|
Altering cancer transcriptomes using epigenomic inhibitors |
80.59 |
|
Altering cancer transcriptomes using epigenomic inhibitors [RNA-Seq] |
80.59 |
|
Aging Human Hematopoietic Stem Cells Manifest Profound Epigenetic Reprogramming of Enhancers That May Predispose to Leukemia (RNA-seq of KLF6 KO) |
67.14 |
|
RNA-seq analysis reveals profound changes in transcript profiles between siCon- and siH19-transfected EVT cells |
54.92 |
|
RNA expression analysis of neuroblastoma cell lines treated with epigenetic drugs |
53.47 |
|
hTERT promotes cell adhesion and migration independent of telomerase activity |
51.81 |
|
Functional interactions between Mi-2β and AP1 complexes control response and recovery from barrier disruption |
39.43 |
|
Cleavage Factor Im as a key regulator of 3’ UTR length |
39.05 |
|
MYCi975 regulates MYC target genes |
37.04 |
|
An evolutionarily conserved function of polycomb silences the MHC class I antigen presentation pathway and enables immune evasion in cancer |
36.31 |
|
An evolutionarily conserved function of polycomb silences the MHC class I antigen presentation pathway and enables immune evasion in cancer [RNA-Seq] |
36.31 |
|
Genome-wide RNA-seq from GALNT14-depleted and GALNT14 overexpressing MDA-MB-231 LM2 and Par cells |
34.41 |
|
TALENs-mediated gene disruption of FLT3 in leukemia cells: Using genome-editing approach for exploring the molecular basis of gene abnormality |
32.82 |
|
Early response of human ovarian and fallopian tube surface epithelial cells to norepinephrine |
32.03 |
|
Hijacking of stress response machinery by oncogenes in acute leukaemia [RNA-seq] |
31.87 |
|
Hijacking of stress response machinery by oncogenes in acute leukaemia |
31.87 |
|
Parvovirus B19 NS1 protein induces cell cycle arrest at G2 phase |
29.46 |
|
Bioinformatics analysis of transcriptome related to blood stasis syndrome in diabetes mellitus patients |
27.17 |
|
Sensing self and nonself circular RNAs |
27.1 |
|
Endogenous retroviruses are a source of oncogenic enhancers in acute myeloid leukemia |
26.17 |
|
Endogenous retroviruses are a source of oncogenic enhancers in acute myeloid leukemia [RNA-Seq] |
26.17 |
|
Quantitative analysis of bi-modal binding of BET proteins at promoters predicts I-BET sensitivity |
25.68 |
|
RNA-Seq following PCR-based sorting reveals rare cell transcriptional signatures |
25.58 |
|
Analysis of regulatory element evolution between human and mouse reveals a lack of cis-trans compensation |
24.9 |
|
miCLIP, RNA-Seq, and Ribo-Seq in MOLM13 cells |
24.72 |
|
Changes in CD34 and Erythroid Progenitor Transcriptome After RUNX3 Kock-down |
23.16 |
|
Bladder-cancer-associated mutations in RXRA activate peroxisome proliferator-activated receptors to drive urothelial proliferation |
22.53 |
|
Bladder cancer associated mutations in RXRA activate peroxisome proliferator-activated receptors |
22.53 |
|
MLL-AF4 Spreading Identifies Binding Sites that Are Distinct from Super-Enhancers and that Govern Sensitivity to DOT1L Inhibition in Leukemia. |
22.39 |
|
TFAP2C signalling in human fibroblasts |
22.38 |
|
Hypoxic regulation of gene expression in HUVEC is dominated by EPAS1 |
22.05 |
|
Regulartory effect of HNRNPL and LARP on RNA expression in LNCaP prostate cancer cells |
21.7 |
|
HNRNPL and its RNA Targets in Prostate Cancer |
21.7 |
|
GRHL2 is a key lineage determining factor which collaborates with FOXA1 to establish a targetable collateral pathway in the setting of endocrine therapy-resistant breast cancer (RNA-Seq data set 2) |
21.42 |
|
The pause-initiation limit restricts transcription activation in human cells |
20.75 |
|
An RNA-centric dissection of host complexes controlling flavivirus infection |
20.71 |
|
An RNA-centric dissection of host complexes controlling flavivirus infection [RNA-Seq] |
20.71 |
|
Analysis of transcriptional regulation by Myt1 and Myt1l |
20.07 |
|
Peroxisome Proliferator-activated Receptor gamma- Deficiency in Endothelial Cells Impairs Angiogenic Capacity by Loss-of E2F1 Mediated Wnt Effector Genes |
20.05 |
|
Uridilation by TUT4/7 restricts retrotransposition of human Line-1s |
19.81 |
|
Simultaneous and systematic analysis of cellular and viral gene expression during Enterovirus 71-induced host shutoff |
19.77 |
|
Gene Expression Analysis of Melanoma Cells Treated with 6-Thio-dG In Vitro |
19.68 |
|
mRNA destabilization is the dominant effect of mammalian microRNAs by the time substantial repression ensues (sequencing) |
19.51 |
|
mRNA destabilization is the dominant effect of mammalian microRNAs by the time substantial repression ensues |
19.51 |
|
Human Adult Sorted Live Cell Erythroblasts transduced with Sigma non-targeting shRNA negative control (SHC002V) with puromycin selection RNAseq |
19.27 |
|
Gene expression profiles in response to proanthocyanidins in pancreatic cancer cells |
19.01 |
|
NRDE2 negatively regulates nuclear exosome functions |
18.89 |
|
Ribosomal footprinting of CN34-Parental and CN34-LM1a |
18.56 |
|
Human cell line and subcutaneous tumor |
18.54 |
|
Modeling CADASIL vascular pathologies with patient-derived induced pluripotent stem cells |
18.23 |
|
Transcriptome analysis of total RNA in human osteosarcoma cell line U2OS before and after inhibition of zinc finger protein ZNF768 |
18.19 |
|
Proteinase-Activated Receptor 4 (PAR4) mediates cell membrane blebbing in a Gaq/11, Gai independent, RhoA and ß-arrestin-dependent manner. |
18.11 |
|
Nucleoporin-mediated regulation of cell identity genes |
17.93 |
|
RNA-Seq with and without RNase treatment in PCa cell lines |
17.86 |
|
Hemogenic Endothelium transcriptome along the timeline of hESC differentiation |
17.73 |
|
An improved method for circular RNA purification that efficiently removes linear RNAs containing G-quadruplexes or structured 3’ ends |
17.68 |
|
Ribosomal footprinting of MDA_Ctrl and MDA_Arg overexpression cell lines |
17.56 |
|
RNAseq Analysis in glioblastoma cells treated with Mepazine |
17.34 |
|
A Novel PI3K Regulator, ARID4B, Presents Synthetic Essentiality in PTEN-deficient Prostate Cancer [RNA-seq] |
17.24 |
|
A Novel PI3K Regulator, ARID4B, Presents Synthetic Essentiality in PTEN-deficient Prostate Cancer |
17.24 |
|
Tristetraprolin disables prostate cancer maintenance by impairing proliferation and metabolic function |
17.14 |
|
RNA transcriptome sequencing analysis of SGC-7901 cells transfected with ENST00000431060 shRNA or control shRNA |
17.1 |
|
Ribosomal footprinting of MDA-Parental and MDA-LM2 |
17.07 |
|
The cohesin release factor WAPL restricts chromatin loop extension. [RNA-Seq] |
16.68 |
|
The cohesin release factor WAPL restricts chromatin loop extension. |
16.68 |
|
Knockdown of ADNP in HCT116 colon cancer cells |
