|
Valproic acid attenuates hyperglycemia induced complement and coagulation cascade gene expression |
65.56 |
|
Lysine benzoylation is a novel histone mark |
42.35 |
|
Lysine benzoylation is a novel histone mark [RNA-seq] |
42.35 |
|
miR941 overexpression experiment |
40.14 |
|
MeRIP-seq for heat shock in B-cell lymphoma cells |
33.69 |
|
Next Generation RNA Sequencing Analysis of AMPK Wild Type, AMPKα-KO and AMPKα1-2A U2OS cell Transcriptomes |
33.3 |
|
Human HAP1 cells before and after nutrient deprivation |
31.21 |
|
Transcriptomic profiling of human HAP1 cells before and after nutrient deprivation |
31.21 |
|
Differetially expressed genes after hTR overexpression in U2OS cells |
29.66 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of Retinoblastoma Transcriptomes |
24.99 |
|
Fisetin induces autophagy in pancreatic cancer cells via endoplasmic reticulum stress- and mitochondrial stress-dependent pathways |
24.7 |
|
RNA-seq in transgenic cells |
24.05 |
|
Tracing Enhancer Networks using Epigenetic Traits (TENET) |
23.5 |
|
Impact of ETV7 activity on interferon-stimulated gene expression in 293T cells treated with interferon alpha |
23.49 |
|
ETV7 and interferon response |
23.49 |
|
Fbxo32 mediated gene expression program underlies EMT and metastasis |
22.38 |
|
Inhibition of TNBC metastasis by Gpx1 |
22.31 |
|
DHX36 resolves G-rich structures in mRNA untranslated region to allow their translation [cPDS-RNA-seq] |
20.36 |
|
Drug combination of 17-AAG and Belinostat on MDA-MB-231 breast cancer cells |
19.0 |
|
microRNA suppresses prostate cancer stem cells and metastasis by inhibiting a cohort of pro-metastasis targets including CD44, Rho GTPases and EZH2 |
18.94 |
|
RNA-seq and ChIP-seq analysis of BMI1 or RING1B-silenced prostate cancer cells C4-2 |
18.67 |
|
Interaction with WDR5 recruits MYC to a small cohort of genes required for tumor onset and maintenance |
18.65 |
|
Assembly of methylated LSD1 and CHD1 drives AR-dependent transcription and translocation |
18.61 |
|
Assembly of methylated LSD1 and CHD1 drives AR-dependent transcription and translocation [RNA-Seq] |
18.61 |
|
Genome-wide RNA-seq from GALNT14-depleted and GALNT14 overexpressing MDA-MB-231 LM2 and Par cells |
18.17 |
|
Integrated multi-omics approach reveals a role of ALDH1A1 in lipid metabolism in human colon cancer cells |
17.85 |
|
RNA-seq analysis of CRISPR/Cas9 generated human BMPR2 deficient endothelial cell lines harboring mutations characteristic for hereditary pulmonary hypertension (HPAH) |
17.5 |
|
Effect of CTCF and Rad21 knockdown on SLK cells and KSHV gene expression |
17.18 |
|
Understanding the Mechanistic Contribution of Herbal Extracts in Compound Kushen Injection with Transcriptome Analysis |
17.01 |
|
Gene expression analysis of dengue-infected cells |
16.9 |
|
Mitotically associated long non-coding RNA, MANCR regulates cell cycle in triple negative breast cancer cells |
16.69 |
|
Two dimensional and extracellular matrix based three-dimensional cultures of lung and breast cancer cells |
16.65 |
|
Gene expression profiling in two dimensional and extracellular matrix based three-dimensional cultures of lung and breast cancer cells |
16.65 |
|
RNA-Seq analysis of primary human keratinocytes exposed to Cannabidiol |
16.55 |
|
Elongation Factor TFIIS Prevents Transcription Stress and R-Loop Accumulation to Maintain Genome Stability [ RNA-seq] |
15.95 |
|
Elongation Factor TFIIS Prevents Transcription Stress and R-Loop Accumulation to Maintain Genome Stability |
15.95 |
|
Genome-wide analysis of herpes simplex virus type 1 (HSV-1) infected cells |
15.53 |
|
RNA-sequencing of human liver tissue |
15.2 |
|
Global Promotion of Alternative Internal Exon Usage by mRNA 3' End Formation Factors |
15.15 |
|
Global Regulation of Alternative Internal Exon Usage by mRNA 3' End Formation Factors [RNA-Seq] |
15.15 |
|
FMRP-associated MOV10 facilitates and antagonizes miRNA-mediated regulation |
15.11 |
|
The translation termination factor GSPT1 is a phenotypically relevant off-target of heterobifunctional phthalimide degraders |
15.01 |
|
RNA-seq analysis of uveal melanoma cells treated with FR900359 |
14.95 |
|
A Novel PI3K Regulator, ARID4B, Presents Synthetic Essentiality in PTEN-deficient Prostate Cancer |
14.69 |
|
A Novel PI3K Regulator, ARID4B, Presents Synthetic Essentiality in PTEN-deficient Prostate Cancer [RNA-seq] |
14.69 |
|
Studying iPSCs from a hibernating mammal reveals molecular mechanisms of cold resistance in neural tissues |
14.4 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of transcriptomes of human cord blood CD34+ cells treated with HDAC5 inhibitor |
14.16 |
|
Selective modulation of inflammatory Natural Killer (NK) cell phenotypes following histone H3K27 demethylase inhibition |
14.14 |
|
Selective modulation of inflammatory Natural Killer (NK) cell phenotypes following histone H3K27 demethylase inhibition [RNA-Seq] |
14.14 |
|
SAM68 is required for regulation of Pumilio by the NORAD long noncoding RNA |
14.06 |
|
Intragenic DNA methylation modulates alternative splicing by recruiting MeCP2 to promote exon recognition |
14.03 |
|
Intragenic DNA methylation modulates alternative splicing by recruiting MeCP2 to promote exon recognition [RNA-Seq] |
14.03 |
|
RNAseq Analysis in glioblastoma cells treated with Mepazine |
13.85 |
|
Global transcriptional profiling changes upon knockdown of LKB1 in human glioblastoma cell lines |
13.38 |
|
Transcriptome sequencing of K-562 cells |
12.97 |
|
Rorc disruption in human FG pancreatic cancer cells |
12.69 |
|
Transcriptomic hallmarks of tumor plasticity and stromal interactions in brain metastasis [MultiDisease] |
12.53 |
|
Oncogenic Notch promotes long-range regulatory interactions within hyperconnected 3D cliques [MB157_RNA-seq] |
12.5 |
|
C9orf72 Intermediate Repeats are Associated with Corticobasal Degeneration, Increased C9orf72 Expression and Disruption of Autophagy |
12.37 |
|
METTL3 promotes translation in human cancer cells |
12.33 |
|
Active translatome profiling with RiboLace in MCF7 cells |
12.12 |
|
The RNA binding protein IGF2BP3 promotes hematopoietic progenitor cell proliferation by targeting leukemogenic pathways |
12.04 |
|
RNA-Seq to assess the transcriptional effects of G quadruplex stabilization by the G4 ligand PhenDC3 in HT-1080 cells |
11.93 |
|
RNA-seq data corresponding to: AZD4573 is a highly selective CDK9 inhibitor that suppresses Mcl-1 and induces apoptosis in hematological cancer cells |
11.87 |
|
Nuclear import of the DSCAM-cytoplasmic domain drives signaling capable of inhibiting synapse formation |
11.55 |
|
