-
1
-
-
0023970247
-
Merosin, a protein specific for basement membranes of Schwann cells, striated muscle, and trophoblast, is expressed late in nerve and muscle development
-
Leivo I, Engvall E. Merosin, a protein specific for basement membranes of Schwann cells, striated muscle, and trophoblast, is expressed late in nerve and muscle development. Proc Natl Acad Sci U S A. 1988;85:1544-1548.
-
(1988)
Proc Natl Acad Sci U S A
, vol.85
, pp. 1544-1548
-
-
Leivo, I.1
Engvall, E.2
-
2
-
-
0025494189
-
Distribution and isolation of four laminin variants: Tissue restricted distribution of heterotrimers assembled from five different subunits
-
Engvall E, Earwicker D, Haparanta T, Ruoslahti E, Sanes JR. Distribution and isolation of four laminin variants: tissue restricted distribution of heterotrimers assembled from five different subunits. Cell Regulation. 1990;1:731-740.
-
(1990)
Cell Regulation
, vol.1
, pp. 731-740
-
-
Engvall, E.1
Earwicker, D.2
Haparanta, T.3
Ruoslahti, E.4
Sanes, J.R.5
-
3
-
-
0030465319
-
Merosin/laminin-2 and muscular dystrophy
-
Wewer UM, Engvall E. Merosin/laminin-2 and muscular dystrophy. Neuromusc Disord. 1996;6:409-418.
-
(1996)
Neuromusc Disord.
, vol.6
, pp. 409-418
-
-
Wewer, U.M.1
Engvall, E.2
-
4
-
-
0028098737
-
Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin
-
Higuchi I, Yamada H, Fukunaga H, et al. Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin. J Clin Invest. 1994;94:601-606.
-
(1994)
J Clin Invest.
, vol.94
, pp. 601-606
-
-
Higuchi, I.1
Yamada, H.2
Fukunaga, H.3
-
5
-
-
0029047909
-
Laminin abnormality in severe childhood autosomal recessive muscular dystrophy
-
Yamada H, Tome FMS, Higuchi I, et al. Laminin abnormality in severe childhood autosomal recessive muscular dystrophy. Lab Invest. 1995;72:715-722.
-
(1995)
Lab Invest.
, vol.72
, pp. 715-722
-
-
Yamada, H.1
Tome, F.M.S.2
Higuchi, I.3
-
6
-
-
0027360897
-
Abnormal localization of laminin subunits in muscular dystrophies
-
Hayashi YK, Engvall E, Arikawa-Hirasawa E, et al. Abnormal localization of laminin subunits in muscular dystrophies. J Neurol Sci. 1993;119:53-64.
-
(1993)
J Neurol Sci.
, vol.119
, pp. 53-64
-
-
Hayashi, Y.K.1
Engvall, E.2
Arikawa-Hirasawa, E.3
-
7
-
-
0029007799
-
Expression of laminin subunits in congenital muscular dystrophy
-
Sewry CA, Philpot J, Mahony D, Wilson LA, Muntoni, F, Dubowitz V. Expression of laminin subunits in congenital muscular dystrophy. Neuromusc Disord. 1995; 5:307-316.
-
(1995)
Neuromusc Disord.
, vol.5
, pp. 307-316
-
-
Sewry, C.A.1
Philpot, J.2
Mahony, D.3
Wilson, L.A.4
Muntoni, F.5
Dubowitz, V.6
-
9
-
-
0028835527
-
Diagnostic criteria for the limb-girdle muscular dystrophies: Report of the ENMC consortium on limb-girdle dystrophies
-
Bakker E, Beckmann M, Hamida B, et al. Diagnostic criteria for the limb-girdle muscular dystrophies: report of the ENMC consortium on limb-girdle dystrophies. Neuromusc Disord. 1995;5:71-74.
-
(1995)
Neuromusc Disord.
, vol.5
, pp. 71-74
-
-
Bakker, E.1
Beckmann, M.2
Hamida, B.3
-
10
-
-
0028877455
-
Muscular dystrophies: Diseases of the dystrophin-glycoprotein complex
-
Worton R. Muscular dystrophies: diseases of the dystrophin-glycoprotein complex. Science. 1995;270:755-756.
-
(1995)
Science
, vol.270
, pp. 755-756
-
-
Worton, R.1
-
11
-
-
0031042885
-
Mutations in the sarcoglycan genes in patients with myopathy
-
Duggan DJ, Gorospe JR, Fanin M, Hoffman EP, Angelini C. Mutations in the sarcoglycan genes in patients with myopathy. N Engl J Med. 1997;336:618-624.
-
(1997)
N Engl J Med.
, vol.336
, pp. 618-624
-
-
Duggan, D.J.1
Gorospe, J.R.2
Fanin, M.3
Hoffman, E.P.4
Angelini, C.5
-
12
-
-
0030511827
-
Muscular dystrophy associated with β-dystroglycan deficiency
-
Mustafa A, Salih M, Sunada Y, et al. Muscular dystrophy associated with β-dystroglycan deficiency. Ann Neurol. 1996;40:925-928.
-
(1996)
Ann Neurol.
, vol.40
, pp. 925-928
-
-
Mustafa, A.1
Salih, M.2
Sunada, Y.3
-
13
-
-
0029061267
-
Clinical phenotype in congenital muscular dystrophy: Correlation with expression of merosin in skeletal muscle
-
Philpot J, Sewry C, Pennock J, Dubowitz V. Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscle. Neuromusc Disord. 1994;5:301-305.
-
(1994)
Neuromusc Disord.
