INT284873

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Context Info
Confidence 0.43
First Reported 2008
Last Reported 2008
Negated 0
Speculated 0
Reported most in Abstract
Documents 1
Total Number 2
Disease Relevance 0.35
Pain Relevance 0.06

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

transport (Scn3b) plasma membrane (Scn3b)
Scn3b (Mus musculus)
Pain Link Frequency Relevance Heat
Action potential 52 56.08 Quite High
addiction 10 5.00 Very Low Very Low Very Low
action potential duration 10 5.00 Very Low Very Low Very Low
Eae 6 5.00 Very Low Very Low Very Low
Nav1.1 4 5.00 Very Low Very Low Very Low
sodium channel 2 5.00 Very Low Very Low Very Low
Nav1.9 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Congenital Anomalies 4 98.38 Very High Very High Very High
Targeted Disruption 12 75.00 Quite High
Ventricular Tachycardia 44 34.56 Quite Low
Arrhythmogenic Right Ventricular Dysplasia 26 5.00 Very Low Very Low Very Low
Heart Arrhythmia 18 5.00 Very Low Very Low Very Low
Syndrome 8 5.00 Very Low Very Low Very Low
Body Weight 6 5.00 Very Low Very Low Very Low
Camurati-engelmann Disease 4 5.00 Very Low Very Low Very Low
Adhesions 4 5.00 Very Low Very Low Very Low
Bartter Syndrome 4 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
We report for the first time abnormalities in cardiac ventricular electrophysiology in a genetically modified murine model lacking the Scn3b gene (Scn3b?
Negative_regulation (lacking) of Scn3b associated with congenital anomalies
1) Confidence 0.43 Published 2008 Journal Prog Biophys Mol Biol Section Abstract Doc Link PMC2764399 Disease Relevance 0.17 Pain Relevance 0.03
We report for the first time abnormalities in cardiac ventricular electrophysiology in a genetically modified murine model lacking the Scn3b gene (Scn3b?
Negative_regulation (lacking) of Scn3b associated with congenital anomalies
2) Confidence 0.43 Published 2008 Journal Prog Biophys Mol Biol Section Abstract Doc Link PMC2764399 Disease Relevance 0.17 Pain Relevance 0.03

General Comments

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