|
Expression analysis of genes modulated after knock-down of lncRNA CHROME. |
67.47 |
|
Transcriptional change of THP-1 after HSV-1UL37WT or HSV-1UL37C819S |
66.24 |
|
Transcriptional profile of CAOV2 primary and CAOV2 recurrent cells |
63.33 |
|
Transcriptional responses of human insulinoma cells to acute cytokine exposure |
60.23 |
|
Lineage tracing of acute myeloid leukemia reveals the impact of hypomethylating agents on chemoresistance selection |
59.3 |
|
Genome-wide profiling of siRNA targeting EWS-FLI1 in TC32 Ewing sarcoma cell line |
55.84 |
|
Next Generation RNA Sequencing Analysis of AMPK Wild Type, AMPKα-KO and AMPKα1-2A U2OS cell Transcriptomes |
55.33 |
|
mRNA expression in iPS cells generated by a synthetic self-replicative RNA |
54.46 |
|
IDH3a KO RNA-seq |
52.36 |
|
Crizotinib v. DMSO in SW480 cells |
48.98 |
|
DNA methylation state is associated with the formation of loops and links in hematopoietic stem cells |
46.37 |
|
DNA methylation state is associated with the formation of loops and links in hematopoietic stem cells [RNA-seq] |
46.37 |
|
Characterization of gene regulation and protein interaction networks for Matrin 3 encoding mutations linked to amyotrophic lateral sclerosis and myopathy |
46.24 |
|
HeLa transcriptome induction by IFN gamma and indoleamine 2,3-dioxygenase (IDO) |
45.92 |
|
Overexpression of NFIB and YBX1 in MCF-7 cells |
45.36 |
|
FOXD3 is a novel tumor suppressor in lung cancer |
45.36 |
|
GREB1, a novel target of Wnt signaling, promotes development of hepatoblastoma by suppressing TGFβ signaling |
44.98 |
|
Transcriptomic analysis of trametinib-resistant HCT116 colorectal carcinoma cells compared to the parental control cells |
42.28 |
|
XBP1s Activation Globally Remodels N-Glycan Structure Distribution Patterns |
39.02 |
|
Generation of induced neural stem cells from urine derived cells by synthetic mRNA |
38.49 |
|
Profiles of Long Noncoding RNAs in Human Naive and Memory T Cells |
34.45 |
|
Effect of Influenza virus infection on lncRNA expression in A549 cells |
33.95 |
|
SIRT6 regulates redox homeostasis in human mesenchymal stem cells by the transactivation of NRF2 |
33.71 |
|
Enriched EWSR1 and EWS-FLI1 RNA-seq of HNRNPH1-silenced TC32 Ewing sarcoma and 293T human embryonic kidney cells. |
32.94 |
|
Lipid degradation promotes prostate cancer cell survival |
32.88 |
|
MenSCs inhibit HCC growth through oncogenic pathway suppression via regulating 5-hmC in enhancer elements [RNA-seq] |
32.87 |
|
MenSCs inhibit HCC growth through oncogenic pathway suppression via regulating 5-hmC in enhancer elements |
32.87 |
|
Survival of pancreatic cancer cells lacking KRAS function |
32.26 |
|
Effect of CTCF and Rad21 knockdown on SLK cells and KSHV gene expression |
32.18 |
|
ZEB1 insufficiency causes corneal endothelial cell state transition and altered cellular processing |
32.08 |
|
Supraphysiological Androgens Repress Prostate Cancer Growth and Induce DNA Damage Augmented by PARP Inhibition |
31.87 |
|
Gene expression profile of HGC27 and LMSU gastric cancer cell p53 KO and KD |
31.86 |
|
A non-catalytic function of carbonic anhydrase IX contributes to the glycolytic phenotype and pH regulation in human breast cancer cells |
31.52 |
|
TRIM24 is an oncogenic transcriptional co-activator of STAT3 in glioblastoma |
31.42 |
|
Genome wide characterization of a STAT1-independent antiviral and immunoregulatory transcriptional program induced by IFNβ and TNFα reveals non-canonical STAT2 and IRF9 pathways |
30.55 |
|
Integrative Genomic Analysis Reveals Widespread Enhancer Regulation by p53 in Response to DNA Damage |
29.81 |
|
Differential expression in wild-type and mutant neurofibroma and MPNST cell lines |
