A lire en août...

- Rôle des gènes Olig1 et Olig2 dans la trisomie 21.

- Les mutations de TUBA1A causent différents types de lissencéphalie.

- Analyze du transcriptome dans des cellules 'Rett' clonées.

Ana Borges - Publications

2009

Identification of Different Genomic Deletions and One Duplication in the Dysferlin Gene Using Multiplex Ligation-Dependent Probe Amplification and Genomic Quantitative PCR.

Krahn M, Borges A, Navarro C, Schuit R, Stojkovic T, Torrente Y, Wein N, Pécheux C, Lévy N.

Genetic Testing and Molecular Biomarkers, 2009, sous presse.


2007

Truncation of NHEJ1 in a patient with polymicrogyria.

Cantagrel V, Lossi AM, Lisgo S, Missirian C, Borges A, Philip N, Fernandez C, Cardoso C, Figarella-Branger D, Moncla A, Lindsay S, Dobyns WB, Villard L.

Human Mutation, 2007, 28:356-364.


2006

Migrating and myelinating potential of subventricular zone neural progenitor cells in white matter tracts of the adult rodent brain.

Cayre M, Bancila M, Virard I, Borges A, Durbec P.

Molecular and Cellular Neuroscience, 2006, 31:748-758.