|
A role for p53 in the adaptation to glutamine starvation through the expression of Slc1a3 |
53.64 |
|
Comparison between THP-1 cells obtained from either ATCC or DSMZ biorepository |
33.6 |
|
XPO1 inhibition antagonizes MCL via nuclear retention of IkB: Selinexor demonstrates antitumor activities in both ibr-sensitive and ibr-resistant tumor cells |
30.61 |
|
Splicing towards noncoding isoforms in colorectal carcinoma is associated with tumor hypoxia and the DNA damage response |
24.79 |
|
Genome-wide maps in MCF-7 cells with six2 or CYP4Z1 3'UTR or CYP4Z2P 3'UTR overexpression or not |
23.9 |
|
The LRF/ZBTB7A transcription factor is a BCL11A-independent repressor of fetal hemoglobin |
23.57 |
|
Treatment of multiple myeloma cells with EZH2 small molecule inhibitor |
22.28 |
|
IDH3a KO RNA-seq |
21.44 |
|
Vitamin C Promotes Apoptosis in Breast Cancer Cells by Increasing TRAIL Expression |
20.31 |
|
RNA-sequencing of isogenic primary, pre-malignant immortalized, and Ras-transformed human mammary epithelial cells |
19.57 |
|
Transcriptomic analysis of senescent cells upon PTBP1 knockdown and EXOC7 knockdown |
18.5 |
|
RNA-Seq comparative analysis of human neuroblastoma cells before and after their confrontation to the embryonic microenvironment |
18.46 |
|
Ewing sarcoma resistance to SP-2509 is not mediated through KDM1A/LSD1 mutation I |
17.79 |
|
MYCi361 regulates MYC target genes |
17.73 |
|
p38 SAPK and SKIIP induced changes in alternative splicing patterns upon osmostress |
17.48 |
|
Epigenetic reprogramming of melanoma cells by vitamin C treatment |
16.94 |
|
Peptidomimetic blockade of MYB in acute myeloid leukemia |
16.92 |
|
Peptidomimetic blockade of MYB in acute myeloid leukemia [RNA-seq] |
16.92 |
|
CD95L derived si- and shRNAs kill cancer cells through an RNAi mechanism by targeting survival genes [shL3.shR6.RNAseq.lg] |
16.91 |
|
Targeted degradation of BRD9 reverses oncogenic gene expression in synovial sarcoma |
16.83 |
|
Targeted degradation of BRD9 reverses oncogenic gene expression in synovial sarcoma [RNA-seq] |
16.83 |
|
Genome-wide chromatin analysis of Ewing sarcoma (RNA-seq) |
16.5 |
|
Genome-wide chromatin analysis of Ewing sarcoma |
16.5 |
|
RNA-seq of three Ewing sarcoma cell lines (A673, SK-N-MC, RDES), transfected with either siControl or siMYBL2. |
16.49 |
|
Cooperation of dominant oncogenes with regulatory variants shapes clinical outcomes in pediatric cancer |
16.49 |
|
Global transcriptional changes in the JJN3 myeloma cell line that occur as a result of treatment with 2 pyrrolobenzodiazepine (PBD) monomers |
16.35 |
|
Neurotrophic Tyrosine Kinase Receptor 1 is Epigenetically Regulated by IL-13 and Contributes to Allergic Inflammation |
15.93 |
|
MYT1 attenuates neuroblastoma cell differentiation by inhibiting retinoic acid signaling pathway |
15.64 |
|
A transcriptome-wide divergence in protein translation scales with LIN28B expression |
14.82 |
|
LncRNA-GAS5 negative regulation of YAP-target genes expression |
14.16 |
|
Mapping of DHT-responsive or -independent AR-binding sites induced by activated Src in prostate cancer cell lines [RNA-seq] |
14.0 |
|
Mapping of DHT-responsive or -independent AR-binding sites induced by activated Src in prostate cancer cell lines |
14.0 |
|
Developing a Novel Two-Dimensional Culture System to Enrich Human Prostate Luminal Progenitors That Can Function as a Cell of Origin for Prostate Cancer |
13.9 |
|
Bromodomain inhibition of the transcriptional coactivators CBP/EP300 as a therapeutic strategy to target the IRF4 network in multiple myeloma (RNA-Seq) |
13.74 |
|
Bromodomain inhibition of the transcriptional coactivators CBP/EP300 as a therapeutic strategy to target the IRF4 network in multiple myeloma |
13.74 |
|
Knockdown of ADNP in HCT116 colon cancer cells |
13.74 |
|
Gene expression profile using RNA-seq in WC00060 or SR-0788 cells transfected with siRNA for KPC1 or control |
13.38 |
|
ZBTB48 is both a vertebrate telomere-binding protein and a transcriptional activator |
13.33 |
|
ZBTB48 is both a vertebrate telomere-binding protein and a transcriptional activator [RNA-seq] |
13.33 |
|
Che-1 is targeted by c-Myc to sustain proliferation in pre-B-cell acute lymphoblastic leukemia [RNA-seq] |
13.08 |
|
Che-1 is targeted by c-Myc to sustain proliferation in pre-B-cell acute lymphoblastic leukemia |
13.08 |
|
ARID1A loss impairs enhancer-mediated gene regulation and drives colon cancer in mice |
12.89 |
|
ARID1A loss impairs enhancer-mediated gene regulation and drives colon cancer in mice [HCT116_RNA-seq] |
12.89 |
|
Expression profile of Lo19S state cells in the presence and absence of bortezomib treatment |
12.49 |
|
Transcriptional profile of CAOV2 primary and CAOV2 recurrent cells |
12.31 |
|
High throughput characterization of the m6A demethylase FTO by CLIP and RNAseq |
12.22 |
|
Heterozygous p53-R280T mutation promotes proliferation of NPC cells through activating PI3K/Akt signaling pathway |
12.14 |
|
Maintaining iron homeostasis is the key role of lysosomal acidity for cell proliferation |
12.0 |
|
Treatment of prostate cancer cells with S-adenosylmethionine leads to genomewide alterations of transcription profiles |
11.71 |
|
Multiple mechanisms disrupt let-7 miRNA biogenesis and function in neuroblastoma [longRNA] |
11.55 |
|
SAM68 is required for regulation of Pumilio by the NORAD long noncoding RNA |
11.43 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of miR-29b-1 and miR-29a targets in tamoxifen-sensitive and tamoxifen-resistant human breast cancer cells |
11.23 |
|
Activation of HOTTIP lncRNA perturbs HSC function leading to AML like disease |
11.16 |
|
The NORAD lncRNA assembles a topoisomerase complex critical for genome stability [RNA-seq] |
11.11 |
|
The NORAD lncRNA assembles a topoisomerase complex critical for genome stability |
11.11 |
|
Selective roles of vertebrate PCF11 in premature and full-length transcript termination (chromatin-bound RNA-seq) |
11.08 |
|
Control of prostate tumour growth by the long non-coding RNA GHSROS |
11.05 |
|
Transcriptome-wide identification of splicing defects upon XAB2 knockdown |
10.93 |
|
Gene expression alterations associated with acquired-resistance to the CDK4/6 inhibitor palbociclib [Palbociclib resistance_RNASeq] |
10.79 |
|
TGF-β regulation of miRNA expression in pancreatic cancer |
10.43 |
|
Cajal bodies are linked to genome conformation |
10.41 |
|
Cajal bodies are linked to genome conformation [RNA-Seq] |
