Art

J-GLOBAL ID：201802249766795659   Reference number：18A2058021

Methylome analysis of thyroid ectopy shows no disease-specific DNA methylation signature

異所性甲状腺のメチローム解析は疾患特異的DNAメチル化特性を示さない

Author (5)： Narumi Satoshi (Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan) ,  Narumi Satoshi (Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan) ,  Matsubara Keiko (Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan) ,  Ishii Tomohiro (Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan) ,  Hasegawa Tomonobu (Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan)
Material： Clinical Pediatric Endocrinology  (Clin Pediatr Endocrinol)
Volume： 27  Issue： 4  Page： 235-238(J-STAGE)  Publication year： 2018 
JST Material Number： L4217A  ISSN： 0918-5739  Document type： Article
Article type： 原著論文  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： human ,...
Semi thesaurus term： *Aberrant thyroid

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Author keywords (5)： congenital hypothyroidism ,  thyroid dysgenesis ,  thyroid ectopy ,  epigenetics ,  DNA methylation

JST classification (1)： Endocrine diseases  (GL03000I)

Reference (7)：

• 1. Abu-Khudir, R, Larrivée-Vanier, S, Wasserman, JD, Deladoëy, J. Disorders of thyroid morphogenesis. Best Pract Res Clin Endocrinol Metab 2017;31: 143-59.
• 2. Castanet, M, Polak, M, Bonaïti-Pellié, C, Lyonnet, S, Czernichow, P, Léger, J, AFDPHE (Association Française pour le Dépistage et la Prévention des Handicaps de l’Enfant). Nineteen years of national screening for congenital hypothyroidism: familial cases with thyroid dysgenesis suggest the involvement of genetic factors. J Clin Endocrinol Metab 2001;86: 2009-14.
• 3. Perry, R, Heinrichs, C, Bourdoux, P, Khoury, K, Szöts, F, Dussault, JH, et al. Discordance of monozygotic twins for thyroid dysgenesis: implications for screening and for molecular pathophysiology. J Clin Endocrinol Metab 2002;87: 4072-7.
• 4. De Felice, M, Di Lauro, R. Thyroid development and its disorders: genetics and molecular mechanisms. Endocr Rev 2004;25: 722-46.
• 5. Kondo, T, Nakazawa, T, Ma, D, Niu, D, Mochizuki, K, Kawasaki, T, et al. Epigenetic silencing of TTF-1/NKX2-1 through DNA hypermethylation and histone H3 modulation in thyroid carcinomas. Lab Invest 2009;89: 791-9.

Terms in the title (4)： 異所性甲状腺 ,  解析 ,  疾患 ,  DNAメチル化