-
1
-
-
17344365600
-
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
-
Liu J, Aoki M, Illa I, et al. Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy. Nat Genet 1998;20:31-36
-
(1998)
Nat Genet
, vol.20
, pp. 31-36
-
-
Liu, J.1
Aoki, M.2
Illa, I.3
-
2
-
-
17344363640
-
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
-
Bashir R, Britton S, Strachan T, et al. A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B. Nat Genet 1998;20:37-42
-
(1998)
Nat Genet
, vol.20
, pp. 37-42
-
-
Bashir, R.1
Britton, S.2
Strachan, T.3
-
3
-
-
0034665195
-
The third human FER-1-like protein is highly similar to dysferlin
-
Britton S, Freeman T, Vafiadaki E, et al. The third human FER-1-like protein is highly similar to dysferlin. Genomics 2000;68:313-21
-
(2000)
Genomics
, vol.68
, pp. 313-321
-
-
Britton, S.1
Freeman, T.2
Vafiadaki, E.3
-
4
-
-
0033972161
-
Myoferlin, a candidate gene and potential modifier of muscular dystrophy
-
Davis DB, Delmonte AJ, Ly CT, et al. Myoferlin, a candidate gene and potential modifier of muscular dystrophy. Hum Mol Genet 2000;9:217-26
-
(2000)
Hum Mol Genet
, vol.9
, pp. 217-226
-
-
Davis, D.B.1
Delmonte, A.J.2
Ly, C.T.3
-
5
-
-
0033846745
-
OTOF encodes multiple long and short isoforms: Genetic evidence that the long ones underlie recessive deafness DFNB9
-
Yasunaga S, Grati M, Chardenoux S, et al. OTOF encodes multiple long and short isoforms: Genetic evidence that the long ones underlie recessive deafness DFNB9. Am J Hum Genet 2000;67:591-600
-
(2000)
Am J Hum Genet
, vol.67
, pp. 591-600
-
-
Yasunaga, S.1
Grati, M.2
Chardenoux, S.3
-
6
-
-
0030972880
-
A nematode gene required for sperm vesicle fusion
-
Achanzar WE, Ward S. A nematode gene required for sperm vesicle fusion. J Cell Sci 1997;110:1073-81
-
(1997)
J Cell Sci
, vol.110
, pp. 1073-1081
-
-
Achanzar, W.E.1
Ward, S.2
-
7
-
-
0037738510
-
Defective membrane repair in dysferlin-deficient muscular dystrophy
-
Bansal D, Miyake K, Vogel SS, et al. Defective membrane repair in dysferlin-deficient muscular dystrophy. Nature 2003;423:168-72
-
(2003)
Nature
, vol.423
, pp. 168-172
-
-
Bansal, D.1
Miyake, K.2
Vogel, S.S.3
-
8
-
-
0347379869
-
Dysferlin interacts with annexins A1 and A2 and mediates sarcolemmal wound-healing
-
Lennon NJ, Kho A, Bacskai BJ, et al. Dysferlin interacts with annexins A1 and A2 and mediates sarcolemmal wound-healing. J Biol Chem 2003;50466-73
-
(2003)
J Biol Chem
, pp. 50466-50473
-
-
Lennon, N.J.1
Kho, A.2
Bacskai, B.J.3
-
9
-
-
0035844879
-
A novel integrin-linked kinase-binding protein, affixin, is involved in the early stage of cell-substrate interaction
-
Yamaji S, Suzuki A, Sugiyama Y, et al. A novel integrin-linked kinase-binding protein, affixin, is involved in the early stage of cell-substrate interaction. J Cell Biol 2001;153:1251-64
-
(2001)
J Cell Biol
, vol.153
, pp. 1251-1264
-
-
Yamaji, S.1
Suzuki, A.2
Sugiyama, Y.3
-
10
-
-
0035126590
-
Parvin, a 42 kDa focal adhesion protein, related to the alpha-actinin superfamily
-
