|
Proteasome machinery is instrumental in a common gain-of-function program of the p53 missense mutants in cancer. |
96.65 |
|
Proteasome machinery is instrumental in a common gain-of-function program of the p53 missense mutants in cancer. |
96.65 |
|
EP400 is required for Max and MCPyV mediated gene activation |
52.2 |
|
mRNA cap methyltransferase, RNMT-RAM, promotes RNA pol II transcription |
50.85 |
|
IMP3 regulated gene expression in breast cancer cells |
47.89 |
|
RNA-sequencing of human mammary epithelial cells (HMLEs) transduced in vitro with a shRNA against SOX4 or a scrambled shRNA in untreated and TGF-β-treated (16 hours) conditions |
44.48 |
|
Apoptotic endothelial cells release small extracellular vesicles loaded with immunostimulatory viral-like RNAs |
36.79 |
|
CD73 knockdown effect in pancreatic cancer cell lines |
33.07 |
|
HITS-CLIP analysis uncovers a link between the Kaposi's sarcoma associated herpesvirus ORF57 protein and host pre-mRNA metabolism |
32.25 |
|
Tristetraprolin disables prostate cancer maintenance by impairing proliferation and metabolic function |
31.53 |
|
Effect of 48h treatment with 100nM GSK2879552 on T-ALL cell lines HSB2 and RPMI8402 |
29.36 |
|
Uridylation by TUT4 and TUT7 marks mRNA for degradation |
29.0 |
|
Expression data from human perivascular stem cell-derived extracellular vesicles (PSC-EVs) and PSCs |
27.04 |
|
DHX9 suppresses spurious RNA processing defects originating from the Alu invasion of the human genome [uvCLAP CLIP-seq] |
26.11 |
|
Quantitative comparison between cellular mRNAs and exosomal mRNAs in human iPSC-derived motor neurons |
25.1 |
|
Selective roles of vertebrate PCF11 in premature and full-length transcript termination (chromatin-bound RNA-seq) |
24.61 |
|
Ribo_seq (aka ribosome profiling) analysis of control and Myc-induced U2OS cells |
24.47 |
|
Expression data from miR340 overexpressing human A549 cells |
24.39 |
|
Cleavage Factor Im as a key regulator of 3’ UTR length |
24.03 |
|
Major hnRNP proteins act as general TDP-43 functional modifiers both in Drosophila and human neuronal cells. |
24.01 |
|
Transcript abundance in A-T-derived iPSC: Comparing isogenic cells to unrelated individual |
23.54 |
|
Genome-wide expression change by SHARPIN knockdown in MCF-7 cells |
23.12 |
|
Simultaneous and systematic analysis of cellular and viral gene expression during Enterovirus 71-induced host shutoff |
23.0 |
|
RRAD, IL4I1, CDKN1A, and SERPINE1 genes are potentially co-regulated by NF-κB and p53 transcription factors in cells exposed to high doses of ionizing radiation [RNA-Seq] |
22.57 |
|
Uridylation by TUT4 and TUT7 marks mRNA for degradation [RNA-Seq] |
22.45 |
|
Three-dimensional Oxabicycloheptene sulfonate targets the homologous recombination and repair programs through estrogen receptor α antagonism |
22.36 |
|
Transcriptomic changes mediated by β-amyloid in human aortic endothelial cells (HAOEC) |
22.31 |
|
ChIPseq and RNAseq analysis of T47D cells with/without silencing TRPS1/CHD4 |
21.74 |
|
Survival of pancreatic cancer cells lacking KRAS function |
21.31 |
|
Ribosomal footprinting of MDA-Parental and MDA-LM2 |
21.14 |
|
Effect of 48h treatment with 100nM GSK2879552 on T-ALL cell lines LOUCY and PEER |
20.53 |
|
Ribosomal footprinting of CN34-Parental and CN34-LM1a |
20.28 |
|
Transcriptome analysis of total RNA in human osteosarcoma cell line U2OS before and after inhibition of zinc finger protein ZNF768 |
19.96 |
|
Enhanced T cell responses to IL-6 in type 1 diabetes are associated with early clinical disease and increased IL-6 receptor expression |
19.94 |
|
Genome wide expression change by RNF168 knocking down in MCF-7 cells |
19.83 |
|
Ribosomal footprinting of MDA_Ctrl and MDA_Arg overexpression cell lines |
19.5 |
|
Opposing Effects of Cyclooxygenase-2 (COX-2) on Estrogen Receptor β (ERβ) Response to 5α-reductase Inhibition in Prostate Epithelial Cells |
19.49 |
|
UBL5 is essential for pre-mRNA splicing and sister chromatid cohesion in human cells |
19.48 |
|
Telomere-Dependent and Telomere-Independent Roles of RAP1 in Regulating Human Stem Cell Homeostasis |
19.29 |
|
RNA-seq Transcriptome Analysis of AD169 and AD169-ΔUL26 infected MRC5 fibroblasts. |
19.24 |
|
Small extracellular vesicles are key regulators of non-cell autonomous intercellular communication in senescence via the interferon protein, IFITM3 |
19.09 |
|
Differential expression of genes in AD169-infected MRC5. |
18.94 |
|
The SS18-SSX oncoprotein hijacks KDM2B-PRC1.1 to drive synovial sarcoma [RNA-seq] |
18.89 |
|
The SS18-SSX oncoprotein hijacks KDM2B-PRC1.1 to drive synovial sarcoma |
18.89 |
|
Dissecting the dynamics of signaling events in the BMP,WNT and NODAL cascade during self-organized fate patterning in human gastruloids |
18.68 |
|
Extensive remodeling of DC function by rapid maturation-induced epigenetic gene silencing [RNA-Seq] |
18.45 |
|
Extensive remodeling of DC function by rapid maturation-induced epigenetic gene silencing |
18.45 |
|
Transcriptome profiling of a mouse model of alveolar soft part sarcoma |
18.1 |
|
Effect of CTCF and Rad21 knockdown on SLK cells and KSHV gene expression |
17.91 |
|
Global analysis of ZNF217 chromatin occupancy in the breast cancer cell genome reveals an association with Eralpha |
17.66 |
|
Sensing self and nonself circular RNAs |
17.61 |
|
Regulation of highly expressed hCINAP on translatome |
17.4 |
|
Heterogeneous nuclear ribonucleoprotein C1/C2 links transcriptional and splicing actions of 1,25-dihydroxyvitamin D |
17.08 |
|
The ARID1A tumor suppressor controls global transcription via pausing of RNA Polymerase II |
16.86 |
|
KSDM1b Role in Ewing Sarcoma |
16.34 |
|
Genome wide expression change in LCC2 and MCF-7 cells |
16.32 |
|
Gene expression regulated by CSA and CSB in neuroblastoma cell line |
16.26 |
|
Identification of the role of polydom in neurofibromas |
15.92 |
|
MDM2 and MDM4 are Therapeutic Vulnerabilities in Malignant Rhabdoid Tumors |
15.89 |
|
Biosynthesis of histone messenger RNA employs a specific 3' end endonuclease |
15.82 |
|
Genome-wide RNA-seq from GALNT14-depleted and GALNT14 overexpressing MDA-MB-231 LM2 and Par cells |
15.8 |
|
Differetially expressed genes after hTR overexpression in U2OS cells |
15.66 |
|
Apatinib preferentially inhibits Gefitinib-resistant lung cancer cells by inducing cell cycle arrest and inhibiting VEGFR signaling pathway |
15.64 |
|
Genomic basis for clinical response to histone deacetylase inhibition in advanced urothelial carcinoma |
15.59 |
|
RNA-seq in SUNE-1 cells after downregulation of DANCR expression |
