|
Protein kinase A-mediated phosphorylation regulates STAT3 activation and oncogenic EZH2 activity |
748.48 |
|
Statins modulate endothelial transcriptional profile by inhibiting EZH2 |
167.22 |
|
The transcriptome effect of overexpressing EZH2 in MCF7 |
94.01 |
|
Effect of 48h treatment with 100nM GSK2879552 on T-ALL cell lines LOUCY and PEER |
70.08 |
|
Gene expression analysis of human CD8+ T cells treated with a DOT1L inhibitor |
48.56 |
|
Mitotic stress is an integral part of the oncogene-induced senescence program that promotes multinucleation and cell cycle arrest |
46.98 |
|
Effect of Hotair overexpression in human breast cancer cell lines |
45.72 |
|
Tamoxifen Resistance in Breast Cancer is Regulated by the EZH2-ERa-GREB1 Transcriptional Axis |
45.48 |
|
Comparative Transcriptomics of Triple Negative Breast Cancer Stem Cells and Differentiated Tumor Cells Identifies Teneurin-4 as a Potential Therapeutic Target |
44.4 |
|
The role of PHF19 in promoting H3K27me3 deposition in multiple myeloma (RNA-Seq) |
43.64 |
|
The role of PHF19 in promoting H3K27me3 deposition in multiple myeloma |
43.64 |
|
Transcriptional profiles of normal human mature B cells |
41.97 |
|
RNA-Seq analysis RPE1 cells following exposure to Nutlin-3 to identify target genes of p53 [tpo12] |
40.46 |
|
H3B-8800, a novel oral splicing modulator, induces lethality in spliceosome mutant cancers [Nalm-6] |
40.38 |
|
Benzotriazoles reactivate latent HIV-1 through inactivation of STAT5 SUMOylation (RNA-Seq) |
33.82 |
|
Benzotriazoles reactivate latent HIV-1 through inactivation of STAT5 SUMOylation |
33.82 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of HIV-1 Latency in Central Memory T Cells |
33.06 |
|
Homolog-selective degradation as a strategy to probe the function of CDK6 in AML |
31.34 |
|
Expression profiles of restoration of BAP1 in a BAP1 deficient cell line |
30.69 |
|
Transcriptome analysis of BAP1 knockout and restoration |
30.69 |
|
In vitro differentiation of human low threshold mechanoreceptive (LTMR) neurons from embryonic stem cells |
29.16 |
|
Inhibition of SF3B1 by molecules targeting the spliceosome in Rh18 cells |
27.72 |
|
Modeling human brain evolution using induced pluripotent stem cells: comparative analysis of neuronal development in humans and chimpanzees |
27.71 |
|
Hit-and-run' programing of CAR-T cells using mRNA nanocarriers |
27.44 |
|
Recovery and analysis of nascent RNA |
26.75 |
|
The oncogenic BRD4-NUT chromatin regulator drives aberrant transcription within large topological domains |
26.75 |
|
LINE-1 elements are derepressed in senescent cells and elicit a chronic Type-I Interferon response |
26.44 |
|
Differentially Expressed Genes upon Knockdown of ZRANB1 or EZH2 in LM2 Cells |
24.97 |
|
Transcript abundance in A-T-derived iPSC: Comparing isogenic cells to unrelated individual |
24.93 |
|
The effect of engineered del(7q) on induced pluripotent stem cells (iPSCs) derived from patients with Shwachman Diamond Syndrome (SDS). |
24.65 |
|
Low cytosolic folate cycling is a hallmark of U251 glioblastoma cells reprogramming towards pluripotency |
24.56 |
|
Low cytosolic folate cycling is a hallmark of U251 glioblastoma cells reprogramming towards pluripotency [RNA-seq] |
24.56 |
|
Selective suppression of endothelial cytokine production by progesterone receptor [RNA-seq] |
24.35 |
|
Selective suppression of endothelial cytokine production by progesterone receptor |
24.35 |
|
PTEN suppresses neoplastic transformation of human neural stem cells by transcriptional repression of Pax7 |
23.46 |
|
The RNA helicase DDX6 regulates self-renewal and differentiation of human and mouse stem cells [RNA-Seq] |
23.23 |
|
Genome wide expression change by RNF168 knocking down in MCF-7 cells |
22.61 |
|
Analysis of Th17 gene signature in the presence of CD28 costimulation in human CD4 naïve T cells |
22.41 |
|
MenSCs inhibit HCC growth through oncogenic pathway suppression via regulating 5-hmC in enhancer elements [RNA-seq] |
21.54 |
|
MenSCs inhibit HCC growth through oncogenic pathway suppression via regulating 5-hmC in enhancer elements |
21.54 |
|
Knockdown of ADNP in HCT116 colon cancer cells |
21.16 |
|
A common cell state in Triple Negative Breast Cancers represents a druggable vulnerability |
21.06 |
|
RNA-Seq to assess the transcriptional effects of G quadruplex stabilization by the G4 ligand PhenDC3 in HT-1080 cells |
20.94 |
|
RNA-seq of resting and activated CD4+ T cells +-JQ1 |
20.83 |
|
An aspartyl protease defines a novel pathway for export of Toxoplasma proteins into the host cell |
20.5 |
|
Gene expression changes after depletion of Cyclin F and atypical E2Fs in HeLa cells. |
20.46 |
|
Differential gene expression tools exhibit substandard performance for long non-coding RNA-sequencing data |
20.46 |
|
Defining a microRNA-mRNA targetome for calcineurin inhibitor induced nephrotoxicity |
20.42 |
|
RNAseq of PRMT4KD in human cord blood derived CD34+ cells |
20.31 |
|
Integrative analysis identifies lincRNAs up- and downstream of neuroblastoma driver genes (ALK) |
20.07 |
|
Transcription control by the ENL YEATS domain in acute leukemia [RNA-seq] |
20.07 |
|
Transcription control by the ENL YEATS domain in acute leukemia |
20.07 |
|
Epigenome-wide Effects of Vitamin-D on Bronchial Epithelial Cells using ATAC-Seq and RNA-seq |
19.7 |
|
RNA-Seq analysis of 4N and 2N RPE1 cells following polyploid induction via cytokinesis failure or Aurora kinase inhibition [tpo3] |
19.68 |
|
Elongation Factor TFIIS Prevents Transcription Stress and R-Loop Accumulation to Maintain Genome Stability [ RNA-seq] |
19.34 |
|
Elongation Factor TFIIS Prevents Transcription Stress and R-Loop Accumulation to Maintain Genome Stability |
19.34 |
|
Gene Expression Profiling of Cutaneous CD30+ Lymphoproliferative Disorders by RNA-seq |
19.26 |
|
Resistance to BET inhibitor leads to new therapeutic vulnerabilities in castration resistant prostate cancer |
19.21 |
|
Transcriptional profiling of MCF7 cells treated with H3B05942, E2, or standard of care compounds |
18.97 |
|
Apatinib preferentially inhibits Gefitinib-resistant lung cancer cells by inducing cell cycle arrest and inhibiting VEGFR signaling pathway |
18.97 |
|
Single-cell transcriptomic analysis of tissue resident memory T cells in human lung cancer [ 10x genomics] |
18.82 |
|
Stably-paused genes revealed through inhibition of transcription initiation by the TFIIH inhibitor Triptolide |
18.59 |
|
Gene expression comparison of resting human peripheral-blood NK cells and activated counterparts |
18.5 |
|
Transcriptomic profiling of human HAP1 cells before and after nutrient deprivation |
18.21 |
|
Human HAP1 cells before and after nutrient deprivation |
