
10.1002/ana.20824, 16634037
-
Sveen ML, Schwartz M, Vissing J. High prevalence and phenotype-genotype correlations of limb girdle muscular dystrophy type 2I in Denmark. Ann Neurol 2006, 59:808-815. 10.1002/ana.20824, 16634037.
-
(2006)
Ann Neurol
, vol.59
, pp. 808-815
-
-
Sveen, M.L.1
Schwartz, M.2
Vissing, J.3
-
7
-
-
33646353390
-
High prevalence and phenotype-genotype correlations of limb girdle muscular dystrophy type 2I in Denmark
-
10.1002/ana.20824, 16634037
-
Sveen ML, Schwartz M, Vissing J. High prevalence and phenotype-genotype correlations of limb girdle muscular dystrophy type 2I in Denmark. Ann Neurol 2006, 59:808-815. 10.1002/ana.20824, 16634037.
-
(2006)
Ann Neurol
, vol.59
, pp. 808-815
-
-
Sveen, M.L.1
Schwartz, M.2
Vissing, J.3
-
8
-
-
18144383891
-
LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotype
-
10.1212/01.WNL.0000157654.59374.E5, 15883334
-
Schwartz M, Hertz JM, Sveen ML, Vissing J. LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotype. Neurology 2005, 64:1635-1637. 10.1212/01.WNL.0000157654.59374.E5, 15883334.
-
(2005)
Neurology
, vol.64
, pp. 1635-1637
-
-
Schwartz, M.1
Hertz, J.M.2
Sveen, M.L.3
Vissing, J.4
-
9
-
-
18244375299
-
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C
-
10.1093/hmg/10.25.2851, 11741828
-
Brockington M, Yuva Y, Prandini P, Brown SC, Torelli S, Benson MA, Herrmann R, Anderson LV, Bashir R, Burgunder JM, et al. Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. Hum Mol Genet 2001, 10:2851-2859. 10.1093/hmg/10.25.2851, 11741828.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2851-2859
-
-
Brockington, M.1
Yuva, Y.2
Prandini, P.3
Brown, S.C.4
Torelli, S.5
Benson, M.A.6
Herrmann, R.7
Anderson, L.V.8
Bashir, R.9
Burgunder, J.M.10
-
10
-
-
33646353390
-
High prevalence and phenotype-genotype correlations of limb girdle muscular dystrophy type 2I in Denmark
-
10.1002/ana.20824, 16634037
-
Sveen ML, Schwartz M, Vissing J. High prevalence and phenotype-genotype correlations of limb girdle muscular dystrophy type 2I in Denmark. Ann Neurol 2006, 59:808-815. 10.1002/ana.20824, 16634037.
-
(2006)
Ann Neurol
, vol.59
, pp. 808-815
-
-
Sveen, M.L.1
Schwartz, M.2
Vissing, J.3
-
11
-
-
0020058217
-
Five different types of centrally nucleated muscle fibres in man: elemental composition and morphological criteria. A study of myopathies, fetal tissue and muscle spindle
-
Wroblewski R, Edstrom L, Mair WG. Five different types of centrally nucleated muscle fibres in man: elemental composition and morphological criteria. A study of myopathies, fetal tissue and muscle spindle. J Submicrosc Cytol 1982, 14:377-387.
-
(1982)
J Submicrosc Cytol
, vol.14
, pp. 377-387
-
-
Wroblewski, R.1
Edstrom, L.2
Mair, W.G.3
-
12
-
-
0019966026
-
Fetal myosin heavy chains in regenerating muscle
-
10.1038/298294a0, 7045696
-
Sartore S, Gorza L, Schiaffino S. Fetal myosin heavy chains in regenerating muscle. Nature 1982, 298:294-296. 10.1038/298294a0, 7045696.
-
(1982)
Nature
, vol.298
, pp. 294-296
-
-
Sartore, S.1
Gorza, L.2
Schiaffino, S.3
-
13
-
-
0026805782
-
Identification of skeletal muscle precursor cells in vivo by use of MyoD1 and myogenin probes
-
10.1007/BF00318695, 1310442
-
Grounds MD, Garrett KL, Lai MC, Wright WE, Beilharz MW. Identification of skeletal muscle precursor cells in vivo by use of MyoD1 and myogenin probes. Cell Tissue Res 1992, 267:99-104. 10.1007/BF00318695, 1310442.
