microarray gene expressions profile dataset Search Results


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Giner Inc microarray gene expression profiling
Microarray Gene Expression Profiling, supplied by Giner Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SuperArray Bioscience Corporation gene expression cdna microarrays for profiling genes involved in tgf-b (#mm-023)
Gene Expression Cdna Microarrays For Profiling Genes Involved In Tgf B (#Mm 023), supplied by SuperArray Bioscience Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biotechnology Information gene expression microarray dataset gse103611
Gene Expression Microarray Dataset Gse103611, supplied by Biotechnology Information, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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HEALTH Gene Technologies Co microarray gene expression dataset gse72810
Microarray Gene Expression Dataset Gse72810, supplied by HEALTH Gene Technologies Co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Genechem microarray analysis of msc gene expression profile
<t>Microarray</t> analysis of differentially expressed genes in MSCs during endothelial differentiation. In EC-MSC coculture system, there MSC samples for each group were collected at days 0 and 7, respectively, and sent to microarray analysis of differentially expressed genes. The inclusion criteria for differentially expressed genes were the absolute fold change of RNA levels > 1.5 and P value < 0.05. The analysis yielded 2482 (999 upregulated and 1483 downregulated) genes in MSC-H cells and 1325 (671 upregulated and 654 downregulated) genes in MSC-C cells. These genes were enriched in GO terms ( a ) and KEGG pathways analysis ( b ). The enriched terms that were present in both MSC-C and MSC-H groups were marked by asterisks. The MSC-H cells yielded a cluster of the most enriched terms with high similarity to MSC-C cells. Approximately one-half of the most enriched GO terms and pathways were consistent between them. Nevertheless, multiple pathways were noteworthy of being exclusively enriched in MSC-H cells, including MAPK and p53 signaling. c The number of differentially expressed genes (significance genes) enriched in the shared GO terms was counted and compared between groups. MSC-H cells yielded 1.7-fold (ranged from 1.5 to 1.9-fold) greater number of significance genes than MSC-C cells on average. d The number of differentially expressed genes (significance genes) enriched in the shared signaling pathways was counted and compared between groups. Similarly, MSC-H cells had an average 1.4-fold (ranged from 1.3 to 1.8-fold) increase of significance gene counts than the MSC-H cells
Microarray Analysis Of Msc Gene Expression Profile, supplied by Genechem, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Hielscher Ultrasonics gene expression microarray dataset
<t>Microarray</t> analysis of differentially expressed genes in MSCs during endothelial differentiation. In EC-MSC coculture system, there MSC samples for each group were collected at days 0 and 7, respectively, and sent to microarray analysis of differentially expressed genes. The inclusion criteria for differentially expressed genes were the absolute fold change of RNA levels > 1.5 and P value < 0.05. The analysis yielded 2482 (999 upregulated and 1483 downregulated) genes in MSC-H cells and 1325 (671 upregulated and 654 downregulated) genes in MSC-C cells. These genes were enriched in GO terms ( a ) and KEGG pathways analysis ( b ). The enriched terms that were present in both MSC-C and MSC-H groups were marked by asterisks. The MSC-H cells yielded a cluster of the most enriched terms with high similarity to MSC-C cells. Approximately one-half of the most enriched GO terms and pathways were consistent between them. Nevertheless, multiple pathways were noteworthy of being exclusively enriched in MSC-H cells, including MAPK and p53 signaling. c The number of differentially expressed genes (significance genes) enriched in the shared GO terms was counted and compared between groups. MSC-H cells yielded 1.7-fold (ranged from 1.5 to 1.9-fold) greater number of significance genes than MSC-C cells on average. d The number of differentially expressed genes (significance genes) enriched in the shared signaling pathways was counted and compared between groups. Similarly, MSC-H cells had an average 1.4-fold (ranged from 1.3 to 1.8-fold) increase of significance gene counts than the MSC-H cells
Gene Expression Microarray Dataset, supplied by Hielscher Ultrasonics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Agendia BV genomics platform for tumor gene expression profiling and microarray assay tests
