From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation-Reference-Cited by-同舟云学术

From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation

Published:2016-02-25 Issue:1 Volume:1417 Page:5-22
ISSN:0077-8923
Container-title:Annals of the New York Academy of Sciences
language:en
Short-container-title:Ann. N.Y. Acad. Sci.

Author:

Bacchetta Rosa¹,Barzaghi Federica²,Roncarolo Maria-Grazia¹

Affiliation:

1. Department of Pediatrics; Division of Pediatric Stem Cells, Transplantation and Regenerative Medicine; Stanford University Medical School; Stanford California.

2. San Raffaele Telethon Institute for Gene Therapy; Division of Regenerative Medicine; Stem Cells and Gene Therapy; San Raffaele Scientific Institute; Milan Italy

Publisher

Wiley

Subject

History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/nyas.13011/fullpdf

Reference156 articles.

1. An X-linked syndrome of diarrhea, polyendocrinopathy, and fatal infection in infancy;Powell;J. Pediatr.,1982

2. JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome;Chatila;J. Clin. Invest.,2000

3. X-linked lymphoreticular disease in the scurfy (sf) mutant mouse;Godfrey;Am. J. Pathol.,1991

4. Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse;Brunkow;Nat. Genet.,2001

5. The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3;Bennett;Nat. Genet.,2001

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