|
Adaptation of a RAS pathway activation signature from FF to FFPE tissues in colorectal cancer (FFPE RNA-Seq II) |
154.87 |
|
RNAseq analysis of ESRP regulated splicing events in prostate cancer |
75.32 |
|
Proteomic profiling of VCP substrates links VCP to K6-linked ubiquitylation and c-Myc function |
69.05 |
|
Human HAP1 cells before and after nutrient deprivation |
48.91 |
|
Transcriptomic profiling of human HAP1 cells before and after nutrient deprivation |
48.91 |
|
Differential expression of genes in HCMV-infected fibroblasts regulated by the purinergic receptor P2Y2. |
42.01 |
|
Analysis and expansion of the eosinophilic esophagitis transcriptome by RNA sequencing |
40.86 |
|
Differential expression of genes in AD169-infected MRC5. |
39.04 |
|
RNA-seq in HT-29 colorectal cancer cells after F. nucleatum treatment |
38.23 |
|
Next generation sequencing on knockdown of AC093323.3 in lung cancer cells |
37.02 |
|
A Novel PI3K Regulator, ARID4B, Presents Synthetic Essentiality in PTEN-deficient Prostate Cancer |
33.27 |
|
A Novel PI3K Regulator, ARID4B, Presents Synthetic Essentiality in PTEN-deficient Prostate Cancer [RNA-seq] |
33.27 |
|
Mitochondrial unfolded protein response controls matrix pre-RNA processing and translation |
30.32 |
|
Gene expression analysis of dengue-infected cells |
29.08 |
|
SMUG1 promotes telomere maintenance through telomerase RNA end-processing |
25.59 |
|
Genome-wide profiling of siRNA targeting EWS-FLI1 in TC32 Ewing sarcoma cell line |
23.08 |
|
Maintaining iron homeostasis is the key role of lysosomal acidity for cell proliferation |
22.89 |
|
Tracking of dCas9-methyltransferase footprints |
21.78 |
|
HeLa transcriptome induction by IFN gamma and indoleamine 2,3-dioxygenase (IDO) |
21.29 |
|
microRNAs with an AAGUGC seed motif constitute an integral part of a signaling network driving NSCLC cell proliferation |
21.01 |
|
RC3H1 posttranscriptionally regulates A20 mRNA and modulates the activity of the IKK/NF-kB pathway |
20.75 |
|
RC3H1 posttranscriptionally regulates A20 mRNA and modulates the activity of the IKK/NF-kB pathway [RNA-Seq] |
20.75 |
|
Food-derived Compounds Apigenin and Luteolin Modulate mRNA Splicing of Introns with Weak Splice Sites |
20.58 |
|
DDX54 regulates transcriptome dynamics during DNA damage response [4SU-seq] |
20.4 |
|
ROR-γ drives androgen-receptor expression and represents a therapeutic target in castration-resistant prostate cancer |
20.1 |
|
MOV10 Is a 5' to 3' RNA Helicase Contributing to UPF1 mRNA Target Degradation by Translocation along 3'UTRs (expression) |
19.69 |
|
MOV10 Is a 5' to 3' RNA Helicase Contributing to UPF1 mRNA Target Degradation by Translocation along 3'UTRs |
19.69 |
|
Transcriptomic profiling of normal human cardiac fibroblast treated with halofuginone |
19.49 |
|
Transcriptomes analysis for the regulation of Z36 induced autophagy in HeLa cell death |
19.41 |
|
Time-course expression data from HEK293∆RAF1:ER cells stimulated with 4OHT, U0126, CYHX, ActD, EGF, FGF, or IGF and labelled with 4SU |
18.37 |
|
Time-course expression data from HEK293∆RAF1:ER cells stimulated with 4OHT and labelled with 4SU |
18.37 |
|
Transcriptome analysis in Neobractatin treated cells |
17.99 |
|
Urinary sediment transcriptomic and longitudinal data to investigate renal function decline in type 1 diabetes |
17.94 |
|
EP400 is required for Max and MCPyV mediated gene activation |
17.7 |
|
An improved method for circular RNA purification that efficiently removes linear RNAs containing G-quadruplexes or structured 3’ ends |
17.26 |
|
Effect of MDK expressing Melanoma cells conditioned media in Human LEC |
17.19 |
|
Response of HEK293 Freestyle cells to 36 h of culture in Zn(II)-depleted Freestyle medium |
16.69 |
|
Global gene expression differences between blood- and lymphatic-specific endothelial colony forming cells |
16.63 |
|
Dual inhibition of HDMX and HDM2 as a Therapeutic Strategy in Leukemia |
16.46 |
|
SPOP mutation confers intrinsic BET inhibitor resistance in prostate cancer (BRD4_JQ1_RNA-seq) |
16.18 |
|
Candidate genes and pathways downstream of PAX8 involved in ovarian high-grade serous carcinoma |
16.18 |
|
A non-canonical role of YAP/TEAD is required for activation of estrogen-regulated enhancers in breast cancer [RNA-seq] |
16.01 |
|
A non-canonical role of YAP/TEAD is required for activation of estrogen-regulated enhancers in breast cancer |
16.01 |
|
A combinatorial screen of the CLOUD uncovers a synergy targeting the androgen receptor |
15.86 |
|
Self-organized amniogenesis by human pluripotent stem cells in a biomimetic implantation-like niche |
15.64 |
|
Novel Non-catalytic Substrate-selective p38α-specific MAPK Inhibitors with Endothelial-Stabilizing and Anti-inflammatory Activity |
15.6 |
|
Altering cancer transcriptomes using epigenomic inhibitors [RNA-Seq] |
15.5 |
|
Altering cancer transcriptomes using epigenomic inhibitors |
15.5 |
|
RNA-seq analysis in Cornea epithelial cells (CECs), skin epithelial cells (SECs), LSCs after knocking down PAX6 (3-D shPAX6 LSCs) and SESCs transduced with PAX6(3-D PAX6+ SESCs) upon 3-D differentiation |
15.34 |
|
Global gene expression differences between blood- and lymphatic-specific human dermal microvascular endothelial cells |
15.3 |
|
High RNA polymerase II occupancy on herpes simplex virus 1 late genes early in infection suggests progression to elongation is a critical switch to trigger late viral gene expression |
14.98 |
|
Discovering the anti-cancer potential of non-oncology drugs by systematic PRISM profiling |
14.77 |
|
Mitochondrial unfolded protein response controls matrix pre-RNA processing and translation |
14.76 |
|
ARID1A and PI3-Kinase pathway mutations in the endometrium drive epithelial transdifferentiation and collective invasion |
14.55 |
|
Integrative analysis of mRNA and lncRNA profiles identified pathogenetic lncRNAs in esophageal squamous cell carcinoma |
14.52 |
|
DHX9 suppresses spurious RNA processing defects originating from the Alu invasion of the human genome [uvCLAP CLIP-seq] |
14.37 |
|
RNAseq Study in CC-671 Treated Cal-51 Cells |
14.05 |
|
Genome-wide transcriptome analysis of NIPBL iPSC and commited cardiomyoctes |
13.91 |
|
The human blood-nerve barrier transcriptome |
13.67 |
|
EZH2 inhibitor efficacy in non-Hodgkin lymphoma does not require suppression of H3K27 mono-methylation [RNA-Seq] |
13.62 |
|
EZH2 inhibitor efficacy in non-Hodgkin lymphoma does not require suppression of H3K27 mono-methylation |
13.62 |
|
IRF1 regulates IFN dependent and independent gene expression |
13.37 |