16.38 |
|
Dual role of CSL (RBP-Jk) and NOTCH1 in cancer-associated fibroblast genome stability and expansion [RNA-seq] |
16.26 |
|
Dual role of CSL (RBP-Jk) and NOTCH1 in CAF |
16.26 |
|
SLAM-seq for K562 endogenous mRNA decay |
16.04 |
|
Genes significantly down or Up-regulated upon RNF219 knockdown |
15.89 |
|
Identifying the molecular mode of action of itraconazole in colorectal cancer |
15.88 |
|
Identification of a dynamic core transcriptional network in t(8;21) AML regulating differentiation block and self-renewal [RNA-Seq] |
15.79 |
|
Identification of a dynamic core transcriptional network in t(8;21) AML regulating differentiation block and self-renewal |
15.79 |
|
Identification of Nrf2 regulated genes by RNA sequencing |
15.76 |
|
Nrf2 regulated genes in A549 cells |
15.76 |
|
CD95L derived si- and shRNAs kill cancer cells through an RNAi mechanism by targeting survival genes [shL3.shR6.RNAseq.lg] |
15.71 |
|
Combined Experimental and System-Level Analyses Reveal the Complex Regulatory Network of miR-124 during Human Neurogenesis [ZNF787] |
15.68 |
|
Self-organization of polarized cerebellar plate neuroepithelium in three-dimensional culture of human pluripotent stem cells |
15.52 |
|
Reprogramming of Endothelium Into Hematopoietic Progenitors by Defined Factors and Vascular Induction |
15.47 |
|
Active translatome profiling with RiboLace in MCF7 cells |
15.36 |
|
Codon usage optimization in pluripotent embryonic stem cells [RNA-seq] |
15.03 |
|
Epigenetic and transcriptional analysis of mesoderm progenitor cells identifies HOPX as a novel regulator of hemogenic endothelium |
14.95 |
|
Role of miR-146a in neural stem cell differentiation and neural lineage determination: relevance for neurodevelopmental disorders |
14.86 |
|
Parkinson’s Disease Genetic Risk in a Midbrain Neuronal Cell Line |
14.82 |
|
Genomic expression analysis of K562 cells expressing shRNA targeting lncRNA-IIRX and control cells |
14.68 |
|
MEIS1 regulates hematopoiesis in hPSCs |
14.6 |
|
RNA-seq analysis to identify the genes regulated by p53-SET interplay |
14.46 |
|
RNA-dependent RNA polymerase sequence specificities of capsnatching viruses are tailored to aid viral replication |
14.46 |
|
GCTM-5 positive and negative cells in pancreatic adenocarcinoma cell lines |
14.41 |
|
Transcriptional landscape of epithelial and immune cell populations revealed through FACS-seq of healthy human skin |
14.36 |
|
The inhibitory effect of TIAM1 on TAZ transcriptional activity and TIAM1 differentially expressed genes |
14.32 |
|
List of TIAM1 differentially expressed genes in SW620 cells [RNA-seq] |
14.32 |
|
Transcriptome analysis of U87 cells upon LINC00152 knockdown |
14.32 |
|
H19 regulates hepatic glucose production by epigenetic modification of Hnf4* |
14.09 |
|
Identification of genes regulated by Long noncoding RNA H19 in hepatic cells |
14.09 |
|
RNA sequencing (RNA-SEQ) of Human endothelial cells (HUVEC) in LFS, sFRP2OE, and WT conditioned media |
14.0 |
|
RNA expression analysis upon JMJD1C depletion |
13.98 |
|
JMJD1C is required for the survival of acute myeloid leukemia by functioning as a co-activator for key transcription factors |
13.98 |
|
A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging |
13.94 |
|
Gene expression changes upon drug withdrawal (Mel888 cell line) |
13.78 |
|
Characterization of transcriptomics landscape in HUVEC cells exposed to oxidative stress |
13.74 |
|
Oncogenic Notch promotes long-range regulatory interactions within hyperconnected 3D cliques |
13.4 |
|
CHD7 is Suppressed in the Perinecrotic/Ischemic Microenvironment and is a Novel Regulator of Angiogenesis |
13.37 |
|
Vitamin d receptor-mediated stromal reprogramming suppresses pancreatitis and enhances pancreatic cancer therapy |
13.34 |
|
High capacity of the endoplasmic reticulum to prevent secretion and aggregation of amyloidgenic proteins |
13.26 |
|
Catalogue of differentially expressed long non-coding RNAs following activation of human and mouse innate immunity |
13.21 |
|
Effect of OVO-like 1 knockdown on global transcript expression in differentiated BeWo trophoblast cells |
13.19 |
|
RNA seq_PDX2_SHP099 |
13.1 |
|
Tamoxifen Resistance in Breast Cancer is Regulated by the EZH2-ERa-GREB1 Transcriptional Axis |
13.03 |
|
RRAD, IL4I1, CDKN1A, and SERPINE1 genes are potentially co-regulated by NF-κB and p53 transcription factors in cells exposed to high doses of ionizing radiation [RNA-Seq] |
13.0 |
|
Epigenetic Therapy Increases Therapeutic Efficacy in Myeloproliferative Neoplasms Through Inhibition of Aberrant Inflammatory Signaling |
12.93 |
|
Cooperative and Antagonistic Transcriptional Regulation by BRG/BRM [RNA-seq] |
12.89 |
|
Co-regulation of transcription by BRG1 and Brm, two mutually exclusive SWI/SNF ATPase subunits |
12.89 |
|
LINC00520 is Induced by Src, STAT3, and PI3K and Plays a Functional Role in Breast Cancer |
12.8 |
|
Non-coding regions are the main source of tumor-specific antigens [human] |
12.8 |
|
Non-coding regions are the main source of tumor-specific antigens |
12.8 |
|
Dual inhibition of HDMX and HDM2 as a Therapeutic Strategy in Leukemia |
12.74 |
|
In vitro differentiation of human low threshold mechanoreceptive (LTMR) neurons from embryonic stem cells |
12.61 |
|
Disruption of the exocyst induces podocyte loss and dysfunction |
12.56 |
|
Cell differentiation grade determines distinct FOXA2 contributions to the cis-regulatory networks of pancreatic cancer cells |
12.51 |
|
Cell differentiation grade determines distinct FOXA2 contributions to the cis-regulatory networks of pancreatic cancer cells [RNA-seq] |
12.51 |
|
Cooperation of dominant oncogenes with regulatory variants shapes clinical outcomes in pediatric cancer |
12.3 |
|
RNA-seq of three Ewing sarcoma cell lines (A673, SK-N-MC, RDES), transfected with either siControl or siMYBL2. |
12.3 |
|
Multivalent binding of PWWP2A to H2A.Z-marked transcriptional active chromatin regulates mitosis and organ development |
12.29 |
|
Multivalent binding of PWWP2A to H2A.Z-marked transcriptional active chromatin regulates mitosis and organ development [RNA-seq] |
12.29 |
|
The Short Isoform of BRD4 Promotes HIV-1 Latency by Engaging Repressive SWI/SNF Chromatin Remodeling Complexes |
12.27 |
|
Replicative senescence is associated with nuclear reorganization and DNA methylation at specific transcription factor binding sites |
12.22 |
|
Replicative senescence is associated with nuclear reorganization and DNA methylation at specific transcription factor binding sites (RNA-seq) |
12.22 |
|
Bach1 Regulates the Self-renewal and Mesendodermal Differentiation of Human Embryonic Stem Cells |
12.1 |
|