18.21 |
|
Integrative transcriptome-wide analyses reveal critical HER2-regulated mRNAs and lincRNAs in HER2+ breast cancer |
18.2 |
|
The LIN28B/let-7 axis is a novel therapeutic pathway in Multiple Myeloma |
18.02 |
|
Luminal lncRNAs Regulation by ERα-controlled Enhancers in a Ligand-independent Manner in Breast Cancer Cells |
17.9 |
|
Generation of induced neural stem cells from urine derived cells by synthetic mRNA |
17.75 |
|
Improved genome-wide mapping of uncapped and cleaved transcripts in eukaryotes—GMUCT 2.0 |
17.29 |
|
Messenger RNA expression after silencing or inhibition of MEN1in MCF-7 breast cancer cells |
17.24 |
|
Vitamin d receptor-mediated stromal reprogramming suppresses pancreatitis and enhances pancreatic cancer therapy |
16.91 |
|
The effects of chemokines CCL2/7 on MDA-MB-231-FOXC1 cells |
16.82 |
|
Genome-wide profiling of siRNA targeting EWS-FLI1 in TC32 Ewing sarcoma cell line |
16.61 |
|
Characterization of EZH2-deficient human embryonic stem cells [ChIP-seq and bulk RNA-seq] |
16.28 |
|
Pancreatic cancer-derived exosomes induce apoptosis of T lymphocytes through the p38 MAPK signal transduction pathway |
16.26 |
|
Heterozygous mutations in SMARCA2 lead to impaired neurogenesis due to global retargeting of SMARCA4 |
16.06 |
|
Comprehensive evaluation of differential gene expression analysis methods for RNA-seq data |
15.78 |
|
Locally transplanted human urine-induced nephron progenitor cells contribute to renal repair in mice kidney with diabetic nephropathy |
15.53 |
|
Spliceosomal disruption of the non-canonical BAF complex in cancer |
15.24 |
|
MDM2 and MDM4 are Therapeutic Vulnerabilities in Malignant Rhabdoid Tumors |
15.21 |
|
Transcriptome wide identification of Dicer binding in human and C. elegans reveals a variety of substrates |
15.19 |
|
Activation of the p53 transcriptional program sensitizes cancer cells to Cdk7 inhibitors |
15.19 |
|
Effect of Toxoplasma gondii efector TgIST on global transcriptome of human foreskin fibroblasts (HFFs) upon type I IFN activation |
15.17 |
|
HNRNPM-regulated splicing dependencies in prostate cancer [RNA-Seq] |
15.17 |
|
HNRNPM-regulated splicing dependencies in prostate cancer |
15.17 |
|
Ribosome queuing enables non-AUG translation to be resistant to multiple protein synthesis inhibitors |
15.1 |
|
Activation of Wnt/beta-catenin in Ewing sarcoma cells antagonizes EWS/ETS function and promotes phenotypic transition to more metastatic cell states |
15.01 |
|
Comprehensive comparative analysis of RNA sequencing methods for degraded or low input samples |
14.9 |
|
BET bromodomain inhibitor iBET151 impedes human ILC2 activation and prevents experimental allergic lung inflammation |
14.74 |
|
RNA-sequencing of isogenic primary, pre-malignant immortalized, and Ras-transformed human mammary epithelial cells |
14.72 |
|
Quantitative Analysis of PPARD Transcriptomes in Colon Cancer Cells by Next Generation Sequencing (NGS) |
14.51 |
|
Global transcriptional analysis of human extended pluripotent stem cells, human primed pluripotent stem cells, mouse extended pluripotent stem cells, and mouse embryonic stem cells by RNA-seq |
14.43 |
|
Global transcriptional analysis and genome-wide analysis of chromatin state in extended pluripotent stem cells, primed pluripotent stem cells, and naïve pluripotent stem cells |
14.43 |
|
The Developmental Heterogeneity of Human Natural Killer Cells Defined by Single-cell Transcriptome |
14.32 |
|
Prospective Isolation and Comparison of Human Germinal Matrix and Glioblastoma EGFR+ Populations with Stem Cell Properties |
14.23 |
|
Transcriptome analysis of U87 cells upon LINC00152 knockdown |
14.2 |
|
Triplet nucleotide repeat-based siRNAs are highly toxic to cancer cells |
14.16 |
|
Expression data from A2780 cells treated with DMSO, Olaparib(Ola), Palbociclib(PD), and their combination (Ola/PD) |
14.08 |
|
Gene expression profiles of primary human NK cells before and after expansion on CSTX002 feeder cells, with and without IL-21 stimulation |
14.01 |
|
Identification of global regulators of T-helper cell lineage specification |
14.0 |
|
Identification of global regulators of T-helper cell lineage specification (RNA-Seq) |
14.0 |
|
The impact of pro-inflammatory cytokines on the β-cell regulatory landscape provides insights into the genetics of type 1 diabetes |
13.98 |
|
Gene expression changes in THP1 cells at day 2 and 4 following shRNA knock-down of RUVBL2 |
13.95 |
|
RNA-seq analysis of SKMEL28 melanoma cells following DIRC3 and IGFBP5 ASO knockdown |
13.87 |
|
RNA-seq analysis of YFV-17D specific and total naive CD8 T cells in humans |
13.82 |
|
CD95L derived si- and shRNAs kill cancer cells through an RNAi mechanism by targeting survival genes [shL3.shR6.RNAseq.lg] |
13.76 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of Retinoblastoma Transcriptomes |
13.75 |
|
SPOP mutation confers intrinsic BET inhibitor resistance in prostate cancer (BRD4_JQ1_RNA-seq) |
13.63 |
|
GRHL2 is a key lineage determining factor which collaborates with FOXA1 to establish a targetable collateral pathway in the setting of endocrine therapy-resistant breast cancer (RNA-Seq data set 1) |
13.6 |
|
Distinct structural classes of activating FOXA1 alterations in prostate cancer progression [RNA-Seq] |
13.53 |
|
Distinct structural classes of activating FOXA1 alterations in prostate cancer progression |
13.53 |
|
Identifying lincRNA as prognostic biomarker for clear cell renal cell carcinoma |
13.48 |
|
RNA-seq data corresponding to: AZD4573 is a highly selective CDK9 inhibitor that suppresses Mcl-1 and induces apoptosis in hematological cancer cells |
13.47 |
|
In situ CAPTURE of chromatin interactions by biotinylated dCas9 |
13.44 |
|
RNA-seq transcriptonal profiling in human K562 cells with or without dCas9 and sgRNAs |
13.44 |
|
Epigenetic mechanisms underlie the crosstalk between growth factors and a steroid hormone |
13.4 |
|
Epigenetic mechanisms underlie the crosstalk between growth factors and a steroid hormone [IMR90_MCF7_RNA-Seq] |
13.4 |
|
Human Nonsense-Mediated RNA Decay Initiates Widely by Endonucleolysis and Targets snoRNA Host Genes |
13.34 |
|
Human Adult Sorted Live Cell Erythroblasts transduced with Sigma shRNA Clone TRCN0000005418 targeting RIOK3 with puromycin selection RNAseq |
13.34 |
|
Genome wide expression change in LCC2 and MCF-7 cells |
13.27 |
|
Prediction of bacterial infection outcome using single cell RNA-seq analysis of human immune cells [sorted population Bulk RNA-seq] |
13.22 |
|
Specific modulation of HIV RNA splicing and upregulation of anti-inflammatory miR-124 by the new drug candidate ABX464 |
13.21 |
|