-
(1992)
Cell Tissue Res
, vol.267
, pp. 99-104
-
-
Grounds, M.D.1
Garrett, K.L.2
Lai, M.C.3
Wright, W.E.4
Beilharz, M.W.5
-
14
-
-
0030839605
-
Myogenic regulatory factors during regeneration of skeletal muscle in young, adult, and old rats
-
Marsh DR, Criswell DS, Carson JA, Booth FW. Myogenic regulatory factors during regeneration of skeletal muscle in young, adult, and old rats. J Appl Physiol 1997, 83:1270-1275.
-
(1997)
J Appl Physiol
, vol.83
, pp. 1270-1275
-
-
Marsh, D.R.1
Criswell, D.S.2
Carson, J.A.3
Booth, F.W.4
-
15
-
-
0242467963
-
Satellite cell depletion in degenerative skeletal muscle
-
Jejurikar SS, Kuzon WM. Satellite cell depletion in degenerative skeletal muscle. Apoptosis 2003, 8:573-578.
-
(2003)
Apoptosis
, vol.8
, pp. 573-578
-
-
Jejurikar, S.S.1
Kuzon, W.M.2
-
16
-
-
33646353390
-
High prevalence and phenotype-genotype correlations of limb girdle muscular dystrophy type 2I in Denmark
-
10.1002/ana.20824, 16634037
-
Sveen ML, Schwartz M, Vissing J. High prevalence and phenotype-genotype correlations of limb girdle muscular dystrophy type 2I in Denmark. Ann Neurol 2006, 59:808-815. 10.1002/ana.20824, 16634037.
-
(2006)
Ann Neurol
, vol.59
, pp. 808-815
-
-
Sveen, M.L.1
Schwartz, M.2
Vissing, J.3
-
17
-
-
0142151077
-
Loss of calpain-3 autocatalytic activity in LGMD2A patients with normal protein expression
-
10.1016/S0002-9440(10)63551-1, 1892408, 14578192
-
Fanin M, Nascimbeni AC, Fulizio L, Trevisan CP, Meznaric-Petrusa M, Angelini C. Loss of calpain-3 autocatalytic activity in LGMD2A patients with normal protein expression. Am J Pathol 2003, 163:1929-1936. 10.1016/S0002-9440(10)63551-1, 1892408, 14578192.
-
(2003)
Am J Pathol
, vol.163
, pp. 1929-1936
-
-
Fanin, M.1
Nascimbeni, A.C.2
Fulizio, L.3
Trevisan, C.P.4
Meznaric-Petrusa, M.5
Angelini, C.6
-
18
-
-
43549125190
-
Immobilization of the rabbit tibialis anterior muscle in a lengthened position causes addition of sarcomeres in series and extra-cellular matrix proliferation
-
10.1016/j.jbiomech.2008.03.006, 18460410
-
Ponten E, Friden J. Immobilization of the rabbit tibialis anterior muscle in a lengthened position causes addition of sarcomeres in series and extra-cellular matrix proliferation. J Biomech 2008, 41:1801-1804. 10.1016/j.jbiomech.2008.03.006, 18460410.
-
(2008)
J Biomech
, vol.41
, pp. 1801-1804
-
-
Ponten, E.1
Friden, J.2
-
19
-
-
18644362893
-
Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration
-
10.1016/S0092-8674(02)00907-8, 12230980
-
Cohn RD, Henry MD, Michele DE, Barresi R, Saito F, Moore SA, Flanagan JD, Skwarchuk MW, Robbins ME, Mendell JR, et al. Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration. Cell 2002, 110:639-648. 10.1016/S0092-8674(02)00907-8, 12230980.
-
(2002)
Cell
, vol.110
, pp. 639-648
-
-
Cohn, R.D.1
Henry, M.D.2
Michele, D.E.3
Barresi, R.4
Saito, F.5
Moore, S.A.6
Flanagan, J.D.7
Skwarchuk, M.W.8
Robbins, M.E.9
Mendell, J.R.10
-
20
-
-
0026460270
-
The dystrophin-related protein, utrophin, is expressed on the sarcolemma of regenerating human skeletal muscle fibres in dystrophies and inflammatory myopathies
-
10.1016/0960-8966(92)90004-P, 1483043
-
Helliwell TR, Man NT, Morris GE, Davies KE. The dystrophin-related protein, utrophin, is expressed on the sarcolemma of regenerating human skeletal muscle fibres in dystrophies and inflammatory myopathies. Neuromuscul Disord 1992, 2:177-184. 10.1016/0960-8966(92)90004-P, 1483043.