10.41 |
|
Oncogenic Notch promotes long-range regulatory interactions within hyperconnected 3D cliques [HCC1599_RNA-seq] |
10.36 |
|
PolyA-sequencing in IMR-32 cells treated with THZ531 or DMSO |
10.32 |
|
SNHG12 knockdown in Human Umbilical Vein Cells under ROS conditions. |
10.32 |
|
Analysis of transcriptome changes following SOX2 knockdown in three different Ewing sarcoma cell lines |
10.2 |
|
LNCaP treated with iBET |
10.08 |
|
Transcriptome splicing analysis in K562 cells expressing rare and private spliceosomal mutations |
10.04 |
|
Pervasive transcription read-through promotes aberrant expression of oncogenes and RNA chimeras in renal carcinoma |
9.97 |
|
Myeloid-derived suppressor cells facilitie invasion and metastasis of papillary thyroid cancer cells by repressing miR-486-3p |
9.91 |
|
RNAseq Analysis in glioblastoma cells treated with Mepazine |
9.87 |
|
NF-κB p65 dimerization and DNA-binding is important for inflammatory gene expression |
9.78 |
|
Nuclear Parkin Regulates Transcriptional Response during Hypoxia |
9.67 |
|
Retinoic Acid Induced Transcriptional Repressor HIC1 is Required for Suppressive Function of Human Induced Regulatory T cells [RNA-Seq 1] |
9.62 |
|
Hypoxic transcriptome of SQ20B human head and neck cancer cells |
9.54 |
|
BRG1 governs Glucocorticoid Receptor interactions with chromatin and pioneer factors across the genome |
9.46 |
|
U1 snRNP telescripting regulates size-function stratified human genome |
9.46 |
|
Reversible LSD1 Inhibition with HCI-2509 induces the p53 gene expression signature in high-risk neuroblastoma cells |
9.37 |
|
Rare cell variability and drug-induced reprogramming as a mode of cancer drug resistance [RNA-seq] |
9.32 |
|
LINE-1 elements are derepressed in senescent cells and elicit a chronic Type-I Interferon response |
9.3 |
|
Gene expression changes upon drug withdrawal (Mel888 cell line) |
9.28 |
|
Seletive inhibition of CDK9 in DLBCL cell lines |
9.25 |
|
Epigenetic silencing of the tumor suppressor RASSF4 favors multiple myeloma progression |
9.25 |
|
Identification of Sin3B regulated genes during quiescence |
9.23 |
|
The landscape of alternative splicing in aggressive prostate cancers |
9.21 |
|
DNA breaks and chromatin structural changes enhance the transcription of Autoimmune Regulator target genes [RNA-Seq] |
9.08 |
|
DNA breaks and chromatin structural changes enhance the transcription of Autoimmune Regulator target genes |
9.08 |
|
The Wnt/β-catenin and RAS-ERK Pathways were Activated in Tissues of Chemotherapy-Resistant Gastric Cancer PDX Tumor |
9.05 |
|
RNA-seq analysis of HT-29, MCF10A, and MDA-MB-436 cells |
9.04 |
|
Distinct roles of cohesin-SA1 and cohesin-SA2 in 3D chromosome organization |
8.99 |
|
Super-Enhancers Promote Transcriptional Dysregulation in Nasopharyngeal Carcinoma |
8.81 |
|
Super-Enhancers Promote Transcriptional Dysregulation in Nasopharyngeal Carcinoma [RNA-seq] |
8.81 |
|
Bromodomain-containing Protein 4 (BRD4) is Required for the Maintenance of a Mammary Epithelial Phenotype [RNA-Seq] |
8.8 |
|
Bromodomain-containing Protein 4 (BRD4) is Required for the Maintenance of a Mammary Epithelial Phenotype |
8.8 |
|
Chromatin landscape of human visceral and subcutaneous adipocytes |
8.74 |
|
RNA-seq analysis of FET cells treated with RSPO1 or TGFβ1 |
8.65 |
|
RNA sequencing analysis of selumetinib-resistant CRC cells lines |
8.59 |
|
Characterisation of HIF-dependent alternative isoforms in pancreatic cancer |
8.51 |
|
Chemotherapeutic drugs inhibiting Topoisomerase 1 activity inhibit TNF-induced inflammatory gene expression |
8.43 |
|
Genome-wide analysis of the Integrator complex (HTS) |
8.42 |
|
Genome-wide analysis of the Integrator complex |
8.42 |
|
LncRNA NONHSAT113026 represses renal cell carcinoma tumorigenesis through interacting with NF-κB/p50 and SLUG |
8.37 |
|
Transcriptomic analysis of ERR alpha orphan nuclear receptor |
8.3 |
|
Effect of FGF13 depletion on the H460 cell line |
8.16 |
|
Inhibition of ERG Activity in Patient Derived Prostate Cancer Xenografts using the Small Molecule Inhibitor YK-4-279 |
8.15 |
|
mRNA and RNC-mRNA deep sequencing of three hepatocellular carcinoma cell lines |
8.13 |
|
Ribosome profiling and RNA sequencing of MCF10A-ER-Src and fibroblast cell transformation |
8.12 |
|
Developmental stage specific chromosome architecture in human erythroid cells |
8.05 |
|
Developmental stage specific chromosome architecture in human erythroid cells (RNA-seq) |
8.05 |
|
Genes significantly down or Up-regulated upon RNF219 knockdown |
8.04 |
|
Small-molecule-based Human Genome G4 Profiling Reveals Potential Gene Regulation Activity |
8.03 |
|
Endothelial gene expression analysis |
7.95 |
|
Total RNA deep sequencing (ribosomal depleted) of human umbilical vein endothelial cells exposed to hypoxia (0.2%) for 12h and 24h or kept under normoxic conditions. |
7.95 |
|
Genome-wide analysis of ferroptosis related genes in liver cancer cells. |
7.89 |
|
Domain-focused CRISPR-screen identifies HRI as a fetal hemoglobin regulator in human erythroid cells |
7.85 |
|
RNA-seq of human aneuploid cell lines with Trisomy 21 |
7.84 |
|
ARID1A and PI3-Kinase pathway mutations in the endometrium drive epithelial transdifferentiation and collective invasion |
7.74 |
|
RNA-Seq in two Ewing sarcoma cell lines: A673 and SKNMC |
7.66 |
|
Endogenous retroviruses are a source of oncogenic enhancers in acute myeloid leukemia [RNA-Seq] |
7.63 |
|
Endogenous retroviruses are a source of oncogenic enhancers in acute myeloid leukemia |
7.63 |
|
Inducible three-factor direct reprogramming to nephron progenitors using piggyBac transposons |
7.62 |
|
6mer seed toxicity in tumour suppressive microRNAs |
7.61 |
|
Cancer avatars derived from genetically engineered pluripotent stem cells allow for longitudinal assessment of tumor development |
7.54 |
|
The BCL6 RD2 domain governs commitment of activated B-cells to form germinal centers |
7.41 |
|
Poly(A)-ClickSeq resolves CF25-mediated alternative poly-adenylation, HeLa |
7.25 |
|
Transcriptome Sequencing of Adipose-Derived Mesechymal Stromal Cells |
7.23 |
|
RNA-sequencing of mRNAs from control and CAP-D3 deficient Salmonella infected HT-29 cells |
7.21 |
|
CBFb-SMMHC inhibition triggers apoptosis by disrupting MYC chromatin dynamics in acute myeloid leukemia [RNA-seq] |
7.09 |
|
CBFb-SMMHC inhibition triggers apoptosis by disrupting MYC chromatin dynamics in acute myeloid leukemia |
