To read in august...

- Role of Olig1 and Olig2 in Down syndrome.

- TUBA1A mutations cause wide spectrum lissencephaly.

- Cell cloning-based transcriptome analysis in Rett patients.

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, in press.


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.