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Advanced glycation endproduct-modified superoxide dismutase-1 (SOD1)-positive inclusions are common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutations and transgenic mice expressing human SOD1 with a G85R mutation.
Kato S, Horiuchi S, Liu J, Cleveland DW, Shibata N, Nakashima K, Nagai R, Hirano A, Takikawa M, Kato M, Nakano I, Ohama E. Kato S, et al. Among authors: takikawa m. Acta Neuropathol. 2000 Nov;100(5):490-505. doi: 10.1007/s004010000226. Acta Neuropathol. 2000. PMID: 11045671
Copper chaperone for superoxide dismutase co-aggregates with superoxide dismutase 1 (SOD1) in neuronal Lewy body-like hyaline inclusions: an immunohistochemical study on familial amyotrophic lateral sclerosis with SOD1 gene mutation.
Kato S, Sumi-Akamaru H, Fujimura H, Sakoda S, Kato M, Hirano A, Takikawa M, Ohama E. Kato S, et al. Among authors: takikawa m. Acta Neuropathol. 2001 Sep;102(3):233-8. doi: 10.1007/s004010000355. Acta Neuropathol. 2001. PMID: 11585247
Formation of advanced glycation end-product-modified superoxide dismutase-1 (SOD1) is one of the mechanisms responsible for inclusions common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutation, and transgenic mice expressing human SOD1 gene mutation.
Kato S, Nakashima K, Horiuchi S, Nagai R, Cleveland DW, Liu J, Hirano A, Takikawa M, Kato M, Nakano I, Sakoda S, Asayama K, Ohama E. Kato S, et al. Among authors: takikawa m. Neuropathology. 2001 Mar;21(1):67-81. doi: 10.1046/j.1440-1789.2001.00359.x. Neuropathology. 2001. PMID: 11304045 Review.
New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytes.
Kato S, Takikawa M, Nakashima K, Hirano A, Cleveland DW, Kusaka H, Shibata N, Kato M, Nakano I, Ohama E. Kato S, et al. Among authors: takikawa m. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000 Jun;1(3):163-84. doi: 10.1080/14660820050515160. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000. PMID: 11464950 Review.
102 results