Retinoic acid suppresses MYB in adenoid cystic carcinoma |
13.07 |
|
Retinoic acid suppresses MYB in adenoid cystic carcinoma [RNA-seq] |
13.07 |
|
Landscape of H3K4me3 in human CD19 cells |
12.82 |
|
Identifying ASCL1 target genes in primary GBM stem cell cultures [RNA-seq] |
12.77 |
|
Differential effects of estrogen receptor beta isoforms on glioblastoma progression |
12.76 |
|
SRSF2 mutations impair hematopoiesis and alter exon recognition |
12.69 |
|
Transcriptome of iPSC-derived Neural Cells with Heterozygous Knockout in CHD8 |
12.6 |
|
Gene expression profiles of active and restricted R/G-HIV+ primary human fetal astrocytes |
12.45 |
|
Regulation of protein translation during mitosis |
12.37 |
|
Universal alternative splicing of noncoding exons |
12.31 |
|
Immune-restricted epigenetic reader SP140 maintains macrophage identity and activation states critical to intestinal homeostasis [RNA-seq] |
12.31 |
|
Immune-restricted epigenetic reader SP140 maintains macrophage identity and activation states critical to intestinal homeostasis |
12.31 |
|
Temporal dynamic reorganization of 3D chromatin in hormone-induced breast cancer and endocrine resistance |
12.28 |
|
Inhibition of TNBC metastasis by Gpx1 |
12.27 |
|
Large-scale expansion of human iPSC-derived skeletal muscle cells for disease modeling and cell-based therapeutic strategies |
12.24 |
|
Genome-wide analysis of YAP and TFCP2 occupancy and regulated expression in liver cancer cells |
12.22 |
|
Genome-wide analysis of YAP and TFCP2 down-regulated genes in liver cancer cells |
12.22 |
|
HIV-1 perturbs homeostatic ILCs, unmasks ILC1 plasticity, and boosts TCF7+ memory NK cells |
12.21 |
|
Effect of venetoclax, tedizolid, and combination treatment on gene expression in a venetoclax-resistant AML cell line |
12.13 |
|
Reduced CYFIP1 in human neural progenitors as 15q11.2 deletion model: donor specific dysregulation of schizophrenia/epilepsy genes |
12.08 |
|
Single-cell transcriptomics of the human placenta: inferring the cell communication network of the maternal-fetal interface |
12.05 |
|
CASZ1 directly regulates expression of myogenic genes through regional epigenetic modifications to induce muscle and rhabdomyosarcoma cell differentiation |
12.0 |
|
RNA expression analysis of neuroblastoma cell lines treated with epigenetic drugs |
11.99 |
|
Genome wide transcriptome analysis of palbociclib or GSK3326595 treated A375 cells [Palbociclib_GSK_RNASeq] |
11.99 |
|
Direct interaction of MYCN and p53 regulate transcriptional responses in neuroblastoma |
11.91 |
|
Direct interaction of MYCN and p53 regulate transcriptional responses in neuroblastoma [RNA-Seq] |
11.91 |
|
Dual inhibition of HDMX and HDM2 as a Therapeutic Strategy in Leukemia |
11.88 |
|
The ALK downregulated target gene HBP1 and repressor of MYCN activity as synergistic target for combined PI3K/HDAC inhibition [RNA-Seq] |
11.83 |
|
The ALK downregulated target gene HBP1 and repressor of MYCN activity as synergistic target for combined PI3K/HDAC inhibition |
11.83 |
|
Cranial pericytes derived from neural crest cells reveal an inherent cell type-specific defect in Alzheimer's Disease |
11.8 |
|
Supraphysiological Androgens Repress Prostate Cancer Growth and Induce DNA Damage Augmented by PARP Inhibition |
11.77 |
|
DIGIT regulates endoderm differentiation of human embryonic stem cells |
11.68 |
|
Single cell analysis of HSV-1 infection reveals anti-viral and developmental programs are activated in distinct sub-populations with opposite outcomes |
11.57 |
|
Next Generation Sequencing upon siRNA-mediated knockdown of EIF5A in MCF-7 cells. |
11.55 |
|
Transcriptomic analysis of primary human T cells and murine RAW 264.7 macrophages 3D cultured in different collagen densities |
11.54 |
|
Rare cell variability and drug-induced reprogramming as a mode of cancer drug resistance [RNA-seq] |
11.52 |
|
Changes in RNA expression in human oral cavity carcinoma cells as a result of LDB1 reduction |
11.49 |
|
Effect of Hypoxia in Severe Preeclampsia through Epigenetic Regulation |
11.4 |
|
DGCR8 acts as a novel adaptor for the exosome complex to degrade double-stranded structured RNAs |
11.4 |
|
Transcriptomic analysis reveals novel long non-coding RNAs critical for vertebrate development |
11.37 |
|
Transcriptomic analysis reveals novel long non-coding RNAs critical for vertebrate development [RNA-Seq] |
11.37 |
|
Toxoplasma gondii infection of human retinal pigment epithelial cells |
11.32 |
|
12hr 5-FU treatment vs. DMSO in SJSA cells (from 'A kinase independent role for CDK19 in p53 response') |
11.26 |
|
Transcriptional Profiling of CENPA-Depleted Prostate Cancer Cell Lines |
11.07 |
|
CENPA-Bound Genes and Transcriptional Profiling of CENPA-Depleted Prostate Cancer Cells |
11.07 |
|
CRISPR adenine and cytosine base editors with reduced RNA off-target activities [CBE] |
11.07 |
|
CRISPR adenine and cytosine base editors with reduced RNA off-target activities |
11.07 |
|
UBE3A-mediated regulation of imprinted genes and epigenome-wide marks in human neurons |
11.05 |
|
A novel CRISPR-engineered prostate cancer cell line defines the AR-V transcriptome and identifies PARP inhibitor sensitivities. |
10.94 |
|
Targeting EZH2 in MYCN-amplified Neuroblastoma |
10.92 |
|
Targeting EZH2 in MYCN-amplified Neuroblastoma [RNA-seq] |
10.92 |
|
Proliferation pause as an early blockade of human cellular reprogramming toward pluripotency [RNA-seq analysis] |
10.89 |
|
Gata6 potently initiates reprogramming of pluripotent and differentiated cells to extraembryonic endoderm stem cells [ChIP-Seq & RNA-Seq] |
10.8 |
|
Gata6 potently initiates reprogramming of pluripotent and differentiated cells to extraembryonic endoderm stem cells |
10.8 |
|
Campylobacter concisus pathotypes induce distinct global responses in intestinal epithelial cells [BAA] |
10.78 |
|
Bone marrow derived human B cells [normal proB] |
10.73 |
|
Combined Experimental and System-Level Analyses Reveal the Complex Regulatory Network of miR-124 during Human Neurogenesis [d7+d14] |
10.72 |
|
Transcriptome analysis reveals malignant and hypoxic signature of glioblastoma |
10.7 |
|
Regulation of cellular heterogeneity and rates of symmetric and asymmetric divisions in triple-negative breast cancer |
10.7 |
|
Human RELA haploinsufficiency results in autosomal dominant chronic mucocutaneous ulceration: the transcriptional profile of RelA haploinsufficient patients |
10.69 |
|
Epigenetic reprogramming at estrogen-receptor binding sites alters 3D chromatin landscape in endocrine resistant breast cancer |
10.66 |
|
Epigenetic reprogramming at estrogen-receptor binding sites alters the 3D chromatin landscape in endocrine resistant breast cancer [RNA-seq] |