15.48 |
|
Cyclophosphamide (CTX) Enhances Cancer Antibody Immunotherapy in the Resistant Bone Marrow Niche by Modulating Macrophage FcγR Expression |
15.13 |
|
Epigenome-wide analysis of DNA methylation in lung tissue shows concordance with blood studies and identifies tobacco smoke-inducible enhancers |
14.91 |
|
Analysis of regulatory element evolution between human and mouse reveals a lack of cis-trans compensation |
14.91 |
|
Single-cell Transcriptomic Atlas of the Human Retina Identifies Cell Types Associated with Age-Related Macular Degeneration |
14.77 |
|
SHQ1 regulation of RNA splicing is required for T-lymphoblastic leukemia cell survival |
14.74 |
|
DGCR8 acts as a novel adaptor for the exosome complex to degrade double-stranded structured RNAs |
14.71 |
|
The human blood-nerve barrier transcriptome |
14.68 |
|
Solid phase chemistry to covalently and reversibly capture thiolated RNA |
14.67 |
|
Gene-Centric Functional Dissection of Human Genetic Variation Uncovers Regulators of Hematopoiesis |
14.57 |
|
The cohesin complex prevents Myc-induced replication stress |
14.42 |
|
RNA-Seq analysis of cSCC cells after siRNA-induced gene knockdown of lncRNA PRECSIT |
14.38 |
|
Seletive inhibition of CDK9 in DLBCL cell lines |
14.27 |
|
Genome-Wide Transcriptional Effects of the Anti-Cancer Agent Camptothecin |
14.2 |
|
Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia [shRNA] |
14.2 |
|
circRNA-sequencing |
14.15 |
|
Gene expression profile of HGC27 and LMSU gastric cancer cell p53 KO and KD |
14.02 |
|
Identification of microRNA-668 and microRNA-489 targets by RISC immunoprecipitation |
13.84 |
|
Global analyses of the effect of different cellular contexts on microRNA targeting (RNA-Seq) |
13.81 |
|
Global analyses of the effect of different cellular contexts on microRNA targeting |
13.81 |
|
Safeguarding nucleolar homeostasis by CBX4 alleviates senescence and osteoarthritis |
13.75 |
|
Gene Expression Analysis of Melanoma Cells Treated with 6-Thio-dG In Vitro |
13.6 |
|
High RNA polymerase II occupancy on herpes simplex virus 1 late genes early in infection suggests progression to elongation is a critical switch to trigger late viral gene expression |
13.6 |
|
Human cell line and subcutaneous tumor |
13.54 |
|
RNA helicase A is necessary for KIF1Bβ tumor suppression in neuroblastoma |
13.48 |
|
DHX36 resolves G-rich structures in mRNA untranslated region to allow their translation [ChrRNA-seq] |
13.34 |
|
PTEN suppresses neoplastic transformation of human neural stem cells by transcriptional repression of Pax7 |
13.33 |
|
RNA-seq of HBV-infected Primary Human Hepatocytes treatment by Tazarotene |
13.29 |
|
Global expression profiles in cardiac progenitor cells generated by ISX-9 |
13.28 |
|
Global mRNA expression profile in cardiac progenitor cells generated by ISX-9 |
13.28 |
|
Functional role of SLIT2 and ROBO1 in trophoblasts |
13.22 |
|
Lipid catabolism inhibition sensitizes prostate cancer cells to antiandrogen blockade |
13.21 |
|
Utilizing single-cell variations to reveal environment-dependent tuning of network connectivity in human macrophages (RNA-Seq, CAGE and ChIP-Seq) |
13.08 |
|
Utilizing single-cell variations to reveal environment-dependent tuning of network connectivity in human macrophages |
13.08 |
|
Genomic expression analysis of K562 cells expressing shRNA targeting lncRNA-IIRX and control cells |
13.07 |
|
Genome-wide functional assessment of enhancer activities in the human genome |
13.06 |
|
RNA-seq melanoma |
12.97 |
|
Expression profile and potential functions of circulating long noncoding RNAs in acute ischemic stroke in the Southern Chinese Han population |
12.94 |
|
CD95L derived si- and shRNAs kill cancer cells through an RNAi mechanism by targeting survival genes [shL3.shR6.RNAseq.lg] |
12.81 |
|
A genome-wide long noncoding RNA CRISPRi screen identifies PRANCR as a novel regulator of epidermal homeostasis |
12.8 |
|
Quiescent glioblastoma cells shift to an epithelial-mesenchymal transition-like gene program |
12.74 |
|
H3K27Ac in MCF7 Y537S ER mutant cells and RNAseq with and without treatment with THZ1 |
12.73 |
|
BET bromodomain inhibition |
12.73 |
|
Effect of BET bromodomain inhibition with JQ1 in stressed human derived iPS cardiomyocytes |
12.73 |
|
RUNX2/CBFB modulates the response to MEK inhibitors through activation of receptor tyrosine kinases in KRAS mutant colorectal cancer |
12.64 |
|
Transcriptomic analysis of iPSC and ESC challenged with atmospheric or physiological oxygen |
12.57 |
|
Gene expression profile using RNA-seq in WC00060 or SR-0788 cells transfected with siRNA for KPC1 or control |
12.57 |
|
Proteinase-Activated Receptor 4 (PAR4) mediates cell membrane blebbing in a Gaq/11, Gai independent, RhoA and ß-arrestin-dependent manner. |
12.46 |
|
RUNX1 contributes to higher-order chromatin organization and gene regulation in breast cancer cells. |
12.41 |
|
Neurofibromin is an Estrogen Receptor alpha Transcriptional Co-repressor in Breast cancer |
12.33 |
|
Transcriptome profiling identified a 3-lncRNA regulatory network in transthyretin against glucose induced hRECs dysfunction |
12.22 |
|
The myelin protein PMP2 is regulated by SOX10 and drives melanoma cell invasion |
12.21 |
|
Transcriptional landscape of epithelial and immune cell populations revealed through FACS-seq of healthy human skin |
12.15 |
|
A novel lncRNA lncRNA-AF339830 promotes colorectal carcinogenesis and glucose metabolism by stabilizing and specifying the transcription modification pattern of c-Myc |
12.15 |
|
A novel lncRNA lncRNA-AF339830 promotes colorectal carcinogenesis and glucose metabolism by stabilizing and specifying the transcription modification pattern of c-Myc [RNA-Seq] |
12.15 |
|
An improved method for circular RNA purification that efficiently removes linear RNAs containing G-quadruplexes or structured 3’ ends |
12.15 |
|
Multiple mechanisms disrupt let-7 miRNA biogenesis and function in neuroblastoma |
12.07 |
|
Transcriptome sequencing wide functional analysis of human mesenchymal stem cells |
12.07 |
|
JAK dependent survival of ALK- ALCL |
12.05 |
|
Histone variant H2A.Bbd is associated with active transcription and mRNA processing in human cells |
12.05 |
|
Histone variant H2A.Bbd is associated with active transcription and mRNA processing in human cells [RNA-Seq] |
12.05 |
|
Effect of the knockdown of MLL1 and MLL2 on pediatric high grade glioma |
12.05 |
|
Reassessment of Exosome Composition |
12.03 |
|
Alu RNA modulates the expression of cell cycle genes in human fibroblasts |
11.99 |
|
