|
MeRIP-seq for heat shock in B-cell lymphoma cells |
70.75 |
|
A systematic analysis of nuclear heat-shock protein 90 identifies a metazoan-specific regulatory module |
57.04 |
|
4sU-seq of HFF exposed to salt and heat stress |
56.8 |
|
Transcriptome analysis in Neobractatin treated cells |
37.02 |
|
Genome-wide analysis of YAP and TFCP2 down-regulated genes in liver cancer cells |
33.6 |
|
Genome-wide analysis of YAP and TFCP2 occupancy and regulated expression in liver cancer cells |
33.6 |
|
Studying iPSCs from a hibernating mammal reveals molecular mechanisms of cold resistance in neural tissues |
32.99 |
|
Adaptation of a RAS pathway activation signature from FF to FFPE tissues in colorectal cancer (FFPE RNA-Seq II) |
31.38 |
|
The bromodomain protein BRD4 regulates splicing during heat shock |
28.08 |
|
Development of a selective CDK9 degrader from a multi-targeted CDK inhibitor |
21.55 |
|
Development of a selective CDK9 degrader from a multi-targeted CDK inhibitor [RNA-seq] |
21.55 |
|
Genome-wide view of the impact of Spt5-Pol II inhibitors (SPIs) on mRNA levels [RNA-Seq 2h] |
19.42 |
|
Activation of HOTTIP lncRNA perturbs HSC function leading to AML like disease |
17.72 |
|
Distinct regulation of alternative polyadenylation and gene expression by nuclear poly(A) polymerases |
15.78 |
|
Isolation and Transcriptome Analyses of Human Erythroid Progenitors: BFU-E and CFU-E |
14.9 |
|
A critical but divergent role of PRDM14 in human primordial germ cell fate revealed by inducible degrons [RNA-seq] |
14.33 |
|
A critical but divergent role of PRDM14 in human primordial germ cell fate revealed by inducible degrons |
14.33 |
|
Proteinase-Activated Receptor 4 (PAR4) mediates cell membrane blebbing in a Gaq/11, Gai independent, RhoA and ß-arrestin-dependent manner. |
14.26 |
|
Characterization of human mosaic Rett syndrome brain tissue by single-nucleus RNA sequencing |
14.21 |
|
24hr CA treatment vs. DMSO in HCT116 cells (from 'Identification of CDK8 and CDK19 substrates in human cells using cortistatin A and quantitative phosphoproteomics') |
14.21 |
|
Global analysis of pre-mRNA subcellular localization upon splicing inhibition by spliceostatin A |
14.2 |
|
Mitochondrial unfolded protein response controls matrix pre-RNA processing and translation |
14.02 |
|
Grainyhead-like 2 is essential for androgen receptor expression and activity in prostate cancer (RNA-seq) |
14.01 |
|
Grainyhead-like 2 is essential for androgen receptor expression and activity in prostate cancer |
14.01 |
|
Expression profile of Lo19S state cells in the presence and absence of bortezomib treatment |
13.85 |
|
mRNA expression profiling in MDA-MB-231 (LM1) cells with a tet-incible MBD2 or p66α knock down, or treated with MBD2-targeting small molecule ABA or APC |
13.58 |
|
WNK1 kinase and the termination factor PCF11 connect nuclear mRNA export with transcription |
13.56 |
|
High throughput characterization of the m6A demethylase FTO by CLIP and RNAseq |
13.48 |
|
RNAseq of HEK293 cells after Chtop knockdown |
13.39 |
|
Co-transcriptional loading of RNA export factors shapes the human transcriptome |
13.39 |
|
SPOP mutation confers intrinsic BET inhibitor resistance in prostate cancer (BRD4_JQ1_RNA-seq) |
13.22 |
|
hnRNP C is a key regulator of protein synthesis in mitosis |
13.13 |
|
KLF6-dependent transcription in renal cancer cells |
12.89 |
|
Seletive inhibition of CDK9 in DLBCL cell lines |
12.85 |
|
Global analysis of enhancer targets: Mosaic-seq |
12.81 |
|
Gene expression profiling study by RNA-seq for identifying genes associated with epithelial-mesenchymal transition and acquired resistance to ALK inhibitors |
12.35 |
|
Epithelial-mesenchymal transition and acquired resistance to ALK inhibitors |
12.35 |
|
Identification of genes regulated by Long noncoding RNA H19 in hepatic cells |
12.27 |
|
H19 regulates hepatic glucose production by epigenetic modification of Hnf4* |
12.27 |
|
PolyA-sequencing in IMR-32 cells treated with THZ531 or DMSO |
12.04 |
|
Depicting early human development and germ cell origin with porcine embryos |
11.88 |
|
β-catenin/Tcf7l2 dependent transcriptional regulation of GLUT1 gene expression by Zic family proteins in colon cancer |
11.86 |
|
Transcriptome-wide study of the response of human trabecular meshwork cells to the substrate stiffness increase |
11.8 |
|
Sequencing Universal Human Reference RNA by Smart-seq and early barcoding library preparation methods |
11.72 |
|
Polysome-associated mRNA profiling of cancer cells in response to CXCL12 and IGF1 |
11.6 |
|
Improved genome-wide mapping of uncapped and cleaved transcripts in eukaryotes—GMUCT 2.0 |
11.54 |
|
Expression data from A2780 cells treated with DMSO, Olaparib(Ola), Palbociclib(PD), and their combination (Ola/PD) |
11.37 |
|
FOXD3 is a novel tumor suppressor in lung cancer |
11.34 |
|
Differential roles of human PUS10 in miRNA processing and tRNA pseudouridylation |
11.29 |
|
The comparison of high-throughput single-cell RNA-seq methods |
11.25 |
|
MenSCs inhibit HCC growth through oncogenic pathway suppression via regulating 5-hmC in enhancer elements [RNA-seq] |
11.1 |
|
MenSCs inhibit HCC growth through oncogenic pathway suppression via regulating 5-hmC in enhancer elements |
11.1 |
|
AMPK signaling for naïve pluripotency [Hs] |
11.09 |
|
AMPK signaling for naïve pluripotency |
11.09 |
|
Gene expression profiling of leukemia cells following asparagine depletion |
10.97 |
|
‘Naïve’ ESRRB+ iPSCs with the capacity for rapid neural differentiation |
10.86 |
|
Wnt addiction of genetically defined cancers reversed by PORCN inhibition |
10.62 |
|
RNA-seq in transgenic cells |
10.61 |
|
Expression by CD133+ cells isolated from the adult human exocrine pancreas |
10.26 |
|
Trans-differentiation of human adult peripheral blood T cells into neurons |
10.13 |
|
Identification of transcription start sites for human A549 cell line using ReCappable-seq |
10.11 |
|
Gene expression changes in THP1 cells at day 2 and 4 following shRNA knock-down of RUVBL2 |
10.06 |
|
Transcriptional profile in human S. haematobium infection |
9.91 |
|
RNA-seq analysis of A2780 and OVCAR3 human ovarian cancer cell lines after overexpression of collagen type XI alpha 1 (COL11A1) |
9.84 |
|
Transcriptome analysis of human immortilized astrocytes reprogrammed into dopaminergic neurons |
9.83 |
|
Transcriptional change of THP-1 after HSV-1UL37WT or HSV-1UL37C819S |
9.81 |
|
