Résultat de recherche

New Publication

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Subnuclear re-localization of SOX10 and p54NRB correlates with a unique neurological phenotype associated with SOX10 missense mutations.

Nadège Bondurand, Véronique Pingault

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

Nathalie Lefort

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Intracellular offspring released from SFB filaments are flagellated.

Nadine CERF-BENSUSSAN

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Modulation of the gut microbiota to improve innate resistance.

Nadine CERF-BENSUSSAN

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

Nadine CERF-BENSUSSAN

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Recent advances in celiac disease and refractory celiac disease.

Nadine CERF-BENSUSSAN

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

Jeanne Amiel, Stanislas Lyonnet, Patrick Nitschké, Chris Gordon

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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

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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

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

Jeanne Amiel, Stanislas Lyonnet, Patrick Nitschké, Chris Gordon

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

Jeanne Amiel, Stanislas Lyonnet, Patrick Nitschké, Chris Gordon

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