These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

224 related articles for article (PubMed ID: 11685453)

  • 1. A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA-->AAUGAA) leads to the IPEX syndrome.
    Bennett CL; Brunkow ME; Ramsdell F; O'Briant KC; Zhu Q; Fuleihan RL; Shigeoka AO; Ochs HD; Chance PF
    Immunogenetics; 2001 Aug; 53(6):435-9. PubMed ID: 11685453
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3.
    Bennett CL; Christie J; Ramsdell F; Brunkow ME; Ferguson PJ; Whitesell L; Kelly TE; Saulsbury FT; Chance PF; Ochs HD
    Nat Genet; 2001 Jan; 27(1):20-1. PubMed ID: 11137993
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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. PubMed ID: 17484868
    [TBL] [Abstract][Full Text] [Related]  

  • 4. FOXP3 acts as a rheostat of the immune response.
    Ochs HD; Ziegler SF; Torgerson TR
    Immunol Rev; 2005 Feb; 203():156-64. PubMed ID: 15661028
    [TBL] [Abstract][Full Text] [Related]  

  • 5. IPEX and FOXP3: clinical and research perspectives.
    Wildin RS; Freitas A
    J Autoimmun; 2005; 25 Suppl():56-62. PubMed ID: 16243487
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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. PubMed ID: 16630773
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 18951619
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome.
    Owen CJ; Jennings CE; Imrie H; Lachaux A; Bridges NA; Cheetham TD; Pearce SH
    J Clin Endocrinol Metab; 2003 Dec; 88(12):6034-9. PubMed ID: 14671208
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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. PubMed ID: 18316354
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Treatment of the immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) by allogeneic bone marrow transplantation.
    Baud O; Goulet O; Canioni D; Le Deist F; Radford I; Rieu D; Dupuis-Girod S; Cerf-Bensussan N; Cavazzana-Calvo M; Brousse N; Fischer A; Casanova JL
    N Engl J Med; 2001 Jun; 344(23):1758-62. PubMed ID: 11396442
    [No Abstract]   [Full Text] [Related]  

  • 11. 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. PubMed ID: 17931557
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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. PubMed ID: 17196245
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome.
    Harbuz R; Lespinasse J; Boulet S; Francannet C; Creveaux I; Benkhelifa M; Jouk PS; Lunardi J; Ray PF
    Prenat Diagn; 2010 Nov; 30(11):1072-8. PubMed ID: 20842625
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and molecular findings in IPEX syndrome.
    Myers AK; Perroni L; Costigan C; Reardon W
    Arch Dis Child; 2006 Jan; 91(1):63-4. PubMed ID: 16371377
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Developmental changes of FOXP3-expressing CD4+CD25+ regulatory T cells and their impairment in patients with FOXP3 gene mutations.
    Fuchizawa T; Adachi Y; Ito Y; Higashiyama H; Kanegane H; Futatani T; Kobayashi I; Kamachi Y; Sakamoto T; Tsuge I; Tanaka H; Banham AH; Ochs HD; Miyawaki T
    Clin Immunol; 2007 Dec; 125(3):237-46. PubMed ID: 17916446
    [TBL] [Abstract][Full Text] [Related]  

  • 16. IPEX is a unique X-linked syndrome characterized by immune dysfunction, polyendocrinopathy, enteropathy, and a variety of autoimmune phenomena.
    Bennett CL; Ochs HD
    Curr Opin Pediatr; 2001 Dec; 13(6):533-8. PubMed ID: 11753102
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cutaneous manifestations of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome.
    Halabi-Tawil M; Ruemmele FM; Fraitag S; Rieux-Laucat F; Neven B; Brousse N; De Prost Y; Fischer A; Goulet O; Bodemer C
    Br J Dermatol; 2009 Mar; 160(3):645-51. PubMed ID: 18795917
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked inheritance (IPEX), a syndrome of systemic autoimmunity caused by mutations of FOXP3, a critical regulator of T-cell homeostasis.
    Gambineri E; Torgerson TR; Ochs HD
    Curr Opin Rheumatol; 2003 Jul; 15(4):430-5. PubMed ID: 12819471
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dermatologic and immunologic findings in the immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
    Nieves DS; Phipps RP; Pollock SJ; Ochs HD; Zhu Q; Scott GA; Ryan CK; Kobayashi I; Rossi TM; Goldsmith LA
    Arch Dermatol; 2004 Apr; 140(4):466-72. PubMed ID: 15096376
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 37(4):208-15. PubMed ID: 19912978
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.