The ribonuclease activity of SAMHD1 is required for HIV-1 restriction |
11.92 |
|
Selective silencing of euchromatic L1s revealed by genome-wide screens for L1 regulators |
11.9 |
|
A novel Menin-MLL inhibitor induces specific chromatin changes and eradicates disease in models of MLL-rearranged leukemia [RNA-Seq II] |
11.84 |
|
6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 is essential for p53-null cancer cells |
11.81 |
|
HNF1A deficiency impairs β-cell fate, granule maturation and function |
11.74 |
|
Global transcriptional changes in U87MG glioblastoma cells upon shRNA-mediated TRIM52 knockdown |
11.73 |
|
Circular RNAs are down-regulated in KRAS mutant colon cancer cells and can be transferred to exosomes |
11.71 |
|
Apolipoprotein E4 Expression Causes Gain of Toxic Function in Isogenic Human Induced Pluripotent Stem Cell-Derived Endothelial Cells |
11.69 |
|
Cistromic re-programming by truncating GATA3 mutations promotes mesenchymal transformation in vitro, but not mammary tumour formation in mice [RNA-seq] |
11.68 |
|
Cistromic re-programming by truncating GATA3 mutations promotes mesenchymal transformation in vitro, but not mammary tumour formation in mice |
11.68 |
|
Co-expression of CD163 and CD141 Identifies Human Circulating IL-10-Producing Dendritic Cells (DC-10) |
11.65 |
|
Co-expression of CD163 and CD141 Identifies Human Circulating IL-10-Producing Dendritic Cells (DC-10) [RNA-seq] |
11.65 |
|
Nuclear HNRNPA2B1 HITS-CLIP and RNA-seq |
11.63 |
|
LINC00520 is Induced by Src, STAT3, and PI3K and Plays a Functional Role in Breast Cancer |
11.62 |
|
GRHL2 is a key lineage determining factor which collaborates with FOXA1 to establish a targetable collateral pathway in the setting of endocrine therapy-resistant breast cancer (RNA-Seq data set 2) |
11.49 |
|
GIST cell cycle dysregulation is required for progression to high-risk disease but not for resistance to kinase inhibitors |
11.49 |
|
RNA-seq analysis of A498 cell line treated with siSETD2 or si-NC |
11.44 |
|
MYT1 attenuates neuroblastoma cell differentiation by inhibiting retinoic acid signaling pathway |
11.41 |
|
Illumina Total RNA-seq in HeLa |
11.33 |
|
m6A-seq data analysis of control and PCIF1 knockdown transcriptome |
11.27 |
|
Chemical Enhancement of Direct Cardiac Reprogramming In Vitro and In Vivo |
11.27 |
|
HOXC6 affects the malignant phenotype of esophageal squamous cell carcinoma cells |
11.27 |
|
Expression profiles of restoration of BAP1 in a BAP1 deficient cell line |
11.1 |
|
Transcriptome analysis of BAP1 knockout and restoration |
11.1 |
|
mRNA destabilization is the dominant effect of mammalian microRNAs by the time substantial repression ensues |
11.06 |
|
mRNA destabilization is the dominant effect of mammalian microRNAs by the time substantial repression ensues (sequencing) |
11.06 |
|
Zika virus antagonizes interferon response in patients and disrupts RIG-I-MAVS interaction through its CARD-TM domains |
11.01 |
|
Molecular mechanism underlying increased ischemic damage in the ALDH2*2 genetic polymorphism using a human iPSC model system |
10.96 |
|
Antibody-Mediated Inhibition of MICA/B Shedding Promotes NK Cell-Driven Tumor Immunity |
10.89 |
|
Aortic Valve Tissue: Stenosis vs. Sclerosis |
10.88 |
|
Nutritional control of protein translation |
10.87 |
|
RNAseq of Extracellular vesicle RNAs and cellular RNAs from HPASMCs with or without TGF-b1 or BMP4 treatment |
10.82 |
|
Genome-wide DNA accessibility maps and differential gene expression using ChIP-seq, ATAC-seq and RNA-seq for the human secondary fibroblast cell line hiF-T and whole worms with and without knockdown of FACT complex |
10.81 |
|
Comprehensive analysis of microRNA expression in regionalized human neural progenitor cells reveals microRNA-10 as a caudalizing factor |
10.77 |
|
RNA-Sequencing experiment for effects of PKF115-584 treatment on four T-ALL cell lines (RPMI8402, HPB-ALL, Jurkat, CCRF-CEM). |
10.76 |
|
Epigenome Editing by a CRISPR/Cas9-Based Acetyltransferase Activates Genes from Promoters and Enhancers |
10.76 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and AXL-/- astrocytes Transcriptomes |
10.75 |
|
Chromatin-informed inference of transcriptional programs in gynecologic cancers |
10.75 |
|
Chromatin-informed inference of transcriptional programs in gynecologic cancers [RNA-Seq] |
10.75 |
|
Genome wide expression change by RNF168 knocking down in NEC cells |
10.7 |
|
Mitochondrial dsRNA triggers antiviral signalling in humans |
10.69 |
|
The LINC01138 Drives Malignancies via Activating Arginine Methyltransferase 5 in Hepatocellular Carcinoma |
10.69 |
|
RNAseq of HEK293 cells after Chtop knockdown |
10.68 |
|
Co-transcriptional loading of RNA export factors shapes the human transcriptome |
10.68 |
|
Differential gene expression tools exhibit substandard performance for long non-coding RNA-sequencing data |
10.62 |
|
Identification of the RB loss-induced transcriptome and E2F1 cistrome in prostate cancer |
10.62 |
|
Identification of the RB loss-induced transcriptome in prostate cancer [RNA] |
10.62 |
|
Human lymph nodes maintain a unique subset of resident memory T cells with high functional potential important for protective immunity and immunotherapies |
10.59 |
|
Role of BET proteins in YAP/TAZ-dependent transcription [RNA-seq 1] |
10.59 |
|
EHMT1 and EHMT2 inhibition induce fetal hemoglobin expression |
10.58 |
|
EHMT1 and EHMT2 inhibition induce fetal hemoglobin expression [RNA-seq] |
10.58 |
|
DHX36 resolves G-rich structures in mRNA untranslated region to allow their translation [cPDS-RNA-seq] |
10.57 |
|
RNA-seq analysis of SLIRP knockdown with 1nM DHT in LNCaP cells |
10.54 |
|
Effect of PRDM11 depletion in U2932 cells |
10.54 |
|
Generation of induced neural stem cells from urine derived cells by synthetic mRNA |
10.53 |
|
DDX3X regulation of global translation is impaired by medulloblastoma-associated mutations [RNA-Seq] |
10.49 |
|
DDX3X regulation of global translation is impaired by medulloblastoma-associated mutations |
10.49 |
|
RING-finger protein 6 amplification activates JAK/STAT3 pathway by modifying SHP-1 ubiquitylation and associates with poor outcome in colorectal cancer |
10.46 |
|
Pre-mRNA Splicing is Facilitated by an Optimal RNA Polymerase II Elongation Rate |
10.45 |
|
Characterization of transcriptomics landscape in HUVEC cells exposed to oxidative stress |
10.44 |
|
Identification of Atrial Fibrillation associated genes and functional non-coding variants |
10.43 |
|
Functional Screening in Human Cardiac Organoids Reveals a Metabolic Mechanism for Cardiomyocyte Maturation |
