-
1
-
-
46649093386
-
Developmental expression of the alpha-skeletal actin gene
-
Bertola, L.D., E.B. Ott, S. Griepsma, F.J. Vonk, and C.P. Bagowski. 2008. Developmental expression of the alpha-skeletal actin gene. BMC Evol. Biol. 8:166.
-
(2008)
BMC Evol. Biol.
, vol.8
, pp. 166
-
-
Bertola, L.D.1
Ott, E.B.2
Griepsma, S.3
Vonk, F.J.4
Bagowski, C.P.5
-
2
-
-
0027476102
-
Quantitative analysis of the human α-skeletal actin gene in transgenic mice
-
Brennan, K.J., and E.C. Hardeman. 1993. Quantitative analysis of the human alpha-skeletal actin gene in transgenic mice. J. Biol. Chem. 268:719-725. (Pubitemid 23021382)
-
(1993)
Journal of Biological Chemistry
, vol.268
, Issue.1
, pp. 719-725
-
-
Brennan, K.J.1
Hardeman, E.C.2
-
3
-
-
4444305799
-
Histological parameters for the quantitative assessment of muscular dystrophy in the mdx-mouse
-
DOI 10.1016/j.nmd.2004.06.008, PII S0960896604001750
-
Briguet, A., I. Courdier-Fruh, M. Foster, T. Meier, and J.P. Magyar. 2004. Histological parameters for the quantitative assessment of muscular dystrophy in the mdx-mouse. Neuromuscul. Disord. 14:675-682. (Pubitemid 39194668)
-
(2004)
Neuromuscular Disorders
, vol.14
, Issue.10
, pp. 675-682
-
-
Briguet, A.1
Courdier-Fruh, I.2
Foster, M.3
Meier, T.4
Magyar, J.P.5
-
4
-
-
23744475805
-
Different effects of cardiac versus skeletal muscle regulatory proteins on in vitro measures of actin filament speed and force
-
DOI 10.1113/jphysiol.2005.084194
-
Clemmens, E.W., M. Entezari, D.A. Martyn, and M. Regnier. 2005. Different effects of cardiac versus skeletal muscle regulatory proteins on in vitro measures of actin filament speed and force. J. Physiol. 566:737-746. (Pubitemid 41122657)
-
(2005)
Journal of Physiology
, vol.566
, Issue.3
, pp. 737-746
-
-
Clemmens, E.W.1
Entezari, M.2
Martyn, D.A.3
Regnier, M.4
-
5
-
-
0035864823
-
slow affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathy
-
Corbett, M.A., C.S. Robinson, G.F. Dunglison, N. Yang, J.E. Joya, A.W. Stewart, C. Schnell, P.W. Gunning, K.N. North, and E.C. Hardeman. 2001. A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathy. Hum. Mol. Genet. 10:317-328. (Pubitemid 32166543)
-
(2001)
Human Molecular Genetics
, vol.10
, Issue.4
, pp. 317-328
-
-
Corbett, M.A.1
Robinson, C.S.2
Dunglison, G.F.3
Yang, N.4
Joya, J.E.5
Stewart, A.W.6
Schnell, C.7
Gunning, P.W.8
North, K.N.9
Hardeman, E.C.10
-
6
-
-
0028239920
-
Structure and expression of the human slow twitch skeletal muscle troponin I gene
-
Corin, S.J., O. Juhasz, L. Zhu, P. Conley, L. Kedes, and R. Wade. 1994. Structure and expression of the human slow twitch skeletal muscle troponin I gene. J. Biol. Chem. 269:10651-10659. (Pubitemid 24198270)