RNA-seq analysis reveals profound changes in transcript profiles between siCon- and siH19-transfected uterine smooth muscle cells (USMC) |
9.73 |
|
DHX15 regulates CMTR1-dependent gene expression and cell proliferation |
9.62 |
|
TRIM28 interacts with EZH2 and SWI/SNF to activate genes that promote mammosphere formation |
9.53 |
|
Spliceosomal disruption of the non-canonical BAF complex in cancer |
9.41 |
|
The regulation of ferroptosis by TAZ in epithelial ovarian cancer |
9.4 |
|
Inducible three-factor direct reprogramming to nephron progenitors using piggyBac transposons |
9.37 |
|
Splicing towards noncoding isoforms in colorectal carcinoma is associated with tumor hypoxia and the DNA damage response |
9.36 |
|
The cohesin complex prevents Myc-induced replication stress |
9.26 |
|
Single-cell RNA sequencing-based CRISPRi screening resolves molecular drivers of early human endoderm development [set 1] |
9.23 |
|
Treatment of SW480 colon cancer cell induced xenografts with AZD and DBZ |
9.2 |
|
Tracking distinct RNA populations using efficient and reversible covalent chemistry |
9.19 |
|
Transriptional profiling upon heat shock and recovery in cells deficient for FBXW7 and their wild type counterpart. |
9.09 |
|
FBXW7 modulates stress response by post-translational modification of HSF1 |
9.09 |
|
A non-catalytic function of carbonic anhydrase IX contributes to the glycolytic phenotype and pH regulation in human breast cancer cells |
9.08 |
|
Species-specific maturation profiles of human, chimpanzee and bonobo neural cells |
8.96 |
|
Single-cell transcription profiling in KS1 patient iPSCs and NPCs |
8.95 |
|
Precise Gene Editing Preserves Hematopoietic Stem Cell Function Following Transient p53-Mediate DNA Damage Response |
8.87 |
|
IQGAP3 interacts with Rad17 to activate the MRN/ATM/Chk2 signaling and promote radioresistance in lung cancer |
8.86 |
|
The SPOP-containing Complex Functions as an E3 Ligase for SETD2 to Regulate Gene-Specific H3K36me3-Coupled Alternative Splicing |
8.84 |
|
Effect of REST on cancer invasiveness in MCF-7 and MDA-MB-231 cells using RNA-sequencing (RNA-seq) analysis . |
8.76 |
|
Nuclear import of the DSCAM-cytoplasmic domain drives signaling capable of inhibiting synapse formation |
8.74 |
|
Effect of 48h treatment with 100nM GSK2879552 on T-ALL cell lines LOUCY and PEER |
8.74 |
|
LncRNA-GAS5 negative regulation of YAP-target genes expression |
8.73 |
|
Selectively targeting bromodomain and extraterminal proteins for degradation as a novel anti-glioblastoma strategy [RNA-seq] |
8.64 |
|
RNA-Seq to assess the transcriptional effects of G quadruplex stabilization by the G4 ligand PhenDC3 in HT-1080 cells |
8.62 |
|
TRIM28-Regulated Transposon Repression Is Required for Human Germline Competency and Not Primed or Naive Human Pluripotency |
8.52 |
|
Whole Transcriptomic Sequencing of Metastatic Castration Resistant Prostate Cancer Samples |
8.5 |
|
Gene expression profile of multiple myeloma cell lines treated with CB-5083 |
8.49 |
|
ARID1A loss impairs enhancer-mediated gene regulation and drives colon cancer in mice |
8.42 |
|
ARID1A loss impairs enhancer-mediated gene regulation and drives colon cancer in mice [HCT116_RNA-seq] |
8.42 |
|
Transcriptional profiling of microglia; current state of the art and future perspectives |
8.41 |
|
Alternative splicing of differentiated myeloid cell transcripts after infection by Anaplasma phagocytophilum impacts a selective group of cellular programs |
8.36 |
|
RNA-seq of naive and primed ES cells |
8.25 |
|
The long non-coding RNA MALAT1 contributes to the pathogenesis of multiple sclerosis through alternative splicing and backsplicing regulation |
8.23 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of miR-29b-1 and miR-29a targets in tamoxifen-sensitive and tamoxifen-resistant human breast cancer cells |
8.22 |
|
Biochemical fractionation of HEK293 nuclei and RNA-seq of chromatin-associated and soluble-nuclear RNA |
8.2 |
|
Open chromatin mapping identifies transcriptional networks regulating human epididymis epithelial function [Rnase-Seq] |
8.18 |
|
Open chromatin mapping identifies transcriptional networks regulating human epididymis epithelial function |
8.18 |
|
RNA-dependent RNA polymerase sequence specificities of capsnatching viruses are tailored to aid viral replication |
8.16 |
|
Transcriptome-wide analysis of the role of HTLV-1 Tax PBM in T-Cells from infected humanized-mice (hu-Mice) |
8.15 |
|
MDM2 and MDM4 are Therapeutic Vulnerabilities in Malignant Rhabdoid Tumors |
8.14 |
|
A damaged genome's transcriptional landscape through multilayered expression profiling around in situ-mapped DNA double-strand breaks |
8.04 |
|
Pitfalls in Single Clone CRISPR-Cas9 Mutagenesis to Fine-map Regulatory Intervals |
7.99 |
|
Differential expression of genes in AD169-infected MRC5. |
7.96 |
|
Widespread N6-methyladenosine-dependent RNA Structural Switches Regulate RNA-Protein Interactions |
7.89 |
|
Inhibition of SF3B1 by molecules targeting the spliceosome in Rh18 cells |
7.87 |
|
RNAseq to determine gene expression changes following depletion of SETDB1 in THP-1 AML Cells |
7.87 |
|
DNMT and HDAC inhibitors globally induce cryptic TSSs encoded in long terminal repeats |
7.83 |
|
Comparative principles of DNA methylation reprogramming during human and mouse in vitro primordial germ cell specification [Mouse and Human RNA-seq and BS-seq] |
7.83 |
|
Comparative principles of DNA methylation reprogramming during human and mouse in vitro primordial germ cell specification |
7.83 |
|
Diverse AR-V7 cistromes in castration-resistant prostate cancer are governed by HoxB13 |
7.82 |
|
Aging of hematopoietic stem cells is driven by regional specialization of marrow macrophages |
7.6 |
|
Human CD11b+ macrophages - Aging of hematopoietic stem cells is driven by regional specialization of marrow macrophages |
7.6 |
|
TMED9-gated CNIH4 and TGFa signaling promotes pro-metastatic states in human primary colon cancer cells |
7.57 |
|
Mapping interactions for the TNIP2 hub protein |
7.54 |
|
CROP-Seq in Primary Human T Cells |
7.52 |
|
LINE-1 elements are derepressed in senescent cells and elicit a chronic Type-I Interferon response |
7.49 |
|
Differentially expressed genes post knock down of lincDUSP26 |
7.43 |
|
scRNASeq analysis of cycling cardiomyocytes |
7.4 |
|
An integrative network biology analysis identifies miR-508-3p as the determinant and a prognosis biomarker of the mesenchymal subtype ovarian cancer |