29.22 |
|
Neurofibroma |
29.22 |
|
Decrease in EZH2 histone methyltransferase mediates the effects of fluid shear stress (FSS) in endothelial cells |
28.63 |
|
RNAseq of PRMT4KD in human cord blood derived CD34+ cells |
28.62 |
|
Human Adult Sorted Live Cell Erythroblasts transduced with Sigma shRNA Clone TRCN0000005418 targeting RIOK3 with puromycin selection RNAseq |
28.23 |
|
A role for ZNF598 in post-transcriptional gene regulation |
27.92 |
|
RNA sequencing of erythroid and granulomonocytic colonies differentiated from transduced bone marrow CD34+ cells expressing U2AF1 S34F mutation, U2AF1 wild-type or empty vector control |
27.87 |
|
Differetially expressed genes after hTR overexpression in U2OS cells |
27.86 |
|
Genomic analysis of human parthenogenetic haploid ESCs (hPGES), normal human ESCs(H9) and human forskin fibroblast |
26.92 |
|
mRNA expression data from human parthenogenetic haploid ESCs (hPGES), normal ESCs (H9) and human fibroblast |
26.92 |
|
VAMP8 contributes to TRIM6-mediated type-I interferon antiviral response upon West Nile virus (WNV) infection |
26.36 |
|
A549 cells and MSR-A549 cells |
26.22 |
|
mRNA expression profile of A549 cells and MSR-A549 cells with or without JQ1 treatment |
26.22 |
|
The impact of pro-inflammatory cytokines on the β-cell regulatory landscape provides insights into the genetics of type 1 diabetes |
26.07 |
|
Mitochondrial phosphoenolpyruvate carboxykinase (PCK2) regulates metabolic adaptation and glucose-independent tumor cell growth |
25.93 |
|
Effect of the knockdown of MLL1 and MLL2 on pediatric high grade glioma |
25.78 |
|
Endometrial epithelial cell transcriptome response to co-culture with adipose stromal cells |
25.6 |
|
RNA Sequencing of default, melanocyte biased and enteric human neural crest populations (NC) and neuroectoderm (CNS) |
25.49 |
|
Genome-wide analysis of Dengue virus 2 infected cells |
25.0 |
|
Integrated analyses of early responses to radiation in glioblastoma identify new alterations in RNA processing and candidate targets to improve treatment outcomes |
24.98 |
|
Effector and regulatory T cells roll at high shear stress by inducible tether and sling formation |
24.62 |
|
The inhibitory effect of TIAM1 on TAZ transcriptional activity and TIAM1 differentially expressed genes |
24.39 |
|
List of TIAM1 differentially expressed genes in SW620 cells [RNA-seq] |
24.39 |
|
Global mRNA expression profile in cardiac progenitor cells generated by ISX-9 |
24.37 |
|
Global expression profiles in cardiac progenitor cells generated by ISX-9 |
24.37 |
|
IL-6/Stat3-Dependent Induction of Distinct, Obesity-Associated Natural Killer Cells Deteriorates Energy and Glucose Homeostasis |
24.09 |
|
Identifying transcripts that are transcriptinoally regulated by CBFB and RUNX1 using RNAseq |
23.37 |
|
Transcriptome analysis reveals malignant and hypoxic signature of glioblastoma |
23.31 |
|
A quantitative chemotherapy genetic interaction map identifies new factors associated with PARP inhibitor resistance |
23.09 |
|
Transcriptomic analysis of effect of oncolytic measles virus (MV) on transformed and non-transformed bone marrow-derived mesenchymal stem cells (MSCs) |
23.02 |
|
Replicated transcriptome profiling of Normal and Cancerous Prostate Cells [RNA-Seq] |
22.92 |
|
Transcriptome analysis of human embryonic stem cells (hESCs) and human fibroblasts upon rapamycin |
22.81 |
|
Three-dimensional disorganisation of the cancer genome occurs coincident with long range genetic and epigenetic alterations |
22.64 |
|
Three-dimensional disorganisation of the cancer genome occurs coincident with long range genetic and epigenetic alterations [RNA-seq] |