-
(1994)
Journal of Biological Chemistry
, vol.269
, Issue.14
, pp. 10651-10659
-
-
Corin, S.J.1
Juhasz, O.2
Zhu, L.3
Conley, P.4
Kedes, L.5
Wade, R.6
-
7
-
-
0036311912
-
Mice lacking skeletal muscle actin show reduced muscle strength and growth deficits and die during the neonatal period
-
DOI 10.1128/MCB.22.16.5887-5896.2002
-
Crawford, K., R. Flick, L. Close, D. Shelly, R. Paul, K. Bove, A. Kumar, and J. Lessard. 2002. Mice lacking skeletal muscle actin show reduced muscle strength and growth deficits and die during the neonatal period. Mol. Cell. Biol. 22:5887-5896. (Pubitemid 34815837)
-
(2002)
Molecular and Cellular Biology
, vol.22
, Issue.16
, pp. 5887-5896
-
-
Crawford, K.1
Flick, R.2
Close, L.3
Shelly, D.4
Paul, R.5
Bove, K.6
Kumar, A.7
Lessard, J.8
-
10
-
-
34347236921
-
Organelle isolation: Functional mitochondria from mouse liver, muscle and cultured filroblasts
-
DOI 10.1038/nprot.2006.478, PII NPROT.2006.478
-
Frezza, C., S. Cipolat, and L. Scorrano. 2007. Organelle isolation: functional mitochondria from mouse liver, muscle and cultured fibroblasts. Nat. Protoc. 2:287-295. (Pubitemid 47040043)
-
(2007)
Nature Protocols
, vol.2
, Issue.2
, pp. 287-295
-
-
Frezza, C.1
Cipolat, S.2
Scorrano, L.3
-
11
-
-
10044275521
-
Skeletal muscle pathology in endurance athletes with acquired training intolerance
-
DOI 10.1136/bjsm.2003.006502
-
Grobler, L.A., M. Collins, M.I. Lambert, C. Sinclair-Smith, W. Derman, A. St Clair Gibson, and T.D. Noakes. 2004. Skeletal muscle pathology in endurance athletes with acquired training intolerance. Br. J. Sports Med. 38:697-703. (Pubitemid 39611549)
-
(2004)
British Journal of Sports Medicine
, vol.38
, Issue.6
, pp. 697-703
-
-
Grobler, L.A.1
Collins, M.2
Lambert, M.I.3
Sinclair-Smith, C.4
Derman, W.5
St Clair Gibson, A.6
Noakes, T.D.7
-
12
-
-
36549071997
-
Mutations in smooth muscle α-actin (ACTA2) lead to thoracic aortic aneurysms and dissections
-
DOI 10.1038/ng.2007.6, PII NG20076
-
Guo, D.C., H. Pannu, V. Tran-Fadulu, C.L. Papke, R.K. Yu, N. Avidan, S. Bourgeois, A.L. Estrera, H.J. Safi, E. Sparks, et al. 2007. Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections. Nat. Genet. 39:1488-1493. (Pubitemid 350191352)
-
(2007)
Nature Genetics
, vol.39
, Issue.12
, pp. 1488-1493
-
-
Guo, D.-C.1
Pannu, H.2
Tran-Fadulu, V.3
Papke, C.L.4
Yu, R.K.5
Avidan, N.6
Bourgeois, S.7
Estrera, A.L.8
Safi, H.J.9
Sparks, E.10
Amor, D.11
Ades, L.12
McConnell, V.13
Willoughby, C.E.14
Abuelo, D.15
Willing, M.16
Lewis, R.A.17
Kim, D.H.18
Scherer, S.19
Tung, P.P.20
Ahn, C.21
Buja, L.M.22
Raman, C.S.23
Shete, S.S.24
Milewicz, D.M.25
more..