|
Overexpression of NFIB and YBX1 in MCF-7 cells |
13.28 |
|
RNA-Seq analysis of primary human keratinocytes exposed to Cannabidiol |
13.12 |
|
An alternative CTCF isoform antagonizes canonical CTCF occupancy and changes chromatin architecture to promote apoptosis |
13.03 |
|
Interaction with WDR5 recruits MYC to a small cohort of genes required for tumor onset and maintenance |
13.02 |
|
Transcriptomic analysis of acute mitochondrial pyruvate carrier inhibition using UK5099 in ABL prostate cancer cells |
12.82 |
|
Global analysis of pre-mRNA subcellular localization upon splicing inhibition by spliceostatin A |
12.71 |
|
IMP3 regulated gene expression in breast cancer cells |
12.64 |
|
RNA sequencing of GlyH-101-treated MCF-7 cell line |
12.5 |
|
RNA-Sequencing experiment for effects of PKF115-584 treatment on four T-ALL cell lines (RPMI8402, HPB-ALL, Jurkat, CCRF-CEM). |
12.35 |
|
Analysis of Combined Transcriptomes Identifies Gene Modules Differentially Responding to Pathogenic Stimulation in Vascular Smooth Muscle and Endothelial Cells |
12.06 |
|
RNA-Seq profiling of days 0, 7 and 18 kidney organoids differentiated from three separate vials of starting material |
12.02 |
|
Single-cell transcriptomics of human oocytes: environment-driven metabolic competition and compensatory mechanisms during oocyte maturation |
11.99 |
|
Role of COP1 on MAP kinase transcriptional output in melanoma |
11.82 |
|
m6A-dependent regulation of messenger RNA stability |
11.58 |
|
Role of XRN2 ribonucleolytic activity in RNA metabolism |
11.54 |
|
Characterization of transcriptomics landscape in HUVEC cells exposed to oxidative stress (Total RNA) |
11.53 |
|
Illumina sequencing of vaginal epithelial cells from women using depot medroxyprogesterone acetate or non-hormonal contraception |
11.44 |
|
Small-molecule targeting of brachyury transcription factor addiction in chordoma [rnaseq_sgrna] |
11.4 |
|
Poly(A)-ClickSeq resolves CF25-mediated alternative poly-adenylation, HeLa |
11.4 |
|
Coordinate regulation of alternative pre-mRNA splicing events by the human RNA chaperone proteins hnRNPA1 and DDX5 |
11.35 |
|
Modeling the MYC-driven normal-to-tumour switch in breast cancer. |
11.3 |
|
Gene expression in PANC1 cells treated with Rakicidin |
11.3 |
|
U1 snRNP telescripting regulates size-function stratified human genome |
11.27 |
|
Tristetraprolin disables prostate cancer maintenance by impairing proliferation and metabolic function |
11.26 |
|
Over expression of Receptor Activity Modifying Protein 2 in HEK293T cells |
11.24 |
|
Differential expression in LNCaP cells expressing the wild-type androgen receptor (AR-WT) or the ligand-independent AR-V7 splice variant |
11.1 |
|
mRNA differential expression in LNCaP cells expressing the wild-type androgen receptor (AR-WT) or the ligand-independent AR-V7 splice variant |
11.1 |
|
Gene expression profiling by RNA-seq in hTert-HME1 cell line treated with control or BRCA2 siRNAs and grown with or without EGF (epithelial growth factor) |
11.05 |
|
Campylobacter concisus pathotypes induce distinct global responses in intestinal epithelial cells [UNSWCD] |
10.99 |
|
Transcriptome analysis-identified long noncoding RNA CRNDE in maintaining endothelial cell proliferation, migration, and tube formation |
10.99 |
|
Hypoxic regulation of transcription in HUVEC is mediated by EPAS1 |
10.92 |
|
Mitochondrial unfolded protein response controls matrix pre-RNA processing and translation |
10.82 |
|
Differential responses by human respiratory epithelial cell lines to respiratory syncytial virus reflect distinct patterns of infection control |
10.5 |
|
Depicting early human development and germ cell origin with porcine embryos |
10.5 |
|
RNA sequencing of HepG2 cells treated with estradiol or estrogen receptor agonist |
10.42 |
|
Simultaneous profiling of sexually transmitted bacterial pathogens, microbiome, and concordant host response in cervical samples using whole transcriptome sequencing analysis |
10.38 |
|
CXCR4 regulates extra-medullary myeloma through epithelial-mesenchymal transition-like transcriptional activation |
10.32 |
|
Limiting cholesterol biosynthetic flux engages type I IFN signaling in a STING-dependent manner |
10.2 |
|
Knockdown of ADNP in HCT116 colon cancer cells |
10.18 |
|
ADAR1 controls apoptosis of stressed cells by inhibiting Staufen-mediated mRNA decay |
10.16 |
|
MDM2 and MDM4 are Therapeutic Vulnerabilities in Malignant Rhabdoid Tumors |
10.16 |
|
Vitamin C Promotes Apoptosis in Breast Cancer Cells by Increasing TRAIL Expression |
10.14 |
|
Next Generation Sequencing upon siRNA-mediated knockdown of EIF5A in MCF-7 cells. |
10.02 |
|
The effect of Foxc1 deficiency on undifferentiated and differentiated human primary keratinocytes |
9.98 |
|
NAD+ Analog-sensitive PARPs Reveal a Role for PARP-1 in Transcription Elongation |
9.95 |
|
Fisetin induces autophagy in pancreatic cancer cells via endoplasmic reticulum stress- and mitochondrial stress-dependent pathways |
9.94 |
|
Cell differentiation grade determines distinct FOXA2 contributions to the cis-regulatory networks of pancreatic cancer cells [RNA-seq] |
9.91 |
|
Cell differentiation grade determines distinct FOXA2 contributions to the cis-regulatory networks of pancreatic cancer cells |
9.91 |
|
RNA-Seq with and without RNase treatment in PCa cell lines |
9.9 |
|
NOTCH1 activation in breast cancer confers sensitivity to inhibition of SUMOylation |
9.87 |
|
EWSR1 influences alternative splicing through direct and indirect mechanisms |
9.84 |
|
MeRIP sequencing reveals angiogenic properties of vascular endothelial cells |
9.77 |
|
Genome-wide expression profiling of an in vitro model for studying esophageal epithelial differentiation |
9.74 |
|
DHX15 regulates CMTR1-dependent gene expression and cell proliferation |
9.74 |
|
Effect of from Human Umbilical Vein Endothelial Cells |
9.68 |
|
Lung adenocarcinoma metastasis is suppressed by the alveolar lineage transcription factors GATA6 and HOPX. |
9.62 |
|
The translation termination factor GSPT1 is a phenotypically relevant off-target of heterobifunctional phthalimide degraders |
9.58 |
|
Transcriptomic analysis of IPF lung-associated and normal peripheral blood T cells |
9.52 |
|
iRNA-seq: Computational method for genome wide assessment of acute transcriptional regulation from total RNA-seq data |
9.52 |
|
mRNA cap methyltransferase, RNMT-RAM, promotes RNA pol II transcription |
9.34 |
|
ChIP-seq of ER and RUNX2 in MCF7 breast cancer cell lines |
9.33 |
|
Gene expression and 4sUDRB-seq for NF90/NF110 of human scramble and KD HeLa cells. |
