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Volumn 59, Issue 7, 2007, Pages 747-753

Generation of mice with glial cell dysfunction

Author keywords

Alexander disease; Astrocyte; GFAP; Mlcl; Neuroligin 3

Indexed keywords

GLIAL FIBRILLARY ACIDIC PROTEIN; KAINIC ACID; MUTANT PROTEIN; NEUROLIGIN;

EID: 34447650626     PISSN: 00068969     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (1)

References (9)
  • 1
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    • Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease
    • Brenner M, Johnson AB, Boespflug-Tanguy O, Rodriguez D, Goldman JE, et al: Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease. Nat Genet 27: 117-120, 2001
    • (2001) Nat Genet , vol.27 , pp. 117-120
    • Brenner, M.1    Johnson, A.B.2    Boespflug-Tanguy, O.3    Rodriguez, D.4    Goldman, J.E.5
  • 2
    • 33751073409 scopus 로고    scopus 로고
    • Alexander disease-associated glial fibrillary acidic protein mutations in mice induce Rosenthal fiber formation and a white matter stress response
    • Hagemann TL, Connor JX, Messing A: Alexander disease-associated glial fibrillary acidic protein mutations in mice induce Rosenthal fiber formation and a white matter stress response. J Neurosci 26: 11162-11173, 2006
    • (2006) J Neurosci , vol.26 , pp. 11162-11173
    • Hagemann, T.L.1    Connor, J.X.2    Messing, A.3
  • 3
    • 20044376483 scopus 로고    scopus 로고
    • Experimental autoimmune encephalomyelitis repressed by microglial paralysis
    • Heppner FL, Greter M, Marino D, Falsig J, Raivich G, et al: Experimental autoimmune encephalomyelitis repressed by microglial paralysis. Nat Med 11: 146-152, 2005
    • (2005) Nat Med , vol.11 , pp. 146-152
    • Heppner, F.L.1    Greter, M.2    Marino, D.3    Falsig, J.4    Raivich, G.5
  • 4
    • 0037656313 scopus 로고    scopus 로고
    • Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
    • Jamain S, Quach H, Betancur C, Rastam M, Colineaux C, et al: Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat Genet 34: 27-29, 2003
    • (2003) Nat Genet , vol.34 , pp. 27-29
    • Jamain, S.1    Quach, H.2    Betancur, C.3    Rastam, M.4    Colineaux, C.5
  • 5
    • 0035072651 scopus 로고    scopus 로고
    • Mutations of MLC1 (KIAA0027), encoding a putative membrane protein, cause megalencephalic leukoencephalopathy with subcortical cysts
    • Leegwater PA, Yuan BQ, van der Steen J, Mulders J, Konst AA, et al: Mutations of MLC1 (KIAA0027), encoding a putative membrane protein, cause megalencephalic leukoencephalopathy with subcortical cysts. Am J Hum Genet 68: 831-838, 2001
    • (2001) Am J Hum Genet , vol.68 , pp. 831-838
    • Leegwater, P.A.1    Yuan, B.Q.2    van der Steen, J.3    Mulders, J.4    Konst, A.A.5
  • 6
    • 0031931614 scopus 로고    scopus 로고
    • Fatal encephalopathy with astrocyte inclusions in GFAP transgenic mice
    • Messing A, Head MW, Galles K, Galbreath EJ, Goldman JE, et al: Fatal encephalopathy with astrocyte inclusions in GFAP transgenic mice. Am J Pathol 152: 391-398, 1998
    • (1998) Am J Pathol , vol.152 , pp. 391-398
    • Messing, A.1    Head, M.W.2    Galles, K.3    Galbreath, E.J.4    Goldman, J.E.5
  • 8
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    • Murine model of Alexander disease: Analysis of GFAP aggregate formation and its pathological significance
    • Tanaka KF, Takebayashi H, Yamazaki Y, Ono K, Naruse M, et al: Murine model of Alexander disease: Analysis of GFAP aggregate formation and its pathological significance. Glia 55: 617-631, 2007
    • (2007) Glia , vol.55 , pp. 617-631
    • Tanaka, K.F.1    Takebayashi, H.2    Yamazaki, Y.3    Ono, K.4    Naruse, M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.