Genome-wide transcriptome analysis of NIPBL iPSC and commited cardiomyoctes |
11.96 |
|
A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab [ribosome profiling] |
11.91 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of ALDH+ E-BCSC, CD24-CD44+ M-BCSC and Bulk tumor cell Transcriptomes from MC1 and Vari068 PDX models of TNBC |
11.81 |
|
DHX9 suppresses spurious RNA processing defects originating from the Alu invasion of the human genome [uvCLAP CLIP-seq] |
11.76 |
|
Epigenomic plasticity enables human pancreatic alpha to beta cell reprogramming |
11.75 |
|
Single-cell transcriptomics of the human retinal pigment epithelium and choroid in health and macular degeneration |
11.71 |
|
Investigation into human Tra2 protein-dependent splicing in MDA-MB-231 cells using iCLIP and RNA-seq |
11.7 |
|
Differentially expressed genes from RNA-Seq and functional enrichment results are affected by the choice of single-end versus paired-end reads and stranded versus non-stranded protocols |
11.64 |
|
Proliferation pause as an early blockade of human cellular reprogramming toward pluripotency [RNA-seq analysis] |
11.64 |
|
Global Long Terminal Repeat activation participates in establishing the unique gene expression program of classical Hodgkin Lymphoma [RNA-Seq] |
11.57 |
|
Implication of Long noncoding RNAs in the endothelial cell response to hypoxia revealed by RNA-sequencing. |
11.42 |
|
Gene expression comparison of resting human peripheral-blood NK cells and activated counterparts |
11.38 |
|
Comprehensive analysis of Long non-coding RNA expression in dorsal root ganglion reveals cell type specificity and dysregulation following nerve injury |
11.37 |
|
Comprehensive analysis of Long non-coding RNA expression in dorsal root ganglion reveals cell type specificity and dysregulation following nerve injury [human iPS] |
11.37 |
|
ADAR1 controls apoptosis of stressed cells by inhibiting Staufen-mediated mRNA decay |
11.26 |
|
Global analysis of pre-mRNA subcellular localization upon splicing inhibition by spliceostatin A |
11.22 |
|
ETS family proteins bind glucocorticoid receptor: relevance for treatment of Ewing sarcoma |
11.21 |
|
Chromatin accessibility landscape upon induction of Msgn1, Pax3 and Myf5 in mesodermal cells and identification of conserved Pax3 binding sites and target genes during skeletal myogenesis |
11.18 |
|
SETDB2 links E2A-PBX1 to cell cycle dysregulation in acute leukemia through CDKN2C repression [sequencing] |
11.13 |
|
The Molecular Dissection of the Oncogenic Role of ETS1 in the Mesenchymal Subtypes of Head and Neck Squamous Cell Carcinoma [RNA-seq knock-down] |
11.09 |
|
Irf9 function in immunity in mouse |
11.02 |
|
Transcription profile analysis of wild type and Irf9-/- human monocytic THP1 cells in response to type I interferons |
11.02 |
|
Conservative alteration of chromosomal expression pattern across human solid tumor types |
10.99 |
|
N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis[Ribosome Profiling] |
10.86 |
|
ZNF131 suppresses centrosome fragmentation in Glioblastoma stem-like cells through regulation of HAUS5 |
10.82 |
|
RUNX2/CBFB modulates the response to MEK inhibitors through activation of receptor tyrosine kinases in KRAS mutant colorectal cancer |
10.81 |
|
UBL5 is essential for pre-mRNA splicing and sister chromatid cohesion in human cells |
10.81 |
|
mRNA cap methyltransferase, RNMT-RAM, promotes RNA pol II transcription |
10.76 |
|
NGS based identification of GD2-positive tumor-specific phenotype for cancer diagnostics and therapy |
10.74 |
|
RNA seq data of Hep3B-control, Hep3B-sertraline, Hep3B-XL413, Hep3B-XL413-sertraline, Huh7-control, Huh7-sertraline, Huh7-XL413, Huh7-XL413-sertraline cells |
10.74 |
|
Coordinate regulation of alternative pre-mRNA splicing events by the human RNA chaperone proteins hnRNPA1 and DDX5 |
10.71 |
|
The RNA-binding profile of Acinus, a peripheral component of the Exon junction complex, reveals its role in splicing regulation |
10.68 |
|
Hepatocyte maturation |
10.64 |
|
MiR-CLIP capture of a miRNA targetome uncovers a lincRNA H19-miR-106a interaction |
10.57 |
|
Mechanosensitive ion channel regulates tissue stiffening to promote glioma aggression |
10.53 |
|
Solid phase chemistry to covalently and reversibly capture thiolated RNA |
10.4 |
|
Human Nonsense-Mediated RNA Decay Initiates Widely by Endonucleolysis and Targets snoRNA Host Genes |
10.37 |
|
Transcriptional Regulationand Chromatin Dynamics inHuman Epithelial Cell Differentiation (RNA-seq) |
10.32 |
|
Transcriptional Regulationand Chromatin Dynamics inHuman Epithelial Cell Differentiation |
10.32 |
|
Genome-wide expression change by SHARPIN knockdown in MCF-7 cells |
10.27 |
|
Regulation of protein translation during mitosis |
10.27 |
|
Expression data for HT29 cells treated with 5-aza-deoxy-cytidine [RNA-Seq] |
10.24 |
|
Expression data for HT29 cells treated with 5-aza-deoxy-cytidine |
10.24 |
|
KMT2D regulates p63 target enhancers to coordinate epithelial homeostasis [RNA-Seq] |
10.15 |
|
KMT2D regulates p63 target enhancers to coordinate epithelial homeostasis |
10.15 |
|
Transcriptomic profiling of mesenchymal stem cells (MSC) differentiation into mesangial cells |
10.13 |
|
Transcriptome analysis of human airway epithelium infected by Human Bocavirus 1 |
10.12 |
|
Long non-coding RNA SMILR regulates genes involved in cytokinesis in human vascular smooth muscle cell |
10.04 |
|
Temporal dynamic reorganization of 3D chromatin in hormone-induced breast cancer and endocrine resistance |
10.01 |
|
Genome-scale identification of transcription factors that mediate an inflammatory network during breast cellular transformation |
9.97 |
|
RNA-seq during MCF10A-ER-Src cell transformation and upon factor knockdowns |
9.97 |
|
Progressive motor neuron pathology and the role of astrocytes in a human stem cell model of VCP-related ALS |
9.93 |
|
Comparison of expression profiles of APP-depleted prostate cancer cells (LNCaP) |
9.91 |
|
SREBP1 drives Keratin 80-dependent cytoskeletal changes and invasive behavior in endocrine resistant ERα breast cancer |
9.89 |
|
Cistromic re-programming by truncating GATA3 mutations promotes mesenchymal transformation in vitro, but not mammary tumour formation in mice [RNA-seq] |
9.89 |
|
Cistromic re-programming by truncating GATA3 mutations promotes mesenchymal transformation in vitro, but not mammary tumour formation in mice |
9.89 |
|
FUS mutant human motoneurons transcriptome analysis reveals altered pathways and impairment of microRNA function |
9.82 |
|
Genome-wide maps of chromatin state and mRNA expression patterns in leukemic cell lines |
9.72 |
|
A genome-wide long noncoding RNA CRISPRi screen identifies PRANCR as a novel regulator of epidermal homeostasis |
