INT206764

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Context Info
Confidence 0.05
First Reported 2007
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 8
Total Number 9
Disease Relevance 13.45
Pain Relevance 2.84

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

cytoplasm (AQP4, Nqo1) cytosol (Nqo1) transport (AQP4)
oxidoreductase activity (Nqo1) plasma membrane (AQP4) transmembrane transport (AQP4)
AQP4 (Homo sapiens)
Nqo1 (Mus musculus)
Pain Link Frequency Relevance Heat
Multiple sclerosis 100 100.00 Very High Very High Very High
Demyelination 16 99.46 Very High Very High Very High
medulla 2 95.96 Very High Very High Very High
Spinal cord 52 92.32 High High
Central nervous system 36 90.92 High High
addiction 9 84.08 Quite High
Neuritis 97 81.76 Quite High
imagery 10 74.52 Quite High
Inflammation 59 60.48 Quite High
intrathecal 36 53.36 Quite High
Disease Link Frequency Relevance Heat
Neuromyelitis Optica 481 100.00 Very High Very High Very High
Demyelinating Disease 220 100.00 Very High Very High Very High
Necrosis 6 99.70 Very High Very High Very High
Autonomic Nervous System Disease 2 97.36 Very High Very High Very High
Disease 261 96.04 Very High Very High Very High
Respiratory Failure 5 94.08 High High
Autoimmune Disease 19 92.68 High High
Channelopathies 2 91.72 High High
Central Nervous System Disease 22 90.92 High High
Syndrome 24 87.52 High High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Lennon and colleagues discovered a biomarker for NMO; NMO-IgG is an autoantibody initially detected in the serum of 73% of NMO but less than 5% of CMS patients [10], which binds to aquaporin-4 (AQP4) [11], the most abundant water channel in the CNS [12-14].
AQP4 Binding (binds) of NMO-IgG associated with neuromyelitis optica and multiple sclerosis
1) Confidence 0.05 Published 2010 Journal J Neuroinflammation Section Body Doc Link PMC2941752 Disease Relevance 2.72 Pain Relevance 0.75
Lennon and colleagues discovered a biomarker for NMO; NMO-IgG is an autoantibody initially detected in the serum of 73% of NMO but less than 5% of CMS patients [10], which binds to aquaporin-4 (AQP4) [11], the most abundant water channel in the CNS [12-14].
aquaporin-4 Binding (binds) of NMO-IgG associated with neuromyelitis optica and multiple sclerosis
2) Confidence 0.05 Published 2010 Journal J Neuroinflammation Section Body Doc Link PMC2941752 Disease Relevance 2.72 Pain Relevance 0.74
Thus we hypothesized that AQP4 antibodies in fact characterize NMO patients.


AQP4 Binding (characterize) of NMO associated with neuromyelitis optica
3) Confidence 0.03 Published 2007 Journal PLoS Medicine Section Abstract Doc Link PMC1852124 Disease Relevance 1.17 Pain Relevance 0.17
It is therefore still unclear whether antibodies to AQP4 are specific for NMO and whether testing for these antibodies may be useful for its diagnosis and its distinction from diseases with similar clinical and neuroradiological patterns, such as MS and other autoimmune diseases with involvement of the CNS.
AQP4 Binding (specific) of NMO associated with neuromyelitis optica, multiple sclerosis, autoimmune disease, central nervous system and disease
4) Confidence 0.03 Published 2007 Journal PLoS Medicine Section Body Doc Link PMC1852124 Disease Relevance 1.74 Pain Relevance 0.29
The limited access of circulating IgG to the extracapillary space in the CNS would only permit interaction of NMO-IgG with AQP4 at the glia limitans of BBB: in consequence of these findings, many authors suggest the perivascular space as the primary target site of the pathogenic process.
AQP4 Binding (interaction) of NMO associated with neuromyelitis optica
5) Confidence 0.02 Published 2010 Journal Current Neuropharmacology Section Body Doc Link PMC2923365 Disease Relevance 1.09 Pain Relevance 0.17
Moreover, two pathologic patterns in NMO, both of which were associated with loss of AQP4 immunoreactivity were described [39].
AQP4 Binding (associated) of NMO associated with neuromyelitis optica
6) Confidence 0.02 Published 2010 Journal Current Neuropharmacology Section Body Doc Link PMC2923365 Disease Relevance 1.33 Pain Relevance 0.35
In summary, the intriguing report by Roemer and colleagues [80], describing loss of AQP4 in the absence of demyelination or necrosis suggests that binding of antibody to AQP4 may be the initial pathogenic event in NMO lesions.
AQP4 Binding (binding) of NMO associated with neuromyelitis optica, necrosis and demyelination
7) Confidence 0.02 Published 2010 Journal Current Neuropharmacology Section Body Doc Link PMC2923365 Disease Relevance 1.27 Pain Relevance 0.31
In 70-80% of cases, neuromyelitis optica (NMO) is associated with highly specific serum auto-antibodies to aquaporin-4 (termed AQP4-Ab or NMO-IgG).
aquaporin-4 Binding (associated) of NMO associated with neuromyelitis optica
8) Confidence 0.01 Published 2010 Journal J Neuroinflammation Section Abstract Doc Link PMC2945323 Disease Relevance 0.70 Pain Relevance 0.03
In 70-80% of cases, neuromyelitis optica (NMO) is associated with highly specific serum auto-antibodies to aquaporin-4 (termed AQP4-Ab or NMO-IgG).
AQP4 Binding (associated) of NMO associated with neuromyelitis optica
9) Confidence 0.01 Published 2010 Journal J Neuroinflammation Section Abstract Doc Link PMC2945323 Disease Relevance 0.70 Pain Relevance 0.03

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