Regulation of mRNA half-life by an inhibitor of human decapping enzyme Dcp2 following transcription shutoff in HEK293T cells |
11.51 |
|
DNA breaks and chromatin structural changes enhance the transcription of Autoimmune Regulator target genes |
11.4 |
|
DNA breaks and chromatin structural changes enhance the transcription of Autoimmune Regulator target genes [RNA-Seq] |
11.4 |
|
TGFβ-induced fibroblast activation requires persistent and targeted HDAC-mediated gene repression |
11.37 |
|
RNA-seq in HT-29 colorectal cancer cells after F. nucleatum treatment |
11.3 |
|
Survival of pancreatic cancer cells lacking KRAS function |
11.28 |
|
Transcriptome analysis in HT29 and SW480 cells depleted of Prdx2 |
11.17 |
|
RNA-seq analysis of HT-29, MCF10A, and MDA-MB-436 cells |
11.07 |
|
Human Adult Sorted Live Cell Erythroblasts transduced with Sigma shRNA Clone TRCN0000005418 targeting RIOK3 with puromycin selection RNAseq |
11.0 |
|
SOX21 ensures rostral forebrain identity by suppression of WNT8B during neural regionalization of human embryonic stem cells |
10.95 |
|
Identification of differential expressed genes of JQ1 or JQ1+Bortezomib in colorectal cancer cells |
10.93 |
|
H3B-8800, a novel oral splicing modulator, induces lethality in spliceosome mutant cancers [K562] |
10.88 |
|
ER proteostasis and temperature differentially impact the mutational tolerance of influenza hemagglutinin |
10.79 |
|
HIV-1 perturbs homeostatic ILCs, unmasks ILC1 plasticity, and boosts TCF7+ memory NK cells |
10.79 |
|
Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of TDP-43-dependent neurodegeneration |
10.78 |
|
HDAC inhibition enhances the in vivo efficacy of MEK inhibitor therapy in uveal melanoma |
10.75 |
|
Diverse Compounds from Pleuromutilin Lead to a Thioredoxin Inhibitor and Inducer of Ferroptosis |
10.71 |
|
Tpl-2 small molecule project |
10.59 |
|
Tpl-2 and MEK small molecule inhibitors |
10.59 |
|
Disease Model of GATA4 Mutation Reveals Transcription Factor Cooperativity in Human Cardiogenesis |
10.55 |
|
Disease Model of GATA4 Mutation Reveals Transcription Factor Cooperativity in Human Cardiogenesis [RNA-Seq] |
10.55 |
|
EHMT1 and EHMT2 inhibition induce fetal hemoglobin expression |
10.5 |
|
EHMT1 and EHMT2 inhibition induce fetal hemoglobin expression [RNA-seq] |
10.5 |
|
Gene expression profile in response to HIF-1α inhibition together with PPARα activation and the postnatal factors (T3, IGF-1 and dexamethasone) in hiPSC-CMs |
10.45 |
|
Effect of venetoclax, tedizolid, and combination treatment on gene expression in a venetoclax-resistant AML cell line |
10.34 |
|
Oncogenic Notch promotes long-range regulatory interactions within hyperconnected 3D cliques [HCC1599_RNA-seq] |
10.33 |
|
The landscape of alternative splicing in aggressive prostate cancers |
10.32 |
|
Induction of human SST and PV neurons by expressing a single transcription factor LHX6 |
10.14 |
|
ILF2 Regulates RNA Splicing of DNA Damage Response Genes to Confer Poor Prognosis in 1q21-Amplified Multiple Myeloma |
10.13 |
|
Model systems of DUX4 expression recapitulate the transcriptional profile of FSHD cells |
10.11 |
|
The Jumonji-domain histone demethylase inhibitor JIB-04 deregulates oncogenic programs and increases DNA damage in Ewing Sarcoma, resulting in impaired cell proliferation and survival, and reduced tumor growth |
10.05 |
|
RNA-sequencing analysis for gene expression profiles affected by CASC9 knockdown |
10.0 |
|
Transcriptome analysis of ECFCs treated with GSK-343 and Panobinostat |
9.93 |
|
Transcriptomic profiles of human foreskin fibroblast cells in response to orf virus |
9.86 |
|
Estrogen receptor and mTOR signaling rewires cancer metabolism in obesity-associated breast cancer |
9.76 |
|
EZHIP constrains Polycomb Repressive Complex 2 activity in germ cells (RNA-Seq) |
9.68 |
|
EZHIP constrains Polycomb Repressive Complex 2 activity in germ cells |
9.68 |
|
Gene expression in PANC1 cells treated with Rakicidin |
9.46 |
|
Quantitative Analysis of PPARD Transcriptomes in Colon Cancer Cells by Next Generation Sequencing (NGS) |
9.37 |
|
Genome-wide view of the impact of Spt5-Pol II inhibitors (SPIs) on mRNA levels [RNA-Seq 2h] |
9.34 |
|
Genome-wide CRISPR-Cas9 screen identifies druggable synthetic lethality between LSD1 and MTORC1 in MLL-translocated AML |
9.26 |
|
Transcriptomic hallmarks of tumor plasticity and stromal interactions in brain metastasis |
9.26 |
|
Expression changes in melanoma cell lines under BRAFi treatment timepoints [RNA-Seq.CellLine.batch4] |
9.24 |
|
IRF1 regulates IFN dependent and independent gene expression |
9.23 |
|
ZBTB48 is both a vertebrate telomere-binding protein and a transcriptional activator |
9.16 |
|
ZBTB48 is both a vertebrate telomere-binding protein and a transcriptional activator [RNA-seq] |
9.16 |
|
H3B-8800, a novel oral splicing modulator, induces lethality in spliceosome mutant cancers [Nalm-6] |
9.15 |
|
RNA-seq analysis of BAP1-depleted uveal melanoma cells |
9.15 |
|
HNF1A deficiency impairs β-cell fate, granule maturation and function |
9.11 |
|
Effects of NSUN2 deficiency on the mRNA 5-methylcytosine modification and gene expression profile in HEK293 cells (RNA-Seq) |
9.11 |
|
The stress granule transcriptome reveals principles of mRNA accumulation in stress granules. |
9.01 |
|
CHCHD2 gene KO effect in iPSC drived motor neurons |
8.86 |
|
UBR7 is a novel E3 ubiquitin ligase for H2BK120 and acts as a tumor-suppressor in breast cancer [RNA-Seq] |
8.84 |
|
UBR7 is a novel E3 ubiquitin ligase for H2BK120 and acts as a tumor-suppressor in breast cancer |
8.84 |
|
Transcriptomic but not genomic variability confers phenotype of breast cancer stem cells |
8.83 |
|
Gene expression in mature and immature human ES-derived beta cells, and sorted beta-cells from adult islets |
8.78 |
|
Analysis of the polyA+ RNA of LPS-treated human CD14+ monocytes |
8.58 |
|
DDX3X regulation of global translation is impaired by medulloblastoma-associated mutations [RNA-Seq] |
8.54 |
|
DDX3X regulation of global translation is impaired by medulloblastoma-associated mutations |
8.54 |
|
MPTAC determines APP fragmentation via sensing sulfur amino acid catabolism |
8.5 |
|
A role for p53 in the adaptation to glutamine starvation through the expression of Slc1a3 |
8.5 |
|
Genomic expression analysis of K562 cells expressing shRNA targeting lncRNA-IIRX and control cells |
8.49 |
|
Cohesin and CTCF Differentially Affect the Chromatin Architecture and Gene Expression in Human Cells |
8.48 |
|
Inhibition of DNA methylation promotes breast tumor sensitivity to netrin-1 interference |
8.43 |
|
Inhibition of DNA methylation promotes breast tumor sensitivity to netrin-1 interference [RNA-Seq] |
