메뉴 건너뛰기




Volumn 54, Issue 12, 1997, Pages 1457-1461

Abnormal expression of laminin chain in skeletal muscle of adult-onset limb-girdle muscular dystrophy

Author keywords

[No Author keywords available]

Indexed keywords

LAMININ; MEROSIN; SARCOGLYCAN;

EID: 0030810062     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.1997.00550240013007     Document Type: Article
Times cited : (23)

References (26)
  • 1
    • 0023970247 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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
  • 9
    • 0028835527 scopus 로고
    • 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 scopus 로고
    • 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
  • 12
    • 0030511827 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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
  • 17
    • 0025181051 scopus 로고
    • Structure of the human laminin β1 chain gene
    • Vuolteenaho R, Chow LT, Tryggvason K. Structure of the human laminin β1 chain gene. J Biol Chem. 1990;265:15611-15616.
    • (1990) J Biol Chem. , vol.265 , pp. 15611-15616
    • Vuolteenaho, R.1    Chow, L.T.2    Tryggvason, K.3
  • 18
    • 0029771617 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.