INT300511

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Context Info
Confidence 0.10
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 2
Disease Relevance 2.28
Pain Relevance 0.13

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

extracellular region (Plaur, Vtn) extracellular matrix organization (Vtn) enzyme binding (Plaur)
extracellular space (Vtn) proteinaceous extracellular matrix (Vtn) cell adhesion (Vtn)
Anatomy Link Frequency
extracellular matrix 2
Plaur (Mus musculus)
Vtn (Mus musculus)
Pain Link Frequency Relevance Heat
Inflammation 34 69.56 Quite High
fibrosis 6 5.00 Very Low Very Low Very Low
Freund adjuvant 4 5.00 Very Low Very Low Very Low
cytokine 2 5.00 Very Low Very Low Very Low
Buprenorphine 2 5.00 Very Low Very Low Very Low
alcohol 2 5.00 Very Low Very Low Very Low
antagonist 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Adhesions 2 99.46 Very High Very High Very High
Apoptosis 4 98.64 Very High Very High Very High
Cancer 114 95.16 Very High Very High Very High
Pathologic Processes 2 76.72 Quite High
INFLAMMATION 34 69.56 Quite High
Lymphatic Abnormalities 2 67.92 Quite High
Graft Vs Host Disease 4 63.80 Quite High
Disease 2 61.28 Quite High
Metastasis 16 53.28 Quite High
Age-related Macular Degeneration 2 33.92 Quite Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
The contribution of these proteins in cancer progression relies on their capacity to control various biological processes such as (i) cell proliferation [5]; (ii) cell invasion through plasmin-mediated extracellular matrix degradation [6]; (iii) cell adhesion and migration through the interaction of uPA/uPAR/PAI-1 complex with vitronectin and integrins [7]; and (iv) cell apoptosis through the control of pro-apoptotic factor release [8].
uPAR Binding (complex) of vitronectin in extracellular matrix associated with cancer, apoptosis and adhesions
1) Confidence 0.10 Published 2010 Journal PLoS ONE Section Body Doc Link PMC2836381 Disease Relevance 1.11 Pain Relevance 0.06
The contribution of these proteins in cancer progression relies on their capacity to control various biological processes such as (i) cell proliferation [5]; (ii) cell invasion through plasmin-mediated extracellular matrix degradation [6]; (iii) cell adhesion and migration through the interaction of uPA/uPAR/PAI-1 complex with vitronectin and integrins [7]; and (iv) cell apoptosis through the control of pro-apoptotic factor release [8].
uPAR Binding (interaction) of vitronectin in extracellular matrix associated with cancer, apoptosis and adhesions
2) Confidence 0.10 Published 2010 Journal PLoS ONE Section Body Doc Link PMC2836381 Disease Relevance 1.17 Pain Relevance 0.07

General Comments

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