|
An evolutionarily conserved function of polycomb silences the MHC class I antigen presentation pathway and enables immune evasion in cancer |
31.07 |
|
An evolutionarily conserved function of polycomb silences the MHC class I antigen presentation pathway and enables immune evasion in cancer [RNA-Seq] |
31.07 |
|
The RNA exosome nuclease complex regulates human embryonic stem cell differentiation [RNA-Seq rescue_SS] |
30.32 |
|
CDK12 catalytic activity is rate-limiting for RNAPII processivity on core DNA replication genes and G1/S progression (3' RNA) |
25.26 |
|
Polysome-associated mRNA profiling of cancer cells in response to CXCL12 and IGF1 |
22.04 |
|
The RNA exosome nuclease complex regulates human embryonic stem cell differentiation |
14.6 |
|
MiR-CLIP capture of a miRNA targetome uncovers a lincRNA H19-miR-106a interaction |
14.2 |
|
Expression data from A2780 cells treated with DMSO, Olaparib(Ola), Palbociclib(PD), and their combination (Ola/PD) |
13.82 |
|
To investigate the decay constants (half-lives) of transcript isoforms generated by alternative polyadenylation in proliferating and quiescent cells |
13.47 |
|
Identification of transcription start sites for human A549 cell line using ReCappable-seq |
13.22 |
|
Improved genome-wide mapping of uncapped and cleaved transcripts in eukaryotes—GMUCT 2.0 |
12.95 |
|
Peptidomimetic blockade of MYB in acute myeloid leukemia [RNA-seq] |
12.89 |
|
Peptidomimetic blockade of MYB in acute myeloid leukemia |
12.89 |
|
A comprehensive single cell transcriptional landscape of human hematopoietic progenitors |
12.69 |
|
PolyA-sequencing in IMR-32 cells treated with THZ531 or DMSO |
12.04 |
|
Mutation independent activation of the Notch pathway is associated with Lapatinib resistance in Her2+ breast cancer cell lines |
11.66 |
|
ETV7 and interferon response |
11.14 |
|
Impact of ETV7 activity on interferon-stimulated gene expression in 293T cells treated with interferon alpha |
11.14 |
|
Comprehensive comparative analysis of 5’ end RNA sequencing methods |
10.42 |
|
Isolation and Transcriptome Analyses of Human Erythroid Progenitors: BFU-E and CFU-E |
10.41 |
|
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 |
10.31 |
|
Species-specific maturation profiles of human, chimpanzee and bonobo neural cells |
10.23 |
|
MUC1-C represses the RASSF1A tumor suppressor and activated Kras signaling in human carcinoma cells |
10.17 |
|
A common cell state in Triple Negative Breast Cancers represents a druggable vulnerability |
10.12 |
|
Gene expression profile of LMSU gastric cancer cell p53 KO and KD |
9.99 |
|
Splicing and gene expression changes in human MDAM-MB231 breast cancer cells with TRA2B knockdown |
9.27 |
|
Genome wide mapping of polyadenylation sites in proliferating and contact-inhibited cells and cells with knockdown of cleavage and polyadenylation factors |
9.27 |
|
Transcriptional profile of human STAT1-/- fibroblasts expressing IFI6 or empty control vector |
9.12 |
|
HMGA2 Promotes Long-Term Engraftment and Myelo-Erythroid Differentiation of Human Hematopoietic Stem and Progenitor Cells |
9.09 |
|
Sequencing Universal Human Reference RNA by Smart-seq and early barcoding library preparation methods |
8.79 |
|
The Developmental Heterogeneity of Human Natural Killer Cells Defined by Single-cell Transcriptome |
8.75 |
|
Development of a selective CDK9 degrader from a multi-targeted CDK inhibitor |
8.68 |
|
Development of a selective CDK9 degrader from a multi-targeted CDK inhibitor [RNA-seq] |
8.68 |
|
Enhancement of Arterial Specification in Human Pluripotent Stem Cell Cultures Promotes Definitive Hematoendothelial Program with Broad Myelolymphoid Potential |
8.61 |
|
Global analysis of enhancer targets: Mosaic-seq |
8.54 |
|
Transcriptome splicing analysis in K562 cells expressing rare and private spliceosomal mutations |
8.51 |
|
SNHG5 siRNA knock down in HCT116 cells |
8.29 |
|
Adipocyte-derived lipids mediate melanoma progression via FATP proteins |
8.27 |
|
RNA sequence of mRNA in HUVEC cells after depleting EGFL6 |
7.96 |
|
Effects of Polybrominated Diphenyl Ether (PBDE) Mixture on estrogen receptor positive (ER+) patient-derived tumor xenograft (PDX) model |
7.78 |
|
β-catenin/Tcf7l2 dependent transcriptional regulation of GLUT1 gene expression by Zic family proteins in colon cancer |
7.68 |
|
Splicing towards noncoding isoforms in colorectal carcinoma is associated with tumor hypoxia and the DNA damage response |
7.26 |
|
RNA-seq analysis of Retinoic Acid and Non-treated Control hiPSCs |
7.23 |
|
Gene expression alterations associated with acquired-resistance to the CDK4/6 inhibitor palbociclib [Palbociclib resistance_RNASeq] |
7.11 |
|
RNA-seq of Single-Cell Genotyping of Transcriptomes |
7.09 |
|
Single-Cell Genotyping of Transcriptomes |
7.09 |
|
CROP-Seq in Primary Human T Cells |
6.95 |
|
Seletive inhibition of CDK9 in DLBCL cell lines |
6.85 |
|
RNA-seq and m6A-seq of AML cells with FTO knockdown or inhibition |
6.68 |
|
IGF2BP1 promotes SRF-dependent transcription in cancer in a m6A- and miRNA-dependent manner |
6.62 |
|
IGF2BP1 promotes SRF-dependent transcription in cancer in a m6A- and miRNA-dependent manner [Huh-7] |
6.62 |
|
Precise Gene Editing Preserves Hematopoietic Stem Cell Function Following Transient p53-Mediate DNA Damage Response |
6.57 |
|
High-throughput sequencing of PROMPT-enriched samples. |
6.52 |
|
Retinoic Acid Induced Transcriptional Repressor HIC1 is Required for Suppressive Function of Human Induced Regulatory T cells [RNA-Seq 1] |
6.49 |
|
RNA seq data of Hep3B-control, Hep3B-sertraline, Hep3B-XL413, Hep3B-XL413-sertraline, Huh7-control, Huh7-sertraline, Huh7-XL413, Huh7-XL413-sertraline cells |
6.45 |
|
Interaction with ZMYND11 mediates opposing roles of Ras-responsive transcription factors ETS1 and ETS2 |
6.3 |
|
Interaction with ZMYND11 mediates opposing roles of Ras-responsive transcription factors ETS1 and ETS2 |
6.3 |
|
RNA-Seq to assess the transcriptional effects of G quadruplex stabilization by the G4 ligand PhenDC3 in HT-1080 cells |
6.05 |
|
Identification of global regulators of T-helper cell lineage specification |
6.03 |
|
Identification of global regulators of T-helper cell lineage specification (RNA-Seq) |
6.03 |
|
The dynamics of cellular response to therapeutic perturbation using multiplexed quantification of the proteome and transcriptome at single-cell resolution |
