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Context Info
Confidence 0.39
First Reported 2007
Last Reported 2010
Negated 1
Speculated 0
Reported most in Title
Documents 2
Total Number 2
Disease Relevance 1.17
Pain Relevance 0.09

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

nucleus (Foxc1) DNA binding (Foxc1) transcription factor binding (Foxc1)
cytoplasm (Foxc1)
Anatomy Link Frequency
epithelial cell 1
Foxc1 (Mus musculus)
Pain Link Frequency Relevance Heat
Pain 1 86.16 High High
ketamine 2 5.00 Very Low Very Low Very Low
imagery 2 5.00 Very Low Very Low Very Low
Analgesic 1 5.00 Very Low Very Low Very Low
Inflammation 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Cancer 164 100.00 Very High Very High Very High
Syndrome 3 99.00 Very High Very High Very High
Hydrocephalus 2 97.60 Very High Very High Very High
Deafness 2 97.04 Very High Very High Very High
Intellectual Impairment 1 89.92 High High
Growth Problems 1 88.96 High High
Arthralgia 1 86.40 High High
Eye Malformation 1 81.72 Quite High
Carcinoma 14 50.00 Quite Low
Repression 1 32.96 Quite Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
As shown by qPCR analysis, expression of known regulators of normal and tumor mammary epithelial cell fate and function, namely Ehf [43], Elf5 [44], Etv5 [45], and Foxc1 [46] is stronger in the CD24ahigh subset (Figure 13B), whereas the CD24alow subset is distinguished by a higher expression of the Twist2 gene (Figure 13B), whose product has a function in EMT [38].
Gene_expression (expression) of Foxc1 in epithelial cell associated with cancer
1) Confidence 0.39 Published 2010 Journal PLoS ONE Section Body Doc Link PMC2920333 Disease Relevance 0.26 Pain Relevance 0
Absence of PITX2, BARX1, and FOXC1 mutations in De Hauwere syndrome (Axenfeld-Rieger anomaly, hydrocephaly, hearing loss): a 25-year follow up.
Neg (Absence) Gene_expression (Absence) of FOXC1 associated with deafness, syndrome and hydrocephalus
2) Confidence 0.22 Published 2007 Journal Am. J. Med. Genet. A Section Title Doc Link 17486624 Disease Relevance 0.92 Pain Relevance 0.09

General Comments

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