10.38 |
|
Systematic Functional Dissection of Common Genetic Variation Affecting Red Blood Cell Traits [mRNA-Seq] |
10.36 |
|
Systematic Functional Dissection of Common Genetic Variation Affecting Red Blood Cell Traits |
10.36 |
|
Comparative Analysis of the Transcriptome of Latent Autoimmune Diabetes (LADA) Patients from Eastern China |
10.35 |
|
ADAR1 controls apoptosis of stressed cells by inhibiting Staufen-mediated mRNA decay |
10.31 |
|
KMT2D regulates p63 target enhancers to coordinate epithelial homeostasis |
10.29 |
|
KMT2D regulates p63 target enhancers to coordinate epithelial homeostasis [RNA-Seq] |
10.29 |
|
Rate of elongation by RNA polymerase II is influenced by specific gene features and histone modifications |
10.28 |
|
Temporal dynamic reorganization of 3D chromatin in hormone-induced breast cancer and endocrine resistance |
10.24 |
|
Differentially expressed genes post knock down of lincDUSP26 |
10.14 |
|
Estrogen response in breast cancer cell line MCF-7 is dependent on NR2F2 [RNA-seq] |
10.12 |
|
NR2F2 study |
10.12 |
|
SIRT6 regulates redox homeostasis in human mesenchymal stem cells by the transactivation of NRF2 |
10.06 |
|
The translation termination factor GSPT1 is a phenotypically relevant off-target of heterobifunctional phthalimide degraders |
10.05 |
|
Differential expression of long non‑coding RNA and mRNA in children with Henoch‑Schönlein purpura nephritis |
10.03 |
|
Trisomy of a ‘Down syndrome critical region’ globally amplifies transcription via HMGN1 overexpression |
10.01 |
|
Bioinformatics analysis of transcriptome related to blood stasis syndrome in diabetes mellitus patients |
9.99 |
|
Multivalent binding of PWWP2A to H2A.Z-marked transcriptional active chromatin regulates mitosis and organ development |
9.98 |
|
Multivalent binding of PWWP2A to H2A.Z-marked transcriptional active chromatin regulates mitosis and organ development [RNA-seq] |
9.98 |
|
Diverse AR-V7 cistromes in castration-resistant prostate cancer are governed by HoxB13 |
9.92 |
|
RNA-Seq of polysome profiling fractions and whole cell lysates of UVB-irradiated N-TERT keratinocytes |
9.89 |
|
Species-specific maturation profiles of human, chimpanzee and bonobo neural cells |
9.85 |
|
Gene expression profiles in NORAD knockout and PUMILIO overexpressing cells |
9.78 |
|
FMRP facilitates the nuclear export of N6-methyladenosine-containing mRNAs |
9.74 |
|
Studying iPSCs from a hibernating mammal reveals molecular mechanisms of cold resistance in neural tissues |
9.61 |
|
Effect of disulfiram treatment on pediatric high grade glioma |
9.58 |
|
Uridilation by TUT4/7 restricts retrotransposition of human Line-1s |
9.52 |
|
TT-Seq captures the human transient transcriptome |
9.49 |
|
Precise Gene Editing Preserves Hematopoietic Stem Cell Function Following Transient p53-Mediate DNA Damage Response |
9.49 |
|
mTORC1 balances cellular amino acid supply with demand for protein synthesis through post-transcriptional control of ATF4 |
9.48 |
|
RNA-seq in neutrophils from Juvenile Idiopathic Arthritis |
9.47 |
|
Oncogenic Notch promotes long-range regulatory interactions within hyperconnected 3D cliques [MB157_RNA-seq] |
9.46 |
|
PTBP1 excludes UPF1 to protect long 3'UTRs from nonsense-mediated mRNA decay |
9.46 |
|
Integrated epigenomic and transcriptomic profiling of terminal human erythropoiesis [TMCC2] |
9.39 |
|
Exploring the RNA landscape of endothelial exosomes |
9.34 |
|
Recruiting Endogenous ADARs with Antisense Oligonucleotides to Reprogram the Transcriptome |
9.33 |
|
Measuring the effect of MYC on transcription during the DNA double-strand break response by RNA-seq of newly synthesized transcripts |
9.23 |
|
Noncoding regions are the main source of targetable tumor-specific antigens |
9.21 |
|
Vitamin C–dependent lysine demethylase 6 (KDM6)-mediated demethylation promotes a chromatin state that supports the endothelial-to-hematopoietic transition |
9.03 |
|
Vitamin C dependent KDM6 demethylation specifies a functional chromatin state for endothelial-to-hematopoietic transition [RNA-Seq] |
9.03 |
|
The transcriptome effect of overexpressing EZH2 in MCF7 |
8.9 |
|
Quantitative Analysis of p53 and/or TGFBR2 Knockdown Endothelial Transcriptomes after Irradiation |
8.86 |
|
RNAseq Analysis in glioblastoma cells treated with Mepazine |
8.84 |
|
Genome-wide analysis of ferroptosis related genes in liver cancer cells. |
8.83 |
|
Active translatome profiling with RiboLace in MCF7 cells |
8.79 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of human patient derived primary Glioblastoma (GBM) cancer cell Transcriptomes |
8.78 |
|
mitoCPR - a surveillance pathway that protects mitochondria in response to mitochondrial import stress [human] |
8.75 |
|
mitoCPR - a surveillance pathway that protects mitochondria in response to mitochondrial import stress |
8.75 |
|
Effect of PBK knockdown on C4-2 cell transcriptome |
8.71 |
|
Multiplexed engineering and analysis of endogenous enhancer activity in single cells: Mosaic-Seq of beta-globin locus (separate infection) |
8.68 |
|
Transcriptional Signatures of Hypoxic and Inflammatory Renal Epithelial Injury |
8.67 |
|
Endogenous retroviruses are a source of oncogenic enhancers in acute myeloid leukemia [RNA-Seq] |
8.63 |
|
Endogenous retroviruses are a source of oncogenic enhancers in acute myeloid leukemia |
8.63 |
|
A next generation sequencing based approach to identify extracellular vesicle mediated mRNA transfers between cells |
8.63 |
|
SERPINA3- a novel keratinocyte differentiation promotor mediates epidermal barrier repair response in psoriatic lesion |
8.61 |
|
Pitfalls in Single Clone CRISPR-Cas9 Mutagenesis to Fine-map Regulatory Intervals |
8.61 |
|
Reversible LSD1 Inhibition with HCI-2509 induces the p53 gene expression signature in high-risk neuroblastoma cells |
8.6 |
|
PRC2 specifies ectoderm lineages and maintains pluripotency in primed but not naïve ESCs |
8.6 |
|
Genomic Reorganization of Lamin-Associated Domains in Cardiac Myocytes is Associated with Differential Gene Expression and DNA Methylation in Human Dilated Cardiomyopathy |
8.59 |
|
Genomic Reorganization of Lamin-Associated Domains in Cardiac Myocytes is Associated with Differential Gene Expression and DNA Methylation in Human Dilated Cardiomyopathy [RNA-Seq] |
8.59 |
|
Transcriptome Analysis of CircMRPS35 mediated mRNA expression profiles |
8.39 |
|
RNA sequencing of heart samples of myotonic dystrophic (DM1) patients |
8.24 |
|
Genome-wide identification of cancer-specific alternative splicing in circRNA |
8.15 |
|
