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Matthieu Moreau, Yoann Saillour, Vicente Elorriaga, Amaia OCHANDORENA SAA , Alessandra Pierani, Frédéric Causeret
Source : Dev Cell
2023 Jun 14
Pmid / DOI: 37321213
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Diversity within olfactory sensory derivatives revealed by the contribution of Dbx1 lineages
Frédéric Causeret, Alessandra Pierani
Source : J Comp Neurol
2023 May 1
Pmid / DOI: 37125418
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Alessandra Pierani, Martina Riva, Patrick Azzam, Francesco Dori
Source : Nat Commun
2023 Mar 18
Pmid / DOI: 36934089
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Nasim Ramezanidoraki, Driss EL-OUARDI, Nadia Bahi-Buisson, Alessandra Pierani, Pierre Billuart
Source : Int J Mol Sci
2023 Mar 11
Pmid / DOI: 36982451
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Martina Riva, Sofia Ferreira, Vera Medvedeva, Frédéric Causeret, Nadia Bahi-Buisson, Alessandra Pierani
Source : bioRxiv
2021 May 25
Pmid / DOI: https://doi.org/10.1101/2021.05.25.445586
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Evolutionary Gain of Dbx1 Expression Drives Subplate Identity in the Cerebral Cortex.
Alessandra Pierani, Andrzej W Cwetsch, Yoann Saillour
Source : Cell Rep
2020 Jan 8
Pmid / DOI: 31618633
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Alessandra Pierani, Martina Riva
Source : Elife
2020 Jan 8
Pmid / DOI: 31891351
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Alessandra Pierani
Source : Nat Commun
2020 Jan 3
Pmid / DOI: 31534164
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Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics.
Nadia Bahi-Buisson
Source : Brain
2019 Dec 10
Pmid / DOI: 30879067
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Delineating FOXG1 syndrome: From congenital microcephaly to hyperkinetic encephalopathy.
Nadia Bahi-Buisson, Camille Maillard
Source : Neurol Genet
2019 Nov 20
Pmid / DOI: 30533527
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Kremen1-induced cell death is regulated by homo- and heterodimerization.
Frédéric Causeret, Alessandra Pierani
Source : Cell Death Discov
2019 Nov 20
Pmid / DOI: 31069116
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Lydie Burglen, Nadia Bahi-Buisson
Source : Neuron
2019 Aug 8
Pmid / DOI: 30449657
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Alessandra Pierani
Source : Cereb. Cortex
2019 Jun 17
Pmid / DOI: 31206158
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Recurrent RTTN mutation leading to severe microcephaly, polymicrogyria and growth restriction.
Nadia Bahi-Buisson, Camille Maillard
Source : Eur J Med Genet
2019 Feb 22
Pmid / DOI: 30121372
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Mutations in TBR1 gene leads to cortical malformations and intellectual disability.
Nadia Bahi-Buisson, Camille Maillard
Source : Eur J Med Genet
2019 Feb 22
Pmid / DOI: 30268909