8.43 |
|
RNA-seq and m6A-seq of AML cells with FTO knockdown or inhibition |
8.43 |
|
RNA-seq in neutrophils from Juvenile Idiopathic Arthritis |
8.39 |
|
Hypoxic regulation of transcription in HUVEC is mediated by EPAS1 |
8.38 |
|
Effect of Hotair overexpression in human breast cancer cell lines |
8.35 |
|
Long non-coding RNA RP11-19E11.1 is an E2F1 target required for tumor cell proliferation and survival in basal breast cancer |
8.34 |
|
Gene expression profiling in lung and breast cancer cells treated by Bloom-specific siRNAs |
8.34 |
|
PER2 synchronizes mitotic expansion and decidual transformation of human endometrial stromal cells |
8.32 |
|
RNA expression in primary huamn muscle cells treated with 1,25(OH)2D3 or vehicle |
8.2 |
|
mRNA and miRNA expression in primary human muscle cells treated with 1,25(OH)2D3 or vehicle |
8.2 |
|
ChIP-seq of ER and RUNX2 in MCF7 breast cancer cell lines |
8.11 |
|
Characterization of sperm lncRNA and its differently expression in the sperm of asthenozoospermic patients |
8.11 |
|
CRISPR adenine and cytosine base editors with reduced RNA off-target activities |
8.01 |
|
CRISPR adenine and cytosine base editors with reduced RNA off-target activities [CBE] |
8.01 |
|
NKX2.2 |
7.99 |
|
RNA-Seq analysis of NKX2.2 knockdown in human pancreatic islets |
7.99 |
|
Campylobacter concisus pathotypes induce distinct global responses in intestinal epithelial cells [UNSWCD] |
7.99 |
|
Generation of KRAS signatures using immortalized isogenic lung cells. |
7.98 |
|
Transciptome profiling of NoDice and RNaseIII null cells prior to and after polyIC treatment |
7.97 |
|
Small-molecule-based Human Genome G4 Profiling Reveals Potential Gene Regulation Activity |
7.94 |
|
KANK1 inhibits cell growth by inducing apoptosis though regulating CXXC5 in human malignant peripheral nerve sheath tumors |
7.9 |
|
Mechanistic Model-Guided Study of Embryonic Morphogenesis |
7.88 |
|
Therapeutic targeting of GCB- and ABC-DLBCLs by rationally designed BCL6 inhibitors |
7.84 |
|
PAK4 suppresses RELB to prevent senescence-like growth arrest in breast cancer |
7.84 |
|
Tricyclic Antidepressants Induce Inactivation of Hepatic Stellate Cell (HSC) Myofibroblasts |
7.82 |
|
RNA sequencing for PDX1, NGN3 and MAFA transduced iPSCs cell |
7.8 |
|
Insulin receptor associates with promoters genome-wide and regulates gene expression [RNA-seq 2] |
7.79 |
|
Discovery and verification of liver cancer marker genes and variable scission based on second-generation sequencing data analysis |
7.73 |
|
EZH2 and BCL6 cooperate to assemble CBX8-BCOR Polycomb complex to repress bivalent promoters, mediate germinal center formation and promote lymphomagenesis |
7.7 |
|
EZH2 and BCL6 cooperate to assemble CBX8-BCOR Polycomb complex to repress bivalent promoters, mediate germinal center formation and promote lymphomagenesis [RNA-seq] |
7.7 |
|
Identification of Sin3B regulated genes during quiescence |
7.69 |
|
DIGIT regulates endoderm differentiation of human embryonic stem cells |
7.67 |
|
Species-specific maturation profiles of human, chimpanzee and bonobo neural cells |
7.64 |
|
SIX4 acts as a master regulator of genes associated with the malignant phenotype of non-small cell lung cancer cells |
7.64 |
|
Evidence for HOXC6 as a potential molecular marker for non-small cell lung cancer |
7.62 |
|
LMO1 Synergizes with MYCN to Promotes Neuroblastoma Initiation and Metastasis |
7.52 |
|
Atheroprotective flow alters EZH2/H3K27me3 dependent transcriptional profile in human endothelial cells |
7.52 |
|
Transriptional profiling upon heat shock and recovery in cells deficient for FBXW7 and their wild type counterpart. |
7.51 |
|
FBXW7 modulates stress response by post-translational modification of HSF1 |
7.51 |
|
Loss of CHD1 facilitates oncogenic hijacking of AR during cancer progression |
7.51 |
|
Loss of CHD1 facilitates oncogenic hijacking of AR during cancer progression [RNA-seq] |
7.51 |
|
Transcriptome-profiling (RNA-seq) and Ribosome-profiling (Ribo-seq) of BJ cells treated with Nutlin-3a, an MDM2 inhibitor, which induces p53. |
7.44 |
|
RNAseq analysis of patient-derived luminal breast cancer xenografts treated with progestins |
7.41 |
|
Patient-derived luminal breast cancer xenografts with progestins |
7.41 |
|
Molecular characterization of BRSK2 and BRSK1 kinases as negative regulators of the NRF2 transcription factor |
7.4 |
|
Analyses of a panel of transcripts and construction of RNA networks in hepatocellular carcinoma |
7.36 |
|
Small molecule targets TMED9, promotes lysosomal degradation to reverse proteinopathy |
7.35 |
|
Bach1 Regulates the Self-renewal and Mesendodermal Differentiation of Human Embryonic Stem Cells |
7.33 |
|
5hmC and gene expression data in breast cancer cell lines treated with an antioxidant |
7.29 |
|
Integrator complex regulates NELF-mediated RNA Polymerase II pause/release and processivity at coding genes. |
7.27 |
|
Integrator complex regulates NELF-mediated RNA Polymerase II pause/release and processivity at coding genes [RNA-seq] |
7.27 |
|
RNA-seq data for non-targeting siRNA and CDK11 siRNA transfection in SHhES8 cells |
7.13 |
|
Transcriptional study of ARN8 cells treated with novel DHODH inhibitors |
7.12 |
|
Arginine citrullination at the C-terminal domain controls RNA Polymerase II transcription |
7.12 |
|
T47D RNA-seq and ChrRNA-seq data |
7.12 |
|
Heterogeneous nuclear ribonucleoprotein C1/C2 links transcriptional and splicing actions of 1,25-dihydroxyvitamin D |
7.12 |
|
Mediator kinase inhibition further activates super-enhancer-associated genes in AML |
7.06 |
|
Effect in HCT116 cells of 3hr cortistatin A treatment on gene expression. |
7.06 |
|
Maintaining iron homeostasis is the key role of lysosomal acidity for cell proliferation |
7.03 |
|
Identification of microRNA-dependent gene regulatory networks driving human pancreatic endocrine cell differentiation [RNA-Seq III] |
7.0 |
|
The anti-leukemic effect of R-2HG depends on its acting as an m6A mRNA modifier-RNA Seq-PBS / R-2HG treatment |
7.0 |
|
The effects of chemokines CCL2/7 on MDA-MB-231-FOXC1 cells |
6.99 |
|
DART-seq: an antibody-free method for global m6A detection |
6.96 |
|
Modeling and characterization of the dynamic gene regulatory networks underlying cancer drug resistance based on time-course RNA-seq data |
6.93 |
|
A combinatorial screen of the CLOUD uncovers a synergy targeting the androgen receptor |
6.92 |
|
Topoisomerase 1 inhibition suppresses inflammatory genes and protects from death by inflammation |
6.89 |
|
Topoisomerase 1 inhibition suppresses inflammatory genes and protects from death by inflammation (RNA-Seq) |