-
(1992)
Neuromuscul Disord
, vol.2
, pp. 177-184
-
-
Helliwell, T.R.1
Man, N.T.2
Morris, G.E.3
Davies, K.E.4
-
21
-
-
0030809116
-
Altered expression of the alpha7beta1 integrin in human and murine muscular dystrophies
-
Hodges BL, Hayashi YK, Nonaka I, Wang W, Arahata K, Kaufman SJ. Altered expression of the alpha7beta1 integrin in human and murine muscular dystrophies. J Cell Sci 1997, 110:2873-2881.
-
(1997)
J Cell Sci
, vol.110
, pp. 2873-2881
-
-
Hodges, B.L.1
Hayashi, Y.K.2
Nonaka, I.3
Wang, W.4
Arahata, K.5
Kaufman, S.J.6
-
22
-
-
0029921129
-
Utrophin: a structural and functional comparison to dystrophin
-
10.1111/j.1750-3639.1996.tb00781.x, 8866746
-
Blake DJ, Tinsley JM, Davies KE. Utrophin: a structural and functional comparison to dystrophin. Brain Pathol 1996, 6:37-47. 10.1111/j.1750-3639.1996.tb00781.x, 8866746.
-
(1996)
Brain Pathol
, vol.6
, pp. 37-47
-
-
Blake, D.J.1
Tinsley, J.M.2
Davies, K.E.3
-
23
-
-
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
-
10.1083/jcb.115.6.1695, 2289198, 1757469
-
Nguyen TM, Ellis JM, Love DR, Davies KE, Gatter KC, Dickson G, Morris GE. 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 1991, 115:1695-1700. 10.1083/jcb.115.6.1695, 2289198, 1757469.
-
(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
-
24
-
-
0347757245
-
Asymptomatic carriers for homozygous novel mutations in the FKRP gene: the other end of the spectrum
-
10.1038/sj.ejhg.5201066, 14647208
-
de Paula F, Vieira N, Starling A, Yamamoto LU, Lima B, de Cassia PR, Vainzof M, Nigro V, Zatz M. Asymptomatic carriers for homozygous novel mutations in the FKRP gene: the other end of the spectrum. Eur J Hum Genet 2003, 11:923-930. 10.1038/sj.ejhg.5201066, 14647208.
-
(2003)
Eur J Hum Genet
, vol.11
, pp. 923-930
-
-
de Paula, F.1
Vieira, N.2
Starling, A.3
Yamamoto, L.U.4
Lima, B.5
de Cassia, P.R.6
Vainzof, M.7
Nigro, V.8
Zatz, M.9
-
25
-
-
0035212037
-
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan
-
10.1086/324412, 1235559, 11592034
-
Brockington M, Blake DJ, Prandini P, Brown SC, Torelli S, Benson MA, Ponting CP, Estournet B, Romero NB, Mercuri E, et al. Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan. Am J Hum Genet 2001, 69:1198-1209. 10.1086/324412, 1235559, 11592034.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1198-1209
-
-
Brockington, M.1
Blake, D.J.2
Prandini, P.3
Brown, S.C.4
Torelli, S.5
Benson, M.A.6
Ponting, C.P.7
Estournet, B.8
Romero, N.B.9
Mercuri, E.10
-
26
-
-
18144383891
-
LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotype
-
10.1212/01.WNL.0000157654.59374.E5, 15883334
-
Schwartz M, Hertz JM, Sveen ML, Vissing J. LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotype. Neurology 2005, 64:1635-1637. 10.1212/01.WNL.0000157654.59374.E5, 15883334.