-
13
-
-
0037331148
-
The effect of chelerythrine on depolarization-induced force responses in skinned fast skeletal muscle fibres of the rat
-
DOI 10.1038/sj.bjp.0705035
-
Han, R., and A.J. Bakker. 2003. The effect of chelerythrine on depolarization-induced force responses in skinned fast skeletal muscle fibres of the rat. Br. J. Pharmacol. 138:417-426. (Pubitemid 36269482)
-
(2003)
British Journal of Pharmacology
, vol.138
, Issue.3
, pp. 417-426
-
-
Han, R.1
Bakker, A.J.2
-
14
-
-
0028178197
-
α-Skeletal actin is associated with increased contractility in the mouse heart
-
Hewett, T.E., I.L. Grupp, G. Grupp, and J. Robbins. 1994. Alpha-skeletal actin is associated with increased contractility in the mouse heart. Circ. Res. 74:740-746. (Pubitemid 24088534)
-
(1994)
Circulation Research
, vol.74
, Issue.4
, pp. 740-746
-
-
Hewett, T.E.1
Grupp, I.L.2
Grupp, G.3
Robbins, J.4
-
15
-
-
28244446353
-
Defining α-skeletal and α-cardiac actin expression in human heart and skeletal muscle explains the absence of cardiac involvement in ACTA1 nemaline myopathy
-
DOI 10.1016/j.nmd.2005.08.004, PII S0960896605002531
-
Ilkovski, B., S. Clement, C. Sewry, K.N. North, and S.T. Cooper. 2005. Defining alpha-skeletal and alpha-cardiac actin expression in human heart and skeletal muscle explains the absence of cardiac involvement in ACTA1 nemaline myopathy. Neuromuscul. Disord. 15:829-835. (Pubitemid 41713137)
-
(2005)
Neuromuscular Disorders
, vol.15
, Issue.12
, pp. 829-835
-
-
Ilkovski, B.1
Clement, S.2
Sewry, C.3
North, K.N.4
Cooper, S.T.5
-
16
-
-
15544374741
-
E-Sarcoglycan compensates for lack of α-sarcoglycan in a mouse model of limb-girdle muscular dystrophy
-
DOI 10.1093/hmg/ddi072
-
Imamura, M., Y. Mochizuki, E. Engvall, and S. Takeda. 2005. Epsilon-sarcoglycan compensates for lack of alpha-sarcoglycan in a mouse model of limb-girdle muscular dystrophy. Hum. Mol. Genet. 14:775-783. (Pubitemid 40403274)
-
(2005)
Human Molecular Genetics
, vol.14
, Issue.6
, pp. 775-783
-
-
Imamura, M.1
Mochizuki, Y.2
Engvall, E.3
Takeda, S.4
-
17
-
-
36649009131
-
Novel application of flow cytometry: Determination of muscle fiber types and protein levels in whole murine skeletal muscles and heart
-
DOI 10.1002/cm.20239
-
Jackaman, C., K.J. Nowak, G. Ravenscroft, E.M. Lim, S. Clement, and N.G. Laing. 2007. Novel application of flow cytometry: determination of muscle fiber types and protein levels in whole murine skeletal muscles and heart. Cell Motil. Cytoskeleton. 64:914-925. (Pubitemid 350197279)
-
(2007)
Cell Motility and the Cytoskeleton
, vol.64
, Issue.12
, pp. 914-925
-
-
Jackaman, C.1
Nowak, K.J.2
Ravenscroft, G.3
Lim, E.M.4
Clement, S.5
Laing, N.G.6
-
18
-
-
68549121081
-
Context-dependent functional substitution of (alpha)-skeletal actin by (gamma)-cytoplasmic actin
-
doi:10.1096/fj.09-129783
-
Jaeger, M.A., K.J. Sonnemann, D.P. Fitzsimons, K.W. Prins, and J.M. Ervasti. 2009. Context-dependent functional substitution of (alpha)-skeletal actin by (gamma)-cytoplasmic actin. FASEB J. doi:10.1096/fj.09-129783.
-
(2009)
FASEB J.
-
-
Jaeger, M.A.1
Sonnemann, K.J.2
Fitzsimons, D.P.3
Prins, K.W.4
Ervasti, J.M.5
-
19
-
-
8744305686
-
Missense mutations of ACTA1 cause dominant congenital myopathy with cores
-
DOI 10.1136/jmg.2004.020271
-
Kaindl, A.M., F. Ruschendorf, S. Krause, H.H. Goebel, K. Koehler, C. Becker, D. Pongratz, J. Muller-Hocker, P. Nurnberg, G. Stoltenburg-Didinger, et al. 2004. Missense mutations of ACTA1 cause dominant congenital myopathy with cores. J. Med. Genet. 41:842-848. (Pubitemid 39524311)
-
(2004)
Journal of Medical Genetics
, vol.41
, Issue.11
, pp. 842-848
-
-
Kaindl, A.M.1
Ruschendorf, F.2
Krause, S.3
Goebel, H.-H.4
Koehler, K.5
Becker, C.6
Pongratz, D.7
Muller-Hocker, J.8
Nurnberg, P.9
Stoltenburg-Didinger, G.10
Lochmuller, H.11
Huebner, A.12
-
20
-
-
0031001970
-
Rescue of cardiac α-actin-deficient mice by enteric smooth muscle γ- Actin
-
DOI 10.1073/pnas.94.9.4406
-
Kumar, A., K. Crawford, L. Close, M. Madison, J. Lorenz, T. Doetschman, S. Pawlowski, J. Duffy, J. Neumann, J. Robbins, et al. 1997. Rescue of cardiac alpha-actin-deficient mice by enteric smooth muscle gamma-actin. Proc. Natl. Acad. Sci. USA. 94:4406-4411. (Pubitemid 27194254)
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, Issue.9
, pp. 4406-4411
-
-
Kumar, A.1
Crawford, K.2
Close, L.3
Madison, M.4
Lorenz, J.5
Doetschman, T.6
Pawlowski, S.7
Duffy, J.8
Neumann, J.9
Robbins, J.10
Boivin, G.P.11
O'Toole, B.A.12
Lessard, J.L.13
-
21
-
-
18244383309
-
Transgenic overexpression of cardiac actin in the mouse heart suggests coregulation of cardiac, skeletal and vascular actin expression
-
Kumar, A., K. Crawford, R. Flick, R. Klevitsky, J.N. Lorenz, K.E. Bove, J. Robbins, and J.L. Lessard. 2004. Transgenic overexpression of cardiac actin in the mouse heart suggests coregulation of cardiac, skeletal and vascular actin expression. Transgenic Res. 13:531-540.
