INT157461

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Context Info
Confidence 0.36
First Reported 2009
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 3
Total Number 5
Disease Relevance 6.72
Pain Relevance 2.67

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

cell adhesion (CX3CR1) plasma membrane (CX3CR1) signal transducer activity (CX3CR1)
Anatomy Link Frequency
monocytes 1
anterior 1
natural killer cells 1
T cell 1
CX3CR1 (Homo sapiens)
Pain Link Frequency Relevance Heat
glial activation 1 99.10 Very High Very High Very High
Neuropathic pain 1 98.60 Very High Very High Very High
Inflammation 73 98.28 Very High Very High Very High
rheumatoid arthritis 6 97.08 Very High Very High Very High
Chronic pancreatitis 9 96.96 Very High Very High Very High
chemokine 169 96.62 Very High Very High Very High
fibrosis 4 95.08 Very High Very High Very High
psoriasis 3 94.16 High High
Inflammatory stimuli 1 92.64 High High
Neuritis 5 88.16 High High
Disease Link Frequency Relevance Heat
Neuropathic Pain 1 98.60 Very High Very High Very High
Adhesions 2 98.48 Very High Very High Very High
INFLAMMATION 88 98.28 Very High Very High Very High
Disease 74 97.76 Very High Very High Very High
Rheumatoid Arthritis 15 97.08 Very High Very High Very High
Pancreatitis 9 96.96 Very High Very High Very High
Asthma 6 96.20 Very High Very High Very High
Fibrosis 6 95.08 Very High Very High Very High
Psoriasis 3 94.16 High High
Renal Disease 3 93.72 High High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Furthermore, fractalkine increases neuropathic pain through glial activation, which can be diminished by blocking of its receptor, CX3CR1, through neutralizing antibodies.
CX3CR1 Binding (receptor) of associated with neuropathic pain and glial activation
1) Confidence 0.36 Published 2009 Journal Lab. Invest. Section Abstract Doc Link 19153557 Disease Relevance 1.62 Pain Relevance 1.35
It interacts with the unique receptor CX3CR1 that is expressed on monocytes, natural killer cells, and some T cells.
CX3CR1 Binding (interacts) of in natural killer cells
2) Confidence 0.32 Published 2010 Journal Molecular Vision Section Body Doc Link PMC2874579 Disease Relevance 1.58 Pain Relevance 0.31
Fractalkine/CX3CL1-CX3CR1 interaction contributes to the development of various inflammatory diseases such as rheumatoid arthritis, asthma, Wegener’s granulomatosis, Crohn’s disease, psoriasis, glomerulonephritis, experimental autoimmune anterior uveitis, and atherosclerosis [52-57].
CX3CR1 Binding (interaction) of in anterior associated with psoriasis, renal disease, rheumatoid arthritis, increased venous pressure under development, disease, asthma, inflammation and uveitis
3) Confidence 0.24 Published 2010 Journal Molecular Vision Section Body Doc Link PMC2874579 Disease Relevance 1.61 Pain Relevance 0.28
It interacts with the unique receptor CX3CR1 that is expressed on monocytes, natural killer cells, and some T cells.
CX3CR1 Binding (interacts) of in monocytes
4) Confidence 0.11 Published 2010 Journal Molecular Vision Section Body Doc Link PMC2874579 Disease Relevance 1.58 Pain Relevance 0.31
Lastly, the “CX3C” chemokines (three amino acids between the first two cysteines) are, to date, represented by a single peptide, namely, CX3CL1/fractalkine, which is encoded on human chromosome 16, binds the CX3CR1 receptor and regulates T cell trafficking and adhesion [4].
CX3CR1 receptor Binding (binds) of in T cell associated with chemokine and adhesions
5) Confidence 0.02 Published 2010 Journal Journal of Oncology Section Body Doc Link PMC2798669 Disease Relevance 0.34 Pain Relevance 0.43

General Comments

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