INT312731

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Context Info
Confidence 0.36
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 2
Disease Relevance 0.38
Pain Relevance 0.94

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

endoplasmic reticulum (UGT2B15)
UGT2B15 (Homo sapiens)
Pain Link Frequency Relevance Heat
diclofenac 2 99.70 Very High Very High Very High
cINOD 8 99.60 Very High Very High Very High
Pain 2 86.88 High High
Bioavailability 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
INFLAMMATION 2 99.08 Very High Very High Very High
Pain 2 86.88 High High
Renal Disease 36 61.12 Quite High
Proteinuria 4 42.88 Quite Low
Focal Segmental Glomerulosclerosis 10 40.80 Quite Low
Injury 16 35.28 Quite Low
Keloid Scars 4 33.20 Quite Low
Urinary Tract Infection 2 13.20 Low Low
Chronic Renal Failure 8 10.16 Low Low
Obesity 22 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
However, use of steroids together with NSAIDs will competitively inhibit the steroid glucuronidation activity of UGT2B15.
Negative_regulation (inhibit) of UGT2B15 associated with cinod
1) Confidence 0.36 Published 2010 Journal Subst Abuse Treat Prev Policy Section Body Doc Link PMC2877023 Disease Relevance 0.23 Pain Relevance 0.48
Sten et al. discovered that commonly used over-the-counter (OTC) non steroidal anti-inflammatory drugs (NSAIDs) like diclofenac and ibuprofen inhibited the testosterone glucuronidation activity of UGT2B17, UGT2B15 and some other UGTs that have previously shown low but detectable activity [43].
Negative_regulation (inhibited) of UGT2B15 associated with inflammation, cinod and diclofenac
2) Confidence 0.36 Published 2010 Journal Subst Abuse Treat Prev Policy Section Body Doc Link PMC2877023 Disease Relevance 0.15 Pain Relevance 0.46

General Comments

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