9.27 |
|
JQ1 +/- Vemurafenib in BRAF mutant melanoma (A375) |
9.25 |
|
Biosynthesis of histone messenger RNA employs a specific 3' end endonuclease |
9.24 |
|
Next Generation RNA Sequencing Analysis of AMPK Wild Type, AMPKα-KO and AMPKα1-2A U2OS cell Transcriptomes |
9.2 |
|
Increased Serine and One Carbon Pathway Metabolism by PKCl/i Deficiency Promotes Neuroendocrine Prostate Cancer |
9.09 |
|
Increased Serine and One Carbon Pathway Metabolism by PKCl/i Deficiency Promotes Neuroendocrine Prostate Cancer [RNA-seq] |
9.09 |
|
RNA expression analysis upon JMJD1C depletion |
9.09 |
|
JMJD1C is required for the survival of acute myeloid leukemia by functioning as a co-activator for key transcription factors |
9.09 |
|
RNA-sequencing of human vascular endothelial cells after si-RNA mediated gene silencing of interleukin-6 (IL6) |
9.05 |
|
Cohesin and CTCF Differentially Affect the Chromatin Architecture and Gene Expression in Human Cells |
9.04 |
|
Hepatitis C virus functionally sequesters miR-122 |
8.94 |
|
Hepatitis C virus functionally sequesters miR-122 [RNA-Seq] |
8.94 |
|
CDK12 regulates alternative last exon mRNA splicing and promotes invasion of a breast cancer cell line |
8.93 |
|
RNA-Seq analysis of human lung fibroblasts exposed to TGF-β |
8.9 |
|
The DNM3OS lncRNA is a reservoir of fibromiRs with major functions in fibroblast response to TGF-beta and fibrogenesis |
8.9 |
|
Differentially expressed genes post knock down of lincDUSP26 |
8.9 |
|
Sequencing of freshly produced RNA following exposure of cells to DNA damage-inducing UV mimetic 4-hydroxyaminoquinolone (4-NQO) |
8.89 |
|
A quantitative chemotherapy genetic interaction map identifies new factors associated with PARP inhibitor resistance |
8.88 |
|
Bromodomain-containing Protein 4 (BRD4) is Required for the Maintenance of a Mammary Epithelial Phenotype |
8.75 |
|
Bromodomain-containing Protein 4 (BRD4) is Required for the Maintenance of a Mammary Epithelial Phenotype [RNA-Seq] |
8.75 |
|
Human Nonsense-Mediated RNA Decay Initiates Widely by Endonucleolysis and Targets snoRNA Host Genes |
8.67 |
|
RNA-sequencing time course of Human Intestinal Epithelial Cells (HIECs) following knockdown of miR-30bcd using complementary locked nucleic acids |
8.62 |
|
Transcriptional profiling of JEG3 cells with HLA-G ablation via deletion of Enhancer L |
8.52 |
|
Genome-wide expression from the esophageal biopsies of subjects with and without eosinophilic esophagitis |
8.39 |
|
ATF7IP-mediated stabilization of the histone methyltransferase SETDB1 is essential for heterochromatin formation by the HUSH complex |
8.37 |
|
Assessing the impact of loss of ATF7IP and SETDB1 on the transcriptome |
8.37 |
|
Comparative total RNA and mRNA sequencing and systems analysis reveals nascent transcriptional response to early HIV-1 infection in a CD4+ T cell line |
8.33 |
|
Oncogenic Notch promotes long-range regulatory interactions within hyperconnected 3D cliques [HCC1599_RNA-seq] |
8.24 |
|
SREBP1 drives Keratin 80-dependent cytoskeletal changes and invasive behavior in endocrine resistant ERα breast cancer |
8.22 |
|
CircRNAome diversity in human mature B-cells, T-cells and monocytes |
8.11 |
|
A Unique Epigenomic Landscape Defines Human Erythropoiesis (RNA-seq) |
8.11 |
|
A Unique Epigenomic Landscape Defines Human Erythropoiesis |
8.11 |
|
SNHG12 knockdown in Human Umbilical Vein Cells under ROS conditions. |
8.02 |
|
p38 SAPK and SKIIP induced changes in alternative splicing patterns upon osmostress |
8.01 |
|
nELAVL HITS-CLIP in Alzheimer's Disease patients |
7.97 |
|
The landscape of alternative splicing in aggressive prostate cancers |
7.93 |
|
Treatment of multiple myeloma cells with EZH2 small molecule inhibitor |
7.86 |
|
Effects of Inhibition of CDK8/19 Mediator Kinase by Senexin B in HCT116 cells treated with or without TNF-alpha |
7.84 |
|
Transcriptomic analysis of trametinib-resistant HCT116 colorectal carcinoma cells compared to the parental control cells |
7.83 |
|
LIN28A modulates splicing and gene expression programs in breast cancer cells [RNA-Seq] |
7.82 |
|
LIN28A modulates splicing and gene expression programs in breast cancer cells |
7.82 |
|
Treatment of SW480 colon cancer cell induced xenografts with AZD and DBZ |
7.81 |
|
3’ Uridylation Expands miRNA Target Repertoire |
7.79 |
|
Image based identification and targeting of cancer stem cells in pancreatic adenocarcinoma (PDAC) |
7.76 |
|
Assembly of methylated LSD1 and CHD1 drives AR-dependent transcription and translocation |
7.74 |
|
Assembly of methylated LSD1 and CHD1 drives AR-dependent transcription and translocation [RNA-Seq] |
7.74 |
|
Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation |
7.73 |
|
HIV-1 perturbs homeostatic ILCs, unmasks ILC1 plasticity, and boosts TCF7+ memory NK cells |
7.66 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of Human Pluripotent Stem Cell-Derived Endocardial-like And Primary Cardiac Endothelial Cell Transcriptomes |
7.65 |
|
Transcriptional regulation in pluripotent stem cells by Methyl CpG binding protein 2 (MeCP2) |
7.64 |
|
Identification of Differentially Expressed Splice Variants by the Proteogenomic Pipeline Splicify |
7.6 |
|
Global transcriptional profiling changes upon knockout of USP22 in human Non-small cell lung cancer cells |
7.6 |
|
Systematic discovery of endogenous human ribonucleoprotein complexes |
7.57 |
|
Diffuse Large B Cell Lymphoma cell line with Acquired Resistance to PI3Kδ Inhibitor Idelalisib |
7.55 |
|
BRG1 governs Glucocorticoid Receptor interactions with chromatin and pioneer factors across the genome |
7.55 |
|
Nuclear import of the DSCAM-cytoplasmic domain drives signaling capable of inhibiting synapse formation |
7.54 |
|
LNCaP treated with iBET |
7.54 |
|
NR4A1 Inhibition Synergizes with Ibrutinib in Killing Mantle Cell Lymphoma Cells |
7.53 |
|
Genome-wide analysis of YAP and TFCP2 occupancy and regulated expression in liver cancer cells |
7.44 |
|
Genome-wide analysis of YAP and TFCP2 down-regulated genes in liver cancer cells |
7.44 |
|
TRIM24 is an oncogenic transcriptional co-activator of STAT3 in glioblastoma |
7.43 |
|
Major roles of cyclobutane pyrimidine dimers, nucleotide excision repair and ATR in the alternative splicing response to UV irradiation |
7.39 |
|
Expression data for KDM1B knockdown in Glioma-Initiating Cells (GICs) |
7.39 |
|
Tafazzin Regulates Cell State by Modulating Phosphatidylethanolamine and Phosphatidylserine levels |
7.37 |
|
