2214 résultats correspondant à votre recherche

  • Innovation

    TEST VAC -28:11

  • Institut Imagine

    Quid des maladies génétiques

  • TBC1D8B Loss-of-Function Mutations Lead to X-Linked Nephrotic Syndrome via Defective Trafficking Pathways.

    Corinne Antignac, Guillaume Dorval, Olivier Gribouval, Olivia Boyer, Alexandre Benmerah , Géraldine Mollet

    Source :

    Am. J. Hum. Genet.

    2019 nov 19

    Pmid / DOI:

    30661770

  • 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

  • Somatic genetic rescue in Mendelian haematopoietic diseases.

    Patrick Revy, Alain Fischer

    Source :

    Nat. Rev. Genet.

    2019 sep 18

    Pmid / DOI:

    31186537

  • Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes.

    Frédéric Rieux-Laucat, Jérome Hadjadj, Alain Fischer, Bénédicte Neven, Nicolas Garcelon

    Source :

    Blood

    2019 juil 5

    Pmid / DOI:

    30940614

  • Alessandra Pierani
    Laboratoires de recherche
    Alessandra Pierani
  • Extracellular Pax6 Regulates Tangential Cajal-Retzius Cell Migration in the Developing Mouse Neocortex.

    Alessandra Pierani

    Source :

    Cereb. Cortex

    2019 juin 17

    Pmid / DOI:

    31206158

  • Kremen1-induced cell death is regulated by homo- and heterodimerization.

    Frédéric Causeret, Alessandra Pierani

    Source :

    Cell Death Discov

    2019 nov 20

    Pmid / DOI:

    31069116

  • Cortical developmental death: selected to survive or fated to die.

    Alessandra Pierani, Frédéric Causeret

    Source :

    Curr. Opin. Neurobiol.

    2018 juil 19

    Pmid / DOI:

    29738999

  • Enhanced Abventricular Proliferation Compensates Cell Death in the Embryonic Cerebral Cortex.

    Alessandra Pierani

    Source :

    Cereb. Cortex

    2018 juin 14

    Pmid / DOI:

    27620979