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Medicago microarray expression analyses
Microarray Expression Analyses, supplied by Medicago, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/expression+microarray+analyses/microarray+analysis/pmc04700669-112-18-6
Average 90 stars, based on 1 article reviews
microarray expression analyses - by Bioz Stars, 2026-10
90/100 stars

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Microarray:

Article Title: MYB transcription factors, active players in abiotic stress signaling
Article Snippet: The MYB family of proteins is a group of large, functionally diverse transcription factors, and widely present in all eukaryotes.. The MYB family of proteins in plants is characterized by the presence of a conserved MYB DNA-binding domain that typically contains one to four imperfect repeats.. In the past decades, extensive information has been accumulated on the roles of these proteins in regulating important processes in plants, including development, metabolism, and responses to environmental stresses.

Article Title: <i>Lathyrus sativus</i> Resistance Against the Existing and Emerging Pathogens <i>Erysiphe pisi</i> and <i>E. trifolii</i>: A Case of Commonalities or Total Discrepancy?
Article Snippet: Powdery mildew on Lathyrus sativus (grass pea) is commonly caused by Erysiphe pisi, the causal agent of pea powdery mildew.. E. trifolii could also pose an additional threat to grass pea, as it does to pea (Pisum sativum).. In order to understand the potential threat and the availability of resistance sources, the response to both pathogens was analyzed on a worldwide germplasm collection of 189 grass pea accessions.

Article Title: Transcriptome analysis of secondary cell wall development in Medicago truncatula
Article Snippet: .. To characterize the transcriptome profile during Medicago stem maturation, we collected stem samples for RNA extraction and subsequent microarray expression analyses. .. Five internodes, i.e. the aforementioned internodes 2, 3, 5, 7, and 9 from the Medicago primary stem, were collected in three biological replicates.

Article Title: Regulatory Patterns of a Large Family of Defensin-Like Genes Expressed in Nodules of Medicago truncatula
Article Snippet: .. Various techniques including mutant analysis, reverse genetics, suppressive subtractive hybridization, expressed sequence tag (EST) profiling, and macroarray and microarray gene expression analysis , have been used to identify plant genes involved in nodule development and function in the model legume Medicago truncatula, hereafter referred to as Medicago. ..

Article Title: The functional balance between the WUSCHEL-RELATED HOMEOBOX1 gene and the phytohormone auxin is a key factor for cell proliferation in Arabidopsis seedlings
Article Snippet: .. The microarray analysis using a mutant of the WOX1 homolog of Medicago truncatula ( stenofolia ) revealed the decreased expression of the PIN1 homolog and the increased expression of auxin-responsive SAUR homologous genes ( Tadege et al. 2011 ), which is consistent with our results. ..

Article Title: Unified Transcriptomic Signature of Arbuscular Mycorrhiza Colonization in Roots of Medicago truncatula by Integration of Machine Learning, Promoter Analysis, and Direct Merging Meta-Analysis
Article Snippet: The Microarray studies belonged to Medicago truncatula A17. .. The microarray experiment (Floss et al., ) was originally designed to compare gene expression in roots of Medicago truncatula A17 and Medicago truncatula mutant mtpt4-1 colonized with Gigaspora gigantea . ..

Article Title: The er2 gene resistance against powdery mildew infection is associated with enhanced antioxidative protection and defense gene expression
Article Snippet: 32 The present study was aimed at analyzing host responses of JI-2480 a resistant pea genotype 33 carrying a recessive gene er2 and Arkela commercial cultivar susceptible to powdery mildew 34 infection caused by Erysiphe pisi.. The cellular responses were analyzed through biochemical, 35 histo-chemical and defense gene expression in a time-course manner.. The reactive oxygen 36 species (ROS) scavenging enzymes showed higher activity in JI-2480 post-inoculation compared 37 to Arkel suggesting antioxidant enzymes role in suppressing pathogen-induced oxidative burst.

Article Title: Genome-wide analysis of the basic leucine zipper (bZIP) transcription factor gene family in six legume genomes
Article Snippet: Microarray expression values for Medicago and Lotus were downloaded from http://mtgea.noble.org/v3/ [ , ] and http://ljgea.noble.org/ v2/ [ ]. .. To identify candidate bZIP genes responsive to drought and/or salt stresses, microarray gene expression data in Medicago were downloaded from Zhang et al. [ ] and Li et al. [ ], respectively. ..

