<p>The analysis compared 789 oligo probes corresponding to 537 human genes significantly differentially expressed (fold change >1.5, <i>q</i> <0.05) between twins discordant for SAID. The upper horizontal axis (blue bars) describe the association of the data set with a given pathway (-log (<i>p</i> value)). The cutoff threshold value (defined as <i>p</i> = 0.05) is shown by the vertical red line. The ratio of the number of genes from the data set that map to a given pathway divided by the total number of molecules that comprise the pathway is shown on the horizontal axis (green triangles). Previously reported viral-related signaling pathways are in bold print.</p
<p>Ingenuity pathway analysis was used to assemble a network based upon 22 differentially expressed ...
<p>Ingenuity Pathway analysis (IPA) was performed for genes exhibiting preferential H3K4Me3 enrichme...
<p>The Ingenuity Pathway Analysis tool was used to identify significant genes that are related to he...
<p>(A) The pathway analysis indicated that a large number of differentially expressed genes belong t...
<p>A) IPA software v7.6 (Ingenuity® Systems, USA) was used to identify the top canonical pathways in...
<p>A: hierarchical analysis of the number of genes in each pathway for each condition. Numbers of ge...
<p>All genes that were significant at a p<0.05 level were subjected to pathway analysis (Ingenuity P...
Using the Impact Analysis method in iPathway (Advaita Corporation), we conducted unbiased pathway an...
<p>In this analysis, genes were tested for significant association in specific cell functional (A) o...
<p>624 genes downregulated in the CA1 subregion of rTg4510 were subjected subjected to Ingenuity Pat...
<p>Twenty-nine probe sets (representing 26 genes) were identified as uniquely dysregulated in the di...
<p>The top ranked Ingenuity canonical pathways resulting from differentially upregulated gene expres...
<p>Intensity of the red color indicates the degree of upregulation. Intensity of the green color ind...
<p>Ingenuity pathway analysis was used to assemble a network based upon 20 differentially expressed ...
<p>Pathway analysis at different time points was done using the Ingenuity curated database of gene i...
<p>Ingenuity pathway analysis was used to assemble a network based upon 22 differentially expressed ...
<p>Ingenuity Pathway analysis (IPA) was performed for genes exhibiting preferential H3K4Me3 enrichme...
<p>The Ingenuity Pathway Analysis tool was used to identify significant genes that are related to he...
<p>(A) The pathway analysis indicated that a large number of differentially expressed genes belong t...
<p>A) IPA software v7.6 (Ingenuity® Systems, USA) was used to identify the top canonical pathways in...
<p>A: hierarchical analysis of the number of genes in each pathway for each condition. Numbers of ge...
<p>All genes that were significant at a p<0.05 level were subjected to pathway analysis (Ingenuity P...
Using the Impact Analysis method in iPathway (Advaita Corporation), we conducted unbiased pathway an...
<p>In this analysis, genes were tested for significant association in specific cell functional (A) o...
<p>624 genes downregulated in the CA1 subregion of rTg4510 were subjected subjected to Ingenuity Pat...
<p>Twenty-nine probe sets (representing 26 genes) were identified as uniquely dysregulated in the di...
<p>The top ranked Ingenuity canonical pathways resulting from differentially upregulated gene expres...
<p>Intensity of the red color indicates the degree of upregulation. Intensity of the green color ind...
<p>Ingenuity pathway analysis was used to assemble a network based upon 20 differentially expressed ...
<p>Pathway analysis at different time points was done using the Ingenuity curated database of gene i...
<p>Ingenuity pathway analysis was used to assemble a network based upon 22 differentially expressed ...
<p>Ingenuity Pathway analysis (IPA) was performed for genes exhibiting preferential H3K4Me3 enrichme...
<p>The Ingenuity Pathway Analysis tool was used to identify significant genes that are related to he...