9.69 |
|
hMTR4 plays a central role in creating balanced nuclear RNA pools for degradation and export |
9.69 |
|
Poly(A)-specific ribonuclease (PARN) mediates 3' end maturation of the telomerase RNA component |
9.68 |
|
Biased Expression of the FOXP3Δ3 Isoform in Aggressive Bladder Cancer Mediates Differentiation and Cisplatin Chemotherapy Resistance |
9.63 |
|
Exploring the RNA landscape of endothelial exosomes |
9.62 |
|
Integrin signaling regulates YAP/TAZ to control skin homeostasis |
9.61 |
|
Hematopoietic Stem and Progenitor Cells from Human Pluripotent Stem Cells via Transcription Factor Conversion of Hemogenic Endothelium |
9.6 |
|
Functional Cardiac Fibroblasts Derived from Human Pluripotent Stem Cells via Second Heart Field Progenitors |
9.55 |
|
Convergent exaptation of Alu and B/ID SINEs for Staufen-mediated mRNA decay |
9.51 |
|
The ZZ-type zinc finger of ZZZ3 modulates the ATAC complex-mediated histone acetylation and gene activation |
9.49 |
|
Pericyte-like cells generated from human pluripotent stem cells support hematopoietic stem and progenitors ex vivo |
9.44 |
|
Nickel induced transcriptional changes persist post exposure through epigenetic reprograming |
9.43 |
|
RNASEQ Analysis of sh-TRC and sh-MIR100HG in the triplex negative breast cancer |
9.41 |
|
Human Adipocytes Regulate Gene Expression in Triple-negative Breast Cancer Assessed by NGS Sequencing |
9.4 |
|
Transcriptomic analysis of trametinib-resistant HCT116 colorectal carcinoma cells compared to the parental control cells |
9.38 |
|
The LINC01138 Drives Malignancies via Activating Arginine Methyltransferase 5 in Hepatocellular Carcinoma |
9.33 |
|
Opposing Effects of Cyclooxygenase-2 (COX-2) on Estrogen Receptor β (ERβ) Response to 5α-reductase Inhibition in Prostate Epithelial Cells |
9.32 |
|
Whole-Transcriptome Profiling of Canine and Human in Vitro Models Exposed to a G-Quadruplex Binding Small Molecule |
9.3 |
|
Genome-wide discovery of human splicing branchpoints [RNAse] |
9.29 |
|
Global transcriptional profiling changes upon knockout of USP22 in human Non-small cell lung cancer cells |
9.19 |
|
Gene expression profiles of primary human NK cells before and after expansion on CSTX002 feeder cells, with and without IL-21 stimulation |
9.12 |
|
An alternative CTCF isoform antagonizes canonical CTCF occupancy and changes chromatin architecture to promote apoptosis |
9.01 |
|
Pan-cancer transcriptomic analysis associates long non-coding RNAs with key mutational driver events |
8.99 |
|
RNA-seq expression data from EB-HSPC after AM580 treatment compated to DMSO-trated and FL-HSPCs |
8.98 |
|
Bromodomain inhibition of the co-activators CBP/EP300 facilitates reprogramming |
8.94 |
|
Bromodomain inhibition of the co-activators CBP/EP300 facilitates reprogramming (RNA-seq fibroblasts) |
8.94 |
|
ZBTB10 binds the telomeric variant repeat TTGGGG and interacts with TRF2 |
8.93 |
|
ZBTB10 binds the telomeric variant repeat TTGGGG and interacts with TRF2 [RNA-Seq] |
8.93 |
|
Essential Roles of SETD7 as Transcriptional Activator and Co-regulator of H3K36me in Cardiac Lineage Commitment |
8.93 |
|
Decrease in EZH2 histone methyltransferase mediates the effects of fluid shear stress (FSS) in endothelial cells |
8.9 |
|
The ARID1A tumor suppressor controls global transcription via pausing of RNA Polymerase II |
8.89 |
|
Innate-like activation of mucosal-associated invariant T cells in mycobacterial infection |
8.85 |
|
Transcriptome-profiling (RNA-seq) and Ribosome-profiling (Ribo-seq) of BJ cells treated with Nutlin-3a, an MDM2 inhibitor, which induces p53. |
8.82 |
|
Developmental origins define epigenomic differences between subcutaneous and visceral adipocytes |
8.82 |
|
Interaction with ZMYND11 mediates opposing roles of Ras-responsive transcription factors ETS1 and ETS2 |
8.78 |
|
Interaction with ZMYND11 mediates opposing roles of Ras-responsive transcription factors ETS1 and ETS2 |
8.78 |
|
BASP1 modifies the Tamoxifen response |
8.78 |
|
Non-transmissible measles virus vector with segmented RNA genome establishes different types of iPSCs from hematopoietic cells |
8.72 |
|
mRNA sequencing of highly and lowly metastatic human colorectal cancer PDXs |
8.71 |
|
Long Non-coding RNA PICSAR Promotes Growth of Cutaneous Squamous Cell Carcinoma by Regulating ERK1/2 Activity |
8.7 |
|
FMRP facilitates the nuclear export of N6-methyladenosine-containing mRNAs |
8.7 |
|
The identification of RBM47 binding sites and RBM47-dependent alternative splicing events in brain metastatic breast cancer cells |
8.69 |
|
Identification of alternatively spliced transcripts in brain metastatic derivatives of MDA-MB-231 breast cancer cells in response to RBM47 expression |
8.69 |
|
RNA-sequencing of human liver tissue |
8.69 |
|
A role for ZNF598 in post-transcriptional gene regulation |
8.65 |
|
Transcriptomics-based drug repurposing approach identifies novel drugs against sorafenib-resistant hepatocellular carcinoma |
8.64 |
|
HBEC-shp53-PCHD7 |
8.62 |
|
Inhibition of DNA methylation promotes breast tumor sensitivity to netrin-1 interference [RNA-Seq] |
8.58 |
|
Inhibition of DNA methylation promotes breast tumor sensitivity to netrin-1 interference |
8.58 |
|
Novel Targeting of Transcription and Metabolism in Glioblastoma |
8.57 |
|
The transcriptomic differences between Th1, Tr1, and Tneg cells in controlled human malaria infection |
8.54 |
|
Acetylation of spliceosome protein PHF5A modulates stress responses and colorectal carcinogenesis through alternative splicing mediated upregulation of KDM3A |
8.5 |
|
Effect of Ro 08-2750 treatment on gene expression of human leukemia cell lines MOLM13 and K562 |
8.4 |
|
Axitinib exposure triggers endothelial cells senescence through ROS accumulation and ATM activation |
8.4 |
|
Integrative Analysis of Tamoxifen-resistant Cell Line Models Based on Sequencing Genomes, Transcriptomes and Epigenomes [seq] |
8.33 |
|
Integrative Analysis of Tamoxifen-resistant Cell Line Models Based on Sequencing Genomes, Transcriptomes and Epigenomes |
8.33 |
|
H3K27Ac in MCF7 Y537S ER mutant cells and RNAseq with and without treatment with THZ1 |
8.33 |
|
Patient-derived organoids (PDOs) model treatment response of metastatic gastrointestinal cancers. |
8.31 |
|
Evolving Spindlin1 Small Molecule Inhibitors Using Protein Microarrays |
8.26 |
|
Functional studies of missense TREM2 mutations in human stem cell-derived microglia |
8.18 |
|
MLL-AF4 binds directly to a BCL-2 specific enhancer and impacts H3K27 acetylation |
8.14 |
|
Reducing the structure bias of RNA-Seq reveals a large number of non-annotated non-coding RNA |
8.12 |
|