RNA Extraction:

Article Title: Transcriptome analysis of secondary cell wall development in Medicago truncatula
Article Snippet: .. To characterize the transcriptome profile during Medicago stem maturation, we collected stem samples for RNA extraction and subsequent microarray expression analyses. .. Five internodes, i.e. the aforementioned internodes 2, 3, 5, 7, and 9 from the Medicago primary stem, were collected in three biological replicates.

Expressing:

Article Title: Transcriptome analysis of secondary cell wall development in Medicago truncatula
Article Snippet: .. To characterize the transcriptome profile during Medicago stem maturation, we collected stem samples for RNA extraction and subsequent microarray expression analyses. .. Five internodes, i.e. the aforementioned internodes 2, 3, 5, 7, and 9 from the Medicago primary stem, were collected in three biological replicates.

Article Title: The functional balance between the WUSCHEL-RELATED HOMEOBOX1 gene and the phytohormone auxin is a key factor for cell proliferation in Arabidopsis seedlings
Article Snippet: .. The microarray analysis using a mutant of the WOX1 homolog of Medicago truncatula ( stenofolia ) revealed the decreased expression of the PIN1 homolog and the increased expression of auxin-responsive SAUR homologous genes ( Tadege et al. 2011 ), which is consistent with our results. ..

Mutagenesis:

Article Title: Regulatory Patterns of a Large Family of Defensin-Like Genes Expressed in Nodules of Medicago truncatula
Article Snippet: .. Various techniques including mutant analysis, reverse genetics, suppressive subtractive hybridization, expressed sequence tag (EST) profiling, and macroarray and microarray gene expression analysis , have been used to identify plant genes involved in nodule development and function in the model legume Medicago truncatula, hereafter referred to as Medicago. ..

Article Title: The functional balance between the WUSCHEL-RELATED HOMEOBOX1 gene and the phytohormone auxin is a key factor for cell proliferation in Arabidopsis seedlings
Article Snippet: .. The microarray analysis using a mutant of the WOX1 homolog of Medicago truncatula ( stenofolia ) revealed the decreased expression of the PIN1 homolog and the increased expression of auxin-responsive SAUR homologous genes ( Tadege et al. 2011 ), which is consistent with our results. ..

Article Title: Unified Transcriptomic Signature of Arbuscular Mycorrhiza Colonization in Roots of Medicago truncatula by Integration of Machine Learning, Promoter Analysis, and Direct Merging Meta-Analysis
Article Snippet: The Microarray studies belonged to Medicago truncatula A17. .. The microarray experiment (Floss et al., ) was originally designed to compare gene expression in roots of Medicago truncatula A17 and Medicago truncatula mutant mtpt4-1 colonized with Gigaspora gigantea . ..

Hybridization:

Article Title: Regulatory Patterns of a Large Family of Defensin-Like Genes Expressed in Nodules of Medicago truncatula
Article Snippet: .. Various techniques including mutant analysis, reverse genetics, suppressive subtractive hybridization, expressed sequence tag (EST) profiling, and macroarray and microarray gene expression analysis , have been used to identify plant genes involved in nodule development and function in the model legume Medicago truncatula, hereafter referred to as Medicago. ..

Sequencing:

Article Title: Regulatory Patterns of a Large Family of Defensin-Like Genes Expressed in Nodules of Medicago truncatula
Article Snippet: .. Various techniques including mutant analysis, reverse genetics, suppressive subtractive hybridization, expressed sequence tag (EST) profiling, and macroarray and microarray gene expression analysis , have been used to identify plant genes involved in nodule development and function in the model legume Medicago truncatula, hereafter referred to as Medicago. ..

Gene Expression:

Article Title: Regulatory Patterns of a Large Family of Defensin-Like Genes Expressed in Nodules of Medicago truncatula
Article Snippet: .. Various techniques including mutant analysis, reverse genetics, suppressive subtractive hybridization, expressed sequence tag (EST) profiling, and macroarray and microarray gene expression analysis , have been used to identify plant genes involved in nodule development and function in the model legume Medicago truncatula, hereafter referred to as Medicago. ..

Article Title: Unified Transcriptomic Signature of Arbuscular Mycorrhiza Colonization in Roots of Medicago truncatula by Integration of Machine Learning, Promoter Analysis, and Direct Merging Meta-Analysis
Article Snippet: The Microarray studies belonged to Medicago truncatula A17. .. The microarray experiment (Floss et al., ) was originally designed to compare gene expression in roots of Medicago truncatula A17 and Medicago truncatula mutant mtpt4-1 colonized with Gigaspora gigantea . ..

