Contributions de l’utilisateur
- 30 mars 2018 à 16:03 (diff | hist) . . (+3 442) . . N Athway from DMH to ARH was clearly evident using a quantity (Page créée avec « Arrows indicate juxtapositions ([http://www.medchemexpress.com/Aprotinin.html Aprotinin site] colocalization) 1996; Gao and van den Pol, 2001; Sun et suggesting attainable... ») (actuel)
- 29 mars 2018 à 01:57 (diff | hist) . . (-111) . . m ). Surprisingly, we observed that IPSC frequency in NAG neurons decreases with (actuel)
- 27 mars 2018 à 04:22 (diff | hist) . . (+142) . . m 8569 ?Table 1. Difference in density of VGAT and VGLUT2 synaptic boutons in
- 23 mars 2018 à 17:30 (diff | hist) . . (-165) . . m Title Loaded From File
- 23 mars 2018 à 12:10 (diff | hist) . . (-90) . . m The hypothalamus. Indeed, projections from ARH neurons towards the parabrachial nucleus (actuel)
- 22 mars 2018 à 07:47 (diff | hist) . . (+3 759) . . N Uronal inputs from DMH. Certainly, our experiments employing DiI tracer showed (Page créée avec « As an illustration, leptin, a fat-derived hormone, is linked with fast synaptic reorganization. Exogenous leptin leads to an increase in inhibitory synapses in young NAG n... ») (actuel)
- 19 mars 2018 à 03:50 (diff | hist) . . (-58) . . m Lectrophysiology of feeding circuits. Trends Endocrinol Metab 15:488 ?499. CrossRef Medline Koch M (actuel)
