-
1
-
-
0242607215
-
Mutations in the γ-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26)
-
Zhu M., Yang T., Wei S., et al. Mutations in the γ-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26). Am J Hum Genet 2003, 73:1082-1091.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 1082-1091
-
-
Zhu, M.1
Yang, T.2
Wei, S.3
-
2
-
-
1642503807
-
A mutation in the γ actin gene 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)
-
van Wijk E., Kreiger E., Kemperman M.H., et al. A mutation in the γ actin gene 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26). J Med Genet 2003, 40:879-884.
-
(2003)
J Med Genet
, vol.40
, pp. 879-884
-
-
van Wijk, E.1
Kreiger, E.2
Kemperman, M.H.3
-
3
-
-
33749042566
-
A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment
-
Rendtorff N.D., Zhu M., Fagerheim T., et al. A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment. Eur J Hum Genet 2006, 14:1097-1105.
-
(2006)
Eur J Hum Genet
, vol.14
, pp. 1097-1105
-
-
Rendtorff, N.D.1
Zhu, M.2
Fagerheim, T.3
-
4
-
-
51749098016
-
Novel ACTG1 mutation causing autosomal dominant non-syndromic hearing impairment in a Chinese family
-
Liu P., Li H., Ren X., et al. Novel ACTG1 mutation causing autosomal dominant non-syndromic hearing impairment in a Chinese family. J Genet Genomics 2008, 35:553-558.
-
(2008)
J Genet Genomics
, vol.35
, pp. 553-558
-
-
Liu, P.1
Li, H.2
Ren, X.3
-
5
-
-
0033587759
-
A heterozygous mutation of β-actin associated with neutrophil dysfunction and recurrent infection
-
Nunoi H., Yamazaki T., Tsuchiya H., et al. A heterozygous mutation of β-actin associated with neutrophil dysfunction and recurrent infection. Proc Natl Acad Sci USA 1999, 96:8693-8698.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 8693-8698
-
-
Nunoi, H.1
Yamazaki, T.2
Tsuchiya, H.3
-
6
-
-
33646873916
-
A mutation of β-actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia
-
Procaccio V., Salazar G., Ono S., et al. A mutation of β-actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia. Am J Hum Genet 2006, 78:947-960.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 947-960
-
-
Procaccio, V.1
Salazar, G.2
Ono, S.3
-
7
-
-
36549071997
-
Mutations in smooth muscle α-actin (ACTA2) lead to thoracic aortic aneurysms and dissections
-
Guo D.C., Pannu H., Tran-Fadulu V., et al. Mutations in smooth muscle α-actin (ACTA2) lead to thoracic aortic aneurysms and dissections. Nat Genet 2007, 39:1488-1493.
-
(2007)
Nat Genet
, vol.39
, pp. 1488-1493
-
-
Guo, D.C.1
Pannu, H.2
Tran-Fadulu, V.3
-
8
-
-
65149088429
-
Mutations in smooth muscle α-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease
-
Guo D.C., Papke C.L., Tran-Fadulu V., et al. Mutations in smooth muscle α-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease. Am J Hum Genet 2009, 84:617-627.
-
(2009)
Am J Hum Genet
, vol.84
, pp. 617-627
-
-
Guo, D.C.1
Papke, C.L.2
Tran-Fadulu, V.3
-
9
-
-
0032076955
-
Actin mutations in dilated cardiomyopathy, a heritable form of heart failure
-
Olson T.M., Michels V.V., Thibodeau S.N., Tai Y.S., Keating M.T. Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science 1998, 280:750-752.
-
(1998)
Science
, vol.280
, pp. 750-752
-
-
Olson, T.M.1
Michels, V.V.2
Thibodeau, S.N.3
Tai, Y.S.4
Keating, M.T.5
-
10
-
-
18744433901
-
α-Cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy
-
Mogensen J., Klausen I.C., Pedersen A.K., et al. α-Cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy. J Clin Invest 1999, 103:R39-R43.