Article Title: Genome-wide analysis of the basic leucine zipper (bZIP) transcription factor gene family in six legume genomes
Article Snippet: Microarray expression values for Medicago and Lotus were downloaded from http://mtgea.noble.org/v3/ [ , ] and http://ljgea.noble.org/ v2/ [ ]. .. To identify candidate bZIP genes responsive to drought and/or salt stresses, microarray gene expression data in Medicago were downloaded from Zhang et al. [ ] and Li et al. [ ], respectively. ..



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Image Search Results


A hierarchical heatmap comparing global mRNA levels to RISC-IP mRNA levels in U-87 astrocytoma and primary astrocytes. MRNAs included in the heatmap had a fold change >1.4 and were significantly expressed (p<0.01).

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: A hierarchical heatmap comparing global mRNA levels to RISC-IP mRNA levels in U-87 astrocytoma and primary astrocytes. MRNAs included in the heatmap had a fold change >1.4 and were significantly expressed (p<0.01).

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques:

RISC-immunoprecipitated  mRNA  compared to global cellular  mRNA  in U-87 astrocytoma cells and primary  astrocytes  with a fold change > ±1.8 (p <0.01).

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: RISC-immunoprecipitated mRNA compared to global cellular mRNA in U-87 astrocytoma cells and primary astrocytes with a fold change > ±1.8 (p <0.01).

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques: RNA Binding Assay, Sequencing

( A ) MRNA microarray validation with qRT-PCR analysis in grouped RISC-IP U-87 astrocytoma and primary astrocytes samples. Grouped RISC-IP data were compared to the grouped global mRNA from U-87 astrocytoma and primary astrocytes samples. Eight mRNAs were selected from the grouped mRNA microarray dataset and examined by qRT-PCR. Fold change from the mRNA microarray are given by log2 values (left y-axis, light grey bars). Fold change from the qRT-PCR was determined using the 2 -ΔΔCt method and all mRNA expression values were normalized to the beta-actin endogenous control (right y-axis, dark grey bars). Error bars represent the standard deviation of the mean (SD). Importantly, the fold change (y-axis) cannot be directly compared between assays due to differences in calculation methods, but the general trend of up-regulation and down-regulation can be compared. ( B ) MRNAs in RISC compared to the global cellular milieu in U-87 astrocytoma cells. MRNA expression in U-87 astrocytoma cells were normalized to primary astrocytes mRNA expression. All mRNAs had a fold change >2.5 and were significantly expressed (p<0.01). Green and red arrows indicate decreased and increased levels respectively.

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: ( A ) MRNA microarray validation with qRT-PCR analysis in grouped RISC-IP U-87 astrocytoma and primary astrocytes samples. Grouped RISC-IP data were compared to the grouped global mRNA from U-87 astrocytoma and primary astrocytes samples. Eight mRNAs were selected from the grouped mRNA microarray dataset and examined by qRT-PCR. Fold change from the mRNA microarray are given by log2 values (left y-axis, light grey bars). Fold change from the qRT-PCR was determined using the 2 -ΔΔCt method and all mRNA expression values were normalized to the beta-actin endogenous control (right y-axis, dark grey bars). Error bars represent the standard deviation of the mean (SD). Importantly, the fold change (y-axis) cannot be directly compared between assays due to differences in calculation methods, but the general trend of up-regulation and down-regulation can be compared. ( B ) MRNAs in RISC compared to the global cellular milieu in U-87 astrocytoma cells. MRNA expression in U-87 astrocytoma cells were normalized to primary astrocytes mRNA expression. All mRNAs had a fold change >2.5 and were significantly expressed (p<0.01). Green and red arrows indicate decreased and increased levels respectively.

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques: Microarray, Quantitative RT-PCR, Expressing, Standard Deviation

RISC-immunoprecipitated  mRNA  in human U-87 astrocytoma cells compared to RISC-immunoprecipitated  mRNA  in primary human  astrocytes  with a fold change >±2.6 (p <0.01).

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: RISC-immunoprecipitated mRNA in human U-87 astrocytoma cells compared to RISC-immunoprecipitated mRNA in primary human astrocytes with a fold change >±2.6 (p <0.01).

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques:

Bar charts display the relative number (-log(p-value)) of mRNAs with a fold change >2.5 and were considered significant (p<0.01). RISC-IP mRNA were indicated with dark blue bars and the global mRNA were indicated with light blue bars. The threshold (yellow lines) were set at p<0.01 and were calculated using Fischer's exact p-value test using IPA software.