6.0 |
|
RNA-sequencing of isogenic primary, pre-malignant immortalized, and Ras-transformed human mammary epithelial cells |
5.98 |
|
MenSCs inhibit HCC growth through oncogenic pathway suppression via regulating 5-hmC in enhancer elements |
5.98 |
|
MenSCs inhibit HCC growth through oncogenic pathway suppression via regulating 5-hmC in enhancer elements [RNA-seq] |
5.98 |
|
The landscape of alternative splicing in aggressive prostate cancers |
5.81 |
|
Distinct gene expression profile of Huh7 cell lines stably overexpressing CRABP1 or 2 |
5.78 |
|
Nickel induced transcriptional changes persist post exposure through epigenetic reprograming (RNA-seq dataset) |
5.77 |
|
A novel Menin-MLL inhibitor induces specific chromatin changes and eradicates disease in models of MLL-rearranged leukemia [RNA-Seq II] |
5.77 |
|
Activation of HOTTIP lncRNA perturbs HSC function leading to AML like disease |
5.6 |
|
Cell-to-cell variation in defective virus expression and effect on host response during influenza virus infection |
5.57 |
|
Synergy from Gene Expression and Network Mining (SynGeNet) method predicts genotype-specific synergistic drug combinations in melanoma |
5.57 |
|
WNK1 kinase and the termination factor PCF11 connect nuclear mRNA export with transcription |
5.23 |
|
Che-1 is targeted by c-Myc to sustain proliferation in pre-B-cell acute lymphoblastic leukemia |
5.22 |
|
Che-1 is targeted by c-Myc to sustain proliferation in pre-B-cell acute lymphoblastic leukemia [RNA-seq] |
5.22 |
|
mRNA expression profile of A549 cells and MSR-A549 cells with or without JQ1 treatment |
5.21 |
|
A549 cells and MSR-A549 cells |
5.21 |
|
scRNASeq analysis of cycling cardiomyocytes |
5.08 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of HIV-1 Latency in Central Memory T Cells |
5.07 |
|
HNF1A deficiency impairs β-cell fate, granule maturation and function |
5.06 |
|
LNCaP treated with iBET |
4.91 |
|
Proteinase-Activated Receptor 4 (PAR4) mediates cell membrane blebbing in a Gaq/11, Gai independent, RhoA and ß-arrestin-dependent manner. |
4.86 |
|
Dioxin and AHR impairs mesoderm gene expression and cardiac differentiation in human embryonic stem cells |
4.79 |
|
Dioxin and AHR impairs mesoderm gene expression and cardiac differentiation in human embryonic stem cells (RNA-Seq) |
4.79 |
|
High throughput characterization of the m6A demethylase FTO by CLIP and RNAseq |
4.77 |
|
CHD7 is Suppressed in the Perinecrotic/Ischemic Microenvironment and is a Novel Regulator of Angiogenesis |
4.69 |
|
Trans-differentiation of human adult peripheral blood T cells into neurons |
4.66 |
|
DNMT and HDAC inhibitors globally induce cryptic TSSs encoded in long terminal repeats |
4.65 |
|
DGCR8 acts as a novel adaptor for the exosome complex to degrade double-stranded structured RNAs |
4.61 |
|
A TFIID-SAGA perturbation that targets MYB and suppresses acute myeloid leukemia (RNA-seq) |
4.6 |
|
A TFIID-SAGA perturbation that targets MYB and suppresses acute myeloid leukemia |
4.6 |
|
Vitamin C Promotes Apoptosis in Breast Cancer Cells by Increasing TRAIL Expression |
4.59 |
|
Tafazzin Regulates Cell State by Modulating Phosphatidylethanolamine and Phosphatidylserine levels |
4.59 |
|
RNAseq Study in CC-671 Treated Cal-51 Cells |
4.57 |
|
The regulation of ferroptosis by TAZ in epithelial ovarian cancer |
4.54 |
|
Defining the Transcriptional Landscape during Cytomegalovirus Latency with Single-Cell RNA Sequencing |
4.51 |
|
RNA-seq of MDA-MB-231 cells with TET1 knockout |
4.46 |
|
Silencing p300 in MCF7 cells to study expression and alternative splicing |
4.46 |
|
LncRNA NMR knockdown and overexpression in esophageal squamous cell carcinoma cell lines |
4.42 |
|
Histone Demethylase-Assisted Somatic Cell Nuclear Transfer Facilitates Derivation of Human Pluripotent Stem Cells |
4.42 |
|
PolyA-sequencing in Kelly and Kelly E9R neuroblastoma cells treated with THZ531 or DMSO |
4.41 |
|
Knock-down of Ror1 in MDA-MB-231 cell line decreases cell invasiveness |
4.39 |
|
Characterization of sperm lncRNA and its differently expression in the sperm of asthenozoospermic patients |
4.38 |
|
Single-cell transcriptome of human epithelial cells reveals novel insights into early innate immune responses to influenza virus and viral antagonism |
4.36 |
|
MBNL1-dependent modulation of gene expression in MDA-MB-231 breast cancer cells |
4.35 |
|
Muscleblind-like 1 suppresses breast cancer metastatic colonization and stabilizes metastasis suppressor transcripts |
4.35 |
|
ZNF599 and DNMT3A coordinately control nuclear envelope organization by repression of SUN4 expression |
4.34 |
|
Measuring the effect of MYC on transcription during the DNA double-strand break response by RNA-seq of newly synthesized transcripts |
4.33 |
|
Human CD4+CD103+ cutaneous resident memory T cells are found in the circulation of healthy subjects |
4.32 |
|
Transcriptome analysis of immature and matured human oocytes from patients of young and advanced maternal age |
4.32 |
|
AZ1366: An inhibitor of tankyrase and the canonical Wnt pathway that limits the persistence of non-small cell lung cancer cells following EGFR inhibition |
4.31 |
|
Single-cell RNA sequencing-based CRISPRi screening resolves molecular drivers of early human endoderm development [set 1] |
4.31 |
|
A quantitative chemotherapy genetic interaction map identifies new factors associated with PARP inhibitor resistance |
4.31 |
|
Glioblastoma stem cells infected by ZIKA virus |
4.29 |
|
Transcriptomics-based drug repurposing approach identifies novel drugs against sorafenib-resistant hepatocellular carcinoma |
4.28 |
|
Crizotinib v. DMSO in SW480 cells |
4.22 |
|
O-glcnAc reprograms cellular energetics |
4.22 |
|
Downregulation of DDX5/DDX17 and REST |
4.21 |
|
Genome-wide probing of RNA structure reveals active unfolding of mRNA structures in vivo |
4.2 |
|
RNA-Seq in two Ewing sarcoma cell lines: A673 and SKNMC |
4.2 |
|
Polyol pathway links glucose metabolism to the aggressiveness of cancer cells |
4.17 |
|
Characterization of human CDK12 and CDK13 in the regulation of RNA processing |
4.14 |
|
Patient-derived luminal breast cancer xenografts with progestins |
4.13 |
|
RNAseq analysis of patient-derived luminal breast cancer xenografts treated with progestins |
4.13 |
|
