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Tournier, N, S Goutal, S Mairinger, IH Lozano, T Filip, M Sauberer, F Caillé, et al. “Complete Inhibition of ABC and ABC at the Blood-Brain Barrier by Co-Infusion of Erlotinib and Tariquidar to Improve Brain Delivery of the Model ABC/ABC Substrate [11C]Erlotinib.”https://doi.org/10.1177/0271678X20965500__Journal of Cerebral Blood Flow and Metabolism. SAGE Publications, 2021.https://doi.org/10.1177/0271678X20965500 .
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Morandell, Jasmin, Lena A Schwarz, Bernadette Basilico, Saren Tasciyan, Georgi A Dimchev, Armel Nicolas, Christoph M Sommer, et al. “Cul3 Regulates Cytoskeleton Protein Homeostasis and Cell Migration during a Critical Window of Brain Development.”https://doi.org/10.1038/s41467-021-23123-x__Nature Communications. Springer Nature, 2021.https://doi.org/10.1038/s41467-021-23123-x .
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Avagliano, Laura, Ilaria Parenti, Paolo Grazioli, Elisabetta Di Fede, Chiara Parodi, Milena Mariani, Frank J. Kaiser, Angelo Selicorni, Cristina Gervasini, and Valentina Massa. “Chromatinopathies: A Focus on Cornelia de Lange Syndrome.”https://doi.org/10.1111/cge.13674__Clinical Genetics. Wiley, 2020.https://doi.org/10.1111/cge.13674 .
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Weinert, Stefanie, Niclas Gimber, Dorothea Deuschel, Till Stuhlmann, Dmytro Puchkov, Zohreh Farsi, Carmen F. Ludwig, et al. “Uncoupling Endosomal CLC Chloride/Proton Exchange Causes Severe Neurodegeneration.”https://doi.org/10.15252/embj.2019103358__EMBO Journal. EMBO Press, 2020.https://doi.org/10.15252/embj.2019103358 .
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Parenti, Ilaria, Farah Diab, Sara Ruiz Gil, Eskeatnaf Mulugeta, Valentina Casa, Riccardo Berutti, Rutger W.W. Brouwer, et al. “MA and NIPBL Variants Impair the Heterodimerization of the Cohesin Loader Subunits and Cause Cornelia de Lange Syndrome.”https://doi.org/10.1016/j.celrep.2020.107647__Cell Reports. Elsevier, 2020.https://doi.org/10.1016/j.celrep.2020.107647 .
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Parenti, Ilaria, Luis E Garcia Rabaneda, Hanna Schön, and Gaia Novarino. “Neurodevelopmental Disorders: From Genetics to Functional Pathways.”https://doi.org/10.1016/j.tins.2020.05.004__Trends in Neurosciences. Elsevier, 2020.https://doi.org/10.1016/j.tins.2020.05.004 .
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Morandell, Jasmin. “Illuminating the Role of Cul3 in Autism Spectrum Disorder Pathogenesis.”https://doi.org/10.15479/AT:ISTA:8620__Institute of Science and Technology Austria, 2020.https://doi.org/10.15479/AT:ISTA:8620 .
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Morandell, Jasmin, Lena A Schwarz, Bernadette Basilico, Saren Tasciyan, Armel Nicolas, Christoph M Sommer, Caroline Kreuzinger, et al. “Cul3 Regulates Cytoskeleton Protein Homeostasis and Cell Migration during a Critical Window of Brain Development.”https://doi.org/10.1101/2020.01.10.902064 __BioRxiv. Cold Spring Harbor Laboratory, n.d.https://doi.org/10.1101/2020.01.10.902064  .
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Basilico, Bernadette, Jasmin Morandell, and Gaia Novarino. “Molecular Mechanisms for Targeted ASD Treatments.”https://doi.org/10.1016/j.gde.2020.06.004__Current Opinion in Genetics and Development. Elsevier, 2020.https://doi.org/10.1016/j.gde.2020.06.004 .
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