INT237347

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Context Info
Confidence 0.36
First Reported 2008
Last Reported 2008
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.44
Pain Relevance 0.03

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

cell differentiation (Bin1) nucleus (Bin1) cytoplasm (Bin1)
Bin1 (Mus musculus)
Pain Link Frequency Relevance Heat
sodium channel 1 52.16 Quite High
Inflammation 2 5.00 Very Low Very Low Very Low
ketamine 1 5.00 Very Low Very Low Very Low
anesthesia 1 5.00 Very Low Very Low Very Low
Sciatic nerve 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Congenital Structural Myopathies 17 100.00 Very High Very High Very High
Frailty 2 98.08 Very High Very High Very High
Muscle Weakness 4 97.60 Very High Very High Very High
Paralysis 1 59.92 Quite High
Demyelinating Disease 2 8.88 Low Low
Cytomegalovirus Infection 13 5.00 Very Low Very Low Very Low
Disease 5 5.00 Very Low Very Low Very Low
Muscle Disease 5 5.00 Very Low Very Low Very Low
Charcot Marie Tooth Disease 4 5.00 Very Low Very Low Very Low
Death 2 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Recently, mutations in the amphyphisin 2/Bin1 gene in patients with an autosomal recessive form of CNM were shown to alter its membrane tubulation properties and interaction with dynamin 2 (6).
Bin1 Binding (interaction) of associated with congenital structural myopathies
1) Confidence 0.36 Published 2008 Journal Human Molecular Genetics Section Body Doc Link PMC2441725 Disease Relevance 0.44 Pain Relevance 0.03

General Comments

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