The role of X-linked FOXP3 in the autoimmune susceptibility of Turner Syndrome patients
Turner Syndrome patients have an absent second sex chromosome and a predisposition to autoimmune disease. We hypothesized that the autoimmune susceptibility in Turner Syndrome may be due to an alteration in the expression of the X-linked FOXP3 gene. FOXP3 is important in the development of regulator...
Ausführliche Beschreibung
Bibliographische Detailangaben
| Veröffentlicht in: | Clinical immunology (Orlando, Fla.). - 1999. - 131(2009), 1 vom: 01. Apr., Seite 139-44
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| 1. Verfasser: |
Su, Maureen A
(VerfasserIn) |
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| Weitere Verfasser: |
Stenerson, Matthew,
Liu, Weihong,
Putnam, Amy,
Conte, Felix,
Bluestone, Jeffrey A,
Anderson, Mark S |
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| Format: | Online-Aufsatz
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| Sprache: | English |
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| Veröffentlicht: |
2009
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| Zugriff auf das übergeordnete Werk: | Clinical immunology (Orlando, Fla.)
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| Schlagworte: | Journal Article
Research Support, N.I.H., Extramural
FOXP3 protein, human
Forkhead Transcription Factors |
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