Generating Patterned Kidney Organoids for Studying Development and Diseases |
4.1 |
|
RNA-seq analysis of control and ZC3H18-depleted ovarian cancer cells |
4.04 |
|
Genome-wide transcriptome analysis of NIPBL iPSC and commited cardiomyoctes |
4.0 |
|
Identification of renal resident macrophages across species |
4.0 |
|
Abnormal RNA splicing and genomic instability after induction of DNMT3A mutations by CRISPR/Cas9 gene editing [RNA-Seq] |
3.97 |
|
Abnormal RNA splicing and genomic instability after induction of DNMT3A mutations by CRISPR/Cas9 gene editing |
3.97 |
|
Effect of drugs on transcriptomic profiles |
3.93 |
|
B-cell activating factor (BAFF) stimulation of Burkitt Lymphoma cell line |
3.93 |
|
B-cell activating factor (BAFF) stimulation of Burkitt Lymphoma cell line [RNA-Seq] |
3.93 |
|
The ZZ-type zinc finger of ZZZ3 modulates the ATAC complex-mediated histone acetylation and gene activation |
3.92 |
|
Dynamics of the human and viral m6A RNA methylomes during HIV-1 infection of T cells |
3.88 |
|
Assessing the effect of SUPT4H1 RNAi on the transcription of a repeat-containing reporter construct |
3.87 |
|
Genome-wide maps in MCF-7 cells with six2 or CYP4Z1 3'UTR or CYP4Z2P 3'UTR overexpression or not |
3.87 |
|
miR-191 regulates human cell proliferation and directly targets multiple oncogenes [seq] |
3.83 |
|
Genome wide miR-191 target profile determined by RIP and gene expression profiling |
3.83 |
|
mRNA and RNC-mRNA deep sequencing of three hepatocellular carcinoma cell lines |
3.82 |
|
Super-Enhancers Promote Transcriptional Dysregulation in Nasopharyngeal Carcinoma |
3.82 |
|
Super-Enhancers Promote Transcriptional Dysregulation in Nasopharyngeal Carcinoma [RNA-seq] |
3.82 |
|
Transcription control by the ENL YEATS domain in acute leukemia |
3.81 |
|
Transcription control by the ENL YEATS domain in acute leukemia [RNA-seq] |
3.81 |
|
Human embryonic stem cell, chimpanzee induced pluripotent stem cell, orangutan induced pluripotent stem cell, rhesus embryonic stem cell, and their derived cortical organoid RNA-seq |
3.79 |
|
Time series single-cell transcriptomic analysis of AEC2 directed differentiation |
3.77 |
|
Transcriptome sequencing of K-562 cells |
3.77 |
|
The RNA binding protein IGF2BP3 promotes hematopoietic progenitor cell proliferation by targeting leukemogenic pathways |
3.77 |
|
Interleukin-1β induces mitochondrial DAMP production to activate STING-dependent innate immune programs |
3.76 |
|
Ex-vivo Human Hematopoietic Stem Cell Expansion Requires Coordination of Cellular Reprogramming with Mitochondrial Remodeling and P53 Activation |
3.75 |
|
IGF2BP3 controls cancer cell invasiveness by modulation RISC function |
3.72 |
|
The Polycomb protein BMI1 induces an invasive gene expression signature in melanoma that promotes metastasis and chemoresistance. |
3.65 |
|
Targeting HuH7 cells with JumonjiC Lysine Demethylase Inhibitors (RNA-Seq) |
3.62 |
|
High Resolution Mapping of RNA Polymerases Identifies Mechanisms of Sensitivity and Resistance to BET Inhibitors in t(8;21) AML |
3.61 |
|
Neurotrophic Tyrosine Kinase Receptor 1 is Epigenetically Regulated by IL-13 and Contributes to Allergic Inflammation |
3.58 |
|
Impact of dieldrin on transcription in Jurkat T cells |
3.55 |
|
Investigation into human Tra2 protein-dependent splicing in MDA-MB-231 cells using iCLIP and RNA-seq |
3.52 |
|
Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation |
3.49 |
|
A Unique Epigenomic Landscape Defines Human Erythropoiesis |
3.48 |
|
A Unique Epigenomic Landscape Defines Human Erythropoiesis (RNA-seq) |
3.48 |
|
RNA-sequencing of mRNAs from control and CAP-D3 deficient Salmonella infected HT-29 cells |
3.48 |
|
DART-seq: an antibody-free method for global m6A detection |
3.48 |
|
The MLL-AF9 and MLL-AF4 oncofusion proteins bind a distinct enhancer repertoire and target the RUNX1 program in MLLr AML |
3.47 |
|
EIF1AX-A113 splice and RAS mutations cooperate to drive thyroid tumorigenesis through ATF4 and c-MYC |
3.46 |
|
The effects of chemokines CCL2/7 on MDA-MB-231-FOXC1 cells |
3.44 |
|
Translating transcriptome of cancer cells in situ in mesenchymal-rich tumor microenvironment |
3.42 |
|
Total RNA-seq in ALL-SIL upon TLX1 knockdown |
3.41 |
|
The cohesin complex prevents Myc-induced replication stress |
3.39 |
|
RNA-seq in SUNE-1 cells after downregulation of DANCR expression |
3.38 |
|
Nickel induced transcriptional changes persist post exposure through epigenetic reprograming (ChIP-seq & RNA-seq datasets) |
3.38 |
|
A non-catalytic function of carbonic anhydrase IX contributes to the glycolytic phenotype and pH regulation in human breast cancer cells |
3.37 |
|
Transcriptome of activated human and mouse MAIT cells |
3.37 |
|
Transciptome profiling of NoDice and RNaseIII null cells prior to and after polyIC treatment |
3.36 |
|
Gene expression analysis of the impact of TDP-43 knockout in human cells. |
3.35 |
|
Exploiting Prmt5-orchestrated intron detention signatures to treat splicing-addicted malignant glioma tumors |
3.35 |
|
Lysine benzoylation is a novel histone mark |
3.32 |
|
Lysine benzoylation is a novel histone mark [RNA-seq] |
3.32 |
|
The p30 isoform of CEBPA uncovers a silent enhancer to drive the expression of the tumor promotive factor CD73 in CEBPA mutant AML |
3.32 |
|
H3B-8800, a novel oral splicing modulator, induces lethality in spliceosome mutant cancers [Nalm-6] |
3.31 |
|
PolyA-sequencing in IMR-32 neuroblastoma cells with shRNA mediated depletion of CDK12, CDK13 or GFP. |
3.3 |
|
Trisomy of a ‘Down syndrome critical region’ globally amplifies transcription via HMGN1 overexpression |
3.3 |
|
Targeted reactivation of FMR1 transcription in FXS embryonic stem cells |
3.29 |
|
RNA-Seq of over-expression and knockdown of the lncRNA SLNCR1 in melanoma cells |
3.27 |
|
RNA-seq, ChIP-seq and single cell RNA-seq of human skin Langerhans cells |
3.26 |
|
RNAseq of CD8+ and CD8- MAIT cells in human peripheral blood |
3.24 |
|
RNA-seq analysis of human cardiosphere cells with different tubule supportive potential |
3.23 |
|
Single cell analysis of HSV-1 infection reveals anti-viral and developmental programs are activated in distinct sub-populations with opposite outcomes |
3.23 |
|
Loss of 9p21 regulatory hub promotes kidney cancer progression by upregulating HOXB13 |
3.21 |
|
Differential mRNA expression upon 9p21 deletion in HEK TE single-cell derived clones |
