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.
211 related articles for article (PubMed ID: 30368009)
21. 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]
22. 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]
23. 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]
24. 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]
25. The FOXP3Δ2 isoform supports Treg cell development and protects against severe IPEX syndrome. Frith K; Joly AL; Ma CS; Tangye SG; Lohse Z; Seitz C; Verge CF; Andersson J; Gray P J Allergy Clin Immunol; 2019 Jul; 144(1):317-320.e8. PubMed ID: 30904640 [No Abstract] [Full Text] [Related]
26. Identification of a novel nonsense mutation in the FOXP3 gene in a fetus with hydrops--Expanding the phenotype of IPEX syndrome. Reichert SL; McKay EM; Moldenhauer JS Am J Med Genet A; 2016 Jan; 170A(1):226-32. PubMed ID: 26395338 [TBL] [Abstract][Full Text] [Related]
27. 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]
28. Prenatal Bowel Findings in Male Siblings With a Confirmed FOXP3 Mutation. Griswold C; Durica AR; Dennis LG; Jewell AF J Ultrasound Med; 2018 Apr; 37(4):1033-1037. PubMed ID: 28960390 [TBL] [Abstract][Full Text] [Related]
29. IPEX syndrome from diagnosis to cure, learning along the way. Bacchetta R; Roncarolo MG J Allergy Clin Immunol; 2024 Mar; 153(3):595-605. PubMed ID: 38040040 [TBL] [Abstract][Full Text] [Related]
30. Fecal microbiota transplantation before hematopoietic stem cell transplantation in a pediatric case of chronic diarrhea with a FOXP3 mutation. Wu W; Shen N; Luo L; Deng Z; Chen J; Tao Y; Mo X; Cao Q Pediatr Neonatol; 2021 Mar; 62(2):172-180. PubMed ID: 33358585 [TBL] [Abstract][Full Text] [Related]
31. 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]
32. 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]
33. Foxp3: a genetic foundation for regulatory T cell differentiation and function. Ramsdell F; Rudensky AY Nat Immunol; 2020 Jul; 21(7):708-709. PubMed ID: 32577010 [No Abstract] [Full Text] [Related]
34. T cell gene therapy to treat immunodeficiency. Panchal N; Ghosh S; Booth C Br J Haematol; 2021 Feb; 192(3):433-443. PubMed ID: 33280098 [TBL] [Abstract][Full Text] [Related]
35. Somatic and germline FOXP3 mosaicism in the mother of a boy with IPEX syndrome. Lin Y; Xu A; Zeng C; Cheng J; Li N; Niu H; Liu L; Li X Eur J Immunol; 2018 May; 48(5):885-887. PubMed ID: 29400909 [TBL] [Abstract][Full Text] [Related]
36. Analyses of a Mutant Foxp3 Allele Reveal BATF as a Critical Transcription Factor in the Differentiation and Accumulation of Tissue Regulatory T Cells. Hayatsu N; Miyao T; Tachibana M; Murakami R; Kimura A; Kato T; Kawakami E; Endo TA; Setoguchi R; Watarai H; Nishikawa T; Yasuda T; Yoshida H; Hori S Immunity; 2017 Aug; 47(2):268-283.e9. PubMed ID: 28778586 [TBL] [Abstract][Full Text] [Related]
37. Recurrent Non Immune Fetal Hydrops Associated With IPEX Syndrome. Shanes E; Propst L; Ouyang DW; Ernst LM Pediatr Dev Pathol; 2019 Oct; 22(5):465-471. PubMed ID: 30813833 [TBL] [Abstract][Full Text] [Related]
38. Opinion and Special Articles: Cerebellar Ataxia and Liver Failure Complicating IPEX Syndrome. Rim J; Byler M; Soldatos A; Notarangelo L; Leibovitch E; Jacobson S; Gorman M; Lebel RR; Werner K Neurology; 2021 Feb; 96(6):e956-e959. PubMed ID: 33168705 [No Abstract] [Full Text] [Related]
39. Familial IPEX syndrome: different glomerulopathy in two siblings. Park E; Chang HJ; Shin JI; Lim BJ; Jeong HJ; Lee KB; Moon KC; Kang HG; Ha IS; Cheong HI Pediatr Int; 2015 Apr; 57(2):e59-61. PubMed ID: 25712815 [TBL] [Abstract][Full Text] [Related]
40. [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] [Previous] [Next] [New Search]