Art
J-GLOBAL ID:202202229999826153   Reference number:22A1019393

The Molecular Basis of Spinocerebellar Ataxia Type 7

脊髄小脳失調症7型の分子基盤【JST・京大機械翻訳】
Author (13):
Material:
Volume: 16  Page: 818757  Publication year: 2022 
JST Material Number: U7087A  ISSN: 1662-453X  Document type: Article
Article type: 文献レビュー  Country of issue: Switzerland (CHE)  Language: ENGLISH (EN)
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Spinocerebellar ataxia (SCA) t...
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Genetic variation  ,  Nervous system diseases  ,  Biological function 
Reference (141):
  • Ahmad S. I. (2012). Neurodegenerative Diseases. New York: Springer-Verlag.
  • Alves S., Cormier-Dequaire F., Marinello M., Marais T., Muriel M. P., Beaumatin F., et al (2014). The autophagy/lysosome pathway is impaired in SCA7 patients and SCA7 knock-in mice. Acta Neuropathol. 128 705-722. doi: 10.1007/s00401-014-1289-8
  • Ansorge O., Giunti P., Michalik A., Van Broeckhoven C., Harding B., Wood N., et al (2004). Ataxin-7 aggregation and ubiquitination in infantile SCA7 with 180 CAG repeats. Ann. Neurol. 56 448-452. doi: 10.1002/ana.20230
  • Arnoriaga Rodríguez M., Blasco G., Coll C., Biarnés C., Contreras-Rodríguez O., Garre-Olmo J., et al (2019). Glycated Hemoglobin, but not Insulin Sensitivity, is Associated with Memory in Subjects with Obesity. Obesity 27 932-942. doi: 10.1002/oby.22457
  • Arrasate M., Mitra S., Schweitzer E. S., Segal M. R., Finkbeiner S. (2004). Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death. Nature 431 805-810. doi: 10.1038/nature02998
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