10.66 |
|
Generation, transcriptome profiling, and functional validation of cone-enriched human retinal organoids |
10.65 |
|
Generation of KRAS signatures using immortalized isogenic lung cells. |
10.63 |
|
Expression analysis of primary human monocytes stimulated with an anti-TLR10 mAb (5C2C5) |
10.57 |
|
Genistein and bisphenol A exposure cause estrogen receptor 1 to bind thousands of binding sites in a cell type-specific manner |
10.55 |
|
BET-Bromodomain Inhibitors Engage The Host Immune System And Regulate Expression Of The Immune Checkpoint Ligand PD-L1 [3mRNA-seq] |
10.53 |
|
BET-Bromodomain Inhibitors Engage The Host Immune System And Regulate Expression Of The Immune Checkpoint Ligand PD-L1 |
10.53 |
|
Proteostasis by STUB1/HSP70 complex controls sensitivity to androgen receptor targeted therapy in advanced prostate cancer |
10.51 |
|
Proteostasis by STUB1/HSP70 complex controls sensitivity to androgen receptor targeted therapy in advanced prostate cancer (RNA-Seq) |
10.51 |
|
DJ-1 is dispensable for human stem cell homeostasis |
10.48 |
|
Bach1 Regulates the Self-renewal and Mesendodermal Differentiation of Human Embryonic Stem Cells |
10.46 |
|
Transcriptional alteration after ionizing radiation exposure in human fibroblasts, iPSCs and NPCs |
10.45 |
|
Estrogen deprivation triggers and immunosuppressive phenotype in breast cancer cells |
10.45 |
|
Genome-wide transcriptional response to random aneuploidy in human cells |
10.44 |
|
ZNF804A transcriptome networks in differentiating human neurons derived from induced pluripotent stem cells |
10.43 |
|
Genome-wide probing of RNA structure reveals active unfolding of mRNA structures in vivo |
10.38 |
|
Noncoding regions are the main source of targetable tumor-specific antigens |
10.36 |
|
FBXW7 modulates stress response by post-translational modification of HSF1 |
10.34 |
|
Transriptional profiling upon heat shock and recovery in cells deficient for FBXW7 and their wild type counterpart. |
10.34 |
|
ChIP-seq of ER and RUNX2 in MCF7 breast cancer cell lines |
10.3 |
|
Neurofibroma |
10.29 |
|
Differential expression in wild-type and mutant neurofibroma and MPNST cell lines |
10.29 |
|
Overexpression of UGT2B17 in MEC1 and JVM2 leukemia cell lines |
10.22 |
|
Combinatorial Reprogramming of Estrogen Signaling by the Nuclear Receptor Family 3C |
10.19 |
|
Antibodies That Convert Bone Marrow Into Trafficking Microglia-Like Cells Reduce Brain Amyloid |
10.13 |
|
Induced pluripotent stem cell modeling of bone marrow failure and MDS identifies therapeutic targets |
10.07 |
|
RNA-seq in acute myeloid leukemia (AML) cells with and without knockdown of METTL14 |
10.03 |
|
MKL1 augments megakaryocyte maturation by enhancing the SRF regulatory axis |
9.99 |
|
MKL1 augments megakaryocyte maturation by enhancing the SRF regulatory axis [RNA-seq] |
9.99 |
|
Genome-wide chromatin analysis of Ewing sarcoma (RNA-seq) |
9.99 |
|
Genome-wide chromatin analysis of Ewing sarcoma |
9.99 |
|
NR4A1 Inhibition Synergizes with Ibrutinib in Killing Mantle Cell Lymphoma Cells |
9.9 |
|
ILF2 Regulates RNA Splicing of DNA Damage Response Genes to Confer Poor Prognosis in 1q21-Amplified Multiple Myeloma |
9.9 |
|
shRNA-mediated knockdown of ETV4 and MED25 in the prostate cell line PC3 reveals set of genes potentially coregulated by MED25 and ETV4 |
9.88 |
|
Genome-wide occupancy of FLAG-MED25 and ETV4 and expression profiling of shRNA-mediated knockdown of ETV4 and MED25 in the prostate cell line PC3 |
9.88 |
|
Whole transcriptome analysis of PBMCs stimulated with either a P. aeruginosa phage PNM lysate or with its bacterial host P. aeruginosa |
9.86 |
|
Gene expression analysis of immortalized human liver progenitor-like cells in culture |
9.85 |
|
Identification of transcripts altered upon LIN-41 knockdown in human embryonic stem cells |
9.84 |
|
Three congruent human Schwann cell models of CMT1A reveal a converged phenotype |
9.83 |
|
A TFIID-SAGA perturbation that targets MYB and suppresses acute myeloid leukemia (RNA-seq) |
9.82 |
|
A TFIID-SAGA perturbation that targets MYB and suppresses acute myeloid leukemia |
9.82 |
|
A single cell reference map for human blood and tissue T cell activation |
9.81 |
|
Oncogenic Notch promotes long-range regulatory interactions within hyperconnected 3D cliques |
9.8 |
|
Wnt addiction of genetically defined cancers reversed by PORCN inhibition |
9.75 |
|
Effect of from Human Umbilical Vein Endothelial Cells |
9.72 |
|
The effects of U1 snRNA mutation in chronic lymphocytic leukemia cell lines |
9.69 |
|
Compared performance of Affymetrix HTA arrays and Illumina RNAseq for the analysis of tumours [RNA-seq] |
9.65 |
|
Compared performance of Affymetrix HTA arrays and Illumina RNAseq for the analysis of tumours |
9.65 |
|
Allosteric Antagonist Modulation of TRPV2 by Piperlongumine Impairs Glioblastoma Progression |
9.65 |
|
Targeting MYC dependency in ovarian cancer through inhibition of CDK7 and CDK12/13 |
9.62 |
|
RIG-I and MDA5 fRIP during KSHV lytic reactivation |
9.59 |
|
A code of mono-phosphorylation modulates the function of RB. |
9.59 |
|
Transcriptome-wide identification of splicing defects upon XAB2 knockdown |
9.55 |
|
Expression profile of HNF1A knockdown and overexpression in 22RV1 and LNCaP cells respectively |
9.5 |
|
A map of gene expression in neutrophil-like cell lines |
9.47 |
|
Identification of the networks that regulate human monocytic myeloid-derived suppressor cell differentiation into inflammatory macrophages |
9.45 |
|
Transcriptome-wide identification of CELF2 functional targets in T cells |
9.42 |
|
The transcriptomic differences between Th1, Tr1, and Tneg cells in controlled human malaria infection |
9.4 |
|
The role of FAM46C in myeloma cells [sequencing] |
9.39 |
|
The role of FAM46C in myeloma cells |
9.39 |
|
Proteasome machinery is instrumental in a common gain-of-function program of the p53 missense mutants in cancer. |
9.37 |
|
Proteasome machinery is instrumental in a common gain-of-function program of the p53 missense mutants in cancer. |
9.37 |
|
RNA sequencing of human macrophages treated with iron chelator deferiprone (DEF), with and without lipopolysaccharide (LPS) |
9.36 |
|
Differential RNA-seq analysis comparing APC-defective and APC-restored SW480 colorectal cancer cells |
9.34 |
|
Differential expression of human parthenogenic stem cells, neural stem cells and DA progenitors. |
9.33 |
|
Gene expression profiling in two dimensional and extracellular matrix based three-dimensional cultures of lung and breast cancer cells |
9.33 |
|
Two dimensional and extracellular matrix based three-dimensional cultures of lung and breast cancer cells |
