INT210831

From wiki-pain
Jump to: navigation, search
Context Info
Confidence 0.67
First Reported 2007
Last Reported 2008
Negated 0
Speculated 0
Reported most in Body
Documents 7
Total Number 7
Disease Relevance 1.69
Pain Relevance 0.32

This is a graph with borders and nodes. Maybe there is an Imagemap used so the nodes may be linking to some Pages.

transport (Abca4) ATPase activity (Abca4) transmembrane transport (Abca4)
Abca4 (Mus musculus)
Pain Link Frequency Relevance Heat
Inflammation 116 98.04 Very High Very High Very High
Neuropeptide 6 84.72 Quite High
imagery 10 83.04 Quite High
Potency 30 78.96 Quite High
5HT 12 44.28 Quite Low
antagonist 12 30.12 Quite Low
agonist 78 10.00 Low Low
Hippocampus 15 5.28 Low Low
Opioid 12 5.00 Very Low Very Low Very Low
cytokine 9 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
INFLAMMATION 123 98.04 Very High Very High Very High
Infection 81 94.08 High High
Targeted Disruption 23 93.72 High High
Congenital Anomalies 43 84.40 Quite High
Overweight 6 79.76 Quite High
Obesity 78 76.88 Quite High
Hydrocephalus 1 70.56 Quite High
Congenital Toxoplasmosis 3 68.72 Quite High
Body Weight 31 64.48 Quite High
Disease 31 63.12 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
It is of interest that expression of the ABCA4 gene is localized to the periventricular/perihippocampal area (Figure 9) and that this same area is noted to be prominently involved in the MRIs (Figure 3) and histopathology (Figure 6) of the chronically infected mice.
Gene_expression (expression) of ABCA4
1) Confidence 0.67 Published 2008 Journal J Neuroinflammation Section Body Doc Link PMC2588578 Disease Relevance 0.61 Pain Relevance 0.16
Rm1 and Rm2 are well-expressed at the cell-surface and do not respond to other endogenous ligands, such as ?
Gene_expression (expressed) of Rm1
2) Confidence 0.01 Published 2007 Journal PLoS ONE Section Body Doc Link PMC1930153 Disease Relevance 0 Pain Relevance 0
Alternatively, retrovirus-mediated hypothalamic expression of RM1 and Rm2 in adult MC4R-deficient mice could be used as a first step in evaluating Rm1 and Rm2 in vivo.
Gene_expression (expression) of RM1
3) Confidence 0.01 Published 2007 Journal PLoS ONE Section Body Doc Link PMC1930153 Disease Relevance 0.48 Pain Relevance 0
Rm1 and Rm2 are well-expressed at the cell-surface and do not respond to other endogenous ligands, such as ?
Gene_expression (expressed) of Rm2
4) Confidence 0.01 Published 2007 Journal PLoS ONE Section Body Doc Link PMC1930153 Disease Relevance 0 Pain Relevance 0
To this end, we measured cAMP release in transiently transfected cells expressing wild-type MC4R, Rm1, and Rm2 in response to increasing concentrations of ?
Gene_expression (expressing) of Rm1
5) Confidence 0.01 Published 2007 Journal PLoS ONE Section Body Doc Link PMC1930153 Disease Relevance 0.06 Pain Relevance 0.08
Alternatively, retrovirus-mediated hypothalamic expression of RM1 and Rm2 in adult MC4R-deficient mice could be used as a first step in evaluating Rm1 and Rm2 in vivo.
Gene_expression (expression) of Rm2
6) Confidence 0.01 Published 2007 Journal PLoS ONE Section Body Doc Link PMC1930153 Disease Relevance 0.48 Pain Relevance 0
To this end, we measured cAMP release in transiently transfected cells expressing wild-type MC4R, Rm1, and Rm2 in response to increasing concentrations of ?
Gene_expression (expressing) of Rm2
7) Confidence 0.01 Published 2007 Journal PLoS ONE Section Body Doc Link PMC1930153 Disease Relevance 0.06 Pain Relevance 0.08

General Comments

This test has worked.

Personal tools
Namespaces

Variants
Actions
Navigation
Toolbox