408 related articles for article (PubMed ID: 25468195)
1. Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like disorder caused by loss-of-function mutations in LRBA.
Charbonnier LM; Janssen E; Chou J; Ohsumi TK; Keles S; Hsu JT; Massaad MJ; Garcia-Lloret M; Hanna-Wakim R; Dbaibo G; Alangari AA; Alsultan A; Al-Zahrani D; Geha RS; Chatila TA
J Allergy Clin Immunol; 2015 Jan; 135(1):217-27. PubMed ID: 25468195
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Regulatory T-cell dysfunction induces autoantibodies to bullous pemphigoid antigens in mice and human subjects.
Muramatsu K; Ujiie H; Kobayashi I; Nishie W; Izumi K; Ito T; Yoshimoto N; Natsuga K; Iwata H; Shimizu H
J Allergy Clin Immunol; 2018 Dec; 142(6):1818-1830.e6. PubMed ID: 29704593
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. DOCK8 Deficiency Presenting as an IPEX-Like Disorder.
Alroqi FJ; Charbonnier LM; Keles S; Ghandour F; Mouawad P; Sabouneh R; Mohammed R; Almutairi A; Chou J; Massaad MJ; Geha RS; Baz Z; Chatila TA
J Clin Immunol; 2017 Nov; 37(8):811-819. PubMed ID: 29058101
[TBL] [Abstract][Full Text] [Related]
7. Role of human forkhead box P3 in early thymic maturation and peripheral T-cell homeostasis.
Santoni de Sio FR; Passerini L; Restelli S; Valente MM; Pramov A; Maccari ME; Sanvito F; Roncarolo MG; Porteus M; Bacchetta R
J Allergy Clin Immunol; 2018 Dec; 142(6):1909-1921.e9. PubMed ID: 29705245
[TBL] [Abstract][Full Text] [Related]
8. Molecular feature and therapeutic perspectives of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
Huang Q; Liu X; Zhang Y; Huang J; Li D; Li B
J Genet Genomics; 2020 Jan; 47(1):17-26. PubMed ID: 32081609
[TBL] [Abstract][Full Text] [Related]
9. The imbalance of circulating T helper subsets and regulatory T cells in patients with LRBA deficiency: Correlation with disease severity.
Azizi G; Mirshafiey A; Abolhassani H; Yazdani R; Ghanavatinejad A; Noorbakhsh F; Rezaei N; Aghamohammadi A
J Cell Physiol; 2018 Nov; 233(11):8767-8777. PubMed ID: 29806698
[TBL] [Abstract][Full Text] [Related]
10. Single-cell analysis of FOXP3 deficiencies in humans and mice unmasks intrinsic and extrinsic CD4
Zemmour D; Charbonnier LM; Leon J; Six E; Keles S; Delville M; Benamar M; Baris S; Zuber J; Chen K; Neven B; Garcia-Lloret MI; Ruemmele FM; Brugnara C; Cerf-Bensussan N; Rieux-Laucat F; Cavazzana M; André I; Chatila TA; Mathis D; Benoist C
Nat Immunol; 2021 May; 22(5):607-619. PubMed ID: 33833438
[TBL] [Abstract][Full Text] [Related]
11. Quantitative analysis of tissue inflammation and responses to treatment in immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome, and review of literature.
Chen CA; Chung WC; Chiou YY; Yang YJ; Lin YC; Ochs HD; Shieh CC
J Microbiol Immunol Infect; 2016 Oct; 49(5):775-782. PubMed ID: 26748735
[TBL] [Abstract][Full Text] [Related]
12. The immunological and genetic basis of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
Bin Dhuban K; Piccirillo CA
Curr Opin Allergy Clin Immunol; 2015 Dec; 15(6):525-32. PubMed ID: 26485097
[TBL] [Abstract][Full Text] [Related]
13. IPEX due to an exon 7 skipping FOXP3 mutation with autoimmune diabetes mellitus cured by selective T
Magg T; Wiebking V; Conca R; Krebs S; Arens S; Schmid I; Klein C; Albert MH; Hauck F
Clin Immunol; 2018 Jun; 191():52-58. PubMed ID: 29567430
[TBL] [Abstract][Full Text] [Related]
14. From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation.
Bacchetta R; Barzaghi F; Roncarolo MG
Ann N Y Acad Sci; 2018 Apr; 1417(1):5-22. PubMed ID: 26918796
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Exaggerated follicular helper T-cell responses in patients with LRBA deficiency caused by failure of CTLA4-mediated regulation.
Alroqi FJ; Charbonnier LM; Baris S; Kiykim A; Chou J; Platt CD; Algassim A; Keles S; Al Saud BK; Alkuraya FS; Jordan M; Geha RS; Chatila TA
J Allergy Clin Immunol; 2018 Mar; 141(3):1050-1059.e10. PubMed ID: 28601686
[TBL] [Abstract][Full Text] [Related]
17. [Girl with IPEX syndrome with low expression of Foxp3].
Horiuchi S; Ishiguro A; Nakagawa T; Shoji K; Nagai A; Arai K; Horikawa R; Kawai T; Watanabe N; Onodera M
Nihon Rinsho Meneki Gakkai Kaishi; 2012; 35(6):526-32. PubMed ID: 23291488
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy, and enteropathy, and implications for clinical management.
Baxter SK; Walsh T; Casadei S; Eckert MM; Allenspach EJ; Hagin D; Segundo G; Lee MK; Gulsuner S; Shirts BH; Sullivan KE; Keller MD; Torgerson TR; King MC
J Allergy Clin Immunol; 2022 Jan; 149(1):327-339. PubMed ID: 33864888
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
