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2317 résultats correspondant à votre recherche

  • Striatal progenitors derived from human ES cells mature into DARPP32 neurons in vitro and in quinolinic acid-lesioned rats.

    Nathalie Lefort

    Source :

    Proc. Natl. Acad. Sci. U.S.A.

    2008 déc 1

    Pmid / DOI:

    18922775

  • Intracellular offspring released from SFB filaments are flagellated.

    Nadine CERF-BENSUSSAN

    Source :

    Nat Microbiol

    2019 déc 10

    Pmid / DOI:

    31819216

  • Modulation of the gut microbiota to improve innate resistance.

    Nadine CERF-BENSUSSAN

    Source :

    Curr. Opin. Immunol.

    2019 aoû 8

    Pmid / DOI:

    30205357

  • Scratching Beneath the Surface: Linking Skin Pathology with Food Allergy.

    Nadine CERF-BENSUSSAN

    Source :

    Immunity

    2019 oct 8

    Pmid / DOI:

    31117007

  • Recent advances in celiac disease and refractory celiac disease.

    Nadine CERF-BENSUSSAN

    Source :

    F1000Res

    2019 juil 14

    Pmid / DOI:

    31297187

  • De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development.

    Jeanne Amiel, Stanislas Lyonnet, Patrick Nitschké, Chris Gordon

    Source :

    Nat. Genet.

    2017 sep 5

    Pmid / DOI:

    28067911

  • Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in Infancy.

    Jeanne Amiel, Stanislas Lyonnet, Loïc de Pontual, Damien Bonnet, Patrick Nitschké, Chris Gordon, Anne Guimier

    Source :

    Am. J. Hum. Genet.

    2017 mai 2

    Pmid / DOI:

    27523598

  • MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates.

    Jeanne Amiel, Chris Gordon, Stanislas Lyonnet, Patrick Nitschké, Loïc de Pontual, Damien Bonnet, Anne Guimier

    Source :

    Nat. Genet.

    2016 mar 7

    Pmid / DOI:

    26437028

  • Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia.

    Jeanne Amiel, Stanislas Lyonnet, Patrick Nitschké, Chris Gordon

    Source :

    Am. J. Hum. Genet.

    2015 mai 29

    Pmid / DOI:

    25772936

  • Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears.

    Jeanne Amiel, Stanislas Lyonnet, Patrick Nitschké, Chris Gordon

    Source :

    Am. J. Hum. Genet.

    2014 fév 12

    Pmid / DOI:

    24268655

  • EFTUD2 haploinsufficiency leads to syndromic oesophageal atresia.

    Jeanne Amiel, Stanislas Lyonnet, Loïc de Pontual, Sandrine Marlin, Chris Gordon

    Source :

    J. Med. Genet.

    2013 juin 13

    Pmid / DOI:

    23188108

  • Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans.

    Jeanne Amiel

    Source :

    Nat. Genet.

    2011 nov 21

    Pmid / DOI:

    21892160