Résultat de recherche

1801 results found for your search

  • Benefit Corporation: a path to affordable gene therapies?

    Source :

    Nat. Med.

    2019 Nov 26

    Pmid / DOI:

    31768067

  • XPO1 regulates erythroid differentiation and is a new target for the treatment of β-thalassemia.

    Olivier Hermine

    Source :

    Haematologica

    2019 Nov 22

    Pmid / DOI:

    31753924

  • A TP63 mutation causes prominent alopecia with mild ectodermal dysplasia.

    Alain Hovnanian , Patrick Nitschké, Christine Bole

    Source :

    J. Invest. Dermatol.

    2019 Nov 4

    Pmid / DOI:

    31682841

  • Imagine Institute

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    TEST VAC -28:11 VA

  • Imagine Institute

    What genetic diseases

  • 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 Jul 5

    Pmid / DOI:

    30940614

  • Alessandra Pierani
    Laboratoires de recherche
    Alessandra Pierani