3.21 |
|
Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of TDP-43-dependent neurodegeneration |
3.2 |
|
Human Treg IL-12 stimulation |
3.18 |
|
TRIM28 interacts with EZH2 and SWI/SNF to activate genes that promote mammosphere formation |
3.18 |
|
Selectively targeting bromodomain and extraterminal proteins for degradation as a novel anti-glioblastoma strategy [RNA-seq] |
3.17 |
|
Multiplexed engineering and analysis of endogenous enhancer activity in single cells: Mosaic-Seq of beta-globin locus (separate infection) |
3.17 |
|
Inhibition of DNA methylation promotes breast tumor sensitivity to netrin-1 interference |
3.16 |
|
Inhibition of DNA methylation promotes breast tumor sensitivity to netrin-1 interference [RNA-Seq] |
3.16 |
|
N6-methyladenine DNA Modification in Glioblastoma [RNA-seq] |
3.15 |
|
N6-methyladenine DNA Modification in Glioblastoma |
3.15 |
|
Gene expression analysis of BRD4 knockdown in HT-29 and HCT116 cells |
3.11 |
|
Designer epigenome modifiers enable robust and sustained gene silencing in clinically relevant human cells |
3.11 |
|
Designer epigenome modifiers enable robust and sustained gene silencing in clinically relevant human cells [RNA-seq] |
3.11 |
|
RNAseq to determine gene expression changes following depletion of SETDB1 in THP-1 AML Cells |
3.08 |
|
Global analysis of ZNF217 chromatin occupancy in the breast cancer cell genome reveals an association with Eralpha |
3.08 |
|
RNA seq with AML (NB4) cells upon FTO inhibition |
3.05 |
|
Interactions of aCPs with Cytosine-rich Polypyrimidine Tracts Enhance Splicing of Cassette Exons |
3.05 |
|
Cajal bodies are linked to genome conformation |
3.04 |
|
Cajal bodies are linked to genome conformation [RNA-Seq] |
3.04 |
|
JQ1 +/- Vemurafenib in BRAF mutant melanoma (A375) |
3.01 |
|
Circular RNAs are down-regulated in KRAS mutant colon cancer cells and can be transferred to exosomes |
3.01 |
|
Lyophilized human cells stored at room temperature preserve multiple RNA species at excellent quality for RNA sequencing |
3.0 |
|
The SPOP-containing Complex Functions as an E3 Ligase for SETD2 to Regulate Gene-Specific H3K36me3-Coupled Alternative Splicing |
3.0 |
|
INO80 governs super-enhancer-mediated oncogenic transcription and tumor growth in melanoma [RNA-seq] |
2.98 |
|
INO80 governs super-enhancer-mediated oncogenic transcription and tumor growth in melanoma |
2.98 |
|
The X-linked DDX3X RNA helicase dictates translation re-programming and metastasis in melanoma |
2.97 |
|
RNA-seq analysis of control and Myc-induced U2OS cells |
2.97 |
|
Stably-paused genes revealed through inhibition of transcription initiation by the TFIIH inhibitor Triptolide |
2.96 |
|
Gene expression and 4sUDRB-seq for NF90/NF110 of human scramble and KD HeLa cells. |
2.96 |
|
DDX3X regulation of global translation is impaired by medulloblastoma-associated mutations [RNA-Seq] |
2.94 |
|
DDX3X regulation of global translation is impaired by medulloblastoma-associated mutations |
2.94 |
|
VAMP8 contributes to TRIM6-mediated type-I interferon antiviral response upon West Nile virus (WNV) infection |
2.91 |
|
RNA-seq of UGP2 mutant human embryonic stem cells and in vitro differentiated neural stem cells |
2.91 |
|
Depicting early human development and germ cell origin with porcine embryos |
2.91 |
|
pSILAC mass spectrometry reveals ZFP91 as novel IMiD dependent substrate of the CRL4CRBN ligase |
2.9 |
|
THZ1 targeting CDK7 suppresses STAT transcriptional activity and sensitizes T-cell lymphomas to BCL2 inhibitors |
2.88 |
|
Single-cell analysis of adult human ovary using 10X genomics |
2.88 |
|
Medial Ganglionic Eminence and Cortical Organoids Model Human Brain Development and Interneuron Migration |
2.87 |
|
Gene expression in control and DOCK8 CRISPR KHYG1 NK cells |
2.87 |
|
RNAseq to determine whether bidirectional transcription occurs over transposable elements following depletion of SETDB1 in THP-1 AML Cells |
2.85 |
|
Poly(A)-ClickSeq resolves CF25-mediated alternative poly-adenylation, HeLa |
2.81 |
|
Single-cell Map of Diverse Immune Phenotypes in the Breast Tumor Microenvironment - 5' RNA sequencing and TCR sequencing |
2.8 |
|
Selective expression of long non-coding RNAs in a breast cancer cell progression model |
2.8 |
|
circ-ZNF609 regulates G1-S progression in Rhabdomyosarcoma |
2.8 |
|
Grainyhead-like 2 is essential for androgen receptor expression and activity in prostate cancer (RNA-seq) |
2.8 |
|
Grainyhead-like 2 is essential for androgen receptor expression and activity in prostate cancer |
2.8 |
|
Transcriptome analysis in a radiosensitive and a radioresistant cell line after ionizing radiation |
2.78 |
|
ATF4 inhibition by p62 represses stromal metabolic reprogramming and tumorigenesis II |
2.77 |
|
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity |
2.76 |
|
Identification of a core p53 transcriptional program with highly fractionated tumor suppressive activity |
2.75 |
|
GRO-seq from HCT116, MCF7 and SJSA cell lines treated with DMSO and Nutlin |
2.75 |
|
Direct interaction of MYCN and p53 regulate transcriptional responses in neuroblastoma [RNA-Seq] |
2.73 |
|
Direct interaction of MYCN and p53 regulate transcriptional responses in neuroblastoma |
2.73 |
|
RNA-seq of ASXL2 shRNA KD in SKNO-1 cells |
2.73 |
|
Bromodomain inhibition of the transcriptional coactivators CBP/EP300 as a therapeutic strategy to target the IRF4 network in multiple myeloma (RNA-Seq) |
2.72 |
|
Bromodomain inhibition of the transcriptional coactivators CBP/EP300 as a therapeutic strategy to target the IRF4 network in multiple myeloma |
2.72 |
|
Genome-wide discovery of human splicing branchpoints [RNAse] |
2.71 |
|
Divergent effects of eRF3 and Upf1 on the expression of uORF carrying mRNAs and ribosome protein genes |
2.69 |
|
GREB1 amplifies androgen receptor output in prostate cancer and contributes to antiandrogen resistance |
2.67 |
|
Nucleotide stress induction of HEXIM1 suppresses melanoma by modulating cancer cell-specific gene transcription |
2.65 |
|
ZFR coordinates crosstalk between RNA decay and transcription in innate immunity |
2.61 |
|
Transcription-dependent control of stem cell self-renewal and differentiation by the splicing factor U2AF1 |
2.59 |
|
Accurate annotation of human protein-coding small open reading frames |