The RNA-binding profile of Acinus, a peripheral component of the Exon junction complex, reveals its role in splicing regulation |
7.33 |
|
Overexpression of UGT2B17 in MEC1 and JVM2 leukemia cell lines |
7.31 |
|
The transcriptomic differences between Th1, Tr1, and Tneg cells in controlled human malaria infection |
7.25 |
|
Vitamin d receptor-mediated stromal reprogramming suppresses pancreatitis and enhances pancreatic cancer therapy |
7.24 |
|
Gene expression profiles of brain endothelial cells during embryonic development at bulk and single-cell levels |
7.22 |
|
FMRP facilitates the nuclear export of N6-methyladenosine-containing mRNAs |
7.16 |
|
SLIGRL-induced gene expression changes in NHEK cells |
7.15 |
|
Human cell line and subcutaneous tumor |
7.14 |
|
List of TIAM1 differentially expressed genes in SW620 cells [RNA-seq] |
7.13 |
|
The inhibitory effect of TIAM1 on TAZ transcriptional activity and TIAM1 differentially expressed genes |
7.13 |
|
Regulation of mRNA half-life by an inhibitor of human decapping enzyme Dcp2 following transcription shutoff in HEK293T cells |
7.09 |
|
HEK293 TFAM Knockout Expression Study |
7.02 |
|
Gene-Edited Human Kidney Organoids Reveal Mechanisms of Disease in Podocyte Development |
7.02 |
|
A global identification of PUM1 and PUM2 mRNA targets and their protein cofactors in human seminoma TCam-2 cells |
7.0 |
|
Expression profile of LNCaP/AR cells with or without HNF4G expression grown for long term in charcoal stripped-serum (CSS) media |
7.0 |
|
Effect of FGF13 depletion on the H460 cell line |
6.93 |
|
Characterizing the contrasting roles of JMJD3 and UTX histone demethylases in T cell acute lymphoblastic leukemia [short_hairpins_RNA-seq] |
6.92 |
|
Nickel induced transcriptional changes persist post exposure through epigenetic reprograming (RNA-seq dataset) |
6.87 |
|
RNA-Seq of Kaposi’s sarcoma reveal alterations in glucose and lipid metabolism |
6.83 |
|
Transcriptome-wide analysis links the short-term expression of the b isoforms of T-cell intracellular antigens to protective proteostasis-mediated survival and quiescence |
6.79 |
|
Hierarchy of mono- and bi-allelic TP53 alterations in Multiple Myeloma cell fitness |
6.79 |
|
Integrative analysis identifies targetable CREB1/FoxA1 transcriptional co-regulation as a predictor of prostate cancer recurrence |
6.78 |
|
The MLL-AF9 and MLL-AF4 oncofusion proteins bind a distinct enhancer repertoire and target the RUNX1 program in MLLr AML |
6.77 |
|
Biochemical fractionation of HEK293 nuclei and RNA-seq of chromatin-associated and soluble-nuclear RNA |
6.74 |
|
siRNA-mediated silencing of ORAI3 in MDA-MB-468 breast cancer cells exposed to hypoxia |
6.69 |
|
POU2AF1 Functions in the Human Airway Epithelium to Regulate Expression of Host Defense Genes |
6.68 |
|
POU2AF1 Functions in the Human Airway Epithelium to Regulate Expression of Host Defense Genes [RNA-Seq] |
6.68 |
|
Genome-wide view of the impact of Spt5-Pol II inhibitors (SPIs) on mRNA levels [RNA-Seq 24h] |
6.62 |
|
Expression data from A2780 cells treated with DMSO, Olaparib(Ola), Palbociclib(PD), and their combination (Ola/PD) |
6.6 |
|
RNA-seq data corresponding to: AZD4573 is a highly selective CDK9 inhibitor that suppresses Mcl-1 and induces apoptosis in hematological cancer cells |
6.58 |
|
Bromodomain protein BRD4 is a transcriptional repressor of autophagy and lysosomal function |
6.58 |
|
MYT1 attenuates neuroblastoma cell differentiation by inhibiting retinoic acid signaling pathway |
6.54 |
|
The RNA exosome nuclease complex regulates human embryonic stem cell differentiation [RNA-Seq rescue_SS] |
6.54 |
|
Effect of PBK knockdown on C4-2 cell transcriptome |
6.51 |
|
R430: A potent inbibitor of DNA and RNA viruses |
6.48 |
|
Genome-wide analysis of STAT3 in diffuse large B-cell lymphoma |
6.47 |
|
The pause-initiation limit restricts transcription activation in human cells |
6.42 |
|
RNA-sequencing experiment: Treatment of MCF-7 breast cancer cells with the novel small molecule ZNA |
6.41 |
|
BAF controls genome accessibility |
6.36 |
|
Cleavage Factor Im as a key regulator of 3’ UTR length |
6.34 |
|
Open chromatin mapping identifies transcriptional networks regulating human epididymis epithelial function |
6.33 |
|
Open chromatin mapping identifies transcriptional networks regulating human epididymis epithelial function [Rnase-Seq] |
6.33 |
|
Gene expression profiling of leukemia cells following asparagine depletion |
6.28 |
|
ADAR1-editing of cellular and measles virus-derived duplex RNA |
6.27 |
|
ADAR1-editing in HeLa, p150-KO and ADAR1-KO transcriptomes |
6.27 |
|
Effect of 48h treatment with 100nM GSK2879552 on T-ALL cell lines LOUCY and PEER |
6.25 |
|
Targeting Glioblastoma Stem Cells through Disruption of the Circadian Clock |
6.23 |
|
Targeting Glioblastoma Stem Cells through Disruption of the Circadian Clock [RNA-Seq] |
6.23 |
|
Epigenetic silencing of the tumor suppressor RASSF4 favors multiple myeloma progression |
6.16 |
|
Tumor suppressor SMARCB1 suppresses super-enhancers to govern hESC lineage determination |
6.07 |
|
Targeting Taxane-Platin Resistant Lung Cancers with JumonjiC Lysine Demethylase Inhibitors (RNA-Seq) |
6.06 |
|
Targeting Taxane-Platin Resistant Lung Cancers with JumonjiC Lysine Demethylase Inhibitors |
6.06 |
|
Transcriptome analysis of total RNA in human osteosarcoma cell line U2OS before and after inhibition of zinc finger protein ZNF768 |
6.04 |
|
Genome-wide discovery of human splicing branchpoints [RNAse] |
5.99 |
|
Stem cell and neurogenic gene-expression profiles link prostate basal cells to aggressive prostate cancer |
5.98 |
|
MOF acetyl transferase regulates transcription and respiration in mitochondria |
5.93 |
|
The Polycomb Repressor Complex 1 Drives Double-Negative Prostate Cancer Metastasis by Coordinating Stemness and Immune Suppression |
5.91 |
|
Parkinson’s Disease Genetic Risk in a Midbrain Neuronal Cell Line |
5.89 |
|
Epithelial-mesenchymal transition and acquired resistance to ALK inhibitors |
5.86 |
|
Gene expression profiling study by RNA-seq for identifying genes associated with epithelial-mesenchymal transition and acquired resistance to ALK inhibitors |
5.86 |
|
Regulation of Lipids is Central to Replicative Senescence |
5.83 |
|
Transcriptomic Reprogramming of Prostate Cancer Cells Driven by Stroma-Derived AREG |
5.82 |
|
UBR7 is a novel E3 ubiquitin ligase for H2BK120 and acts as a tumor-suppressor in breast cancer |
5.81 |
|
UBR7 is a novel E3 ubiquitin ligase for H2BK120 and acts as a tumor-suppressor in breast cancer [RNA-Seq] |
5.81 |
|
CD73 knockdown effect in pancreatic cancer cell lines |
