Art

J-GLOBAL ID：201302208791131159   Reference number：13A0312788

細胞内小器官と神経難病 繊毛病と神経症状

Author (1)： KUMAMOTO NATSUKO (名古屋市大 大学院医学研究科 機能組織学)
Material： 脳21  (Brain 21)
Volume： 16  Issue： 1  Page： 78-82  Publication year： Jan. 20, 2013 
JST Material Number： L3821A  ISSN： 1344-0128  Document type： Article
Article type： 解説  Country of issue： Japan (JPN)  Language： JAPANESE (JA)

Thesaurus term： *hereditary disease ,...
Semi thesaurus term： *Ciliopathy ,...

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JST classification (2)： Congenital diseases,deformities in general.  (GD03010V) ,  Clinical neurology in general  (GN01030H)

Reference (18)：

• 1) Gerdes JM, et al : The vertebrate primary cilium in de-velopment, homeostasis, and disease. Cell 137 : 32-45, 2009.
• 2) Goetz SC, Anderson KV : The primary cilium : a signal-ling centre during vertebrate development. Nat Rev Genet 11 : 331-344, 2010.
• 3) Pazour GJ, et al : Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella. J Cell Biol 151 : 709-718, 2000.
• 4) Qin H, et al : An autosomal recessive polycystic kidney disease gene homolog is involved in intraflagellar trans-port in C. elegans ciliated sensory neurons. Curr Biol 11 : 457-461, 2001.
• 5) Yoder BK, et al : Insertional mutagenesis and molecu-lar analysis of a new gene associated with polycystic kidney disease. Proc Assoc Am Physicians 107 : 314- 323, 1995.

Terms in the title (4)： 細胞内小器官 ,  神経難病 ,  繊毛病 ,  神経症状