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Martina Riva, Sofia Ferreira, Yoann Saillour, Frédéric Causeret, Charles-Joris Roux, Nadia Bahi-Buisson, Alessandra Pierani
Source :
J Clin Invest2024 juil 9Pmid / DOI:
38980724 -
Martina Riva, Sofia Ferreira, Yoann Saillour, Vera Medvedeva, Frédéric Causeret, Nadia Bahi-Buisson, Alessandra Pierani
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J Clin Invest2024 juil 9Pmid / DOI:
38980724 -
Matthieu Moreau, Yoann Saillour, Vicente Elorriaga, Amaia OCHANDORENA SAA , Alessandra Pierani, Frédéric Causeret
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Dev Cell2023 juin 14Pmid / DOI:
37321213 -
Diversity within olfactory sensory derivatives revealed by the contribution of Dbx1 lineages
Frédéric Causeret, Alessandra Pierani
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J Comp Neurol2023 mai 1Pmid / DOI:
37125418 -
Transient perinatal metabolic shifts determine neuronal survival and functional circuit formation
Alessandra Pierani
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Cell2023 avr 27Pmid / DOI:
37116467 -
Alessandra Pierani, Martina Riva, Patrick Azzam, Francesco Dori
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Nat Commun2023 mar 18Pmid / DOI:
36934089 -
Nasim Ramezanidoraki, Driss EL-OUARDI, Nadia Bahi-Buisson, Alessandra Pierani, Pierre Billuart
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Int J Mol Sci2023 mar 11Pmid / DOI:
36982451 -
Cajal-retzius cells: Recent advances in identity and function
Vicente Elorriaga, Alessandra Pierani, Frédéric Causeret
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Curr Opin Neurobiol2023 fév 10Pmid / DOI:
36774666 -
Martina Riva, Sofia Ferreira, Vera Medvedeva, Frédéric Causeret, Nadia Bahi-Buisson, Alessandra Pierani
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bioRxiv2021 mai 25Pmid / DOI:
https://doi.org/10.1101/2021.05.25.445586 -
Evolutionary Gain of Dbx1 Expression Drives Subplate Identity in the Cerebral Cortex.
Alessandra Pierani, Andrzej W Cwetsch, Yoann Saillour
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Cell Rep2020 jan 8Pmid / DOI:
31618633 -
Alessandra Pierani, Martina Riva
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Elife2020 jan 8Pmid / DOI:
31891351 -
Alessandra Pierani
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Nat Commun2020 jan 3Pmid / DOI:
31534164 -
Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics.
Nadia Bahi-Buisson
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Brain2019 déc 10Pmid / DOI:
30879067 -
Kremen1-induced cell death is regulated by homo- and heterodimerization.
Frédéric Causeret, Alessandra Pierani
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Cell Death Discov2019 nov 20Pmid / DOI:
31069116 -
Delineating FOXG1 syndrome: From congenital microcephaly to hyperkinetic encephalopathy.
Nadia Bahi-Buisson, Camille Maillard
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Neurol Genet2019 nov 20Pmid / DOI:
30533527