2.57 |
|
Single-cell RNA sequencing-based CRISPRi screening resolves molecular drivers of early human endoderm development |
2.56 |
|
FBP2 inhibits sarcoma progression by restraining mitochondrial biogenesis |
2.55 |
|
Probing the Global Cellular Responses to Lipotoxicity Caused by Saturated Fatty Acids |
2.55 |
|
Analysis of transcriptomes of healthy donor and CD46 deficient CD8 T cells |
2.52 |
|
Transcriptome analysis of CD8+ T cells from healthy controls and patients wth CD46 deficiency |
2.52 |
|
RNA transcriptome analysis of IRF1 and IRF3 knockout in immortalized primary hepatocytes infected with hepatitis A virus |
2.52 |
|
CXCR4 is a host factor that regulates Plasmodium development in hepatocytes |
2.5 |
|
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 |
2.5 |
|
Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation (Ribo-seq, RNA-seq) |
2.5 |
|
Effect of low-dose sorafenib and alkylating agents in inflammation and angiogenesis in breast cancer |
2.48 |
|
Oncogenic Serine-Threonine Kinase Receptor Associated Protein Supports Hepatocellular Carcinoma Cell Growth by Enhancing Wnt/β-catenin Signaling |
2.47 |
|
p38 SAPK and SKIIP induced changes in alternative splicing patterns upon osmostress |
2.47 |
|
ARID1A regulates condensin II distribution and chromosomal partition |
2.46 |
|
ARID1A regulates condensin II distribution and chromosomal partition [RNA-seq] |
2.46 |
|
Molecular characterization of BRSK2 and BRSK1 kinases as negative regulators of the NRF2 transcription factor |
2.46 |
|
Biosynthesis of histone messenger RNA employs a specific 3' end endonuclease |
2.45 |
|
Generation and persistence of human tissue-resident memory T cells in lung transplantation |
2.44 |
|
Mitotically associated long non-coding RNA, MANCR regulates cell cycle in triple negative breast cancer cells |
2.42 |
|
Identification of altered developmental pathways in human juvenile HD iPSC with 71Q and 109Q using transcriptome profiling |
2.4 |
|
A zebrafish melanoma model reveals emergence of neural crest identity during melanoma initiation |
2.4 |
|
A zebrafish melanoma model reveals emergence of neural crest identity during melanoma initiation [human cell line RNA-seq] |
2.4 |
|
Transcriptional profiling of JEG3 cells with HLA-G ablation via deletion of Enhancer L |
2.38 |
|
Ex-vivo Human Hematopoietic Stem Cell Expansion Requires Coordination of Cellular Reprogramming with Mitochondrial Remodeling and P53 Activation [bulk] |
2.37 |
|
High-resolution liver cancer genomic profiling links etiology, epigenetic and mutation signatures |
2.35 |
|
High-resolution liver cancer genomic profiling links etiology, epigenetic and mutation signatures [RNA-Seq] |
2.35 |
|
RNA-sequencing of the GSI treatment of the CUTLL1 cell line |
2.34 |
|
RC3H1 posttranscriptionally regulates A20 mRNA and modulates the activity of the IKK/NF-kB pathway |
2.33 |
|
RC3H1 posttranscriptionally regulates A20 mRNA and modulates the activity of the IKK/NF-kB pathway [RNA-Seq] |
2.33 |
|
Functional role of SLIT2 and ROBO1 in trophoblasts |
2.32 |
|
Gene expression, methylome and splicing of THP-1 monocytic cells and THP-1-derived macrophage |
2.31 |
|
Expression profile of wild type (WT) vs miR-155-/- in FLT3-ITD+ AML (MV4-11) cell lines |
2.27 |
|
Genome-wide CRISPR-Cas9 screen identifies functionally relevant microRNAs in AML |
2.27 |
|
Integrated single cell analysis of blood and cerebrospinal fluid leukocytes in multiple sclerosis |
2.26 |
|
Regulating Interleukin-2 activity with engineered receptor signaling clamps |
2.25 |
|
Binding to SMN2 pre-mRNA-Protein complex elicits specificity for small molecule splicing modifiers |
2.22 |
|
Induction of human hemogenesis in adult fibroblasts by defined factors and hematopoietic co-culture |
2.22 |
|
PRDM1 inhibits proliferation of human colon cancer organoids |
2.21 |
|
EHMT1 and EHMT2 inhibition induce fetal hemoglobin expression |
2.2 |
|
EHMT1 and EHMT2 inhibition induce fetal hemoglobin expression [RNA-seq] |
2.2 |
|
An Argonaute phosphorylation cycle promotes microRNA-mediated silencing [whole transcriptome RNA-seq] |
2.2 |
|
Small molecule inhibition of ERK dimerization prevents tumorigenesis by Ras-ERK pathway oncogenes |
2.17 |
|
Chronic cadmium exposure decreases the dependency of MCF7 breast cancer cells on ERα |
2.17 |
|
Increased Serine and One Carbon Pathway Metabolism by PKCl/i Deficiency Promotes Neuroendocrine Prostate Cancer [RNA-seq] |
2.15 |
|
Increased Serine and One Carbon Pathway Metabolism by PKCl/i Deficiency Promotes Neuroendocrine Prostate Cancer |
2.15 |
|
The anti-leukemic effect of R-2HG depends on its acting as an m6A mRNA modifier-RNA Seq-PBS / R-2HG treatment |
2.13 |
|
ARID1A loss impairs enhancer-mediated gene regulation and drives colon cancer in mice |
2.13 |
|
ARID1A loss impairs enhancer-mediated gene regulation and drives colon cancer in mice [HCT116_RNA-seq] |
2.13 |
|
Transcriptomic analysis of ERR alpha orphan nuclear receptor |
2.11 |
|
Antioxidant metabolism in activated CD8+ T cells regulates stem-like human memory T cell formation and anti-tumor immunity |
2.1 |
|
Group A Streptococcus M1T1 Intracellular Infection of Primary Tonsil Epithelial Cells Dampens Levels of Secreted IL-8 Through the Action of SpyCEP |
2.09 |
|
Cockayne syndrome A and B proteins regulate the transcription arrest upon genotoxic stress through a ubiquitin/proteasome degradation process (RNA-seq) |
2.08 |
|
Cockayne syndrome A and B proteins regulate the transcription arrest upon genotoxic stress through a ubiquitin/proteasome degradation process |
2.08 |
|
mRNA profiles of JMJD3 overexpression- and JMJD3 knockout- HL-60 cells |
2.08 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of transcriptomes of human cord blood CD34+ cells treated with HDAC5 inhibitor |
2.05 |
|
The NORAD lncRNA assembles a topoisomerase complex critical for genome stability |
2.02 |
|
The NORAD lncRNA assembles a topoisomerase complex critical for genome stability [RNA-seq] |
2.02 |
|
Transcriptome analysis of PRMT6 knock-out in NT2/D1 cells |
2.01 |
|
Genomic location of PRMT6-dependent H3R2 methylation is decisive for the transcriptional outcome of associated genes |
2.01 |
|
Oncogenic MYC induces a dependency on the spliceosome in human cancer |
1.99 |
|
Spliceosomal disruption of the non-canonical BAF complex in cancer |