-
(1999)
J Clin Invest
, vol.103
-
-
Mogensen, J.1
Klausen, I.C.2
Pedersen, A.K.3
-
11
-
-
0033799445
-
Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy
-
Olson T.M., Doan T.P., Kishimoto N.Y., Whitby F.G., Ackerman M.J., Fananapazir L. Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy. J Mol Cell Cardiol 2000, 32:1687-1694.
-
(2000)
J Mol Cell Cardiol
, vol.32
, pp. 1687-1694
-
-
Olson, T.M.1
Doan, T.P.2
Kishimoto, N.Y.3
Whitby, F.G.4
Ackerman, M.J.5
Fananapazir, L.6
-
12
-
-
0041663609
-
Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy
-
Van Driest S.L., Ellsworth E.G., Ommen S.R., Tajik A.J., Gersh B.J., Ackerman M.J. Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy. Circulation 2003, 108:445-451.
-
(2003)
Circulation
, vol.108
, pp. 445-451
-
-
Van Driest, S.L.1
Ellsworth, E.G.2
Ommen, S.R.3
Tajik, A.J.4
Gersh, B.J.5
Ackerman, M.J.6
-
13
-
-
27844611696
-
Gene mutations in apical hypertrophic cardiomyopathy
-
Arad M., Penas-Lado M., Montserrat M., et al. Gene mutations in apical hypertrophic cardiomyopathy. Circulation 2005, 112:2805-2811.
-
(2005)
Circulation
, vol.112
, pp. 2805-2811
-
-
Arad, M.1
Penas-Lado, M.2
Montserrat, M.3
-
14
-
-
0032858915
-
Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy
-
Nowak K.J., Wattanasirichaigoon D., Goebel H.H., et al. Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy. Nat Genet 1999, 23:208-212.
-
(1999)
Nat Genet
, vol.23
, pp. 208-212
-
-
Nowak, K.J.1
Wattanasirichaigoon, D.2
Goebel, H.H.3
-
15
-
-
0042071493
-
Muscle disease caused by mutations in the skeletal muscle α-actin gene, ACTA1
-
Sparrow J.C., Nowak K., Durling H.J., et al. Muscle disease caused by mutations in the skeletal muscle α-actin gene, ACTA1. Neuromuscul Disord 2003, 13:519-531.
-
(2003)
Neuromuscul Disord
, vol.13
, pp. 519-531
-
-
Sparrow, J.C.1
Nowak, K.2
Durling, H.J.3
-
16
-
-
69549129388
-
Mutations and polymorphisms of the skeletal muscle α-actin gene (ACTA1)
-
Laing N.G., Dye D.E., Wallgren-Pettersson C., et al. Mutations and polymorphisms of the skeletal muscle α-actin gene (ACTA1). Hum mutat 2009, 30:1-11.
-
(2009)
Hum mutat
, vol.30
, pp. 1-11
-
-
Laing, N.G.1
Dye, D.E.2
Wallgren-Pettersson, C.3
-
17
-
-
9144245756
-
Actin mutations are one cause of congenital fibre-type disproportion
-
Laing N.G., Clarke N.F., Dye D.E., et al. Actin mutations are one cause of congenital fibre-type disproportion. Ann Neurol 2004, 56:689-694.
-
(2004)
Ann Neurol
, vol.56
, pp. 689-694
-
-
Laing, N.G.1
Clarke, N.F.2
Dye, D.E.3
-
18
-
-
0031020004
-
Infantile intranuclear rod myopathy
-
Goebel H.H., Piirsoo A., Warlo I., Schofer O., Kehr S., Gaude M. Infantile intranuclear rod myopathy. J Child Neurol 1997, 12:22-30.
