Francis / Goutebroze

Les publications de l'équipe Francis / Goutebroze.

Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex.

Bizzotto S, Uzquiano A, Dingli F, Ershov D, Houllier A, Arras G, Richards M, Loew D, Minc N, Croquelois A, Houdusse A, Francis F.
2017 Sci Rep. 11;7(1):17308.

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Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical development.

Broix L, Asselin L, Silva C, Ivanova EL, Tilly P, Gilet JG, Lebrun N, Jagline H, Muraca G, Saillour Y, Drouot N, Reilly ML, Francis F, Benmerah A, Bahi-Buisson N, Belvindrah R, Nguyen L, Godin JD, Chelly J, Hinckelmann MV.
2017 Hum Mol Genet.doi: 10.1093/hmg/ddx384. [Epub ahead of print]

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Early born neurons are abnormally positioned in the doublecortin knockout hippocampus

Khalaf-Nazzal R, Stouffer MA, Olaso R, Muresan L, Roumegous A, Lavilla V, Carpentier W, Moutkine I, Dumont S, Albaud B, Cagnard N, Roest Crollius H, Francis F.
2017 Hum Mol Genet.1;26(1):90-108

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Genetics and mechanisms leading to human cortical malformations

Romero DM, Bahi-Buisson N, Francis F.
2017 Semin Cell Dev Biol. S1084-9521(17)30239-2.

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Schwannomin-interacting Protein 1 Isoform IQCJ-SCHIP1 Is a Multipartner Ankyrin- and Spectrin-binding Protein Involved in the Organization of Nodes of Ranvier.

Martin PM,  Cifuentes-Diaz C, Devaux J,  Garcia M, , Bureau J, Thomasseau S, Klingler E, Girault JA,  Goutebroze L.
2017 J Biol Chem. 2017 10;292(6):2441-2456

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