Nadine Bruneau

发表

PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine

P. Genton, Ying-Hui Fu, A. Hunter, 2012, Neurology.

GRIN2A mutations cause epilepsy-aphasia spectrum disorders

J. Shendure, G. Carvill, I. Scheffer, 2013, Nature Genetics.

Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsy

G. Carvill, I. Scheffer, H. Mefford, 2016, European Journal of Human Genetics.

Functional Properties of Human NMDA Receptors Associated with Epilepsy-Related Mutations of GluN2A Subunit

N. Burnashev, S. Antonov, R. Giniatullin, 2017, Front. Cell. Neurosci..

GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction

Anne de Saint Martin, N. Burnashev, T. Tsintsadze, 2013, Nature Genetics.

Magnetofection™ of NMDA Receptor Subunits GluN1 and GluN2A Expression Vectors in Non-Neuronal Host Cells.

Nadine Bruneau, P. Szepetowski, N. Bruneau, 2017, Methods in molecular biology.

SRPX2 mutations in disorders of language cortex and cognition.

Marie-Noëlle Metz-Lutz, Edouard Hirsch, Sandrine Pereira, 2006, Human molecular genetics.

The Epilepsy of Infancy With Migrating Focal Seizures: Identification of de novo Mutations of the KCNT2 Gene That Exert Inhibitory Effects on the Corresponding Heteromeric KNa1.1/KNa1.2 Potassium Channel

L. Aniksztejn, H. Becq, Nadine Bruneau, 2020, Frontiers in Cellular Neuroscience.

Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions.

J. Jankovic, A. Bowcock, K. Bhatia, 2012, Cell reports.

Tubacin prevents neuronal migration defects and epileptic activity caused by rat Srpx2 silencing in utero.

Y. Ben-Ari, N. Burnashev, A. Represa, 2013, Brain : a journal of neurology.

A subset of genomic alterations detected in rolandic epilepsies contains candidate or known epilepsy genes including GRIN2A and PRRT2

P. Ryvlin, A. Arzimanoglou, E. Hirsch, 2014, Epilepsia.

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.

Edouard Hirsch, Simon E Fisher, S. Fisher, 2010, Human molecular genetics.

Infantile Convulsions with Paroxysmal Dyskinesia (ICCA Syndrome) and Copy Number Variation at Human Chromosome 16p11

G. Lathrop, P. Dessen, V. Lazar, 2010, PloS one.

The role of the urokinase receptor in epilepsy, in disorders of language, cognition, communication and behavior, and in the central nervous system.

Nadine Bruneau, P. Szepetowski, 2011, Current pharmaceutical design.

In Utero Administration of Drugs Targeting Microglia Improves the Neurodevelopmental Outcome Following Cytomegalovirus Infection of the Rat Fetal Brain

F. Michel, P. Gressens, S. Bauer, 2018, Front. Cell. Neurosci..

Cytomegalovirus Infection of the Rat Developing Brain In Utero Prominently Targets Immune Cells and Promotes Early Microglial Activation

P. Gressens, S. Bauer, F. Watrin, 2016, PloS one.

Mutations in the Novel Protein PRRT2 Cause Infantile Convulsions with Paroxysmal Kinesigenic Dyskinesia

Lynch, J. Jankovic, A. Bowcock, 2012 .