mrna gene levels Search Results


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  • 99
    Thermo Fisher mrna levels
    CDK4and CDK6 gene and protein expression levels in physiological placental villous explants treated with culture media conditioned by normal or PE-PDMSC. (A) CDK4 <t>mRNA</t> (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time <t>PCR</t> and Western Blot analysis. B) CDK6 mRNA (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time PCR and Western Blot analysis. Statistical significance (*) has been considered as p
    Mrna Levels, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 14181 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher gene chip mrna levels
    CDK4and CDK6 gene and protein expression levels in physiological placental villous explants treated with culture media conditioned by normal or PE-PDMSC. (A) CDK4 <t>mRNA</t> (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time <t>PCR</t> and Western Blot analysis. B) CDK6 mRNA (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time PCR and Western Blot analysis. Statistical significance (*) has been considered as p
    Gene Chip Mrna Levels, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 93/100, based on 21 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Illumina Inc mrna seq prep kit gene expression levels
    Differentially expressed genes and KEGG pathways in NTD embryos. a Scatter plot of differentially expressed mRNAs between the NTDs and normal rat embryos. Red dots indicate upregulated mRNAs, blue dots indicate equally expressed mRNAs, and green dots indicate downregulated mRNAs. The cut-off criteria were FDR ≤ 0.001 and |log2Ratio|≥ 1. Ratio = NTD <t>embryos-RPKM/normal</t> embryos-RPKM. b KEGG pathway analysis of differentially expressed genes (DEGs). The signaling pathways included the focal adhesion pathway, regulation of actin cytoskeleton pathway, tight junction pathway, ECM-receptor interaction pathway, and cell adhesion molecular pathway. The pathways of interest are indicated with circles. The red circles indicate the pathways with more upregulated genes. The green circle indicates the pathway with more downregulated genes. c Relative <t>mRNA</t> expression of the differentially expressed genes with |log2 fold change| > 0.5, fold change = NTD embryos /normal embryos. (* P
    Mrna Seq Prep Kit Gene Expression Levels, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 84/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Illumina Inc gene expression arrays mrna expression levels
    Expression of <t>Nox/Duox</t> isoforms in benign and malignant prostate cell lines. RNA from benign (EP156T and RWPE1) and malignant (DU145, LNCaP, PC‐3, and VCaP) prostate epithelial cell lines was prepared and relative expression levels of the indicated genes determined by qPCR. Values represent mean fold change (±SEM) in gene expression from triplicates in three independent experiments relative to EP156T cells and normalized against the housekeeping gene B2M. <t>mRNA</t> levels of PSA are shown as a positive control, as DU145 cells are considered to lack PSA expression 33 , a threshold cut‐off score was arbitrarily set at a value of 10, below which the indicated genes were not considered to be expressed.
    Gene Expression Arrays Mrna Expression Levels, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher gene expression profiling mrna expression levels
    Expression of <t>Nox/Duox</t> isoforms in benign and malignant prostate cell lines. RNA from benign (EP156T and RWPE1) and malignant (DU145, LNCaP, PC‐3, and VCaP) prostate epithelial cell lines was prepared and relative expression levels of the indicated genes determined by qPCR. Values represent mean fold change (±SEM) in gene expression from triplicates in three independent experiments relative to EP156T cells and normalized against the housekeeping gene B2M. <t>mRNA</t> levels of PSA are shown as a positive control, as DU145 cells are considered to lack PSA expression 33 , a threshold cut‐off score was arbitrarily set at a value of 10, below which the indicated genes were not considered to be expressed.
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    Thermo Fisher mouse gapd gapdh endogenous control
    Expression of <t>Nox/Duox</t> isoforms in benign and malignant prostate cell lines. RNA from benign (EP156T and RWPE1) and malignant (DU145, LNCaP, PC‐3, and VCaP) prostate epithelial cell lines was prepared and relative expression levels of the indicated genes determined by qPCR. Values represent mean fold change (±SEM) in gene expression from triplicates in three independent experiments relative to EP156T cells and normalized against the housekeeping gene B2M. <t>mRNA</t> levels of PSA are shown as a positive control, as DU145 cells are considered to lack PSA expression 33 , a threshold cut‐off score was arbitrarily set at a value of 10, below which the indicated genes were not considered to be expressed.
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    Thermo Fisher gapdh housekeeping gene mrna levels
    Expression of <t>Nox/Duox</t> isoforms in benign and malignant prostate cell lines. RNA from benign (EP156T and RWPE1) and malignant (DU145, LNCaP, PC‐3, and VCaP) prostate epithelial cell lines was prepared and relative expression levels of the indicated genes determined by qPCR. Values represent mean fold change (±SEM) in gene expression from triplicates in three independent experiments relative to EP156T cells and normalized against the housekeeping gene B2M. <t>mRNA</t> levels of PSA are shown as a positive control, as DU145 cells are considered to lack PSA expression 33 , a threshold cut‐off score was arbitrarily set at a value of 10, below which the indicated genes were not considered to be expressed.
    Gapdh Housekeeping Gene Mrna Levels, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies level 3 agilent 244k custom gene expression g4502a 07 platform mrna microarray data