5.79 |
|
O-GlcNAc transferase fine-tunes MYC-dependent transcription to promote cell cycle |
5.78 |
|
O-GlcNAc transferase fine-tunes MYC-dependent transcription to promote cell cycle [RNA-seq] |
5.78 |
|
mRNA recovered upon RNF219 IP. [RNA-IP] |
5.75 |
|
Quantitative Analysis of negative control and overexpression-TRIB1 in PC3 and DU145 Transcriptomes |
5.75 |
|
Chromatin-informed inference of transcriptional programs in gynecologic cancers |
5.74 |
|
Chromatin-informed inference of transcriptional programs in gynecologic cancers [RNA-Seq] |
5.74 |
|
CREB5 promotes resistance to androgen-receptor antagonists and androgen deprivation in prostate cancer |
5.73 |
|
Human embryonic stem cells in E8 and AKIT culture medium |
5.73 |
|
Growth factor-free, chemically-defined culture system for expansion and derivation of human pluripotent stem cells |
5.73 |
|
Comprehensive comparative analysis of RNA sequencing methods for degraded or low input samples |
5.72 |
|
Tracking distinct RNA populations using efficient and reversible covalent chemistry |
5.6 |
|
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 |
5.59 |
|
shRNA-mediated knockdown of ETV4 and MED25 in the prostate cell line PC3 reveals set of genes potentially coregulated by MED25 and ETV4 |
5.59 |
|
Targeted reactivation of FMR1 transcription in FXS embryonic stem cells |
5.59 |
|
CHD1 loss sensitizes prostate cancer to DNA damaging therapy by promoting error-prone double-strand break repair |
5.58 |
|
Determining mRNA half-lives on a transcriptome-wide scale |
5.58 |
|
RNA-sequencing transcriptome profiling of normal human keratinocytes differentiation |
5.58 |
|
RNA-sequencing of cells derived from the site of inflammation of Juvenile Idiopathic Arthritis patients |
5.58 |
|
Epigenetic profiling and RNA-sequencing of Juvenile Idiopathic Arthritits (JIA) patients |
5.58 |
|
RNA-seq of naive and primed ES cells (NHSM) |
5.58 |
|
Gene expression analysis of the impact of TDP-43 knockout in human cells. |
5.56 |
|
Three-dimensional disorganisation of the cancer genome occurs coincident with long range genetic and epigenetic alterations [RNA-seq] |
5.5 |
|
Three-dimensional disorganisation of the cancer genome occurs coincident with long range genetic and epigenetic alterations |
5.5 |
|
Selective expression of long non-coding RNAs in a breast cancer cell progression model |
5.48 |
|
Differential effects of estrogen receptor beta isoforms on glioblastoma progression |
5.44 |
|
Replicated transcriptome profiling of Normal and Cancerous Prostate Cells [RNA-Seq] |
5.44 |
|
Human co-transcriptional splicing kinetics and coordination revealed by direct nascent RNA sequencing |
5.41 |
|
ICE1 promotes the link between splicing and nonsense-mediated mRNA decay |
5.4 |
|
Distinct roles of cohesin-SA1 and cohesin-SA2 in 3D chromosome organization |
5.38 |
|
Genome wide association study of bone size yields eleven loci that also affect height, bone density, osteoarthritis and fractures |
5.38 |
|
Cooperation of GRSF1 and the mitochondrial degradosome (hSuv3-PNPase complex) in degradation of mitochondrial RNA |
5.38 |
|
RNAseq of T-ALL upon long non coding rna purturbation |
5.36 |
|
Glioma Stem Cell Specific Super Enhancer Drives Polyunsaturated Fatty Acid Synthesis to Support EGFR Signaling |
5.35 |
|
Uridylation-mediated RNA quality control pathway in mammalian cytoplasm [RNA-Seq] |
5.35 |
|
TUT-DIS3L2 is a mammalian surveillance pathway for aberrant structured non-coding RNAs. |
5.35 |
|
Next-generation sequencing of human dermal fibroblasts transdifferentiated towards the otic lineage |
5.33 |
|
Cockayne syndrome A and B proteins regulate the transcription arrest upon genotoxic stress through a ubiquitin/proteasome degradation process (RNA-seq) |
5.32 |
|
Cockayne syndrome A and B proteins regulate the transcription arrest upon genotoxic stress through a ubiquitin/proteasome degradation process |
5.32 |
|
The human cellular nucleic acid binding protien binds G-rich elements close to translation initiation sires and promotes translation. |
5.3 |
|
The human cellular nucleic acid binding protien binds G-rich elements close to translation initiation sires and promotes translation. [RNA-Seq] |
5.3 |
|
Treatment of prostate cancer cells with S-adenosylmethionine leads to genomewide alterations of transcription profiles |
5.2 |
|
MYCL and EP400 are required for Max and MCPyV mediated gene activation |
5.2 |
|
Strand-specific Dual RNA-seq of Bronchial Epithelial cells Infected with Influenza A/H3N2 Viruses Reveals Splicing of Gene Segment 6 and Novel Host-Virus Interactions |
5.17 |
|
The Polycomb protein BMI1 induces an invasive gene expression signature in melanoma that promotes metastasis and chemoresistance. |
5.16 |
|
Mapping interactions for the TNIP2 hub protein |
5.15 |
|
Splicing and epigenetic factors jointly regulate epidermal differentiation |
5.12 |
|
Comparison of expression profiles of APP-depleted prostate cancer cells (LNCaP) |
5.11 |
|
PT2385 HIF2A inhibitor treatment of patient derived orthotopic xenograft neuroblastoma cells in the presence or absence of hypoxia |
5.06 |
|
Transcriptome profiling of Normal and Cancerous Prostate Cells |
4.98 |
|
LIN28A Over-expression RNAseq |
4.96 |
|
mRNA Sequencing of Human PromoCells Using Random Primed mRNA-Sequencing Technique |
4.89 |
|
Developing a Novel Two-Dimensional Culture System to Enrich Human Prostate Luminal Progenitors That Can Function as a Cell of Origin for Prostate Cancer |
4.87 |
|
Tumor hypoxia causes DNA hypermethylation by reducing TET activity |
4.82 |
|
Tumor hypoxia causes DNA hypermethylation by reducing TET activity (RNA-Seq) |
4.82 |
|
Clinical and genomic crosstalk between glucocorticoid receptor and estrogen receptor α in endometrial cancer [RNA-seq] |
4.8 |
|
Clinical and genomic crosstalk between glucocorticoid receptor and estrogen receptor α in endometrial cancer |
4.8 |
|
Transcriptome of U251 cells overexpression complement component 7 |
4.78 |
|
The cohesin complex prevents Myc-induced replication stress |
4.75 |
|
Knockout human reveal an essential role for Paternally Expressed 10 (PEG10) in JEG3 cell line development |
4.72 |
|
Disease modelling of core pre-mRNA splicing factor haploinsufficiency |
4.7 |
|
Chromatin remodeling mediated by ARID1A is indispensable for normal hematopoiesis in mice (human RNA-Seq) |
4.66 |
|
Small molecule targets TMED9, promotes lysosomal degradation to reverse proteinopathy |
4.66 |
|
Integrated Profiling of mRNAs and microRNAs to Identify Potential Biomarkers for Oral Malignant Transformation [mRNA-Seq] |