High resolution ChIP sequencing reveals novel bindings targets and prognostic role for SOX11 in Mantle cell lymphoma |
8.12 |
|
High resolution ChIP sequencing reveals novel bindings targets and prognostic role for SOX11 in Mantle cell lymphoma (RNA-Seq) |
8.12 |
|
Global Mapping of Human RNA-RNA Interactions |
8.11 |
|
The human cellular nucleic acid binding protien binds G-rich elements close to translation initiation sires and promotes translation. |
8.1 |
|
The human cellular nucleic acid binding protien binds G-rich elements close to translation initiation sires and promotes translation. [RNA-Seq] |
8.1 |
|
Low carbohydrate diet study for non-alcoholic fatty liver disease patients |
8.07 |
|
NOTCH signaling is activated in and contributes to resistance in enzalutamide-resistant prostate cancer cells |
8.07 |
|
Transcriptome wide analysis of translation efficiency in MCF7 cells using polysome profiling with and without eIF4A inhibition by hippuristanol treatment |
7.99 |
|
Effect of ILF3 on translation during homeostasis and the antiviral response |
7.96 |
|
Tamoxifen Resistance in Breast Cancer is Regulated by the EZH2-ERa-GREB1 Transcriptional Axis |
7.94 |
|
RNA-sequencing of highly pure synovial tissue macrophages reveals two distinct osteoarthritis subgroups that indicate different disease mechanisms. |
7.84 |
|
Transcriptomic Profiling of Posterior Polymorphous Corneal Dystrophy |
7.84 |
|
Transciptomic profiling of human fetal lung samples |
7.76 |
|
Unraveling cis-regulatory elements by mapping structural changes in mRNAs |
7.75 |
|
Cellular gene expression during Hepatitis C Virus replication revealed by Ribosome profiling |
7.73 |
|
RNAseq of cell lines with knocked in ESR1 mutations |
7.68 |
|
Transcriptome wide identification of Dicer binding in human and C. elegans reveals a variety of substrates |
7.66 |
|
Whole Transcriptome RNASeq Data for Cell-Sorted Antibody Secreting Cells (ASC) |
7.61 |
|
RNA-seq of RKO cells with cTAZ KO or putback |
7.55 |
|
Non-transmissible measles virus vector with segmented RNA genome establishes different types of iPSCs from hematopoietic cells |
7.55 |
|
Enhancement of Arterial Specification in Human Pluripotent Stem Cell Cultures Promotes Definitive Hematoendothelial Program with Broad Myelolymphoid Potential |
7.5 |
|
Glioma-derived miRNA-containing extracellular vesicles induce angiogenesis by reprogramming brain endothelial cells (longRNA-seq) |
7.43 |
|
Glioma-derived miRNA-containing extracellular vesicles induce angiogenesis by reprogramming brain endothelial cells |
7.43 |
|
Synaptic dysfunction in human neurons with Autism associated deletions in PTCHD1-AS |
7.32 |
|
Luminal subtype-specific circRNAs in breast cancer cells by a novel tool for external data analysis. |
7.25 |
|
Lyophilized human cells stored at room temperature preserve multiple RNA species at excellent quality for RNA sequencing |
7.22 |
|
A non-canonical role of YAP/TEAD is required for activation of estrogen-regulated enhancers in breast cancer |
7.22 |
|
A non-canonical role of YAP/TEAD is required for activation of estrogen-regulated enhancers in breast cancer [RNA-seq] |
7.22 |
|
Genome-scale identification of transcription factors that mediate an inflammatory network during breast cellular transformation |
7.21 |
|
RNA-seq during MCF10A-ER-Src cell transformation and upon factor knockdowns |
7.21 |
|
Transcriptome data from human endocrine cells recovered from mouse grafts with pre-engraftment controls |
7.19 |
|
Genome-wide expression analysis of human hTert immortalized fibroblasts after donwregulation of MCM7 |
7.18 |
|
PT2385 HIF2A inhibitor treatment of patient derived orthotopic xenograft neuroblastoma cells in the presence or absence of hypoxia |
7.16 |
|
Prolyl Hydroxylase Substrate Adenylosuccinate Lyase Is An Oncogenic Driver In Triple Negative Breast Cancer |
7.15 |
|
Modulation of gene transcription and epigenetics of colon carcinoma cells by bacterial membrane vesicles |
7.11 |
|
Total RNAseq of human putamen and caudate nucleus tissues in healthy control and Bipolar Disorder individuals |
7.08 |
|
Effect of Polybrominated diphenyl ethers (PBDEs) on gene expression of MCF7 cells |
6.9 |
|
COMBINING BET AND MEK INHIBITORS SYNERGISTICALLY TARGETS NRAS MUTANT MELANOMA |
6.88 |
|
Transcriptome landscape of HeLa response upon triamcinolone acetonide |
6.79 |
|
LHX9 rescues KRAS suppression through transcriptional regulation of YAP1 |
6.76 |
|
LHX9 rescues KRAS suppression through transcriptional regulation of YAP1 [RNA-Seq] |
6.76 |
|
H3K27ac ChIP-Seq and mRNA-Seq analysis of five human B-lymphoblastoid cell lines (LCLs) prepared from the same healthy male individual (CEPH/UTAH). |
6.72 |
|
RNAseq in Alzheimer's Disease patients |
6.64 |
|
Distinct roles of cohesin-SA1 and cohesin-SA2 in 3D chromosome organization |
6.62 |
|
High-throughput RNA sequencing on circular RNA profiles of human pancreatic cancer cell lines and gemcitabine resistant pancreatic cancer cell lines. |
6.57 |
|
Transcriptome Profiling of Influenza A Virus-infected Lung Epithelial (A549) Cells with Lariciresinol-4-β-D-glucopyranoside Treatment |
6.54 |
|
CBFβ-MYH11 fusion blocks hematopoietic differentiation via repression of a GATA2 gene program |
6.49 |
|
Cystathionine-β-Synthase Promotes Colon Carcinogenesis |
6.47 |
|
RNA-Sequencing approach for the identification of novel long non-coding RNA biomarkers in colorectal cancer |
6.46 |
|
The Short Isoform of BRD4 Promotes HIV-1 Latency by Engaging Repressive SWI/SNF Chromatin Remodeling Complexes |
6.42 |
|
Toxicogenomics of the flame retardant tris (2-butoxyethyl) phosphate in HepG2 cells using RNA-seq. |
6.32 |
|
Gene expression profiles in response to proanthocyanidins in pancreatic cancer cells |
6.31 |
|
Transcriptome of human keratinocytes with or without HPV16 oncogene expression |
6.27 |
|
ETS1 acts as a tumor suppressor in breast cancer by inhibiting growth-related factors |
6.24 |
|
TrapSeq: An RNA Sequencing-based pipeline for the identification of genetrap insertions in mammalian cells |
6.22 |
|
Defective structural RNA processing in relapsing-remitting multiple sclerosis |
6.17 |
|
Genome-wide CRISPR-Cas9 screen identifies SLC1A3 as a key contributor to L-asparaginase Resistance in Solid tumors |
6.11 |
|
lncRNA-PCAT1 knockdown effect on the gene expression of androgen independent LNCaP (LNCaP-AI) cell line |
6.11 |
|
Molecular Criteria for Defining the Naive Human Pluripotent State |
6.07 |
|
Interaction between mitoNEET and NAF-1 in cancer cells |
6.02 |
|
