234 related articles for article (PubMed ID: 21984607)
41. Disruption of immunological tolerance: role of AIRE gene in autoimmunity.
Rizzi M; Ferrera F; Filaci G; Indiveri F
Autoimmun Rev; 2006 Feb; 5(2):145-7. PubMed ID: 16431348
[TBL] [Abstract][Full Text] [Related]
42. Lessons on immune tolerance from the monogenic disease APS1.
DeVoss JJ; Anderson MS
Curr Opin Genet Dev; 2007 Jun; 17(3):193-200. PubMed ID: 17466510
[TBL] [Abstract][Full Text] [Related]
43. 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]
44. Autoimmunity in severe combined immunodeficiency (SCID): lessons from patients and experimental models.
Milner JD; Fasth A; Etzioni A
J Clin Immunol; 2008 May; 28 Suppl 1():S29-33. PubMed ID: 18193342
[TBL] [Abstract][Full Text] [Related]
45. FOXP3: genetic and epigenetic implications for autoimmunity.
Katoh H; Zheng P; Liu Y
J Autoimmun; 2013 Mar; 41():72-8. PubMed ID: 23313429
[TBL] [Abstract][Full Text] [Related]
46. A defect of regulatory T cells in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy.
Kekäläinen E; Tuovinen H; Joensuu J; Gylling M; Franssila R; Pöntynen N; Talvensaari K; Perheentupa J; Miettinen A; Arstila TP
J Immunol; 2007 Jan; 178(2):1208-15. PubMed ID: 17202386
[TBL] [Abstract][Full Text] [Related]
47. Lessons from primary immunodeficiencies: Autoimmune regulator and autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy.
Constantine GM; Lionakis MS
Immunol Rev; 2019 Jan; 287(1):103-120. PubMed ID: 30565240
[TBL] [Abstract][Full Text] [Related]
48. 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]
49. 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]
50. AIRE expression controls the peripheral selection of autoreactive B cells.
Sng J; Ayoglu B; Chen JW; Schickel JN; Ferre EMN; Glauzy S; Romberg N; Hoenig M; Cunningham-Rundles C; Utz PJ; Lionakis MS; Meffre E
Sci Immunol; 2019 Apr; 4(34):. PubMed ID: 30979797
[TBL] [Abstract][Full Text] [Related]
51. 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]
52. 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]
53. Recent insights into the role and molecular mechanisms of the autoimmune regulator (AIRE) gene in autoimmunity.
Fierabracci A
Autoimmun Rev; 2011 Jan; 10(3):137-43. PubMed ID: 20850570
[TBL] [Abstract][Full Text] [Related]
54. AIRE-mutations and autoimmune disease.
Bruserud Ø; Oftedal BE; Wolff AB; Husebye ES
Curr Opin Immunol; 2016 Dec; 43():8-15. PubMed ID: 27504588
[TBL] [Abstract][Full Text] [Related]
55. A potential screening tool for IPEX syndrome.
Heltzer ML; Choi JK; Ochs HD; Sullivan KE; Torgerson TR; Ernst LM
Pediatr Dev Pathol; 2007; 10(2):98-105. PubMed ID: 17378693
[TBL] [Abstract][Full Text] [Related]
56. Infections in the monogenic autoimmune syndrome APECED.
Oikonomou V; Break TJ; Gaffen SL; Moutsopoulos NM; Lionakis MS
Curr Opin Immunol; 2021 Oct; 72():286-297. PubMed ID: 34418591
[TBL] [Abstract][Full Text] [Related]
57. Single centre experience of haematopoietic SCT for patients with immunodysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
Nademi Z; Slatter M; Gambineri E; Mannurita SC; Barge D; Hodges S; Bunn S; Thomas J; Haugk B; Hambleton S; Flood T; Cant A; Abinun M; Gennery A
Bone Marrow Transplant; 2014 Feb; 49(2):310-2. PubMed ID: 24270390
[No Abstract] [Full Text] [Related]
58. APECED and the place of AIRE in the puzzle of the immune network associated with autoimmunity.
Aytekin ES; Cagdas D
Scand J Immunol; 2023 Aug; 98(2):e13299. PubMed ID: 38441333
[TBL] [Abstract][Full Text] [Related]
59. FOXP3 deficiency, from the mechanisms of the disease to curative strategies.
Borna S; Meffre E; Bacchetta R
Immunol Rev; 2024 Mar; 322(1):244-258. PubMed ID: 37994657
[TBL] [Abstract][Full Text] [Related]
60. Primary immunodeficiencies unravel critical aspects of the pathophysiology of autoimmunity and of the genetics of autoimmune disease.
Coutinho A; Carneiro-Sampaio M
J Clin Immunol; 2008 May; 28 Suppl 1():S4-10. PubMed ID: 18293069
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
