INT202183

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Context Info
Confidence 0.11
First Reported 2006
Last Reported 2006
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 1.25
Pain Relevance 0.21

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

signal transduction (PLAU, PLAUR) extracellular region (PLAU, PLAUR) plasma membrane (PLAU, PLAUR)
peptidase activity (PLAU) extracellular space (PLAU) enzyme binding (PLAUR)
Anatomy Link Frequency
extracellular matrix 2
PLAU (Homo sapiens)
PLAUR (Homo sapiens)
Pain Link Frequency Relevance Heat
chemokine 1 94.56 High High
Inflammation 5 87.84 High High
cytokine 1 84.24 Quite High
metalloproteinase 2 5.00 Very Low Very Low Very Low
COX2 1 5.00 Very Low Very Low Very Low
anesthesia 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Cancer 29 98.92 Very High Very High Very High
Wound Healing 5 96.60 Very High Very High Very High
Adhesions 1 96.32 Very High Very High Very High
Metastasis 2 93.88 High High
INFLAMMATION 5 87.84 High High
Injury 5 65.20 Quite High
Breast Cancer 15 54.08 Quite High
Carcinoma 1 41.76 Quite Low
Apoptosis 1 27.76 Quite Low
Aggression 1 7.36 Low Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
For example, uPA, uPAR and its inhibitor PAI-1 are responsible for the degradation and remodeling of the extracellular matrix, and are further involved in angiogenesis, cell adhesion and migration necessary for tumor cell invasion and metastasis [31,32].
uPA Regulation (responsible) of Protein_catabolism (degradation) of uPAR in extracellular matrix associated with cancer, metastasis and adhesions
1) Confidence 0.11 Published 2006 Journal Breast Cancer Res Section Body Doc Link PMC1779463 Disease Relevance 1.25 Pain Relevance 0.21

General Comments

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