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Journal of Autoimmunity|September 16, 2022
Regulatory B cells in patients suffering from inborn errors of immunity with severe immune dysregulationShahrzad Bakhtiar, Celia Kaffenberger, Emilia Salzmann-Manrique, et al.Journal of Clinical Immunology|March 26, 2026
A Novel Pathogenic Variant in TRAC Gene Associated with SCID Phenotype: Expanding the Genetic and Clinical SpectrumMehmet Ali Karaselek, Mehmet Yavuz Ozbey, Vedat Uygun, et al.Central-European Journal of Immunology|October 30, 2023
Intraoral and maxillofacial abnormalities in patients with autosomal dominant hyper-IgE syndromeIldikó Tar, Márta Szegedi, Ewa Krasuska-Sławińska, et al.The Journal of Allergy and Clinical Immunology|December 4, 2014
Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like disorder caused by loss-of-function mutations in LRBALouis-Marie Charbonnier, Erin Janssen, Janet Chou, et al.Frontiers in Immunology|November 1, 2024
Newborn screening for SCID: the very first prospective pilot study from TürkiyeSule Haskologlu, Senem Kocak, Lale Satiroglu Tufan, et al.Science Immunology|September 23, 2022
A Stk4-Foxp3-NF-κB p65 transcriptional complex promotes T<sub>reg</sub> cell activation and homeostasisYe Cui, Mehdi Benamar, Klaus Schmitz-Abe, et al.Proceedings of the National Academy of Sciences of the United States of America|November 6, 2023
Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sitesPeng Zhang, Matthieu Chaldebas, Masato Ogishi, et al.Nature Immunology|April 9, 2021
Single-cell analysis of FOXP3 deficiencies in humans and mice unmasks intrinsic and extrinsic CD4<sup>+</sup> T cell perturbationsDavid Zemmour, Louis-Marie Charbonnier, Juliette Leon, et al.Blood|April 15, 2018
Patients with <i>CD3G</i> mutations reveal a role for human CD3γ in T<sub>reg</sub> diversity and suppressive functionJared H Rowe, Ottavia M Delmonte, Sevgi Keles, et al.The Journal of Allergy and Clinical Immunology|November 21, 2017
Type I IFN-related NETosis in ataxia telangiectasia and Artemis deficiencyErsin Gul, Esra Hazar Sayar, Bilgi Gungor, et al.Pageof 10