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Molecular Immunology|November 6, 2007
EphA and ephrin-A proteins regulate integrin-mediated T lymphocyte interactionsNigel Sharfe, Martina Nikolic, Lorand Cimpeon, et al.Journal of Autoimmunity|September 20, 2015
The effects of RelB deficiency on lymphocyte development and functionNigel Sharfe, Daniele Merico, Ariana Karanxha, et al.The Journal of Allergy and Clinical Immunology|November 19, 2013
Fatal combined immunodeficiency associated with heterozygous mutation in STAT1Nigel Sharfe, Amit Nahum, Andrea Newell, et al.The Journal of Allergy and Clinical Immunology|September 27, 2020
Combined immunodeficiency caused by a novel homozygous NFKB1 mutationAmarilla B Mandola, Nigel Sharfe, Zahra Nagdi, et al.The Journal of Allergy and Clinical Immunology|November 29, 2017
Dual loss of p110δ PI3-kinase and SKAP (KNSTRN) expression leads to combined immunodeficiency and multisystem syndromic featuresNigel Sharfe, Ariana Karanxha, Harjit Dadi, et al.Blood|July 26, 2003
Inhibition of acute lymphoblastic and myeloid leukemias by a novel kinase inhibitorThomas Grunberger, Peter Demin, Olga Rounova, et al.Frontiers in Immunology|February 7, 2022
Case Report: Eosinophilic Esophagitis in a Patient With a Novel STAT1 Gain-of-Function Pathogenic VariantOri Scott, Nigel Sharfe, Harjit Dadi, et al.The Journal of Allergy and Clinical Immunology|August 23, 2017
Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11)Harjit Dadi, Tyler A Jones, Daniele Merico, et al.Journal of Autoimmunity|November 19, 2022
NFκB pathway dysregulation due to reduced RelB expression leads to severe autoimmune disorders and declining immunityNigel Sharfe, Ilan Dalal, Zahra Naghdi, et al.The Journal of Allergy and Clinical Immunology|August 6, 2025
Autosomal-dominant Roquin-1 immunodeficiency and hyperinflammationAmit Nahum, Nigel Sharfe, Daniele Merico, et al.Pageof 3