Art

J-GLOBAL ID：200902259439630529   Reference number：09A0818437

Recent progress in understanding molecular pathogenesis of Fanconi anemia

Fanconi貧血の分子病態-最近の進歩

Author (3)： YAMASHITA TAKAYUKI (群馬大学生体調節研究所) ,  ODA TSUKASA (群馬大学生体調節研究所) ,  SEKIMOTO TAKAYUKI (群馬大学生体調節研究所)
Material： 臨床血液  (Japanese Journal of Clinical Hematology)
Volume： 50  Issue： 7  Page： 538-546 (J-STAGE)  Publication year： 2009 
JST Material Number： Z0688A  ISSN： 0485-1439  Document type： Article
Article type： 解説  Country of issue： Japan (JPN)  Language： JAPANESE (JA)

Thesaurus term： human ,...
Semi thesaurus term： genetic variation ,...

Register(free) or Log In to access     To see more with JDream III (charged).   {{ this.onShowAbsJLink("http://jdream3.com/lp/jglobal/index.html?docNo=09A0818437&from=J-GLOBAL&jstjournalNo=Z0688A") }}

JST classification (3)： Hematologic diseases  (GK03000F) ,  Congenital diseases,deformities in general.  (GD03010V) ,  Molecular genetics in general  (EC02010J)

Reference (91)：

• TANIGUCHI, T. Molecular pathogenesis of Fanconi anemia : recent progress. Blood. 2006, 107, 4223-4233
• WANG, W. Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins. Nat Rev Genet. 2007, 8, 735-748
• DE WINTER, JP. The genetic and molecular basis of Fanconi anemia. Mutat Res. 2008, 2008, Nov 14
• STRATHDEE, CA. Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9. Nat Genet. 1992, 1, 196-198
• STRATHDEE, CA. Cloning of cDNAs for Fanconi's anaemia by functional complementation. Nature. 1992, 356, 763-767

Terms in the title (2)： Fanconi貧血 ,  分子病態