-
(2004)
Transgenic Res.
, vol.13
, pp. 531-540
-
-
Kumar, A.1
Crawford, K.2
Flick, R.3
Klevitsky, R.4
Lorenz, J.N.5
Bove, K.E.6
Robbins, J.7
Lessard, J.L.8
-
22
-
-
9144245756
-
Actin mutations are one cause of congenital fibre type disproportion
-
DOI 10.1002/ana.20260
-
Laing, N.G., N.F. Clarke, D.E. Dye, K. Liyanage, K.R. Walker, Y. Kobayashi, S. Shimakawa, T. Hagiwara, R. Ouvrier, J.C. Sparrow, et al. 2004. Actin mutations are one cause of congenital fibre type disproportion. Ann. Neurol. 56:689-694. (Pubitemid 39540749)
-
(2004)
Annals of Neurology
, vol.56
, Issue.5
, pp. 689-694
-
-
Laing, N.G.1
Clarke, N.F.2
Dye, D.E.3
Liyanage, K.4
Walker, K.R.5
Kobayashi, Y.6
Shimakawa, S.7
Hagiwara, T.8
Ouvrier, R.9
Sparrow, J.C.10
Nishino, I.11
North, K.N.12
Nonaka, I.13
-
23
-
-
0027934071
-
Passive and active tension in single cardiac myofibrils
-
Linke, W.A., V.I. Popov, and G.H. Pollack. 1994. Passive and active tension in single cardiac myofibrils. Biophys. J. 67:782-792. (Pubitemid 24235407)
-
(1994)
Biophysical Journal
, vol.67
, Issue.2
, pp. 782-792
-
-
Linke, W.A.1
Popov, V.I.2
Pollack, G.H.3
-
24
-
-
18744433901
-
α-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy
-
Mogensen, J., I.C. Klausen, A.K. Pedersen, H. Egeblad, P. Bross, T.A. Kruse, N. Gregersen, P.S. Hansen, U. Baandrup, and A.D. Borglum. 1999. Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy. J. Clin. Invest. 103:R39-R43. (Pubitemid 29535504)
-
(1999)
Journal of Clinical Investigation
, vol.103
, Issue.10
-
-
Mogensen, J.1
Klausen, I.C.2
Pedersen, A.K.3
Egeblad, H.4
Bross, P.5
Kruse, T.A.6
Gregersen, N.7
Hansen, P.S.8
Baandrup, U.9
Borglum, A.D.10
-
25
-
-
0022403599
-
Identification of amino acid substitutions differentiating actin isoforms in their interaction with myosin
-
DOI 10.1111/j.1432-1033.1985.tb09313.x
-
Mossakowska, M., and H. Strzelecka-Golaszewska. 1985. Identification of amino acid substitutions differentiating actin isoforms in their interaction with myosin. Eur. J. Biochem. 153:373-381. (Pubitemid 16209839)
-
(1985)
European Journal of Biochemistry
, vol.153
, Issue.2
, pp. 373-381
-
-
Mossakowska, M.1
Strzelecka-Golaszewska, H.2
-
26
-
-
60549108053
-
Therapeutic approaches for the sarcomeric protein diseases
-
N.G. Laing, editor. Landes Bioscience, Austin, TX
-
Nowak, K.J. 2008. Therapeutic approaches for the sarcomeric protein diseases. In The Sarcomere and Skeletal Muscle Disease. vol.642. N.G. Laing, editor. Landes Bioscience, Austin, TX. 207-223.