22.64 |
|
An evolutionarily conserved function of polycomb silences the MHC class I antigen presentation pathway and enables immune evasion in cancer |
22.62 |
|
An evolutionarily conserved function of polycomb silences the MHC class I antigen presentation pathway and enables immune evasion in cancer [RNA-Seq] |
22.62 |
|
Exploring ILF2 regulatory genes by next-generation sequencing |
22.47 |
|
Antibodies That Convert Bone Marrow Into Trafficking Microglia-Like Cells Reduce Brain Amyloid |
22.33 |
|
Reprogramming by de-bookmarking somatic transcriptional program via targeting the BET bromodomains |
21.91 |
|
Valproic acid attenuates hyperglycemia induced complement and coagulation cascade gene expression |
21.73 |
|
Transcriptome-wide analysis of the role of HTLV-1 Tax PBM in T-Cells from infected humanized-mice (hu-Mice) |
21.54 |
|
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 |
21.34 |
|
Locally transplanted human urine-induced nephron progenitor cells contribute to renal repair in mice kidney with diabetic nephropathy |
21.22 |
|
Mitotic stress is an integral part of the oncogene-induced senescence program that promotes multinucleation and cell cycle arrest |
21.09 |
|
Hepatitis C virus functionally sequesters miR-122 [RNA-Seq] |
21.0 |
|
Hepatitis C virus functionally sequesters miR-122 |
21.0 |
|
Generation and functional characterization of MDSC-like cells |
20.9 |
|
Helios enhances the preferential differentiation of human fetal CD4+ naïve T cells into regulatory T cells. [RNA-Seq - ex vivo] |
20.54 |
|
RNA-sequencing of isogenic primary, pre-malignant immortalized, and Ras-transformed human mammary epithelial cells |
20.51 |
|
Paxillin regulates genomic networks in prostate cancer [LNCaP] |
20.49 |
|
Transcriptional profiling of MCF7 cells treated with H3B05942, E2, or standard of care compounds |
20.48 |
|
Gene Expression of Breast Cancer Cell Lines Across Biomaterial Platforms |
20.47 |
|
An integrative network biology analysis identifies miR-508-3p as the determinant and a prognosis biomarker of the mesenchymal subtype ovarian cancer |
20.36 |
|
Reciprocal Reprogramming of Cancer Cells and Associated Mesenchymal Stem Cells in Gastric Cancer. |
20.25 |
|
Transcriptional alteration after ionizing radiation exposure in human fibroblasts, iPSCs and NPCs |
20.22 |
|
Interferon-γ Represses M2 Gene Expression in Human Macrophages by Disassembling Enhancers Bound by the Transcription Factor MAF |
20.2 |
|
IFN-γ Represses M2 Gene Expression in Human Macrophages by Suppressing and Disassembling MAF-binding Enhancers [RNA-seq] |
20.2 |
|
MeRIP sequencing reveals angiogenic properties of vascular endothelial cells |
20.17 |
|
CD95L derived si- and shRNAs and the CD95L mRNA kill cancer cells through an RNAi mechanism by targeting survival genes [siL3.RNAseq.lg] |
20.11 |
|
MYCi361 regulates MYC target genes |
20.1 |
|
STRIPAK directs PP2A activity to promote oncogenic transformation |
19.99 |
|
Bladder cancer associated mutations in RXRA activate peroxisome proliferator-activated receptors |
19.94 |
|
Bladder-cancer-associated mutations in RXRA activate peroxisome proliferator-activated receptors to drive urothelial proliferation |
19.94 |
|
Gene induction by the USP6 oncogene in response to interferon |
19.83 |
|
The cohesin complex prevents Myc-induced replication stress |
19.8 |
|
Transcriptome profiling of Normal and Cancerous Prostate Cells |
19.25 |
|
Maturation of human iNSCs |
19.19 |
|
Gene-Edited Human Kidney Organoids Reveal Mechanisms of Disease in Podocyte Development |
19.16 |
|
Effects of Inhibition of CDK8/19 Mediator Kinase by Senexin B in HCT116 cells treated with or without TNF-alpha |
