INT268127

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Context Info
Confidence 0.14
First Reported 2009
Last Reported 2010
Negated 0
Speculated 1
Reported most in Body
Documents 2
Total Number 2
Disease Relevance 0
Pain Relevance 0.05

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

small molecule metabolic process (MARCKS) plasma membrane (MARCKS) cytoplasm (MARCKS)
Anatomy Link Frequency
band 1
telomere 1
MARCKS (Homo sapiens)
Pain Link Frequency Relevance Heat
imagery 2 90.28 High High
Kinase C 65 50.00 Quite Low
Central nervous system 10 5.00 Very Low Very Low Very Low
Inflammation 4 5.00 Very Low Very Low Very Low
antagonist 2 5.00 Very Low Very Low Very Low
Neuronal excitability 2 5.00 Very Low Very Low Very Low
Hippocampus 2 5.00 Very Low Very Low Very Low
Lasting pain 1 5.00 Very Low Very Low Very Low
long-term potentiation 1 5.00 Very Low Very Low Very Low
Neurobehavioral 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Virus Diseases 89 50.00 Quite Low
Borna Disease 4 50.00 Quite Low
Infection 29 5.00 Very Low Very Low Very Low
Ataxia 23 5.00 Very Low Very Low Very Low
Disease 19 5.00 Very Low Very Low Very Low
Cold Sores 18 5.00 Very Low Very Low Very Low
Targeted Disruption 14 5.00 Very Low Very Low Very Low
Sprains And Strains 12 5.00 Very Low Very Low Very Low
Factor Viii Deficiency 8 5.00 Very Low Very Low Very Low
Epstein-barr Virus 6 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Quantification of protein phosphorylation was carried out by measuring the intensity of fluorescence of the band corresponding to the phosphorylated protein normalized by ß-tubulin expression, due to inefficient stripping of phospho-MARCKS and phospho-SNAP-25 antibodies binding.
phospho-MARCKS Binding (binding) of in band
1) Confidence 0.14 Published 2009 Journal PLoS Pathogens Section Body Doc Link PMC2673689 Disease Relevance 0 Pain Relevance 0.05
Accordingly, it was established that MACs can be formed in HT1080 cells from either linear or circular input DNA, with circular alphoid constructs being very effective at forming MACs, whether or not human telomere sequences are added.
MACs Spec (whether) Binding (formed) of in telomere
2) Confidence 0.08 Published 2010 Journal Journal of Biomedicine and Biotechnology Section Body Doc Link PMC2938438 Disease Relevance 0 Pain Relevance 0

General Comments

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