Translocation of dense granule effectors across the parasitophorous vacuole membrane in Toxoplasma-infected cells requires the activity of ROP17, a rhoptry protein kinase |
5.95 |
|
RNA-seq of naive and primed ES cells |
5.93 |
|
Functional Cardiac Fibroblasts Derived from Human Pluripotent Stem Cells via Second Heart Field Progenitors |
5.89 |
|
SREBP1 drives Keratin 80-dependent cytoskeletal changes and invasive behavior in endocrine resistant ERα breast cancer |
5.86 |
|
High capacity of the endoplasmic reticulum to prevent secretion and aggregation of amyloidgenic proteins |
5.78 |
|
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 |
5.6 |
|
N6-methyladenosine (m6A) profiling of EndoC-bH1 cell line and RNA seq of Mettl14 knockout mice beta cell |
5.6 |
|
Regulation of stem cell property and drug resistance of cancer cells by targeting transcriptional machinery via inhibition of neddylation |
5.53 |
|
The dynamic landscape of coding and non-coding RNAs in the innate immune response to microbial pathogens |
5.44 |
|
Next Generation Sequencing and m6A sequencing Facilitates Quantitative Analysis of Wild Type and genetic FTO knockdown ccRCC cells Transcriptomes |
5.42 |
|
SLIGRL-induced gene expression changes in NHEK cells |
5.31 |
|
Profiling of lung tumor-infiltrating CD8 T cells according to their expression status of CD39 |
5.2 |
|
Identification of altered developmental pathways in human juvenile HD iPSC with 71Q and 109Q using transcriptome profiling |
5.11 |
|
High-throughput RNAi cell viability screen to identify selective targets for EWS-FLI1 positive Ewing sarcoma |
5.03 |
|
Pain-driven transcriptome changes in synovium of knee osteoarthritis patients |
4.96 |
|
LncPRESS1 is a p53-regulated lncRNA that safeguards pluripotency by disrupting SIRT6 mediated de-acetylation of histone H3K56 |
4.91 |
|
MEF2C phosphorylation is required for chemotherapy resistance in acute myeloid leukemia [mutant MEF2C] |
4.86 |
|
MicroRNA targetome analysis during HCMV infection |
4.86 |
|
C9/ALS Human Embryonic Stem Cells and C9/ALS Induced Pluripotent Stem Cells |
4.84 |
|
Identification of transcripts altered upon LIN-41 knockdown in human embryonic stem cells |
4.82 |
|
Ribosomal protein RPL26 is the principal target of UFMylation |
4.8 |
|
K562 polyA RNA-Seq |
4.72 |
|
Identification and validation of differentially expressed transcripts by RNA-Sequencing of formalin-fixed, paraffin-embedded (FFPE) lung tissue from patients with Idiopathic Pulmonary Fibrosis |
4.66 |
|
Expression analysis of PC3 cells treated with scramble AON or AON directed against MBNL1 |
4.62 |
|
Transcriptomic profile of human embryonic renal corpuscles |
4.59 |
|
The Genetic Landscape of Diamond-Blackfan Anemia |
4.46 |
|
Discovery of Drug Candidates that Inhibit and Eliminate Zika Virus Infection in Fetal and Adult Brain |
4.39 |
|
Apoptosis enhancing drugs overcome innate platinum resistance in CA125 negative tumor initiating populations of high grade serous ovarian cancer |
4.38 |
|
Molecular Signature of CAID Syndrome: Noncanonical Roles of SGO1 in Regulation of TGF-β Signaling and Epigenomics. [RNA-seq] |
4.36 |
|
Molecular Signature of CAID Syndrome: Noncanonical Roles of SGO1 in Regulation of TGF-β Signaling and Epigenomics. |
4.36 |
|
Tracing Enhancer Networks using Epigenetic Traits (TENET) |
4.35 |
|
mRNA expression in human DAOY cells |
4.34 |
|
Transcriptome of iPSC-derived Cerebral Organoids with Heterozygous Knockout in CHD8 |
4.25 |
|
A transcriptome dataset revealing the molecular features of breast cancer stem cells |
4.23 |
|
Direct identification of endogenous SMG6 targets and a preferred motif spanning SMG6 cleavage sites by parallel analysis of RNA ends in human cells |
4.22 |
|
O-glcnAc reprograms cellular energetics |
4.22 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of SW480 cells and HPSE-knockdown SW480 cells Transcriptomes |
4.09 |
|
PML2-mediated thread-like nuclear bodies mark late senescence in Hutchinson–Gilford progeria syndrome |
4.07 |
|
PML2‐mediated thread‐like nuclear bodies mark late senescence in Hutchinson–Gilford progeria syndrome [RNA-seq] |
4.07 |
|
Newly defined ABCB5+ dermal mesenchymal stem cells promote healing of chronic iron overload wounds via secretion of interleukin-1 receptor antagonist |
4.05 |
|
BCL6 confers KRAS-mutant NSCLCs resistance to BET inhibitors |
4.04 |
|
mRNA sequencing of highly and lowly metastatic human colorectal cancer PDXs |
4.0 |
|
RNA Sequencing of Human iPS derived Cardiomyocytes |
3.98 |
|
RNA-seq analysis of PRMT5-regulated genes in irradiated/non-irradiated LNCaP cells |
3.89 |
|
Transcriptome analysis of SH-SY5Y cells after knockdown of circSLC45A4 |
3.88 |
|
The contribution of Alu exons to the human proteome |
3.86 |
|
Determination of tRNA aminoacylation levels by high throughput sequencing |
3.86 |
|
Identifying transcripts that are transcriptinoally regulated by CBFB and RUNX1 using RNAseq |
3.83 |
|
Gene expression profiling by RNA-seq of SW480 TGM2 knockdown cells |
3.77 |
|
MicroRNA-125a-5p overexpression in human macrophages |
3.74 |
|
IGF2BP1 promotes SRF-dependent transcription in cancer in a m6A- and miRNA-dependent manner |
3.74 |
|
IGF2BP1 promotes SRF-dependent transcription in cancer in a m6A- and miRNA-dependent manner [Huh-7] |
3.74 |
|
RNA seq_PDX2_SHP099 |
3.68 |
|
EPCR Expression Defines the Most Primitive Subset of Human HSPC and Is Required for Their In Vivo Activity |
3.68 |
|
Induction of Sertoli-like cells from human fibroblasts by NR5A1 and GATA4 |
3.64 |
|
Arrayed molecular barcoding identifies TNFSF13 as a positive regulator of acute myeloid leukemia-initiating cells |
3.58 |
|
Measure transcript integrity using RNA-seq data |
3.5 |
|
mRNA-sequencing of 293T-no dice transfected with miR-16, miR-214, or KSHV-miR-K6-5p |
3.5 |
|
lncRNA expression analysis in patients with eosinophilic and neutrophilic asthma |
3.43 |
|
Nucleotide stress induction of HEXIM1 suppresses melanoma by modulating cancer cell-specific gene transcription [RNA-Seq1] |
3.41 |
|
Gene expression profiles of rescue with wild type or SUMO double mutant TRIM24 |
3.3 |
|
Mutant p63 disrupts the key specification switch from the multipotent cell state to stratified epithelia during epithelial differentiation/in ectodermal dysplasia disorders |
3.22 |
|
Effects of plasticizers (bisphenol A, bisphenol AF) and an herbicide in MCF7 human breast cancer cells |
3.2 |
|
Transcriptional regulation of autophagy-lysosomal function in BRAF-driven melanoma progression and chemoresistance |
3.12 |
|
