G. Laforet

Are there multiple pathways in the pathogenesis of Huntington's disease?

Manho Kim, N. Aronin, M. Kim, 1999, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

The molecular pathology of rett syndrome

S. Akbarian, Yan Jiang, G. Laforet, 2007, NeuroMolecular Medicine.

Mutant Huntingtin Expression in Clonal Striatal Cells: Dissociation of Inclusion Formation and Neuronal Survival by Caspase Inhibition

D. Tagle, A. Heller, Manho Kim, 1999, The Journal of Neuroscience.

Changes in Cortical and Striatal Neurons Predict Behavioral and Electrophysiological Abnormalities in a Transgenic Murine Model of Huntington's Disease

C. Cepeda, M. Levine, C. Calvert, 2001, The Journal of Neuroscience.

Forskolin and dopamine D1 receptor activation increase Huntingtin's association with endosomes in immortalized neuronal cells of striatal origin

M. Hayden, J. Velier, A. Heller, 1999, Neuroscience.

Analysis of huntingtin‐associated protein 1 in mouse brain and immortalized striatal neurons

P. Bhide, J. Velier, A. Heller, 1999, The Journal of comparative neurology.