J. Massalas

发表

Motor and behavioral phenotype in conditional mutants with targeted ablation of cortical D1 dopamine receptor-expressing cells

J. Waddington, M. Ehrlich, A. Lawrence, 2015, Neurobiology of Disease.

Early direct and transneuronal effects in mice with targeted expression of a toxin gene to D1 dopamine receptor neurons

J. Drago, D. Finkelstein, J. Massalas, 1999, Neuroscience.

Role of α4‐ and α6‐containing nicotinic receptors in the acquisition and maintenance of nicotine self‐administration

A. Lawrence, J. Drago, J. Massalas, 2015, Addiction biology.

Proconvulsant-induced seizures in α4 nicotinic acetylcholine receptor subunit knockout mice

M. Horne, S. Berkovic, J. Drago, 2002, Neuropharmacology.

Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development.

F. Alt, D. Bodine, J. Drago, 1997, Development.

Neurochemical changes in dopamine D1, D3 and D1/D3 receptor knockout mice.

J. Waddington, M. Horne, J. Drago, 2003, European journal of pharmacology.

Phenotypic Characterization of an α4 Neuronal Nicotinic Acetylcholine Receptor Subunit Knock-Out Mouse

I. Scheffer, J. Waddington, M. Horne, 2000, The Journal of Neuroscience.

Resolving pathobiological mechanisms relating to Huntington disease: Gait, balance, and involuntary movements in mice with targeted ablation of striatal D1 dopamine receptor cells

J. Waddington, M. Ehrlich, A. Lawrence, 2014, Neurobiology of Disease.

Phenotyping dividing cells in mouse models of neurodegenerative basal ganglia diseases

M. Ehrlich, A. Lawrence, J. Drago, 2013, BMC Neuroscience.

Late direct and transneuronal effects in mice with targeted expression of a toxin gene to D1 dopamine receptor neurons

J. Drago, J. Massalas, J. Wong, 1999, Neuroscience.

Essential conservation of D1 mutant phenotype at the level of individual topographies of behaviour in mice lacking both D1 and D3 dopamine receptors

J. Waddington, J. Drago, J. Massalas, 2003, Psychopharmacology.

Nicotine-Induced Dystonic Arousal Complex in a Mouse Line Harboring a Human Autosomal-Dominant Nocturnal Frontal Lobe Epilepsy Mutation

Tristan D. McClure-Begley, H. Lester, J. Waddington, 2007, The Journal of Neuroscience.