K562 single cell RNA-seq study
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View SamplesMicroRNA down-regulation and noise regulation
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View SamplesThis project aims to discover canonical gene fusion events from mixed human tissue cell lines.
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View SamplesThe SCH9 null strain has smaller cell size, grows at a slower rate and survives three times longer than wide-type yeast.
Comparative analyses of time-course gene expression profiles of the long-lived sch9Delta mutant.
Age
View SamplesThe three yeast mutants sch9, ras2, tor1 show extended chronological life span up to three folds.
Significant and systematic expression differentiation in long-lived yeast strains.
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View SamplesWe examined skin biopsies from a diverse cohort of 23 SSc patients (including lesional forearm and non-lesional back samples) by RNA-seq. Metagenomic filtering and annotation was performed using the Integrated Metagenomic Sequencing Analysis (IMSA). Associations between microbiome composition and gene expression were analyzed using single-sample gene set enrichment analysis (ssGSEA).
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Sex, Age, Specimen part
View SamplesEstrogens have been shown to elicit anti-cancer effects against estrogen receptor alpha (ER)-positive breast cancer. We sought to determine the underlying mechanism of therapeutic response. Response to estrogen treatment was assessed in ER+ breast cancer models of anti-estrogen resistant disease: WHIM16 patient-derived xenografts, C7-2-HI and C4-HI murine mammary adenocarcinomas, and long-term estrogen-deprived MCF-7 cells.
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Sex, Age, Specimen part
View SamplesMicroenvironmental secreted factor screening revealed cytokines that modulate drug sensitivity in ER+ breast cancer cells. BMP4 was a top hit that is not normally expressed in ER+ breast cancer, and was found to enhance efficacy of anti-estrogens and CDK4/6i in anti-estrogen-sensitive and -resistant ER+ breast cancer cells. The anti-cancer effects of BMP4 were mediated by ALK3 and canonical BMP pathway signaling, leading to downstream p21 induction and cell cycle arrest. The clinical relevance of this phenotype was confirmed in analyses of 3 cohorts of patients with ER+ breast cancer, highlighting BMP4 pathway activation as a potential therapeutic opportunity in ER+ breast cancer.
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Sex, Age, Specimen part
View SamplesIn the semi-dominant mouse model, Nan (neonatal anemia), heterozygotes suffer hemolytic anemia at birth and throughout life due to a missense mutation (E339D) in transcription factor KLF1 (Krüppel-like factor 1; formerly EKLF, erythroid Krüppel-like factor) Here, we focus on erythropoiesis in the adult spleen. We performed RNAseq in flow-sorted spleen erythroid precursors from adult Nan and WT littermates rendered anemic by phlebotomy as a means to identify global transcriptome changes specific to the Nan KLF1 defect, as opposed to those characterizing anemia generally. We show that (1) expression variation in adult Nan spleen is driven primarily by cell maturation, (2) genotype influences on gene expression are most prominent in late stages of erythroid differentiation when Klf1 expression is highest, (3) Nan-KLF1 produces tissue-specific differential gene expression, and (4) suboptimal stress and basal erythropoiesis with increased reactive oxygen species (ROS) contribute to anemia in adult Nan mice.
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Sex, Specimen part, Cell line
View Samples46BR.1G1 cell line is impaired in DNA ligase 1 (LIG1) activity resulting in an increased level of endogenous single (SSBs) and double stranded DNA breaks (DSBs). 46BR.1G1 fibroblastoid cells represent a suitable model system to investigate how cells cope with low levels of chronic DNA damage, a condition frequently encountered in tumors. Transcriptional alterations in 46BR.1G1 cells were determined by RNAseq by comparison with 7A3, a cell line in which the defect was rescued by stable expression of ectopic wild-type Lig1. The identification of genes differentially expressed in 46BR.1G1 cells would contribute to the elucidation of DNA damage response (DDR) mechanisms.
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