In: Social Cognitive and Affective Neuroscience, 2016, vol. 11, no. 6, p. 1017-1025
|
In: Social Cognitive and Affective Neuroscience, 2017, vol. 12, no. 4, p. 618-634
|
In: Cerebral Cortex, 2017, vol. 27, no. 10, p. 4946-4959
|
In: Behavior Genetics, 1997, vol. 27, no. 6, p. 565-572
|
In: Documenta Ophthalmologica, 2006, vol. 112, no. 3, p. 209-215
|
In: European Archives of Psychiatry and Clinical Neuroscience, 2005, vol. 255, no. 1, p. 33-39
|
In: Psychological Medicine, 2013, vol. 43, no. 12, p. 2571-2582
|
In: Human Reproduction, 1992, vol. 7, no. 2, p. 180-183
|
In: Current Biology, 2016, vol. 26, no. 5, p. 661–669
Dopaminergic neurons serve multiple functions, including reinforcement processing during associative learning [1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12]. It is thus warranted to understand which dopaminergic neurons mediate which function. We study larval Drosophila, in which only approximately 120 of a total of 10,000 neurons are dopaminergic, as judged by the expression of tyrosine...
|
In: European Journal of Neuroscience, 2012, p. -
Recent work has shown that infusion of brain-derived neurotrophic factor (BDNF) into the ventral tegmental area (VTA) promotes a switch in the mechanisms mediating morphine motivation, from a dopamine-independent to a dopamine-dependent pathway. Here we showed that a single infusion of intra-VTA BDNF also promoted a switch in the mechanisms mediating ethanol motivation, from a dopamine-dependent...
|