9.33 |
|
Synaptic dysfunction in human neurons with Autism associated deletions in PTCHD1-AS |
9.3 |
|
Overexpression and knockdown experiment for circCSNK1G3 |
9.29 |
|
Transcriptomes of human monocytes after ex vivo exposure to uric acid |
9.28 |
|
Co-Stimulation–Induced AP-1 Activity is Required for Chromatin Opening During T Cell Activation [RNA-seq] |
9.22 |
|
Co-Stimulation–Induced AP-1 Activity is Required for Chromatin Opening During T Cell Activation. |
9.22 |
|
Expression data for KDM1B knockdown in Glioma-Initiating Cells (GICs) |
9.2 |
|
Transcriptome-wide analysis of the role of HTLV-1 Tax PBM in T-Cells from infected humanized-mice (hu-Mice) |
9.16 |
|
ELF4 is a target of miR-124 and promotes neuroblastoma proliferation and undifferentiated state |
9.14 |
|
Dioxin and AHR impairs mesoderm gene expression and cardiac differentiation in human embryonic stem cells (RNA-Seq) |
9.12 |
|
Dioxin and AHR impairs mesoderm gene expression and cardiac differentiation in human embryonic stem cells |
9.12 |
|
Lineage specific differentiation is influenced by state of human pluripotency [RNA-seq] |
9.04 |
|
Lineage specific differentiation is influenced by state of human pluripotency |
9.04 |
|
Studying the selectivity of a small molecule Synucleozid on transcriptome |
9.03 |
|
Prolyl Hydroxylase Substrate Adenylosuccinate Lyase Is An Oncogenic Driver In Triple Negative Breast Cancer |
9.01 |
|
A novel lncRNA lncRNA-AK096729 promotes colorectal carcinogenesis and glucose metabolism by stabilizing and specifying the transcription modification pattern of c-Myc |
8.99 |
|
Base-resolution mapping reveals distinct classes of N1-methyladenosine methylome in nuclear- and mitochondrial-encoded transcripts |
8.97 |
|
CHD1 loss sensitizes prostate cancer to DNA damaging therapy by promoting error-prone double-strand break repair |
8.96 |
|
Co-transcriptional loading of RNA export factors shapes the human transcriptome |
8.96 |
|
RNAseq of HEK293 cells after Chtop knockdown |
8.96 |
|
Transcriptomic profile of T cell acute lymphoblastic leukemia (T-ALL) cell from patients in CHCQMU |
8.92 |
|
mRNA-Seq profiling of human developing kidney |
8.92 |
|
NET-CAGE Characterizes the Dynamics and Topology of Human Transcribed Cis-regulatory Elements |
8.87 |
|
Whole-transcriptome profilings between a pair of HCA7-derived KRAS-wildtype cetuximab sensitive and resistant colon cancer cells from 3D culture |
8.87 |
|
Patient iPSC-derived neural stem cells display progressive enlargement of lysosomes and disruptions of glycosaminoglycan pathway and autophagy in concordance with clinical severity of Mucopolysaccharidosis I |
8.86 |
|
Transcriptomic profiles of human foreskin fibroblast cells in response to orf virus |
8.86 |
|
Implication of Long noncoding RNAs in the endothelial cell response to hypoxia revealed by RNA-sequencing. |
8.84 |
|
Mitochondrial phosphoenolpyruvate carboxykinase (PCK2) regulates metabolic adaptation and glucose-independent tumor cell growth |
8.82 |
|
Effect of hyperfractionated irradiation (HFRT) of prostate primary basal cells (PrEPs) on the transcriptome |
8.81 |
|
In Vitro and In Vivo Modulation of Alternative Splicing by the Biguanide Metformin. |
8.77 |
|
Expression data from fresh human embryonic lung epithelial tip and stalk cells and cultured organoids derived from tip and stalk. |
8.75 |
|
RNA sequencing analysis of triple cytokine-captured human CD4 T cells |
8.74 |
|
Lung adenocarcinoma metastasis is suppressed by the alveolar lineage transcription factors GATA6 and HOPX. |
8.71 |
|
RNA Sequencing of default, melanocyte biased and enteric human neural crest populations (NC) and neuroectoderm (CNS) |
8.7 |
|
PTHrP overexpression in MCF7 cells |
8.7 |
|
Gene expression profiles of tumor-infiltrating CD8 T cells in hepatocellular carcinoma |
8.67 |
|
Adaptive resistance of melanoma cells to RAF inhibition via reversible induction of a slowly-dividing de-differentiated state |
8.67 |
|
REPROGRAMMING IDENTIFIES FUNCTIONALLY DISTINCT STAGES OF CLONAL EVOLUTION IN MYELODYSPLASTIC SYNDROMES |
8.66 |
|
Exploiting Prmt5-orchestrated intron detention signatures to treat splicing-addicted malignant glioma tumors |
8.63 |
|
SAM68 is required for regulation of Pumilio by the NORAD long noncoding RNA |
8.58 |
|
Maintaining iron homeostasis is the key role of lysosomal acidity for cell proliferation |
8.57 |
|
Gene expression profile of LMSU gastric cancer cell p53 KO and KD |
8.54 |
|
Biological effect of chronic mistranslation in mammalian cells |
8.54 |
|
The mechanism of HHT in treating acute myeloid leukemia on RNA level. |
8.52 |
|
Trisomy of a ‘Down syndrome critical region’ globally amplifies transcription via HMGN1 overexpression |
8.52 |
|
A Primate lncRNA Mediates Notch Signaling During Neuronal Development by Sequestering miRNA [SHSY5Y cells] |
8.5 |
|
Regulation of PRMT5-MDM4 axis is critical in the response to CDK4/6 inhibitors in melanoma |
8.47 |
|
Extensive remodeling of DC function by rapid maturation-induced epigenetic gene silencing |
8.4 |
|
Extensive remodeling of DC function by rapid maturation-induced epigenetic gene silencing [RNA-Seq] |
8.4 |
|
LMO1 Synergizes with MYCN to Promotes Neuroblastoma Initiation and Metastasis |
8.38 |
|
IgG immunocomplexes sensitize human monocytes for inflammatory hyperactivity via transcriptomic and epigenetic reprogramming in Rheumatoid Arthritis |
8.38 |
|
Effect of ER stress on MUC1 kidney disease patient derived cells and and treatment by BRD4780 |
8.35 |
|
A SRp55-regulated alternative splicing network controls pancreatic beta cell survival and function |
8.29 |
|
Alarmin S100A11 initiates a chemokine response to the human pathogen Toxoplasma gondii |
8.27 |
|
Distinct gene expression profile of Huh7 cell lines stably overexpressing CRABP1 or 2 |
8.26 |
|
Chromatin accessibility landscape upon induction of Msgn1, Pax3 and Myf5 in mesodermal cells and identification of conserved Pax3 binding sites and target genes during skeletal myogenesis |
8.26 |
|
Global transcriptional changes in the JJN3 myeloma cell line that occur as a result of treatment with 2 pyrrolobenzodiazepine (PBD) monomers |
8.23 |
|
LED, a long non-coding RNA activator of enhancer RNAs, is hypermethylated in human cancers |
8.23 |
|
Identification of differentially spliced genes by wild type or S34F mutation of U2AF1 |
8.19 |
|
mTOR hyperactivation in Down Syndrome mediates deficits in autophagy induction, autophagosome formation, and mitophagy |
8.17 |
|
Paired Related Homeobox Protein 1 Regulates Quiescence in Human Oligodendrocyte Progenitors |
8.16 |
|
Widespread intronic polyadenylation diversifies immune cell transcriptomes |