7.37 |
|
CREB5 promotes resistance to androgen-receptor antagonists and androgen deprivation in prostate cancer |
7.31 |
|
Effect of disulfiram treatment on pediatric high grade glioma |
7.25 |
|
HuR controls apoptosis and activation response without effects on cytokine 3′ UTRs |
7.23 |
|
Characterization of human CDK12 and CDK13 in the regulation of RNA processing |
7.22 |
|
SLAM-seq for K562 endogenous mRNA decay |
7.19 |
|
Human embryonic stem cell, chimpanzee induced pluripotent stem cell, orangutan induced pluripotent stem cell, rhesus embryonic stem cell, and their derived cortical organoid RNA-seq |
7.13 |
|
Transcriptional landscape changes during human embryonic stem cell derivation |
7.07 |
|
BRG1 governs Glucocorticoid Receptor interactions with chromatin and pioneer factors across the genome |
6.98 |
|
Epigenetic reprogramming at estrogen-receptor binding sites alters the 3D chromatin landscape in endocrine resistant breast cancer [RNA-seq] |
6.98 |
|
Epigenetic reprogramming at estrogen-receptor binding sites alters 3D chromatin landscape in endocrine resistant breast cancer |
6.98 |
|
miR-191 regulates human cell proliferation and directly targets multiple oncogenes [seq] |
6.93 |
|
Genome wide miR-191 target profile determined by RIP and gene expression profiling |
6.93 |
|
Lysine benzoylation is a novel histone mark |
6.87 |
|
Lysine benzoylation is a novel histone mark [RNA-seq] |
6.87 |
|
RNA-Seq with and without RNase treatment in PCa cell lines |
6.87 |
|
Regulation of protein translation during mitosis |
6.86 |
|
Identification of renal resident macrophages across species |
6.85 |
|
Genome-wide functional assessment of enhancer activities in the human genome |
6.8 |
|
Genome expression analysis of Lung Progenitors matured in the presence of constitutively active or pharmacologically inhibited Glycogen Synthase Kinase 3 |
6.77 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of HIV-1 Latency in Central Memory T Cells |
6.72 |
|
Gene expression analysis of C4-2 cells treated with ACLY inhibitor and Enzalutamide |
6.72 |
|
RUNX2/CBFB modulates the response to MEK inhibitors through activation of receptor tyrosine kinases in KRAS mutant colorectal cancer |
6.71 |
|
Hijacking of stress response machinery by oncogenes in acute leukaemia [RNA-seq] |
6.71 |
|
Hijacking of stress response machinery by oncogenes in acute leukaemia |
6.71 |
|
The stress granule transcriptome reveals principles of mRNA accumulation in stress granules. |
6.69 |
|
Transcriptome analysis of SKI knock-out in HL60 cells |
6.67 |
|
Combined cistrome and transcriptome analysis of SKI in AML cells identifies SKI as a co-repressor for RUNX1 |
6.67 |
|
The hepatitis C viral protein NS5A stabilizes growth-regulatory human transcripts |
6.63 |
|
Integrating single-cell transcriptomic data across different conditions, technologies, and species |
6.62 |
|
Cell-to-cell variation in defective virus expression and effect on host response during influenza virus infection |
6.62 |
|
Medial Ganglionic Eminence and Cortical Organoids Model Human Brain Development and Interneuron Migration |
6.56 |
|
Transcriptome analysis of dominant-negative Brd4 mutants identifies Brd4-specific target genes of BET inhibitor JQ1 |
6.48 |
|
Poly(ADP-ribosyl)ation dependent changes in CTCF-chromatin binding and gene expression in breast cells |
6.46 |
|
3’READS+, a sensitive and accurate method for 3’ end sequencing of polyadenylated RNA |
6.45 |
|
The MLL-AF9 and MLL-AF4 oncofusion proteins bind a distinct enhancer repertoire and target the RUNX1 program in MLLr AML |
6.42 |
|
Tumors with TSC mutations are sensitive to CDK7 inhibition through NRF2 and glutathione depletion |
6.39 |
|
Generating Patterned Kidney Organoids for Studying Development and Diseases |
6.36 |
|
RNA-Seq gene profiling comparison from human cDC subsets and pre-cDC subsets |
6.3 |
|
The LIN28B/let-7 axis is a novel therapeutic pathway in Multiple Myeloma |
6.29 |
|
Transcription-dependent control of stem cell self-renewal and differentiation by the splicing factor U2AF1 |
6.28 |
|
Perivascular signals alter global genomic profile of glioblastoma and response to temozolomide in a gelatin hydrogel |
6.26 |
|
Next generation sequencing on knockdown of AC093323.3 in lung cancer cells |
6.25 |
|
The landscape of alternative splicing in aggressive prostate cancers |
6.22 |
|
Genome-wide CRISPR-Cas9 screen identifies druggable synthetic lethality between LSD1 and MTORC1 in MLL-translocated AML |
6.22 |
|
A Unique Epigenomic Landscape Defines Human Erythropoiesis |
6.21 |
|
A Unique Epigenomic Landscape Defines Human Erythropoiesis (RNA-seq) |
6.21 |
|
Innate-like activation of mucosal-associated invariant T cells in mycobacterial infection |
6.2 |
|
Bromodomain-containing Protein 4 (BRD4) is Required for the Maintenance of a Mammary Epithelial Phenotype [RNA-Seq] |
6.16 |
|
Bromodomain-containing Protein 4 (BRD4) is Required for the Maintenance of a Mammary Epithelial Phenotype |
6.16 |
|
The mechanism of HHT in treating acute myeloid leukemia on RNA level. |
6.16 |
|
Combined inhibition of STAT3 and DNA repair in palbociclib-resistant ER-positive breast cancer |
6.15 |
|
The Developmental Heterogeneity of Human Natural Killer Cells Defined by Single-cell Transcriptome |
6.13 |
|
DART-seq: an antibody-free method for global m6A detection |
6.09 |
|
Comparative transcriptomic analysis of human and Drosophila extracellular vesicles reveals extensive conservation |
6.08 |
|
Genome-wide analysis of STAT3 in diffuse large B-cell lymphoma |
6.08 |
|
Transcriptome-wide off-target RNA editing induced by CRISPR-guided DNA base editors [Modifications - screen] |
6.06 |
|
RNA editing in nascent RNA affects pre-mRNA splicing |
6.03 |
|
Control of prostate tumour growth by the long non-coding RNA GHSROS (LNCaP) |
6.02 |
|
Single-cell Map of Diverse Immune Phenotypes in the Breast Tumor Microenvironment - 5' RNA sequencing and TCR sequencing |
6.01 |
|
NRDE2 negatively regulates nuclear exosome functions |
6.0 |
|
RNA-seq analyisis of PUM2 knockout cells |
5.97 |
|
Region-specific Innate Antiviral Responses of the Human Epididymis |
5.93 |
|
Ex-vivo Human Hematopoietic Stem Cell Expansion Requires Coordination of Cellular Reprogramming with Mitochondrial Remodeling and P53 Activation |
5.9 |
|
Trans-chromosomal regulation by a novel lincRNA required for adipogenesis that escapes X-chromosome inactivation |