7.09 |
|
Modeling the MYC-driven normal-to-tumour switch in breast cancer. |
7.08 |
|
A TFIID-SAGA perturbation that targets MYB and suppresses acute myeloid leukemia (RNA-seq) |
7.05 |
|
A TFIID-SAGA perturbation that targets MYB and suppresses acute myeloid leukemia |
7.05 |
|
Androgen Receptor-regulated genes in prostate cancer cells |
7.02 |
|
RNA-seq profiling identifies Androgen Receptor-regulated genes in prostate cancer cells |
7.02 |
|
RNA-sequencing experiment: Treatment of MCF-7 breast cancer cells with the novel small molecule ZNA |
7.0 |
|
The MLL-AF9 and MLL-AF4 oncofusion proteins bind a distinct enhancer repertoire and target the RUNX1 program in MLLr AML |
7.0 |
|
A non-catalytic function of carbonic anhydrase IX contributes to the glycolytic phenotype and pH regulation in human breast cancer cells |
6.9 |
|
Deletion of DXZ4 on the human inactive X chromosome eliminates superdomains and impairs gene silencing |
6.88 |
|
SMN2 splicing modifiers improve motor function and longevity in mice with spinal muscular atrophy |
6.85 |
|
Genome wide mapping of long noncoding (lnc) RNAs in hepatic stellate cells |
6.82 |
|
Inhibition of TNBC metastasis by Gpx1 |
6.78 |
|
Divergent effects of eRF3 and Upf1 on the expression of uORF carrying mRNAs and ribosome protein genes |
6.76 |
|
Effects of Cardiac Glycosides on RNA Expression in Prostate Cancer LNCaP-abl Cells |
6.74 |
|
Cohesin and CTCF Differentially Affect the Chromatin Architecture and Gene Expression in Human Cells |
6.7 |
|
ARID1A is a critical regulator of luminal identity and therapeutic response in oestrogen receptor-positive breast cancer (RNA-Seq) |
6.69 |
|
Biosynthesis of histone messenger RNA employs a specific 3' end endonuclease |
6.66 |
|
Gene expression changes upon drug withdrawal (A375/451Lu cell lines) |
6.61 |
|
Reprogramming postnatal human epidermal keratinocytes toward functional neural crest fates |
6.59 |
|
Stem cell and neurogenic gene-expression profiles link prostate basal cells to aggressive prostate cancer |
6.55 |
|
High resolution ChIP sequencing reveals novel bindings targets and prognostic role for SOX11 in Mantle cell lymphoma |
6.54 |
|
High resolution ChIP sequencing reveals novel bindings targets and prognostic role for SOX11 in Mantle cell lymphoma (RNA-Seq) |
6.54 |
|
Gene expression profiles of isogenic single-cell derived clones of BRAF-mutated SK-MEL-5 melanoma cell lines |
6.53 |
|
LSD1 pharmacological inhibition in SET-2 containing wild type and mutant LSD1 [RNA-Seq] |
6.5 |
|
LSD1 pharmacological inhibition in SET-2 containing wild type and mutant LSD1 |
6.5 |
|
Overexpression of NFIB and YBX1 in MCF-7 cells |
6.48 |
|
RNA-seq analysis of human cardiosphere cells with different tubule supportive potential |
6.45 |
|
Impact of DNA MMR activity on antiviral gene expression in H441 cells infected with influenza A virus |
6.38 |
|
Enhancer Domains in Gastrointestinal Stromal Tumor Regulate KIT Expression and are Targetable by BET Bromodomain Inhibition |
6.22 |
|
Enhancer Domains in Gastrointestinal Stromal Tumor Regulate KIT Expression and are Targetable by BET Bromodomain Inhibition [RNA-seq] |
6.22 |
|
Implication of Long noncoding RNAs in the endothelial cell response to hypoxia revealed by RNA-sequencing. |
6.19 |
|
RNA-sequencing (RNA-seq) in BxPC-3 and S2-007 cell lines |
6.18 |
|
Targeting MYC dependency in ovarian cancer through inhibition of CDK7 and CDK12/13 |
6.18 |
|
Targeting HuH7 cells with JumonjiC Lysine Demethylase Inhibitors (RNA-Seq) |
6.17 |
|
Transient stabilization, rather than inhibition of MYC amplifies extrinsic apoptosis and therapeutic responses in refractory B-cell lymphoma |
6.17 |
|
miR-191 regulates human cell proliferation and directly targets multiple oncogenes [seq] |
6.15 |
|
Genome wide miR-191 target profile determined by RIP and gene expression profiling |
6.15 |
|
Expression profile of LNCaP/AR cells with or without HNF4G expression grown for long term in charcoal stripped-serum (CSS) media |
6.07 |
|
Global host gene expression changes in KSHV+ PEL cells upon KSHV reactivation |
6.07 |
|
Transcription factor p63 bookmarks genomic loci in epithelial cells and regulates a subset of target genes during epidermal differentiation through dynamic enhancers |
6.06 |
|
Transcription factor p63 bookmarks genomic loci in epithelial cells and regulates a subset of target genes during epidermal differentiation through dynamic enhancers (RNA-Seq) |
6.06 |
|
Regulation of PRMT5-MDM4 axis is critical in the response to CDK4/6 inhibitors in melanoma |
6.05 |
|
NOTCH1 activation in breast cancer confers sensitivity to inhibition of SUMOylation |
6.04 |
|
Gene expression in control and DOCK8 CRISPR KHYG1 NK cells |
6.01 |
|
Genome wide expression change by RNF168 knocking down in NEC cells |
5.98 |
|
Transcriptomic analysis of trametinib-resistant HCT116 colorectal carcinoma cells compared to the parental control cells |
5.97 |
|
Next Generation Sequencing Quantitative Analysis of Wild Type and AML1-ETO Related Fusion Circular RNA (F-CircAE) Knockdown Kasumi-1 Cells Transcriptomes |
5.96 |
|
BASP1 modifies the Tamoxifen response |
5.93 |
|
Gene expression analysis of BRD4 knockdown in HT-29 and HCT116 cells |
5.85 |
|
Benzotriazoles reactivate latent HIV-1 through inactivation of STAT5 SUMOylation |
5.82 |
|
Benzotriazoles reactivate latent HIV-1 through inactivation of STAT5 SUMOylation (RNA-Seq) |
5.82 |
|
H3K27ac ChIP-Seq and mRNA-Seq analysis of five human B-lymphoblastoid cell lines (LCLs) prepared from the same healthy male individual (CEPH/UTAH). |
5.79 |
|
Transcriptomes analysis for the regulation of Z36 induced autophagy in HeLa cell death |
5.74 |
|
A Unique Epigenomic Landscape Defines Human Erythropoiesis (RNA-seq) |
5.73 |
|
A Unique Epigenomic Landscape Defines Human Erythropoiesis |
5.73 |
|
RNAseq Study in CC-671 Treated Cal-51 Cells |
5.72 |
|
Mesenchymal stem/stromal cell engulfment reveals metastatic advantage in breast cancer |
5.7 |
|
Gene Expression Profiling of SPOP Knocked Down Cell |
5.69 |
|
TMED9-gated CNIH4 and TGFa signaling promotes pro-metastatic states in human primary colon cancer cells |
5.68 |
|
Multiple mechanisms disrupt let-7 miRNA biogenesis and function in neuroblastoma |
5.65 |
|
Global hypomethylation mediated changes regulate constitutive PD-L1 expression in melanoma |
5.64 |
|