6.89 |
|
Spatially Constrained Tandem Bromodomain Inhibition Bolsters Sustained Repression of BRD4 Transcriptional Activity for TNBC Cell Growth |
6.89 |
|
Next generation sequencing analysis of transcriptomes at different timepoints after chlorprothixene treatment in NB4 and Kasumi-1 cells |
6.87 |
|
Bromodomain protein BRD4 is required for estrogen receptor-dependent transcription and enhancer activation |
6.87 |
|
Bromodomain protein BRD4 is required for estrogen receptor-dependent transcription and enhancer activation [RNA-Seq] |
6.87 |
|
Genome-wide analysis of YAP and TFCP2 down-regulated genes in liver cancer cells |
6.83 |
|
Genome-wide analysis of YAP and TFCP2 occupancy and regulated expression in liver cancer cells |
6.83 |
|
Discovery of naturally occurring ESR1 mutations during acquisition of resistance to endocrine therapy in widely used estrogen receptor positive breast cancer cell lines [RNA-Seq] |
6.82 |
|
Discovery of naturally occurring ESR1 mutations during acquisition of resistance to endocrine therapy in widely used estrogen receptor positive breast cancer cell lines |
6.82 |
|
Gene expression profiling of leukemia cells following asparagine depletion |
6.79 |
|
SMUG1 promotes telomere maintenance through telomerase RNA end-processing |
6.78 |
|
Tracking of dCas9-methyltransferase footprints |
6.77 |
|
Glioblastoma stem cells infected by ZIKA virus |
6.74 |
|
Proteomic profiling of VCP substrates links VCP to K6-linked ubiquitylation and c-Myc function |
6.74 |
|
IL-6/Stat3-Dependent Induction of Distinct, Obesity-Associated Natural Killer Cells Deteriorates Energy and Glucose Homeostasis |
6.73 |
|
Overexpression of NFIB and YBX1 in MCF-7 cells |
6.73 |
|
The bromodomain protein BRD4 regulates splicing during heat shock |
6.72 |
|
High-throughput sequencing of pluripotent cells |
6.69 |
|
The influence of PPFIA1 silencing to gene expression in breast carcinoma cell line and head and neck squamous cell carcinoma cell lines by RNA-sequencing in three dimensional collagen I |
6.67 |
|
RNA binding protein CPEB1 remodels host and viral RNA landscapes [RNA-Seq] |
6.66 |
|
Altering cancer transcriptomes using epigenomic inhibitors [RNA-Seq] |
6.62 |
|
Altering cancer transcriptomes using epigenomic inhibitors |
6.62 |
|
Next generation sequencing of human hepatic stellate cell line, LX-2 treated with recombinant human TGF-β1, with DMSO or ML290 (5 µM) for 72h. |
6.61 |
|
Neutrophils in systemic onset Juvenile Idiopathic Arthritis display sepsis-like features which can be reverted by IL-1 blockade |
6.6 |
|
Genome wide association study of bone size yields eleven loci that also affect height, bone density, osteoarthritis and fractures |
6.58 |
|
Gene expression in TAL1-driven T-cell ALL in response to TAL1-KD, UTX-KD, and GSKJ4 treatment |
6.57 |
|
T-cell ALL in response to TAL1-KD, UTX-KD, and GSKJ4 treatment |
6.57 |
|
TGF-β regulation of miRNA expression in pancreatic cancer |
6.56 |
|
Trisomy of a ‘Down syndrome critical region’ globally amplifies transcription via HMGN1 overexpression |
6.55 |
|
Nudt3 is a mRNA Decapping Enzyme That Modulates Cell Migration |
6.53 |
|
RNA transcriptome analysis during HSV-1 infection |
6.5 |
|
A non-canonical role of YAP/TEAD is required for activation of estrogen-regulated enhancers in breast cancer [RNA-seq] |
6.5 |
|
A non-canonical role of YAP/TEAD is required for activation of estrogen-regulated enhancers in breast cancer |
6.5 |
|
Systems-level analyses reveal a convergent pathway for progression of diffuse astrocytoma and potential role for resveratrol in delaying high-grade transformation |
6.49 |
|
Hypertonic saline attenuates the cytokine-induced pro-inflammatory signature in primary human lung epithelia |
6.46 |
|
Gene expression changes in THP1 cells at day 2 and 4 following shRNA knock-down of RUVBL2 |
6.43 |
|
Transcriptome profiling identified a 3-lncRNA regulatory network in transthyretin against glucose induced hRECs dysfunction |
6.42 |
|
RNA-seq analysis of A498 cell line treated with siSETD2 or si-NC |
6.42 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of Human Pluripotent Stem Cell-Derived Endocardial-like And Primary Cardiac Endothelial Cell Transcriptomes |
6.4 |
|
FMRP facilitates the nuclear export of N6-methyladenosine-containing mRNAs |
6.37 |
|
RNA-seq of naive and primed ES cells (NHSM) |
6.36 |
|
AhR activity directs BRAF inhibitors resistance in metastastic melanoma |
6.34 |
|
Human iPSC-derived cells and microengineered Organ-Chip enhance neural development. |
6.34 |
|
NAD+ Analog-sensitive PARPs Reveal a Role for PARP-1 in Transcription Elongation |
6.34 |
|
Human iPSC-based Modeling of Late-Onset Disease using Progerin-induced Aging |
6.31 |
|
Transcriptomes analysis for the regulation of Z36 induced autophagy in HeLa cell death |
6.31 |
|
Silencing p300 in MCF7 cells to study expression and alternative splicing |
6.29 |
|
Distinct Roles of BET Family Members in ERα Enhancer Function and Gene Regulation in Breast Cancer Cells [RNA-seq] |
6.26 |
|
Distinct Roles of BET Family Members in ERα Enhancer Function and Gene Regulation in Breast Cancer Cells |
6.26 |
|
An Alternative Splicing Event Amplifies Evolutionary Differences Between Vertebrates |
6.19 |
|
Campylobacter concisus pathotypes induce distinct global responses in intestinal epithelial cells |
6.19 |
|
Transcriptomic characterization of a human in vitro model of arrhythmogenic cardiomyopathy under topological and mechanical stimuli |
6.16 |
|
Vitamin C Promotes Apoptosis in Breast Cancer Cells by Increasing TRAIL Expression |
6.1 |
|
5hmC dynamically correlated with enhancer's activities during hES-to-Pancreatic endoderm cell differentiation |
6.1 |
|
5hmC dynamically correlated with enhancer's activities during hES-to-Pancreatic endoderm cell differentiation (RNA-Seq) |
6.1 |
|
Super-enhancer-driven CCAT1 is co-activated by SOX2 and TP63 and promotes squamous cancer from esophagus, head and neck and lung [RNA-seq] |
6.08 |
|
Super-enhancer-driven CCAT1 is co-activated by SOX2 and TP63 and promotes squamous cancer from esophagus, head and neck and lung |
6.08 |
|
Control of prostate tumour growth by the long non-coding RNA GHSROS |
6.07 |
|
SOX17 Is a Critical Specifier of Human Primordial Germ Cell Fate |
6.06 |
|
Tumors with TSC mutations are sensitive to CDK7 inhibition through NRF2 and glutathione depletion |
5.98 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of mesoderm posterior bHLH transcription factor 1(MESP1)+ and MESP1- cells' Transcriptomes |
5.9 |
|
Toxicogenomics of the flame retardant tris (2-butoxyethyl) phosphate in HepG2 cells using RNA-seq. |