-
(2008)
The Sarcomere and Skeletal Muscle Disease
, vol.642
, pp. 207-223
-
-
Nowak, K.J.1
-
27
-
-
16644402070
-
Duchenne muscular dystrophy and dystrophin: Pathogenesis and opportunities for treatment
-
Nowak, K.J., and K.E. Davies. 2004. Duchenne muscular dystrophy and dystrophin: pathogenesis and opportunities for treatment. EMBO Rep. 5:872-876.
-
(2004)
EMBO Rep.
, vol.5
, pp. 872-876
-
-
Nowak, K.J.1
Davies, K.E.2
-
28
-
-
0032858915
-
Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy
-
DOI 10.1038/13837
-
Nowak, K.J., D. Wattanasirichaigoon, H.H. Goebel, M. Wilce, K. Pelin, K. Donner, R.L. Jacob, C. Hubner, K. Oexle, J.R. Anderson, et al. 1999. Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy. Nat. Genet. 23:208-212. (Pubitemid 29455395)
-
(1999)
Nature Genetics
, vol.23
, Issue.2
, pp. 208-212
-
-
Nowak, K.J.1
Wattanasirichaigoon, D.2
Goebel, H.H.3
Wilce, M.4
Pelin, K.5
Donner, K.6
Jacob, R.L.7
Hubner, C.8
Oexle, K.9
Anderson, J.R.10
Verity, C.M.11
North, K.N.12
Iannaccone, S.T.13
Muller, C.R.14
Nurnberg, P.15
Muntoni, F.16
Sewry, C.17
Hughes, I.18
Sutphen, R.19
Lacson, A.G.20
Swoboda, K.J.21
Vigneron, J.22
Wallgren-Pettersson, C.23
Beggs, A.H.24
Laing, N.G.25
more..
-
29
-
-
33847623295
-
Nemaline myopathy caused by absence of α-skeletal muscle actin
-
DOI 10.1002/ana.21035
-
Nowak, K.J., C.A. Sewry, C. Navarro, W. Squier, C. Reina, J.R. Ricoy, S.S. Jayawant, A.M. Childs, J.A. Dobbie, R.E. Appleton, et al. 2007. Nemaline myopathy caused by absence of alpha-skeletal muscle actin. Ann. Neurol. 61:175-184. (Pubitemid 46363844)
-
(2007)
Annals of Neurology
, vol.61
, Issue.2
, pp. 175-184
-
-
Nowak, K.J.1
Sewry, C.A.2
Navarro, C.3
Squier, W.4
Reina, C.5
Ricoy, J.R.6
Jayawant, S.S.7
Childs, A.-M.8
Dobbie, J.A.9
Appleton, R.E.10
Mountford, R.C.11
Walker, K.R.12
Clement, S.13
Barois, A.14
Muntoni, F.15
Romero, N.B.16
Laing, N.G.17
-
30
-
-
0033587759
-
A heterozygous mutation of β-actin associated with neutrophil dysfunction and recurrent infection
-
DOI 10.1073/pnas.96.15.8693
-
Nunoi, H., T. Yamazaki, H. Tsuchiya, S. Kato, H.L. Malech, I. Matsuda, and S. Kanegasaki. 1999. A heterozygous mutation of beta-actin associated with neutrophil dysfunction and recurrent infection. Proc. Natl. Acad. Sci. USA. 96:8693-8698. (Pubitemid 29354853)
-
(1999)
Proceedings of the National Academy of Sciences of the United States of America
, vol.96
, Issue.15
, pp. 8693-8698
-
-
Nunoi, H.1
Yamazaki, T.2
Tsuchiya, H.3
Kato, S.4
Malech, H.L.5
Matsuda, I.6
Kanegasaki, S.7
-
31
-
-
0032076955
-
Actin mutations in dilated cardiomyopathy, a heritable form of heart failure
-
DOI 10.1126/science.280.5364.750
-
Olson, T.M., V.V. Michels, S.N. Thibodeau, Y.S. Tai, and M.T. Keating. 1998. Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science. 280:750-752. (Pubitemid 28243352)
-
(1998)
Science
, vol.280
, Issue.5364
, pp. 750-752
-
-
Olson, T.M.1
Michels, V.V.2
Thibodeau, S.N.3
Tai, Y.-S.4
Keating, M.T.5
-
32
-
-
0023013586
-
The skeletal and cardiac α-actin genes are coexpressed in early embryonic striated muscle
-
DOI 10.1016/0012-1606(86)90315-5
-
Ordahl, C.P. 1986. The skeletal and cardiac alpha-actin genes are coexpressed in early embryonic striated muscle. Dev. Biol. 117:488-492. (Pubitemid 17170361)
-
(1986)
Developmental Biology
, vol.117
, Issue.2
, pp. 488-492
-
-
Ordahl, C.P.1
-
33
-
-
56149099711
-
Sarcospan reduces dystrophic pathology: Stabilization of the utrophin-glycoprotein complex
-
Peter, A.K., J.L. Marshall, and R.H. Crosbie. 2008. Sarcospan reduces dystrophic pathology: stabilization of the utrophin-glycoprotein complex. J. Cell Biol. 183:419-427.