5.88 |
|
Characterisation of HIF-dependent alternative isoforms in pancreatic cancer |
5.81 |
|
Global response to chemotherapy-induced apoptosis |
5.81 |
|
Gene expression by high-throughput sequencing of T47D-MTVL human breast cancer cells upon H1.4 knock-down and multiple H1 variants |
5.81 |
|
Histone Demethylase-Assisted Somatic Cell Nuclear Transfer Facilitates Derivation of Human Pluripotent Stem Cells |
5.8 |
|
RNA-seq Transcriptome Analysis of AD169 and AD169-ΔUL26 infected MRC5 fibroblasts. |
5.75 |
|
Distinct gene expression profile of Huh7 cell lines stably overexpressing CRABP1 or 2 |
5.75 |
|
Transcriptomic analysis of T84 colon carcinoma cell line treated with trametinib, JQ1 or their combination |
5.69 |
|
CRISPR adenine and cytosine base editors with reduced RNA off-target activities [CBE] |
5.69 |
|
CRISPR adenine and cytosine base editors with reduced RNA off-target activities |
5.69 |
|
The Short Isoform of BRD4 Promotes HIV-1 Latency by Engaging Repressive SWI/SNF Chromatin Remodeling Complexes |
5.67 |
|
Circular RNAs are down-regulated in KRAS mutant colon cancer cells and can be transferred to exosomes |
5.6 |
|
Cohesin and CTCF Differentially Affect the Chromatin Architecture and Gene Expression in Human Cells |
5.53 |
|
Epigenetic Therapy Increases Therapeutic Efficacy in Myeloproliferative Neoplasms Through Inhibition of Aberrant Inflammatory Signaling |
5.53 |
|
Maintaining iron homeostasis is the key role of lysosomal acidity for cell proliferation |
5.45 |
|
MKL1 augments megakaryocyte maturation by enhancing the SRF regulatory axis [RNA-seq] |
5.45 |
|
MKL1 augments megakaryocyte maturation by enhancing the SRF regulatory axis |
5.45 |
|
Domain-focused CRISPR-screen identifies HRI as a fetal hemoglobin regulator in human erythroid cells |
5.42 |
|
Aging Human Hematopoietic Stem Cells Manifest Profound Epigenetic Reprogramming of Enhancers That May Predispose to Leukemia (RNA-Seq of LMNA KD) |
5.38 |
|
Polyol pathway links glucose metabolism to the aggressiveness of cancer cells |
5.36 |
|
A common cell state in Triple Negative Breast Cancers represents a druggable vulnerability |
5.35 |
|
Pan-cancer transcriptomic analysis associates long non-coding RNAs with key mutational driver events |
5.33 |
|
MYC dependent mRNA translation shapes gene expression and cell biology |
5.32 |
|
Total RNA-seq in ALL-SIL upon JQ1 inhibition |
5.29 |
|
Apatinib preferentially inhibits Gefitinib-resistant lung cancer cells by inducing cell cycle arrest and inhibiting VEGFR signaling pathway |
5.29 |
|
Mitochondrial unfolded protein response controls matrix pre-RNA processing and translation |
5.29 |
|
SnapShot-Seq: a method for extracting genome-wide, in vivo mRNA dynamics from a single total RNA sample |
5.22 |
|
Rational targeting of cooperating layers of the epigenome yields enhanced therapeutic efficacy against AML |
5.17 |
|
Dynamic incorporation of histone H3 variants into chromatin is essential for acquisition of aggressive traits and metastatic colonization |
5.16 |
|
A quantitative chemotherapy genetic interaction map identifies new factors associated with PARP inhibitor resistance |
5.15 |
|
RNA-seq of resting and activated CD4+ T cells +-JQ1 |
5.14 |
|
Total RNA-seq in ALL-SIL upon TLX1 knockdown |
5.12 |
|
RNA sequencing of GlyH-101-treated MCF-7 cell line |
5.12 |
|
Next Generation Sequencing of control (Untreated), PAN injured and Adriamycin injured human podocytes |
5.1 |
|
An epigenetic mark of polycomb response elements implemented by Trx/MLL/COMPASS |
5.1 |
|
An Alternative Splicing Event Amplifies Evolutionary Differences Between Vertebrates |
5.08 |
|
GRO-seq from HCT116, MCF7 and SJSA cell lines treated with DMSO and Nutlin |
5.05 |
|
Identification of a core p53 transcriptional program with highly fractionated tumor suppressive activity |
5.05 |
|
SMYD2 specificly regulate BIX-01294 induced TP53 target genes revealed by RNA-Seq |
5.05 |
|
TFPa/HADHA is required for fatty acid beta-oxidation and cardiolipin re-modeling in human cardiomyocytes |
5.04 |
|
mRNA sequencing identifies differential gene expresssion profiles between ASCC3 knock-down cells and control cells |
5.02 |
|
Transcriptome sequencing after MAGOHB knockdown in MAGOH-deleted or non-deleted cancer cells |
5.01 |
|
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 |
5.01 |
|
Nickel induced transcriptional changes persist post exposure through epigenetic reprograming (ChIP-seq & RNA-seq datasets) |
5.0 |
|
Effect of FGF13 depletion on the H460 cell line |
4.99 |
|
RNAseq to determine whether bidirectional transcription occurs over transposable elements following depletion of SETDB1 in THP-1 AML Cells |
4.97 |
|
EHMT1 and EHMT2 inhibition induce fetal hemoglobin expression [RNA-seq] |
4.97 |
|
EHMT1 and EHMT2 inhibition induce fetal hemoglobin expression |
4.97 |
|
K562 polyA RNA-Seq |
4.92 |
|
Genome-wide discovery of human splicing branchpoints [RNAse] |
4.9 |
|
Activation of a SOX2-dependent transcriptional regulatory circuit drives glioblastoma. |
4.9 |
|
Transcriptome splicing analysis in K562 cells expressing rare and private spliceosomal mutations |
4.9 |
|
RNA-Seq analysis of breast cancer cells after shikonin treatment |
4.86 |
|
mRNA profiles of JMJD3 overexpression- and JMJD3 knockout- HL-60 cells |
4.85 |
|
Loss of 9p21 regulatory hub promotes kidney cancer progression by upregulating HOXB13 |
4.8 |
|
Differential mRNA expression upon 9p21 deletion in HEK TE single-cell derived clones |
4.8 |
|
Analysis of HPV16 E2 host gene expression using TERT immortalized keratinocytes (NOKs) cell lines and RNA-sequencing |
4.79 |
|
Genomic deletion of malic enzyme 2 confers collateral lethality in pancreas cancer |
4.78 |
|
CD97 is a Critical Regulator of Acute Myeloid Leukemia Stem Cell Function |
4.77 |
|
Comprehensive comparative analysis of 5’ end RNA sequencing methods |
4.73 |
|
ChIP-seq and RNA-Seq analyses of epithelial and mesenchymal cells - HMLE, N8, N8-CTx |
4.71 |
|
RNA-Seq comparisons of gene expression profiles of epithelial and mesenchymal cells - HMLE, N8, N8-CTx |
4.71 |
|
Expression profiling of ILC transitional populations and Aiolos accessability and H3K27ac histone modifications in transfected MNK3 cells |
4.71 |
|
RNA-Seq from human ILC transitional populations |
4.71 |
|
Single-cell RNA sequencing-based CRISPRi screening resolves molecular drivers of early human endoderm development |
4.68 |
|