The effect of very-high-molecular-mass hyaluronan (vHMM-HA) on IMR90 transcriptome |
8.08 |
|
Inhibition of ERG Activity in Patient Derived Prostate Cancer Xenografts using the Small Molecule Inhibitor YK-4-279 |
8.06 |
|
RNAseq analysis of the human neutrophil transcriptome, with and without in vitro cytokine stimulation |
8.02 |
|
RBPJ Maintains Brain Tumor Initiating Cells through CDK9-mediated Transcriptional Elongation |
8.01 |
|
RNA-seq Profiles in RBPJ Maintains Brain Tumor Initiating Cells through CDK9-mediated Transcriptional Elongation |
8.01 |
|
A systematic analysis of nuclear heat-shock protein 90 identifies a metazoan-specific regulatory module |
7.97 |
|
The role of antigen presenting cells in the induction of HIV-1 latency in resting CD4+ T-cells |
7.88 |
|
Glioma-derived miRNA-containing extracellular vesicles induce angiogenesis by reprogramming brain endothelial cells (longRNA-seq) |
7.87 |
|
Glioma-derived miRNA-containing extracellular vesicles induce angiogenesis by reprogramming brain endothelial cells |
7.87 |
|
Transcriptional regulation of autophagy-lysosomal function in BRAF-driven melanoma progression and chemoresistance |
7.85 |
|
Differential expression of pancreatic cancer PANC1 cells treated with pilocarpine |
7.84 |
|
Identification of miR-100 and miR-125b targets by AGO2 RIP-seq and RNA-seq after ectopic expression of miR-100 or miR-125b and evaluation of the TGFb expression signature in PANC-1 cells by RNA-seq |
7.82 |
|
Evidence for rRNA 2'-O-methylation plasticity: control of intrinsic translational capabilities of human ribosomes |
7.75 |
|
Gene-Edited Human Kidney Organoids Reveal Mechanisms of Disease in Podocyte Development |
7.72 |
|
Transcriptome sequencing wide functional analysis of human mesenchymal stem cells |
7.67 |
|
Transcriptome-wide response to synthetic chromatin protein PcTF |
7.62 |
|
Genome-wide analysis of ferroptosis related genes in liver cancer cells. |
7.56 |
|
Thymine DNA Glycosylase as a novel target for melanoma: effect of TDG silencing on gene expression in SK-mel-28 melanoma cells |
7.55 |
|
TrapSeq: An RNA Sequencing-based pipeline for the identification of genetrap insertions in mammalian cells |
7.55 |
|
RNA-sequencing and MeDIP-sequencing of shSRC-1 and shNT tamoxifen treated LY2 cells |
7.52 |
|
RNA-sequencing of shSRC-1 and shNT tamoxifen treated LY2 cells |
7.52 |
|
Rapid neurogenesis through transcriptional activation in human stem cell (RNA-Seq) |
7.45 |
|
Induced DNA demethylation, genome instability and transcription |
7.42 |
|
Impact of DNA demethylation agents (5-azacytidine or vitamin C) on gene expression in glioblastoma HSR-GBM1 cells |
7.42 |
|
Gene expression profile in breast cancer cells |
7.4 |
|
Genome-wide profile of cJun and p27 and gene expression profile in breast cancer cells |
7.4 |
|
Improved genome-wide mapping of uncapped and cleaved transcripts in eukaryotes—GMUCT 2.0 |
7.31 |
|
FGF2 regulation of gene expression in stable inducible Neurons |
7.23 |
|
Smad5 acts as an intracellular pH messenger and maintains bioenergetic homoeostasis |
7.17 |
|
Comprehensive analysis of microRNA expression in regionalized human neural progenitor cells reveals microRNA-10 as a caudalizing factor |
7.11 |
|
RNA-seq of HBV-infected Primary Human Hepatocytes treatment by Tazarotene |
7.11 |
|
Noncoding regions are the main source of targetable tumor-specific antigens |
6.99 |
|
Effect of PBK knockdown on C4-2 cell transcriptome |
6.97 |
|
Lineage tracing of acute myeloid leukemia reveals the impact of hypomethylating agents on chemoresistance selection |
6.95 |
|
Contribution of SRF and Nkx2-5 to androgen-dependent gene expression in prostate cancer |
6.91 |
|
Pre-mRNA Splicing is Facilitated by an Optimal RNA Polymerase II Elongation Rate |
6.88 |
|
Reassessment of Exosome Composition |
6.83 |
|
RNA sequencing analysis of triple cytokine-captured human CD4 T cells |
6.83 |
|
Tracing transcriptome profiles of human oocyte cultured by growth hormone or not in vitro by single cell RNA-seq |
6.7 |
|
CRISPR-Cas9 combinatorial KO of epigenetic regulators in human ovarian cancer cells |
6.63 |
|
Distinct changes in transcriptional profiles and epigenetic patterns mediated by EZH2 inhibitors in sensitive and insensitive prostate cancer cells |
6.57 |
|
EZH2 inhibitor-mediated transcriptional profiling in prostate cancer cells [RNA-seq] |
6.57 |
|
Genome-wide CRISPR-Cas9 screen identifies SLC1A3 as a key contributor to L-asparaginase Resistance in Solid tumors |
6.46 |
|
Reprogramming of human stem cells towards a rejuvenated and transformation-resisting state by recoding a single nucleotide |
6.44 |
|
The LRF/ZBTB7A transcription factor is a BCL11A-independent repressor of fetal hemoglobin |
6.4 |
|
RNA-seq of RKO cells with cTAZ KO or putback |
6.32 |
|
A non-canonical role of YAP/TEAD is required for activation of estrogen-regulated enhancers in breast cancer |
6.25 |
|
A non-canonical role of YAP/TEAD is required for activation of estrogen-regulated enhancers in breast cancer [RNA-seq] |
6.25 |
|
Transcriptome analysis of BAP1 knockout and restoration |
6.24 |
|
Expression profiles of restoration of BAP1 in a BAP1 deficient cell line |
6.24 |
|
Gene expression changes after depletion of Cyclin F and atypical E2Fs in HeLa cells. |
6.19 |
|
Transcriptional responses of melanoma cells to BRAF inhibition |
6.18 |
|
Programmable RNA N6-methyladenosine editing by CRISPR-Cas9 conjugates |
6.11 |
|
Isolation of highly enriched cardiac mesoderm from differentiating human embryonic stem cells |
6.1 |
|
CD13 and ROR2 permit isolation of highly enriched cardiac mesoderm from differentiating human embryonic stem cells |
6.1 |
|
CDK12 mediated transcriptional regulation in U2OS cells |
6.08 |
|
To identify transcripts that are differentially expressed in the MYCN amplified vs MYCN non-amplified cell lines using Next Generation Sequencing |
5.98 |
|
Sequencing-based analyses characterize a tumor suppressive role of mir-1271 repressed by DNA hypermethylation in gastric cancer |
5.97 |
|
The IMiDs, through loss of Ikaros and Aiolos, primes myeloma cells for daratumumab mediated killing by upregulation of CD38 |
5.88 |
|
Gene expression analysis of a panel of human fibroblasts that generate an aligned (anisotropic) vs non-aligned extracellular matrix |
5.87 |
|
NF-κB p65 dimerization and DNA-binding is important for inflammatory gene expression |
5.84 |
|
Transcriptome-wide identification of CELF2 functional targets in T cells |
5.79 |
|
Generation of Brain Region-specific Organoids using a Miniaturized Spinning Bioreactor and Modelling ZIKV Exposure |
5.7 |
|
Role of COP1 on MAP kinase transcriptional output in melanoma |
5.7 |
|
