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Correction: Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder.
J Exp Med. 2023 Jan 2;220(1):e2022049812012022c. doi: 10.1084/jem.2022049812012022c. Epub 2022 Dec 7.
J Exp Med. 2023.
PMID: 36480208
Free PMC article.
No abstract available.
Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder.
Kaiser FMP, Gruenbacher S, Oyaga MR, Nio E, Jaritz M, Sun Q, van der Zwaag W, Kreidl E, Zopf LM, Dalm VASH, Pel J, Gaiser C, van der Vliet R, Wahl L, Rietman A, Hill L, Leca I, Driessen G, Laffeber C, Brooks A, Katsikis PD, Lebbink JHG, Tachibana K, van der Burg M, De Zeeuw CI, Badura A, Busslinger M.
Kaiser FMP, et al. Among authors: gruenbacher s.
J Exp Med. 2022 Sep 5;219(9):e20220498. doi: 10.1084/jem.20220498. Epub 2022 Aug 10.
J Exp Med. 2022.
PMID: 35947077
Free PMC article.
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Transcriptional function of E2A, Ebf1, Pax5, Ikaros and Aiolos analyzed by in vivo acute protein degradation in early B cell development.
Fedl AS, Tagoh H, Gruenbacher S, Sun Q, Schenk RL, Froussios K, Jaritz M, Busslinger M, Schwickert TA.
Fedl AS, et al. Among authors: gruenbacher s.
Nat Immunol. 2024 Sep;25(9):1663-1677. doi: 10.1038/s41590-024-01933-7. Epub 2024 Aug 23.
Nat Immunol. 2024.
PMID: 39179932
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Essential role of the Pax5 C-terminal domain in controlling B cell commitment and development.
Gruenbacher S, Jaritz M, Hill L, Schäfer M, Busslinger M.
Gruenbacher S, et al.
J Exp Med. 2023 Dec 4;220(12):e20230260. doi: 10.1084/jem.20230260. Epub 2023 Sep 19.
J Exp Med. 2023.
PMID: 37725138
Free PMC article.
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