19.04 |
|
ncRNA (non-coding RNA) signature in endothelial cells during hypoxia [RNA-seq] |
18.95 |
|
ncRNA (non-coding RNA) signature in endothelial cells during hypoxia |
18.95 |
|
24hr CA treatment vs. DMSO in HCT116 cells (from 'Identification of CDK8 and CDK19 substrates in human cells using cortistatin A and quantitative phosphoproteomics') |
18.83 |
|
Transcriptomes of oxLDL exposed trained monocytes |
18.79 |
|
oxLDL exposed trained monocytes |
18.79 |
|
RNA-seq of UGP2 mutant human embryonic stem cells and in vitro differentiated neural stem cells |
18.7 |
|
Retinoic Acid Induced Transcriptional Repressor HIC1 is Required for Suppressive Function of Human Induced Regulatory T cells [RNA-Seq 1] |
18.67 |
|
Proteinase-Activated Receptor 4 (PAR4) mediates cell membrane blebbing in a Gaq/11, Gai independent, RhoA and ß-arrestin-dependent manner. |
18.34 |
|
RNA-seq differential expression studies: more sequence, or more replication? |
18.34 |
|
Transcriptomic analysis of iPSC and ESC challenged with atmospheric or physiological oxygen |
18.3 |
|
RNA-Seq study of Cell lines rendered resistant to idelalisib and ibrutinib |
18.3 |
|
Axitinib exposure triggers endothelial cells senescence through ROS accumulation and ATM activation |
18.28 |
|
Transcriptome sequencing wide functional analysis of human mesenchymal stem cells (Poly(I:C) and LPS) |
18.22 |
|
Gene expression, methylome and splicing of THP-1 monocytic cells and THP-1-derived macrophage |
18.03 |
|
Gene expression analysis of ER+ and ER- breast cancer cell lines with acquired resistance to palbociclib |
17.99 |
|
Tracking of dCas9-methyltransferase footprints |
17.96 |
|
Different Temporal Effects of Ebola Virus VP35 and VP24 Proteins on Global Gene Expression in Human Dendritic Cells |
17.93 |
|
Differentially Expressed Genes upon Knockdown of ZRANB1 or EZH2 in LM2 Cells |
17.92 |
|
Effects of Freeze-Thawing and Intravenous Infusion on Mesenchymal Stromal Cell Gene Expression |
17.92 |
|
Modulation of Indoleamine 2, 3-dioxygenase 1 Expression by Activated Human T cells in Breast Cancer Cells is Controlled by DNA Promoter Methylation |
17.85 |
|
The Unfolded Protein Response Regulator, ATF6, Promotes Mesodermal Differentiation |
17.63 |
|
Integrative analysis identifies lincRNAs up- and downstream of neuroblastoma driver genes (ALK) |
17.59 |
|
Single-cell RNA-Seq Investigation of Foveal and Peripheral Expression in the Human Retina |
17.47 |
|
RNA-seq transcriptional profiling in human primary fetal and adult CD34+ hematopoietic stem/progenitor cells (HSPCs) erythroid progenitor cells (ProEs) |
17.42 |
|
Co-expression of CD163 and CD141 Identifies Human Circulating IL-10-Producing Dendritic Cells (DC-10) [RNA-seq] |
17.33 |
|
Co-expression of CD163 and CD141 Identifies Human Circulating IL-10-Producing Dendritic Cells (DC-10) |
17.33 |
|
Effect of Toxoplasma gondii efector TgIST on global transcriptome of human foreskin fibroblasts (HFFs) upon type I IFN activation |
17.26 |
|
Bacterial Infection Remodels the DNA Methylation Landscape of Human Dendritic Cells (mRNA-Seq) |
17.2 |
|
Oncogenic Notch promotes long-range regulatory interactions within hyperconnected 3D cliques |
17.06 |
|
The Notch driven long non-coding RNA repertoire in T-cell acute lymphoblastic leukemia |
16.97 |
|
Transcriptional profile of CAOV2 ovarian cancer cells with TAZ silencing |
16.89 |
|
Therapeutic targeting of KDM1A/LSD1 in Ewing sarcoma engages the ER-stress response II |
16.87 |
|
Gene expression profiling via RNA sequencing of patient brain tumors cultured in 3D bioengineered cultures |
16.83 |
|
Generation of targeted homozygosity in the genome of human induced pluripotent stem cells |
