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 *

325 related articles for article (PubMed ID: 21400500)

  • 1. Functional type 1 regulatory T cells develop regardless of FOXP3 mutations in patients with IPEX syndrome.
    Passerini L; Di Nunzio S; Gregori S; Gambineri E; Cecconi M; Seidel MG; Cazzola G; Perroni L; Tommasini A; Vignola S; Guidi L; Roncarolo MG; Bacchetta R
    Eur J Immunol; 2011 Apr; 41(4):1120-31. PubMed ID: 21400500
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Defective regulatory and effector T cell functions in patients with FOXP3 mutations.
    Bacchetta R; Passerini L; Gambineri E; Dai M; Allan SE; Perroni L; Dagna-Bricarelli F; Sartirana C; Matthes-Martin S; Lawitschka A; Azzari C; Ziegler SF; Levings MK; Roncarolo MG
    J Clin Invest; 2006 Jun; 116(6):1713-22. PubMed ID: 16741580
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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. PubMed ID: 21802372
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) and IPEX-related disorders: an evolving web of heritable autoimmune diseases.
    Verbsky JW; Chatila TA
    Curr Opin Pediatr; 2013 Dec; 25(6):708-14. PubMed ID: 24240290
    [TBL] [Abstract][Full Text] [Related]  

  • 5. IPEX and the role of Foxp3 in the development and function of human Tregs.
    Le Bras S; Geha RS
    J Clin Invest; 2006 Jun; 116(6):1473-5. PubMed ID: 16741571
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Demethylation analysis of the FOXP3 locus shows quantitative defects of regulatory T cells in IPEX-like syndrome.
    Barzaghi F; Passerini L; Gambineri E; Ciullini Mannurita S; Cornu T; Kang ES; Choe YH; Cancrini C; Corrente S; Ciccocioppo R; Cecconi M; Zuin G; Discepolo V; Sartirana C; Schmidtko J; Ikinciogullari A; Ambrosi A; Roncarolo MG; Olek S; Bacchetta R
    J Autoimmun; 2012 Feb; 38(1):49-58. PubMed ID: 22264504
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Treatment with rapamycin can restore regulatory T-cell function in IPEX patients.
    Passerini L; Barzaghi F; Curto R; Sartirana C; Barera G; Tucci F; Albarello L; Mariani A; Testoni PA; Bazzigaluppi E; Bosi E; Lampasona V; Neth O; Zama D; Hoenig M; Schulz A; Seidel MG; Rabbone I; Olek S; Roncarolo MG; Cicalese MP; Aiuti A; Bacchetta R
    J Allergy Clin Immunol; 2020 Apr; 145(4):1262-1271.e13. PubMed ID: 31874182
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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. PubMed ID: 23534974
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Mutation in the Transcription Factor Foxp3 Drives T Helper 2 Effector Function in Regulatory T Cells.
    Van Gool F; Nguyen MLT; Mumbach MR; Satpathy AT; Rosenthal WL; Giacometti S; Le DT; Liu W; Brusko TM; Anderson MS; Rudensky AY; Marson A; Chang HY; Bluestone JA
    Immunity; 2019 Feb; 50(2):362-377.e6. PubMed ID: 30709738
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Point mutants of forkhead box P3 that cause immune dysregulation, polyendocrinopathy, enteropathy, X-linked have diverse abilities to reprogram T cells into regulatory T cells.
    McMurchy AN; Gillies J; Allan SE; Passerini L; Gambineri E; Roncarolo MG; Bacchetta R; Levings MK
    J Allergy Clin Immunol; 2010 Dec; 126(6):1242-51. PubMed ID: 21036387
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 103(17):6659-64. PubMed ID: 16617117
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome: A systematic review.
    Park JH; Lee KH; Jeon B; Ochs HD; Lee JS; Gee HY; Seo S; Geum D; Piccirillo CA; Eisenhut M; van der Vliet HJ; Lee JM; Kronbichler A; Ko Y; Shin JI
    Autoimmun Rev; 2020 Jun; 19(6):102526. PubMed ID: 32234571
    [TBL] [Abstract][Full Text] [Related]  

  • 15. IPEX as a result of mutations in FOXP3.
    van der Vliet HJ; Nieuwenhuis EE
    Clin Dev Immunol; 2007; 2007():89017. PubMed ID: 18317533
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. The immunogenetics of immune dysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome.
    d'Hennezel E; Bin Dhuban K; Torgerson T; Piccirillo CA
    J Med Genet; 2012 May; 49(5):291-302. PubMed ID: 22581967
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 19189134
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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):304-309. PubMed ID: 21595732
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.