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) |
4.63 |
|
ICE1 promotes the link between splicing and nonsense-mediated mRNA decay |
4.63 |
|
Gene expression profile in endometrial organoids cultured in normal follicular phase vs PCOS-like hormone profile |
4.6 |
|
Global transcriptome analysis of HAP1 cells |
4.58 |
|
Genetic-to-epigenetic Therapy for Pancreatic Cancer |
4.56 |
|
Retinoic Acid Induced Transcriptional Repressor HIC1 is Required for Suppressive Function of Human Induced Regulatory T cells [RNA-Seq 1] |
4.5 |
|
pSILAC mass spectrometry reveals ZFP91 as novel IMiD dependent substrate of the CRL4CRBN ligase |
4.48 |
|
GREB1 amplifies androgen receptor output in prostate cancer and contributes to antiandrogen resistance |
4.47 |
|
TimeLapse-seq: adding a temporal dimension to RNA sequencing through nucleoside recoding |
4.46 |
|
Vitamin C Promotes Apoptosis in Breast Cancer Cells by Increasing TRAIL Expression |
4.45 |
|
Stretch-Enhancers Delineate Disease-Associated Regulatory Nodes in T Cells |
4.44 |
|
MicroRNA targetome analysis during HCMV infection |
4.44 |
|
Systematic discovery of endogenous human ribonucleoprotein complexes |
4.42 |
|
Profile of gene expression in U87-MG xenografts expressing control vector (V0), the ubiquitin ligase KPC1 or the p50 subunit of the NF-kB transcription factor, using RNASeq analysis of transcripts mapped independently to the human and murine genomes |
4.41 |
|
RNA-sequencing of mRNAs from control and CAP-D3 deficient Salmonella infected HT-29 cells |
4.41 |
|
An integrative analysis of non-coding regulatory DNA variations associated with autism |
4.4 |
|
Pancreatic cancer-derived exosomes induce apoptosis of T lymphocytes through the p38 MAPK signal transduction pathway |
4.38 |
|
IGF2BP1 promotes SRF-dependent transcription in cancer in a m6A- and miRNA-dependent manner [Huh-7] |
4.35 |
|
IGF2BP1 promotes SRF-dependent transcription in cancer in a m6A- and miRNA-dependent manner |
4.35 |
|
Characterization of transcriptomics landscape in HUVEC cells exposed to oxidative stress (Total RNA) |
4.33 |
|
Club cells surviving influenza A virus infection induce temporary non-specific anti-viral immunity |
4.33 |
|
The NORAD lncRNA assembles a topoisomerase complex critical for genome stability [RNA-seq] |
4.33 |
|
The NORAD lncRNA assembles a topoisomerase complex critical for genome stability |
4.33 |
|
RNA sequencing of primary human platelets and in vitro cell lines |
4.26 |
|
Global transcriptional changes in the JJN3 myeloma cell line that occur as a result of treatment with 2 pyrrolobenzodiazepine (PBD) monomers |
4.17 |
|
Cell responses to dysregulated VZV-induced cell-cell fusion |
4.17 |
|
Lyophilized human cells stored at room temperature preserve multiple RNA species at excellent quality for RNA sequencing |
4.16 |
|
Knock-down of Ror1 in MDA-MB-231 cell line decreases cell invasiveness |
4.11 |
|
Pseudotime Ordering of Single Human Beta-Cells Reveals States of Insulin Production and Unfolded Protein Response |
4.08 |
|
Identification of Differentially Expressed Splice Variants by the Proteogenomic Pipeline Splicify |
4.07 |
|
RNA-Guided Human Gene Activation by Cas9/CRISPR-Based Engineered Transcription Factors |
4.06 |
|
Antioxidant metabolism in activated CD8+ T cells regulates stem-like human memory T cell formation and anti-tumor immunity |
4.02 |
|
Stem and effector CD8 T-cells from human cancers |
3.98 |
|
Human naïve pluripotent stem cells exhibit X chromosome dampening and X-inactivation (RNA-Seq) |
3.97 |
|
Characterization of human ILC2 subsets |
3.96 |
|
In vitro differentiation of human embryonic stem cells into ovarian follicle-like cells |
3.92 |
|
Complete deconvolution of cellular mixtures based on linearity of transcriptional signatures |
3.89 |
|
Ex-vivo Human Hematopoietic Stem Cell Expansion Requires Coordination of Cellular Reprogramming with Mitochondrial Remodeling and P53 Activation [bulk] |
3.86 |
|
Long non-coding RNA TYKRIL controls pericyte function and survival in the cardiovascular and central nervous system through regulation of p53 activity and PDGFRß expression |
3.86 |
|
Comprehensive comparative analysis of RNA sequencing methods for degraded or low input samples |
3.85 |
|
Regulation of the glucocorticoid receptor via a BET-dependent enhancer drives antiandrogen resistance in prostate cancer |
3.81 |
|
CRISPR Display: A modular method for locus-specific targeting of long noncoding RNAs and synthetic RNA devices in vivo [RNA-Seq] |
3.79 |
|
CRISPR Display: A modular method for locus-specific targeting of long noncoding RNAs and synthetic RNA devices in vivo |
3.79 |
|
Identification of altered developmental pathways in human juvenile HD iPSC with 71Q and 109Q using transcriptome profiling |
3.77 |
|
Sirt6 Oncogene Mediates PI3K/Akt Signaling Activation in Diffuse Large B-Cell Lymphoma |
3.76 |
|
Transcriptomic analysis of the effect of histone H4 K31R mutation in U2OS cells |
3.75 |
|
Integration of genome-wide DNA methylome and transcriptome of human intestinal fibroblasts reveals novel candidate gene signatures in Crohn’s disease-associated fibrosis |
3.75 |
|
The RNA helicase DDX6 regulates self-renewal and differentiation of human and mouse stem cells [RNA-seq] |
3.75 |
|
RNA-sequencing of the GSI treatment of the CUTLL1 cell line |
3.74 |
|
HBEC-shp53-PCHD7 |
3.72 |
|
ETV4 is necessary for estrogen signaling and growth in endometrial cancer cells |
3.7 |
|
ETV4 is necessary for estrogen signaling and growth in endometrial cancer cells [RNA-seq] |
3.7 |
|
Transcriptomic analysis of acute mitochondrial pyruvate carrier inhibition using UK5099 in ABL prostate cancer cells |
3.68 |
|
Arginine methylation controls cell proliferation by integrating E2F activity with the splicing machinery (RNA-seq data set) |
3.62 |
|
Arginine methylation controls cell proliferation by integrating E2F activity with the splicing machinery |
3.62 |
|
Enhancement of Arterial Specification in Human Pluripotent Stem Cell Cultures Promotes Definitive Hematoendothelial Program with Broad Myelolymphoid Potential |
3.61 |
|
Mitochondrial unfolded protein response controls matrix pre-RNA processing and translation |
3.61 |
|
Targeting HuH7 cells with JumonjiC Lysine Demethylase Inhibitors (RNA-Seq) |
3.57 |
|
Expanding the Nucleoside Recoding Toolkit: Revealing RNA Population Dynamics with 6-thioguanisine |
3.57 |
|
