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Publications of the Francis / Goutebroze Team

CORTICAL DEVELOPMENT AND PATHOLOGY

A human dynein heavy chain mutation impacts cortical progenitor cells causing developmental defects, reduced brain size and altered brain architecture

Romero DM, Zaidi D, Cifuentes-Diaz C, Maillard C, Grannec G, Selloum M, Birling MC, Bahi-Buisson N, Francis F Neurobiol Dis. 2023 May;180:106085.

PMID :
36933672

Differential impacts of Cntnap2 heterozygosity and Cntnap2 null homozygosity on axon and myelinated fiber development in mouse

Cifuentes-Diaz C, Canali G, Garcia M, Druart M, Manett T, Savariradjane M, Guillaume C, Le Magueresse C, Goutebroze L Front Neurosci. 2023 Jan 30;17:1100121.

PMID :
36793543

Primary Cilia Influence Progenitor Function during Cortical Development.

Zaidi D, Chinnappa K, Francis F. Cells. 2022 Sep 16;11(18):2895.

PMID :
36139475

Inflammation and Autophagy: A Convergent Point between Autism Spectrum Disorder (ASD)-Related Genetic and Environmental Factors: Focus on Aluminum Adjuvants.

Angrand L, Masson JD, Rubio-Casillas A, Nosten-Bertrand M, Crépeaux G. Toxics. 2022 Aug 31;10(9):518.

PMID :
36136483

RAB6 and dynein drive post-Golgi apical transport to prevent neuronal progenitor delamination

Brault JB, Bardin S, Lampic M, Carpentieri JA, Coquand L, Penisson M, Lachuer H, Victoria GS, Baloul S, El Marjou F, Boncompain G, Miserey-Lenkei S, Belvindrah R, Fraisier V, Francis F, Perez F, Goud B, Baffet AD EMBO Rep. 2022 Aug 18:e54605

PMID :
35979738

Novel role of the synaptic scaffold protein Dlgap4 in ventricular surface integrity and neuronal migration during cortical development

Romero DM, Poirier K, Belvindrah R, Moutkine I, Houllier A, LeMoing AG, Petit F, Boland A, Collins SC, Soiza-Reilly M, Yalcin B, Chelly J, Deleuze JF, Bahi-Buisson N, Francis F Nat Commun. (2022) 13, 2746

PMID :
35585091

Visualising the cytoskeletal machinery in neuronal growth cones using cryo-electron tomography

Atherton J, Stouffer M, Francis F, Moores CA J Cell Sci. (2022) 135

PMID :
35383828

Doublecortin mutation leads to persistent defects in the Golgi apparatus and mitochondria in adult hippocampal pyramidal cells

Stouffer MA, Khalaf-Nazzal R, Cifuentes-Diaz C, Albertini G, Bandet E, Grannec G, Lavilla V, Deleuze JF, Olaso R, Nosten-Bertrand M, Francis F Neurobiol Dis. (2022) 168, 105702

PMID :
35339680

Human cerebral organoids reveal progenitor pathology in EML1-linked cortical malformation

Jabali A, Hoffrichter A, Uzquiano A, Marsoner F, Wilkens R, Siekmann M, Bohl B, Rossetti AC, Horschitz S, Koch P, Francis F, Ladewig J EMBO Rep. (2022) e54027 Epub ahead of print

PMID :
35289477

CADPS functional mutations in patients with bipolar disorder increase the sensitivity to stress.

Sitbon J, Nestvogel D, Kappeler C, Nicolas A, Maciuba S, Henrion A, Troudet R, Courtois E, Grannec G, Latapie V, Barau C, Le Corvoisier P, Pietrancosta N, Henry C, Leboyer M, Etain B, Nosten-Bertrand M, Martin TFJ, Rhee J, Jamain S. Mol Psychiatry. 2022 Feb;27(2):1145-1157.

PMID :
35169262

Lis1 mutation prevents basal radial glia-like cell production in the mouse.

Penisson M, Jin M, Wang S, Hirotsune S, Francis F, Belvindrah R Hum Mol Genet. (2022) 31, 942-957

PMID :
34635911

Mapping the molecular and cellular complexity of cortical malformations

Klingler E, Francis F, Jabaudon D, Cappello S Science (2021) 371: eaba4517

PMID :
33479124
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