5.87 |
|
Designer epigenome modifiers enable robust and sustained gene silencing in clinically relevant human cells |
5.86 |
|
Designer epigenome modifiers enable robust and sustained gene silencing in clinically relevant human cells [RNA-seq] |
5.86 |
|
Genome-wide Gene Expression Profiling in DLBCL Cell Lines Treated with CUDC-907 |
5.85 |
|
A novel lncRNA lncRNA-AF339830 promotes colorectal carcinogenesis and glucose metabolism by stabilizing and specifying the transcription modification pattern of c-Myc |
5.85 |
|
A novel lncRNA lncRNA-AF339830 promotes colorectal carcinogenesis and glucose metabolism by stabilizing and specifying the transcription modification pattern of c-Myc [RNA-Seq] |
5.85 |
|
Profiling of circular RNAs in gastric cancer tissues and adjacent normal tissues |
5.83 |
|
Epigenomic profiling reveals the key function of histone H3K9 methylation during tumor transformation process |
5.83 |
|
Effect of estrogen (E2) treatment on the C4-12 relative to the MCF7 cells |
5.79 |
|
Gene expression profiling associated with knockdown of RNF20 in human normal and malignant lung epithelial cell lines |
5.78 |
|
Functional role of SLIT2 and ROBO1 in trophoblasts |
5.78 |
|
Expression data for HT29 cells treated with 5-aza-deoxy-cytidine |
5.77 |
|
Expression data for HT29 cells treated with 5-aza-deoxy-cytidine [RNA-Seq] |
5.77 |
|
Distinct gene expression profile of Huh7 cell lines stably overexpressing CRABP1 or 2 |
5.76 |
|
Effect of CRISPR-Cas9 mediated knock-out of integrin alpha2 on the transcriptome of DU145 prostate cancer cell grown as a spheroid culture |
5.74 |
|
LINE-2 transposable elements are a source of functional human microRNAs and target sites |
5.71 |
|
SUV420H2 knockdown in PANC-1 |
5.68 |
|
Effects of Polybrominated Diphenyl Ether (PBDE) Mixture on estrogen receptor positive (ER+) patient-derived tumor xenograft (PDX) model |
5.65 |
|
Genetic Tagging During Human Mesoderm Differentiation Reveals Tripotent Lateral Plate Mesodermal Progenitors |
5.61 |
|
Studying the selectivity of a targeted small molecule degrading a hypoxia-associated non-coding RNA |
5.61 |
|
Nuclear Parkin Regulates Transcriptional Response during Hypoxia |
5.61 |
|
Ambient O2 pressure induces NF-kB1/RelA related inflammatory response in human lung epithelial cells in vitro |
5.6 |
|
Evaluation of RNA amplification and RNA-Seq library preparation protocols for spermatozoa RNA profiling |
5.59 |
|
Targeting HuH7 cells with JumonjiC Lysine Demethylase Inhibitors (RNA-Seq) |
5.58 |
|
Global transcriptional profiling changes upon knockout of USP22 in human Non-small cell lung cancer cells |
5.56 |
|
Repression of stress-induced LINE-1 expression protects cancer cell populations from lethal drug-exposures |
5.55 |
|
Repression of stress-induced LINE-1 expression protects cancer cell populations from lethal drug-exposures [RNA-Seq] |
5.55 |
|
Heterozygous and homozygous knock-in of PIK3CA-H1047R into human iPSCs |
5.55 |
|
RNA-sequencing of milk cells extracted from pre-partum secretions and longitudinally from mature human milk across the first year of lactation |
5.53 |
|
H3K27Ac in MCF7 Y537S ER mutant cells and RNAseq with and without treatment with THZ1 |
5.52 |
|
Small RNA-seq of human granulosa cells reveals miRNAs in FSHR and aromatase genes |
5.47 |
|
High-throughput RNA sequencing of human preovulatory cumulus and mural granulosa cells (mRNA) |
5.47 |
|
Coordinate regulation of alternative pre-mRNA splicing events by the human RNA chaperone proteins hnRNPA1 and DDX5 |
5.47 |
|
RNA-seq of H1299 cells in which either PRKCI or SOX2 was silenced by validated lentiviral shRNA constructs |
5.44 |
|
RNA-sequencing WT vs SOCS3 knockout Glioblastoma stem-cells |
5.4 |
|
Patterned human microvascular grafts enable rapid vascularization and increase perfusion in infarcted hearts |
5.39 |
|
Integrin αvβ3 acting as membrane receptor for thyroid hormones mediates angiogenesis in malignant T cells |
5.38 |
|
Transcriptome-wide profiling of poly(A)-tail length, translation efficiency and mRNA stability using TED-seq, mRNA-seq, Ribo-seq and PRO-seq in ER stress conditions |
5.37 |
|
RNA-Guided Human Gene Activation by Cas9/CRISPR-Based Engineered Transcription Factors |
5.27 |
|
Global transcriptional analysis of human extended pluripotent stem cells, human primed pluripotent stem cells, mouse extended pluripotent stem cells, and mouse embryonic stem cells by RNA-seq |
5.23 |
|
Global transcriptional analysis and genome-wide analysis of chromatin state in extended pluripotent stem cells, primed pluripotent stem cells, and naïve pluripotent stem cells |
5.23 |
|
Resistance to BET inhibitor leads to new therapeutic vulnerabilities in castration resistant prostate cancer |
5.22 |
|
The Adenovirus E1A C Terminus Suppresses a Delayed Antiviral Response and Modulates RAS Signaling |
5.21 |
|
The Adenovirus E1A C Terminus Suppresses a Delayed Antiviral Response and Modulates RAS Signaling [RNA-seq] |
5.21 |
|
Targeting MYC dependency in ovarian cancer through inhibition of CDK7 and CDK12/13 |
5.19 |
|
Impact of GDF15 expression of ovarian cancer cell on stroma and Cisplatin responses |
5.16 |
|
JMJD3 and UTX Determine Fidelity and Lineage Specification of Human Neural Progenitor Cells |
5.11 |
|
JMJD3 and UTX Determine Fidelity and Lineage Specification of Human Neural Progenitor Cells [RNA-seq] |
5.11 |
|
SERPINA3- a novel keratinocyte differentiation promotor mediates epidermal barrier repair response in psoriatic lesion |
5.11 |
|
EZH2 inhibitor efficacy in non-Hodgkin lymphoma does not require suppression of H3K27 mono-methylation [RNA-Seq] |
5.07 |
|
EZH2 inhibitor efficacy in non-Hodgkin lymphoma does not require suppression of H3K27 mono-methylation |
5.07 |
|
RNA-sequencing |
5.05 |
|
RNA-Seq analysis of human Tr1, Tregs and IL10neg cells |
4.98 |
|
Dissection of estrogen receptor alpha signaling pathways in osteoblasts using RNA-sequencing |
4.95 |
|
The RNA-binding protein RBM47 suppresses metastatic breast cancer progression |
4.92 |
|
Human Sandhoff Disease Cerebral Organoids Exhibit Enlarged Size, Increased Cellular Proliferation, and Impaired Differentiation |
4.87 |
|
Bacterial Infection Remodels the DNA Methylation Landscape of Human Dendritic Cells (mRNA-Seq) |
4.87 |
|
Cis-SAGe fusion RNAs in transcription splicing factors knocking-down 293T cells |
4.87 |
|
Transcriptomic analysis of the effect of trastuzumab in human iPSC-CMs |
4.82 |
|
Connexin 32-mediated cell-cell communication is essential for hepatic differentiation from human embryonic stem cells |
4.81 |
|
RNA-seq differential expression studies: more sequence, or more replication? |