Cap-specific terminal N6-methylation of RNA by an RNA polymerase II-associated methyltransferase. |
3.52 |
|
Expression alterations induced by restoration of AXIN1 expression in SNU449 hepatocellular carcinoma cells |
3.49 |
|
A novel compound that blocks HIV-1 replication inhibits the splicing regulatory function of SRSF10 |
3.48 |
|
RNA-seq of PC3 prostate cancer cell line xenografts in mice administered the ghrelin receptor antagonist [D-Lys3]-GHRP-6 or PBS for two weeks |
3.48 |
|
Analysis of the Clustered Protocadherin (cPcdh) Locus in Human Pluripotent Stem and Derived Cells [RNA-seq II our of II] |
3.4 |
|
Transcriptional impact of MTHFD2 in Human Aortic Endothelial Cells |
3.39 |
|
RNA-sequencing of healthy human skeletal myocytes |
3.39 |
|
Interactions of aCPs with Cytosine-rich Polypyrimidine Tracts Enhance Splicing of Cassette Exons |
3.38 |
|
Multiplexed engineering and analysis of endogenous enhancer activity in single cells: Mosaic-Seq of beta-globin locus (separate infection) |
3.36 |
|
SPOP mutation confers intrinsic BET inhibitor resistance in prostate cancer |
3.35 |
|
Activation Dynamics and Immunoglobulin Evolution of Pre-existing and Newly Generated Human Memory B-cell Responses to Influenza Hemagglutinin |
3.35 |
|
CHD7 is Suppressed in the Perinecrotic/Ischemic Microenvironment and is a Novel Regulator of Angiogenesis |
3.33 |
|
TALEN-based knockout of mir-141 and mir-200c in SK-BR-3 cells |
3.33 |
|
Next Generation Sequencing Quantitative Analysis of Wild Type and AML1-ETO Related Fusion Circular RNA (F-CircAE) Knockdown Kasumi-1 Cells Transcriptomes |
3.32 |
|
Human cells contain natural double-stranded RNAs with potential regulatory capacity |
3.28 |
|
The pause-initiation limit restricts transcription activation in human cells |
3.25 |
|
Designer epigenome modifiers enable robust and sustained gene silencing in clinically relevant human cells [RNA-seq] |
3.25 |
|
Designer epigenome modifiers enable robust and sustained gene silencing in clinically relevant human cells |
3.25 |
|
Transcriptomics profiling of Alzheimer’s disease reveal novel molecular targets |
3.21 |
|
MBNL1-dependent modulation of gene expression in MDA-MB-231 breast cancer cells |
3.17 |
|
Muscleblind-like 1 suppresses breast cancer metastatic colonization and stabilizes metastasis suppressor transcripts |
3.17 |
|
Generation and persistence of human tissue-resident memory T cells in lung transplantation |
2.98 |
|
Global host gene expression changes in KSHV+ PEL cells upon KSHV reactivation |
2.97 |
|
RNA-seq analysis upon ARID1B overexpression |
2.94 |
|
Single-cell RNA-seq reveals differentiation of bona fide human pDCs and cDC1s in cultures of cord blood CD34+ progenitors, and a newly identified terminal differentiation step of cDC1s |
2.89 |
|
Transcriptome profiling of HepG2 cells upon treatment of the menin-MLL inhibitor MI-503 or DMSO |
2.84 |
|
Regulatory network controlling tumor-promoting inflammation in human cancers |
2.82 |
|
Regulatory network controlling tumor-promoting inflammation in human cancers [RNA-seq] |
2.82 |
|
Positively selected enhancer elements endow tumor cells with metastatic competence |
2.78 |
|
KDM1A confers invasive and metastatic attributes in lung adenocarcinoma by modulating a non-canonical Integrin ß3-KRAS signaling pathway |
2.77 |
|
Bulk RNA-sequencing of cell types isolated by FACS from normal human prostates |
2.75 |
|
Multiplexed engineering and analysis of endogenous enhancer activity in single cells: Mosaic-Seq of beta-globin locus (pooled infection) |
2.74 |
|
An atlas of TNF-α-responsive promoters and enhancers in the intestinal epithelial cell model Caco-2 |
2.74 |
|
Platelet Transcriptome Profiling in HIV and ABCC4 as a Biomarker of Platelet Activity |
2.68 |
|
RNA-Seq data of NCI-H82 cells expressing a Dox-On pRB (pTripZ RB1) grown in the presence or absence of DOX and then treated with vehicle or AZD2811. |
2.65 |
|
RNAseq of ribosomal fractionation to assess the effect of CBFB on translation regulation |
2.64 |
|
MicroRNA-125a-5p overexpression in human macrophages |
2.62 |
|
Transcriptome analysis of the HepG2 cells expressing hepatic transcription factors |
2.61 |
|
Expression analysis of THP1 cells following shRNA knock-down of RUVBL2 |
2.56 |
|
O-GlcNAc transferase fine-tunes MYC-dependent transcription to promote cell cycle [RNA-seq] |
2.56 |
|
O-GlcNAc transferase fine-tunes MYC-dependent transcription to promote cell cycle |
2.56 |
|
CRISPR/Cas9-mediated ASXL1 mutation in U937 cells perturbs myeloid differentiation |
2.56 |
|
Single-cell Transcriptomics reveals multi-step adaptations to endocrine therapy |
2.49 |
|
Evolutionary origin and functional divergence of stem cell homeobox genes in eutherian mammals |
2.43 |
|
RNA-Seq analysis of Head and Neck Squamous cell carcinoma cell-lines |
2.42 |
|
Tracing the temporal-spatial transcriptomic landscapes of the human fetal digestive tract by single cell RNA-seq analysis [adult tissues] |
2.41 |
|
LncRNA NMR knockdown and overexpression in esophageal squamous cell carcinoma cell lines |
2.36 |
|
Lipid catabolism inhibition sensitizes prostate cancer cells to antiandrogen blockade |
2.36 |
|
Single cell transcriptomics reveals new insights on the dynamical function of transcription factors during blood stem and progenitor cell formation |
2.33 |
|
Single-cell RNAseq analysis of the empty and i8TF cell lines after 3 days of BL-CFC culture |
2.33 |
|
RNA-seq of HEK293T cells overexpressing TET1-FL or TET1-ALT |
2.29 |
|
RNA-seq, ChIP-seq and single cell RNA-seq of human skin Langerhans cells |
2.24 |
|
The DPYSL2 gene connects mTOR and schizophrenia |
2.23 |
|
Next generation sequencing of small RNAs isolated from exosomes in human semen |
2.23 |
|
Gene expression in control and DOCK8 CRISPR KHYG1 NK cells |
2.18 |
|
Impact of library preparation on downstream analysis and interpretation of RNA-seq data: comparison between Illumina PolyA and NuGEN Ovation protocol |
2.18 |
|
SNHG15 is a bifunctional MYC-regulated noncoding locus encoding a lncRNA that promotes cell proliferation, invasion and drug resistance in colorectal cancer by interacting with AIF |
2.17 |
|
PolyA+ RNA-seq in ALL-SIL upon TLX1 knockdown |
2.17 |
|
Rnase L reprograms translation by widespread mRNA turnover escaped by antiviral mRNAs |
2.17 |
|
Gene expression profile of HGC27 gastric cancer cell p53 KO and KD |
2.17 |
|
Evidence for rRNA 2'-O-methylation plasticity: control of intrinsic translational capabilities of human ribosomes |