    Expression of <t>Nox/Duox</t> isoforms in benign and malignant prostate cell lines. RNA from benign (EP156T and RWPE1) and malignant (DU145, LNCaP, PC‐3, and VCaP) prostate epithelial cell lines was prepared and relative expression levels of the indicated genes determined by qPCR. Values represent mean fold change (±SEM) in gene expression from triplicates in three independent experiments relative to EP156T cells and normalized against the housekeeping gene B2M. <t>mRNA</t> levels of PSA are shown as a positive control, as DU145 cells are considered to lack PSA expression 33 , a threshold cut‐off score was arbitrarily set at a value of 10, below which the indicated genes were not considered to be expressed.
    Level 3 Agilent 244k Custom Gene Expression G4502a 07 Platform Mrna Microarray Data, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 86/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies level 3 mrna gene expression data
    Expression of <t>Nox/Duox</t> isoforms in benign and malignant prostate cell lines. RNA from benign (EP156T and RWPE1) and malignant (DU145, LNCaP, PC‐3, and VCaP) prostate epithelial cell lines was prepared and relative expression levels of the indicated genes determined by qPCR. Values represent mean fold change (±SEM) in gene expression from triplicates in three independent experiments relative to EP156T cells and normalized against the housekeeping gene B2M. <t>mRNA</t> levels of PSA are shown as a positive control, as DU145 cells are considered to lack PSA expression 33 , a threshold cut‐off score was arbitrarily set at a value of 10, below which the indicated genes were not considered to be expressed.
    Level 3 Mrna Gene Expression Data, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Illumina Inc level 3 illumina hiseq rnaseqv2 rsem gene level normalized mrna expression data
    Expression of <t>Nox/Duox</t> isoforms in benign and malignant prostate cell lines. RNA from benign (EP156T and RWPE1) and malignant (DU145, LNCaP, PC‐3, and VCaP) prostate epithelial cell lines was prepared and relative expression levels of the indicated genes determined by qPCR. Values represent mean fold change (±SEM) in gene expression from triplicates in three independent experiments relative to EP156T cells and normalized against the housekeeping gene B2M. <t>mRNA</t> levels of PSA are shown as a positive control, as DU145 cells are considered to lack PSA expression 33 , a threshold cut‐off score was arbitrarily set at a value of 10, below which the indicated genes were not considered to be expressed.
    Level 3 Illumina Hiseq Rnaseqv2 Rsem Gene Level Normalized Mrna Expression Data, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 91/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies level 3 normalized agilent 244k gene expression mrna array data
    Expression of <t>Nox/Duox</t> isoforms in benign and malignant prostate cell lines. RNA from benign (EP156T and RWPE1) and malignant (DU145, LNCaP, PC‐3, and VCaP) prostate epithelial cell lines was prepared and relative expression levels of the indicated genes determined by qPCR. Values represent mean fold change (±SEM) in gene expression from triplicates in three independent experiments relative to EP156T cells and normalized against the housekeeping gene B2M. <t>mRNA</t> levels of PSA are shown as a positive control, as DU145 cells are considered to lack PSA expression 33 , a threshold cut‐off score was arbitrarily set at a value of 10, below which the indicated genes were not considered to be expressed.
    Level 3 Normalized Agilent 244k Gene Expression Mrna Array Data, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    88
    Thermo Fisher refseq gene mrna level
    Expression of <t>Nox/Duox</t> isoforms in benign and malignant prostate cell lines. RNA from benign (EP156T and RWPE1) and malignant (DU145, LNCaP, PC‐3, and VCaP) prostate epithelial cell lines was prepared and relative expression levels of the indicated genes determined by qPCR. Values represent mean fold change (±SEM) in gene expression from triplicates in three independent experiments relative to EP156T cells and normalized against the housekeeping gene B2M. <t>mRNA</t> levels of PSA are shown as a positive control, as DU145 cells are considered to lack PSA expression 33 , a threshold cut‐off score was arbitrarily set at a value of 10, below which the indicated genes were not considered to be expressed.
    Refseq Gene Mrna Level, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 88/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Thermo Fisher target mrna levels taqman gene expression assays
    Expression of <t>Nox/Duox</t> isoforms in benign and malignant prostate cell lines. RNA from benign (EP156T and RWPE1) and malignant (DU145, LNCaP, PC‐3, and VCaP) prostate epithelial cell lines was prepared and relative expression levels of the indicated genes determined by qPCR. Values represent mean fold change (±SEM) in gene expression from triplicates in three independent experiments relative to EP156T cells and normalized against the housekeeping gene B2M. <t>mRNA</t> levels of PSA are shown as a positive control, as DU145 cells are considered to lack PSA expression 33 , a threshold cut‐off score was arbitrarily set at a value of 10, below which the indicated genes were not considered to be expressed.
    Target Mrna Levels Taqman Gene Expression Assays, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    CDK4and CDK6 gene and protein expression levels in physiological placental villous explants treated with culture media conditioned by normal or PE-PDMSC. (A) CDK4 mRNA (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time PCR and Western Blot analysis. B) CDK6 mRNA (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time PCR and Western Blot analysis. Statistical significance (*) has been considered as p

