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Appears in Networks 2

In-Edges 6

a(CHEBI:"glutamate(1-)") association path(MESH:D008568) View Subject | View Object

The capacity for thinking and remembering is derived from various input and output pathways between the hippocampus and the neocortex,9 and all such pathways rely on signaling mediated by the neurotransmitter glutamate. PubMed:16273023

bp(MESH:D017774) association path(MESH:D008568) View Subject | View Object

It is believed that LTP, which can persist at a given synapse for periods ranging from hours to months, models the processes of learning and memory, and a number of studies have demonstrated a loss of LTP in animal models of Alzheimer's disease. PubMed:16273023

a(MESH:D006624) association path(MESH:D008568) View Subject | View Object

The capacity for thinking and remembering is derived from various input and output pathways between the hippocampus and the neocortex,9 and all such pathways rely on signaling mediated by the neurotransmitter glutamate. PubMed:16273023

a(MESH:D019579) association path(MESH:D008568) View Subject | View Object

The capacity for thinking and remembering is derived from various input and output pathways between the hippocampus and the neocortex,9 and all such pathways rely on signaling mediated by the neurotransmitter glutamate. PubMed:16273023

a(MESH:D059329) association path(MESH:D008568) View Subject | View Object

Cholinergic neurons within the nucleus basalis (NB) and the septal diagonal band complex provide the major source of cholinergic innervation to the cerebral cortex and hippocampus, respectively, and play a key role in memory and attentional function [11–13]. PubMed:18986241

path(MESH:D000544) association path(MESH:D008568) View Subject | View Object

Alzheimer’s disease (AD) is a progressive and fatal neurodegenerative disorder manifested by cognitive and memory decline and progressive impairment of activities of daily living, as well as a variety of neuropsychiatric symptoms and behavioral dysfunctions. PubMed:18986241

Out-Edges 6

path(MESH:D008568) association a(MESH:D006624) View Subject | View Object

The capacity for thinking and remembering is derived from various input and output pathways between the hippocampus and the neocortex,9 and all such pathways rely on signaling mediated by the neurotransmitter glutamate. PubMed:16273023

path(MESH:D008568) association a(MESH:D019579) View Subject | View Object

The capacity for thinking and remembering is derived from various input and output pathways between the hippocampus and the neocortex,9 and all such pathways rely on signaling mediated by the neurotransmitter glutamate. PubMed:16273023

path(MESH:D008568) association a(CHEBI:"glutamate(1-)") View Subject | View Object

The capacity for thinking and remembering is derived from various input and output pathways between the hippocampus and the neocortex,9 and all such pathways rely on signaling mediated by the neurotransmitter glutamate. PubMed:16273023

path(MESH:D008568) association bp(MESH:D017774) View Subject | View Object

It is believed that LTP, which can persist at a given synapse for periods ranging from hours to months, models the processes of learning and memory, and a number of studies have demonstrated a loss of LTP in animal models of Alzheimer's disease. PubMed:16273023

path(MESH:D008568) association path(MESH:D000544) View Subject | View Object

Alzheimer’s disease (AD) is a progressive and fatal neurodegenerative disorder manifested by cognitive and memory decline and progressive impairment of activities of daily living, as well as a variety of neuropsychiatric symptoms and behavioral dysfunctions. PubMed:18986241

path(MESH:D008568) association a(MESH:D059329) View Subject | View Object

Cholinergic neurons within the nucleus basalis (NB) and the septal diagonal band complex provide the major source of cholinergic innervation to the cerebral cortex and hippocampus, respectively, and play a key role in memory and attentional function [11–13]. PubMed:18986241

About

BEL Commons is developed and maintained in an academic capacity by Charles Tapley Hoyt and Daniel Domingo-Fernández at the Fraunhofer SCAI Department of Bioinformatics with support from the IMI project, AETIONOMY. It is built on top of PyBEL, an open source project. Please feel free to contact us here to give us feedback or report any issues. Also, see our Publishing Notes and Data Protection information.

If you find BEL Commons useful in your work, please consider citing: Hoyt, C. T., Domingo-Fernández, D., & Hofmann-Apitius, M. (2018). BEL Commons: an environment for exploration and analysis of networks encoded in Biological Expression Language. Database, 2018(3), 1–11.