Olski TM, Noegel AA, Korenbaum E. Parvin, a 42 kDa focal adhesion protein, related to the alpha-actinin superfamily. J Cell Sci 2001;114:525-38
-
(2001)
J Cell Sci
, vol.114
, pp. 525-538
-
-
Olski, T.M.1
Noegel, A.A.2
Korenbaum, E.3
-
11
-
-
0033595539
-
Dysferlin is a surface membrane-associated protein that is absent in Miyoshi myopathy
-
Matsuda C, Aoki M, Hayashi YK, et al. Dysferlin is a surface membrane-associated protein that is absent in Miyoshi myopathy. Neurology 1999;53:1119-22
-
(1999)
Neurology
, vol.53
, pp. 1119-1122
-
-
Matsuda, C.1
Aoki, M.2
Hayashi, Y.K.3
-
12
-
-
0032955751
-
Dysferlin is a plasma membrane protein and is expressed early in human development
-
Anderson LV, Davison K, Moss JA, et al. Dysferlin is a plasma membrane protein and is expressed early in human development [published erratum appears in Hum Mol Genet 1999 Jun;8(6):1141]. Hum Mol Genet 1999;8:855-61
-
(1999)
Hum Mol Genet
, vol.8
, pp. 855-861
-
-
Anderson, L.V.1
Davison, K.2
Moss, J.A.3
-
13
-
-
0032969289
-
-
published erratum appears Jun
-
Anderson LV, Davison K, Moss JA, et al. Dysferlin is a plasma membrane protein and is expressed early in human development [published erratum appears in Hum Mol Genet 1999 Jun;8(6):1141]. Hum Mol Genet 1999;8:855-61
-
(1999)
Hum Mol Genet
, vol.8
, Issue.6
, pp. 1141
-
-
-
14
-
-
0035838362
-
Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy
-
Hayashi YK, Ogawa M, Tagawa K, et al. Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy. Neurology 2001;57:115-21
-
(2001)
Neurology
, vol.57
, pp. 115-121
-
-
Hayashi, Y.K.1
Ogawa, M.2
Tagawa, K.3
-
15
-
-
0038629355
-
Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patients
-
Tagawa K, Ogawa M, Kawabe K, et al. Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patients. J Neurol Sci 2003;211:23-28
-
(2003)
J Neurol Sci
, vol.211
, pp. 23-28
-
-
Tagawa, K.1
Ogawa, M.2
Kawabe, K.3
-
16
-
-
0035880516
-
The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle
-
Matsuda C, Hayashi YK, Ogawa M, et al. The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle. Hum Mol Genet 2001;10:1761-66
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1761-1766
-
-
Matsuda, C.1
Hayashi, Y.K.2
Ogawa, M.3
-
17
-
-
0033673056
-
Intracellular accumulation and reduced sarcolemmal expression of dysferlin in limb-girdle muscular dystrophies
-
Piccolo F, Moore SA, Ford GC, et al. Intracellular accumulation and reduced sarcolemmal expression of dysferlin in limb-girdle muscular dystrophies. Ann Neurol 2000;48:902-12
-
(2000)
Ann Neurol
, vol.48
, pp. 902-912
-
-
Piccolo, F.1
Moore, S.A.2
Ford, G.C.3
-
18
-
-
10744219571
-
Dysferlin mutations in Japanese Miyoshi myopathy: Relationship to phenotype
-
Takahashi T, Aoki M, Tateyama M, et al. Dysferlin mutations in Japanese Miyoshi myopathy: Relationship to phenotype. Neurology 2003;60:1799-804
-
(2003)
Neurology
, vol.60
, pp. 1799-1804
-
-
Takahashi, T.1
Aoki, M.2
Tateyama, M.3
-
19
-
-
0035215432
-
Novel protein domains and repeats in Drosophila melanogaster: Insights into structure, function, and evolution