16.81 |
|
Transcriptome analysis of human airway epithelium infected by Human Bocavirus 1 |
16.72 |
|
RNA-seq analysis of FET cells treated with RSPO1 or TGFβ1 |
16.59 |
|
Effect of from Human Umbilical Vein Endothelial Cells |
16.48 |
|
Discovery of first-in-class reversible dual small molecule inhibitors against G9a and DNMTs with in vivo activity in hematological malignancies [RNA-Seq] |
16.43 |
|
Discovery of first-in-class reversible dual small molecule inhibitors against G9a and DNMTs with in vivo activity in hematological malignancies |
16.43 |
|
Benzotriazoles reactivate latent HIV-1 through inactivation of STAT5 SUMOylation (RNA-Seq) |
16.28 |
|
Benzotriazoles reactivate latent HIV-1 through inactivation of STAT5 SUMOylation |
16.28 |
|
Chromatin Topology Reorganization and Transcription Repression by PML/RARα in Acute Promyeloid Leukemia (RNA-seq) |
16.26 |
|
Chromatin Topology Reorganization and Transcription Repression by PML/RARα in Acute Promyeloid Leukemia |
16.26 |
|
The ALK downregulated target gene HBP1 and repressor of MYCN activity as synergistic target for combined PI3K/HDAC inhibition |
16.25 |
|
The ALK downregulated target gene HBP1 and repressor of MYCN activity as synergistic target for combined PI3K/HDAC inhibition [RNA-Seq] |
16.25 |
|
Heterozygous mutations in SMARCA2 lead to impaired neurogenesis due to global retargeting of SMARCA4 |
16.2 |
|
UBC9 knockdown in bladder cancer T24 cell lines |
16.2 |
|
Parkinson’s Disease Genetic Risk in a Midbrain Neuronal Cell Line |
16.17 |
|
Estrogen deprivation triggers and immunosuppressive phenotype in breast cancer cells |
16.15 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of miR-29b-1 and miR-29a targets in tamoxifen-sensitive and tamoxifen-resistant human breast cancer cells |
16.15 |
|
Large-Scale Atlas of Mutant IDH1-Dependent Chromatin State Reprogramming, Reversibility, and Persistence |
16.13 |
|
Large-Scale Atlas of Mutant IDH1-Dependent Chromatin State Reprogramming, Reversibility, and Persistence [RNA-seq] |
16.13 |
|
Analysis of the polyA+ RNA of LPS-treated human CD14+ monocytes |
16.09 |
|
PTEN suppresses neoplastic transformation of human neural stem cells by transcriptional repression of Pax7 |
15.97 |
|
Quantitative Analysis of p53 and/or TGFBR2 Knockdown Endothelial Transcriptomes after Irradiation |
15.96 |
|
Hypoxic transcriptome of SQ20B human head and neck cancer cells |
15.94 |
|
The effects of U1 snRNA mutation in chronic lymphocytic leukemia cell lines |
15.91 |
|
Nuclear Actin Regulates Inducible Transcription by Enhancing RNA Polymerase II Clustering |
15.86 |
|
AZ1366: An inhibitor of tankyrase and the canonical Wnt pathway that limits the persistence of non-small cell lung cancer cells following EGFR inhibition |
15.81 |
|
Heterozygous p53-R280T mutation promotes proliferation of NPC cells through activating PI3K/Akt signaling pathway |
15.78 |
|
Involvement of Condensin in Cellular Senescence through Gene Regulation and Compartmental Reorganization |
15.77 |
|
The effect of PPARG inhibition on human angiomyolipoma cells |
15.75 |
|
The effect of Abl kinases,or Ponatinib challenging on breast cancer cells' global transcriptome |
15.69 |
|
RNASeq of mouse, human, and non-human primate primary dermal fibroblasts to poly(I:C) transfection |
15.69 |
|
Splicing towards noncoding isoforms in colorectal carcinoma is associated with tumor hypoxia and the DNA damage response |
15.68 |
|
Epigenome regulation during epidermal lineage commitment [ATAC-seq, RNA-seq] |
15.68 |
|
Transcriptomic analysis reveals novel long non-coding RNAs critical for vertebrate development [RNA-Seq] |