    Journal: Cell Cycle

    Article Title: Altered expression of G1/S phase cell cycle regulators in placental mesenchymal stromal cells derived from preeclamptic pregnancies with fetal-placental compromise

    doi: 10.1080/15384101.2016.1261766

    Figure Lengend Snippet: CDK4and CDK6 gene and protein expression levels in physiological placental villous explants treated with culture media conditioned by normal or PE-PDMSC. (A) CDK4 mRNA (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time PCR and Western Blot analysis. B) CDK6 mRNA (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time PCR and Western Blot analysis. Statistical significance (*) has been considered as p

    Article Snippet: Gene expressions levels of JunB, CyclinD1, p16INK4A , p18INK4C , CDK4, CDK6 and PARP1 were determined by Real Time PCR using specific TaqMan primers and probes (Life Technologies, Cat. No 4331182). mRNA levels were normalized using endogenous 18s as internal reference (Life Technologies, Cat. No 4333760F).

    Techniques: Expressing, Real-time Polymerase Chain Reaction, Western Blot

    JunB and Cyclin D1 gene and protein expression levels in physiological placental villous explants treated with culture media conditioned by normal or PE-PDMSC. (A)JunB mRNA (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time PCR and Western Blot analysis. B) Cyclin D1 mRNA (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time PCR and Western Blot analysis. Statistical significance (*) has been considered as p

    Journal: Cell Cycle

    Article Title: Altered expression of G1/S phase cell cycle regulators in placental mesenchymal stromal cells derived from preeclamptic pregnancies with fetal-placental compromise

    doi: 10.1080/15384101.2016.1261766

    Figure Lengend Snippet: JunB and Cyclin D1 gene and protein expression levels in physiological placental villous explants treated with culture media conditioned by normal or PE-PDMSC. (A)JunB mRNA (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time PCR and Western Blot analysis. B) Cyclin D1 mRNA (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time PCR and Western Blot analysis. Statistical significance (*) has been considered as p

    Article Snippet: Gene expressions levels of JunB, CyclinD1, p16INK4A , p18INK4C , CDK4, CDK6 and PARP1 were determined by Real Time PCR using specific TaqMan primers and probes (Life Technologies, Cat. No 4331182). mRNA levels were normalized using endogenous 18s as internal reference (Life Technologies, Cat. No 4333760F).

    Techniques: Expressing, Real-time Polymerase Chain Reaction, Western Blot

    P16 INK4A and p18 INK4C gene and protein expression levels in physiological placental villous explants treated with culture media conditioned by normal or PE-PDMSC. (A) P16 INK4A mRNA (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time PCR and Western Blot analysis. B) and p18 INK4C mRNA (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time PCR and Western Blot analysis. Statistical significance (*) has been considered as p

    Journal: Cell Cycle

    Article Title: Altered expression of G1/S phase cell cycle regulators in placental mesenchymal stromal cells derived from preeclamptic pregnancies with fetal-placental compromise

    doi: 10.1080/15384101.2016.1261766

    Figure Lengend Snippet: P16 INK4A and p18 INK4C gene and protein expression levels in physiological placental villous explants treated with culture media conditioned by normal or PE-PDMSC. (A) P16 INK4A mRNA (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time PCR and Western Blot analysis. B) and p18 INK4C mRNA (left panels) and protein (right panels) expression levels in physiological villous explants treated with unconditioned media (CTRL, n = 16 explants) or media conditioned by normal (N CM, n = 16 explants) and preeclamptic (PE CM, n = 16 explants) PDMSCs as assessed by Real Time PCR and Western Blot analysis. Statistical significance (*) has been considered as p

    Article Snippet: Gene expressions levels of JunB, CyclinD1, p16INK4A , p18INK4C , CDK4, CDK6 and PARP1 were determined by Real Time PCR using specific TaqMan primers and probes (Life Technologies, Cat. No 4331182). mRNA levels were normalized using endogenous 18s as internal reference (Life Technologies, Cat. No 4333760F).