-
Ponting CP, Mott R, Bork P, et al. Novel protein domains and repeats in Drosophila melanogaster: Insights into structure, function, and evolution. Genome Res 2001;11:1996-2008
-
(2001)
Genome Res
, vol.11
, pp. 1996-2008
-
-
Ponting, C.P.1
Mott, R.2
Bork, P.3
-
20
-
-
0037850992
-
C. elegans PAT-6/actopaxin plays a critical role in the assembly of integrin adhesion complexes in vivo
-
Lin X, Qadota H, Moerman DG, et al. C. elegans PAT-6/actopaxin plays a critical role in the assembly of integrin adhesion complexes in vivo. Curr Biol 2003;13:922-32
-
(2003)
Curr Biol
, vol.13
, pp. 922-932
-
-
Lin, X.1
Qadota, H.2
Moerman, D.G.3
-
21
-
-
3242887228
-
Annexin 2 is a phosphatidylinositol (4, 5)-bisphosphate binding protein recruited to actin assembly sites at cellular membranes
-
Rescher U, Ruhe D, Ludwig C, et al. Annexin 2 is a phosphatidylinositol (4, 5)-bisphosphate binding protein recruited to actin assembly sites at cellular membranes. J Cell Sci 2004;117:3473-80
-
(2004)
J Cell Sci
, vol.117
, pp. 3473-3480
-
-
Rescher, U.1
Ruhe, D.2
Ludwig, C.3
-
22
-
-
2542468783
-
Affixin interacts with alpha-actinin and mediates integrin signaling for reorganization of F-actin induced by initial cell-substrate interaction
-
Yamaji S, Suzuki A, Kanamori H, et al. Affixin interacts with alpha-actinin and mediates integrin signaling for reorganization of F-actin induced by initial cell-substrate interaction. J Cell Biol 2004;165:539-51
-
(2004)
J Cell Biol
, vol.165
, pp. 539-551
-
-
Yamaji, S.1
Suzuki, A.2
Kanamori, H.3
-
23
-
-
0036500836
-
Repairing a torn cell surface: Make way, lysosomes to the rescue
-
McNeil PL. Repairing a torn cell surface: Make way, lysosomes to the rescue. J Cell Sci 2002;115:873-79
-
(2002)
J Cell Sci
, vol.115
, pp. 873-879
-
-
McNeil, P.L.1
-
24
-
-
0037439424
-
Interaction of alphaPIX (ARHGEF6) with beta-parvin (PARVB) suggests an involvement of alphaPIX in integrin-mediated signaling
-
Rosenberger G, Jantke I, Gal A, et al. Interaction of alphaPIX (ARHGEF6) with beta-parvin (PARVB) suggests an involvement of alphaPIX in integrin-mediated signaling. Hum Mol Genet 2003;12:155-67
-
(2003)
Hum Mol Genet
, vol.12
, pp. 155-167
-
-
Rosenberger, G.1
Jantke, I.2
Gal, A.3
-
25
-
-
12144291549
-
The first CH domain of affixin activates Cdc42 and Rac1 through alphaPIX, a Cdc42/Rac1-specific guanine nucleotide exchanging factor
-
Mishima W, Suzuki A, Yamaji S, et al. The first CH domain of affixin activates Cdc42 and Rac1 through alphaPIX, a Cdc42/Rac1-specific guanine nucleotide exchanging factor. Genes Cells 2004;9:193-204
-
(2004)
Genes Cells
, vol.9
, pp. 193-204
-
-
Mishima, W.1
Suzuki, A.2
Yamaji, S.3
-
26
-
-
0031610579
-
PAK kinases are directly coupled to the PIX family of nucleotide exchange factors
-
Manser E, Loo TH, Koh CG, et al. PAK kinases are directly coupled to the PIX family of nucleotide exchange factors. Mol Cell 1998;1:183-92
-
(1998)
Mol Cell
, vol.1
, pp. 183-192
-
-
Manser, E.1
Loo, T.H.2
Koh, C.G.3
|