15.58 |
|
Transcriptomic analysis reveals novel long non-coding RNAs critical for vertebrate development |
15.58 |
|
A novel lncRNA lncRNA-AF339830 promotes colorectal carcinogenesis and glucose metabolism by stabilizing and specifying the transcription modification pattern of c-Myc [RNA-Seq] |
15.58 |
|
A novel lncRNA lncRNA-AF339830 promotes colorectal carcinogenesis and glucose metabolism by stabilizing and specifying the transcription modification pattern of c-Myc |
15.58 |
|
ABCB5 is activated by MITF and b-catenin and is associated with melanoma differentiation |
15.56 |
|
Transcriptional Signatures of Hypoxic and Inflammatory Renal Epithelial Injury |
15.53 |
|
RNA-seq analysis of YFV-17D specific and total naive CD8 T cells in humans |
15.4 |
|
The ETS transcription factor ELF1 regulates a critical, broadly antiviral program distinct from the type I interferon response |
15.35 |
|
The ETS transcription factor ELF1 regulates a critical, broadly antiviral program distinct from the type I interferon response |
15.35 |
|
High-throughput RNA sequencing of human preovulatory cumulus and mural granulosa cells (mRNA) |
15.26 |
|
Small RNA-seq of human granulosa cells reveals miRNAs in FSHR and aromatase genes |
15.26 |
|
Total RNA deep sequencing (ribosomal depleted) of human umbilical vein endothelial cells exposed to hypoxia (0.2%) for 12h and 24h or kept under normoxic conditions. |
15.1 |
|
Endothelial gene expression analysis |
15.1 |
|
Human Adipocytes Regulate Gene Expression in Triple-negative Breast Cancer Assessed by NGS Sequencing |
14.91 |
|
Candidate genes and pathways downstream of PAX8 involved in ovarian high-grade serous carcinoma |
14.87 |
|
naive T cell heterogeneity after neonatal thymectomy |
14.84 |
|
The regulartory role of ZCCHC24 in splicing machinery |
14.83 |
|
Exogenous pyruvate represses histone gene expression to inhibit cancer cell proliferation via the NAMPT-NAD + -SIRT1 pathway |
14.74 |
|
Error-free and error-prone DNA repair gene expression through reprogramming and passage in human iPS cells |
14.73 |
|
SHP2 Drives Adaptive Resistance to ERK Signaling Inhibition in Molecularly Defined Subsets of ERK-dependent Tumors |
14.69 |
|
Triplet nucleotide repeat-based siRNAs are highly toxic to cancer cells |
14.65 |
|
Combined inhibition of STAT3 and DNA repair in palbociclib-resistant ER-positive breast cancer |
14.6 |
|
Transcriptome wide analysis of classically and alternatively activated macrophages |
14.59 |
|
Gene expression changes associated with resistance to tagraxofusp (SL-401) |
14.57 |
|
SMN deficiency in spinal muscular atrophy causes widespread intron retention and DNA damage |
14.55 |
|
Effect of 48h treatment with 100nM GSK2879552 on T-ALL cell lines HSB2 and RPMI8402 |
14.45 |
|
Exploring the role of macroH2A1 in transcription regulation in IMR90 primary human lung fibroblasts with RNA-seq and ChIP-seq |
14.44 |
|
RNA-seq from control and macroH2A1-depleted IMR90 primary human lung fibroblasts |
14.44 |
|
Genetic-to-epigenetic Therapy for Pancreatic Cancer |
14.39 |
|
Genome-wide CRISPR-Cas9 screen identifies SLC1A3 as a key contributor to L-asparaginase Resistance in Solid tumors |
14.32 |
|
Human iPSC-derived glomeruli provide an advanced model to interrogate podocyte biology and accurately recapitulate podocytopathy |
14.27 |
|
Controlling for gene expression changes in transcription factor protein networks. |
14.27 |
|
Control of prostate tumour growth by the long non-coding RNA GHSROS (LNCaP) |
14.26 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of transcriptomes of human cord blood CD34+ cells treated with HDAC5 inhibitor |
14.23 |
|