, vol.5
, pp. 301-305
-
-
Philpot, J.1
Sewry, C.2
Pennock, J.3
Dubowitz, V.4
-
14
-
-
0029877803
-
Congenital muscular dystrophy: Clinical and pathologic study of 50 patients with the classical (occidental) merosin-positive form
-
Kobayashi O, Hayashi Y, Arahata K, Ozawa E, Nonaka I. Congenital muscular dystrophy: clinical and pathologic study of 50 patients with the classical (occidental) merosin-positive form. Neurology. 1996;46:815-818.
-
(1996)
Neurology
, vol.46
, pp. 815-818
-
-
Kobayashi, O.1
Hayashi, Y.2
Arahata, K.3
Ozawa, E.4
Nonaka, I.5
-
15
-
-
0029396750
-
Laminin β2 chain and adhalin deficiency in the skeletal muscle of Walker-Warburg syndrome (cerebro-ocular dysplasia-muscular dystrophy)
-
Wewer UM, Durkin ME, Zhang X, et al. Laminin β2 chain and adhalin deficiency in the skeletal muscle of Walker-Warburg syndrome (cerebro-ocular dysplasia-muscular dystrophy). Neurology. 1995;45:2099-2101.
-
(1995)
Neurology
, vol.45
, pp. 2099-2101
-
-
Wewer, U.M.1
Durkin, M.E.2
Zhang, X.3
-
16
-
-
0029124239
-
Expression of laminin subunits in human fetal skeletal muscle
-
Sewry CA, Chevallay M, Tome FMS. Expression of laminin subunits in human fetal skeletal muscle. Histochem J. 1995;27:497-504.
-
(1995)
Histochem J.
, vol.27
, pp. 497-504
-
-
Sewry, C.A.1
Chevallay, M.2
Tome, F.M.S.3
-
18
-
-
0029771617
-
Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures
-
Joost Jobsis G, Keizers H, Vreijling JP, et al. Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures. Nat Genet. 1996;14:113-115.
-
(1996)
Nat Genet.
, vol.14
, pp. 113-115
-
-
Joost Jobsis, G.1
Keizers, H.2
Vreijling, J.P.3
-
19
-
-
0029970098
-
Defective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophy
-
Gache Y, Chavanas S, Lacour JP, et al. Defective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophy. J Clin Invest. 1996;97: 2289-2298.
-
(1996)
J Clin Invest.
, vol.97
, pp. 2289-2298
-
-
Gache, Y.1
Chavanas, S.2
Lacour, J.P.3
-
20
-
-
9444272226
-
Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization
-
Irwin Mclean WH, Pulkkinen L, Smith FJD, et al. Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization. Genes Dev. 1996;10:1724-1735.
-
(1996)
Genes Dev.
, vol.10
, pp. 1724-1735
-
-
Irwin Mclean, W.H.1
Pulkkinen, L.2
Smith, F.J.D.3
-
21
-
-
9344248374
-
Plectin deficiency results in muscular dystrophy with epidermolysis bullosa
-
Smith FJD, Eady RAJ, Leigh IM, et al. Plectin deficiency results in muscular dystrophy with epidermolysis bullosa. Nat Genet. 1996;13:450-457.
-
(1996)
Nat Genet.
, vol.13
, pp. 450-457
-
-
Smith, F.J.D.1
Eady, R.A.J.2
Leigh, I.M.3
-
22
-
-
0013897332
-
Ultrastructural observations of skeletal muscle in myopathy and neuropathy with special reference to muscular dystrophy
-
Fisher ER, Cohn RE, Danowski TS. Ultrastructural observations of skeletal muscle in myopathy and neuropathy with special reference to muscular dystrophy. Lab Invest. 1966;15:778-793.
-
(1966)
Lab Invest.
, vol.15
, pp. 778-793
-
-
Fisher, E.R.1
Cohn, R.E.2
Danowski, T.S.3
-
23
-
-
0014508701
-
Fine structure of the human skeletal muscle in myopathy
-
Santa T. Fine structure of the human skeletal muscle in myopathy. Arch Neurol. 1969;20:479-489.
-
(1969)
Arch Neurol.
, vol.20
, pp. 479-489
-
-
Santa, T.1
-
24
-
-
0029921917
-
Basement membrane abnormality in merosin-negative congenital muscular dystrophy
-
Osari S, Kobayashi O, Yamashita Y, et al. Basement membrane abnormality in merosin-negative congenital muscular dystrophy. Acta Neuropathol. 1996;91:332-336.
-
(1996)
Acta Neuropathol.
, vol.91
, pp. 332-336
-
-
Osari, S.1
Kobayashi, O.2
Yamashita, Y.3
-
25
-
-
0029992191
-
Disruption of muscle basal lamina in congenital muscular dystrophy with merosin deficiency
-
Minetti C, Bado M, Morreale G, Pedemonte M, Cordone G. Disruption of muscle basal lamina in congenital muscular dystrophy with merosin deficiency. Neurology. 1996;46:1354-1358.
-
(1996)
Neurology
, vol.46
, pp. 1354-1358
-
-
Minetti, C.1
Bado, M.2
Morreale, G.3
Pedemonte, M.4
Cordone, G.5
-
26
-
-
0030922711
-
Early onset autosomal dominant myopathy with rigidity of the spine: A possible role for laminin β1?
-
Taylor J, Muntoni F, Robb S, Dubowitz V, Sewry C. Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin β1? Neuromusc Disord. 1997;7:211-216.
-
(1997)
Neuromusc Disord.
, vol.7
, pp. 211-216
-
-
Taylor, J.1
Muntoni, F.2
Robb, S.3
Dubowitz, V.4
Sewry, C.5
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