-
(2005)
Neurology
, vol.64
, pp. 1635-1637
-
-
Schwartz, M.1
Hertz, J.M.2
Sveen, M.L.3
Vissing, J.4
-
27
-
-
0037380737
-
Phenotypic spectrum associated with mutations in the fukutin-related protein gene
-
10.1002/ana.10559, 12666124
-
Mercuri E, Brockington M, Straub V, Quijano-Roy S, Yuva Y, Herrmann R, Brown SC, Torelli S, Dubowitz V, Blake DJ, et al. Phenotypic spectrum associated with mutations in the fukutin-related protein gene. Ann Neurol 2003, 53:537-542. 10.1002/ana.10559, 12666124.
-
(2003)
Ann Neurol
, vol.53
, pp. 537-542
-
-
Mercuri, E.1
Brockington, M.2
Straub, V.3
Quijano-Roy, S.4
Yuva, Y.5
Herrmann, R.6
Brown, S.C.7
Torelli, S.8
Dubowitz, V.9
Blake, D.J.10
-
28
-
-
75649132196
-
A COX-2 inhibitor reduces muscle soreness, but does not influence recovery and adaptation after eccentric exercise
-
10.1111/j.1600-0838.2009.00947.x, 19522751
-
Paulsen G, Egner IM, Drange M, Langberg H, Benestad HB, Fjeld JG, Hallen J, Raastad T. A COX-2 inhibitor reduces muscle soreness, but does not influence recovery and adaptation after eccentric exercise. Scand J Med Sci Sports 2010, 20:e195-e207. 10.1111/j.1600-0838.2009.00947.x, 19522751.
-
(2010)
Scand J Med Sci Sports
, vol.20
-
-
Paulsen, G.1
Egner, I.M.2
Drange, M.3
Langberg, H.4
Benestad, H.B.5
Fjeld, J.G.6
Hallen, J.7
Raastad, T.8
-
30
-
-
77949470763
-
Satellite cell characterization from aging human muscle
-
10.1179/174313209X385725, 20092696
-
Corbu A, Scaramozza A, Badiali-DeGiorgi L, Tarantino L, Papa V, Rinaldi R, D'Alessandro R, Zavatta M, Laus M, Lattanzi G, et al. Satellite cell characterization from aging human muscle. Neurol Res 2010, 32:63-72. 10.1179/174313209X385725, 20092696.
-
(2010)
Neurol Res
, vol.32
, pp. 63-72
-
-
Corbu, A.1
Scaramozza, A.2
Badiali-DeGiorgi, L.3
Tarantino, L.4
Papa, V.5
Rinaldi, R.6
D'Alessandro, R.7
Zavatta, M.8
Laus, M.9
Lattanzi, G.10
-
31
-
-
0019488377
-
Embryonic and foetal myosins in human skeletal muscle. The presence of foetal myosins in duchenne muscular dystrophy and infantile spinal muscular atrophy
-
10.1016/0022-510X(81)90018-6, 7310440
-
Fitzsimons RB, Hoh JF. Embryonic and foetal myosins in human skeletal muscle. The presence of foetal myosins in duchenne muscular dystrophy and infantile spinal muscular atrophy. J Neurol Sci 1981, 52:367-384. 10.1016/0022-510X(81)90018-6, 7310440.
-
(1981)
J Neurol Sci
, vol.52
, pp. 367-384
-
-
Fitzsimons, R.B.1
Hoh, J.F.2
-
32
-
-
0022447078
-
Fetal myosin immunoreactivity in human dystrophic muscle
-
10.1002/mus.880090108, 3513005
-
Schiaffino S, Gorza L, Dones I, Cornelio F, Sartore S. Fetal myosin immunoreactivity in human dystrophic muscle. Muscle Nerve 1986, 9:51-58. 10.1002/mus.880090108, 3513005.
-
(1986)
Muscle Nerve
, vol.9
, pp. 51-58
-
-
Schiaffino, S.1
Gorza, L.2
Dones, I.3
Cornelio, F.4
Sartore, S.5
-
33
-
-
0032722122
-
NCAM, vimentin and neonatal myosin heavy chain expression in human muscle diseases
-
10.1046/j.1365-2990.1999.00178.x, 10564532
-
Winter A, Bornemann A. NCAM, vimentin and neonatal myosin heavy chain expression in human muscle diseases. Neuropathol Appl Neurobiol 1999, 25:417-424. 10.1046/j.1365-2990.1999.00178.x, 10564532.
