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Showing results for jens schuster
Search for Jens Schröter instead (1 results)
KRIT1 heterozygous mutations are sufficient to induce a pathological phenotype in patient-derived iPSC models of cerebral cavernous malformation.
Arce M, Erzar I, Yang F, Senthilkumar N, Onyeogaziri FC, Ronchi D, Ahlstrand FC, Noll N, Lugano R, Richards M, Scola E, Corada M, Lazzaroni F, Meggiolaro L, Schuster J, Dahl N, Niemelä M, Jahromi BR, Dimberg A, Lanfraconi S, Latini R, Magnusson PU. Arce M, et al. Among authors: schuster j. Cell Rep. 2025 May 27;44(5):115576. doi: 10.1016/j.celrep.2025.115576. Epub 2025 Apr 14. Cell Rep. 2025. PMID: 40238631 Free article.
Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy.
Fatima A, Hoeber J, Schuster J, Koshimizu E, Maya-Gonzalez C, Keren B, Mignot C, Akram T, Ali Z, Miyatake S, Tanigawa J, Koike T, Kato M, Murakami Y, Abdullah U, Ali MA, Fadoul R, Laan L, Castillejo-López C, Liik M, Jin Z, Birnir B, Matsumoto N, Baig SM, Klar J, Dahl N. Fatima A, et al. Among authors: schuster j. Am J Hum Genet. 2022 Mar 3;109(3):542-546. doi: 10.1016/j.ajhg.2022.02.007. Am J Hum Genet. 2022. PMID: 35245475 Free PMC article. No abstract available.
Comprehensive transcriptome assessment in PBMCs of post-COVID patients at a median follow-up of 28 months after a mild COVID infection reveals upregulation of JAK/STAT signaling and a prolonged immune response.
Fineschi S, Klar J, Lopez Egido JR, Schuster J, Bergquist J, Kaden R, Dahl N. Fineschi S, et al. Among authors: schuster j. Front Immunol. 2025 May 30;16:1589589. doi: 10.3389/fimmu.2025.1589589. eCollection 2025. Front Immunol. 2025. PMID: 40519915 Free PMC article.
52 results