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Single cell analysis of autism patient with bi-allelic NRXN1-alpha deletion reveals skewed fate choice in neural progenitors and impaired neuronal functionality.
Lam M, Moslem M, Bryois J, Pronk RJ, Uhlin E, Ellström ID, Laan L, Olive J, Morse R, Rönnholm H, Louhivuori L, Korol SV, Dahl N, Uhlén P, Anderlid BM, Kele M, Sullivan PF, Falk A. Lam M, et al. Among authors: uhlin e. Exp Cell Res. 2019 Oct 1;383(1):111469. doi: 10.1016/j.yexcr.2019.06.014. Epub 2019 Jul 12. Exp Cell Res. 2019. PMID: 31302032 Free article.
SQSTM1/p62-Directed Metabolic Reprogramming Is Essential for Normal Neurodifferentiation.
Calvo-Garrido J, Maffezzini C, Schober FA, Clemente P, Uhlin E, Kele M, Stranneheim H, Lesko N, Bruhn H, Svenningsson P, Falk A, Wedell A, Freyer C, Wredenberg A. Calvo-Garrido J, et al. Among authors: uhlin e. Stem Cell Reports. 2019 Apr 9;12(4):696-711. doi: 10.1016/j.stemcr.2019.01.023. Epub 2019 Feb 28. Stem Cell Reports. 2019. PMID: 30827875 Free PMC article.
A proposal for an international Code of Conduct for data sharing in genomics.
Matar A, Hansson M, Slokenberga S, Panagiotopoulos A, Chassang G, Tzortzatou O, Pormeister K, Uhlin E, Cardone A, Beauvais M. Matar A, et al. Among authors: uhlin e. Dev World Bioeth. 2023 Dec;23(4):344-357. doi: 10.1111/dewb.12381. Epub 2022 Oct 21. Dev World Bioeth. 2023. PMID: 36269885