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Molecular rescue of Tsc1-ablated cortical tuber mice.
Robens B, Becker AJ. Robens B, et al. Oncotarget. 2017 Jan 24;8(4):5678-5679. doi: 10.18632/oncotarget.14239. Oncotarget. 2017. PMID: 28031543 Free PMC article. No abstract available.
Ste20-like Kinase Is Critical for Inhibitory Synapse Maintenance and Its Deficiency Confers a Developmental Dendritopathy.
Schoch S, Quatraccioni A, Robens BK, Maresch R, van Loo KMJ, Cases-Cunillera S, Kelly T, Opitz T, Borger V, Dietrich D, Pitsch J, Beck H, Becker AJ. Schoch S, et al. Among authors: robens bk. J Neurosci. 2021 Sep 29;41(39):8111-8125. doi: 10.1523/JNEUROSCI.0352-21.2021. Epub 2021 Aug 16. J Neurosci. 2021. PMID: 34400520 Free PMC article.
Biallelic variants in ZNF526 cause a severe neurodevelopmental disorder with microcephaly, bilateral cataract, epilepsy and simplified gyration.
Dentici ML, Alesi V, Quinodoz M, Robens B, Guerin A, Lebon S, Poduri A, Travaglini L, Graziola F, Afenjar A, Keren B, Licursi V, Capuano A, Dallapiccola B, Superti-Furga A, Novelli A. Dentici ML, et al. Among authors: robens b. J Med Genet. 2022 Mar;59(3):262-269. doi: 10.1136/jmedgenet-2020-107430. Epub 2021 Jan 4. J Med Genet. 2022. PMID: 33397746