4.75 |
|
Global analysis of alternative splicing regulated by RBM10 |
4.73 |
|
X-Ray induced DNA-Hydroxymethylation changes |
4.71 |
|
Modulation of gene transcription and epigenetics of colon carcinoma cells by bacterial membrane vesicles |
4.69 |
|
CAR T cell trogocytosis and cooperative killing regulate tumour antigen escape |
4.69 |
|
EZH2 inhibitor-mediated transcriptional profiling in prostate cancer cells [RNA-seq] |
4.68 |
|
Distinct changes in transcriptional profiles and epigenetic patterns mediated by EZH2 inhibitors in sensitive and insensitive prostate cancer cells |
4.68 |
|
Investigation into human Tra2 protein-dependent splicing in MDA-MB-231 cells using iCLIP and RNA-seq |
4.66 |
|
Transcriptome wide analysis of translation efficiency in MCF7 cells using polysome profiling with and without eIF4A inhibition by hippuristanol treatment |
4.65 |
|
Acquired resistance to MEK-CDK4/6 inhibitor combinations in cutaneous melanoma |
4.64 |
|
Pomalidomide inhibits PD-L1 induction to promote anti-tumor immunity |
4.62 |
|
RNA-Sequencing of HUVEC treated with Tie2 activating antibody |
4.58 |
|
AUF-1 affected genes in human skin cells |
4.57 |
|
The RNA helicase DDX39B regulates IL7R alternative splicing reducing the risk of Multiple Sclerosis |
4.51 |
|
Identification of ADAR1 adenosine deaminase dependency in a subset of cancer cells |
4.44 |
|
Differential mRNA expression upon 9p21 deletion in HEK TE single-cell derived clones |
4.42 |
|
Loss of 9p21 regulatory hub promotes kidney cancer progression by upregulating HOXB13 |
4.42 |
|
RNAseq analysis of the human neutrophil transcriptome, with and without in vitro cytokine stimulation |
4.37 |
|
Prolyl Hydroxylase Substrate Adenylosuccinate Lyase Is An Oncogenic Driver In Triple Negative Breast Cancer |
4.36 |
|
Gene expressions of H9s in different culture systems |
4.35 |
|
RNA-SEQ assay for wild type and CRISPR induced endoglin knockout human pulmonary artery smooth muscle cells (PASMC) |
4.35 |
|
Differential expression of pancreatic cancer PANC1 cells treated with pilocarpine |
4.31 |
|
Silencing SPIB in attached and floating state of H1703 lung cancer cells |
4.31 |
|
RNA-sequencing with micro-dissected boundary organoid into anterior, posterior, and boundary regions |
4.27 |
|
Analysis of chromosomal aberrations and recombination by allelic bias in RNA-Seq |
4.25 |
|
RNA sequencing of mechanically strained NHEKs and control NHEKs |
4.24 |
|
Determining effects of microbial metabolite, Urolithin A on colon epithelial cells |
4.24 |
|
Comparison of small cell lung cancer PDX model FHSC04 for response to LSD1 inhibitor RG6016/ORY1001 |
4.24 |
|
Transcriptome splicing analysis in K562 cells expressing rare and private spliceosomal mutations |
4.2 |
|
Tracking transcriptional changes in a species-specific manner during experimental hepatoblastoma progression in vivo |
4.18 |
|
The SUMO Pathway as a Therapeutic Option in Pancreatic Cancer |
4.12 |
|
Expression changes in melanoma cell lines pre MAPKi treatment vs. post-MAPKi resistance (RNA-seq_CellLine.batch2) |
4.1 |
|
RNA-Seq study of Cell lines rendered resistant to idelalisib and ibrutinib |
4.07 |
|
MARCKS and lnc-MARCKS act as inflammation regulators |
4.06 |
|
Targeting Glioblastoma Stem Cells through Disruption of the Circadian Clock |
3.88 |
|
Targeting Glioblastoma Stem Cells through Disruption of the Circadian Clock [RNA-Seq] |
3.88 |
|
SHANK2 mutations associated with autism spectrum disorder cause hyperconnectivity of human neurons |
3.86 |
|
RNA sequencing of MDA-MB231 and U2OS cancer cell lines exposed to the alkylating agent methyl methanesufonate (MMS) and classical chemotherapeutics |
3.83 |
|
Efficient and precise editing of endogenous transcripts with SNAP-tagged ADARs |
3.81 |
|
Epigenetic reprogramming at estrogen-receptor binding sites alters 3D chromatin landscape in endocrine resistant breast cancer |
3.79 |
|
Epigenetic reprogramming at estrogen-receptor binding sites alters the 3D chromatin landscape in endocrine resistant breast cancer [RNA-seq] |
3.79 |
|
RNA sequencing of CACO-2 cells incubated with Bifidobacteria breve grown on human milk oligosaccharides. |
3.76 |
|
Acriflavine inhibits the epithelial-to-mesenchymal transition in vitro in liver and pancreatic cancer cells (part of study on HepG2) |
3.74 |
|
A Suv39H1-low chromatin state drives migratory cell populations in cervical cancer [RNA-Seq] |
3.61 |
|
A Suv39H1-low chromatin state drives migratory cell populations in cervical cancer |
3.61 |
|
Disease-associated mutation in SRSF2 misregulates splicing by altering RNA binding affinities |
3.6 |
|
Generation of Brain Region-specific Organoids using a Miniaturized Spinning Bioreactor and Modelling ZIKV Exposure |
3.6 |
|
Decoding breast cancer tissue-stroma interactions using species-specific sequencing |
3.57 |
|
Disruption of GRIN2B impairs differentiation in human neurons |
3.55 |
|
Gene expression from AsPC-1 cells treated with PTC596 and DMSO |
3.46 |
|
RB tumor suppressor promotes cancer immunity through downregulating PD-L1 expression |
3.46 |
|
RNA-seq of HDAC2-disrupted 293FT cells by CRISPR-Cas9 |
3.45 |
|
Histone deacetylase inhibition enhances antimicrobial peptide but not inflammatory cytokine expression upon bacterial challenge |
3.44 |
|
A systematic analysis of nuclear heat-shock protein 90 identifies a metazoan-specific regulatory module |
3.43 |
|
Myeloid-derived suppressor cells facilitie invasion and metastasis of papillary thyroid cancer cells by repressing miR-486-3p |
3.34 |
|
Response of triple negative breast cancer to BAZ2A/B inhibition and BET bromodomain inhibition alone and in combination (RNAseq) |
3.28 |
|
Response of triple negative breast cancer to BAZ2A/B inhibition and BET bromodomain inhibition alone and in combination |
3.28 |
|
Differential responses by human respiratory epithelial cell lines to respiratory syncytial virus reflect distinct patterns of infection control |
3.25 |
|
Expression analysis of genes modulated after knock-down of lncRNA CHROME. |
3.13 |
|
Protein kinase A-mediated phosphorylation regulates STAT3 activation and oncogenic EZH2 activity |
3.1 |
|
Ribosomal protein RPL26 is the principal target of UFMylation |
3.08 |
|
Expansion, in vivo-ex vivo cycling and genetic manipulation of primary human hepatocytes |
3.06 |
|
In Vitro and In Vivo Modulation of Alternative Splicing by the Biguanide Metformin. |
3.0 |
|
Genome-wide detection of DNase I hypersensitive sites in single cells and FFPE tissue samples |
2.98 |
|
RNA sequencing quantitative analysis of RNA editing levels in ADAR1, ADAR2, AIMP2 overexpression and wild type HEK293 cells |
