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A possible mechanism of such remapping is collateral sprouting (a rather slow process); another prevailing hypothesis is that such referred pathway may be preexisting but latent, and are unmasked after deafferentation [ 85, 86] presumably by disinhibition [ 86- 89].
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In addition, we recently showed that one Flo11p-independent mat formation pathway, referred to as the biofilm pathway, involves the class E vacuolar protein sorting (vps) components of the MVB pathway.
By pathways, we refer to pathways of various different metabolism as defined by biochemists, and as found in biochemistry textbooks (such as [ 10]) and atlases (such as [ 11]).
IPA also projects molecules in the data set to known biological pathways (referred to as "canonical pathways") and finds significantly associated canonical pathways by calculating the ratio of molecules in the data set mapped to canonical pathway divided by total number of molecules in the canonical pathway and by using Fisher's exact test to assign significance to observed association.
Affected KEGG pathways were ranked in order of classical p-values as well as gamma corrected p-values, which refers to pathway impact analysis or a measure of the probability of a pathway being significantly regulated.
These pathways refer to polyol pathway [ 6], nonenzymatic glycation and advanced glycation end products (AGEs) [ 7], diacylglycerol-protein kinase C (DAG-PKC) [ 8], and hexosamine pathways [ 9].
It contains parallel excitatory pathways referred to as the trisynaptic pathway (which carries information as follows: entorhinal cortex → dentate gyrus → CA3 → CA1 → entorhinal cortex) and the monosynaptic pathway (entorhinal cortex → CA1 → entorhinal cortex).
These inconsistencies cause troubles for researchers wishing to refer to pathway information in a large-scale manner across different databases.
As some studies are already using data in IntPath [ 21], we believe our work here can facilitate a variety of works that need to refer to pathway information.
We use a simplified version of the clinical pathway, referred to here as the 'test-treatment pathway', to illustrate the key concepts.
The simulation results showed that the extracellular opening on the receptor surface was the most frequently observed egress point (referred to as pathway A), and a few other pathways through interhelical clefts were also observed with significantly lower frequencies.
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