bulk rna sequencing Search Results


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Monensin An up-regulates mitochondrially encoded genes. (A) Overview of the monensin A mediated alteration of gene expression on HACAT cells using bulk <t>RNA-seq.</t> (B) Pathway enrichment analysis arranging the top up-regulated pathways according to the adjusted p-value (left). The altered information on the top-ranking pathway was further excavated (right). (C) Heatmap shows monensin A-triggered actively expressed genes involved in the top-ranking pathway. Data are color-coded to reflect the relative expression level of mitochondrially encoded genes. All data are normalized to their matched control. (D) PCR-based validation of the mRNA expression of mitochondrial genes in HACAT cells treated with or without monensin A (125 nM) for 3 h. Data are represented as mean ± SD. Two-tailed Student's unpaired t -test (D). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Bulk Rna Sequencing, supplied by LC Sciences, 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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Monensin An up-regulates mitochondrially encoded genes. (A) Overview of the monensin A mediated alteration of gene expression on HACAT cells using bulk <t>RNA-seq.</t> (B) Pathway enrichment analysis arranging the top up-regulated pathways according to the adjusted p-value (left). The altered information on the top-ranking pathway was further excavated (right). (C) Heatmap shows monensin A-triggered actively expressed genes involved in the top-ranking pathway. Data are color-coded to reflect the relative expression level of mitochondrially encoded genes. All data are normalized to their matched control. (D) PCR-based validation of the mRNA expression of mitochondrial genes in HACAT cells treated with or without monensin A (125 nM) for 3 h. Data are represented as mean ± SD. Two-tailed Student's unpaired t -test (D). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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Monensin An up-regulates mitochondrially encoded genes. (A) Overview of the monensin A mediated alteration of gene expression on HACAT cells using bulk <t>RNA-seq.</t> (B) Pathway enrichment analysis arranging the top up-regulated pathways according to the adjusted p-value (left). The altered information on the top-ranking pathway was further excavated (right). (C) Heatmap shows monensin A-triggered actively expressed genes involved in the top-ranking pathway. Data are color-coded to reflect the relative expression level of mitochondrially encoded genes. All data are normalized to their matched control. (D) PCR-based validation of the mRNA expression of mitochondrial genes in HACAT cells treated with or without monensin A (125 nM) for 3 h. Data are represented as mean ± SD. Two-tailed Student's unpaired t -test (D). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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A Volcano plots of glucose metabolism-related genes that are induced in WT versus TRPM7KO cells. Genes with a fold-change ≥2 and P value of < 0.05 are shown. B RT-qPCR analysis validating the decreased expression of glucose catabolic genes from <t>RNA-seq</t> in TRPM7KO cells. C Immunofluorescent staining of TRPM7, SLC2A3 and DAPI in the xenograft tumor (scale bars, 100 μm). D Immunohistochemical staining for TRPM7, SLC2A1 and SLC2A3 in tumor tissue (scale bars, 100 μm). E , F Increased SLC2A3 in naltriben-induced (25 μM, 24 h) WT cells but not TRPM7KO cells. Quantification of protein was below. Two groups of samples were compared by unpaired two-tailed Student’s t -test. Multiple groups were compared by ANOVA.
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A Volcano plots of glucose metabolism-related genes that are induced in WT versus TRPM7KO cells. Genes with a fold-change ≥2 and P value of < 0.05 are shown. B RT-qPCR analysis validating the decreased expression of glucose catabolic genes from <t>RNA-seq</t> in TRPM7KO cells. C Immunofluorescent staining of TRPM7, SLC2A3 and DAPI in the xenograft tumor (scale bars, 100 μm). D Immunohistochemical staining for TRPM7, SLC2A1 and SLC2A3 in tumor tissue (scale bars, 100 μm). E , F Increased SLC2A3 in naltriben-induced (25 μM, 24 h) WT cells but not TRPM7KO cells. Quantification of protein was below. Two groups of samples were compared by unpaired two-tailed Student’s t -test. Multiple groups were compared by ANOVA.
Brb Seq Or ‘Bulk Rna Barcoding And Sequencing, supplied by BioSpyder Technologies, 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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SCHOTT bulk rna sequencing
Summary of 15 studies identified investigating obesity as a variable related to human or animal model osteoarthritis using transcriptomics or metabolomics. Publications with associated Gene Expression Omnibus dataset accession numbers (GSE) are indicated.
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Summary of 15 studies identified investigating obesity as a variable related to human or animal model osteoarthritis using transcriptomics or metabolomics. Publications with associated Gene Expression Omnibus dataset accession numbers (GSE) are indicated.
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Summary of 15 studies identified investigating obesity as a variable related to human or animal model osteoarthritis using transcriptomics or metabolomics. Publications with associated Gene Expression Omnibus dataset accession numbers (GSE) are indicated.
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Summary of 15 studies identified investigating obesity as a variable related to human or animal model osteoarthritis using transcriptomics or metabolomics. Publications with associated Gene Expression Omnibus dataset accession numbers (GSE) are indicated.
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Summary of 15 studies identified investigating obesity as a variable related to human or animal model osteoarthritis using transcriptomics or metabolomics. Publications with associated Gene Expression Omnibus dataset accession numbers (GSE) are indicated.
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Image Search Results