2.16 |
|
Identification of transcripts altered upon LIN-41 knockdown in human embryonic stem cells |
2.14 |
|
Molecular Criteria for Defining the Naive Human Pluripotent State |
2.13 |
|
ZNF599 and DNMT3A coordinately control nuclear envelope organization by repression of SUN4 expression |
2.05 |
|
RNA seq with AML (NB4) cells upon FTO inhibition |
2.04 |
|
Tumor- and cytokine-primed human natural killer cells exhibit distinct phenotypic and transcriptional signatures [RNA-seq] |
2.03 |
|
Tumor- and cytokine-primed human natural killer cells exhibit distinct phenotypic and transcriptional signatures |
2.03 |
|
Role of cervicovaginal microbiota in genital inflammation |
2.01 |
|
B cells expressing the IgA receptor FcRL4 participate in the autoimmune response in patients with rheumatoid arthritis |
2.01 |
|
Trisomy of a ‘Down syndrome critical region’ globally amplifies transcription via HMGN1 overexpression [NALM6 RNA-Seq] |
2.01 |
|
JUNB is a critical AP1 component for SMAD2/3 binding after TGFβ stimulation [RNA-seq] |
2.0 |
|
SMAD2/3 are redirected to novel sites in MCF10A MII after prolonged TGFβ stimulation |
2.0 |
|
Human Treg IL-12 stimulation |
1.91 |
|
Measuring the effect of MYC on transcription during the DNA double-strand break response by RNA-seq of newly synthesized transcripts |
1.86 |
|
Time series single-cell transcriptomic analysis of AEC2 directed differentiation |
1.85 |
|
Widespread Transcription beyond mRNA 3’ Ends Yields Abundant Regulatory RNAs |
1.85 |
|
Next Generation Sequencing identifying the dosage compensation state in human endometrial carcinoma and adjacent tissues |
1.84 |
|
Genome Wide Chromatin Mapping of accessibility (ATAC-seq) and H3K27ac histone modifications in CD56bright and CD56dim natural killer cells |
1.83 |
|
RG/RGG boxes are common binding motifs in RNA-G-quadruplex-interacting proteins |
1.82 |
|
Primate transcript and protein expression levels evolve under compensatory selection pressures |
1.82 |
|
The effect of slow and rapid H2S production on the levels of LPS-induced proinflammatory mediators and transcription in different human cell cultures |
1.81 |
|
Effect of ILF3 on translation during homeostasis and the antiviral response |
1.81 |
|
Race-specific transcriptome and Long non-coding RNA of ADT-resistant African-American prostate cancer cell models. |
1.77 |
|
Genome-wide analysis of the Integrator complex (HTS) |
1.77 |
|
Genome-wide analysis of the Integrator complex |
1.77 |
|
Identification of biomarkers for amyotrophic lateral sclerosis by comprehensive analysis of exosomal mRNAs in human cerebrospinal fluid. |
1.73 |
|
5hmC and gene expression data in breast cancer cell lines treated with an antioxidant |
1.73 |
|
Induction of human regulatory innate lymphoid cells from group 2 innate lymphoid cells by retinoic acid |
1.7 |
|
Co-regulation of transcription by BRG1 and Brm, two mutually exclusive SWI/SNF ATPase subunits |
1.67 |
|
Cooperative and Antagonistic Transcriptional Regulation by BRG/BRM [RNA-seq] |
1.67 |
|
Treatment of prostate cancer cells with S-adenosylmethionine leads to genomewide alterations of transcription profiles |
1.66 |
|
RNA-Sequencing approach for the identification of novel long non-coding RNA biomarkers in colorectal cancer |
1.64 |
|
Enhancement of Human B Cell Differentiation and Function in Lymph Nodes by the TLR9 Agonist MGN1703 |
1.63 |
|
Global transcriptome analysis in the MYCN-amplified neuroblastoma cell line IMR5-75 upon inducible MYCN-knockdown |
1.63 |
|
Transcriptomics analysis of gene expression in normal and METTL3 or WTAP deficient Human HeLa cells |
1.57 |
|
Effect of PDZ domain binding Kinase inhibition using TOPK-32 (called PBKi) on C4-2 cell transcriptome |
1.55 |
|
Remodeling of Ago2-mRNA interactions upon cellular stress reflects miRNA complementarity and correlates with altered translation rates |
1.43 |
|
Remodeling of Ago2-mRNA interactions upon cellular stress reflects miRNA complementarity and correlates with altered translation rates (part 4) |
1.43 |
|
A20 regulates canonical wnt-signaling through an interaction with RIPK4 |
1.41 |
|
Single-cell RNA-Seq Investigation of Foveal and Peripheral Expression in the Human Retina |
1.4 |
|
Role of BET proteins in YAP/TAZ-dependent transcription [RNA-seq 2] |
1.4 |
|
Functional significance of the HIV-1 Tat signature amino acid residues |
1.39 |
|
Drug combination of 17-AAG and Belinostat on MDA-MB-231 breast cancer cells |
1.38 |
|
RNA-seq analysis of Retinoic Acid and Non-treated Control hiPSCs |
1.37 |
|
ETS1 induction by the omental microenvironment promotes ovarian cancer metastasis |
1.36 |
|
ETS1 induction by the omental microenvironment promotes ovarian cancer metastasis [RNA-Seq] |
1.36 |
|
single cell RNA-seq from GM12878 (ENCSR673UIY) |
1.35 |
|
The MEF2B Regulatory Network - RNA-seq data |
1.35 |
|
The MEF2B Regulatory Network |
1.35 |
|
Circular RNA profiling reveals the different distribution/characteristic and possible transport mechanism among the subcellular fractions |
1.34 |
|
Uridylation-mediated RNA quality control pathway in mammalian cytoplasm [RNA-Seq] |
1.25 |
|
TUT-DIS3L2 is a mammalian surveillance pathway for aberrant structured non-coding RNAs. |
1.25 |
|
siRNA-mediated knockdown |
1.21 |
|
Unraveling cis-regulatory elements by mapping structural changes in mRNAs |
1.18 |
|
Single Cell RNASeq profiling of stromal vascular fraction from Subcutaneous and visceral adipose tissue |
1.18 |
|
Identification of trans regulators of ADAR and A-to-I RNA editing using RNA-seq |
1.13 |
|
Unbiased identification of trans regulators of ADAR and A-to-I RNA editing |
1.13 |
|
The p30 isoform of CEBPA uncovers a silent enhancer to drive the expression of the tumor promotive factor CD73 in CEBPA mutant AML |
1.13 |
|
Trisomy of a ‘Down syndrome critical region’ globally amplifies transcription via HMGN1 overexpression [SLAM-Seq] |
1.11 |
|
RNA-seq data |
1.08 |
|
Molecular characterization of BRSK2 and BRSK1 kinases as negative regulators of the NRF2 transcription factor |
1.06 |
|
Estrogen-independent molecular actions of mutant estrogen receptor alpha in endometrial cancer |
1.04 |
|
Estrogen-independent molecular actions of mutant estrogen receptor alpha in endometrial cancer [RNA-seq] |
1.04 |
|
Small-molecule targeting of brachyury transcription factor addiction in chordoma [rnaseq_compound] |
0.99 |
|