<t>Microarray</t> analysis of differentially expressed genes in MSCs during endothelial differentiation. In EC-MSC coculture system, there MSC samples for each group were collected at days 0 and 7, respectively, and sent to microarray analysis of differentially expressed genes. The inclusion criteria for differentially expressed genes were the absolute fold change of RNA levels > 1.5 and P value < 0.05. The analysis yielded 2482 (999 upregulated and 1483 downregulated) genes in MSC-H cells and 1325 (671 upregulated and 654 downregulated) genes in MSC-C cells. These genes were enriched in GO terms ( a ) and KEGG pathways analysis ( b ). The enriched terms that were present in both MSC-C and MSC-H groups were marked by asterisks. The MSC-H cells yielded a cluster of the most enriched terms with high similarity to MSC-C cells. Approximately one-half of the most enriched GO terms and pathways were consistent between them. Nevertheless, multiple pathways were noteworthy of being exclusively enriched in MSC-H cells, including MAPK and p53 signaling. c The number of differentially expressed genes (significance genes) enriched in the shared GO terms was counted and compared between groups. MSC-H cells yielded 1.7-fold (ranged from 1.5 to 1.9-fold) greater number of significance genes than MSC-C cells on average. d The number of differentially expressed genes (significance genes) enriched in the shared signaling pathways was counted and compared between groups. Similarly, MSC-H cells had an average 1.4-fold (ranged from 1.3 to 1.8-fold) increase of significance gene counts than the MSC-H cells
Genomics Platform For Tumor Gene Expression Profiling And Microarray Assay Tests, supplied by Agendia BV, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Agendia BV rna isolation and gene expression profiling through microarray
<t>Microarray</t> analysis of differentially expressed genes in MSCs during endothelial differentiation. In EC-MSC coculture system, there MSC samples for each group were collected at days 0 and 7, respectively, and sent to microarray analysis of differentially expressed genes. The inclusion criteria for differentially expressed genes were the absolute fold change of RNA levels > 1.5 and P value < 0.05. The analysis yielded 2482 (999 upregulated and 1483 downregulated) genes in MSC-H cells and 1325 (671 upregulated and 654 downregulated) genes in MSC-C cells. These genes were enriched in GO terms ( a ) and KEGG pathways analysis ( b ). The enriched terms that were present in both MSC-C and MSC-H groups were marked by asterisks. The MSC-H cells yielded a cluster of the most enriched terms with high similarity to MSC-C cells. Approximately one-half of the most enriched GO terms and pathways were consistent between them. Nevertheless, multiple pathways were noteworthy of being exclusively enriched in MSC-H cells, including MAPK and p53 signaling. c The number of differentially expressed genes (significance genes) enriched in the shared GO terms was counted and compared between groups. MSC-H cells yielded 1.7-fold (ranged from 1.5 to 1.9-fold) greater number of significance genes than MSC-C cells on average. d The number of differentially expressed genes (significance genes) enriched in the shared signaling pathways was counted and compared between groups. Similarly, MSC-H cells had an average 1.4-fold (ranged from 1.3 to 1.8-fold) increase of significance gene counts than the MSC-H cells
Rna Isolation And Gene Expression Profiling Through Microarray, supplied by Agendia BV, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biotechnology Information microarray datasets of mirnas and gene expression profiling
<t>Microarray</t> analysis of differentially expressed genes in MSCs during endothelial differentiation. In EC-MSC coculture system, there MSC samples for each group were collected at days 0 and 7, respectively, and sent to microarray analysis of differentially expressed genes. The inclusion criteria for differentially expressed genes were the absolute fold change of RNA levels > 1.5 and P value < 0.05. The analysis yielded 2482 (999 upregulated and 1483 downregulated) genes in MSC-H cells and 1325 (671 upregulated and 654 downregulated) genes in MSC-C cells. These genes were enriched in GO terms ( a ) and KEGG pathways analysis ( b ). The enriched terms that were present in both MSC-C and MSC-H groups were marked by asterisks. The MSC-H cells yielded a cluster of the most enriched terms with high similarity to MSC-C cells. Approximately one-half of the most enriched GO terms and pathways were consistent between them. Nevertheless, multiple pathways were noteworthy of being exclusively enriched in MSC-H cells, including MAPK and p53 signaling. c The number of differentially expressed genes (significance genes) enriched in the shared GO terms was counted and compared between groups. MSC-H cells yielded 1.7-fold (ranged from 1.5 to 1.9-fold) greater number of significance genes than MSC-C cells on average. d The number of differentially expressed genes (significance genes) enriched in the shared signaling pathways was counted and compared between groups. Similarly, MSC-H cells had an average 1.4-fold (ranged from 1.3 to 1.8-fold) increase of significance gene counts than the MSC-H cells
