K. Poirier

Type de document

Co-auteur

J. Chelly

N. Bahi-Buisson

E. Welker

F.P. Tuy

A. Toussaint

N. Revencu

F. Razavi

R. Olaso

R. Oegema

J. Martinovich

M. Marcy-Bonnière

P. Marcorelles

G.M. Mancini

P. Loget

L. Loeuillet

B. Lhermitte

C. Lebrand

A.G. Le Moing

K. Lascelles

A. Laquerrière

M. KIELAR

F. Jossic

F. Guimiot

M. Gonzales

F. Francis

C. Fallet-Bianco

P. Dias

J. F. Deleuze

C. de Juan Romero

A. Croquelois

W. Carpentier

N. Carion

K. Boutourlinsky

D. Boucher

V. Borrell

S. Bizzotto

B. Bessières

P. Berquin

R. Belvindrah

C. Beldjord

M.C. Addor

Date

Source

Serveur académique Lausannois (2)

Mot-clé

Phenotype (2) Human beings (2) Lissencephaly (2) mur (1) vitesse (1) spectacle (1) protéine (1) mutation (1) plomb (1) analyse (1) gène (1) ADN (1) Development (1) Causes (1) Case (1) Cases (1) Genes (1) Tubulins (1) Dysplasia (1) Speed (1) Plate (1) Neurons (1) Neocortex (1) Mice (1) Magnetic resonance imaging (1) Lead (1) Grammar, Comparative and general--Case (1) Fetus (1) Example (1) Epilepsy (1)

Documents écrit par K. Poirier (2) | parle de K. Poirier (0)

Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly.

C. Fallet-Bianco et al. (2014)

Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human.

M. Kielar et al. (2014)