-
(1997)
J Child Neurol
, vol.12
, pp. 22-30
-
-
Goebel, H.H.1
Piirsoo, A.2
Warlo, I.3
Schofer, O.4
Kehr, S.5
Gaude, M.6
-
19
-
-
0001030415
-
-
Congenital myopathies. In: Engel AG, Franzini-Armstrong C, editors. Myology. New York: McGraw-Hill Inc., 1994
-
Fardeau M, Tome FMS. Congenital myopathies. In: Engel AG, Franzini-Armstrong C, editors. Myology. New York: McGraw-Hill Inc.,; p. 1487-1532.
-
(1994)
-
-
Fardeau, M.1
Tome, F.M.S.2
-
20
-
-
0034213947
-
Report of the 70th ENMC international workshop: nemaline myopathy, 11-13 June 1999, Naarden, The Netherlands
-
Wallgren-Pettersson C., Laing N.G. Report of the 70th ENMC international workshop: nemaline myopathy, 11-13 June 1999, Naarden, The Netherlands. Neuromuscul Disord 2000, 10:299-306.
-
(2000)
Neuromuscul Disord
, vol.10
, pp. 299-306
-
-
Wallgren-Pettersson, C.1
Laing, N.G.2
-
21
-
-
6944241979
-
Homozygous nonsense mutation of the ACTA1 gene - Clinical phenotype and muscle pathology
-
Romero N.B., Barois A., Leroy J.P., et al. Homozygous nonsense mutation of the ACTA1 gene - Clinical phenotype and muscle pathology. Abs Neuromuscul Disord 2003, 13:616.
-
(2003)
Abs Neuromuscul Disord
, vol.13
, pp. 616
-
-
Romero, N.B.1
Barois, A.2
Leroy, J.P.3
-
22
-
-
0019304558
-
Immunofluorescence microscopy of a myopathy - α-actinin is a major constituent of nemaline rods
-
Jockusch B.M., Veldman H., Griffiths G.W., Vanoost B.A., Jennekens F.G.I. Immunofluorescence microscopy of a myopathy - α-actinin is a major constituent of nemaline rods. Exp Cell Res 1980, 127:409-420.
-
(1980)
Exp Cell Res
, vol.127
, pp. 409-420
-
-
Jockusch, B.M.1
Veldman, H.2
Griffiths, G.W.3
Vanoost, B.A.4
Jennekens, F.G.I.5
-
23
-
-
31944440024
-
Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variablity within a kindred
-
Hutchinson D.O., Charlton A., Laing N.G., Ilkovski B., North K.N. Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variablity within a kindred. Neuromuscul Disord 2006, 16:113-121.
-
(2006)
Neuromuscul Disord
, vol.16
, pp. 113-121
-
-
Hutchinson, D.O.1
Charlton, A.2
Laing, N.G.3
Ilkovski, B.4
North, K.N.5
-
24
-
-
36749037144
-
Mechanisms underlying intranuclear rod formation
-
Domazetovska A., Ilkovski B., Cooper S.T., Ghoddusi M., Hardeman E.C., Minamide L.S., et al. Mechanisms underlying intranuclear rod formation. Brain 2007, 130:3275-3284.
-
(2007)
Brain
, vol.130
, pp. 3275-3284
-
-
Domazetovska, A.1
Ilkovski, B.2
Cooper, S.T.3
Ghoddusi, M.4
Hardeman, E.C.5
Minamide, L.S.6
-
25
-
-
0022510684
-
Heat shock induction of intranuclear actin rods in cultured mammalian cells
-
Iida K., Iida H., Yahara I. Heat shock induction of intranuclear actin rods in cultured mammalian cells. Exp Cell Res 1986, 165:207-215.
-
(1986)
Exp Cell Res
, vol.165
, pp. 207-215
-
-
Iida, K.1
Iida, H.2
Yahara, I.3
-
26
-
-
0022379715
-
Morphological study of the mammalian stress response: characterization of changes in cytoplasmic organelles, cytoskeleton, and nucleoli, and appearance of intranuclear actin filaments in rat fibroblasts after heat-shock treatment
-
Welch W.J., Suhan J.P. Morphological study of the mammalian stress response: characterization of changes in cytoplasmic organelles, cytoskeleton, and nucleoli, and appearance of intranuclear actin filaments in rat fibroblasts after heat-shock treatment. J Cell Biol 1985, 101:1198-1211.