1.98 |
|
Induction of human regulatory innate lymphoid cells from group 2 innate lymphoid cells by retinoic acid |
1.98 |
|
Transcriptome landscape of HeLa response upon triamcinolone acetonide |
1.95 |
|
Gene expression changes in THP1 cells at day 2 and 4 following shRNA knock-down of RUVBL2 |
1.95 |
|
CRISPR-Cas9 combinatorial KO of epigenetic regulators in human ovarian cancer cells |
1.95 |
|
Disease modelling of core pre-mRNA splicing factor haploinsufficiency |
1.94 |
|
JMJD3 facilitates C/EBPβ-centered transcriptional program to exert oncorepressor activity in AML |
1.94 |
|
Characterization of transcriptomics landscape in HUVEC cells exposed to oxidative stress (Total RNA) |
1.92 |
|
The RNA exosome nuclease complex regulates human embryonic stem cell differentiation [RNA-Seq SS] |
1.87 |
|
LSD1 mediates MYCN control of epithelial-mesenchymal transition through silencing of metastatic suppressor NDRG1 gene |
1.87 |
|
Inheritable Silencing of Endogenous Genes by Hit-and-Run Targeted Epigenetic Editing |
1.87 |
|
Tracing Enhancer Networks using Epigenetic Traits (TENET) |
1.86 |
|
Human SETMAR is a DNA sequence-specific histone-methylase with a broad effect on the transcriptome |
1.83 |
|
Role of BET proteins in YAP/TAZ-dependent transcription [RNA-seq 1] |
1.83 |
|
Long non-coding RNA RP11-19E11.1 is an E2F1 target required for tumor cell proliferation and survival in basal breast cancer |
1.83 |
|
JUNB is a critical AP1 component for SMAD2/3 binding after TGFβ stimulation [RNA-seq] |
1.82 |
|
SMAD2/3 are redirected to novel sites in MCF10A MII after prolonged TGFβ stimulation |
1.82 |
|
The impact of stanniocalcin 1 on the transcriptome of human cord blood stem/progenitors |
1.79 |
|
Cellular gene expression during Hepatitis C Virus replication revealed by Ribosome profiling |
1.79 |
|
Suppression of ribosomal pausing by eIF5A is necessary to maintain the fidelity of start codon selection (RNA-sequencing) |
1.79 |
|
Suppression of ribosomal pausing by eIF5A is necessary to maintain the fidelity of start codon selection |
1.79 |
|
Single-cell Transcriptomics reveals multi-step adaptations to endocrine therapy |
1.78 |
|
Profiling of protrusion-enriched RNAs from human breast cancer cell line MDA-MB-231 |
1.77 |
|
Dual inhibition of HDMX and HDM2 as a Therapeutic Strategy in Leukemia |
1.76 |
|
Host transcriptome analysis of Aspergillus fumigatus infection in Airway Epithelial Cells |
1.74 |
|
Effect of PRDM11 depletion in U2932 cells |
1.72 |
|
SLAM-seq defines direct gene-regulatory functions of the BRD4-MYC axis [Quant-Seq] |
1.7 |
|
SLAM-seq defines direct gene-regulatory functions of the BRD4-MYC axis |
1.7 |
|
HBEC-shp53-PCHD7 |
1.7 |
|
Gene expression analysis of dengue-infected cells |
1.69 |
|
Cap-specific terminal N6-methylation of RNA by an RNA polymerase II-associated methyltransferase. |
1.68 |
|
An atlas of TNF-α-responsive promoters and enhancers in the intestinal epithelial cell model Caco-2 |
1.64 |
|
SLIGRL-induced gene expression changes in NHEK cells |
1.61 |
|
ARID1A is a critical regulator of luminal identity and therapeutic response in oestrogen receptor-positive breast cancer (RNA-Seq) |
1.61 |
|
Tunable protein synthesis by transcript isoforms in human cells (Transcript Isoforms in Polysomes sequencing: TrIP-seq) |
1.61 |
|
Functional significance of the HIV-1 Tat signature amino acid residues |
1.56 |
|
Perivascular signals alter global genomic profile of glioblastoma and response to temozolomide in a gelatin hydrogel |
1.54 |
|
The hepatitis C viral protein NS5A stabilizes growth-regulatory human transcripts |
1.52 |
|
Impact on erythroid progenitor type on erythroid differntiation |
1.52 |
|
RNA-sequencing of cells derived from the site of inflammation of Juvenile Idiopathic Arthritis patients |
1.51 |
|
Epigenetic profiling and RNA-sequencing of Juvenile Idiopathic Arthritits (JIA) patients |
1.51 |
|
Role of BET proteins in YAP/TAZ-dependent transcription [RNA-seq 2] |
1.51 |
|
Trisomy of a ‘Down syndrome critical region’ globally amplifies transcription via HMGN1 overexpression [NALM6 RNA-Seq] |
1.51 |
|
Pseudotime Ordering of Single Human Beta-Cells Reveals States of Insulin Production and Unfolded Protein Response |
1.5 |
|
Compared performance of Affymetrix HTA arrays and Illumina RNAseq for the analysis of tumours |
1.48 |
|
Compared performance of Affymetrix HTA arrays and Illumina RNAseq for the analysis of tumours [RNA-seq] |
1.48 |
|
Stem cell and neurogenic gene-expression profiles link prostate basal cells to aggressive prostate cancer |
1.47 |
|
RNA-seq analysis of PRMT5-regulated genes in irradiated/non-irradiated LNCaP cells |
1.47 |
|
shRNA knockdown of YAP1 in HCC364 cells, various drug conditions |
1.47 |
|
Hypoxic transcriptome of SQ20B human head and neck cancer cells |
1.46 |
|
Characterisation of the myeloid differentiation process of human hematopoietic stem cells |
1.45 |
|
Transcriptional regulation of autophagy-lysosomal function in BRAF-driven melanoma progression and chemoresistance |
1.43 |
|
Transcriptome of melanoma cell lines resistant to inhibition of the MAPK pathway. |
1.4 |
|
Single-Cell Transcriptome Analysis of Lineage Diversity and Microenvironment in High-Grade Glioma |
1.4 |
|
Single-Cell reconstruction of differentiation trajectory reveals essential dynamics in human cardiac lineage commitment |
1.37 |
|
Global host gene expression changes in KSHV+ PEL cells upon KSHV reactivation |
1.33 |
|
RNA-sequencing of human leukemia cells and mouse hematopoietic progenitors |
1.33 |
|
Genetic and pharmacological restoration of TET2 function blocks stem cell self-renewal and progression of leukemia |
1.33 |
|
Identification of mRNAs with reduced ribosomal loading upon knock-down of translation factor DAP5 from hESCs. |
1.31 |
|
Gene expression profile of HGC27 gastric cancer cell p53 KO and KD |
1.31 |
|
Gene expression profiling associated with knockdown of LKB1 in human intrahepatic cholangiocarcinoma |
1.3 |
|
The long non-coding RNA MALAT1 contributes to the pathogenesis of multiple sclerosis through alternative splicing and backsplicing regulation |
1.3 |
|
Melanoma therapeutic strategies that select against resistance by exploiting MYC-driven evolutionary convergence |
1.29 |
|
hMTR4 plays a central role in creating balanced nuclear RNA pools for degradation and export |
