INT328645

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Context Info
Confidence 0.22
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 3
Total Number 3
Disease Relevance 1.72
Pain Relevance 0.43

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

structural constituent of ribosome (Rpl27a) translation (Rpl27a)
Rpl27a (Mus musculus)
Rpl27a - P27L (2)
Pain Link Frequency Relevance Heat
rheumatoid arthritis 104 96.12 Very High Very High Very High
chemokine 30 50.00 Quite Low
Inflammation 14 5.00 Very Low Very Low Very Low
cytokine 5 5.00 Very Low Very Low Very Low
Crohn's disease 4 5.00 Very Low Very Low Very Low
Arthritis 4 5.00 Very Low Very Low Very Low
antagonist 3 5.00 Very Low Very Low Very Low
methotrexate 2 5.00 Very Low Very Low Very Low
ketamine 2 5.00 Very Low Very Low Very Low
anesthesia 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Targeted Disruption 22 99.88 Very High Very High Very High
Retinal Degeneration 28 99.60 Very High Very High Very High
Rheumatoid Arthritis 123 96.12 Very High Very High Very High
Retina Disease 18 82.64 Quite High
Death 6 25.00 Low Low
Disease 18 5.00 Very Low Very Low Very Low
INFLAMMATION 12 5.00 Very Low Very Low Very Low
Arthritis 5 5.00 Very Low Very Low Very Low
Adhesions 3 5.00 Very Low Very Low Very Low
Cancer 3 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
The PCR reactions were normalised with L27 (L27 ribosomal gene) to allow for comparison between samples.
Gene_expression (gene) of L27
1) Confidence 0.22 Published 2010 Journal Arthritis Res Ther Section Body Doc Link PMC2945064 Disease Relevance 0.86 Pain Relevance 0.43
To determine whether docosahexaenoic acid can protect against hereditary retinal degenerations in transgenic mice expressing the V20G, P23H, and P27L (VPP) rhodopsin mutations.


Gene_expression (expressing) of P27L (P27L) associated with targeted disruption and retinal degeneration
2) Confidence 0.01 Published 2010 Journal Molecular Vision Section Abstract Doc Link PMC2927381 Disease Relevance 0.55 Pain Relevance 0
Mice expressing an opsin transgene containing three (V20G, P23H, and P27L [VPP]) mutations near the N-terminus [36] have been used extensively to study inherited retinal degeneration [37–42].
Gene_expression (expressing) of P27L (P27L) associated with retinal degeneration
3) Confidence 0.00 Published 2010 Journal Molecular Vision Section Body Doc Link PMC2927381 Disease Relevance 0.31 Pain Relevance 0

General Comments

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