The myelin protein PMP2 is regulated by SOX10 and drives melanoma cell invasion |
14.19 |
|
RNA seq_A375 gSMARCB1 + A549 etoposide, Aurora kinases inhibitors treated |
14.15 |
|
RNA-seq analysis of control and Myc-induced U2OS cells |
14.15 |
|
Developmental stage specific chromosome architecture in human erythroid cells (RNA-seq) |
14.15 |
|
Developmental stage specific chromosome architecture in human erythroid cells |
14.15 |
|
EWS-Fli and LNC regulated genes in comparison to GFP samples |
14.08 |
|
Genome-wide probing of RNA structure reveals active unfolding of mRNA structures in vivo |
14.04 |
|
Sequential regulatory loops as key gatekeepers for neuronal reprogramming in human cells |
13.86 |
|
Sequential regulatory loops as key gatekeepers for neuronal reprogramming in human cells [RNA-seq] |
13.86 |
|
ASCL1 mediates neuronal differentiation of primary GBM stem cell cultures upon Notch signalling blockade [RNA-seq] |
13.84 |
|
Induction of human SST and PV neurons by expressing a single transcription factor LHX6 |
13.82 |
|
mRNA cap methyltransferase, RNMT-RAM, promotes RNA pol II transcription |
13.8 |
|
High-efficiency RNA-based reprogramming of human primary fibroblasts |
13.8 |
|
RNA-Sequencing of HUVEC treated with Tie2 activating antibody |
13.76 |
|
Effect of nuclear IL-33 on gene expression |
13.7 |
|
Gene expression changes in human melanoma cell lines compared to primary melanocytes |
13.68 |
|
WRN knockout effects upon gene expression in SW48 and OVK18 |
13.65 |
|
Genome-Wide Transcriptional Regulation Mediated By Biochemically Distinct Forms of SWI/SNF |
13.65 |
|
Combinatorial Regulation Mediated by Biochemically Distinct Forms of SWI/SNF [RNA-Seq] |
13.65 |
|
RNA-sequencing based transcriptome-wide expression profiling of Cynomolgus monkey and human IPSCs in vitro differentiated into endothelial cells |
13.62 |
|
Epigenetic mechanisms underlie the crosstalk between growth factors and a steroid hormone [IMR90_MCF7_RNA-Seq] |
13.55 |
|
Epigenetic mechanisms underlie the crosstalk between growth factors and a steroid hormone |
13.55 |
|
RNA splicing alteration on glioblastoma and normal neural stem cells |
13.53 |
|
Expression data from miR340 overexpressing human A549 cells |
13.51 |
|
High-Throughput Drug Screening identifies Pazopanib and Clofilium tosylate as effective treatments for malignant rhabdoid tumors |
13.51 |
|
Targeted degradation of BRD9 reverses oncogenic gene expression in synovial sarcoma [RNA-seq] |
13.48 |
|
Targeted degradation of BRD9 reverses oncogenic gene expression in synovial sarcoma |
13.48 |
|
Transcriptome analysis in HT29 and SW480 cells depleted of Prdx2 |
13.42 |
|
Whole Transcriptomic Sequencing of Metastatic Castration Resistant Prostate Cancer Samples |
13.42 |
|
RNA-seq analyisis of PUM2 knockout cells |
13.41 |
|
Dynamic incorporation of histone H3 variants into chromatin is essential for acquisition of aggressive traits and metastatic colonization |
13.38 |
|
CircRNAome diversity in human mature B-cells, T-cells and monocytes |
13.36 |
|
RNA sequencing of GlyH-101-treated MCF-7 cell line |
13.28 |
|
Global gene expression analysis of human monocyte-derived dendritic cells (DCs) treated with HMGN1 (N1) and R848 alone or in combination. |
13.24 |
|
Functional role of SLIT2 and ROBO1 in trophoblasts |
13.18 |
|
Robust generation of honemogeneous midbrain organoids with in vivo–like cellular composition facilitates neurotoxin-based Parkinson’s disease modeling |
13.18 |
|
Trnascriptome analysis of HeLa cells infected with rTHOV-wt, -dML, -SW mutant or mock-treated |
13.15 |
|
Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation (Ribo-seq, RNA-seq) |
13.13 |
|
