在日本家族性肌萎缩侧索硬化症中，超氧化物歧化酶1（SOD1）基因存在两个碱基对缺失时Cu/Zn超氧化物歧化酶（SOD1）活性的异常。 - Suppr

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超能文献

Abnormality of Cu/Zn superoxide dismutase (SOD1) activity in Japanese familial amyotrophic lateral sclerosis with two base pair deletion in the SOD1 gene.

作者信息

Nakashima K, Watanabe Y, Kuno N, Nanba E, Takahashi K

机构信息

Division of Neurology, Faculty of Medicine, Tottori University, Yonago, Japan.

出版信息

Neurology. 1995 May;45(5):1019-20. doi: 10.1212/wnl.45.5.1019-a.

DOI:10.1212/wnl.45.5.1019-a

PMID:7746377

Abstract

摘要

相似文献

Abnormality of Cu/Zn superoxide dismutase (SOD1) activity in Japanese familial amyotrophic lateral sclerosis with two base pair deletion in the SOD1 gene.在日本家族性肌萎缩侧索硬化症中，超氧化物歧化酶1（SOD1）基因存在两个碱基对缺失时Cu/Zn超氧化物歧化酶（SOD1）活性的异常。

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A clinicopathological study of a patient with familial amyotrophic lateral sclerosis associated with a two base pair deletion in the copper/zinc superoxide dismutase (SOD1) gene.一名患有家族性肌萎缩侧索硬化症且铜/锌超氧化物歧化酶（SOD1）基因存在两个碱基对缺失的患者的临床病理研究。

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[Identification of the mutation of SOD1 gene in a familial amyotrophic lateral sclerosis].[家族性肌萎缩侧索硬化症中SOD1基因突变的鉴定]

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Anticipation and phenotypic heterogeneity in korean familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutation.韩国超氧化物歧化酶 1 基因突变家族性肌萎缩侧索硬化症的预期和表型异质性。

J Clin Neurol. 2007 Mar;3(1):38-44. doi: 10.3988/jcn.2007.3.1.38. Epub 2007 Mar 20.

Adherent monomer-misfolded SOD1.黏附性单体错误折叠的超氧化物歧化酶1

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Pathological characterization of astrocytic hyaline inclusions in familial amyotrophic lateral sclerosis.

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J Neurol Neurosurg Psychiatry. 1996 Dec;61(6):565-72. doi: 10.1136/jnnp.61.6.565.

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