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 *

377 related articles for article (PubMed ID: 26485097)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. A challenging undertaking: Stem cell transplantation for immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome.
    Kucuk ZY; Bleesing JJ; Marsh R; Zhang K; Davies S; Filipovich AH
    J Allergy Clin Immunol; 2016 Mar; 137(3):953-5.e4. PubMed ID: 26559324
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. Mechanisms of human FoxP3
    Attias M; Al-Aubodah T; Piccirillo CA
    Clin Exp Immunol; 2019 Jul; 197(1):36-51. PubMed ID: 30864147
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. [A case of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome with very early onset inflammatory bowel disease-like changes].
    Bao WT; Li ZL; Li J; Shi XY; Zhang J; Wu H
    Zhonghua Er Ke Za Zhi; 2019 Jul; 57(7):559-561. PubMed ID: 31269558
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 19.