2.96 |
|
Widespread Transcription beyond mRNA 3’ Ends Yields Abundant Regulatory RNAs |
2.89 |
|
HEK293 TFAM Knockout Expression Study |
2.85 |
|
RNA-seq of SOX5 overexpressing primary human neuronal progenitors |
2.85 |
|
Interaction with ZMYND11 mediates opposing roles of Ras-responsive transcription factors ETS1 and ETS2 |
2.84 |
|
Interaction with ZMYND11 mediates opposing roles of Ras-responsive transcription factors ETS1 and ETS2 |
2.84 |
|
Over expression of Receptor Activity Modifying Protein 2 in HEK293T cells |
2.81 |
|
Investigsting the role of NF-ĸB p50 S80 phosphorylation in regulating TNFα-induced transcription in HEK293T cells |
2.72 |
|
The Chromatin-Looping Factor ZNF143 Engages at Looping Promoters to Favor the Estrogen Response in Breast Cancer |
2.64 |
|
The Chromatin-Looping Factor ZNF143 Engages at Looping Promoters to Favor the Estrogen Response in Breast Cancer (RNA-seq) |
2.64 |
|
Enhancement of direct reprogramming from fibroblasts to epithelial lineages by OVOL2-induced mesenchymal-to-epithelial transition [CAGE] |
2.63 |
|
Enhancement of direct reprogramming from fibroblasts to epithelial lineages by OVOL2-induced mesenchymal-to-epithelial transition |
2.63 |
|
Gene expression profile in FTSEC cells (FT190 and FT194 cell lines) transduced with shRNA to knockdown RNF20 or with control shRNA using RNA-seq. |
2.6 |
|
FTSEC cells (FT190 and FT194 cell lines) transduced with shRNA to knockdown RNF20 or with control shRNA |
2.6 |
|
PolyA+ RNA-seq in ALL-SIL upon TLX1 knockdown |
2.55 |
|
Transcriptome profile of HepG2-expressing ATP7B-H1069Q (liver hepatocellular cells) exposed to JNK or p38 Inhibitor |
2.5 |
|
MicroRNA targetome analysis during HCMV infection |
2.47 |
|
DDX54 regulates transcriptome dynamics during DNA damage response [4SU-seq] |
2.44 |
|
Transcriptome-wide analysis to determine miR-200a targets in melanoma cell lines |
2.37 |
|
Effects of transcription factor CEBPA knockdown on vitamin D target gene regulation in THP-1 cells |
2.31 |
|
The pioneer factor CEBPA modulates vitamin D signaling |
2.31 |
|
The transcriptome effect of overexpressing EZH2 in MCF7 |
2.23 |
|
Suppression of NAF-1 in Breast Cancer Cells Reduces their Tumorigenicity by Interfering with Cellular Iron Distribution and Metabolism and Ensuing ROS Formation and Apoptosis |
2.22 |
|
Identification of metabolically distinct adipocyte progenitor cells in human adipose tissues |
2.2 |
|
Effect of drugs on transcriptomic profiles |
2.16 |
|
Gene expression analysis of human hepatocellular cancers |
2.09 |
|
Coronary artery disease genes SMAD3 and TCF21 promote opposing interactive genetic programs that regulate smooth muscle cell differentiation and disease risk [RNA-seq] |
2.06 |
|
Coronary artery disease genes SMAD3 and TCF21 promote opposing interactive genetic programs that regulate smooth muscle cell differentiation and disease risk |
2.06 |
|
Histone H3.1K27 methylation promotes NHEJ by antagonizing FANCD2 on Chromatin |
2.05 |
|
Effects on gene expression of doxorubicin in human stem cells-derived cardiomyocytes |
2.04 |
|
Kidney compartment specific eQTL studies highlight causal genes and pathways for renal disease development |
1.93 |
|
Evaluation of the effectiveness of semen collection and sperm purification methods for spermatozoa transcript profiling |
1.89 |
|
Bioreactor-engineered cancer tissues mimic phenotypes, gene expression profiles and drug resistance mechanisms detectable in xenografts and clinical specimens. |
1.8 |
|
Effect of low-dose sorafenib and alkylating agents in inflammation and angiogenesis in breast cancer |
1.79 |
|
Parvovirus B19 NS1 protein induces cell cycle arrest at G2 phase |
1.73 |
|
Functional Comparison of the HGF/Met and MSP/Ron Systems in a Pancreatic Cancer Model |
1.72 |
|
Defective structural RNA processing in relapsing-remitting multiple sclerosis |
1.68 |
|
Interaction between mitoNEET and NAF-1 in cancer cells |
1.56 |
|
Exploring the gene expression profile upon FXR1 knockdown in H358 cells using RNA-seq |
1.55 |
|
Analysis of gene expression in SKOV3 ovarian cancer cells after knockdown of the long non-coding RNA DNM3OS |
1.54 |
|
Research resource: global identification of estrogen receptor β target genes in triple negative breast cancer cells |
1.52 |
|
Multiplex Enhancer Interference Reveals Collaborative Control of Gene Regulation by Estrogen Receptor Alpha Bound Enhancers |
1.52 |
|
Multiplex Enhancer Interference Reveals Collaborative Control of Gene Regulation by Estrogen Receptor Alpha Bound Enhancers [RNA-Seq] |
1.52 |
|
The transcription and translation landscapes during human cytomegalovirus infection reveal novel host-pathogen interactions |
1.49 |
|
The mithralog EC-7072 is highly cytotoxic to chronic lymphocytic leukemia cells by targeting the B-cell receptor signaling pathway |
1.45 |
|
Noncoding regions are the main source of targetable tumor-specific antigens |
1.34 |
|
FOXA1 upregulation promotes enhancer and transcriptional reprogramming in endocrine-resistant breast cancer |
1.34 |
|
FOXA1 upregulation promotes enhancer and transcriptional reprogramming in endocrine-resistant breast cancer [RNA-seq] |
1.34 |
|
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 |
1.33 |
|
Immune Checkpoint Regulation of Pulmonary Fibrosis [bulk RNA-seq] |
1.33 |
|
α Cell Function and Gene Expression Are Compromised in Type 1 Diabetes |
1.32 |
|
A novel transcriptional network for the Androgen Receptor in human epididymis epithelial cells |
1.31 |
|
A novel transcriptional network for the Androgen Receptor in human epididymis epithelial cells [RNA-Seq] |
1.31 |
|
RNA-sequencing of the GSI treatment of the CUTLL1 cell line |
1.28 |
|
SILAC identifies LAD1 as an oncogenic filamin binder regulating actin dynamics in response to EGF and marking aggressive breast tumors |
1.26 |
|
Conversion of Human Gastric Epithelial Cells to Multipotent Endodermal Progenitors using Defined Small Molecules |
1.26 |
|
Conversion of Human Gastric Epithelial Cells to Multipotent Endodermal Progenitors using Defined Small Molecules [gene expression] |
1.26 |
|
RNA-sequencing of the brain transcriptome implicates dysregulation of neuroplasticity, circadian rhythms, and GTPase binding in bipolar disorder |
1.2 |
|
mRNA-Seq profiling SIX2+ and Foxd1+ cells in mouse embryonic and SIX2+ and SIX2-/MEIS1+ cells human fetal kidney |
1.19 |
|
Transcriptome analysis of the HepG2 cells expressing hepatic transcription factors |
1.19 |
|
IL-21/type I interferon interplay regulates neutrophil-dependent innate immune responses to Staphylococcus aureus |