-
(1985)
J Cell Biol
, vol.101
, pp. 1198-1211
-
-
Welch, W.J.1
Suhan, J.P.2
-
27
-
-
0027258440
-
Colocalization of ADF and cofilin in intranuclear actin rods of cultured muscle cells
-
Ono S., Abe H., Nagaoka R., Obinata T. Colocalization of ADF and cofilin in intranuclear actin rods of cultured muscle cells. J Muscle Res Cell Motil 1993, 14:195-204.
-
(1993)
J Muscle Res Cell Motil
, vol.14
, pp. 195-204
-
-
Ono, S.1
Abe, H.2
Nagaoka, R.3
Obinata, T.4
-
28
-
-
0034468480
-
Novel actin cytoskeleton: actin tubules
-
Sameshima M., Kishi Y., Osumi M., Mahadeo D., Cotter D.A. Novel actin cytoskeleton: actin tubules. Cell Struct Funct 2000, 25:291-295.
-
(2000)
Cell Struct Funct
, vol.25
, pp. 291-295
-
-
Sameshima, M.1
Kishi, Y.2
Osumi, M.3
Mahadeo, D.4
Cotter, D.A.5
-
29
-
-
0027035159
-
-
'Drosophila actin mutants and the study of myofibrillar assembly and function'. In: El Haj, editor. A molecular biology of muscle. SEB symposia XLVI: company of biologists, Cambridge; 1992
-
Sparrow JC, Drummond DR, Hennessey ES, Clayton JD, Lindegaard FB. 'Drosophila actin mutants and the study of myofibrillar assembly and function'. In: El Haj, editor. A molecular biology of muscle. SEB symposia XLVI: company of biologists, Cambridge; 1992. p. 111-119.
-
(1992)
-
-
Sparrow, J.C.1
Drummond, D.R.2
Hennessey, E.S.3
Clayton, J.D.4
Lindegaard, F.B.5
-
30
-
-
0034901458
-
Expression and function of the Drosophila ACT88F actin isoform is not restricted to the indirect flight muscles
-
Nongthomba U., Pasalodos-Sanchez S., Clark S., Clayton J.D., Sparrow J.C. Expression and function of the Drosophila ACT88F actin isoform is not restricted to the indirect flight muscles. J Muscle Res Cell Motil 2001, 22:111-119.
-
(2001)
J Muscle Res Cell Motil
, vol.22
, pp. 111-119
-
-
Nongthomba, U.1
Pasalodos-Sanchez, S.2
Clark, S.3
Clayton, J.D.4
Sparrow, J.C.5
-
31
-
-
0019741511
-
Isolation of Drosophila flightless mutants which affect myofibrillar proteins of indirect flight muscle
-
Mogami K., Hotta Y. Isolation of Drosophila flightless mutants which affect myofibrillar proteins of indirect flight muscle. Mol Gen Genet 1981, 183:409-417.
-
(1981)
Mol Gen Genet
, vol.183
, pp. 409-417
-
-
Mogami, K.1
Hotta, Y.2
-
32
-
-
0028350790
-
Recovery of dominant, autosomal flightless mutants of Drosophila melanogaster and identification of a new gene required for normal muscle structure and function
-
Cripps R.M., Ball E., Stark M., Lawn A., Sparrow J.C. Recovery of dominant, autosomal flightless mutants of Drosophila melanogaster and identification of a new gene required for normal muscle structure and function. Genetics 1994, 137:151-164.
