Art

J-GLOBAL ID：201902291550905470   Reference number：19A2482107

Measurement of Serum Tenascin-X in Joint Hypermobility Syndrome Patients

関節運動過剰症候群患者における血清テネイシンXの測定

Author (9)： Yamada Kazuo (Department of Biosignaling and Radioisotope Experiment, Interdiscipnary Center for Science Research, Organization for Research and Academic Information, Shimane University) ,  Yamada Kazuo (Department of Legal Medicine, Faculty of Medicine, Shimane University) ,  Watanabe Atsushi (Division of Clinical Genetics, Nippon Medical School Hospital) ,  Watanabe Atsushi (Division of Clinical Genetics, Kanazawa University Hospital) ,  Takeshita Haruo (Department of Legal Medicine, Faculty of Medicine, Shimane University) ,  Fujita Atsushi (Department of Human Genetics, Yokohama City University Graduate School of Medicine) ,  Miyake Noriko (Department of Human Genetics, Yokohama City University Graduate School of Medicine) ,  Matsumoto Naomichi (Department of Human Genetics, Yokohama City University Graduate School of Medicine) ,  Matsumoto Ken-ichi (Department of Biosignaling and Radioisotope Experiment, Interdiscipnary Center for Science Research, Organization for Research and Academic Information, Shimane University)
Material： Biological and Pharmaceutical Bulletin (Web)
Volume： 42  Issue： 9  Page： 1596-1599(J-STAGE)  Publication year： 2019 
JST Material Number： U1402A  ISSN： 1347-5215  Document type： Article
Article type： 原著論文  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： human ,...
Semi thesaurus term： *テネイシンX ,...

Register(free) or Log In to access     To see more with JDream III (charged).   {{ this.onShowAbsJLink("http://jdream3.com/lp/jglobal/index.html?docNo=19A2482107&from=J-GLOBAL&jstjournalNo=U1402A") }}

Author keywords (6)： joint hypermobility syndrome ,  Ehlers-Danlos syndrome ,  tenascin-X ,  joint hypermobility syndrome ,  Ehlers-Danlos syndrome ,  tenascin-X

JST classification (2)： Congenital diseases,deformities in general.  (GD03010V) ,  Musculoskeletal diseases  (GG03000T)

Reference (15)：

• 1) Grahame R. Joint hypermobility and genetic collagen disorders: are they related? Arch. Dis. Child., 80, 188-191 (1999).
• 2) Malfait F, Hakim AJ, De Paepe A, Grahame R. The genetic basis of the joint hypermobility syndromes. Rheumatology, 45, 502-507 (2006).
• 3) Tinkle BT, Bird HA, Grahame R, Lavallee M, Levy HP, Sillence D. The lack of clinical distinction between the hypermobility type of Ehlers-Danlos syndrome (a.k.a. hypermobility syndrome). Am. J. Med. Genet. A, 149A, 2368-2370 (2009).
• 4) Schalkwijk J, Zweers MC, Steijlen PM, Dean WB, Taylor G, van Vlijmen IM, van Haren B, Miller WL, Bristow J. A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency. N. Engl. J. Med., 345, 1167-1175 (2001).
• 5) Minamitani T, Ikuta T, Saito Y, Takebe G, Sato M, Sawa H, Nishimura T, Nakamura F, Takahashi K, Ariga H, Matsumoto K. Modulation of collagen fibrillogenesis by tenascin-X and type VI collagen. Exp. Cell Res., 298, 305-315 (2004).

Terms in the title (6)： 関節 ,  運動過剰 ,  症候群 ,  患者 ,  血清 ,  テネイシン