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Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations.
Staels F, De Keukeleere K, Kinnunen M, Keskitalo S, Lorenzetti F, Vanmeert M, Prezzemolo T, Pasciuto E, Lescrinier E, Bossuyt X, Gerbaux M, Willemsen M, Neumann J, Van Loo S, Corveleyn A, Willekens K, Stalmans I, Meyts I, Liston A, Humblet-Baron S, Seppänen M, Varjosalo M, Schrijvers R. Staels F, et al. Among authors: liston a. Front Immunol. 2022 Sep 20;13:973543. doi: 10.3389/fimmu.2022.973543. eCollection 2022. Front Immunol. 2022. PMID: 36203612 Free PMC article.
Regulatory T cells fulfil their promise?
Humblet-Baron S, Baron F, Liston A. Humblet-Baron S, et al. Among authors: liston a. Immunol Cell Biol. 2011 Nov;89(8):825-6. doi: 10.1038/icb.2011.52. Epub 2011 May 24. Immunol Cell Biol. 2011. PMID: 21606944 Free article. No abstract available.
Olmsted syndrome: exploration of the immunological phenotype.
Danso-Abeam D, Zhang J, Dooley J, Staats KA, Van Eyck L, Van Brussel T, Zaman S, Hauben E, Van de Velde M, Morren MA, Renard M, Van Geet C, Schaballie H, Lambrechts D, Tao J, Franckaert D, Humblet-Baron S, Meyts I, Liston A. Danso-Abeam D, et al. Among authors: liston a. Orphanet J Rare Dis. 2013 May 21;8:79. doi: 10.1186/1750-1172-8-79. Orphanet J Rare Dis. 2013. PMID: 23692804 Free PMC article.
Antiapoptotic Mcl-1 is critical for the survival and niche-filling capacity of Foxp3⁺ regulatory T cells.
Pierson W, Cauwe B, Policheni A, Schlenner SM, Franckaert D, Berges J, Humblet-Baron S, Schönefeldt S, Herold MJ, Hildeman D, Strasser A, Bouillet P, Lu LF, Matthys P, Freitas AA, Luther RJ, Weaver CT, Dooley J, Gray DH, Liston A. Pierson W, et al. Among authors: liston a. Nat Immunol. 2013 Sep;14(9):959-65. doi: 10.1038/ni.2649. Epub 2013 Jul 14. Nat Immunol. 2013. PMID: 23852275 Free PMC article.
Gain-of-function mutations in signal transducer and activator of transcription 1 (STAT1): chronic mucocutaneous candidiasis accompanied by enamel defects and delayed dental shedding.
Frans G, Moens L, Schaballie H, Van Eyck L, Borgers H, Wuyts M, Dillaerts D, Vermeulen E, Dooley J, Grimbacher B, Cant A, Declerck D, Peumans M, Renard M, De Boeck K, Hoffman I, François I, Liston A, Claessens F, Bossuyt X, Meyts I. Frans G, et al. Among authors: liston a. J Allergy Clin Immunol. 2014 Nov;134(5):1209-13.e6. doi: 10.1016/j.jaci.2014.05.044. Epub 2014 Jul 18. J Allergy Clin Immunol. 2014. PMID: 25042743 Free PMC article. No abstract available.
Mutant ADA2 in vasculopathies.
Van Eyck L, Liston A, Meyts I. Van Eyck L, et al. Among authors: liston a. N Engl J Med. 2014 Jul 31;371(5):478-9. doi: 10.1056/NEJMc1405506. N Engl J Med. 2014. PMID: 25075846 No abstract available.
Hematopoietic stem cell transplantation rescues the immunologic phenotype and prevents vasculopathy in patients with adenosine deaminase 2 deficiency.
Van Eyck L Jr, Hershfield MS, Pombal D, Kelly SJ, Ganson NJ, Moens L, Frans G, Schaballie H, De Hertogh G, Dooley J, Bossuyt X, Wouters C, Liston A, Meyts I. Van Eyck L Jr, et al. Among authors: liston a. J Allergy Clin Immunol. 2015 Jan;135(1):283-7.e5. doi: 10.1016/j.jaci.2014.10.010. Epub 2014 Nov 25. J Allergy Clin Immunol. 2015. PMID: 25457153 Free PMC article. No abstract available.
381 results