The hematopoietic master transcription factor PU.1 requires its interaction with the SWI/SNF remodeler to access chromatin de novo [RNA-seq] |
0.96 |
|
The hematopoietic master transcription factor PU.1 requires its interaction with the SWI/SNF remodeler to access chromatin de novo |
0.96 |
|
MicroRNA-28 replacement for non-Hodgkin lymphoma therapy |
0.95 |
|
Non-inflammatory tumor microenvironment of Diffuse Intrinsic Pontine Glioma (DIPG) |
0.94 |
|
Epigenetic reprogramming of melanoma cells by vitamin C treatment |
0.91 |
|
RNA-Seq of SHEP TET21N cells upon Doxorubicin treatment |
0.91 |
|
Transient stabilization, rather than inhibition of MYC amplifies extrinsic apoptosis and therapeutic responses in refractory B-cell lymphoma |
0.88 |
|
High-throughput single cell transcriptome analysis and CRISPR screen identify key β cell-specific disease genes |
0.86 |
|
Assessing the effect of SUPT4H1 RNAi on the transcription of a repeat-containing reporter construct |
0.85 |
|
Consequences of Ribosomal Protein Haploinsufficiency in Human Hematopoiesis |
0.8 |
|
Global transcriptomic analyses of bronchial epithelial cells exposed to 5 ng/mL TGF-β1 and 10 nM Estrogen individually and in combination |
0.78 |
|
Dynamic gene regulatory networks of human myeloid differentiation [RNA-seq_siRNA] |
0.74 |
|
Apoptosis enhancing drugs overcome innate platinum resistance in CA125 negative tumor initiating populations of high grade serous ovarian cancer |
0.66 |
|
Modeling genome-wide transcriptional cis-regulation in n LNCaP-abl cell line after siRNA knock down of a series of gene factors [RNA-seq] |
0.64 |
|
Identification of a unique gene expression signature in mercury and 2,3,7,8-tetrachlorodibenzo-p-dioxin co-exposed cells |
0.64 |
|
Transcription factors and stress response gene alterations in human keratinocytes following Solar Simulated Ultra Violet Radiation |
0.63 |
|
Hsa-miR-139-5p/HNRNPF axis modulates gene-transcripts balance in thyroid cancer cells |
0.61 |
|
RNA-sequencing of the brain transcriptome implicates dysregulation of neuroplasticity, circadian rhythms, and GTPase binding in bipolar disorder |
0.6 |
|
Targeting MTHFD2 in Acute Myeloid Leukemia |
0.57 |
|
CENPA-Bound Genes and Transcriptional Profiling of CENPA-Depleted Prostate Cancer Cells |
0.53 |
|
Transcriptional Profiling of CENPA-Depleted Prostate Cancer Cell Lines |
0.53 |
|
Lung adenocarcinoma metastasis is suppressed by the alveolar lineage transcription factors GATA6 and HOPX. |
0.52 |
|
Transcriptional response to the HSP70 inhibitor MAL3-101 in parental rhabdomyosarcoma cells and isogenic acquired-resistance lines. |
0.5 |
|
p53 activity results in DNA replication fork processivity |
0.5 |
|
RNA sequencing of isogenic BRCA2 haploinsufficient vs. wild-type T-ALL cells |
0.46 |
|
Targeting Spt5-Pol II small-molecule inhibitors uncouple distinct activities and reveal additional regulatory roles |
0.46 |
|
Combined MEKi (GDC-0973) and WNT (G007-LK) treatment in APC and KRAS mutant HCT-15 cell line |
0.45 |
|
Functional Significance of U2AF1 S34F Mutation in Lung Adenocarcinomas |
0.45 |
|
Determining mRNA half-lives on a transcriptome-wide scale |
0.44 |
|
Identification of the RB loss-induced transcriptome and E2F1 cistrome in prostate cancer |
0.44 |
|
Identification of the RB loss-induced transcriptome in prostate cancer [RNA] |
0.44 |
|
DNMT1-associated long non-coding RNA regulate global gene expression and DNA methylation in colon cancer |
0.43 |
|
GLIS3 Transcriptionally Activates WNT Genes to Promote Differentiation of Human Embryonic Stem Cells to Posterior Neural Progenitors |
0.37 |
|
Dermal endothelial cells of type 2 diabetic patients |
0.36 |
|
Improving fibroblast characterization using single-cell RNA sequencing: an optimized tissue disaggregation and data processing pipeline |
0.33 |
|
mRNA-Seq profiling SIX2+ and Foxd1+ cells in mouse embryonic and SIX2+ and SIX2-/MEIS1+ cells human fetal kidney |
0.32 |
|
Ribosome profiling of A549 cells depleted of RPLP1 and RPLP2 and infected with DENV. |
0.31 |
|
Genome-wide mapping of DROSHA cleavage sites on primary microRNAs and novel substrates [RNA-seq] |
0.3 |
|
Genome-wide mapping of DROSHA cleavage sites on primary microRNAs and novel substrates |
0.3 |
|
Functional Inflammatory Profiles Distinguish Myelin-Reactive T Cells from Patients with Multiple Sclerosis |
0.29 |
|
Epithelial-mesenchymal transition markers screenedina cell-based model and validated in lung adenocarcinoma |
0.28 |
|
Transcriptional profiling of SF295 cells following MTF1 knockout by CRISPR/Cas9 |
0.28 |
|
Chromatin remodeling mediated by ARID1A is indispensable for normal hematopoiesis in mice (human RNA-Seq) |
0.28 |
|
Concomitant BCORL1 and BRAF mutations in vemurafenib-resistant melanoma cells |
0.27 |
|
Tracing the first hematopoietic stem cell generation in human embryo by single-cell RNA sequencing |
0.23 |
|
JMJD3 facilitates C/EBPβ-centered transcriptional program to exert oncorepressor activity in AML |
0.22 |
|
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 |
0.22 |
|
EGR1-controlled transcriptome of T HESCs |
0.22 |
|
DAOY-Notch1/Notch2 knockout: transcriptome comparison |
0.17 |
|
Epigenome Editing by CRISPR/Cas9 Repressors for Silencing of Distal Regulatory Elements |
0.17 |
|
Genome-wide hsa-miR-503, hsa-miR-103, and hsa-miR-494 target profiles |
0.13 |
|
hsa-miR-503, hsa-miR-103, and hsa-miR-494 genome wide target profiles [RNA-Seq and RIP-Seq] |
0.13 |
|
Identification and mitigation of pervasive off-target activity in CRISPR-Cas9 screens for essential non-coding elements |
0.13 |
|
Preclinical model of obesity and ER-positive breast cancer |
0.13 |
|
Genome-wide maps of WT and over-expressing CenH3/CENP-A in Human HeLa S3 cells |
0.12 |
|
RNA-seq analysis of PRMT5-regulated genes in irradiated/non-irradiated LNCaP cells |
0.11 |
|
Disruption of Na+/H+ exchanger regulatory factor 2 scaffold suppresses colon cancer proliferation |
0.09 |
|
Iron response of HepG2 cells |
0.09 |
|
YTHDF1 Amplifies Wnt/β-Catenin Signaling to Promote Intestinal Stemness |
0.09 |
|
Evaluating and comparing the Transcriptome of (human) Hek 293 based cells, expressing either CHD3 or CHD4 |
0.05 |
|
Targets mediated microRNA arm-imbalance promotes gastric cancer progression [lncRNA] |
0.05 |
|
Global transcriptome analysis of WT versus HEB-/- hESCs |
0.04 |
|
RelA mutants 'reconstituted' and cell cycle synchronized HCT116 Colorectal Cancer Cells |
0.02 |