VAMP1 immunolabelling was weak in the hippocampal fissure, in stratum lacunosum moleculare of CA1 and outer molecular layer of DG (darker layers, Fig. 1a).
As a result all forms of plasticity in the molecular layer of the cerebellar cortex will be expressed with opposite effects in terms of directionality2.
Thereafter, entorhino-hippocampal fibers were cut and the outer molecular layer of the fascia dentata was denervated.
The lateral perforant path (LPP) was stimulated at the dentate outer molecular layer of hippocampal slices.
High frequency stimuli were delivered to the outer molecular layer of the dentate to tetanize the LPP.
Similarly, [125I]CGRP binding was observed in the molecular layer of human cerebellum.
When the ipsilateral entorhinal cortex is completely removed, the outer 70-75% of the molecular layer of the dentate gyrus is almost completely denervated.
Synaptic responses were evoked with a tungsten bipolar electrode in the outer molecular layer of the dentate gyrus.
Mice that survived pilocarpine-induced SE had robust mossy fiber sprouting into the inner molecular layer of the dentate gyrus.
Reduced dendrite growth in AD has been also related to loss of entorhinal projections to the molecular layer of DG and lack of input signal [82], [83].
To quantify the colocalization of GFP with endogenous Synapsin and MAGUK, 4 volumes (20×20×2 mm each) from the molecular layer of the cerebellum were analyzed.