1.29 |
|
Human Embryoid Body Transcriptomes Reveal Maturation Differences Influenced by Size and Formation in Custom Microarrays |
1.28 |
|
RNA seq comparison between scrambled and shGRP78 cells |
1.28 |
|
Domain-focused CRISPR-screen identifies HRI as a fetal hemoglobin regulator in human erythroid cells |
1.28 |
|
Carcinoma-astrocyte gap junctions promote brain metastasis by cytosolic dsDNA response transfer |
1.28 |
|
RNA-seq of cells with TET1 knockout |
1.25 |
|
Tracing the temporal-spatial transcriptomic landscapes of the human fetal digestive tract by single cell RNA-seq analysis [adult tissues] |
1.23 |
|
Mucosal Profiling of Pediatric-Onset Colitis and IBD Reveals Common Pathogenics and Therapeutic Pathways |
1.21 |
|
p53 activity results in DNA replication fork processivity |
1.19 |
|
SEUSS: A scalable screening platform to assess transcriptomic and fitness effects of transcription factor overexpression |
1.19 |
|
A Non-Canonical Nuclear Activity Triggered by Small RNAs and Argonaute Proteins in Human Cells |
1.17 |
|
MARS Seq data from human cortical organoids |
1.15 |
|
CD48-dependent protective autophagy in conventional human T cells promotes restimulation-induced cell death resistance |
1.15 |
|
Regulation of stem cell property and drug resistance of cancer cells by targeting transcriptional machinery via inhibition of neddylation |
1.14 |
|
Analysis of gene expression in SKOV3 ovarian cancer cells after knockdown of the long non-coding RNA DNM3OS |
1.14 |
|
U1 snRNP telescripting regulates size-function stratified human genome |
1.13 |
|
Epigenetic reprogramming of melanoma cells by vitamin C treatment |
1.12 |
|
Small-molecule targeting of brachyury transcription factor addiction in chordoma [rnaseq_compound] |
1.12 |
|
mRNA sequencing of highly and lowly metastatic human colorectal cancer PDXs |
1.11 |
|
Human Treg NaCl stimulation |
1.11 |
|
RNA-seq of HEK293T cells overexpressing TET1-FL or TET1-ALT |
1.1 |
|
Does osteogenic potential of clonal human bone marrow mesenchymal stem/stromal cells correlate with their vascular supportive ability? |
1.1 |
|
Effects of Inhibition of CDK8/19 Mediator Kinase by Senexin B in HEK293 cells treated with or without TNF-alpha |
1.09 |
|
MEF2C phosphorylation is required for chemotherapy resistance in acute myeloid leukemia [mutant MEF2C] |
1.08 |
|
LSD1 mediates AKT activity in PIK3CA mutant colorectal cancer |
1.08 |
|
LSD1 mediates AKT activity in PIK3CA mutant colorectal cancer [RNA-Seq] |
1.08 |
|
Gene expression in TAL1-driven T-cell ALL in response to TAL1-KD, UTX-KD, and GSKJ4 treatment |
1.07 |
|
T-cell ALL in response to TAL1-KD, UTX-KD, and GSKJ4 treatment |
1.07 |
|
Regulation of the glucocorticoid receptor via a BET-dependent enhancer drives antiandrogen resistance in prostate cancer |
1.02 |
|
Lipid catabolism inhibition sensitizes prostate cancer cells to antiandrogen blockade |
1.0 |
|
Effect of nuclear IL-33 on gene expression |
1.0 |
|
Comparative Transcriptomic Analysis of Hematopoietic System Across Species by Microwell-Seq |
0.98 |
|
SLAM-seq for K562 endogenous mRNA decay |
0.95 |
|
RNA deep sequencing to compare genome-wide differences between PRMT5/knockdown and control AML cells |
0.95 |
|
UPF1/SMG7-dependent MicroRNA-mediated Gene Regulation |
0.92 |
|
HEXIM1 is induced by DHODH inhibition to suppress melanoma [Gro-Seq] |
0.91 |
|
HEXIM1 is induced by DHODH inhibition to suppress melanoma |
0.91 |
|
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 |
0.89 |
|
Ribosome profiling upon inhibition of eIF4A |
0.86 |
|
Discovering human diabetes-risk gene function with genetics and physiological assays |
0.86 |
|
Activation of the p53 transcriptional program sensitizes cancer cells to Cdk7 inhibitors |
0.85 |
|
A Reproducibility-Based Computational Framework Identifies An Inducible, Enhanced Antiviral Dendritic Cell State In HIV-1 Elite Controllers (scRNA-Seq) |
0.8 |
|
Direct Isolation and Characterization of Human Nephron Progenitors. |
0.79 |
|
Mutational landscape of splicing genes and functional consequences across 33 cancer types |
0.78 |
|
Changes in CD34 and Erythroid Progenitor Transcriptome After RUNX3 Kock-down |
0.78 |
|
Transient stabilization, rather than inhibition of MYC amplifies extrinsic apoptosis and therapeutic responses in refractory B-cell lymphoma |
0.78 |
|
Preclinical model of obesity and ER-positive breast cancer |
0.75 |
|
KDM1A confers invasive and metastatic attributes in lung adenocarcinoma by modulating a non-canonical Integrin ß3-KRAS signaling pathway |
0.75 |
|
A Basal Stem Cell Signature Identifies Aggressive Prostate Cancer Phenotypes |
0.74 |
|
GATA2 is Dispensable for Generation of Hemogenic Endothelium But Required for Endothelial-to-Hematopoietic Transition |
0.72 |
|
Class I histone deacetylases HDAC1, 2 and 3 are histone decrotonylases |
0.72 |
|
IQGAP3 interacts with Rad17 to activate the MRN/ATM/Chk2 signaling and promote radioresistance in lung cancer |
0.7 |
|
Human muscle-derived CLEC14A-positive cells regenerate muscle independent of PAX7 |
0.7 |
|
RNA-seq data |
0.68 |
|
RNA-seq of cancer cell lines treated with T-025 |
0.64 |
|
A20 regulates canonical wnt-signaling through an interaction with RIPK4 |
0.63 |
|
Role of NuRD subunits CHD3 and CHD4 in human melanoma cells |
0.62 |
|
Role of NuRD subunits CHD3 and CHD4 in human melanoma cells (RNA-seq) |
0.62 |
|
Identification of transcripts altered upon LIN-41 knockdown in human embryonic stem cells |
0.6 |
|
Transcriptome profiling of HepG2 cells upon treatment of the menin-MLL inhibitor MI-503 or DMSO |
0.59 |
|
Identification of a LIF-responsive replication-competent human β cell |
0.59 |
|
Effect of PDZ domain binding Kinase inhibition using TOPK-32 (called PBKi) on C4-2 cell transcriptome |
0.58 |
|
Heterogeneous maintenance of human tissue resident memory T cells based on efflux capacities |
0.57 |
|
Remodeling of Ago2-mRNA interactions upon cellular stress reflects miRNA complementarity and correlates with altered translation rates (part 4) |
0.56 |
|
Remodeling of Ago2-mRNA interactions upon cellular stress reflects miRNA complementarity and correlates with altered translation rates |
0.56 |
|
RNA sequencing of isogenic BRCA2 haploinsufficient vs. wild-type T-ALL cells |
0.54 |
|
4sUDRB-seq: measuring transcription elongation and initiation genomewide |
