INT211028

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Context Info
Confidence 0.47
First Reported 2007
Last Reported 2007
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.73
Pain Relevance 0.11

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

mRNA binding (Celf4) mRNA processing (Celf4) RNA binding (Celf4)
nucleus (Celf4) cytoplasm (Celf4)
Celf4 (Mus musculus)
Pain Link Frequency Relevance Heat
fluoxetine 2 71.84 Quite High
Serotonin 3 69.80 Quite High
Hippocampus 10 5.00 Very Low Very Low Very Low
Pyramidal cell 3 5.00 Very Low Very Low Very Low
cerebral cortex 2 5.00 Very Low Very Low Very Low
Analgesic 1 5.00 Very Low Very Low Very Low
Neurotransmitter 1 5.00 Very Low Very Low Very Low
Neuronal excitability 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Targeted Disruption 7 99.36 Very High Very High Very High
Epilepsy 21 95.68 Very High Very High Very High
Convulsion 53 87.04 High High
Sprains And Strains 9 66.40 Quite High
Absence Epilepsy 5 30.24 Quite Low
Weight Gain 2 24.04 Low Low
Attention Deficit Hyperactivity Disorder 2 22.92 Low Low
Inborn Genetic Diseases 1 18.80 Low Low
Disease 5 15.04 Low Low
Brain Injury 2 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
The origin of the disorder is a transgenic insertion in the Brunol4 gene, resulting in very little Brunol4 transcript in homozygotes and accordingly reduced amount in heterozygotes—suggesting haploinsufficiency.
Positive_regulation (resulting) of Transcription (transcript) of Brunol4 associated with targeted disruption
1) Confidence 0.47 Published 2007 Journal PLoS Genetics Section Body Doc Link PMC1934399 Disease Relevance 0.73 Pain Relevance 0.11

General Comments

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