-
(1994)
Genetics
, vol.137
, pp. 151-164
-
-
Cripps, R.M.1
Ball, E.2
Stark, M.3
Lawn, A.4
Sparrow, J.C.5
-
33
-
-
0030602907
-
Isolation of 88F actin mutant of Drosophila melanogaster and possible alterations in the mutant actin structures
-
An H., Mogami K. Isolation of 88F actin mutant of Drosophila melanogaster and possible alterations in the mutant actin structures. J Mol Biol 1996, 260:492-505.
-
(1996)
J Mol Biol
, vol.260
, pp. 492-505
-
-
An, H.1
Mogami, K.2
-
34
-
-
0025794119
-
Characterisation of missense mutations in the Act88F gene of Drosophila melanogaster
-
Drummond D.R., Hennessey E.S., Sparrow J.C. Characterisation of missense mutations in the Act88F gene of Drosophila melanogaster. Mol Gen Genet 1991, 226:70-80.
-
(1991)
Mol Gen Genet
, vol.226
, pp. 70-80
-
-
Drummond, D.R.1
Hennessey, E.S.2
Sparrow, J.C.3
-
35
-
-
0033214659
-
Actin residue Glu93 is identified as an amino acid affecting myosin binding
-
Razzaq A., Schmitz S., Veigel C., Molloy J.E., Geeves M.A., Sparrow J.C. Actin residue Glu93 is identified as an amino acid affecting myosin binding. J Biol Chem 1999, 274:28321-28328.
-
(1999)
J Biol Chem
, vol.274
, pp. 28321-28328
-
-
Razzaq, A.1
Schmitz, S.2
Veigel, C.3
Molloy, J.E.4
Geeves, M.A.5
Sparrow, J.C.6
-
36
-
-
0034602920
-
Drosophila ACT88F indirect flight muscle-specific actin is not N-terminally acetylated: a mutation in N-terminal processing affects actin function
-
Schmitz S., Clayton J., Nongthomba U., Veigel C., Geeves M., Sparrow J.C. Drosophila ACT88F indirect flight muscle-specific actin is not N-terminally acetylated: a mutation in N-terminal processing affects actin function. J Mol Biol 2000, 295:201-210.
-
(2000)
J Mol Biol
, vol.295
, pp. 201-210
-
-
Schmitz, S.1
Clayton, J.2
Nongthomba, U.3
Veigel, C.4
Geeves, M.5
Sparrow, J.C.6
-
37
-
-
0025822949
-
Development of the indirect flight muscles of Drosophila
-
Fernandes J., Bate M., VijayRaghavan K. Development of the indirect flight muscles of Drosophila. Development 1991, 113:67-77.
-
(1991)
Development
, vol.113
, pp. 67-77
-
-
Fernandes, J.1
Bate, M.2
VijayRaghavan, K.3
-
38
-
-
0032829026
-
A direct screen identifies new flight muscle mutants on the Drosophila second chromosome
-
Nongthomba U., Ramachandra N.B. A direct screen identifies new flight muscle mutants on the Drosophila second chromosome. Genetics 1999, 153:261-274.
-
(1999)
Genetics
, vol.153
, pp. 261-274
-
-
Nongthomba, U.1
Ramachandra, N.B.2
-
39
-
-
0029070405
-
Defects in the Drosophila myosin rod permit sarcomere assembly but cause flight muscle degeneration
-
Kronert W.A., O'Donnell P.T., Fieck A., et al. Defects in the Drosophila myosin rod permit sarcomere assembly but cause flight muscle degeneration. J Mol Biol 1995, 249:111-125.
-
(1995)
J Mol Biol
, vol.249
, pp. 111-125
-
-
Kronert, W.A.1
O'Donnell, P.T.2
Fieck, A.3
-
40
-
-
0022419472
-
Rigor crossbridge structure in tilted single filament layers and flared-X formations from insect flight muscle
-
Reedy M.K., Reedy M.C. Rigor crossbridge structure in tilted single filament layers and flared-X formations from insect flight muscle. J Mol Biol 1985, 185:145-176.