4.64 |
|
Integrated Profiling of mRNAs and microRNAs to Identify Potential Biomarkers for Oral Malignant Transformation |
4.64 |
|
RNASeq of 4SU labelled nascent RNA in MV4;11 cell treated with DMSO, I-BET, SGC0946 and combination of I-BET and SGC0946 |
4.59 |
|
FOXA1 upregulation promotes enhancer and transcriptional reprogramming in endocrine-resistant breast cancer [RNA-seq] |
4.58 |
|
FOXA1 upregulation promotes enhancer and transcriptional reprogramming in endocrine-resistant breast cancer |
4.58 |
|
RBM25 is a global splicing factor promoting inclusion of alternatively spliced exons |
4.55 |
|
Ets homologous factor has critical roles in epithelial dysfunction in airway disease [RNA-seq] |
4.54 |
|
Ets homologous factor has critical roles in epithelial dysfunction in airway disease |
4.54 |
|
Cajal bodies are linked to genome conformation |
4.52 |
|
Cajal bodies are linked to genome conformation [RNA-Seq] |
4.52 |
|
Grainyhead-like 2 is essential for androgen receptor expression and activity in prostate cancer |
4.51 |
|
Grainyhead-like 2 is essential for androgen receptor expression and activity in prostate cancer (RNA-seq) |
4.51 |
|
U2AF1 mutations alter splice site recognition in hematological malignancies |
4.48 |
|
Transcription factor p63 bookmarks genomic loci in epithelial cells and regulates a subset of target genes during epidermal differentiation through dynamic enhancers |
4.46 |
|
Transcription factor p63 bookmarks genomic loci in epithelial cells and regulates a subset of target genes during epidermal differentiation through dynamic enhancers (RNA-Seq) |
4.46 |
|
Long non-coding RNA SMILR regulates genes involved in cytokinesis in human vascular smooth muscle cell |
4.45 |
|
Integrin signaling regulates YAP/TAZ to control skin homeostasis |
4.42 |
|
5hmC dynamically correlated with enhancer's activities during hES-to-Pancreatic endoderm cell differentiation |
4.42 |
|
5hmC dynamically correlated with enhancer's activities during hES-to-Pancreatic endoderm cell differentiation (RNA-Seq) |
4.42 |
|
Investigation into human Tra2 protein-dependent splicing in MDA-MB-231 cells using iCLIP and RNA-seq |
4.39 |
|
Interactions of aCPs with Cytosine-rich Polypyrimidine Tracts Enhance Splicing of Cassette Exons |
4.36 |
|
DART-seq: an antibody-free method for global m6A detection |
4.3 |
|
Gene expression analysis of C4-2 cells treated with ACLY inhibitor and Enzalutamide |
4.29 |
|
Determination of a comprehensive alternative splicing regulatory network and the combinatorial regulation by key factors during Epithelial-to-Mesenchymal Transition [RBM47 KD] |
4.29 |
|
mRNA profiles of JMJD3 overexpression- and JMJD3 knockout- HL-60 cells |
4.25 |
|
Identification of altered developmental pathways in human juvenile HD iPSC with 71Q and 109Q using transcriptome profiling |
4.24 |
|
Selective Inhibition of the Second Bromodomain of BET Family Maintains Anti-Tumor Efficacy and Improves Tolerability |
4.24 |
|
Selective Inhibition of the Second Bromodomain of BET Family Maintains Anti-Tumor Efficacy and Improves Tolerability (22RV1 RNA-seq) |
4.24 |
|
RNA-sequencing analysis examining how the Vibrio cholerae MARTX toxin and its inidividual effector domains modulate the transcriptome of human intestinal epithelial cells. |
4.19 |
|
Analysis of regulatory element evolution between human and mouse reveals a lack of cis-trans compensation |
4.16 |
|
Direct identification of endogenous SMG6 targets and a preferred motif spanning SMG6 cleavage sites by parallel analysis of RNA ends in human cells |
4.13 |
|
Targeting the androgen receptor N-terminus via the cochaperone Bag-1L [RNA-seq C-terminal mutant] |
4.12 |
|
Luminal subtype-specific circRNAs in breast cancer cells by a novel tool for external data analysis. |
4.1 |
|
Transriptional profiling upon heat shock and recovery in cells deficient for FBXW7 and their wild type counterpart. |
4.07 |
|
FBXW7 modulates stress response by post-translational modification of HSF1 |
4.07 |
|
Transcriptional Profiling of CENPA-Depleted Prostate Cancer Cell Lines |
4.06 |
|
CENPA-Bound Genes and Transcriptional Profiling of CENPA-Depleted Prostate Cancer Cells |
4.06 |
|
HNRNPM-regulated splicing dependencies in prostate cancer |
4.06 |
|
HNRNPM-regulated splicing dependencies in prostate cancer [RNA-Seq] |
4.06 |
|
Mutually Exclusive CBC-Containing Complexes Contribute to RNA Fate. |
4.03 |
|
CDK4/6 inhibitor resistance in prostate cancer |
4.01 |
|
RNA-sequencing analysis of glucose and acetate regulated transcripts in glioblastoma cells |
4.0 |
|
Bioreactor-engineered cancer tissues mimic phenotypes, gene expression profiles and drug resistance mechanisms detectable in xenografts and clinical specimens. |
3.92 |
|
N6-methyladenine DNA Modification in Glioblastoma [RNA-seq] |
3.89 |
|
N6-methyladenine DNA Modification in Glioblastoma |
3.89 |
|
A SRp55-regulated alternative splicing network controls pancreatic beta cell survival and function |
3.88 |
|
Determination of tRNA aminoacylation levels by high throughput sequencing |
3.86 |
|
lncRNA-PCAT1 knockdown effect on the gene expression of androgen independent LNCaP (LNCaP-AI) cell line |
3.84 |
|
Epigenome Editing by a CRISPR/Cas9-Based Acetyltransferase Activates Genes from Promoters and Enhancers |
3.83 |
|
Transcriptome analysis upon C6orf203 silencing |
3.8 |
|
Effect of CHKA knockdown on C4-2 cell transcriptome |
3.73 |
|
Characterization and therapeautic application of mesenchymal stem cells with neuromesodermal origin from human pluripotent stem cells |
3.67 |
|
RNA-sequencing analysis for gene expression profiles affected by CASC9 knockdown |
3.61 |
|
Proteostasis by STUB1/HSP70 complex controls sensitivity to androgen receptor targeted therapy in advanced prostate cancer (RNA-Seq) |
3.58 |
|
Proteostasis by STUB1/HSP70 complex controls sensitivity to androgen receptor targeted therapy in advanced prostate cancer |
3.58 |
|
Integrated multi-omics approach reveals a role of ALDH1A1 in lipid metabolism in human colon cancer cells |
3.56 |
|
Anti-Inflammatory Effects of Budesonide in Human Fetal Lung |
3.56 |
|
Non-transmissible measles virus vector with segmented RNA genome establishes different types of iPSCs from hematopoietic cells |
3.54 |
|
Cap-specific terminal N6-methylation of RNA by an RNA polymerase II-associated methyltransferase. |
3.52 |
|
RNA-Seq analysis of prostate cancer cell line LNCaP treated with vehicle, androgen, androgen and IMTPPE, androgen and JJ-(+)-450, androgen and JJ-(-)450, androgen and enzalutamide |
