-
1
-
-
0027724243
-
Overexpression and abnormal modification of the stress protein αβ-crystallin and HSP27 in Alexander disease
-
Head MW, Corbin E., Goldman JE Overexpression and abnormal modification of the stress protein αβ-crystallin and HSP27 in Alexander disease. Am J Pathol. 1993; 143: 743-1753.
-
(1993)
Am J Pathol.
, vol.143
, pp. 743-1753
-
-
Head, M.W.1
Corbin, E.2
Goldman, J.E.3
-
2
-
-
0024446498
-
On grid immunogold labeling of glial immediate filaments in epoxy-embedded tissue
-
Johnson AB, Bettica A. On grid immunogold labeling of glial immediate filaments in epoxy-embedded tissue. Am J Anat. 1989; 185: 335-341.
-
(1989)
Am J Anat.
, vol.185
, pp. 335-341
-
-
Johnson, A.B.1
Bettica, A.2
-
3
-
-
0035163913
-
Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease
-
Brenner M., Jonhson AB, Boespflug-Tanguy O., et al. Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease. Nat Genet. 2001; 27: 117-120.
-
(2001)
Nat Genet.
, vol.27
, pp. 117-120
-
-
Brenner, M.1
Jonhson, A.B.2
Boespflug-Tanguy, O.3
-
4
-
-
13544271858
-
Glial fibrillary acidic protein mutations in a Chinese girl with infantile Alexander disease
-
Ma HW, Lu JF, Jiang J., et al. Glial fibrillary acidic protein mutations in a Chinese girl with infantile Alexander disease. Chin J Med Genet. 2005; 22: 79-81.
-
(2005)
Chin J Med Genet.
, vol.22
, pp. 79-81
-
-
Ma, H.W.1
Lu, J.F.2
Jiang, J.3
-
6
-
-
0042011502
-
Alexander disease: GFAP mutations unify young and old
-
Brenner M., Messing A. Alexander disease: GFAP mutations unify young and old. Lancet Neurol. 2003; 2: 75.
-
(2003)
Lancet Neurol.
, vol.2
, pp. 75
-
-
Brenner, M.1
Messing, A.2
-
7
-
-
14844300130
-
Alexander disease: Combined gene analysis and MRI clarify pathogenesis and extend phenotype
-
Moser HW Alexander disease: Combined gene analysis and MRI clarify pathogenesis and extend phenotype. Ann Neurol. 2005; 57: 307-308.
-
(2005)
Ann Neurol.
, vol.57
, pp. 307-308
-
-
Moser, H.W.1
-
8
-
-
20044372525
-
Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease
-
Li R., Jonhson AB, Salomons G., et al. Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease. Ann Neurol. 2005; 57: 310-326.
-
(2005)
Ann Neurol.
, vol.57
, pp. 310-326
-
-
Li, R.1
Jonhson, A.B.2
Salomons, G.3
-
9
-
-
3142748164
-
Alexander disease: A leukoencephalopathy caused by a mutation in GFAP
-
Johnson AB Alexander disease: A leukoencephalopathy caused by a mutation in GFAP. Neurochem Res. 2004; 29: 961-964.
-
(2004)
Neurochem Res.
, vol.29
, pp. 961-964
-
-
Johnson, A.B.1
-
12
-
-
0037188379
-
Molecular findings in symptomatic and pre-symptomatic Alexander disease patients
-
Gorospe JR, Naidu S., Johnson AB, et al. Molecular findings in symptomatic and pre-symptomatic Alexander disease patients. Neurology. 2002; 58: 1494-1500.
-
(2002)
Neurology
, vol.58
, pp. 1494-1500
-
-
Gorospe, J.R.1
Naidu, S.2
Johnson, A.B.3
-
13
-
-
1242351783
-
Alexander disease: Putative mechanisms of an astrocytic encephalopathy
-
Mignot C., Boespflu-Tanguy O., Gelot A., et al. Alexander disease: putative mechanisms of an astrocytic encephalopathy. Cell Mol Life Sci. 2004; 61: 369-385.
-
(2004)
Cell Mol Life Sci.
, vol.61
, pp. 369-385
-
-
Mignot, C.1
Boespflu-Tanguy, O.2
Gelot, A.3
-
14
-
-
0037086445
-
Conserved segments 1A and 2B of intermediate filament dimer: Their atomic structures and role in filament assembly
-
Strelkov SV, Herrmann H., Geisler N., et al. Conserved segments 1A and 2B of intermediate filament dimer: Their atomic structures and role in filament assembly. EMBO J. 2002; 21: 1255-1266.
-
(2002)
EMBO J.
, vol.21
, pp. 1255-1266
-
-
Strelkov, S.V.1
Herrmann, H.2
Geisler, N.3
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