Microarray Datasets Of Mirnas And Gene Expression Profiling, supplied by Biotechnology Information, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Almac Inc gene expression dna microarray dataset
A: Supervised hierarchical clustering displaying the genes significantly modulated between the resistant and sensitive cell lines (52 under‐ and 51 over‐expressed in resistant cell lines) using a cutoff of twofold change on expression and FDR < 0.01. B: Fold difference in gene expression between sensitive and resistant cell lines detected by qRT‐PCR analyses. Seven genes were selected from the list of altered genes for this analysis. The results from sensitive or resistant cell lines were pooled to obtain an estimated fold change. C: Correlation between the qRT‐PCR and the <t>microarray</t> expression data. The fold difference detected by qRT‐PCR between sensitive and resistant cell lines correlated significantly confirming the microarray results (Pearson's correlation or ρ = 0.739, p ‐value = 0.013).
Gene Expression Dna Microarray Dataset, supplied by Almac Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biotechnology Information tbi gene expression microarray dataset
A: Supervised hierarchical clustering displaying the genes significantly modulated between the resistant and sensitive cell lines (52 under‐ and 51 over‐expressed in resistant cell lines) using a cutoff of twofold change on expression and FDR < 0.01. B: Fold difference in gene expression between sensitive and resistant cell lines detected by qRT‐PCR analyses. Seven genes were selected from the list of altered genes for this analysis. The results from sensitive or resistant cell lines were pooled to obtain an estimated fold change. C: Correlation between the qRT‐PCR and the <t>microarray</t> expression data. The fold difference detected by qRT‐PCR between sensitive and resistant cell lines correlated significantly confirming the microarray results (Pearson's correlation or ρ = 0.739, p ‐value = 0.013).
Tbi Gene Expression Microarray Dataset, supplied by Biotechnology Information, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biotechnology Information ncbi gene expression omnibus microarray dataset gse32537
A: Supervised hierarchical clustering displaying the genes significantly modulated between the resistant and sensitive cell lines (52 under‐ and 51 over‐expressed in resistant cell lines) using a cutoff of twofold change on expression and FDR < 0.01. B: Fold difference in gene expression between sensitive and resistant cell lines detected by qRT‐PCR analyses. Seven genes were selected from the list of altered genes for this analysis. The results from sensitive or resistant cell lines were pooled to obtain an estimated fold change. C: Correlation between the qRT‐PCR and the <t>microarray</t> expression data. The fold difference detected by qRT‐PCR between sensitive and resistant cell lines correlated significantly confirming the microarray results (Pearson's correlation or ρ = 0.739, p ‐value = 0.013).
Ncbi Gene Expression Omnibus Microarray Dataset Gse32537, supplied by Biotechnology Information, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Microarray analysis of differentially expressed genes in MSCs during endothelial differentiation. In EC-MSC coculture system, there MSC samples for each group were collected at days 0 and 7, respectively, and sent to microarray analysis of differentially expressed genes. The inclusion criteria for differentially expressed genes were the absolute fold change of RNA levels > 1.5 and P value < 0.05. The analysis yielded 2482 (999 upregulated and 1483 downregulated) genes in MSC-H cells and 1325 (671 upregulated and 654 downregulated) genes in MSC-C cells. These genes were enriched in GO terms ( a ) and KEGG pathways analysis ( b ). The enriched terms that were present in both MSC-C and MSC-H groups were marked by asterisks. The MSC-H cells yielded a cluster of the most enriched terms with high similarity to MSC-C cells. Approximately one-half of the most enriched GO terms and pathways were consistent between them. Nevertheless, multiple pathways were noteworthy of being exclusively enriched in MSC-H cells, including MAPK and p53 signaling. c The number of differentially expressed genes (significance genes) enriched in the shared GO terms was counted and compared between groups. MSC-H cells yielded 1.7-fold (ranged from 1.5 to 1.9-fold) greater number of significance genes than MSC-C cells on average. d The number of differentially expressed genes (significance genes) enriched in the shared signaling pathways was counted and compared between groups. Similarly, MSC-H cells had an average 1.4-fold (ranged from 1.3 to 1.8-fold) increase of significance gene counts than the MSC-H cells