8.15 |
|
Regionally specified human pluripotent stem cell-derived astrocytes |
8.09 |
|
A Suv39H1-low chromatin state drives migratory cell populations in cervical cancer |
8.09 |
|
A Suv39H1-low chromatin state drives migratory cell populations in cervical cancer [RNA-Seq] |
8.09 |
|
Crizotinib v. DMSO in SW480 cells |
7.94 |
|
Transcriptomic insights into human decidual and peripheral blood CD8 T cells |
7.9 |
|
Nudt3 is a mRNA Decapping Enzyme That Modulates Cell Migration |
7.9 |
|
JQ1 +/- Vemurafenib in BRAF mutant melanoma (A375) |
7.7 |
|
Gene expression profiles of 4-1BB+PD-1-high, 4-1BB-PD-1-high, and PD-1-int tumor-infiltrating CD8 T cells in hepatocellular carcinoma |
7.69 |
|
HEK293 Heat-shock experiment |
7.67 |
|
Characterization of transcriptomics landscape in HUVEC cells exposed to oxidative stress (Total RNA) |
7.66 |
|
Mapping interactions for the TNIP2 hub protein |
7.65 |
|
Downregulation of DDX5/DDX17 and REST |
7.62 |
|
HeLa transcriptome induction by IFN gamma and indoleamine 2,3-dioxygenase (IDO) |
7.56 |
|
RNA-seq analysis of hPSC-derived brain pericyte-like cells, hPSC-derived neural crest stem cells, and primary human brain pericytes |
7.56 |
|
Effect of Polybrominated diphenyl ethers (PBDEs) on gene expression of MCF7 cells |
7.54 |
|
Enhancer Domains in Gastrointestinal Stromal Tumor Regulate KIT Expression and are Targetable by BET Bromodomain Inhibition |
7.54 |
|
Enhancer Domains in Gastrointestinal Stromal Tumor Regulate KIT Expression and are Targetable by BET Bromodomain Inhibition [RNA-seq] |
7.54 |
|
Recapitulating and Deciphering Tumor-stroma Microenvironment by Using a “LEGO” like 3D printed microfluidic device |
7.47 |
|
Polycomb- and Methylation-Independent Roles of EZH2 as a Transcription Activator [RNA-seq] |
7.42 |
|
Polycomb- and Methylation-Independent Roles of EZH2 as a Transcription Activator |
7.42 |
|
Role of SUMOylation in differential ERα transcriptional repression by SERMs and pure antiestrogens in breast cancer cells |
7.37 |
|
Targeted differentiation of regional ventral neuroprogenitors and related neuronal subtypes from human pluripotent stem cells |
7.37 |
|
Transcriptional profiling of MDA-MB-231 and its ρ0 cells (lacking mtDNA) after 48h arginine depletion by arginine deiminase (ADI). |
7.34 |
|
Effect of Ro 08-2750 treatment on gene expression of human leukemia cell lines MOLM13 and K562 |
7.19 |
|
The immediate impact of exoribonucleolysis on nuclear RNA processing, turnover and transcriptional control revealed by rapid depletion of DIS3, EXOSC10 or XRN2 from human cells |
7.14 |
|
RNA-Seq analysis of 4N and 2N RPE1 cells following polyploid induction via cytokinesis failure by siRNA knockdown of Anillin [tpo8] |
7.03 |
|
RNA-seq transcriptonal profiling in human primary adult erythroid progenitor cells (ProEs) after shRNA-mediated depletion of TFAM and PHB2 expression |
6.97 |
|
ARID1A loss impairs enhancer-mediated gene regulation and drives colon cancer in mice |
6.87 |
|
ARID1A loss impairs enhancer-mediated gene regulation and drives colon cancer in mice [HCT116_RNA-seq] |
6.87 |
|
Smad5 acts as an intracellular pH messenger and maintains bioenergetic homoeostasis |
6.83 |
|
Targets of ROR2 overexpression in MCF-7 cells revealed a differentially regulated module of non-canonical WNT signaling pathway |
6.76 |
|
A cell-permeable stapled peptide inhibitor of the estrogen receptor/coactivator interaction |
6.69 |
|
Genome wide characterization of a STAT1-independent antiviral and immunoregulatory transcriptional program induced by IFNβ and TNFα reveals non-canonical STAT2 and IRF9 pathways |
6.67 |
|
Gene expression profile of HGC27 gastric cancer cell p53 KO and KD |
6.64 |
|
Perivascular signals alter global genomic profile of glioblastoma and response to temozolomide in a gelatin hydrogel |
6.63 |
|
Flura-seq identifies organ-specific adaptations in metastasis-initiating cells |
6.63 |
|
Whole transcriptome splicing analysis in isogenic lung epithelial and adenocarcinoma cell lines with or without a recurrent splicing factor mutation, U2AF1 (S34F) |
6.5 |
|
Novel Form of JARID2 is Required to Regulate Differentiation in Keratinocytes. |
6.49 |
|
Epigenetic profiling and RNA-sequencing of Juvenile Idiopathic Arthritits (JIA) patients |
6.48 |
|
RNA-sequencing of cells derived from the site of inflammation of Juvenile Idiopathic Arthritis patients |
6.48 |
|
Transcriptome sequencing after MAGOHB knockdown in MAGOH-deleted or non-deleted cancer cells |
6.35 |
|
CHD7 is Suppressed in the Perinecrotic/Ischemic Microenvironment and is a Novel Regulator of Angiogenesis |
6.27 |
|
Genome models integrating chromatin contacts and nuclear lamin-genome interactions reveal implications of laminopathy-causing lamin mutations on genome architecture |
6.17 |
|
Nucleotide excision repair capacity increases during differentiation of human embryonic carcinoma cells into neurons and muscle cells |
6.16 |
|
Stranded RNA-seq were performed on total RNA following ribosomal RNAs depletion (Ribo-zero removal kit, illumina) for 3 brain , 8 IDHwt and 5 IDHmut glioma samples. |
6.1 |
|
The anti-leukemic effect of R-2HG depends on its acting as an m6A mRNA modifier-RNA Seq-PBS / R-2HG treatment |
5.98 |
|
Downregulation of LATS kinases alters p53 to promote cell migration |
5.98 |
|
Precise Gene Editing Preserves Hematopoietic Stem Cell Function Following Transient p53-Mediate DNA Damage Response [bulk RNA-seq] |
5.95 |
|
Whole transcriptome profile of citrulline-specific B cells from patients with rheumatoid arthritis |
5.94 |
|
Targeted enhancer activation by a subunit of the integrator complex |
5.92 |
|
Non-coding and coding transcriptional profiles are significantly altered in pediatric Retinoblastoma tumors |
5.89 |
|
SLAM-seq defines direct gene-regulatory functions of the BRD4-MYC axis [Quant-Seq] |
5.88 |
|
SLAM-seq defines direct gene-regulatory functions of the BRD4-MYC axis |
5.88 |
|
Identification of Sin3B regulated genes during quiescence |
5.85 |
|
Next Generation Sequencing of human SMA and healthy control Motor Neurons |
5.63 |
|
Characterization of human ILC2 subsets |
5.62 |
|
Targeting MTHFD2 in Acute Myeloid Leukemia |
5.56 |
|
The contribution of adenosine receptor 3-mediated signaling to TLR4-induced responses by human dendritic cells |
5.54 |
|
Interferon receptor signaling pathways regulating PD-L1 and PD-L2 expression |
5.46 |
|
The ZZ-type zinc finger of ZZZ3 modulates the ATAC complex-mediated histone acetylation and gene activation |
5.44 |
|
SQSTM1/p62-directed metabolic reprogramming is essential for normal neurodifferentiation |
5.44 |
|
