-
1
-
-
0029731663
-
Structure-function analysis of the motor domain of myosin
-
Ruppel KM, Spudich JA. Structure-function analysis of the motor domain of myosin. Annu Rev Cell Dev Biol 1996;12: 543-573.
-
(1996)
Annu Rev Cell Dev Biol
, vol.12
, pp. 543-573
-
-
Ruppel, K.M.1
Spudich, J.A.2
-
2
-
-
0025653451
-
Cellular and molecular diversities of mammalian skeletal muscle fibers
-
Pette D, Staron RS. Cellular and molecular diversities of mammalian skeletal muscle fibers. Rev Physiol Biochem Pharmacol 1990;116:1-76.
-
(1990)
Rev Physiol Biochem Pharmacol
, vol.116
, pp. 1-76
-
-
Pette, D.1
Staron, R.S.2
-
3
-
-
0034687697
-
Autosomal dominant myopathy: Missense mutation (Glu-706 → Lys) in the myosin heavy chain IIa gene
-
Martinsson T, Oldfors A, Darin N, et al. Autosomal dominant myopathy: missense mutation (Glu-706 → Lys) in the myosin heavy chain IIa gene. Proc Natl Acad Sci USA 2000;97: 14614-14619.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 14614-14619
-
-
Martinsson, T.1
Oldfors, A.2
Darin, N.3
-
4
-
-
0141535360
-
Myosin storage myopathy associated with a heterozygous missense mutation in MYH7
-
Tajsharghi H, Thornell LE, Lindberg C, et al. Myosin storage myopathy associated with a heterozygous missense mutation in MYH7. Ann Neurol 2003;54:494-500.
-
(2003)
Ann Neurol
, vol.54
, pp. 494-500
-
-
Tajsharghi, H.1
Thornell, L.E.2
Lindberg, C.3
-
5
-
-
4544374719
-
Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause Laing early-onset distal myopathy (MPD1)
-
Meredith C, Herrmann R, Parry C, et al. Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause Laing early-onset distal myopathy (MPD1). Am J Hum Genet 2004;75:703-708.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 703-708
-
-
Meredith, C.1
Herrmann, R.2
Parry, C.3
-
6
-
-
0031830345
-
Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles
-
Darin N, Kyllerman M, Wahlstrom J, et al. Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles. Ann Neurol 1998;44:242-248.
-
(1998)
Ann Neurol
, vol.44
, pp. 242-248
-
-
Darin, N.1
Kyllerman, M.2
Wahlstrom, J.3
-
7
-
-
0037066098
-
Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age
-
Tajsharghi H, Thornell LE, Darin N, et al. Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age. Neurology 2002;58:780-786.
-
(2002)
Neurology
, vol.58
, pp. 780-786
-
-
Tajsharghi, H.1
Thornell, L.E.2
Darin, N.3
-
8
-
-
0031768071
-
Sporadic inclusion-body myositis and hereditary inclusion-body myopathies: Current concepts of diagnosis and pathogenesis
-
Askanas V, Engel WK. Sporadic inclusion-body myositis and hereditary inclusion-body myopathies: current concepts of diagnosis and pathogenesis. Curr Opin Rheumatol 1998;10:530-542.
-
(1998)
Curr Opin Rheumatol
, vol.10
, pp. 530-542
-
-
Askanas, V.1
Engel, W.K.2
-
9
-
-
0000372029
-
Muscle: Structure, function, and development
-
Priess JR, ed. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press
-
Moerman DG, Fire A. Muscle: structure, function, and development. In: Priess JR, ed. C. elegans II. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press, 1997:417-470.
-
(1997)
C. Elegans II
, pp. 417-470
-
-
Moerman, D.G.1
Fire, A.2
-
10
-
-
0000182225
-
Methods
-
Wood WB, ed. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory
-
Sulston JE, Hodgkin JA. Methods. In: Wood WB, ed. The nematode Caenorhabditis elegans. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory, 1988:587-606.
-
(1988)
The Nematode Caenorhabditis Elegans
, pp. 587-606
-
-
Sulston, J.E.1
Hodgkin, J.A.2
-
11
-
-
0027451263
-
Sequence requirements for myosin gene expression and regulation in Caenorhabditis elegans
-
Okkema PG, Harrison SW, Plunger V, et al. Sequence requirements for myosin gene expression and regulation in Caenorhabditis elegans. Genetics 1993;135:385-404.
-
(1993)
Genetics
, vol.135
, pp. 385-404
-
-
Okkema, P.G.1
Harrison, S.W.2
Plunger, V.3
-
12
-
-
0021878067
-
Sequence analysis of mutations that affect the synthesis, assembly and enzymatic activity of the unc-54 myosin heavy chain of Caenorhabditis elegans
-
Dibb NJ, Brown DM, Karn J, et al. Sequence analysis of mutations that affect the synthesis, assembly and enzymatic activity of the unc-54 myosin heavy chain of Caenorhabditis elegans. J Mol Biol 1985;183:543-551.
-
(1985)
J Mol Biol
, vol.183
, pp. 543-551
-
-
Dibb, N.J.1
Brown, D.M.2
Karn, J.3
-
13
-
-
0016063911
-
The genetics of Caenorhabditis elegans
-
Brenner S. The genetics of Caenorhabditis elegans. Genetics 1974;77:71-94.
-
(1974)
Genetics
, vol.77
, pp. 71-94
-
-
Brenner, S.1
-
15
-
-
0033787336
-
The diabetes autoantigen ICA69 and its Caenorhabditis elegans homologue, ric-19, are conserved regulators of neuroendocrine secretion
-
Pilon M, Peng XR, Spence AM, et al. The diabetes autoantigen ICA69 and its Caenorhabditis elegans homologue, ric-19, are conserved regulators of neuroendocrine secretion. Mol Biol Cell 2000;11:3277-3288.
-
(2000)
Mol Biol Cell
, vol.11
, pp. 3277-3288
-
-
Pilon, M.1
Peng, X.R.2
Spence, A.M.3
-
16
-
-
0000823299
-
Muscle
-
Wood WB, ed. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press
-
Waterston RH. Muscle. In: Wood WB, ed. The Nematode Caenorhabditis elegans. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press, 1988:281-335.
-
(1988)
The Nematode Caenorhabditis Elegans
, pp. 281-335
-
-
Waterston, R.H.1
-
17
-
-
13444292382
-
Dynamics of actomyosin interactions in relation to the cross-bridge cycle
-
Zeng W, Conibear PB, Dickens JL, et al. Dynamics of actomyosin interactions in relation to the cross-bridge cycle. Philos Trans R Soc Lond B Biol Sci 2004;359:1843-1855.
-
(2004)
Philos Trans R Soc Lond B Biol Sci
, vol.359
, pp. 1843-1855
-
-
Zeng, W.1
Conibear, P.B.2
Dickens, J.L.3
-
18
-
-
0034597588
-
Muscular dystrophy: The worm turns to genetic disease
-
Chamberlain JS, Benian GM. Muscular dystrophy: the worm turns to genetic disease. Curr Biol 2000;10:R795-R797.
-
(2000)
Curr Biol
, vol.10
-
-
Chamberlain, J.S.1
Benian, G.M.2
|