Global hypomethylation mediated changes regulate constitutive PD-L1 expression in melanoma [RNA-Seq] |
5.64 |
|
Patient Derived Xenograft for Delivery of Precision Medicine in Castrate Resistant Prostate Cancer |
5.64 |
|
Gene expression profile of melanoma cell lines after overexpression or knockdown of KPC1 |
5.64 |
|
Gene expression changes caused by KRAS in MCF-10A |
5.63 |
|
Lineage tracing of acute myeloid leukemia reveals the impact of hypomethylating agents on chemoresistance selection |
5.62 |
|
Muscleblind-like 1 suppresses breast cancer metastatic colonization and stabilizes metastasis suppressor transcripts |
5.62 |
|
MBNL1-dependent modulation of gene expression in MDA-MB-231 breast cancer cells |
5.62 |
|
EIF1AX-A113 splice and RAS mutations cooperate to drive thyroid tumorigenesis through ATF4 and c-MYC |
5.61 |
|
RNA-Seq analysis of cSCC cells after siRNA-induced gene knockdown of lncRNA PRECSIT |
5.59 |
|
mRNA gene expression profiling in a human AML cell line treated with small molecule inhibitors that impact different RNA polymerase transcription complexes, or their combination, in comparison to a global DNA-damaging anthracycline compound |
5.52 |
|
RNA-Seq of SHEP TET21N cells upon Doxorubicin treatment |
5.51 |
|
Estrogen deprivation triggers and immunosuppressive phenotype in breast cancer cells |
5.47 |
|
Differential gene expression analysis between proliferating and quiescent human dermal fibroblasts |
5.43 |
|
ILF2 Regulates RNA Splicing of DNA Damage Response Genes to Confer Poor Prognosis in 1q21-Amplified Multiple Myeloma |
5.42 |
|
HOXC6 affects the malignant phenotype of esophageal squamous cell carcinoma cells |
5.4 |
|
FUS KO mRNA sequencing and anti-FUS RNA immunoprecipitation sequencing |
5.39 |
|
Epigenome regulation during epidermal lineage commitment [ATAC-seq, RNA-seq] |
5.35 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of HIV-1 Latency in Central Memory T Cells |
5.31 |
|
To identify transcripts that are differentially expressed in the MYCN amplified vs MYCN non-amplified cell lines using Next Generation Sequencing |
5.28 |
|
Mining the stiffness-sensitive transcriptome in human vascular smooth muscle cells identifies long non-coding RNA stiffness regulators |
5.27 |
|
PT2385 HIF2A inhibitor treatment of patient derived orthotopic xenograft neuroblastoma cells in the presence or absence of hypoxia |
5.25 |
|
Sirt6 Oncogene Mediates PI3K/Akt Signaling Activation in Diffuse Large B-Cell Lymphoma |
5.24 |
|
shRNA-mediated knockdown of ETV4 and MED25 in the prostate cell line PC3 reveals set of genes potentially coregulated by MED25 and ETV4 |
5.23 |
|
Genome-wide occupancy of FLAG-MED25 and ETV4 and expression profiling of shRNA-mediated knockdown of ETV4 and MED25 in the prostate cell line PC3 |
5.23 |
|
Long Non-coding RNA PICSAR Promotes Growth of Cutaneous Squamous Cell Carcinoma by Regulating ERK1/2 Activity |
5.16 |
|
Loss of histone macroH2A1 in hepatocellular carcinoma cells promotes paracrine-mediated chemoresistance and CD4+CD25+ T regulatory cells activation |
5.14 |
|
Mutation independent activation of the Notch pathway is associated with Lapatinib resistance in Her2+ breast cancer cell lines |
5.13 |
|
Expression alterations induced by restoration of AXIN1 expression in SNU449 hepatocellular carcinoma cells |
5.12 |
|
The LIN28B/let-7 axis is a novel therapeutic pathway in Multiple Myeloma |
5.09 |
|
Changes in CD34 and Erythroid Progenitor Transcriptome After RUNX3 Kock-down |
5.08 |
|
Acquisition of a hybrid E/M state is essential for tumorigenicity of basal breast cancer cells |
5.07 |
|
Click chemistry enables comprehensive preclinical evaluation of targeted epigenetic therapies [RNA-seq] |
5.05 |
|
Click chemistry enables comprehensive preclinical evaluation of targeted epigenetic therapies |
5.05 |
|
FOXD3 is a novel tumor suppressor in lung cancer |
5.04 |
|
ADAR1-editing of cellular and measles virus-derived duplex RNA |
5.03 |
|
ADAR1-editing in HeLa, p150-KO and ADAR1-KO transcriptomes |
5.03 |
|
Genes altered in expression by Cisplatin treatment in lung cancer cell lines |
5.03 |
|
Distinct Roles of BET Family Members in ERα Enhancer Function and Gene Regulation in Breast Cancer Cells |
5.03 |
|
Distinct Roles of BET Family Members in ERα Enhancer Function and Gene Regulation in Breast Cancer Cells [RNA-seq] |
5.03 |
|
Bromodomain and extraterminal proteins foster the core transcriptional regulatory programs and confer vulnerability in liposarcoma (RNA-Seq) |
5.0 |
|
Bromodomain and extraterminal proteins foster the core transcriptional regulatory programs and confer vulnerability in liposarcoma |
5.0 |
|
Poly(ADP-ribosyl)ation dependent changes in CTCF-chromatin binding and gene expression in breast cells |
5.0 |
|
RNAseq of PRMT4KD in human cord blood derived CD34+ cells |
4.99 |
|
THZ1 targeting CDK7 suppresses STAT transcriptional activity and sensitizes T-cell lymphomas to BCL2 inhibitors |
4.98 |
|
Long non-coding RNA RP11-19E11.1 is an E2F1 target required for tumor cell proliferation and survival in basal breast cancer |
4.93 |
|
The Promyelocytic Leukemia Zinc Finger Dependent Transcriptome during Human Endometrial Stromal Cell Decidualization |
4.92 |
|
The Polycomb Repressor Complex 1 Drives Double-Negative Prostate Cancer Metastasis by Coordinating Stemness and Immune Suppression |
4.9 |
|
Gene expression and 4sUDRB-seq for NF90/NF110 of human scramble and KD HeLa cells. |
4.89 |
|
RUNX1-ETO and RUNX1-EVI-1 differentially program the chromatin landscape in t(3;21) and t(8;21) AML but share global C/EBP-alpha dysfunction (RNA-Seq) |
4.89 |
|
RUNX1-ETO and RUNX1-EVI-1 differentially program the chromatin landscape in t(3;21) and t(8;21) AML but share global C/EBP-alpha dysfunction |
4.89 |
|
Next-generation sequencing analysis of transcriptom in gemcitabine resistant pancreatic cancer cells |
4.89 |
|
SNHG5 siRNA knock down in HCT116 cells |
4.88 |
|
Quantitative mass spectrometry-based proteomics reveals the dynamic protein landscape during initiation of human Th17 cell polarization |
4.87 |
|
MUC1-C represses the RASSF1A tumor suppressor and activated Kras signaling in human carcinoma cells |
4.86 |
|
RNA sequencing of BT142 and TS603 cell lines |
4.83 |
|
Metabolic Reprogramming Associated with Aggressiveness Occurs in the G-CIMP-High Molecular Subtypes of IDH1mut Lower Grade Gliomas |
4.83 |
|
Novel Non-catalytic Substrate-selective p38α-specific MAPK Inhibitors with Endothelial-Stabilizing and Anti-inflammatory Activity |