-
(1985)
J Mol Biol
, vol.185
, pp. 145-176
-
-
Reedy, M.K.1
Reedy, M.C.2
-
41
-
-
0019042936
-
Immunochemistry on ultrathin frozen sections
-
Tokuyasu K.T. Immunochemistry on ultrathin frozen sections. Histochem J 1980, 12:381-403.
-
(1980)
Histochem J
, vol.12
, pp. 381-403
-
-
Tokuyasu, K.T.1
-
42
-
-
0025131273
-
Identification and localization of high molecular weight proteins in insect flight and leg muscle
-
Lakey A., Ferguson C., Labeit S., et al. Identification and localization of high molecular weight proteins in insect flight and leg muscle. EMBO J 1990, 9:3459-3467.
-
(1990)
EMBO J
, vol.9
, pp. 3459-3467
-
-
Lakey, A.1
Ferguson, C.2
Labeit, S.3
-
43
-
-
2342425887
-
Troponin I is required for myofibrillogenesis and sarcomere formation in Drosophila flight muscle
-
Nongthomba U., Clark S., Cummins M., Ansari M., Stark M., Sparrow J.C. Troponin I is required for myofibrillogenesis and sarcomere formation in Drosophila flight muscle. J Cell Sci 2004, 117:1795-1805.
-
(2004)
J Cell Sci
, vol.117
, pp. 1795-1805
-
-
Nongthomba, U.1
Clark, S.2
Cummins, M.3
Ansari, M.4
Stark, M.5
Sparrow, J.C.6
-
44
-
-
0001089240
-
Actin gene mutations in Drosophila; heat shock activation in the indirect flight muscles
-
Hiromi Y., Hotta Y. Actin gene mutations in Drosophila; heat shock activation in the indirect flight muscles. EMBO J 1985, 4:1681-1687.
-
(1985)
EMBO J
, vol.4
, pp. 1681-1687
-
-
Hiromi, Y.1
Hotta, Y.2
-
45
-
-
0000519384
-
Molecular characterization of mutant actin genes which induce heat-shock proteins in Drosophila flight muscles
-
Okamoto H., Hiromi Y., Ishikawa E., et al. Molecular characterization of mutant actin genes which induce heat-shock proteins in Drosophila flight muscles. EMBO J 1986, 5:589-596.
-
(1986)
EMBO J
, vol.5
, pp. 589-596
-
-
Okamoto, H.1
Hiromi, Y.2
Ishikawa, E.3
-
46
-
-
0025604603
-
Drosophila melanogaster troponin-T mutations engender three distinct syndromes of myofibrillar abnormalities
-
Fyrberg E., Fyrberg C.C., Beall C., Saville D. Drosophila melanogaster troponin-T mutations engender three distinct syndromes of myofibrillar abnormalities. J Mol Biol 1990, 216:657-675.
-
(1990)
J Mol Biol
, vol.216
, pp. 657-675
-
-
Fyrberg, E.1
Fyrberg, C.C.2
Beall, C.3
Saville, D.4
-
47
-
-
35048817015
-
Aberrant splicing of an alternative exon in the Drosophila troponin-T gene affects flight muscle development
-
Nongthomba U., Ansari M., Thimmaiya D., Stark M., Sparrow J. Aberrant splicing of an alternative exon in the Drosophila troponin-T gene affects flight muscle development. Genetics 2007, 177:295-306.
-
(2007)
Genetics
, vol.177
, pp. 295-306
-
-
Nongthomba, U.1
Ansari, M.2
Thimmaiya, D.3
Stark, M.4
Sparrow, J.5
-
48
-
-
0016661085
-
Zebra body myopathy. Clinical, histochemical and ultrastructural studies
-
Lake B.D., Wilson J. Zebra body myopathy. Clinical, histochemical and ultrastructural studies. J Neurol Sci 1975, 24:437-446.
