259 related articles for article (PubMed ID: 23291488)
1. [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]
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. 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]
4. Persistent Enteropathy in a Toddler with a Novel FOXP3 Mutation and Normal FOXP3 Protein Expression.
Seghezzo S; Bleesing JJ; Kucuk ZY
J Pediatr; 2017 Jul; 186():183-185. PubMed ID: 28457527
[TBL] [Abstract][Full Text] [Related]
5. Unusual and early onset IPEX syndrome: a case report.
Doğruel D; Gürbüz F; Turan İ; Altıntaş DU; Yılmaz M; Yüksel B
Turk J Pediatr; 2019; 61(4):580-584. PubMed ID: 31990476
[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. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. CD4⁺ T cells from IPEX patients convert into functional and stable regulatory T cells by FOXP3 gene transfer.
Passerini L; Rossi Mel E; Sartirana C; Fousteri G; Bondanza A; Naldini L; Roncarolo MG; Bacchetta R
Sci Transl Med; 2013 Dec; 5(215):215ra174. PubMed ID: 24337481
[TBL] [Abstract][Full Text] [Related]
13. Lentiviral Gene Therapy in HSCs Restores Lineage-Specific Foxp3 Expression and Suppresses Autoimmunity in a Mouse Model of IPEX Syndrome.
Masiuk KE; Laborada J; Roncarolo MG; Hollis RP; Kohn DB
Cell Stem Cell; 2019 Feb; 24(2):309-317.e7. PubMed ID: 30639036
[TBL] [Abstract][Full Text] [Related]
14. Clinical and structural impact of mutations affecting the residue Phe367 of FOXP3 in patients with IPEX syndrome.
Colobran R; Álvarez de la Campa E; Soler-Palacín P; Martín-Nalda A; Pujol-Borrell R; de la Cruz X; Martínez-Gallo M
Clin Immunol; 2016 Feb; 163():60-5. PubMed ID: 26748374
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Novel pathogenic variants in FOXP3 in fetuses with echogenic bowel and skin desquamation identified by ultrasound.
Louie RJ; Tan QK; Gilner JB; Rogers RC; Younge N; Wechsler SB; McDonald MT; Gordon B; Saski CA; Jones JR; Chapman SJ; Stevenson RE; Sleasman JW; Friez MJ
Am J Med Genet A; 2017 May; 173(5):1219-1225. PubMed ID: 28317311
[TBL] [Abstract][Full Text] [Related]
18. [A novel missense mutation of FOXP3 causes immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in a Chinese child].
An YF; Zhao XD; Xu F; Yang XQ
Zhonghua Er Ke Za Zhi; 2009 Nov; 47(11):824-8. PubMed ID: 20078992
[TBL] [Abstract][Full Text] [Related]
19. [New mutation in FOXP3 gene identified in an infant with chronic diarrhea as manifestation of autoinmune enteropathy - IPEX syndrome].
Plata García C; Martín-Marín L; Soler-Ramírez A; Rojas JA; Salazar MP
Rev Chil Pediatr; 2020 Aug; 91(4):584-590. PubMed ID: 33399737
[TBL] [Abstract][Full Text] [Related]
20. FOXP3 mutations causing early-onset insulin-requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
Hwang JL; Park SY; Ye H; Sanyoura M; Pastore AN; Carmody D; Del Gaudio D; Wilson JF; Hanis CL; Liu X; Atzmon G; Glaser B; Philipson LH; Greeley SAW;
Pediatr Diabetes; 2018 May; 19(3):388-392. PubMed ID: 29193502
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]