4.83 |
|
Silencing p300 in MCF7 cells to study expression and alternative splicing |
4.79 |
|
Glutaminolysis is a metabolic dependency in FLT3 ITD Acute Myeloid Leukemia unmasked by FLT3 Tyrosine Kinase Inhibition |
4.79 |
|
Global gene expression profile of dasatinib-resistant RCH-ACV cells |
4.76 |
|
Gene expression analysis of human CD8+ T cells treated with a DOT1L inhibitor |
4.71 |
|
Expression profile of wild type (WT) vs miR-155-/- in FLT3-ITD+ AML (MV4-11) cell lines |
4.69 |
|
Genome-wide CRISPR-Cas9 screen identifies functionally relevant microRNAs in AML |
4.69 |
|
Oxaliplatin resistance is enhanced by saracatinib via upregulation of ABCG1 and Wnt/β-catenin signaling in hepatocellular carcinoma |
4.68 |
|
METTL3 promotes translation in human cancer cells |
4.68 |
|
Tracking of dCas9-methyltransferase footprints |
4.68 |
|
RNA sequencing of GlyH-101-treated MCF-7 cell line |
4.65 |
|
Transcriptome of human keratinocytes with or without HPV16 oncogene expression |
4.64 |
|
Functional Comparison of the HGF/Met and MSP/Ron Systems in a Pancreatic Cancer Model |
4.61 |
|
24hr CA treatment vs. DMSO in HCT116 cells (from 'Identification of CDK8 and CDK19 substrates in human cells using cortistatin A and quantitative phosphoproteomics') |
4.55 |
|
Binding to SMN2 pre-mRNA-Protein complex elicits specificity for small molecule splicing modifiers |
4.54 |
|
SRSF1 role in cellular gene expression and splicing |
4.52 |
|
Impact of ETV7 activity on interferon-stimulated gene expression in 293T cells treated with interferon alpha |
4.52 |
|
ETV7 and interferon response |
4.52 |
|
Melanoma therapeutic strategies that select against resistance by exploiting MYC-driven evolutionary convergence |
4.49 |
|
Ewing sarcoma resistance to SP-2509 is not mediated through KDM1A/LSD1 mutation II |
4.48 |
|
Abnormal RNA splicing and genomic instability after induction of DNMT3A mutations by CRISPR/Cas9 gene editing [RNA-Seq] |
4.45 |
|
Abnormal RNA splicing and genomic instability after induction of DNMT3A mutations by CRISPR/Cas9 gene editing |
4.45 |
|
Next Generation Sequencing upon siRNA-mediated knockdown of EIF5A in MCF-7 cells. |
4.44 |
|
PRMT5 Interacts with the BCL6 Oncoprotein and is Required for Germinal Center Formation and Lymphoma Cell Survival |
4.44 |
|
Gene expression profile of LMSU gastric cancer cell p53 KO and KD |
4.42 |
|
Assessing the impact of loss of ATF7IP and SETDB1 on the transcriptome |
4.4 |
|
ATF7IP-mediated stabilization of the histone methyltransferase SETDB1 is essential for heterochromatin formation by the HUSH complex |
4.4 |
|
Tyrosine-1 of RNAPII CTD controls global termination of gene transcription in mammals |
4.39 |
|
β-catenin/Tcf7l2 dependent transcriptional regulation of GLUT1 gene expression by Zic family proteins in colon cancer |
4.36 |
|
Cooptation of tandem DNA repeats for the control of epithelial-to-mesenchymal transition [RNA-Seq] |
4.33 |
|
Cooptation of tandem DNA repeats for the control of epithelial-to-mesenchymal transition. |
4.33 |
|
The DPYSL2 gene connects mTOR and schizophrenia |
4.33 |
|
CD95/Fas ligand mRNA is toxic to cells |
4.32 |
|
Modulation of ESRP2 and MBNL2 in normal kidney and clear cell renal cell carcinoma cell lines for analysis of stability programs |
4.26 |
|
Expression data from A2780 cells treated with DMSO, Olaparib(Ola), Palbociclib(PD), and their combination (Ola/PD) |
4.23 |
|
Effects of Polybrominated Diphenyl Ether (PBDE) Mixture on estrogen receptor positive (ER+) patient-derived tumor xenograft (PDX) model |
4.22 |
|
Polarized B -cell functions |
4.21 |
|
RNA-Seq and ChIP-Seq reveals SQSTM1/p62 as a key mediator of JunB suppression of NF-kB-dependent inflammation |
4.2 |
|
JunB control of keratinocyte-mediated inflammation [RNA-seq] |
4.2 |
|
Integrin signaling regulates YAP/TAZ to control skin homeostasis |
4.19 |
|
RNA-Seq of polysome profiling fractions and whole cell lysates of UVB-irradiated N-TERT keratinocytes |
4.16 |
|
Proliferation pause as an early blockade of human cellular reprogramming toward pluripotency [RNA-seq analysis] |
4.16 |
|
Heterogeneous effects of massive hypoxia pathway activation in kidney cancer |
4.13 |
|
Prostate Cancer Cell RNA-Seq (PC3E and GS689.Li) |
4.12 |
|
RNA-sequencing of the GSI treatment of the CUTLL1 cell line |
4.12 |
|
hMTR4 plays a central role in creating balanced nuclear RNA pools for degradation and export II |
4.11 |
|
RNA-seq analysis of SKMEL28 melanoma cells following DIRC3 and IGFBP5 ASO knockdown |
4.1 |
|
E2F1 orchestrates transcriptomics and oxidative metabolism in Wharton’s jelly derived mesenchymal stem cells from growth-restricted neonates |
4.1 |
|
Gene expression analysis in U251 and U87 cells transduced with NANEP5 vector. |
4.1 |
|
Transcriptome Analysis of CircMRPS35 mediated mRNA expression profiles |
4.1 |
|
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 |
4.09 |
|
Real-time observation of light-controlled transcription in living cells |
4.06 |
|
Probing the Global Cellular Responses to Lipotoxicity Caused by Saturated Fatty Acids |
4.03 |
|
Repression of stress-induced LINE-1 expression protects cancer cell populations from lethal drug-exposures |
4.03 |
|
Repression of stress-induced LINE-1 expression protects cancer cell populations from lethal drug-exposures [RNA-Seq] |
4.03 |
|
Analysis of the senescent transcriptome upon expression of a ZFP36L1 phosphomutant |
4.02 |
|
Total RNA-seq in ALL-SIL upon TLX1 knockdown |
4.02 |
|
Study functions of ADAR proteins using next generation sequencing of genome and transcriptome |
4.0 |
|
Knockout of miR-221 and miR-222 reveals overlapping and specific function between paralogous miRNAs |
3.99 |
|
Nucleotide stress induction of HEXIM1 suppresses melanoma by modulating cancer cell-specific gene transcription [RNA-Seq2] |
3.95 |
|
POU2AF1 Functions in the Human Airway Epithelium to Regulate Expression of Host Defense Genes [RNA-Seq] |
3.93 |
|
POU2AF1 Functions in the Human Airway Epithelium to Regulate Expression of Host Defense Genes |
3.93 |
|
Exploiting Prmt5-orchestrated intron detention signatures to treat splicing-addicted malignant glioma tumors |
3.93 |
|
A pooled single-cell genetic screen identifies regulatory barriers in the continuum of the epithelial-to-mesenchymal transition |
3.92 |
|
Characterization of parental and rociletinib-resistant derived H1975 cell lines |
3.91 |
|