RNA-sequencing of the brain transcriptome implicates dysregulation of neuroplasticity, circadian rhythms, and GTPase binding in bipolar disorder |
3.06 |
|
RNA-seq after siRNA targeting DDX24 applied to iHUVECs cell lines |
3.04 |
|
Epithelial-mesenchymal transition markers screenedina cell-based model and validated in lung adenocarcinoma |
3.04 |
|
Oxaliplatin resistance is enhanced by saracatinib via upregulation of ABCG1 and Wnt/β-catenin signaling in hepatocellular carcinoma |
2.96 |
|
Transcriptomic analysis of differential expressed genes of human tonsillar epithelial cells UT-SCC-60B in response to EV71 infection |
2.88 |
|
Sodium butyrate ameliorates aSyn-induced transcription deregulation and DNA damage |
2.87 |
|
MEF2C phosphorylation is required for chemotherapy resistance in acute myeloid leukemia |
2.84 |
|
RNA sequencing of isogenic BRCA2 haploinsufficient vs. wild-type T-ALL cells |
2.65 |
|
RNA-Seq of PRMT1 overexpression ECA109 cells |
2.65 |
|
Aging-associated patterns in the expression of human endogenous retroviruses |
2.64 |
|
Mutually Exclusive CBC-Containing Complexes Contribute to RNA Fate. |
2.59 |
|
Regulatory network controlling tumor-promoting inflammation in human cancers |
2.57 |
|
Regulatory network controlling tumor-promoting inflammation in human cancers [RNA-seq] |
2.57 |
|
Class I histone deacetylases HDAC1, 2 and 3 are histone decrotonylases |
2.52 |
|
Transcriptome analysis in a radiosensitive and a radioresistant cell line after ionizing radiation |
2.5 |
|
Mitochondrial unfolded protein response controls matrix pre-RNA processing and translation |
2.48 |
|
Global hypomethylation mediated changes regulate constitutive PD-L1 expression in melanoma |
2.47 |
|
Global hypomethylation mediated changes regulate constitutive PD-L1 expression in melanoma [RNA-Seq] |
2.47 |
|
Circular RNA expression signature of low-glucose-treated MIA PaCa-2 cells |
2.41 |
|
Copper Regulation of HIF-1 Transcription Activity [RNA-seq] |
2.38 |
|
Copper Regulation of HIF-1 Transcription Activity |
2.38 |
|
The mRNA expression analysis of psoriasis skin lesion mesenchymal stem cell |
2.38 |
|
RNA-sequencing study of peripheral blood monocytes for chronic periodontitis |
2.36 |
|
Identification of microRNA-dependent gene regulatory networks driving human pancreatic endocrine cell differentiation [H1 RNA-seq] |
2.23 |
|
Gene expression profile of differentially recognized Mtb-epitopes as a function of disease history |
2.21 |
|
An siRNA screen identifies CHD4 as a target for epigenetic therapy |
2.19 |
|
CT Irradiation Induced Changes of Gene Expression within Peripheral Blood Cells |
2.17 |
|
The impact of stanniocalcin 1 on the transcriptome of human cord blood stem/progenitors |
2.06 |
|
In search for materials able to be colonized by a normal endothelium: сharacterization and NGS gene expression profiling of human primary endotheliocytes cultivated on electrospun 3D matrices |
2.06 |
|
Molecular characterization of BRSK2 and BRSK1 kinases as negative regulators of the NRF2 transcription factor |
1.96 |
|
H3K36 mutations promote sarcomagenesis through genome-wide remodeling of H3K36 and H3K27 methylation |
1.96 |
|
H3K36 mutations promote sarcomagenesis through genome-wide remodeling of H3K36 and H3K27 methylation [RNA_Chondroblastoma_H3K36M_H3WT] |
1.96 |
|
HMGA2 Promotes Long-Term Engraftment and Myelo-Erythroid Differentiation of Human Hematopoietic Stem and Progenitor Cells |
1.95 |
|
Genome-wide RNA deep sequencing of CAL-101 or AKTi primed human T cells in comparison to traditionally expanded T cells |
1.94 |
|
Gene expression profiles of isogenic single-cell derived clones of BRAF-mutated SK-MEL-5 melanoma cell lines |
1.88 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and SMAD4 Y95 Mutation Transcriptomes |
1.8 |
|
Role of SUMOylation in differential ERα transcriptional repression by SERMs and pure antiestrogens in breast cancer cells |
1.79 |
|
Campylobacter concisus pathotypes induce distinct global responses in intestinal epithelial cells [Toxin] |
1.79 |
|
Medial Ganglionic Eminence and Cortical Organoids Model Human Brain Development and Interneuron Migration [RNA-seq2] |
1.77 |
|
Histone Demethylases KDM3A and KDM4C regulate mesenchymal stromal cell senescence and bone aging through condensin-mediated heterochromatin organization |
1.75 |
|
RNA-sequencing of Wnt-dependent and Wnt-independent of Glioblastoma stem cell cultures |
1.74 |
|
naive T cell heterogeneity after neonatal thymectomy |
1.74 |
|
Structural basis for human respiratory syncytial virus NS1-mediated modulation of host responses |
1.72 |
|
Transcription elongation regulates genome 3D structure |
1.64 |
|
Gene expression profiling of neural crest progenitor cultures derived from human embryonic stem cells carrying nonsense mutations in the Polycomb gene ASXL1 |
1.61 |
|
Oncogenic roles of ARID5B in T-ALL |
1.6 |
|
RNA-seq analysis in knockdown Jurkat samples for each factor of TAL1 complex |
1.6 |
|
Global Transcriptome Analysis and Enhancer Landscape of Human Primary T Follicular Helper and T Effector Lymphocytes |
1.59 |
|
Global Transcriptome Analysis and Enhancer Landscape of Human Primary T Follicular Helper and T Effector Lymphocytes (RNA-Seq) |
1.59 |
|
A novel non-canonical signaling pathway mediates TGF-β1-induced glucocorticoid insensitivity in epithelial cells |
1.58 |
|
RNA sequencing from FOXM1 knockout HEK293T cells reconstituted with FOXM1 isoforms a, b and c. |
1.58 |
|
mRNA recovered upon RNF219 IP. [RNA-IP] |
1.49 |
|
The p30 isoform of CEBPA uncovers a silent enhancer to drive the expression of the tumor promotive factor CD73 in CEBPA mutant AML |
1.48 |
|
Role of NuRD subunits CHD3 and CHD4 in human melanoma cells (RNA-seq) |
1.47 |
|
Role of NuRD subunits CHD3 and CHD4 in human melanoma cells |
1.47 |
|
Exploring ILF2 regulatory genes by next-generation sequencing |
1.43 |
|
HMGA1 and FOXM1 synergistically regulate a common gene network modulating angiogenesis in breast cancer |
1.37 |
|
WNT signaling memory is required for ACTIVIN to function as a morphogen |
1.35 |
|
Splicing and epigenetic factors jointly regulate epidermal differentiation |
1.34 |
|
Genome-wide expression analysis of human hTert immortalized fibroblasts after downregulation of MCM2 & MCM7 |
1.32 |
|
Identification of global XBP1s target gene expression in human prostate cancer cells |
1.31 |
|
RNA-Seq data of NCI-H82 cells expressing a Dox-On pRB (pTripZ RB1) grown in the presence or absence of DOX and then treated with vehicle or AZD2811. |
1.3 |
|
TFPa/HADHA is required for fatty acid beta-oxidation and cardiolipin re-modeling in human cardiomyocytes |