0.52 |
|
Mutant p53 controls tumor metabolism and metastasis by regulating PGC-1α |
0.51 |
|
Functional TRIM24 degraders via conjugation of ineffectual bromodomain and VHL ligands [RNA-seq] |
0.5 |
|
Nucleotide stress induction of HEXIM1 suppresses melanoma by modulating cancer cell-specific gene transcription [RNA-Seq1] |
0.48 |
|
Multiplexed engineering and analysis of endogenous enhancer activity in single cells: Mosaic-Seq of beta-globin locus (pooled infection) |
0.48 |
|
CENPA-Bound Genes and Transcriptional Profiling of CENPA-Depleted Prostate Cancer Cells |
0.47 |
|
Transcriptional Profiling of CENPA-Depleted Prostate Cancer Cell Lines |
0.47 |
|
Genome-wide analysis of the Integrator complex (HTS) |
0.47 |
|
Genome-wide analysis of the Integrator complex |
0.47 |
|
Rnase L reprograms translation by widespread mRNA turnover escaped by antiviral mRNAs |
0.46 |
|
The mRNA export receptor NXF1 coordinates transcriptional dynamics, alternative polyadenylation and mRNA export |
0.45 |
|
Identification of Resistance Genes to BRAF Inhibitor in Melanoma by piggyBac Transposon Activation Mutagenesis Screen |
0.45 |
|
BET-Bromodomain Inhibitors Engage The Host Immune System And Regulate Expression Of The Immune Checkpoint Ligand PD-L1 [3mRNA-seq] |
0.44 |
|
BET-Bromodomain Inhibitors Engage The Host Immune System And Regulate Expression Of The Immune Checkpoint Ligand PD-L1 |
0.44 |
|
Hyperactive mTOR and MNK1 phosphorylation of eIF4E confer tamoxifen resistance and estrogen independence through selective mRNA translation reprogramming |
0.43 |
|
The hematopoietic master transcription factor PU.1 requires its interaction with the SWI/SNF remodeler to access chromatin de novo [RNA-seq] |
0.43 |
|
The hematopoietic master transcription factor PU.1 requires its interaction with the SWI/SNF remodeler to access chromatin de novo |
0.43 |
|
DAOY-Notch1/Notch2 knockout: transcriptome comparison |
0.38 |
|
Genome-wide maps of WT and over-expressing CenH3/CENP-A in Human HeLa S3 cells |
0.38 |
|
CDK12 mediated transcriptional regulation in U2OS cells |
0.38 |
|
Chromatin remodeling mediated by ARID1A is indispensable for normal hematopoiesis in mice (human RNA-Seq) |
0.33 |
|
The transcriptomic landscape of MAIT cell development in the thymus (NN41 RNAseq data set) |
0.32 |
|
RNA-Seq of SHEP TET21N cells upon Doxorubicin treatment |
0.31 |
|
Human Treg IFNg/IL-10 subpopulations |
0.27 |
|
A novel compound that blocks HIV-1 replication inhibits the splicing regulatory function of SRSF10 |
0.26 |
|
Epigenome Editing by CRISPR/Cas9 Repressors for Silencing of Distal Regulatory Elements |
0.25 |
|
Hsa-miR-139-5p/HNRNPF axis modulates gene-transcripts balance in thyroid cancer cells |
0.24 |
|
Medial Ganglionic Eminence and Cortical Organoids Model Human Brain Development and Interneuron Migration [RNA-seq2] |
0.23 |
|
Polysome profiling RNAseq of cells transfected with an oligonucleotide targeting the ES6S region of the 40S subunit |
0.22 |
|
Stapled peptide inhibitors of RAB25 target context-specific phenotypes in cancer |
0.21 |
|
Regulation of PRMT5-MDM4 axis is critical in the response to CDK4/6 inhibitors in melanoma |
0.21 |
|
Induction of extracellular adenosine salvage and metabolic quiescence regulate the transitional to follicular B cell checkpoint in humans. |
0.18 |
|
Low-dose decitabine priming endows CAR T cells with enhanced and persistent anti-tumor potential by epigenetic reprogramming |
0.18 |
|
Interactome (iCLIP) and Translatome ( Polysome profiling) of Musashi 2 (MSI2) targets in K562 |
0.16 |
|
Uridylation-mediated RNA quality control pathway in mammalian cytoplasm [RNA-Seq] |
0.15 |
|
TUT-DIS3L2 is a mammalian surveillance pathway for aberrant structured non-coding RNAs. |
0.15 |
|
Genome-wide mapping of DROSHA cleavage sites on primary microRNAs and novel substrates [RNA-seq] |
0.13 |
|
Genome-wide mapping of DROSHA cleavage sites on primary microRNAs and novel substrates |
0.13 |
|
RNAseq of ribosomal fractionation to assess the effect of CBFB on translation regulation |
0.11 |
|
siRNA-mediated knockdown |
0.1 |
|
Effect of Ro 08-2750 treatment on gene expression of human leukemia cell lines MOLM13 and K562 |
0.09 |
|
Functional genomic analysis of the haploinsufficient tumor suppressor, CUX1 |
0.09 |
|
Transcriptome profiling of A2M treated A549 Cell Line Samples |
0.08 |
|
HNRNPM-regulated splicing dependencies in prostate cancer |
0.08 |
|
HNRNPM-regulated splicing dependencies in prostate cancer [RNA-Seq] |
0.08 |
|
GLIS3 Transcriptionally Activates WNT Genes to Promote Differentiation of Human Embryonic Stem Cells to Posterior Neural Progenitors |
0.07 |
|
Concomitant BCORL1 and BRAF mutations in vemurafenib-resistant melanoma cells |
0.06 |
|
Function and hormonal regulation of GATA3 in human first trimester placentation |
0.06 |
|
CD133hi, Notchhi, DP (double positive) and DN (double negative) in GBML8 and GBML20, both patient-derived glioblastoma tumorsphere cultures |
0.06 |
|
O-GlcNAc transferase fine-tunes MYC-dependent transcription to promote cell cycle |
0.06 |
|
O-GlcNAc transferase fine-tunes MYC-dependent transcription to promote cell cycle [RNA-seq] |
0.06 |
|
Single cell transcriptomics reveals new insights on the dynamical function of transcription factors during blood stem and progenitor cell formation |
0.05 |
|
Single-cell RNAseq analysis of the empty and i8TF cell lines after 3 days of BL-CFC culture |
0.05 |
|
DNMT1-associated long non-coding RNA regulate global gene expression and DNA methylation in colon cancer |
0.04 |
|
Pseudouridylation of tRNA-derived fragments steers translation control in stem cells [Polysome-Seq] |
0.03 |
|
Genome-wide hsa-miR-503, hsa-miR-103, and hsa-miR-494 target profiles |
0.03 |
|
hsa-miR-503, hsa-miR-103, and hsa-miR-494 genome wide target profiles [RNA-Seq and RIP-Seq] |
0.03 |
|
Genome wide characterization of a STAT1-independent antiviral and immunoregulatory transcriptional program induced by IFNβ and TNFα reveals non-canonical STAT2 and IRF9 pathways |
0.03 |
|
MicroRNA-125a-5p overexpression in human macrophages |
0.03 |
|
Transcriptomic analysis of the effect of histone H4 K31R mutation in U2OS cells |
0.03 |
|
RNA seq analysis of human Fetal and adult derived Enterospheres |
0.03 |
|
Targeting MTHFD2 in Acute Myeloid Leukemia |
0.0 |