INT303974

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Context Info
Confidence 0.79
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 2
Total Number 2
Disease Relevance 0.24
Pain Relevance 0.06

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

nuclear envelope (LBR) small molecule metabolic process (LBR) nucleus (LBR)
DNA binding (LBR)
Anatomy Link Frequency
lamina 1
T lymphocytes 1
LBR (Homo sapiens)
Pain Link Frequency Relevance Heat
cytokine 24 62.04 Quite High
endometriosis 1 55.80 Quite High
Inflammation 9 5.00 Very Low Very Low Very Low
chemokine 3 5.00 Very Low Very Low Very Low
Inflammatory stimuli 2 5.00 Very Low Very Low Very Low
withdrawal 1 5.00 Very Low Very Low Very Low
Pain 1 5.00 Very Low Very Low Very Low
Inflammatory response 1 5.00 Very Low Very Low Very Low
spinal inflammation 1 5.00 Very Low Very Low Very Low
antagonist 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Herpes Virus Infection 1 99.58 Very High Very High Very High
Adhesions 2 81.28 Quite High
Endometriosis (extended) 1 55.80 Quite High
Pressure And Volume Under Development 1 43.08 Quite Low
Obesity 22 32.20 Quite Low
Apoptosis 8 26.36 Quite Low
Retinoblastoma 51 5.00 Very Low Very Low Very Low
Infection 13 5.00 Very Low Very Low Very Low
INFLAMMATION 12 5.00 Very Low Very Low Very Low
Viral Infection 10 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
However, when T lymphocytes are costimulated with PHA or concanavalin A (Con A), leptin dose-dependently enhances the proliferation and activation of cultured T lymphocytes, achieving maximal effect at 10?
Phosphorylation (costimulated) of PHA in T lymphocytes
1) Confidence 0.79 Published 2010 Journal Mediators of Inflammation Section Body Doc Link PMC2846344 Disease Relevance 0.14 Pain Relevance 0.06
Although experiments of this type are often cited as evidence that CHPK-mediated lamin A/C phosphorylation directly leads to lamina disruption, we note that they cannot rule out other mechanisms for lamina disruption upon CHPK expression or herpesvirus infection (such as lamin B or lamin receptor phosphorylation) in addition to or instead of lamin A/C phosphorylation.


Phosphorylation (phosphorylation) of lamin receptor in lamina associated with herpes virus infection
2) Confidence 0.05 Published 2010 Journal PLoS Pathogens Section Body Doc Link PMC2936540 Disease Relevance 0.10 Pain Relevance 0

General Comments

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