3.47 |
|
SLAM-seq for K562 endogenous mRNA decay |
3.45 |
|
The splicing factor RBM25 controls MYC activity in Acute Myeloid Leukemia |
3.41 |
|
RB tumor suppressor promotes cancer immunity through downregulating PD-L1 expression |
3.41 |
|
Oncogenic roles of ARID5B in T-ALL |
3.39 |
|
RNA-seq analysis in knockdown Jurkat samples for each factor of TAL1 complex |
3.39 |
|
Differential Protein Occupancy Profiling of the mRNA Transcriptome |
3.36 |
|
Expression analysis of PC3 cells treated with scramble AON or AON directed against MBNL1 |
3.28 |
|
Identification of HOXB13 target genes responsive to BET inhibitors |
3.16 |
|
PRDM1 inhibits proliferation of human colon cancer organoids |
3.14 |
|
The circadian transcriptional landscape in primary human mammary epithelial cells |
3.13 |
|
Transient stabilization, rather than inhibition of MYC amplifies extrinsic apoptosis and therapeutic responses in refractory B-cell lymphoma |
3.12 |
|
The cytokine environment influence on human skin-derived T cells |
3.11 |
|
Gene expression profiling of neural crest progenitor cultures derived from human embryonic stem cells carrying nonsense mutations in the Polycomb gene ASXL1 [HOM] |
3.09 |
|
Discovery of Drug Candidates that Inhibit and Eliminate Zika Virus Infection in Fetal and Adult Brain |
3.07 |
|
DNMT1-associated long non-coding RNA regulate global gene expression and DNA methylation in colon cancer |
3.07 |
|
RNA-Seq and ChIP-Seq reveals SQSTM1/p62 as a key mediator of JunB suppression of NF-kB-dependent inflammation |
2.98 |
|
JunB control of keratinocyte-mediated inflammation [RNA-seq] |
2.98 |
|
JAG1 Mediated Notch Signaling Regulates Secretory Cell Differentiation of the Human Airway Epithelium |
2.97 |
|
Widespread backtracking by RNA pol II is a major effector of gene activation, 5’ pause release, termination and transcription elongation rate |
2.91 |
|
mRNA-seq from Nutlin-3a, doxorubicin, and DMSO treated HCT116 p21-/- cells |
2.84 |
|
Activation of the p53 transcriptional program sensitizes cancer cells to Cdk7 inhibitors |
2.83 |
|
Epigenetic reprogramming of melanoma cells by vitamin C treatment |
2.82 |
|
A rare subpopulation of melanoma cells with low expression of metastasis suppressor NME1 has a neural crest-like phenotype and is highly metastatic in vivo |
2.78 |
|
Chemotherapeutic drugs inhibiting Topoisomerase 1 activity inhibit TNF-induced inflammatory gene expression |
2.77 |
|
Direct Isolation and Characterization of Human Nephron Progenitors. |
2.7 |
|
Systematic Functional Dissection of Common Genetic Variation Affecting Red Blood Cell Traits |
2.66 |
|
Systematic Functional Dissection of Common Genetic Variation Affecting Red Blood Cell Traits [mRNA-Seq] |
2.66 |
|
Regulation of the glucocorticoid receptor via a BET-dependent enhancer drives antiandrogen resistance in prostate cancer |
2.66 |
|
Small-molecule targeting of brachyury transcription factor addiction in chordoma [rnaseq_compound] |
2.65 |
|
pSILAC mass spectrometry reveals ZFP91 as novel IMiD dependent substrate of the CRL4CRBN ligase |
2.62 |
|
Unbiased evaluation of cell-free amniotic fluid transcriptome of term and preterm infants to detect fetal maturity |
2.6 |
|
Transcriptome-wide identification of CELF2 functional targets in T cells |
2.58 |
|
Transcriptional regulation of autophagy-lysosomal function in BRAF-driven melanoma progression and chemoresistance |
2.55 |
|
Azithromycin induces epidermal differentiation and multivesicular bodies in airway epithelia |
2.54 |
|
RNA sequencing, chromatin accesibility and ChIP seq analysis of BAP1 -/- human liver organoids |
2.54 |
|
Effect of low-dose sorafenib and alkylating agents in inflammation and angiogenesis in breast cancer |
2.49 |
|
A MYC/GCN2/eIF2alpha negative feedback loop limits protein synthesis to prevent MYC-dependent apoptosis in colorectal cancer |
2.42 |
|
Global loss of epigenetic and transcriptional fidility defines a subclass of cancer with immunotherapy resistance |
2.38 |
|
Histone deacetylase inhibition enhances antimicrobial peptide but not inflammatory cytokine expression upon bacterial challenge |
2.34 |
|
RNA sequencing of human mammary epithelial cells |
2.31 |
|
An Argonaute phosphorylation cycle promotes microRNA-mediated silencing [whole transcriptome RNA-seq] |
2.3 |
|
Estrogen-independent molecular actions of mutant estrogen receptor alpha in endometrial cancer [RNA-seq] |
2.27 |
|
Estrogen-independent molecular actions of mutant estrogen receptor alpha in endometrial cancer |
2.27 |
|
Ewing sarcoma resistance to SP-2509 is not mediated through KDM1A/LSD1 mutation II |
2.16 |
|
The cohesin release factor WAPL restricts chromatin loop extension. |
2.15 |
|
The cohesin release factor WAPL restricts chromatin loop extension. [RNA-Seq] |
2.15 |
|
Modeling genome-wide transcriptional cis-regulation in n LNCaP-abl cell line after siRNA knock down of a series of gene factors [RNA-seq] |
2.12 |
|
TOP2B disturbed the quality of human oocytes with advanced maternal age |
1.99 |
|
Locally transplanted human urine-induced nephron progenitor cells contribute to renal repair in mice kidney with diabetic nephropathy |
1.96 |
|
HLA peptides derived from tumor antigens induced by inhibition of DNA methylation for development of drug-facilitated immunotherapy |
1.87 |
|
Genes altered in expression by Cisplatin treatment in lung cancer cell lines |
1.87 |
|
MLL-AF4 Spreading Identifies Binding Sites that Are Distinct from Super-Enhancers and that Govern Sensitivity to DOT1L Inhibition in Leukemia. |
1.86 |
|
KAP1 regulates ERVs in differentiated human cells and contributes to innate immune control |
1.86 |
|
SPOP mutation confers intrinsic BET inhibitor resistance in prostate cancer |
1.82 |
|
Specific labeling of stem cell activity in human colorectal organoids using an ASCL2-responsive minigene |
1.81 |
|
Recapitulating and Deciphering Tumor-stroma Microenvironment by Using a “LEGO” like 3D printed microfluidic device |
1.78 |
|
The NFkB subunit RELA is a master transcriptional regulator of the committed epithelial-mesenchymal transition in airway epithelial cells |
1.77 |
|
CDK12 mediated transcriptional regulation in U2OS cells |
1.69 |
|
Truncation of LOC100288798 (SLC38A4-AS) lncRNA in human haploid KBM7 cell line |
1.68 |
|
Investigsting the role of NF-ĸB p50 S80 phosphorylation in regulating TNFα-induced transcription in HEK293T cells |
1.63 |
|
Genome-wide modelling of transcription kinetics reveals patterns of RNA processing delays |
1.62 |
|