Journal: Stem Cell Research & Therapy

Article Title: HMGB1-modified mesenchymal stem cells attenuate radiation-induced vascular injury possibly via their high motility and facilitation of endothelial differentiation

doi: 10.1186/s13287-019-1197-x

Figure Lengend Snippet: Microarray analysis of differentially expressed genes in MSCs during endothelial differentiation. In EC-MSC coculture system, there MSC samples for each group were collected at days 0 and 7, respectively, and sent to microarray analysis of differentially expressed genes. The inclusion criteria for differentially expressed genes were the absolute fold change of RNA levels > 1.5 and P value < 0.05. The analysis yielded 2482 (999 upregulated and 1483 downregulated) genes in MSC-H cells and 1325 (671 upregulated and 654 downregulated) genes in MSC-C cells. These genes were enriched in GO terms ( a ) and KEGG pathways analysis ( b ). The enriched terms that were present in both MSC-C and MSC-H groups were marked by asterisks. The MSC-H cells yielded a cluster of the most enriched terms with high similarity to MSC-C cells. Approximately one-half of the most enriched GO terms and pathways were consistent between them. Nevertheless, multiple pathways were noteworthy of being exclusively enriched in MSC-H cells, including MAPK and p53 signaling. c The number of differentially expressed genes (significance genes) enriched in the shared GO terms was counted and compared between groups. MSC-H cells yielded 1.7-fold (ranged from 1.5 to 1.9-fold) greater number of significance genes than MSC-C cells on average. d The number of differentially expressed genes (significance genes) enriched in the shared signaling pathways was counted and compared between groups. Similarly, MSC-H cells had an average 1.4-fold (ranged from 1.3 to 1.8-fold) increase of significance gene counts than the MSC-H cells

Article Snippet: Microarray analysis of MSC gene expression profile was performed by GeneChem (Shanghai, China).

Techniques: Microarray, Protein-Protein interactions

A: Supervised hierarchical clustering displaying the genes significantly modulated between the resistant and sensitive cell lines (52 under‐ and 51 over‐expressed in resistant cell lines) using a cutoff of twofold change on expression and FDR < 0.01. B: Fold difference in gene expression between sensitive and resistant cell lines detected by qRT‐PCR analyses. Seven genes were selected from the list of altered genes for this analysis. The results from sensitive or resistant cell lines were pooled to obtain an estimated fold change. C: Correlation between the qRT‐PCR and the microarray expression data. The fold difference detected by qRT‐PCR between sensitive and resistant cell lines correlated significantly confirming the microarray results (Pearson's correlation or ρ = 0.739, p ‐value = 0.013).

Journal: The Journal of Pathology: Clinical Research

Article Title: A 12‐gene signature to distinguish colon cancer patients with better clinical outcome following treatment with 5‐fluorouracil or FOLFIRI

doi: 10.1002/cjp2.17

Figure Lengend Snippet: A: Supervised hierarchical clustering displaying the genes significantly modulated between the resistant and sensitive cell lines (52 under‐ and 51 over‐expressed in resistant cell lines) using a cutoff of twofold change on expression and FDR < 0.01. B: Fold difference in gene expression between sensitive and resistant cell lines detected by qRT‐PCR analyses. Seven genes were selected from the list of altered genes for this analysis. The results from sensitive or resistant cell lines were pooled to obtain an estimated fold change. C: Correlation between the qRT‐PCR and the microarray expression data. The fold difference detected by qRT‐PCR between sensitive and resistant cell lines correlated significantly confirming the microarray results (Pearson's correlation or ρ = 0.739, p ‐value = 0.013).

Article Snippet: Hence, we used a publically available gene expression DNA microarray dataset generated by Almac Diagnostics on 359 FFPE tissue specimens from stage II colon cancer that did not receive adjuvant chemotherapy.

Techniques: Expressing, Gene Expression, Quantitative RT-PCR, Microarray