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

S. Kato; Seiko Horiuchi; Jian Liu; Don W. Cleveland; Noriyuki Shibata; Kenji Nakashima; Ryoji Nagai; Asao Hirano; Miki Takikawa; Masako Kato; Imaharu Nakano; Eisaku Ohama

doi:10.1007/s004010000226

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

Acta Neuropathologica ◽

10.1007/s004010000226 ◽

2000 ◽

Vol 100 (5) ◽

pp. 490-505 ◽

Cited By ~ 48

Author(s):

S. Kato ◽

Seiko Horiuchi ◽

Jian Liu ◽

Don W. Cleveland ◽

Noriyuki Shibata ◽

...

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Gene Mutations ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Advanced Glycation ◽

Sod1 Gene ◽

Advanced Glycation Endproduct ◽

Human Sod1 ◽

Lateral Sclerosis

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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

Neuropathology ◽

10.1046/j.1440-1789.2001.00359.x ◽

2001 ◽

Vol 21 (1) ◽

pp. 67-81 ◽

Cited By ~ 21

Author(s):

Shinsuke Kato ◽

Kenji Nakashima ◽

Seikoh Horiuchi ◽

Ryoji Nagai ◽

Don W. Cleveland ◽

...

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Gene Mutation ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Advanced Glycation ◽

Sod1 Gene ◽

Advanced Glycation End Product ◽

Human Sod1 ◽

Lateral Sclerosis

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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

Neuropathology ◽

10.1111/j.1440-1789.2001.00359.x ◽

2001 ◽

Vol 21 (1) ◽

pp. 67-81 ◽

Cited By ~ 1

Author(s):

Shinsuke Kato ◽

Kenji Nakashima ◽

Seikoh Horiuchi ◽

Ryoji Nagai ◽

Don W. Cleveland ◽

...

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Gene Mutation ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Advanced Glycation ◽

Sod1 Gene ◽

Advanced Glycation End Product ◽

Human Sod1 ◽

Lateral Sclerosis

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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

Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders ◽

10.1080/14660820050515160 ◽

2000 ◽

Vol 1 (3) ◽

pp. 163-184 ◽

Cited By ~ 106

Author(s):

Shinsuke Kato ◽

Miki Takikawa ◽

Kenji Nakashima ◽

Asao Hirano ◽

Don W Cleveland ◽

...

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Gene Mutations ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Sod1 Gene ◽

Lateral Sclerosis

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Astrocytic hyaline inclusions contain advanced glycation endproducts in familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutation: immunohistochemical and immunoelectron microscopical analyses

Acta Neuropathologica ◽

10.1007/s004010050983 ◽

1999 ◽

Vol 97 (3) ◽

pp. 260-266 ◽

Cited By ~ 18

Author(s):

S. Kato ◽

Seikoh Horiuchi ◽

Kenji Nakashima ◽

Asao Hirano ◽

Noriyuki Shibata ◽

...

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Gene Mutation ◽

Advanced Glycation Endproducts ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Advanced Glycation ◽

Glycation Endproducts ◽

Hyaline Inclusions ◽

Lateral Sclerosis

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Advanced glycation endproducts are deposited in neuronal hyaline inclusions: a study on familial amyotrophic lateral sclerosis with superoxide dismutase-1 mutation

Acta Neuropathologica ◽

10.1007/s004010050980 ◽

1999 ◽

Vol 97 (3) ◽

pp. 240-246 ◽

Cited By ~ 19

Author(s):

N. Shibata ◽

Asao Hirano ◽

Shinsuke Kato ◽

Ryoji Nagai ◽

Seikoh Horiuchi ◽

...

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Advanced Glycation Endproducts ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Advanced Glycation ◽

Glycation Endproducts ◽

Hyaline Inclusions ◽

Lateral Sclerosis

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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

Acta Neuropathologica ◽

10.1007/s004010000355 ◽

2001 ◽

Vol 102 (3) ◽

pp. 233-238 ◽

Cited By ~ 36

Author(s):

Shinsuke Kato ◽

Hisae Sumi-Akamaru ◽

Harutoshi Fujimura ◽

Saburo Sakoda ◽

Masako Kato ◽

...

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Lewy Body ◽

Immunohistochemical Study ◽

Familial Amyotrophic Lateral Sclerosis ◽

Copper Chaperone ◽

Superoxide Dismutase 1 ◽

Sod1 Gene ◽

Hyaline Inclusions ◽

Lateral Sclerosis

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Transgenic mouse model for familial amyotrophic lateral sclerosis with superoxide dismutase-1 mutation

Neuropathology ◽

10.1046/j.1440-1789.2001.00361.x ◽

2001 ◽

Vol 21 (1) ◽

pp. 82-92 ◽

Cited By ~ 72

Author(s):

Noriyuki Shibata

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Mouse Model ◽

Transgenic Mouse ◽

Transgenic Mouse Model ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Lateral Sclerosis

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Neuropathology of familial amyotrophic lateral sclerosis patients with superoxide dismutase 1 gene mutation

Neuropathology ◽

10.1111/j.1440-1789.1998.tb00132.x ◽

1998 ◽

Vol 18 (4) ◽

pp. 363-369 ◽

Cited By ~ 14

Author(s):

Asao Hirano

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Gene Mutation ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Lateral Sclerosis

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MRI detects early hindlimb muscle atrophy in Gly93Ala superoxide dismutase-1 (G93A SOD1) transgenic mice, an animal model of familial amyotrophic lateral sclerosis

NMR in Biomedicine ◽

10.1002/nbm.861 ◽

2004 ◽

Vol 17 (1) ◽

pp. 28-32 ◽

Cited By ~ 27

Author(s):

Keith J. Brooks ◽

Mark D. W. Hill ◽

Paul D. Hockings ◽

David G. Reid

Keyword(s):

Animal Model ◽

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Transgenic Mice ◽

Muscle Atrophy ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Hindlimb Muscle ◽

G93a Sod1 ◽

Lateral Sclerosis

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Familial Amyotrophic Lateral Sclerosis with a Novel G85S Mutation of Superoxide Dismutase 1 Gene: Clinical Features of Lower Motor Neuron Disease

Internal Medicine ◽

10.2169/internalmedicine.49.2720 ◽

2010 ◽

Vol 49 (2) ◽

pp. 183-186 ◽

Cited By ~ 4

Author(s):

Takanori Takazawa ◽

Ken Ikeda ◽

Takehisa Hirayama ◽

Kiyokazu Kawabe ◽

Yoshikazu Nakamura ◽

...

Keyword(s):

Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase ◽

Motor Neuron ◽

Motor Neuron Disease ◽

Clinical Features ◽

Lower Motor Neuron ◽

Familial Amyotrophic Lateral Sclerosis ◽

Superoxide Dismutase 1 ◽

Lower Motor Neuron Disease ◽

Lateral Sclerosis

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