The effect of PPARG inhibition on human angiomyolipoma cells |
3.88 |
|
RNA-seq of RKO cells with cTAZ KO or putback |
3.87 |
|
Direct identification of endogenous SMG6 targets and a preferred motif spanning SMG6 cleavage sites by parallel analysis of RNA ends in human cells |
3.87 |
|
PRDM1 inhibits proliferation of human colon cancer organoids |
3.86 |
|
The inhibitory effect of TIAM1 on TAZ transcriptional activity and TIAM1 differentially expressed genes |
3.84 |
|
List of TIAM1 differentially expressed genes in SW620 cells [RNA-seq] |
3.84 |
|
RNA-seq of HEK293T cells overexpressing TET1-FL or TET1-ALT |
3.84 |
|
Genome-wide maps of WT and over-expressing CenH3/CENP-A in Human HeLa S3 cells |
3.84 |
|
RNA sequence of mRNA in HUVEC cells after depleting EGFL6 |
3.83 |
|
PAK4 suppresses RELB to prevent senescence-like growth arrest in breast cancer |
3.82 |
|
MYCi975 regulates MYC target genes |
3.82 |
|
The regulation of ferroptosis by TAZ in epithelial ovarian cancer |
3.75 |
|
Effect on small molecule RBPJ inhibitor (RIN1) on gene expression in Jurkat cells compared to gamma secretase inhibition and siRNA knockdown of RBPJ |
3.74 |
|
Gene-Centric Functional Dissection of Human Genetic Variation Uncovers Regulators of Hematopoiesis |
3.73 |
|
Transcriptional Down-regulation of CCR5 in a Subset of HIV+ Controllers |
3.72 |
|
Transcriptional Down-regulation of CCR5 in a Subset of HIV+ Controllers (RNA-Seq) |
3.72 |
|
SLIGRL-induced gene expression changes in NHEK cells |
3.71 |
|
Gene expression profiling by RNA-seq in hTert-HME1 cell line treated with control or BRCA2 siRNAs and grown with or without EGF (epithelial growth factor) |
3.69 |
|
Host transcriptome analysis of Aspergillus fumigatus infection in Airway Epithelial Cells |
3.68 |
|
Silencing SPIB in attached and floating state of H1703 lung cancer cells |
3.68 |
|
Identification of differential expressed genes of JQ1 or JQ1+Bortezomib in colorectal cancer cells |
3.67 |
|
Sequencing of ponatinib-resistant LC-2/ad derivatives (PR1 and PR2) and parental LC-2/ad cells |
3.64 |
|
Salmonella activation of STAT3 signaling by SarA effector promotes intracellular replication and production of IL-10 |
3.63 |
|
RNA transcriptome analysis of IRF1 and IRF3 knockout in immortalized primary hepatocytes infected with hepatitis A virus |
3.61 |
|
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 |
3.59 |
|
ZFR coordinates crosstalk between RNA decay and transcription in innate immunity |
3.55 |
|
CRISPR-Cas9 combinatorial KO of epigenetic regulators in human ovarian cancer cells |
3.52 |
|
Gene Expression Analysis of HUVEC Seeded rBEL Contructs at Low and High Phases of Glucose Consumption |
3.48 |
|
The multiple myeloma risk allele at 5q15 lowers ELL2 expression and increases ribosomal gene expression [ELL2 KO] |
3.47 |
|
Targeting the androgen receptor N-terminus via the cochaperone Bag-1L [RNA-Seq KO] |
3.42 |
|
HeLa transcriptome induction by IFN gamma and indoleamine 2,3-dioxygenase (IDO) |
3.38 |
|
CLIC5: a novel ETV6 target gene in childhood acute lymphoblastic leukemia |
3.37 |
|
Genome models integrating chromatin contacts and nuclear lamin-genome interactions reveal implications of laminopathy-causing lamin mutations on genome architecture |
3.36 |
|
RNA-seq in transgenic cells |
3.36 |
|
Transcriptomic Reprogramming of Prostate Cancer Cells Driven by Stroma-Derived AREG |
3.34 |
|
Acquired resistance to MEK-CDK4/6 inhibitor combinations in cutaneous melanoma |
3.32 |
|
Overexpression of PHF8 promotes an EMT-related gene signature in MCF10A cells |
3.31 |
|
Regulation of stem cell property and drug resistance of cancer cells by targeting transcriptional machinery via inhibition of neddylation |
3.26 |
|
transcriptome studies of BRD4 inhibitor BDF-1253 on renal clear carcinoma 786-O cells |
3.24 |
|
MKL1 augments megakaryocyte maturation by enhancing the SRF regulatory axis [RNA-seq] |
3.22 |
|
MKL1 augments megakaryocyte maturation by enhancing the SRF regulatory axis |
3.22 |
|
KLF4 as a rheostat of osteolysis and osteogenesis in prostate tumors in the bone |
3.21 |
|
Illumina Total RNA-seq in HeLa |
3.15 |
|
Genome-wide effect of inhibition of glutamine transporter ASCT2 in PC-3 cells by BenSer or GPNA |
3.09 |
|
Alarmin S100A11 initiates a chemokine response to the human pathogen Toxoplasma gondii |
3.07 |
|
Chromatin Topology Reorganization and Transcription Repression by PML/RARα in Acute Promyeloid Leukemia (RNA-seq) |
3.05 |
|
Chromatin Topology Reorganization and Transcription Repression by PML/RARα in Acute Promyeloid Leukemia |
3.05 |
|
Knock-down of Ror1 in MDA-MB-231 cell line decreases cell invasiveness |
3.05 |
|
Effect of drugs on transcriptomic profiles |
3.02 |
|
Wide-scale analysis of alternative polyadenylation (APA) associated with proliferation and transformation using 3'-Seq |
3.0 |
|
N6-methyladenosine mRNA marking promotes selective translation of regulons required for human erythropoiesis [RNA-Seq] |
2.99 |
|
Neurofibromin is an Estrogen Receptor alpha Transcriptional Co-repressor in Breast cancer |
2.99 |
|
Transcriptomic analysis of LSD1 |
2.95 |
|
Targeting Chromatin Regulators Inhibits Leukemogenic Gene Expression in NPM1 Mutant Leukemia |
2.94 |
|
SMAD2/3 are redirected to novel sites in MCF10A MII after prolonged TGFβ stimulation |
2.92 |
|
JUNB is a critical AP1 component for SMAD2/3 binding after TGFβ stimulation [RNA-seq] |
2.92 |
|
Characterization of human CDK12 and CDK13 in the regulation of RNA processing |
2.83 |
|
mRNA expression profiling in MDA-MB-231 (LM1) cells with a tet-incible MBD2 or p66α knock down, or treated with MBD2-targeting small molecule ABA or APC |
2.71 |
|
Positively selected enhancer elements endow tumor cells with metastatic competence |
2.7 |
|
Study of dynamic transcriptome profiling in DNA damage-induced cellular senescence and transient cell-cycle arrest |
2.68 |
|
Searching for target genes of miR-508/509/506/514 in HCT116 cells |
2.65 |
|
ELF1 expression in prostate cells reduces oncogenic ETS functions and promotes senescence and sensitivity to chemotherapy through distinct gene expression programs [RNA-seq] |
2.57 |
|
ELF1 expression in prostate cells reduces oncogenic ETS functions and promotes senescence and sensitivity to chemotherapy through distinct gene expression programs |
2.57 |
|
RNA-Seq of SLNCR1 over-expression in the melanoma cell line A375 |
2.56 |
|