Epigenome Editing by CRISPR/Cas9 Repressors for Silencing of Distal Regulatory Elements |
1.6 |
|
4sUDRB-seq: measuring transcription elongation and initiation genomewide |
1.57 |
|
Single cell analysis of HSV-1 infection reveals anti-viral and developmental programs are activated in distinct sub-populations with opposite outcomes |
1.51 |
|
Long non-coding RNA expression profile associated with malignant progression of oral submucous fibrosis |
1.49 |
|
RNA binding protein CPEB1 remodels host and viral RNA landscapes [RNA-Seq] |
1.43 |
|
Gene expression profile of CRC-derived HILEC |
1.36 |
|
ERK signaling regulates opposing functions of JUN family transcription factors in prostate cancer cell migration |
1.35 |
|
Global transcriptome analysis of WT versus HEB-/- hESCs |
1.29 |
|
Generation of KRAS signatures using immortalized isogenic lung cells. |
1.29 |
|
Expression analysis of genes modulated after knock-down of lncRNA CHROME. |
1.28 |
|
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. |
1.26 |
|
Methylation DNA mediated KLF4 binding activity in glioblastoma cells |
1.25 |
|
Unbiased identification of trans regulators of ADAR and A-to-I RNA editing |
1.25 |
|
Identification of trans regulators of ADAR and A-to-I RNA editing using RNA-seq |
1.25 |
|
RNA sequencing of MDA-MB231 and U2OS cancer cell lines exposed to the alkylating agent methyl methanesufonate (MMS) and classical chemotherapeutics |
1.15 |
|
RG/RGG boxes are common binding motifs in RNA-G-quadruplex-interacting proteins |
1.09 |
|
Gene expression profiling of neural crest progenitor cultures derived from human embryonic stem cells carrying nonsense mutations in the Polycomb gene ASXL1 |
1.09 |
|
Integrated epigenomic and transcriptomic profiling of terminal human erythropoiesis [TMCC2] |
1.09 |
|
CD48-dependent protective autophagy in conventional human T cells promotes restimulation-induced cell death resistance |
0.97 |
|
CNOT1 and Transcriptomic Landscape of a HeLa Cell Line |
0.93 |
|
Next Generation Sequencing (RNA-Sequencing) for the analysis of RUNX3 targets in H460, H460-ERT2-RUNX3 WT and H460-ERT2-RUNX3 MT(K94/171R mutation) |
0.86 |
|
C19ORF66 broadly escapes viral-induced endonuclease cleavage and restricts Kaposi’s Sarcoma Associated Herpesvirus (KSHV) |
0.8 |
|
RNA-sequencing of tamoxifen-resistant and -sensitive breast cancer cell lines. |
0.79 |
|
eVIP2: Expression-based variant impact phenotyping to predict the function of gene variants |
0.77 |
|
Human Adult Sorted Live Cell Erythroblasts RNA-Seq. |
0.76 |
|
Modulation of nonsense-mediated decay by rapamycin |
0.71 |
|
Small-molecule targeting of brachyury transcription factor addiction in chordoma |
0.7 |
|
Single-cell RNAseq analysis of the empty and i8TF cell lines after 3 days of BL-CFC culture |
0.66 |
|
Single cell transcriptomics reveals new insights on the dynamical function of transcription factors during blood stem and progenitor cell formation |
0.66 |
|
Human Treg IFNg/IL-10 subpopulations |
0.65 |
|
Oncogenic Antisense LncRNA P14AS Regulates Expression of ANRIL through AUF1 Binding |
0.64 |
|
WNT signaling memory is required for ACTIVIN to function as a morphogen |
0.64 |
|
Transcriptomic Alterations in Lung Adenocarcinoma Unveil New Mechanisms Targeted by the TBX2 Subfamily of Tumor Suppressor Genes |
0.61 |
|
Integrative classification of human coding and non-coding genes based on RNA metabolism profiles |
0.6 |
|
rG4-seq reveals widespread formation of G-quadruplex structures in the human transcriptome |
0.58 |
|
Defective transcription elongation in a subset of cancers confers immunotherapy resistance (human cell lines RNA-Seq) |
0.55 |
|
RNA-Seq of CD4+ T cells treated with AS1842856 or DMSO |
0.53 |
|
Genome-wide maps of WT and over-expressing CenH3/CENP-A in Human HeLa S3 cells |
0.52 |
|
CRISPR Display: A modular method for locus-specific targeting of long noncoding RNAs and synthetic RNA devices in vivo [RNA-Seq] |
0.51 |
|
CRISPR Display: A modular method for locus-specific targeting of long noncoding RNAs and synthetic RNA devices in vivo |
0.51 |
|
Profiling of protrusion-enriched RNAs from human breast cancer cell line MDA-MB-231 |
0.51 |
|
Gene expression changes due to PARP knockdown in human cells |
0.48 |
|
Gene expression profiling by RNA-seq in hTert-HME1 cell line treated with control or BRCA2 siRNAs and grown with or without EGF (epithelial growth factor) II |
0.45 |
|
Hypoxic transcriptome of SQ20B human head and neck cancer cells |
0.44 |
|
A Non-Canonical Nuclear Activity Triggered by Small RNAs and Argonaute Proteins in Human Cells |
0.44 |
|
Effect of estrogen (E2) treatment on the C4-12 relative to the MCF7 cells |
0.42 |
|
Transcriptional changes after overexpression of proliferation drivers in human mammary epithelial cells. |
0.41 |
|
Cooptation of tandem DNA repeats for the control of epithelial-to-mesenchymal transition. |
0.41 |
|
Cooptation of tandem DNA repeats for the control of epithelial-to-mesenchymal transition [RNA-Seq] |
0.41 |
|
ARS2 is a general suppressor of pervasive transcription [RNAseq] |
0.38 |
|
A compendium of promoter-centered long-range chromatin interactions in diverse human tissues and cell types |
0.37 |
|
YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction. |
0.31 |
|
YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction [RNA-seq] |
0.31 |
|
RNA-Seq of SLNCR1 over-expression in the melanoma cell line A375 |
0.3 |
|
Risk SNPs mediated promoter-enhancer switching promotes prostate cancer progression through lncRNA PCAT19 |
0.25 |
|
Risk SNPs mediated promoter-enhancer switching promotes prostate cancer progression through lncRNA PCAT19 (RNA-seq data sets) |
0.25 |
|
Transcriptomic analysis of LSD1 |
0.2 |
|
Primate-specific gene TMEM14B promotes cortical expansion and folding |
0.19 |
|
HBEC-shp53-PCHD7 |
0.19 |
|
Quantitative mass spectrometry-based proteomics reveals the dynamic protein landscape during initiation of human Th17 cell polarization |
0.13 |
|
An intramolecular salt bridge linking TDP43’s RNA recognition motifs dictates RNA binding, protein stability and TDP43-dependent neurodegeneration |
0.13 |
|
RNA-sequencing of mRNAs from control and CAP-D3 deficient Salmonella infected HT-29 cells |
0.1 |
|
Characterisation of the EZH2 regulated transcriptome in de novo transformed cells (RNA-Seq) |
0.05 |
|
The Small Molecule ISRIB Reverses the Effects of eIF2α Phosphorylation on Translation and Stress Granule Assembly |
0.04 |
|
Targets mediated microRNA arm-imbalance promotes gastric cancer progression [lncRNA] |
0.01 |