INT133255
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
The up-regulated candidate genes ANXA2 and S100A8 encode two Ca2+-modulated proteins expressed in microglia and are implicated in the intracellular and extracellular regulation of inflammatory responses [92,93]. | |||||||||||||||
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In the present study defense signaling comprises the only up-regulated GO categories in the SALS motor cortex, and is represented by numerous candidate genes, whose differential expression likely promotes (FCGBP, YWHAH, ANXA2, S100A8, EDN1, CEBPD) or suppresses (EGR1, metallothioneins) inflammatory responses, respectively. | |||||||||||||||
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TNC expression was detected with increased frequency in the progression from PanIN-1 lesions to PDAC, and a parallel switch from cytoplasmic to cell surface expression of annexin II was observed. | |||||||||||||||
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Tenascin C and annexin II expression in the process of pancreatic carcinogenesis. | |||||||||||||||
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The mRNA and protein levels of TNC and of annexin II were analysed in pancreatic tissues by DNA array, quantitative reverse transcriptase-polymerase chain reaction (QRT-PCR) and immunohistochemistry. | |||||||||||||||
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In conclusion, the expression of TNC and cell surface annexin II increases in the progression from low-grade PanIN lesions to pancreatic cancer. | |||||||||||||||
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WNT1-induced secreted protein 1 (WISP1), a WNT target gene, is also expressed during fracture healing, and overexpression of this gene increases proliferation but decreases the differentiation in a chondrocytic cell line [21]. | |||||||||||||||
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A comparative study using Plasmodium berghei ANKA infected C57BL/6 and BALB/c mice indicated th at both strains of mice expressed CXCL10 (interferon-induced protein 10, IP-10) and CCL2 (monocyte chemotactic protein-1, MCP-1) chemokine genes as early as 24 hours post-infection [12]. | |||||||||||||||
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Our previous studies demonstrated that CIAPIN1 confers multidrug resistance in gastric cancer cells possibly by upregulating multidrug resistance gene-1 and multidrug-related protein-1 expression (16). | |||||||||||||||
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