Amiloride, an old diuretic drug, is a potential therapeutic agent for multiple myeloma |
2.53 |
|
Multi-omic measurements of heterogeneity in HeLa cells across laboratories |
2.45 |
|
In Vitro and In Vivo Modulation of Alternative Splicing by the Biguanide Metformin. |
2.45 |
|
Adenovirus Small E1A Employs the Lysine Acetylases p300/CBP and Tumor Suppressor Rb to Repress Select Host Genes and Promote Productive Virus Infection [RNA-seq] |
2.4 |
|
Adenovirus Small E1A Employs the Lysine Acetylases p300/CBP and Tumor Suppressor Rb to Repress Select Host Genes and Promote Productive Virus Infection |
2.4 |
|
U2AF1 mutations alter splice site recognition in hematological malignancies |
2.38 |
|
RNA-seq of synchronized S phase or G2 phase cells treated with an ATR inhibitor |
2.37 |
|
RNA-seq analysis of the role of HBO1 (KAT7/MYST2) in the ovarian cancer cell line UWB1.289. |
2.33 |
|
single cell RNA-seq from GM12878 (ENCSR673UIY) |
2.32 |
|
Expression analysis of PC3 cells treated with scramble AON or AON directed against MBNL1 |
2.29 |
|
A Hybrid Mechanism of Action for BCL6 in B Cells Defined by Formation of Functionally Distinct Complexes at Enhancers and Promoters |
2.25 |
|
A novel Menin-MLL inhibitor induces specific chromatin changes and eradicates disease in models of MLL-rearranged leukemia [RNA-Seq II] |
2.2 |
|
Histone demethylase LSD1 is required for germinal center formation and BCL6 driven lymphomagenesis |
2.2 |
|
Transcriptional changes in lymphoma cells induced by LSD1 depletion |
2.2 |
|
Lipid catabolism inhibition sensitizes prostate cancer cells to antiandrogen blockade |
2.16 |
|
Genome-wide modelling of transcription kinetics reveals patterns of RNA processing delays |
2.14 |
|
HEK293 TFAM Knockout Expression Study |
2.14 |
|
NSD2 overexpression links drives clustered chromatin and transcriptional changes in a subset of insulated domains of insulated domains |
2.13 |
|
Microenvironmental-derived Regulation of HIF-Signaling Drives Transcriptional Heterogeneity in Glioblastoma Multiforme |
2.13 |
|
LSD1 mediates MYCN control of epithelial-mesenchymal transition through silencing of metastatic suppressor NDRG1 gene |
2.1 |
|
ATRX is necessary for cellular senescence and represses HRAS to drive cells from quiescence into senescence |
2.07 |
|
ATRX is necessary for cellular senescence and represses HRAS to drive cells from quiescence into senescence [RNA-Seq] |
2.07 |
|
LIN28A modulates splicing and gene expression programs in breast cancer cells [RNA-Seq] |
2.03 |
|
LIN28A modulates splicing and gene expression programs in breast cancer cells |
2.03 |
|
SF3B1 Degron knockdown RNA-seq |
2.03 |
|
Oncogenic Notch promotes long-range regulatory interactions within hyperconnected 3D cliques [MB157_RNA-seq] |
2.0 |
|
RNA-Seq analysis of HIF-2a-responsive genes in clear-cell renal cell carcinoma |
2.0 |
|
Analysis of gene expression in SKOV3 ovarian cancer cells after knockdown of the long non-coding RNA DNM3OS |
1.96 |
|
Selective expression of long non-coding RNAs in a breast cancer cell progression model |
1.94 |
|
Stable oxidative cytosine modifications accumulate in cardiac mesenchymal cells from Type2 diabetes patients: rescue by alpha-ketoglutarate and TET-TDG |
1.93 |
|
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] |
1.93 |
|
Race-specific transcriptome and Long non-coding RNA of ADT-resistant African-American prostate cancer cell models. |
1.92 |
|
ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing |
1.91 |
|
ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing (RNA-seq) |
1.91 |
|
Transcriptomic responses to Ivacaftor and prediction of Ivacaftor clinical responsiveness |
1.91 |
|
Mitochondrial unfolded protein response controls matrix pre-RNA processing and translation |
1.88 |
|
Modulation of SF3B1 causes global intron retention and downregulation of the B-cell receptor pathway in chronic lymphocytic leukemia |
1.86 |
|
KSDM1b Role in Ewing Sarcoma |
1.82 |
|
UPF1/SMG7-dependent MicroRNA-mediated Gene Regulation |
1.65 |
|
Human Cord Blood Sorted Live Cell Erythroblasts RNA-Seq |
1.64 |
|
A histone H3.3 Lysine 36 Trimethylation Reader Connects Chromatin to Regulated Pre-mRNA Processing |
1.59 |
|
Disruption of Na+/H+ exchanger regulatory factor 2 scaffold suppresses colon cancer proliferation |
1.58 |
|
CDK4/6 inhibitor resistance in prostate cancer |
1.57 |
|
RNA-seq analysis of control and CDK12-depleted ovarian cancer cells |
1.54 |
|
Genome wide association study of bone size yields eleven loci that also affect height, bone density, osteoarthritis and fractures |
1.54 |
|
Selective roles of vertebrate PCF11 in premature and full-length transcript termination (human 3' mRNA-seq) |
1.53 |
|
Truncation of LOC100288798 (SLC38A4-AS) lncRNA in human haploid KBM7 cell line |
1.52 |
|
SILAC identifies LAD1 as an oncogenic filamin binder regulating actin dynamics in response to EGF and marking aggressive breast tumors |
1.52 |
|
Effect of TUNAR silencing and GSK3 inhibition on human b-cell transcriptome |
1.51 |
|
Transcriptomics analysis of gene expression in normal and METTL3 or WTAP deficient Human HeLa cells |
1.5 |
|
Stochastic genome - nuclear lamina contacts are linked to histone H3K9 dimethylation |
1.49 |
|
Stochastic genome - nuclear lamina contacts are linked to histone H3K9 dimethylation (RNA-seq data) |
1.49 |
|
c-Jun promotes cell migration and drives expression of the motility factor ENPP2 in soft tissue sarcomas |
1.47 |
|
c-Jun promotes cell migration and drives expression of the motility factor ENPP2 in soft tissue sarcomas [RNA-Seq] |
1.47 |
|
Folate modulation induces chromosomal instability and higher proliferation of immortalized human keratinocytes |
1.43 |
|
RNA-seq analysis upon ARID1B overexpression |
1.42 |
|
RNA deep sequencing to compare genome-wide differences between PRMT5/knockdown and control AML cells |
1.42 |
|
LKB1, Salt-Inducible Kinases, and MEF2C are linked dependencies in acute myeloid leukemia (RNA-Seq) |
1.4 |
|
LKB1, Salt-Inducible Kinases, and MEF2C are linked dependencies in acute myeloid leukemia |
1.4 |
|
Chromatin remodeling mediated by ARID1A is indispensable for normal hematopoiesis in mice (human RNA-Seq) |
1.36 |
|
Integrative analysis of RNA, translation and protein levels reveals distinct regulatory variation across humans |
1.32 |
|
A20 regulates canonical wnt-signaling through an interaction with RIPK4 |
1.29 |
|
RB tumor suppressor promotes cancer immunity through downregulating PD-L1 expression |