Expression analysis of THP1 cells following shRNA knock-down of RUVBL2 |
5.7 |
|
Subclonal cooperation drives metastasis through modulating local and systemic immune microenvironments |
5.66 |
|
Identification of downstream genes regulated by YAP1 through knockdown and overexpression of YAP1 in U251 cell with a stably expression of mutant APP |
5.65 |
|
Transcriptomic changes mediated by β-amyloid in human aortic endothelial cells (HAOEC) |
5.64 |
|
Oncogenic changes and EMT in normal human bile duct epithelial cells are caused by parasite-derived materials and N-nitrosodimethylamine |
5.61 |
|
High-throughput sequencing of PROMPT-enriched samples. |
5.59 |
|
Convergent roles of ATF3 and CSL in chromatin control of CAF activation [RNA-seq] |
5.58 |
|
Convergent roles of ATF3 and CSL in chromatin control of CAF activation |
5.58 |
|
Chemical Enhancement of Direct Cardiac Reprogramming In Vitro and In Vivo |
5.57 |
|
Transcriptome Analysis of CircMRPS35 mediated mRNA expression profiles |
5.49 |
|
Ex vivo Dynamics of Human Glioblastoma Cells in a Microvasculature-on-a-Chip System Correlates with Tumor Heterogeneity and Subtypes |
5.43 |
|
SOX11 knockdown in B-ALL cell lines |
5.42 |
|
RNA-Seq analysis of cSCC cells after siRNA-induced gene knockdown of lncRNA PRECSIT |
5.38 |
|
Transcriptomic profiles of human foreskin fibroblast cells in response to orf virus |
5.36 |
|
TimeLapse-seq: adding a temporal dimension to RNA sequencing through nucleoside recoding |
5.36 |
|
RNA-Seq analysis of human neutrophils isolated by different protocols (Polymorphprep and negative selection) and incubated with and without in vitro cytokine stimulation |
5.26 |
|
C9/ALS Human Embryonic Stem Cells and C9/ALS Induced Pluripotent Stem Cells |
5.26 |
|
Gene Expression Profiling of WT and KDM3A Knocked out Cell |
5.25 |
|
Genome-wide maps of chromatin state and Gene Expression Profiling in HCT116 cells |
5.25 |
|
Enhancement of direct reprogramming from fibroblasts to epithelial lineages by OVOL2-induced mesenchymal-to-epithelial transition [CAGE] |
5.23 |
|
Enhancement of direct reprogramming from fibroblasts to epithelial lineages by OVOL2-induced mesenchymal-to-epithelial transition |
5.23 |
|
Improved post thaw function and genetic changes for mesenchymal stromal cells cryopreserved using multicomponent osmolyte solutions |
5.23 |
|
Newly defined ABCB5+ dermal mesenchymal stem cells promote healing of chronic iron overload wounds via secretion of interleukin-1 receptor antagonist |
5.21 |
|
Evolution of an lncRNA leads to a primate specific modulation of alternative splicing |
5.21 |
|
Insulin receptor associates with promoters genome-wide and regulates gene expression [RNA-seq 2] |
5.18 |
|
Knockout human reveal an essential role for Paternally Expressed 10 (PEG10) in JEG3 cell line development |
5.18 |
|
Low carbohydrate diet study for non-alcoholic fatty liver disease patients |
5.12 |
|
Whole Transcriptomic Sequencing of Metastatic Castration Resistant Prostate Cancer Samples |
5.1 |
|
The transcriptome effect of overexpressing EZH2 in MCF7 |
4.99 |
|
Prolyl Hydroxylase Substrate Adenylosuccinate Lyase Is An Oncogenic Driver In Triple Negative Breast Cancer |
4.9 |
|
Toxicogenomics of the flame retardant tris (2-butoxyethyl) phosphate in HepG2 cells using RNA-seq. |
4.87 |
|
RNA-seq analysis of BORIS/CTCFL knockdown in K562 cell line |
4.76 |
|
RNA-seq and small RNA-seq analysis of BORIS/CTCFL knockdown in K562 cell line |
4.76 |
|
Targeted differentiation of regional ventral neuroprogenitors and related neuronal subtypes from human pluripotent stem cells |
4.68 |
|
Expanding the Nucleoside Recoding Toolkit: Revealing RNA Population Dynamics with 6-thioguanisine |
4.68 |
|
STX4 Over-Expression in Human islets |
4.67 |
|
The human cellular nucleic acid binding protien binds G-rich elements close to translation initiation sires and promotes translation. [RNA-Seq] |
4.65 |
|
The human cellular nucleic acid binding protien binds G-rich elements close to translation initiation sires and promotes translation. |
4.65 |
|
Gene expression profiles of BxPC-3, MiaPaCa-2 and PANC-1 cell lines treated with DMSO and THZ1 respectively |
4.63 |
|
RNA-seq analysis upon ARID1B overexpression |
4.59 |
|
Identification of microRNA-dependent gene regulatory networks driving human pancreatic endocrine cell differentiation [H1 RNA-seq] |
4.57 |
|
RNA-SEQ assay for wild type and CRISPR induced endoglin knockout human pulmonary artery smooth muscle cells (PASMC) |
4.45 |
|
CXCR4 is a host factor that regulates Plasmodium development in hepatocytes |
4.44 |
|
Nickel exposure induces persistent mesenchymal phenotype in human lung epithelial cells through epigenetic activation of ZEB1 |
4.35 |
|
Nucleotide stress induction of HEXIM1 suppresses melanoma by modulating cancer cell-specific gene transcription [RNA-Seq2] |
4.31 |
|
PER2 synchronizes mitotic expansion and decidual transformation of human endometrial stromal cells |
4.25 |
|
Antibody-Mediated Inhibition of MICA/B Shedding Promotes NK Cell-Driven Tumor Immunity |
4.25 |
|
Transcriptomic analysis of differential expressed genes of human tonsillar epithelial cells UT-SCC-60B in response to EV71 infection |
4.17 |
|
Acquisition of a hybrid E/M state is essential for tumorigenicity of basal breast cancer cells |
4.16 |
|
Identifying transcripts that are transcriptinoally regulated by CBFB and RUNX1 using RNAseq |
4.11 |
|
GATA2 promotes hematopoietic development and represses cardiac differentiation of human mesoderm |
4.08 |
|
RNA-seq transcriptonal profiling in human K562 cells with or without dCas9 and sgRNAs |
3.99 |
|
In situ CAPTURE of chromatin interactions by biotinylated dCas9 |
3.99 |
|
LSD1 mediates MYCN control of epithelial-mesenchymal transition through silencing of metastatic suppressor NDRG1 gene |
3.97 |
|
RNA-seq analysis in knockdown Jurkat samples for each factor of TAL1 complex |
3.96 |
|
Oncogenic roles of ARID5B in T-ALL |
3.96 |
|
Mitochondrial dsRNA triggers antiviral signalling in humans |
3.92 |
|
Improving fibroblast characterization using single-cell RNA sequencing: an optimized tissue disaggregation and data processing pipeline |
3.91 |
|
Interaction between mitoNEET and NAF-1 in cancer cells |
3.77 |
|
The X-linked DDX3X RNA helicase dictates translation re-programming and metastasis in melanoma |
3.75 |
|
Re-programing chromatin with a bifunctional LSD1/HDAC inhibitor induces therapeutic differentiation in DIPG |
3.7 |
|
Re-programing chromatin with a bifunctional LSD1/HDAC inhibitor induces therapeutic differentiation in DIPG [RNA-seq] |
3.7 |
|
Melanoma therapeutic strategies that select against resistance by exploiting MYC-driven evolutionary convergence |