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: Bar charts display the relative number (-log(p-value)) of mRNAs with a fold change >2.5 and were considered significant (p<0.01). RISC-IP mRNA were indicated with dark blue bars and the global mRNA were indicated with light blue bars. The threshold (yellow lines) were set at p<0.01 and were calculated using Fischer's exact p-value test using IPA software.

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques: Software

Bar charts display the relative number (-log(p-value)) of mRNAs with a fold change >2.5 and were considered significant (p<0.01). RISC-IP mRNA were indicated with dark blue bars and the global mRNA were indicated with light blue bars. The threshold (yellow lines) were set at p<0.01 and were calculated using Fischer's exact p-value test using IPA software.

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: Bar charts display the relative number (-log(p-value)) of mRNAs with a fold change >2.5 and were considered significant (p<0.01). RISC-IP mRNA were indicated with dark blue bars and the global mRNA were indicated with light blue bars. The threshold (yellow lines) were set at p<0.01 and were calculated using Fischer's exact p-value test using IPA software.

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques: Software

Specific  messenger RNA  fold change linked to the increased levels of miR-34a in U-87  astrocytoma  RISC.

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: Specific messenger RNA fold change linked to the increased levels of miR-34a in U-87 astrocytoma RISC.

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques: Permeability, Migration, Expressing, Binding Assay, Isolation

Specific  messenger RNA  fold change linked to increased levels of miR-195 in U-87  astrocytoma  RISC.

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: Specific messenger RNA fold change linked to increased levels of miR-195 in U-87 astrocytoma RISC.

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques: Transduction

Target recognition by the miR-142-3p/−1 and miR-K10a/+1 5′-isomiRs. ( A , B ) Overlap of binding sites for the miR-142-3p and miR-K10a 5′-isomiRs identified in Ago2-PAR-CLIP data from ( A ) BC-1 and ( B ) BC-3 PEL cell lines . ( C ) Minimum base-pairing required for the miR-142-3p ( upper panel) and miR-K10a ( lower panel) 5′-isomiRs to share canonical binding sites. ( D ) Principal component analysis of microarray data of HEK293T cells transfected with individual 5′-isomiRs. ( E – I ) Sylamer enrichment landscape plots for 7mer 3′-UTR matches to miR-142-3p and miR-K10a 5′-isomiRs using microarray data from 293T cells transfected with individual miRNA mimics ( E – H , this study) or from published microarray data from miR-142 −/− mouse megakaryocytes (GEO data set GSE52141, ). The x -axis represents the ranked gene lists. miR-155 sites (pink and black lines) served as negative controls in addition to all random 7mers (gray). Enrichment plots for hexamer motifs are shown in Supplemental Figure S2.

Journal: RNA

Article Title: Divergent target recognition by coexpressed 5′-isomiRs of miR-142-3p and selective viral mimicry

doi: 10.1261/rna.048876.114

Figure Lengend Snippet: Target recognition by the miR-142-3p/−1 and miR-K10a/+1 5′-isomiRs. ( A , B ) Overlap of binding sites for the miR-142-3p and miR-K10a 5′-isomiRs identified in Ago2-PAR-CLIP data from ( A ) BC-1 and ( B ) BC-3 PEL cell lines . ( C ) Minimum base-pairing required for the miR-142-3p ( upper panel) and miR-K10a ( lower panel) 5′-isomiRs to share canonical binding sites. ( D ) Principal component analysis of microarray data of HEK293T cells transfected with individual 5′-isomiRs. ( E – I ) Sylamer enrichment landscape plots for 7mer 3′-UTR matches to miR-142-3p and miR-K10a 5′-isomiRs using microarray data from 293T cells transfected with individual miRNA mimics ( E – H , this study) or from published microarray data from miR-142 −/− mouse megakaryocytes (GEO data set GSE52141, ). The x -axis represents the ranked gene lists. miR-155 sites (pink and black lines) served as negative controls in addition to all random 7mers (gray). Enrichment plots for hexamer motifs are shown in Supplemental Figure S2.

Article Snippet: For an unbiased comparison of the regulatory potential of these isomiRs, we therefore performed Illumina microarray gene expression analyses of HEK293T cells transfected with mimics of the individual isomiRs.

Techniques: Binding Assay, Microarray, Transfection