Human cells contain natural double-stranded RNAs with potential regulatory capacity |
5.43 |
|
Toxoplasma controls host cyclin E expression through the use of a novel MYR1-dependent effector protein, HCE1 |
5.43 |
|
SPOP mutation confers intrinsic BET inhibitor resistance in prostate cancer |
5.38 |
|
Tumor- and cytokine-primed human natural killer cells exhibit distinct phenotypic and transcriptional signatures |
5.36 |
|
Tumor- and cytokine-primed human natural killer cells exhibit distinct phenotypic and transcriptional signatures [RNA-seq] |
5.36 |
|
Post-transcriptional remodelling is temporally deregulated during motor neurogenesis in human ALS models |
5.33 |
|
K562 polyA RNA-Seq |
5.22 |
|
Hypoxic transcriptome of SQ20B human head and neck cancer cells |
5.13 |
|
scRNASeq analysis of cycling cardiomyocytes |
5.07 |
|
shRNA knockdown of YAP1 in HCC364 cells, various drug conditions |
5.07 |
|
Race-specific transcriptome and Long non-coding RNA of ADT-resistant African-American prostate cancer cell models. |
4.99 |
|
Comparison of small cell lung cancer PDX model FHSC04 for response to LSD1 inhibitor RG6016/ORY1001 |
4.96 |
|
RNA-seq of hiPSCs-derived NPCs from 3 pairs of dizygotic discordant twins for Congenital Zika syndrome |
4.95 |
|
Cooptation of tandem DNA repeats for the control of epithelial-to-mesenchymal transition [RNA-Seq] |
4.94 |
|
Cooptation of tandem DNA repeats for the control of epithelial-to-mesenchymal transition. |
4.94 |
|
ELAVL2-regulated transcriptional networks in human neurons link atlernative splicing, autism and human neocortical evolution |
4.9 |
|
Cis-Regulatory Circuits Regulating NEK6 Kinase Overexpression in Transformed B Cells Are Super-Enhancer-Independent |
4.8 |
|
Cis-Regulatory Circuits Regulating NEK6 Kinase Overexpression in Transformed B Cells Are Super-Enhancer-Independent (RNA-seq) |
4.8 |
|
The effect of doxycycline-induced expression of host-cell-factor 2 (HCF-2) proteins on the global gene expression in HEK-293 cells |
4.78 |
|
Molecular characterization of BRSK2 and BRSK1 kinases as negative regulators of the NRF2 transcription factor |
4.78 |
|
Disruption of the TFAP2A regulatory domain causes Branchio-Oculo-Facial Syndrome (BOFS) and illuminates pathomechanisms for other human neurocristopathies [RNA-seq data set 2] |
4.76 |
|
Identification of HOXB13 target genes responsive to BET inhibitors |
4.75 |
|
Oxaliplatin resistance is enhanced by saracatinib via upregulation of ABCG1 and Wnt/β-catenin signaling in hepatocellular carcinoma |
4.65 |
|
Transcriptomic analysis of healthy donor and Sickle Cell Disease (SCD) hematopoietic stem/progenitor cells |
4.57 |
|
Different Temporal Effects of Ebola Virus VP35 and VP24 Proteins on Global Gene Expression in Human Dendritic Cells |
4.48 |
|
The hepatitis C viral protein NS5A stabilizes growth-regulatory human transcripts |
4.3 |
|
Function and hormonal regulation of GATA3 in human first trimester placentation |
4.28 |
|
Induction of human regulatory innate lymphoid cells from group 2 innate lymphoid cells by retinoic acid |
4.28 |
|
Re-programing chromatin with a bifunctional LSD1/HDAC inhibitor induces therapeutic differentiation in DIPG [RNA-seq] |
4.25 |
|
Re-programing chromatin with a bifunctional LSD1/HDAC inhibitor induces therapeutic differentiation in DIPG |
4.25 |
|
Cancer-Causing Mutations in SF3B1 Alter Splicing by Disrupting Interaction with SUGP1 |
4.23 |
|
Comparative Analysis of Cas9 Activators Across Multiple Species |
4.14 |
|
miR-126 Orchestrates an Oncogenic Program in B-Cell Precursor Acute Lymphoblastic Leukemia |
4.08 |
|
Transcriptomic analysis of cultured isogenic myotonic dystrophy type 1 myoblasts with and without the DMPK CTG repeat |
4.07 |
|
Mesenchymal stem/stromal cell engulfment reveals metastatic advantage in breast cancer |
4.04 |
|
Bioreactor-engineered cancer tissues mimic phenotypes, gene expression profiles and drug resistance mechanisms detectable in xenografts and clinical specimens. |
4.02 |
|
Systematic Functional Perturbations Uncover a Prognostic Genetic Network Driving Human Breast Cancer [RNA-Seq] |
3.99 |
|
Systematic Functional Perturbations Uncover a Prognostic Genetic Network Driving Human Breast Cancer |
3.99 |
|
RNASeq of MV4;11 cell treated with DMSO, I-BET, SGC0946 and combination of I-BET and SGC0946 |
3.92 |
|
Functional interdependency of BRD4 and DOT1L in MLL leukaemia |
3.92 |
|
Transcriptomic analysis of iPSC and ESC challenged with atmospheric or physiological oxygen |
3.91 |
|
Transcriptomic analysis of human neural progenitor cells differentiation into astrocytes |
3.86 |
|
Human Treg NaCl stimulation |
3.84 |
|
Human Treg IFNg/IL-10 subpopulations |
3.72 |
|
RNA-sequencing of mRNAs from control and CAP-D3 deficient Salmonella infected HT-29 cells |
3.68 |
|
Identifying markers predicting successful graft outcome for clinical translation of hESC-based cell therapy for Parkinson’s disease |
3.67 |
|
Rate of elongation by RNA polymerase II is influenced by specific gene features and histone modifications |
3.6 |
|
Genome-wide RNA deep sequencing of CAL-101 or AKTi primed human T cells in comparison to traditionally expanded T cells |
3.53 |
|
Role of BET proteins in YAP/TAZ-dependent transcription [RNA-seq 1] |
3.35 |
|
Assessing the impact of loss of ATF7IP and SETDB1 on the transcriptome |
3.3 |
|
ATF7IP-mediated stabilization of the histone methyltransferase SETDB1 is essential for heterochromatin formation by the HUSH complex |
3.3 |
|
Trisomy of a ‘Down syndrome critical region’ globally amplifies transcription via HMGN1 overexpression [SLAM-Seq] |
3.24 |
|
Primate-specific gene TMEM14B promotes cortical expansion and folding |
2.99 |
|
Identification of renal resident macrophages across species [C1] |
2.89 |
|
Cystathionine-β-Synthase Promotes Colon Carcinogenesis |
2.88 |
|
Expression changes in MAPKi resistant M229 melanoma lines co-cultured with PD-1 overexpressing HEK293T cells [CellLine.FPKM.batch5] |
2.85 |
|
SF3B1 Degron knockdown RNA-seq |
2.84 |
|
RNA-Seq analysis of cSCC cells followed by siRNA-induced gene knockdown of C1s. |
2.82 |
|
T-bet recruits P-TEFb to super-enhancers to regulate T helper cell differentiation |
2.73 |
|
T-bet recruits P-TEFb to super-enhancers to regulate T helper cell differentiation (RNA-Seq) |
2.73 |
|
Transcriptional profiling of CD45RO+CD57+CD4+ T cells |
2.71 |
|
NOTCH signaling is activated in and contributes to resistance in enzalutamide-resistant prostate cancer cells |
2.7 |
|
TAF1 is critical for AE driven leukemogenesis [RNA-seq] |
2.65 |
|
TAF1 is critical for AE driven leukemogenesis |
2.65 |
|
Gene expression analysis of CD4+ and CD4- ILC1 subsets by RNAseq |
2.63 |
|