    Techniques: Expressing, Real-time Polymerase Chain Reaction, Western Blot

    Differentially expressed genes and KEGG pathways in NTD embryos. a Scatter plot of differentially expressed mRNAs between the NTDs and normal rat embryos. Red dots indicate upregulated mRNAs, blue dots indicate equally expressed mRNAs, and green dots indicate downregulated mRNAs. The cut-off criteria were FDR ≤ 0.001 and |log2Ratio|≥ 1. Ratio = NTD embryos-RPKM/normal embryos-RPKM. b KEGG pathway analysis of differentially expressed genes (DEGs). The signaling pathways included the focal adhesion pathway, regulation of actin cytoskeleton pathway, tight junction pathway, ECM-receptor interaction pathway, and cell adhesion molecular pathway. The pathways of interest are indicated with circles. The red circles indicate the pathways with more upregulated genes. The green circle indicates the pathway with more downregulated genes. c Relative mRNA expression of the differentially expressed genes with |log2 fold change| > 0.5, fold change = NTD embryos /normal embryos. (* P

    Journal: Cell Death & Disease

    Article Title: Transamniotic mesenchymal stem cell therapy for neural tube defects preserves neural function through lesion-specific engraftment and regeneration

    doi: 10.1038/s41419-020-2734-3

    Figure Lengend Snippet: Differentially expressed genes and KEGG pathways in NTD embryos. a Scatter plot of differentially expressed mRNAs between the NTDs and normal rat embryos. Red dots indicate upregulated mRNAs, blue dots indicate equally expressed mRNAs, and green dots indicate downregulated mRNAs. The cut-off criteria were FDR ≤ 0.001 and |log2Ratio|≥ 1. Ratio = NTD embryos-RPKM/normal embryos-RPKM. b KEGG pathway analysis of differentially expressed genes (DEGs). The signaling pathways included the focal adhesion pathway, regulation of actin cytoskeleton pathway, tight junction pathway, ECM-receptor interaction pathway, and cell adhesion molecular pathway. The pathways of interest are indicated with circles. The red circles indicate the pathways with more upregulated genes. The green circle indicates the pathway with more downregulated genes. c Relative mRNA expression of the differentially expressed genes with |log2 fold change| > 0.5, fold change = NTD embryos /normal embryos. (* P

    Article Snippet: RNA sequencing libraries were constructed using the Illumina mRNA-seq Prep Kit Gene expression levels were calculated using the RPKM (Reads Per kb per Million reads) method.

    Techniques: Expressing

    Expression of Nox/Duox isoforms in benign and malignant prostate cell lines. RNA from benign (EP156T and RWPE1) and malignant (DU145, LNCaP, PC‐3, and VCaP) prostate epithelial cell lines was prepared and relative expression levels of the indicated genes determined by qPCR. Values represent mean fold change (±SEM) in gene expression from triplicates in three independent experiments relative to EP156T cells and normalized against the housekeeping gene B2M. mRNA levels of PSA are shown as a positive control, as DU145 cells are considered to lack PSA expression 33 , a threshold cut‐off score was arbitrarily set at a value of 10, below which the indicated genes were not considered to be expressed.

    Journal: Molecular Carcinogenesis

    Article Title: ROS signaling by NADPH oxidase 5 modulates the proliferation and survival of prostate carcinoma cells

    doi: 10.1002/mc.22255

    Figure Lengend Snippet: Expression of Nox/Duox isoforms in benign and malignant prostate cell lines. RNA from benign (EP156T and RWPE1) and malignant (DU145, LNCaP, PC‐3, and VCaP) prostate epithelial cell lines was prepared and relative expression levels of the indicated genes determined by qPCR. Values represent mean fold change (±SEM) in gene expression from triplicates in three independent experiments relative to EP156T cells and normalized against the housekeeping gene B2M. mRNA levels of PSA are shown as a positive control, as DU145 cells are considered to lack PSA expression 33 , a threshold cut‐off score was arbitrarily set at a value of 10, below which the indicated genes were not considered to be expressed.

    Article Snippet: Illumina Gene Expression Arrays mRNA expression levels of Nox/Duox isoforms in benign and malignant tissue of radical prostatectomy specimens were extracted from a global gene array expression analysis performed with macro‐dissected tissue samples using Illumina Human Sentrix‐12 BeadChip arrays (Illumina, San Diego, CA) as described .

    Techniques: Expressing, Real-time Polymerase Chain Reaction, Positive Control