Zobrazeno 1 - 8
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pro vyhledávání: '"Tucewicz A"'
Akademický článek
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Autor:
Bruna Paulsen, Silvia Velasco, Amanda J. Kedaigle, Martina Pigoni, Giorgia Quadrato, Anthony J. Deo, Xian Adiconis, Ana Uzquiano, Rafaela Sartore, Sung Min Yang, Sean K. Simmons, Panagiotis Symvoulidis, Kwanho Kim, Kalliopi Tsafou, Archana Podury, Catherine Abbate, Ashley Tucewicz, Samantha N. Smith, Alexandre Albanese, Lindy Barrett, Neville E. Sanjana, Xi Shi, Kwanghun Chung, Kasper Lage, Edward S. Boyden, Aviv Regev, Joshua Z. Levin, Paola Arlotta
Publikováno v:
Nature. 602:268-273
Genetic risk for autism spectrum disorder (ASD) is associated with hundreds of genes spanning a wide range of biological functions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bd53e57f536ce5e648278370de37b1d
https://doi.org/10.1038/s41586-021-04358-6
https://doi.org/10.1038/s41586-021-04358-6
Autor:
Martina Pigoni, Ana Uzquiano, Bruna Paulsen, Amanda Kedaigle, Sung Min Yang, Panagiotis Symvoulidis, Xian Adiconis, Silvia Velasco, Rafaela Sartore, Kwanho Kim, Ashley Tucewicz, Kalliopi Tsafou, Xin Jin, Lindy Barrett, Fei Chen, Ed Boyden, Aviv Regev, Joshua Z. Levin, Paola Arlotta
De novoheterozygous loss-of-function mutations inPTENare strongly associated with Autism spectrum disorders (ASD); however, it is unclear how heterozygous mutations in this gene affects different cell types during human brain development, and how the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0ee470a25841a9324dc4983abd14711
https://doi.org/10.1101/2022.11.15.516664
https://doi.org/10.1101/2022.11.15.516664
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Ana Uzquiano, Amanda J. Kedaigle, Martina Pigoni, Bruna Paulsen, Xian Adiconis, Kwanho Kim, Tyler Faits, Surya Nagaraja, Noelia Antón-Bolaños, Chiara Gerhardinger, Ashley Tucewicz, Evan Murray, Xin Jin, Jason Buenrostro, Fei Chen, Silvia Velasco, Aviv Regev, Joshua Z. Levin, Paola Arlotta
Realizing the full utility of brain organoids as experimental systems to study human cortical development requires understanding whether organoids replicate the cellular and molecular events of this complex process precisely, reproducibly, and with f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b05221f5be4c8356051a37014a0f136d
https://doi.org/10.1101/2022.03.17.484798
https://doi.org/10.1101/2022.03.17.484798
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Ana Uzquiano, Amanda J. Kedaigle, Martina Pigoni, Bruna Paulsen, Xian Adiconis, Kwanho Kim, Tyler Faits, Surya Nagaraja, Noelia Antón-Bolaños, Chiara Gerhardinger, Ashley Tucewicz, Evan Murray, Xin Jin, Jason Buenrostro, Fei Chen, Silvia Velasco, Aviv Regev, Joshua Z. Levin, Paola Arlotta
Publikováno v:
Cell. 185:3770-3788.e27
Realizing the full utility of brain organoids to study human development requires understanding whether organoids precisely replicate endogenous cellular and molecular events, particularly since acquisition of cell identity in organoids can be impair
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab72a5eb25f151edae483321cce01486
https://doi.org/10.1016/j.cell.2022.09.010
https://doi.org/10.1016/j.cell.2022.09.010
Autor:
Ashley Tucewicz, Anthony Deo, Sean Simmons, Kwanho Kim, Kasper Lage, Giorgia Quadrato, Paola Arlotta, Xian Adiconis, Samantha Smith, Martina Pigoni, Bruna Paulsen, Kwanghun Chung, Aviv Regev, Kalliopi Tsafou, Joshua Z. Levin, Catherine Abbate, Alex Albanese, Silvia Velasco, Rafaela C. Sartore, Amanda J. Kedaigle, Ana Uzquiano
Genetic risk for autism spectrum disorder (ASD) has been associated with hundreds of genes spanning a wide range of biological functions. The phenotypic alterations in the human brain resulting from mutations in ASD risk genes remain unclear, and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e491090536d8832a3365b8e531ba8b4
https://doi.org/10.1101/2020.11.10.376509
https://doi.org/10.1101/2020.11.10.376509