3.68 |
|
The contribution of Alu exons to the human proteome |
3.59 |
|
Discovery of Drug Candidates that Inhibit and Eliminate Zika Virus Infection in Fetal and Adult Brain |
3.57 |
|
The Developmental Heterogeneity of Human Natural Killer Cells Defined by Single-cell Transcriptome |
3.56 |
|
MEIS2 is a novel oncogenic partner in AML1-ETO positive AML [RNA-Seq human] |
3.52 |
|
MEIS2 is a novel oncogenic partner in AML1-ETO positive AML |
3.52 |
|
RNA deep sequencing analysis of glioma stem cells(GSCs) and non-GSCs |
3.47 |
|
Immune Checkpoint Regulation of Pulmonary Fibrosis [bulk RNA-seq] |
3.44 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of colorectal cancer cells transfected with NC siRNA or RPL9 siRNA |
3.43 |
|
BBBomics - Human Blood Brain Barrier Transcriptomics Hub |
3.4 |
|
BBBomics - Human Blood Brain Barrier Transcriptomics Hub [RNA-seq] |
3.4 |
|
Stable oxidative cytosine modifications accumulate in cardiac mesenchymal cells from Type2 diabetes patients: rescue by alpha-ketoglutarate and TET-TDG |
3.38 |
|
Stable oxidative cytosine modifications accumulate in cardiac mesenchymal cells from Type2 diabetes patients: rescue by alpha-ketoglutarate and TET-TDG functional reactivation [human cells RNA-seq] |
3.38 |
|
The MEF2B Regulatory Network |
3.25 |
|
The MEF2B Regulatory Network - RNA-seq data |
3.25 |
|
N6-methyladenosine Recruits HNRNPG for Alternative Splicing Regulation |
3.17 |
|
Indoxyl sulfate stimulates angiogenesis by regulating reactive oxygen species production via CYP1B1 |
3.09 |
|
RNA G-quadruplexes mark repressive upstream open reading frames in human mRNAs |
3.04 |
|
ETS1 induction by the omental microenvironment promotes ovarian cancer metastasis |
3.03 |
|
ETS1 induction by the omental microenvironment promotes ovarian cancer metastasis [RNA-Seq] |
3.03 |
|
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 |
3.0 |
|
RNA-seq analysis of human KMT2A rearranged MV4;11 AML cell line treated with DOT1L and/or EZH2 inhibitor |
2.99 |
|
Parallel T-cell cloning and deep sequencing of the transcripts of human MAIT cells reveal stable oligoclonal TCRβ repertoire |
2.95 |
|
Regulatory network controlling tumor-promoting inflammation in human cancers [RNA-seq] |
2.88 |
|
Regulatory network controlling tumor-promoting inflammation in human cancers |
2.88 |
|
A Stable Transcription Factor Complex Nucleated by Dimeric AML1-ETO Controls Leukaemogenesis |
2.83 |
|
LHX9 rescues KRAS suppression through transcriptional regulation of YAP1 [RNA-Seq] |
2.63 |
|
LHX9 rescues KRAS suppression through transcriptional regulation of YAP1 |
2.63 |
|
The anti-leukemic effect of R-2HG depends on its acting as an m6A mRNA modifier-RNA Seq-Resistant, sensitive and healthy control |
2.56 |
|
Small extracellular vesicles are key regulators of non-cell autonomous intercellular communication in senescence via the interferon protein, IFITM3 |
2.54 |
|
HMGA1 and FOXM1 synergistically regulate a common gene network modulating angiogenesis in breast cancer |
2.5 |
|
Targeting the androgen receptor N-terminus via the cochaperone Bag-1L [RNA-seq C-terminal mutant] |
2.42 |
|
A code of mono-phosphorylation modulates the function of RB. |
2.42 |
|
Identification of global XBP1s target gene expression in human prostate cancer cells |
2.42 |
|
Targeting Chromatin Regulators Inhibits Leukemogenic Gene Expression in NPM1 Mutant Leukemia |
2.38 |
|
Translating transcriptome of cancer cells in situ in mesenchymal-rich tumor microenvironment |
2.33 |
|
Sequencing of ponatinib-resistant LC-2/ad derivatives (PR1 and PR2) and parental LC-2/ad cells |
2.25 |
|
RNA-seq after siRNA targeting DDX24 applied to iHUVECs cell lines |
2.15 |
|
SLAM-seq defines direct gene-regulatory functions of the BRD4-MYC axis [Quant-Seq] |
2.13 |
|
SLAM-seq defines direct gene-regulatory functions of the BRD4-MYC axis |
2.13 |
|
Long-term in vitro expansion of epithelial stem cells enabled by pharmacological inhibition of PAK1-ROCK-Myosin II and TGF-β signaling |
2.11 |
|
Long-term in vitro expansion of epithelial stem cells enabled by pharmacological inhibition of PAK1-ROCK-Myosin II and TGF-β signaling (RNA-seq) |
2.11 |
|
Circular RNA expression signature of low-glucose-treated MIA PaCa-2 cells |
2.03 |
|
Vammin induces a highly efficient angiogenic response through VEGFR-2/NRP-1 and bypasses the regulatory function of VEGFR-1 |
2.0 |
|
Aneuploidy triggers an immune response |
1.98 |
|
Transcriptome profiling of H1-iCas9 cells grown on laminin and on MEFs |
1.9 |
|
LncRNA NONHSAT113026 represses renal cell carcinoma tumorigenesis through interacting with NF-κB/p50 and SLUG |
1.9 |
|
Differentiation of human embryonic stem cells to HOXA+ hemogenic vasculature that resembles the aorta-gonad-mesonephros |
1.88 |
|
A cell-permeable stapled peptide inhibitor of the estrogen receptor/coactivator interaction |
1.86 |
|
mRNA-Seq profiling of human developing kidney |
1.85 |
|
RNA sequencing quantitative analysis of RNA editing levels in ADAR1, ADAR2, AIMP2 overexpression and wild type HEK293 cells |
1.81 |
|
Androgen receptor functions as transcriptional repressor of Cancer Associated Fibroblast (CAF) activation [RNA-seq] |
1.78 |
|
Androgen receptor functions as transcriptional repressor of Cancer Associated Fibroblast (CAF) activation |
1.78 |
|
Structure and degradation of circular RNAs regulate PKR activation in innate immunity |
1.75 |
|
WNT signaling memory is required for ACTIVIN to function as a morphogen |
1.73 |
|
Epigenetic silencing of the tumor suppressor RASSF4 favors multiple myeloma progression |
1.69 |
|
Ets homologous factor has critical roles in epithelial dysfunction in airway disease [RNA-seq] |
1.68 |
|
Ets homologous factor has critical roles in epithelial dysfunction in airway disease |
1.68 |
|
Genome-wide DNA accessibility maps and differential gene expression using ChIP-seq, ATAC-seq and RNA-seq for the human secondary fibroblast cell line hiF-T and whole worms with and without knockdown of FACT complex |
1.67 |
|
Nudt3 is a mRNA Decapping Enzyme That Modulates Cell Migration |
1.66 |
|
Toxoplasma controls host cyclin E expression through the use of a novel MYR1-dependent effector protein, HCE1 |
1.62 |
|
Molecular Signatures Associated with ZIKV Exposure in Human Cortical Neural Progenitors |
1.62 |
|
N6-methyladenine DNA Modification in Glioblastoma |
1.6 |
|
N6-methyladenine DNA Modification in Glioblastoma [RNA-seq] |
1.6 |
|
Medial Ganglionic Eminence and Cortical Organoids Model Human Brain Development and Interneuron Migration [RNA-seq2] |
1.52 |
|
Time series single-cell transcriptomic analysis of AEC2 directed differentiation |
1.51 |
|
Copper Regulation of HIF-1 Transcription Activity [RNA-seq] |
