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Items: 1 to 20 of 288

1.

IPEX, FOXP3 and regulatory T-cells: a model for autoimmunity.

Ochs HD, Gambineri E, Torgerson TR.

Immunol Res. 2007;38(1-3):112-21. Review.

PMID:
17917016
2.

Immune reconstitution and recovery of FOXP3 (forkhead box P3)-expressing T cells after transplantation for IPEX (immune dysregulation, polyendocrinopathy, enteropathy, X-linked) syndrome.

Zhan H, Sinclair J, Adams S, Cale CM, Murch S, Perroni L, Davies G, Amrolia P, Qasim W.

Pediatrics. 2008 Apr;121(4):e998-1002. doi: 10.1542/peds.2007-1863. Epub 2008 Mar 3.

PMID:
18316354
3.

Immune dysregulation, polyendocrinopathy, enteropathy, X-linked: forkhead box protein 3 mutations and lack of regulatory T cells.

Torgerson TR, Ochs HD.

J Allergy Clin Immunol. 2007 Oct;120(4):744-50; quiz 751-2. Review.

PMID:
17931557
4.

Clinical and molecular aspects of autoimmune enteropathy and immune dysregulation, polyendocrinopathy autoimmune enteropathy X-linked syndrome.

Ruemmele FM, Moes N, de Serre NP, Rieux-Laucat F, Goulet O.

Curr Opin Gastroenterol. 2008 Nov;24(6):742-8. doi: 10.1097/MOG.0b013e32830c9022. Review.

PMID:
19122524
5.

From autoimmune enteropathy to the IPEX (immune dysfunction, polyendocrinopathy, enteropathy, X-linked) syndrome.

Blanco QuirĂ³s A, Arranz Sanz E, Bernardo Ordiz D, Garrote Adrados JA.

Allergol Immunopathol (Madr). 2009 Jul-Aug;37(4):208-15. doi: 10.1016/j.aller.2009.04.002. Epub 2009 Aug 26. Review.

PMID:
19912978
6.

Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: a model of immune dysregulation.

Torgerson TR, Ochs HD.

Curr Opin Allergy Clin Immunol. 2002 Dec;2(6):481-7. Review.

PMID:
14752330
7.

Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity.

Gambineri E, Perroni L, Passerini L, Bianchi L, Doglioni C, Meschi F, Bonfanti R, Sznajer Y, Tommasini A, Lawitschka A, Junker A, Dunstheimer D, Heidemann PH, Cazzola G, Cipolli M, Friedrich W, Janic D, Azzi N, Richmond E, Vignola S, Barabino A, Chiumello G, Azzari C, Roncarolo MG, Bacchetta R.

J Allergy Clin Immunol. 2008 Dec;122(6):1105-1112.e1. doi: 10.1016/j.jaci.2008.09.027. Epub 2008 Oct 25.

PMID:
18951619
8.

CD25 deficiency causes an immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like syndrome, and defective IL-10 expression from CD4 lymphocytes.

Caudy AA, Reddy ST, Chatila T, Atkinson JP, Verbsky JW.

J Allergy Clin Immunol. 2007 Feb;119(2):482-7. Epub 2006 Dec 27.

PMID:
17196245
9.

Single-cell analysis of normal and FOXP3-mutant human T cells: FOXP3 expression without regulatory T cell development.

Gavin MA, Torgerson TR, Houston E, DeRoos P, Ho WY, Stray-Pedersen A, Ocheltree EL, Greenberg PD, Ochs HD, Rudensky AY.

Proc Natl Acad Sci U S A. 2006 Apr 25;103(17):6659-64. Epub 2006 Apr 14. Erratum in: Proc Natl Acad Sci U S A. 2006 Jun 13;103(24):9373.

10.

IPEX and FOXP3: clinical and research perspectives.

Wildin RS, Freitas A.

J Autoimmun. 2005;25 Suppl:56-62. Epub 2005 Oct 21. Review.

PMID:
16243487
11.

Regulatory T-cell functions are subverted and converted owing to attenuated Foxp3 expression.

Wan YY, Flavell RA.

Nature. 2007 Feb 15;445(7129):766-70. Epub 2007 Jan 14.

PMID:
17220876
12.

Clinical and molecular characteristics of immunodysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China.

An YF, Xu F, Wang M, Zhang ZY, Zhao XD.

Scand J Immunol. 2011 Sep;74(3):304-9. doi: 10.1111/j.1365-3083.2011.02574.x.

13.

Identification of FOXP3-negative regulatory T-like (CD4(+)CD25(+)CD127(low)) cells in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.

Otsubo K, Kanegane H, Kamachi Y, Kobayashi I, Tsuge I, Imaizumi M, Sasahara Y, Hayakawa A, Nozu K, Iijima K, Ito S, Horikawa R, Nagai Y, Takatsu K, Mori H, Ochs HD, Miyawaki T.

Clin Immunol. 2011 Oct;141(1):111-20. doi: 10.1016/j.clim.2011.06.006. Epub 2011 Jul 12.

PMID:
21802372
14.

Severe food allergy as a variant of IPEX syndrome caused by a deletion in a noncoding region of the FOXP3 gene.

Torgerson TR, Linane A, Moes N, Anover S, Mateo V, Rieux-Laucat F, Hermine O, Vijay S, Gambineri E, Cerf-Bensussan N, Fischer A, Ochs HD, Goulet O, Ruemmele FM.

Gastroenterology. 2007 May;132(5):1705-17. Epub 2007 Feb 23.

PMID:
17484868
16.

Clinical and molecular findings in IPEX syndrome.

Myers AK, Perroni L, Costigan C, Reardon W.

Arch Dis Child. 2006 Jan;91(1):63-4.

17.

Mechanistic associations of a mild phenotype of immunodysregulation, polyendocrinopathy, enteropathy, x-linked syndrome.

De Benedetti F, Insalaco A, Diamanti A, Cortis E, Muratori F, Lamioni A, Carsetti R, Cusano R, De Vito R, Perroni L, Gambarara M, Castro M, Bottazzo GF, Ugazio AG.

Clin Gastroenterol Hepatol. 2006 May;4(5):653-9.

PMID:
16630773
18.

Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.

Hashimura Y, Nozu K, Kanegane H, Miyawaki T, Hayakawa A, Yoshikawa N, Nakanishi K, Takemoto M, Iijima K, Matsuo M.

Pediatr Nephrol. 2009 Jun;24(6):1181-6. doi: 10.1007/s00467-009-1119-8. Epub 2009 Feb 3.

PMID:
19189134
19.

IPEX as a result of mutations in FOXP3.

van der Vliet HJ, Nieuwenhuis EE.

Clin Dev Immunol. 2007;2007:89017. doi: 10.1155/2007/89017. Review.

20.

Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndrome.

Uzel G, Sampaio EP, Lawrence MG, Hsu AP, Hackett M, Dorsey MJ, Noel RJ, Verbsky JW, Freeman AF, Janssen E, Bonilla FA, Pechacek J, Chandrasekaran P, Browne SK, Agharahimi A, Gharib AM, Mannurita SC, Yim JJ, Gambineri E, Torgerson T, Tran DQ, Milner JD, Holland SM.

J Allergy Clin Immunol. 2013 Jun;131(6):1611-23. doi: 10.1016/j.jaci.2012.11.054. Epub 2013 Mar 25.

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