-
(2008)
J. Cell Biol.
, vol.183
, pp. 419-427
-
-
Peter, A.K.1
Marshall, J.L.2
Crosbie, R.H.3
-
34
-
-
33646873916
-
A mutation of β-actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia
-
DOI 10.1086/504271
-
Procaccio, V., G. Salazar, S. Ono, M.L. Styers, M. Gearing, A. Davila, R. Jimenez, J. Juncos, C.A. Gutekunst, G. Meroni, et al. 2006. A mutation of beta-actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia. Am. J. Hum. Genet. 78:947-960. (Pubitemid 43787687)
-
(2006)
American Journal of Human Genetics
, vol.78
, Issue.6
, pp. 947-960
-
-
Procaccio, V.1
Salazar, G.2
Ono, S.3
Styers, M.L.4
Gearing, M.5
Davila, A.6
Jimenez, R.7
Juncos, J.8
Gutekunst, C.-A.9
Meroni, G.10
Fontanella, B.11
Sontag, E.12
Sontag, J.M.13
Faundez, V.14
Wainer, B.H.15
-
35
-
-
56949105123
-
Expression of cardiac alpha-actin spares extraocular muscles in skeletal muscle alpha-actin diseases - Quantification of striated alpha-actins by MRM-mass spectrometry
-
Ravenscroft, G., S.M. Colley, K.R. Walker, S. Clement, S. Bringans, R. Lipscombe, V. Fabian, N.G. Laing, and K.J. Nowak. 2008. Expression of cardiac alpha-actin spares extraocular muscles in skeletal muscle alpha-actin diseases - quantification of striated alpha-actins by MRM-mass spectrometry. Neuromuscul. Disord. 18:953-958.
-
(2008)
Neuromuscul. Disord.
, vol.18
, pp. 953-958
-
-
Ravenscroft, G.1
Colley, S.M.2
Walker, K.R.3
Clement, S.4
Bringans, S.5
Lipscombe, R.6
Fabian, V.7
Laing, N.G.8
Nowak, K.J.9
-
36
-
-
0025457288
-
The functional importance of multiple actin isoforms
-
Rubenstein, P.A. 1990. The functional importance of multiple actin isoforms. Bioessays. 12:309-315. (Pubitemid 120034469)
-
(1990)
BioEssays
, vol.12
, Issue.7
, pp. 309-315
-
-
Rubenstein, P.A.1
-
38
-
-
0042160140
-
Molecular regulation of individual skeletal muscle fibre types
-
DOI 10.1046/j.1365-201X.2003.01158.x
-
Spangenburg, E.E., and F.W. Booth. 2003. Molecular regulation of individual skeletal muscle fibre types. Acta Physiol. Scand. 178:413-424. (Pubitemid 36960433)
-
(2003)
Acta Physiologica Scandinavica
, vol.178
, Issue.4
, pp. 413-424
-
-
Spangenburg, E.E.1
Booth, F.W.2
-
39
-
-
0042071493
-
Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1)
-
DOI 10.1016/S0960-8966(03)00101-9
-
Sparrow, J.C., K.J. Nowak, H.J. Durling, A.H. Beggs, C. Wallgren-Pettersson, N. Romero, I. Nonaka, and N.G. Laing. 2003. Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1). Neuromuscul. Disord. 13:519-531. (Pubitemid 36961341)
-
(2003)
Neuromuscular Disorders
, vol.13
, Issue.7-8
, pp. 519-531
-
-
Sparrow, J.C.1
Nowak, K.J.2
Durling, H.J.3
Beggs, A.H.4
Wallgren-Pettersson, C.5
Romero, N.6
Nonaka, I.7
Laing, N.G.8
-
40
-
-
0029906168
-
Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene
-
DOI 10.1038/384349a0
-