-
(1975)
J Neurol Sci
, vol.24
, pp. 437-446
-
-
Lake, B.D.1
Wilson, J.2
-
49
-
-
0023663064
-
Arthrin, a myofibrillar protein of insect flight muscle, is an actin-ubiquitin conjugate
-
Ball E., Karlik C.C., Beall C.J., et al. Arthrin, a myofibrillar protein of insect flight muscle, is an actin-ubiquitin conjugate. Cell 1987, 51:221-228.
-
(1987)
Cell
, vol.51
, pp. 221-228
-
-
Ball, E.1
Karlik, C.C.2
Beall, C.J.3
-
50
-
-
4143063984
-
Structural studies of arthrin: monoubiquitinated actin
-
Burgess S., Walker M., Knight P.J., et al. Structural studies of arthrin: monoubiquitinated actin. J Mol Biol 2004, 341:1161-1173.
-
(2004)
J Mol Biol
, vol.341
, pp. 1161-1173
-
-
Burgess, S.1
Walker, M.2
Knight, P.J.3
-
51
-
-
0037462928
-
The location of ubiquitin in Lethocerus arthrin
-
Galkin V.E., Orlova A., Lukoyanova N., et al. The location of ubiquitin in Lethocerus arthrin. J Mol Biol 2003, 325:623-628.
-
(2003)
J Mol Biol
, vol.325
, pp. 623-628
-
-
Galkin, V.E.1
Orlova, A.2
Lukoyanova, N.3
-
52
-
-
8744305686
-
Missense mutations of ACTA1 cause dominant congenital myopathy with cores
-
Kaindl A.M., Ruschendorf F., Krause S., et al. Missense mutations of ACTA1 cause dominant congenital myopathy with cores. J Med Genet 2004, 41:842-848.
-
(2004)
J Med Genet
, vol.41
, pp. 842-848
-
-
Kaindl, A.M.1
Ruschendorf, F.2
Krause, S.3
-
53
-
-
0024617347
-
Genetic dissection of Drosophila myofibril formation: effects of actin and myosin heavy chain null alleles
-
Beall C.J., Sepanski M.A., Fyrberg E.A. Genetic dissection of Drosophila myofibril formation: effects of actin and myosin heavy chain null alleles. Genes Devel 1989, 3:131-140.
-
(1989)
Genes Devel
, vol.3
, pp. 131-140
-
-
Beall, C.J.1
Sepanski, M.A.2
Fyrberg, E.A.3
-
54
-
-
0025258860
-
Alteration in crossbridge kinetics caused by mutations in actin
-
Drummond D.R., Peckham M., Sparrow J.C., White D.C. Alteration in crossbridge kinetics caused by mutations in actin. Nature 1990, 348:440-442.
-
(1990)
Nature
, vol.348
, pp. 440-442
-
-
Drummond, D.R.1
Peckham, M.2
Sparrow, J.C.3
White, D.C.4
-
55
-
-
0026332295
-
Functional and ultrastructural effects of a missense mutation in the indirect flight muscle-specific actin gene of Drosophila melanogaster
-
Sparrow J., Reedy M., Ball E., et al. Functional and ultrastructural effects of a missense mutation in the indirect flight muscle-specific actin gene of Drosophila melanogaster. J Mol Biol 1991, 222:963-982.
-
(1991)
J Mol Biol
, vol.222
, pp. 963-982
-
-
Sparrow, J.1
Reedy, M.2
Ball, E.3
-
56
-
-
0032536820
-
Nuclear export of actin: a novel mechanism regulating the subcellular localization of a major cytoskeletal protein
-
Wada A., Fukuda M., Mishima M., Nishida E. Nuclear export of actin: a novel mechanism regulating the subcellular localization of a major cytoskeletal protein. EMBO J 1998, 17:1635-1641.
-
(1998)
EMBO J
, vol.17
, pp. 1635-1641
-
-
Wada, A.1
Fukuda, M.2
Mishima, M.3
Nishida, E.4
-
57
-
-
77953121313
-
-
Drosophila indirect flight muscles as a model system for the study of human thin filament myopathies. Ph.D. thesis, University of York, 2009.