-
(1999)
Neuropathol Appl Neurobiol
, vol.25
, pp. 417-424
-
-
Winter, A.1
Bornemann, A.2
-
34
-
-
0019966026
-
Fetal myosin heavy chains in regenerating muscle
-
10.1038/298294a0, 7045696
-
Sartore S, Gorza L, Schiaffino S. Fetal myosin heavy chains in regenerating muscle. Nature 1982, 298:294-296. 10.1038/298294a0, 7045696.
-
(1982)
Nature
, vol.298
, pp. 294-296
-
-
Sartore, S.1
Gorza, L.2
Schiaffino, S.3
-
35
-
-
0024585540
-
Myosin heavy chain composition of muscle fibers in spinal muscular atrophy
-
10.1002/mus.880120109, 2664503
-
Biral D, Scarpini E, Angelini C, Salviati G, Margreth A. Myosin heavy chain composition of muscle fibers in spinal muscular atrophy. Muscle Nerve 1989, 12:43-51. 10.1002/mus.880120109, 2664503.
-
(1989)
Muscle Nerve
, vol.12
, pp. 43-51
-
-
Biral, D.1
Scarpini, E.2
Angelini, C.3
Salviati, G.4
Margreth, A.5
-
36
-
-
0032722122
-
NCAM, vimentin and neonatal myosin heavy chain expression in human muscle diseases
-
10.1046/j.1365-2990.1999.00178.x, 10564532
-
Winter A, Bornemann A. NCAM, vimentin and neonatal myosin heavy chain expression in human muscle diseases. Neuropathol Appl Neurobiol 1999, 25:417-424. 10.1046/j.1365-2990.1999.00178.x, 10564532.
-
(1999)
Neuropathol Appl Neurobiol
, vol.25
, pp. 417-424
-
-
Winter, A.1
Bornemann, A.2
-
37
-
-
0022447078
-
Fetal myosin immunoreactivity in human dystrophic muscle
-
10.1002/mus.880090108, 3513005
-
Schiaffino S, Gorza L, Dones I, Cornelio F, Sartore S. Fetal myosin immunoreactivity in human dystrophic muscle. Muscle Nerve 1986, 9:51-58. 10.1002/mus.880090108, 3513005.
-
(1986)
Muscle Nerve
, vol.9
, pp. 51-58
-
-
Schiaffino, S.1
Gorza, L.2
Dones, I.3
Cornelio, F.4
Sartore, S.5
-
38
-
-
0026805782
-
Identification of skeletal muscle precursor cells in vivo by use of MyoD1 and myogenin probes
-
10.1007/BF00318695, 1310442
-
Grounds MD, Garrett KL, Lai MC, Wright WE, Beilharz MW. Identification of skeletal muscle precursor cells in vivo by use of MyoD1 and myogenin probes. Cell Tissue Res 1992, 267:99-104. 10.1007/BF00318695, 1310442.
-
(1992)
Cell Tissue Res
, vol.267
, pp. 99-104
-
-
Grounds, M.D.1
Garrett, K.L.2
Lai, M.C.3
Wright, W.E.4
Beilharz, M.W.5
-
39
-
-
0030839605
-
Myogenic regulatory factors during regeneration of skeletal muscle in young, adult, and old rats
-
Marsh DR, Criswell DS, Carson JA, Booth FW. Myogenic regulatory factors during regeneration of skeletal muscle in young, adult, and old rats. J Appl Physiol 1997, 83:1270-1275.
-
(1997)
J Appl Physiol
, vol.83
, pp. 1270-1275
-
-
Marsh, D.R.1
Criswell, D.S.2
Carson, J.A.3
Booth, F.W.4
-
40
-
-
24044503385
-
L-arginine improves dystrophic phenotype in mdx mice
-
10.1016/j.nbd.2005.02.010, 16137573
-
Voisin V, Sebrie C, Matecki S, Yu H, Gillet B, Ramonatxo M, Israel M, De la PS. L-arginine improves dystrophic phenotype in mdx mice. Neurobiol Dis 2005, 20:123-130. 10.1016/j.nbd.2005.02.010, 16137573.
-
(2005)
Neurobiol Dis
, vol.20
, pp. 123-130
-
-
Voisin, V.1
Sebrie, C.2
Matecki, S.3
Yu, H.4
Gillet, B.5
Ramonatxo, M.6
Israel, M.7
De la, P.S.8
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