1.28 |
|
Virus-like vesicles of Kaposi’s Sarcoma-Associated Herpesvirus activate lytic replication through triggering differentiation signaling (mRNA) |
1.28 |
|
Virus-like vesicles of Kaposi’s Sarcoma-Associated Herpesvirus activate lytic replication through triggering differentiation signaling |
1.28 |
|
An epigenetic mark of polycomb response elements implemented by Trx/MLL/COMPASS |
1.26 |
|
MicroRNA-28 replacement for non-Hodgkin lymphoma therapy |
1.2 |
|
Effect of low-dose sorafenib and alkylating agents in inflammation and angiogenesis in breast cancer |
1.18 |
|
ARS2 is a general suppressor of pervasive transcription [RNAseq] |
1.15 |
|
CD86 regulates a pro-survival signal in myeloma cells |
1.12 |
|
An Argonaute phosphorylation cycle promotes microRNA-mediated silencing [whole transcriptome RNA-seq] |
1.06 |
|
Xrn2 accelerates termination by RNA polymerase II, which is underpinned by CPSF73 activity |
1.0 |
|
Extracellular matrix (ECM) stiffness and collagen-1 (col-1) responsive genes in 3D cultured mammary epithelial cells |
0.98 |
|
JAG1 Mediated Notch Signaling Regulates Secretory Cell Differentiation of the Human Airway Epithelium |
0.98 |
|
Low MITF/AXL ratio predicts early resistance to multiple targeted drugs in melanoma |
0.97 |
|
BET-Bromodomain Inhibitors Engage The Host Immune System And Regulate Expression Of The Immune Checkpoint Ligand PD-L1 [3mRNA-seq] |
0.92 |
|
BET-Bromodomain Inhibitors Engage The Host Immune System And Regulate Expression Of The Immune Checkpoint Ligand PD-L1 |
0.92 |
|
Gene expression profiling by RNA-seq in hTert-HME1 cell line treated with control or BRCA2 siRNAs and grown with or without EGF (epithelial growth factor) II |
0.87 |
|
Effect of BB608 on Gene Expression in HNSCC Cell Line |
0.83 |
|
CNOT1 and Transcriptomic Landscape of a HeLa Cell Line |
0.82 |
|
Epigenome Editing by CRISPR/Cas9 Repressors for Silencing of Distal Regulatory Elements |
0.82 |
|
Critical role of transient activation of human endogenous retroviruses during reprogramming toward pluripotency (RNA-Seq) |
0.81 |
|
Critical role of transient activation of human endogenous retroviruses during reprogramming toward pluripotency |
0.81 |
|
RNA-seq of cancer cell lines treated with T-025 |
0.79 |
|
Hyper-activation of HUSH complex function by Charcot-Marie-Tooth disease mutation in MORC2 |
0.71 |
|
Gene expression for surgically treated pancreatic cancer after one neoadjuvant vaccine dose |
0.68 |
|
Effect of Polybrominated diphenyl ethers (PBDEs) on gene expression of MCF7 cells |
0.66 |
|
Network-based, cross-cohort discovery of transcriptional mechanisms presiding over maintenance of high-risk neuroblastoma subtype state |
0.65 |
|
m6A-RNA mapping, SND1-RNA binding profile mapping and SND1-depletion in KSHV-infected B-lymphocytes |
0.64 |
|
The multiple myeloma risk allele at 5q15 lowers ELL2 expression and increases ribosomal gene expression [ELL2 rescue] |
0.63 |
|
RNA editing in nascent RNA affects pre-mRNA splicing |
0.62 |
|
Functional Significance of U2AF1 S34F Mutation in Lung Adenocarcinomas |
0.61 |
|
HIV Reprograms Human Airway Basal Stem/Progenitor Cells to Acquire a Tissue Destructive Phenotype |
0.6 |
|
KAP1 regulates ERVs in differentiated human cells and contributes to innate immune control |
0.58 |
|
Transcriptomics analysis of gene expression in normal and YTHDC1, SRSF1, SRSF3, SRSF7, SRSF9 or SRSF10 deficient human HeLa cells |
0.57 |
|
Transcriptome profiling of A2M treated A549 Cell Line Samples |
0.57 |
|
Targeting MTHFD2 in Acute Myeloid Leukemia |
0.52 |
|
Downregulation of LATS kinases alters p53 to promote cell migration |
0.51 |
|
Regulation of mRNA half-life by an inhibitor of human decapping enzyme Dcp2 following transcription shutoff in HEK293T cells |
0.5 |
|
Systematic analysis of gene expression profiles controlled by hnRNP Q and hnRNP R, two closely related human heterogeneous nuclear ribonucleoproteins. |
0.49 |
|
YTHDF1 Amplifies Wnt/β-Catenin Signaling to Promote Intestinal Stemness |
0.45 |
|
PolyA-sequencing in Kelly and Kelly E9R neuroblastoma cells treated with THZ531 or DMSO |
0.44 |
|
DNMT1-associated long non-coding RNA regulate global gene expression and DNA methylation in colon cancer |
0.42 |
|
Effect of ILF3 depletion in HeLa cells on RNA steady state levels |
0.38 |
|
Azithromycin induces epidermal differentiation and multivesicular bodies in airway epithelia |
0.37 |
|
Functional genomic analysis of the haploinsufficient tumor suppressor, CUX1 |
0.35 |
|
Gene expression changes due to PARP knockdown in human cells |
0.29 |
|
Xeno-free and Chemically Defined Human System for Culturing Human Epidermal Keratinocytes |
0.25 |
|
Transcriptional response of human endocervical epithelial A2EN cells to infection with wild-type or CpoS-deficient Chlamydia trachomatis L2/434/Bu |
0.21 |
|
RelA mutants 'reconstituted' and cell cycle synchronized HCT116 Colorectal Cancer Cells |
0.18 |
|
Transcriptomic analysis of the role of the integrin a6b4 in detached cells |
0.17 |
|
Genome-wide search for differentially expressed RNAs responsible for the effects induced by Ebola virus replication and transcription |
0.15 |
|
Smoking Dysregulates the Human Airway Basal Cell Transcriptome at COPD-linked Risk Locus 19q13.2 |
0.15 |
|
Role of OSGIN1 in Mediating Smoking-induced Autophagy in the Human Airway Epithelium |
0.15 |
|
Role of OSGIN1 in Mediating Smoking-induced Autophagy in the Human Airway Epithelium [RNA-Seq] |
0.15 |
|
KRASG12C inhibition produces a driver-limited state revealing collateral dependencies |
0.09 |
|
Compare of gene expression between p16INK4A positive and negative regions of colon cancer from five patients |
0.09 |
|
O-GlcNAc transferase fine-tunes MYC-dependent transcription to promote cell cycle [RNA-seq] |
0.08 |
|
O-GlcNAc transferase fine-tunes MYC-dependent transcription to promote cell cycle |
0.08 |
|
Evaluating and comparing the Transcriptome of (human) Hek 293 based cells, expressing either CHD3 or CHD4 |
0.07 |
|
Gene expression analysis of breast cancer cell-lines |
0.07 |
|
Gene expression and genome-wide location analysis of breast cancer cell-lines |
0.07 |
|
Identification of Differentially Expressed Splice Variants by the Proteogenomic Pipeline Splicify |
0.07 |
|
Comprehensive molecular phenotypic effects of the large deletion on chromosome 22q11.2 |
0.06 |
|
6mer seed toxicity in viral microRNAs |
0.0 |