Tinsley, J.M., A.C. Potter, S.R. Phelps, R. Fisher, J.I. Trickett, and K.E. Davies. 1996. Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene. Nature. 384:349-353. (Pubitemid 26408514)
-
(1996)
Nature
, vol.384
, Issue.6607
, 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
-
41
-
-
0031727771
-
Expression of full-length utrophin prevents muscular dystrophy in mdx mice
-
DOI 10.1038/4033
-
Tinsley, J., N. Deconinck, R. Fisher, D. Kahn, S. Phelps, J.M. Gillis, and K. Davies. 1998. Expression of full-length utrophin prevents muscular dystrophy in mdx mice. Nat. Med. 4:1441-1444. (Pubitemid 28553471)
-
(1998)
Nature Medicine
, vol.4
, Issue.12
, 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
-
42
-
-
0018276994
-
At least six different actins are expressed in a higher mammal: An analysis based on the amino acid sequence of the amino-terminal tryptic peptide
-
Vandekerckhove, J., and K. Weber. 1978. At least six different actins are expressed in a higher mammal: an analysis based on the amino acid sequence of the amino-terminal tryptic peptide. J. Mol. Biol. 126:783-802.
-
(1978)
J. Mol. Biol.
, vol.126
, pp. 783-802
-
-
Vandekerckhove, J.1
Weber, K.2
-
43
-
-
0022974690
-
Simultaneous expression of skeletal muscle and heart actin proteins in various striated muscle tissues and cells. a quantitative determination of the two actin isoforms
-
Vandekerckhove, J., G. Bugaisky, and M. Buckingham. 1986. Simultaneous expression of skeletal muscle and heart actin proteins in various striated muscle tissues and cells. A quantitative determination of the two actin isoforms. J. Biol. Chem. 261:1838-1843. (Pubitemid 17205023)
-
(1986)
Journal of Biological Chemistry
, vol.261
, Issue.4
, pp. 1838-1843
-
-
Vandekerckhove, J.1
Bugaisky, G.2
Buckingham, M.3
-
44
-
-
4344649461
-
Genotype-phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle α-actin
-
DOI 10.1016/j.nmd.2004.03.006, PII S0960896604000872
-
Wallgren-Pettersson, C., K. Pelin, K.J. Nowak, F. Muntoni, N.B. Romero, H.H. Goebel, K.N. North, A.H. Beggs, and N.G. Laing. 2004. Genotype-phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle alpha-actin. Neuromuscul. Disord. 14:461-470. (Pubitemid 39141700)
-
(2004)
Neuromuscular Disorders
, vol.14
, Issue.8-9
, pp. 461-470
-
-
Wallgren-Pettersson, C.1
Pelin, K.2
Nowak, K.J.3
Muntoni, F.4
Romero, N.B.5
Goebel, H.H.6
North, K.N.7
Beggs, A.H.8
Laing, N.G.9
-
45
-
-
0242607215
-
Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26)
-
DOI 10.1086/379286
-
Zhu, M., T. Yang, S. Wei, A.T. DeWan, R.J. Morell, J.L. Elfenbein, R.A. Fisher, S.M. Leal, R.J. Smith, and K.H. Friderici. 2003. Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26). Am. J. Hum. Genet. 73:1082-1091. (Pubitemid 37414221)
-
(2003)
American Journal of Human Genetics
, vol.73
, Issue.5
, pp. 1082-1091
-
-
Zhu, M.1
Yang, T.2
Wei, S.3
Dewan, A.T.4
Morell, R.J.5
Elfenbein, J.L.6
Fisher, R.A.7
Leal, S.M.8
Smith, R.J.H.9
Friderici, K.H.10
|