-
Sevdali M. Drosophila indirect flight muscles as a model system for the study of human thin filament myopathies. Ph.D. thesis, University of York, 2009.
-
(2009)
-
-
Sevdali, M.1
-
58
-
-
0034992606
-
Nemaline myopathy caused by mutations in the muscle α-skeletal actin gene
-
Ilkovski B., Cooper S.T., Nowak K., et al. Nemaline myopathy caused by mutations in the muscle α-skeletal actin gene. Am J Hum Genet 2001, 68:1333-1343.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1333-1343
-
-
Ilkovski, B.1
Cooper, S.T.2
Nowak, K.3
-
59
-
-
7944233824
-
α-Actin gene mutations and polymorphisms in Italian patients with nemaline myopathy
-
Graziano C., Bertini E., Minetti C., Porfirio B. α-Actin gene mutations and polymorphisms in Italian patients with nemaline myopathy. Int J Mol Med 2004, 13:805-809.
-
(2004)
Int J Mol Med
, vol.13
, pp. 805-809
-
-
Graziano, C.1
Bertini, E.2
Minetti, C.3
Porfirio, B.4
-
60
-
-
0025075839
-
Atomic model of the actin filament
-
Holmes K.C., Popp D., Gebhard W., Kabsch W. Atomic model of the actin filament. Nature 1990, 347:44-49.
-
(1990)
Nature
, vol.347
, pp. 44-49
-
-
Holmes, K.C.1
Popp, D.2
Gebhard, W.3
Kabsch, W.4
-
61
-
-
4344656639
-
Myopathy mutations in α-skeletal-muscle actin cause a range of molecular defects
-
Costa C.F., Rommelaere H., Waterschoot D., et al. Myopathy mutations in α-skeletal-muscle actin cause a range of molecular defects. J Cell Sci 2004, 117:3367-3377.
-
(2004)
J Cell Sci
, vol.117
, pp. 3367-3377
-
-
Costa, C.F.1
Rommelaere, H.2
Waterschoot, D.3
-
62
-
-
77951170096
-
Dominant negative mutant actins identified in flightless Drosophila can be classified into three classes
-
Noguchi T.Q., Gomibuchi Y., Murakami K., et al. Dominant negative mutant actins identified in flightless Drosophila can be classified into three classes. J Biol Chem 2010, 285:4337-4347.
-
(2010)
J Biol Chem
, vol.285
, pp. 4337-4347
-
-
Noguchi, T.Q.1
Gomibuchi, Y.2
Murakami, K.3
-
63
-
-
58849125703
-
Genotype-phenotype correlations in ACTA1 mutations that cause congenital myopathies
-
Feng J.-J., Marston S. Genotype-phenotype correlations in ACTA1 mutations that cause congenital myopathies. Neuromuscul Disord 2009, 19:6-16.
-
(2009)
Neuromuscul Disord
, vol.19
, pp. 6-16
-
-
Feng, J.-J.1
Marston, S.2
-
64
-
-
0033613918
-
Association of kettin with actin in the Z-disc of insect flight muscle
-
van Straaten M., Goulding D., Kolmerer B., et al. Association of kettin with actin in the Z-disc of insect flight muscle. J Mol Biol 1999, 285:1549-1562.
-
(1999)
J Mol Biol
, vol.285
, pp. 1549-1562
-
-
van Straaten, M.1
Goulding, D.2
Kolmerer, B.3
-
65
-
-
0027133588
-
Ultrastructure of developing flight muscle in Drosophila I. Assembly of myofibrils
-
Reedy M.C., Beall C. Ultrastructure of developing flight muscle in Drosophila I. Assembly of myofibrils. Dev Biol 1993, 160:443-465.
-
(1993)
Dev Biol
, vol.160
, pp. 443-465
-
-
Reedy, M.C.1
Beall, C.2
|