1.28 |
|
ZNF599 and DNMT3A coordinately control nuclear envelope organization by repression of SUN4 expression |
1.26 |
|
KRASG12C inhibition produces a driver-limited state revealing collateral dependencies |
1.21 |
|
Epigenetic changes induced by Bacteroides fragilis toxin (BFT) |
1.18 |
|
Epigenetic changes induced by Bacteroides fragilis toxin (BFT) [RNA-seq] |
1.18 |
|
Transcriptomic Alterations in Lung Adenocarcinoma Unveil New Mechanisms Targeted by the TBX2 Subfamily of Tumor Suppressor Genes |
1.17 |
|
EZH1/SUZ12 complex positively regulates the transcription of NF-κB target genes via interaction with UXT |
1.1 |
|
Chromatin accessibility landscape upon induction of Msgn1, Pax3 and Myf5 in mesodermal cells and identification of conserved Pax3 binding sites and target genes during skeletal myogenesis |
1.09 |
|
Ets homologous factor has critical roles in epithelial dysfunction in airway disease |
1.08 |
|
Ets homologous factor has critical roles in epithelial dysfunction in airway disease [RNA-seq] |
1.08 |
|
Transcriptome-wide response to synthetic chromatin protein PcTF |
1.05 |
|
YAP and MRTF-A, transcriptional co-activators of RhoA- mediated gene expression, are critical for glioblastoma tumorigenicity |
0.98 |
|
Thyroid State Regulates Gene Expression in Human Whole Blood Cells |
0.97 |
|
GATA2 is Dispensable for Generation of Hemogenic Endothelium But Required for Endothelial-to-Hematopoietic Transition |
0.92 |
|
eVIP2: Expression-based variant impact phenotyping to predict the function of gene variants |
0.9 |
|
Gene expression alterations of pancreatic intraepithlial neoplasia |
0.86 |
|
Transcriptional Profiling of Werner Syndrome (WS) iPSC-derived MSC and the isogenic gene-edited controls |
0.85 |
|
Gene expression profiles in HMC3 cells after exposure to ketamine or its active metabolites: 2R6R-HNK and 2S6S-HNK |
0.84 |
|
Frailty in middle age is associated with race-specific changes to the transcriptome. |
0.83 |
|
Modulation of nonsense-mediated decay by rapamycin |
0.7 |
|
4C-seq of insulin promoter, knockdown of INS promoter activity and Genome-wide maps of chromatin state in EndoC-βH1 Cells |
0.66 |
|
Viral shRNA Knockdown of INS Promotor Activity in EndoC-βH1 Cells |
0.66 |
|
Transcriptome analysis of Riociguat and Vehicle control treatment in human hematopoietic stem and progenitor cells |
0.64 |
|
nELAVL HITS-CLIP in Alzheimer's Disease patients |
0.64 |
|
Replication defective viral products exploit a cellular pro-survival mechanism to establish persistent infections |
0.62 |
|
Coordinated regulation of synthesis and stability of RNA during the acute TNF-induced proinflammatory response |
0.59 |
|
Urinary sediment transcriptomic and longitudinal data to investigate renal function decline in type 1 diabetes |
0.57 |
|
The secretome of skin cancer cells activates the mTOR/MYC pathway in healthy keratinocytes and converts them into tumorigenic cells |
0.56 |
|
The control of rRNA synthesis during the directed differentiation of human embryonic stem cells precedes heterochromatin formation. |
0.55 |
|
Transcriptomic analysis of human coronary artery endothelial cells stimulated with TNF-alpha in the presence and absence of ACSL3 siRNA |
0.51 |
|
High-throughput single cell transcriptome analysis and CRISPR screen identify key β cell-specific disease genes |
0.5 |
|
HBEC-shp53-PCHD7 |
0.5 |
|
Epigenetic profiling and RNA-sequencing of Juvenile Idiopathic Arthritits (JIA) patients |
0.48 |
|
RNA-sequencing of cells derived from the site of inflammation of Juvenile Idiopathic Arthritis patients |
0.48 |
|
Differentiation of Induced Pluripotent Stem Cells towards Mesenchymal Stromal Cells is Hampered by Culture in 3D Hydrogels |
0.46 |
|
Differentiation of Induced Pluripotent Stem Cells towards Mesenchymal Stromal Cells is Hampered by Culture in 3D Hydrogels [RNA-Seq] |
0.46 |
|
Exogenous rescue of KLHL9 in SF210 cell line |
0.45 |
|
System-wide profiling of RNA-binding proteins uncovers key regulators of virus infection |
0.44 |
|
Triple vectors expand AAV transfer capacity in the retina |
0.44 |
|
Neuronal brain region-specific DNA methylation and chromatin accessibility are associated with neuropsychiatric trait heritability [RNA-Seq] |
0.43 |
|
Neuronal brain region-specific DNA methylation and chromatin accessibility are associated with neuropsychiatric trait heritability |
0.43 |
|
Transcriptome-wide identification of transient RNA G-quadruplexes in human cells |
0.43 |
|
A toxicogenomics approach to screen chlorinated flame retardants tris(2-chloroethyl) phosphate and tris(2-chloroisopropyl) phosphate for potential health effects |
0.41 |
|
Identification of a unique gene expression signature in mercury and 2,3,7,8-tetrachlorodibenzo-p-dioxin co-exposed cells |
0.36 |
|
Human MAIT cells exit peripheral tissues and re-circulate via lymph in steady state conditions |
0.35 |
|
Hsa-miR-139-5p/HNRNPF axis modulates gene-transcripts balance in thyroid cancer cells |
0.33 |
|
RNA-seq and small RNA-seq from WT and ADAR1 knockdown H9 lines and their differentiation to specific types of neurons |
0.33 |
|
Nascent RNA Sequencing after NMYC activation in SH-EP MYCNER cells |
0.25 |
|
The role of CFTR in islet function |
0.24 |
|
Expression profile of MM.1S tumors folloiwing treatment with bortezomib |
0.23 |
|
Dilated cardiomyopathy vs Myocarditis |
0.23 |
|
Toxoplasma controls host cyclin E expression through the use of a novel MYR1-dependent effector protein, HCE1 |
0.23 |
|
A novel compound that blocks HIV-1 replication inhibits the splicing regulatory function of SRSF10 |
0.21 |
|
Transcriptome sequencing analysis of BRAF-mutant melanoma metastases. |
0.18 |
|
Expression of long non-coding RNAs in autoimmunity and linkage to enhancer function and autoimmune disease risk genetic variants |
0.15 |
|
Distinct and shared functions of ALS-associated TDP-43, FUS, and TAF15 revealed by comprehensive multi-system integrative analyses [RNA-Seq_Stability] |
0.1 |
|
The NFkB subunit RELA is a master transcriptional regulator of the committed epithelial-mesenchymal transition in airway epithelial cells |
0.08 |
|
The WNT target SP5 negatively regulates WNT transcriptional programs in human pluripotent stem cells |
0.08 |
|
Kidney compartment specific eQTL studies highlight causal genes and pathways for renal disease development |
0.05 |
|
N6-methyladenine DNA Modification in Glioblastoma [RNA-seq] |
0.05 |
|
N6-methyladenine DNA Modification in Glioblastoma |
0.05 |
|
Preclinical model of obesity and ER-positive breast cancer |
0.04 |