FOXP3 wt Allele

Known as: PIDX, XPID, Forkhead Box P3 wt Allele 
Human FOXP3 wild-type allele is located in the vicinity of Xp11.23 and is approximately 14 kb in length. This allele, which encodes forkhead box… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1948-2017
05101519482016

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Highly Cited
2007
Highly Cited
2007
BACKGROUND Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) results in systemic autoimmunity from birth and… (More)
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Highly Cited
2007
Highly Cited
2007
BACKGROUND & AIMS Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX; OMIM 304930) syndrome is a congenital… (More)
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Highly Cited
2007
Highly Cited
2007
We have found that FOXP3 is an oligomeric component of a large supramolecular complex. Certain FOXP3 mutants with single amino… (More)
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2007
2007
The main purpose of this study was to determine whether the increased glucose transport (GT) found immediately postexercise (IPEX… (More)
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Highly Cited
2006
Highly Cited
2006
The autoimmune disease immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) is caused by mutations in the… (More)
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Highly Cited
2006
Highly Cited
2006
Foxp3 has been shown to be both necessary and sufficient for the development and function of naturally arising CD4+ CD25… (More)
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Highly Cited
2001
Highly Cited
2001
IPEX is a fatal disorder characterized by immune dysregulation, polyendocrinopathy, enteropathy and X-linked inheritance (MIM… (More)
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Highly Cited
2001
Highly Cited
2001
To determine whether human X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome (IPEX; MIM 304930) is the… (More)
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Highly Cited
2001
Highly Cited
2001
The mouse scurfy gene, Foxp3, and its human orthologue, FOXP3, which maps to Xp11.23–Xq13.3, were recently identified by… (More)
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Highly Cited
2000
Highly Cited
2000
X-linked autoimmunity-allergic disregulation syndrome (XLAAD) is an X-linked recessive immunological disorder characterized by… (More)
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