Art

J-GLOBAL ID：201202240971306899   Reference number：12A0539681

Lesions of cortical GABAergic interneurons and acetylcholine neurons in xeroderma pigmentosum group A

色素性乾皮症A群における皮質GABA作動性介在ニューロンとアセチルコリンニューロンの病変

Author (4)： HAYASHI Masaharu (Dep. of Brain Dev. and Neural Regeneration, Tokyo Metropolitan Inst. of Medical Sci., Tokyo, JPN) ,  OHTO Tatsuyuki (Dep. of Pediatrics, Inst. of Clinical Medicine, Medical Branch, Univ. of Tsukuba, Ibaraki, JPN) ,  SHIODA Kei (Dep. of Neuropathology, Saitama Medical Univ., Saitama, JPN) ,  FUKATSU Ryo (Dep. of Neuropathology, Saitama Medical Univ., Saitama, JPN)
Material： Brain & Development  (Brain & Dev)
Volume： 34  Issue： 4  Page： 287-292  Publication year： Apr. 2012 
JST Material Number： W0814A  ISSN： 0387-7604  Document type： Article
Article type： 原著論文  Country of issue： Netherlands (NLD)  Language： ENGLISH (EN)

Thesaurus term： human ,...

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JST classification (2)： Congenital diseases,deformities in general.  (GD03010V) ,  Nervous system diseases  (GN03000O)

Substance index (2)： GABA ,  Acetylcholine

Reference (28)：

• Kraemer KH, Patronas NJ, Schiffmann R, Brooks BP, Tamura D, Digiovanna JJ. Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship. Neuroscience 2007;145:1388-96.
• Hirai Y, Kodama Y, Moriwaki S, Noda A, Cullings HM, Macphess DG, et al. Heterozygous individuals bearing a founder mutation in the XPA DNA repair gene comprise nearly 1% of the Japanese population. Mutat Res 2006;601:171-8.
• Hayashi M. Role of oxidative stress in xeroderma pigmentosum. Adv Exp Med Biol 2008;637:120-7.
• Itoh M, Hayashi M, Shioda K, Minagawa M, Isa F, Tamagawa K, et al. Neurodegeneration in hereditary nucleotide repair disorders. Brain Dev 1999;21:326-33.
• Hayashi M, Araki S, Kohyama J, Shioda K, Fukatsu R, Tamagawa K. Brainstem and basal ganglia lesions in xeroderma pigmentosum group A. J Neuropathol Exp Neurol 2004;63:1048-57.

Terms in the title (5)： 色素性乾皮症 ,  皮質 ,  GABA ,  介在ニューロン ,  病変