Transcriptome analysis of cold-treated leaves (unifoliates) of soybean seedlings were performed. RNAseq analysis was performed using two lanes on a Illumina HiSeq2000 and sequenced on a 100bp, paired-end run. Overall design: Two-weeks old soybean (c.v. 'Williams 82') seedlings were cold-treated (4 °C) starting at 4 h after the lights turned on (Zeitgeber Time, ZT4 h, 18 hours light/6 hours dark) and maintaining 4 °C continuously with the light cycle till harvest time (0, 1, and 24 hours). All treatment samples were performed in triplicate (with n=6 plants per replication).
The Ethylene Signaling Pathway Negatively Impacts CBF/DREB-Regulated Cold Response in Soybean (<i>Glycine max</i>).
Specimen part, Subject
View SamplesThe lung host immune responses following M.tuberculosis infection in the mouse model of tuberculosis were assayed by studying the gene expression profiles at day 0, day 12, 15 and 21 post infection
Profiling early lung immune responses in the mouse model of tuberculosis.
Specimen part, Time
View SamplesTo understand the role of LSD1 in B cell differentiation, mice with B cell conditional deletion of LSD1 were intravenously inoculated with LPS. After 3 days, B220+GL7-CD138- naïve B cells and CD138+ plasmablasts were FACS-sorted from the spleens and RNA-seq was performed to identify LSD1-target regulated genes. Overall design: RNA-seq on control or LSD1-deficient murine naïve B cells or plasmablasts.
The Histone Demethylase LSD1 Regulates B Cell Proliferation and Plasmablast Differentiation.
Sex, Specimen part, Cell line, Subject
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Integrated analysis of global mRNA and protein expression data in HEK293 cells overexpressing PRL-1.
Cell line
View SamplesThe multifunctional protein tyrosine phosphatase PRL-1 (Gene Symbol: PTP4A1) has been identified as an important oncogene with roles in promoting cell proliferation, survival, migration, invasion, and metastasis. However, little is currently known about the signaling pathways through which it mediates its effects.
Integrated analysis of global mRNA and protein expression data in HEK293 cells overexpressing PRL-1.
Cell line
View SamplesTo understand the role of EZH2 in Plasmablast function EZH2 was inducibly deleted using tamoxifen and B cells stimulated to differentiate with LPS in vivo. After 3 days, CD138+ cells were enriched from the spleens and RNA-seq was performed to identify the genes targeted by EZH2 for repression. Overall design: RNAseq on control or EZH2-deficient murine plasmablasts.
EZH2 Represses the B Cell Transcriptional Program and Regulates Antibody-Secreting Cell Metabolism and Antibody Production.
Sex, Specimen part, Cell line, Treatment, Subject
View SamplesCerebral malaria (CM) is a severe complication of Plasmodium falciparum infection, predominantly experienced by children and non-immune adults, which results in great mortality and long-term sequelae. Recent reports based on histology of post-mortem brain tissue suggest that CM may be the common end point for a range of syndromes. Here, we have analysed the gene expression profiles in brain tissue taken from experimental CM (ECM)-susceptible, Plasmodium berghei ANKA (PbA)-infected C57BL/6 (B6) and CBA/CaH (CBA) mice with ECM. Gene expression profiles were largely heterogeneous between the two ECM-susceptible strains. These results, combined with experimental data, support the existence of distinct pathogenic pathways in CM.
Common strategies to prevent and modulate experimental cerebral malaria in mouse strains with different susceptibilities.
Sex, Specimen part
View SamplesThis SuperSeries is composed of the SubSeries listed below.
DOCK8 is critical for the survival and function of NKT cells.
Sex, Specimen part
View SamplesAnalysis of DOCK8 deficient animals revealed a novel marker of NKT cell development, the integrin CD103. The role of CD103 was further investigated by RNA microarray comparing CD103 negative versus positive NKT cells.
DOCK8 is critical for the survival and function of NKT cells.
Sex, Specimen part
View SamplesAnalysis of DOCK8 deficient animals revealed a key role for this protein the survival and maintenance of natural killer T cells. This work lead to the identification of genes regulated by the guanine exchange factor, DOCK8.
DOCK8 is critical for the survival and function of NKT cells.
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