1.49 |
|
Copper Regulation of HIF-1 Transcription Activity |
1.49 |
|
Multiplex Enhancer Interference Reveals Collaborative Control of Gene Regulation by Estrogen Receptor Alpha Bound Enhancers |
1.44 |
|
Multiplex Enhancer Interference Reveals Collaborative Control of Gene Regulation by Estrogen Receptor Alpha Bound Enhancers [RNA-Seq] |
1.44 |
|
Transcriptome of U251 cells overexpression complement component 7 |
1.41 |
|
RB tumor suppressor promotes cancer immunity through downregulating PD-L1 expression |
1.28 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and AXL-/- astrocytes Transcriptomes |
1.22 |
|
RNA splicing alteration on glioblastoma and normal neural stem cells |
1.18 |
|
Human pulmonary artery endothelial cells (hPAECs) with downregulated BMPR2 signaling demonstrate a unique gene expression signature after exposure to overexpression of AdAlox5 |
1.18 |
|
Adenovirus Small E1A Employs the Lysine Acetylases p300/CBP and Tumor Suppressor Rb to Repress Select Host Genes and Promote Productive Virus Infection |
1.17 |
|
Adenovirus Small E1A Employs the Lysine Acetylases p300/CBP and Tumor Suppressor Rb to Repress Select Host Genes and Promote Productive Virus Infection [RNA-seq] |
1.17 |
|
Effects of transcription on genome - nuclear lamina interactions: RNA-seq data |
1.16 |
|
Effects of transcription on genome - nuclear lamina interactions |
1.16 |
|
Transcriptome-wide identification of transient RNA G-quadruplexes in human cells |
1.16 |
|
Aneuploidy-induced cellular stresses limit autophagic degradation. |
1.11 |
|
RNA-seq analysis reveals profound changes in transcript profiles between siCon- and siH19-transfected uterine smooth muscle cells (USMC) |
1.07 |
|
In search for materials able to be colonized by a normal endothelium: сharacterization and NGS gene expression profiling of human primary endotheliocytes cultivated on electrospun 3D matrices |
1.01 |
|
Transcriptomes in healthy and CHB fetal hearts |
0.98 |
|
RNA-sequencing analysis of 5' capped RNAs identifies novel differentially expressed genes in sessile serrated colon polyps (SSPs) |
0.97 |
|
RNA deep sequencing analysis of human brain microvascular endothelial cells (ECs) treated with glioma-conditioned medium (glioma-CM) |
0.97 |
|
RNA sequencing of GLO1-depleted MDA-MB-231 breast cancer cells |
0.96 |
|
Transcriptomic Alterations in Lung Adenocarcinoma Unveil New Mechanisms Targeted by the TBX2 Subfamily of Tumor Suppressor Genes |
0.94 |
|
ERK signaling regulates opposing functions of JUN family transcription factors in prostate cancer cell migration |
0.92 |
|
RNA-sequencing of the human milk fat layer during colostrum, transitional, and mature stages of lactation |
0.88 |
|
Profiles of ribosome-associated mRNAs regulated by expression of wild-type (WT) or R534H variant of DDX3 with or without Sodium Arsenite treatment |
0.82 |
|
Total RNA profiles associated with DDX3 wild-type (WT) or R534H variant expression with or without sodium arsenite treatment [RNA-seq] |
0.82 |
|
Transcriptomic analysis of human coronary artery endothelial cells stimulated with TNF-alpha in the presence and absence of ACSL3 siRNA |
0.77 |
|
Transcriptome analysis on TDP43 and SRSF3 downstream genes and binding RNAs in MDA-MB231 cells by Next Generation Sequencing |
0.77 |
|
polyA RNA Sequencing Analysis of HTR-8/SVneo cells after lnc-SLC4A1-1 overexpression |
0.75 |
|
RNA sequencing of Formalin-Fixed, Paraffin-Embedded Specimens for Gene Expression Quantification and Data Mining |
0.71 |
|
Profiling and bioinformatics analyses reveal differential expression of circular RNA in tongue cancer revealed by high-throughput sequencing |
0.7 |
|
Transcriptome-wide modulation of splicing by the exon junction complex |
0.67 |
|
An siRNA screen identifies CHD4 as a target for epigenetic therapy |
0.66 |
|
A RUNX2-mediated Epigenetic Regulation of the Survival of p53 Defective Cancer Cells |
0.65 |
|
The control of rRNA synthesis during the directed differentiation of human embryonic stem cells precedes heterochromatin formation. |
0.59 |
|
Genome-wide expression analysis of human hTert immortalized fibroblasts after downregulation of MCM2 & MCM7 |
0.58 |
|
EZH1/SUZ12 complex positively regulates the transcription of NF-κB target genes via interaction with UXT |
0.52 |
|
UMI-count modeling and differential expression analysis for single-cell RNA sequencing |
0.52 |
|
A toxicogenomics approach to screen chlorinated flame retardants tris(2-chloroethyl) phosphate and tris(2-chloroisopropyl) phosphate for potential health effects |
0.52 |
|
The secretome of skin cancer cells activates the mTOR/MYC pathway in healthy keratinocytes and converts them into tumorigenic cells |
0.43 |
|
Profiling premalignant lesions in lung squamous cell carcinomas identifies mechanisms involved in stepwise carcinogenesis |
0.4 |
|
6mer seed toxicity in viral microRNAs |
0.39 |
|
eVIP2: Expression-based variant impact phenotyping to predict the function of gene variants |
0.37 |
|
Modulation of nonsense-mediated decay by rapamycin |
0.36 |
|
Iron response of HepG2 cells |
0.35 |
|
The NFkB subunit RELA is a master transcriptional regulator of the committed epithelial-mesenchymal transition in airway epithelial cells |
0.34 |
|
RNAseq of Breast cancer PDX samples |
0.33 |
|
Tracking transcriptional changes in a species-specific manner during experimental hepatoblastoma progression in vivo |
0.25 |
|
RNA-seq analysis of control and Myc-induced U2OS cells |
0.22 |
|
Hsa-miR-139-5p/HNRNPF axis modulates gene-transcripts balance in thyroid cancer cells |
0.22 |
|
iPSCs Reveal Protective Modifiers of the BMPR2 mutation in Pulmonary Arterial Hypertension |
0.21 |
|
RNA-seq and small RNA-seq from WT and ADAR1 knockdown H9 lines and their differentiation to specific types of neurons |
0.19 |
|
rG4-seq reveals widespread formation of G-quadruplex structures in the human transcriptome |
0.18 |
|
Ribosome profiling of TGFb-treated cells indicates reduced leucine availability |
0.15 |
|
Identification of a unique gene expression signature in mercury and 2,3,7,8-tetrachlorodibenzo-p-dioxin co-exposed cells |
0.12 |
|
Role of SUMOylation in differential ERα transcriptional repression by SERMs and pure antiestrogens in breast cancer cells |
0.09 |
|
Distinct and shared functions of ALS-associated TDP-43, FUS, and TAF15 revealed by comprehensive multi-system integrative analyses [RNA-Seq_Stability] |
0.02 |
|
Multiplexed engineering and analysis of endogenous enhancer activity in single cells: Mosaic-Seq of beta-globin locus (pooled infection) |
0.01 |
|
Targets mediated microRNA arm-imbalance promotes gastric cancer progression [lncRNA] |
0.0 |