M. de Chaldée

The striatal kinase DCLK3 produces neuroprotection against mutant huntingtin

M. Guillermier, F. Petit, G. Bonvento, 2018, Brain : a journal of neurology.

Capucin: a novel striatal marker down-regulated in rodent models of Huntington disease.

A. V. D. Vel, C. Brochier, J. Elalouf, 2006, Genomics.

Linkage disequilibrium on the COMT gene in French schizophrenics and controls.

J. Mallet, D. Campion, D. Samolyk, 1999, American journal of medical genetics.

Quantitative assessment of transcriptome differences between brain territories.

J. Buhler, O. Manzoni, J. Bockaert, 2003, Genome research.

Quantitative gene expression profiling of mouse brain regions reveals differential transcripts conserved in human and affected in disease models.

P. Wincker, J. Caboche, C. Dossat, 2008, Physiological genomics.

Loss of the thyroid hormone-binding protein Crym renders striatal neurons more vulnerable to mutant huntingtin in Huntington's disease

D. Houitte, M. Guillermier, F. Petit, 2014, Human molecular genetics.

Quantitative gene expression profiling of mouse brain regions reveals differential transcripts conserved in human and affected in disease models.

P. Wincker, J. Caboche, C. Dossat, 2008, Physiological genomics.