INT101552

From wiki-pain
Jump to: navigation, search
Context Info
Confidence 0.17
First Reported 2002
Last Reported 2010
Negated 0
Speculated 1
Reported most in Body
Documents 2
Total Number 3
Disease Relevance 1.95
Pain Relevance 0.26

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

transmembrane transport (CACNA1F)
CACNA1F (Homo sapiens)
Pain Link Frequency Relevance Heat
Central nervous system 2 95.28 Very High Very High Very High
Migraine 1 93.56 High High
Calcium channel 4 87.08 High High
corticosteroid 1 5.00 Very Low Very Low Very Low
Paresthesia 1 5.00 Very Low Very Low Very Low
Inflammation 1 5.00 Very Low Very Low Very Low
Pain 1 5.00 Very Low Very Low Very Low
backache 1 5.00 Very Low Very Low Very Low
addiction 1 5.00 Very Low Very Low Very Low
peripheral neuropathy 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Night Blindness 1 99.96 Very High Very High Very High
Disease 30 98.16 Very High Very High Very High
Neurological Disease 3 95.68 Very High Very High Very High
Migraine With Aura 1 94.36 High High
Channelopathies 3 94.08 High High
Ataxia 4 92.80 High High
Spinocerebellar Ataxia Type 2 1 92.04 High High
Ovarian Cancer 47 91.40 High High
Cancer 11 86.12 High High
Drug Induced Neurotoxicity 11 84.16 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
JMcC, JMcV and KF performed the statistical analyses and interpreted the results.
JMcC Spec (analyses) Binding (interpreted) of
1) Confidence 0.17 Published 2010 Journal BMC Infect Dis Section Body Doc Link PMC2893181 Disease Relevance 0.07 Pain Relevance 0
The human diseases comprise: 1) a recessive retinal disorder, X-linked congenital stationary night blindness, associated with mutations in the CACNA1F gene, encoding alpha(1)1.4 subunits of L-type channels; and 2) a group of rare allelic autosomal dominant human neurological disorders including familial hemiplegic migraine, episodic ataxia type 2, and spinocerebellar ataxia type 6, all associated with mutations in the CACNA1A gene, encoding alpha(1)2.1 subunits of P/Q-type calcium channels.
CACNA1F gene Binding (associated) of associated with ataxia, neurological disease, calcium channel, migraine, spinocerebellar ataxia type 2, night blindness, disease and migraine with aura
2) Confidence 0.10 Published 2002 Journal Mol. Neurobiol. Section Abstract Doc Link 11890456 Disease Relevance 1.12 Pain Relevance 0.26
Patients were randomized: the control group received JM8 AUC 5 and PTX 175 mg/m2 every 21 days and the experimental group received JM8 AUC 5 and PLD 30 mg/m2 every 28 days.
JM8 Binding (received) of
3) Confidence 0.07 Published 2010 Journal Therapeutics and Clinical Risk Management Section Body Doc Link PMC2952486 Disease Relevance 0.75 Pain Relevance 0

General Comments

This test has worked.

Personal tools
Namespaces

Variants
Actions
Navigation
Toolbox