Ex vivo Dynamics of Human Glioblastoma Cells in a Microvasculature-on-a-Chip System Correlates with Tumor Heterogeneity and Subtypes |
2.62 |
|
RNA-Seq in PWS iPSC-derived neurons |
2.56 |
|
The p30 isoform of CEBPA uncovers a silent enhancer to drive the expression of the tumor promotive factor CD73 in CEBPA mutant AML |
2.47 |
|
Adenovirus Small E1A Employs the Lysine Acetylases p300/CBP and Tumor Suppressor Rb to Repress Select Host Genes and Promote Productive Virus Infection |
2.35 |
|
Adenovirus Small E1A Employs the Lysine Acetylases p300/CBP and Tumor Suppressor Rb to Repress Select Host Genes and Promote Productive Virus Infection [RNA-seq] |
2.35 |
|
RNA-Seq analysis of proliferating 4N and 2N RPE1 cells derived from single cell clones following inhibition of Aurora B to induce polyploidization [tpo10] |
2.33 |
|
Heterogeneous effects of massive hypoxia pathway activation in kidney cancer |
2.28 |
|
Combined MEKi (GDC-0973) and WNT (G007-LK) treatment in APC and KRAS mutant HCT-15 cell line |
2.16 |
|
Gene expression regulated by CSA and CSB in neuroblastoma cell line |
2.08 |
|
Microenvironmental-derived Regulation of HIF-Signaling Drives Transcriptional Heterogeneity in Glioblastoma Multiforme |
2.07 |
|
Human Treg IL-12 stimulation |
1.99 |
|
DLX3-dependent p53 signaling network controls keratinocyte cell cycle and squamous tumor growth |
1.96 |
|
DLX3 alters transcriptomic profile of adhesion, cell cycle, and cell death in Squamous Cell Carcinoma Cells |
1.96 |
|
Pseudouridylation of tRNA-derived fragments steers translation control in stem cells [Polysome-Seq] |
1.92 |
|
RNAseq of CCRF-CEM, a T-cell acute lymphoblastic leukemia cell line, after knockdown with 2 control hairpins and 6 hairpins targeting the PRC2 complex. |
1.92 |
|
Identification of long noncoding RNAs in T-ALL cell lines |
1.72 |
|
Entrectinib Resistance in a Neuroblastoma Xenograft Model |
1.7 |
|
A novel Menin-MLL inhibitor induces specific chromatin changes and eradicates disease in models of MLL-rearranged leukemia [RNA-Seq II] |
1.68 |
|
RelA mutants 'reconstituted' and cell cycle synchronized HCT116 Colorectal Cancer Cells |
1.64 |
|
Methylation DNA mediated KLF4 binding activity in glioblastoma cells |
1.55 |
|
CRISPR-mediated deletion of prostate cancer risk-associated CTCF loop anchors identifies repressive chromatin loops |
1.49 |
|
Selective silencing of euchromatic L1s revealed by genome-wide screens for L1 regulators |
1.41 |
|
Identification and characterization of circular RNAs as a new class of putative biomarkers in human blood |
1.37 |
|
Xrn2 accelerates termination by RNA polymerase II, which is underpinned by CPSF73 activity |
1.28 |
|
RNA sequencing of isogenic BRCA2 haploinsufficient vs. wild-type T-ALL cells |
1.22 |
|
Gene expression profiling by RNA-seq of SW480 TGM2 knockdown cells |
1.18 |
|
Clinker: visualizing fusion genes detected in RNA-seq data |
1.15 |
|
Proliferation-correlated expression |
1.14 |
|
Multiplexed engineering and analysis of endogenous enhancer activity in single cells: Mosaic-Seq of beta-globin locus (separate infection) |
1.1 |
|
Transcriptional profiling of growing and senescent WT and IL-1R-depleted IMR90 cells |
1.1 |
|
RNA-seq transcriptional profiling in primary human erythroid progenitor cells upon shRNA-mediated knockdown of PRC2 core subunits |
1.02 |
|
ChIP-seq and RNA-seq analysis of PRC2 core subunits in primary human erythroid progenitor cells |
1.02 |
|
A stably self-renewing adult blood-derived induced neural stem cell exhibiting patternability and epigenetic rejuvenation |
1.0 |
|
Multiplexed engineering and analysis of endogenous enhancer activity in single cells: Mosaic-Seq of beta-globin locus (pooled infection) |
0.95 |
|
Specific molecular signatures underlie response to decitabine in CMML [RNA-seq] |
0.85 |
|
Specific molecular signatures underlie response to decitabine in CMML |
0.85 |
|
HSB-2 cells stably expressing LDB1 or mutant LDB1 proteins |
0.84 |
|
INO80 governs super-enhancer-mediated oncogenic transcription and tumor growth in melanoma [RNA-seq] |
0.78 |
|
INO80 governs super-enhancer-mediated oncogenic transcription and tumor growth in melanoma |
0.78 |
|
An evolutionarily conserved function of polycomb silences the MHC class I antigen presentation pathway and enables immune evasion in cancer [RNA-Seq] |
0.75 |
|
An evolutionarily conserved function of polycomb silences the MHC class I antigen presentation pathway and enables immune evasion in cancer |
0.75 |
|
Analysis of gene expression in primary human foreskin keratinocytes +/- HPV16 E7 or PTPN14 knockout |
0.73 |
|
Hsa-miR-371a-5p and hsa-miR-518a-3p regulated genes in choriocarcinoma cells |
0.71 |
|
RNA sequencing of hiPSC derived neural crest populations from Familial Dysautonomia patients |
0.7 |
|
Long non-coding RNA profiling of human lymphoid progenitors reveals transcriptional divergence of B cell and T cell lineages |
0.65 |
|
Pluripotent stem cell model of Nakajo-Nishimura syndrome untangles proinflammatory pathways mediated by oxidative stress |
0.63 |
|
SNHG5 siRNA knock down in HCT116 cells |
0.58 |
|
RNA-seq and small RNA-seq from WT and ADAR1 knockdown H9 lines and their differentiation to specific types of neurons |
0.49 |
|
Modulation of nonsense-mediated decay by rapamycin |
0.48 |
|
rG4-seq reveals widespread formation of G-quadruplex structures in the human transcriptome |
0.47 |
|
RNA sequencing reveals levamisole target genes PTPRZ1 and MDK and their links to interferon pathway in human podocytes |
0.41 |
|
Mechanism suppressing H3K9 trimethylation in pluripotent stem cells and its demise by polyQ-expanded huntingtin mutations [RNA-seq] |
0.38 |
|
Mechanism suppressing H3K9 trimethylation in pluripotent stem cells and its demise by polyQ-expanded huntingtin mutations |
0.38 |
|
RNA sequencing analysis of human podocytes reveals glucocorticoid regulated gene networks targeting non-immune pathways |
0.34 |
|
RNA-Seq of SHEP TET21N cells upon Doxorubicin treatment |
0.13 |
|
Long-term expandable SOX9+ chondrogenic ectomesenchymal cells from human pluripotent stem cells |
0.1 |
|
YTHDF1 Amplifies Wnt/β-Catenin Signaling to Promote Intestinal Stemness |
0.1 |
|
ADAR1-editing in HeLa, p150-KO and ADAR1-KO transcriptomes |
0.03 |
|
ADAR1-editing of cellular and measles virus-derived duplex RNA |
0.03 |
|
4C-seq of insulin promoter, knockdown of INS promoter activity and Genome-wide maps of chromatin state in EndoC-βH1 Cells |
0.03 |
|
Viral shRNA Knockdown of INS Promotor Activity in EndoC-βH1 Cells |
0.03 |
|
RUVBL1/RUVBL2 ATPase Activity Drives PAQosome Maturation, DNA Replication and Radioresistance in Lung Cancer |
0.02 |