1.18 |
|
Characterizing the contrasting roles of JMJD3 and UTX histone demethylases in T cell acute lymphoblastic leukemia [GSKJ4_RNA-seq] |
1.17 |
|
Antiviral and anti-inflammatory properties of novel anti-HIV candidate ABX464 promotes specifics RNA splicing while preserving cellular RNA integrity. |
1.12 |
|
Expression data from fresh human embryonic lung epithelial tip and stalk cells and cultured organoids derived from tip and stalk. |
1.1 |
|
Study of dynamic transcriptome profiling in DNA damage-induced cellular senescence and transient cell-cycle arrest |
1.06 |
|
Gene expression analysis upon mtDNA depletion [RNA-seq] |
1.06 |
|
Gene expression analysis upon mtDNA depletion |
1.06 |
|
Characterization of EZH2-deficient human embryonic stem cells [ChIP-seq and bulk RNA-seq] |
1.03 |
|
Enhancer divergence and cis-regulatory evolution in the human and chimpanzee neural crest |
0.99 |
|
Transcriptome analysis of V336Y mutant mitochondrial ribosomal protein in human HEK293 cell line |
0.96 |
|
Nickel exposure induces persistent mesenchymal phenotype in human lung epithelial cells through epigenetic activation of ZEB1 |
0.95 |
|
Identification of epigenetic interactions between miRNA and DNA methylation associated with polycystic ovarian syndrome |
0.95 |
|
Transcriptome Profiling Reveals the key genes and pathways involved in polycystic ovary syndrome [RNA-seq] |
0.95 |
|
High Resolution Mapping of RNA Polymerases Identifies Mechanisms of Sensitivity and Resistance to BET Inhibitors in t(8;21) AML |
0.94 |
|
Histone demethylase LSD1 is required for germinal center formation and BCL6 driven lymphomagenesis |
0.94 |
|
Transcriptional changes in lymphoma cells induced by LSD1 depletion |
0.94 |
|
Ribosome profiling upon inhibition of eIF4A |
0.92 |
|
Combined MEKi (GDC-0973) and WNT (G007-LK) treatment in APC and KRAS mutant HCT-15 cell line |
0.9 |
|
Human Adult Sorted Live Cell Erythroblasts RNA-Seq. |
0.9 |
|
Heterogeneous effects of massive hypoxia pathway activation in kidney cancer |
0.88 |
|
Identification of a unique gene expression signature in mercury and 2,3,7,8-tetrachlorodibenzo-p-dioxin co-exposed cells |
0.83 |
|
Targets of ROR2 overexpression in MCF-7 cells revealed a differentially regulated module of non-canonical WNT signaling pathway |
0.77 |
|
RNA-sequencing of the human milk fat layer during colostrum, transitional, and mature stages of lactation |
0.77 |
|
Transcriptome profiling of omental adipose tissues in human obesity by RNA-Seq |
0.77 |
|
Disruption of the TFAP2A regulatory domain causes Branchio-Oculo-Facial Syndrome (BOFS) and illuminates pathomechanisms for other human neurocristopathies [RNA-seq data set 2] |
0.76 |
|
Transcriptome analysis of human embryonic stem cells (hESCs) upon siRNA-mediated knockdown of hESC-essential genes |
0.76 |
|
Comparative transcriptome analysis reveals that ECM-Receptor Interaction contributes to the venous metastases of hepatocellular carcinoma |
0.73 |
|
ETS1 induction by the omental microenvironment promotes ovarian cancer metastasis [RNA-Seq] |
0.72 |
|
ETS1 induction by the omental microenvironment promotes ovarian cancer metastasis |
0.72 |
|
Genetic and Epigenetic Landscapes of Laterally Spreading Tumors of the Colorectum |
0.72 |
|
Inhibition of H3K4 demethylation induces autophagy in cancer cell lines |
0.71 |
|
Identification and mitigation of pervasive off-target activity in CRISPR-Cas9 screens for essential non-coding elements |
0.7 |
|
Gene expression activation in CLL mediated by MSCs contact |
0.69 |
|
Small-molecule targeting of brachyury transcription factor addiction in chordoma [rnaseq_compound] |
0.62 |
|
Genetic-to-epigenetic Therapy for Pancreatic Cancer |
0.57 |
|
Genome-wide transcriptome analysis of organotypic rafts derived from human papillomavirus type 16 infected primary keratinocytes [3D raft] |
0.52 |
|
Identification of microRNA-668 and microRNA-489 targets by RISC immunoprecipitation |
0.49 |
|
The transition from proliferation to quiescence in glioblastoma stem-like cells requires Ca2+ signaling and mitochondria remodeling |
0.37 |
|
Transcriptome profiling of HepG2 cells upon treatment of the menin-MLL inhibitor MI-503 or DMSO |
0.37 |
|
Next Generation Sequencing Study of Circadian Changes in Transcriptome of Human Pineal Gland |
0.36 |
|
Genome-wide search for differentially expressed RNAs responsible for the effects induced by Ebola virus replication and transcription |
0.32 |
|
Activation Dynamics and Immunoglobulin Evolution of Pre-existing and Newly Generated Human Memory B-cell Responses to Influenza Hemagglutinin |
0.3 |
|
System-wide profiling of RNA-binding proteins uncovers key regulators of virus infection |
0.29 |
|
Human Adult Sorted Live Cell Erythroblasts transduced with Sigma non-targeting shRNA negative control (SHC002V) with puromycin selection RNAseq |
0.26 |
|
Novel mutations segregating with Complete Androgen Insensitivity Syndrome and their molecular characteristics. |
0.24 |
|
Inhibition of ERG Activity in Patient Derived Prostate Cancer Xenografts using the Small Molecule Inhibitor YK-4-279 |
0.22 |
|
The lung-enriched p53 mutants V157F and R158L/P regulate a novel transcriptome in lung cancer |
0.17 |
|
Expression analysis of the TAF1 syndrome |
0.17 |
|
Transcriptome-profiling (RNA-seq) and Ribosome-profiling (Ribo-seq) in proliferation, quiescence, senescence and transformed states. |
0.16 |
|
The DPYSL2 gene connects mTOR and schizophrenia |
0.13 |
|
Temporal comparison of transcriptomic alterations in human, mouse and rat primary B lymphocytes exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) |
0.12 |
|
Transcriptional response to the HSP70 inhibitor MAL3-101 in parental rhabdomyosarcoma cells and isogenic acquired-resistance lines. |
0.11 |
|
Domain-focused CRISPR-screen identifies HRI as a fetal hemoglobin regulator in human erythroid cells |
0.1 |
|
RNA sequencing of GLO1-depleted MDA-MB-231 breast cancer cells |
0.1 |
|
Epigenome Editing by CRISPR/Cas9 Repressors for Silencing of Distal Regulatory Elements |
0.09 |
|
A toxicogenomics approach to screen chlorinated flame retardants tris(2-chloroethyl) phosphate and tris(2-chloroisopropyl) phosphate for potential health effects |
0.05 |
|
Transcriptional profiling of growing and senescent WT and IL-1R-depleted IMR90 cells |
0.02 |
|
Human Cord Blood Sorted Live Cell Erythroblasts RNA-Seq |
0.02 |
|
RNA sequencing and pathway analysis identify important pathways involved in hypertrichosis and intellectual disability in patients with Wiedemann-Steiner syndrome |
0.01 |
|
Impact on erythroid progenitor type on erythroid differntiation |
0.0 |