Monensin An up-regulates mitochondrially encoded genes. (A) Overview of the monensin A mediated alteration of gene expression on HACAT cells using bulk RNA-seq. (B) Pathway enrichment analysis arranging the top up-regulated pathways according to the adjusted p-value (left). The altered information on the top-ranking pathway was further excavated (right). (C) Heatmap shows monensin A-triggered actively expressed genes involved in the top-ranking pathway. Data are color-coded to reflect the relative expression level of mitochondrially encoded genes. All data are normalized to their matched control. (D) PCR-based validation of the mRNA expression of mitochondrial genes in HACAT cells treated with or without monensin A (125 nM) for 3 h. Data are represented as mean ± SD. Two-tailed Student's unpaired t -test (D). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Journal: Materials Today Bio

Article Title: Replenishment of mitochondrial Na + and H + by ionophores potentiates cutaneous wound healing in diabetes

doi: 10.1016/j.mtbio.2024.101056

Figure Lengend Snippet: Monensin An up-regulates mitochondrially encoded genes. (A) Overview of the monensin A mediated alteration of gene expression on HACAT cells using bulk RNA-seq. (B) Pathway enrichment analysis arranging the top up-regulated pathways according to the adjusted p-value (left). The altered information on the top-ranking pathway was further excavated (right). (C) Heatmap shows monensin A-triggered actively expressed genes involved in the top-ranking pathway. Data are color-coded to reflect the relative expression level of mitochondrially encoded genes. All data are normalized to their matched control. (D) PCR-based validation of the mRNA expression of mitochondrial genes in HACAT cells treated with or without monensin A (125 nM) for 3 h. Data are represented as mean ± SD. Two-tailed Student's unpaired t -test (D). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Article Snippet: RNA samples were submitted to LC Sciences (Hangzhou, China) for bulk RNA sequencing using the Illumina platform.

Techniques: Gene Expression, RNA Sequencing, Expressing, Control, Biomarker Discovery, Two Tailed Test

A Volcano plots of glucose metabolism-related genes that are induced in WT versus TRPM7KO cells. Genes with a fold-change ≥2 and P value of < 0.05 are shown. B RT-qPCR analysis validating the decreased expression of glucose catabolic genes from RNA-seq in TRPM7KO cells. C Immunofluorescent staining of TRPM7, SLC2A3 and DAPI in the xenograft tumor (scale bars, 100 μm). D Immunohistochemical staining for TRPM7, SLC2A1 and SLC2A3 in tumor tissue (scale bars, 100 μm). E , F Increased SLC2A3 in naltriben-induced (25 μM, 24 h) WT cells but not TRPM7KO cells. Quantification of protein was below. Two groups of samples were compared by unpaired two-tailed Student’s t -test. Multiple groups were compared by ANOVA.

Journal: Cell Death & Disease

Article Title: The TRPM7 channel reprograms cellular glycolysis to drive tumorigenesis and angiogenesis

doi: 10.1038/s41419-023-05701-7

Figure Lengend Snippet: A Volcano plots of glucose metabolism-related genes that are induced in WT versus TRPM7KO cells. Genes with a fold-change ≥2 and P value of < 0.05 are shown. B RT-qPCR analysis validating the decreased expression of glucose catabolic genes from RNA-seq in TRPM7KO cells. C Immunofluorescent staining of TRPM7, SLC2A3 and DAPI in the xenograft tumor (scale bars, 100 μm). D Immunohistochemical staining for TRPM7, SLC2A1 and SLC2A3 in tumor tissue (scale bars, 100 μm). E , F Increased SLC2A3 in naltriben-induced (25 μM, 24 h) WT cells but not TRPM7KO cells. Quantification of protein was below. Two groups of samples were compared by unpaired two-tailed Student’s t -test. Multiple groups were compared by ANOVA.

Article Snippet: The bulk RNA sequencing was performed by Metware Co., LTD.

Techniques: Quantitative RT-PCR, Expressing, RNA Sequencing, Staining, Immunohistochemical staining, Two Tailed Test

Summary of 15 studies identified investigating obesity as a variable related to human or animal model osteoarthritis using transcriptomics or metabolomics. Publications with associated Gene Expression Omnibus dataset accession numbers (GSE) are indicated.

Journal: Osteoarthritis and Cartilage Open

Article Title: Transcriptomics and metabolomics: Challenges of studying obesity in osteoarthritis

doi: 10.1016/j.ocarto.2024.100479

Figure Lengend Snippet: Summary of 15 studies identified investigating obesity as a variable related to human or animal model osteoarthritis using transcriptomics or metabolomics. Publications with associated Gene Expression Omnibus dataset accession numbers (GSE) are indicated.

Article Snippet: Schott et al. (2018) [ ] (GSE98287) , Mouse diet-induced obesity , • Low-fat diet-fed mice • high-fat diet-fed mice , Not Reported , Transcriptomics , Bulk RNA sequencing , Colon.

Techniques: Animal Model, Gene Expression, Comparison, RNA Sequencing, Mouse Assay, Microarray, Clinical Proteomics, Structural Proteomics, Control, Gas Chromatography