CX3CR1/Fractalkine receptor expression separates memory CD8+ T cells with distinct functional profiles (RNA-seq) |
13.12 |
|
CX3CR1/Fractalkine receptor expression separates memory CD8+ T cells with distinct functional profiles |
13.12 |
|
RNA-seq of overgrown interscapular adipose tissue with biallelic MFN2 mutations |
13.11 |
|
The RNA helicase DDX6 regulates self-renewal and differentiation of human and mouse stem cells [RNA-seq2] |
13.11 |
|
Bacterial Infection Remodels the DNA Methylation Landscape of Human Dendritic Cells (wtRNA-Seq) |
13.09 |
|
The acetyllysine reader BRD3R promotes human nuclear reprogramming and regulates mitosis |
12.99 |
|
Human iPSC-derived microglia assume a primary microglia-like state after transplantation into the neonatal mouse brain [Single Cell RNAseq] |
12.93 |
|
Selective expansion of myeloid and NK cells in humanized mice yields human-like vaccine responses (Experiment 2: scRNA-seq) |
12.93 |
|
Profiling of gene expression using RNA-Seq in fibroblasts, iPSCs, iPSC-derived neurons and cells overexpressing Onecut transcription factors |
12.92 |
|
Changes in chromatin accessibility and gene expression induced by overexpression of ONECUT transcription factors |
12.92 |
|
HDAC inhibition enhances the in vivo efficacy of MEK inhibitor therapy in uveal melanoma |
12.91 |
|
The contribution of adenosine receptor 3-mediated signaling to TLR4-induced responses by human dendritic cells |
12.9 |
|
Heterogeneous nuclear ribonucleoprotein C1/C2 links transcriptional and splicing actions of 1,25-dihydroxyvitamin D |
12.84 |
|
RNA sequence analysis of stable versus reversible EMT events and the resultant metastases |
12.84 |
|
KMT2D regulates p63 target enhancers to coordinate epithelial homeostasis [RNA-Seq] |
12.8 |
|
KMT2D regulates p63 target enhancers to coordinate epithelial homeostasis |
12.8 |
|
Poly(A)-specific ribonuclease (PARN) mediates 3' end maturation of the telomerase RNA component |
12.76 |
|
LSD1 mediates MYCN control of epithelial-mesenchymal transition through silencing of metastatic suppressor NDRG1 gene |
12.75 |
|
Polyol pathway links glucose metabolism to the aggressiveness of cancer cells |
12.74 |
|
Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation |
12.73 |
|
RNAseq data from SCCOHT1 and OVCAR8 ovarian cancer cells treated with BET inhibitors |
12.71 |
|
Expression profile of Lo19S state cells in the presence and absence of bortezomib treatment |
12.69 |
|
Novel Form of JARID2 is Required to Regulate Differentiation in Keratinocytes. |
12.62 |
|
Adaptive resistance of melanoma cells to RAF inhibition via reversible induction of a slowly-dividing de-differentiated state |
12.62 |
|
Expression changes in melanoma cell lines under BRAFi treatment timepoints [RNA-Seq.CellLine.batch4] |
12.6 |
|
Targeting HuH7 cells with JumonjiC Lysine Demethylase Inhibitors (RNA-Seq) |
12.59 |
|
Differentially expressed genes from RNA-Seq and functional enrichment results are affected by the choice of single-end versus paired-end reads and stranded versus non-stranded protocols |
12.55 |
|
Identification of biomarkers for amyotrophic lateral sclerosis by comprehensive analysis of exosomal mRNAs in human cerebrospinal fluid. |
12.55 |
|
Comparative gene expression profiling of MHH-CALL4 cells subject to pharmacological JAK2 inhibitor treatment (ruxolitinib or CHZ868) or shRNA-mediated JAK2 depletion in vitro |
12.53 |
|
JAK2 is dispensable for maintenance of JAK2 mutant B-cell acute lymphoblastic leukemias |
12.53 |
|
Bromodomain protein BRD4 is a transcriptional repressor of autophagy and lysosomal function |
12.52 |
|
Functional Cardiac Fibroblasts Derived from Human Pluripotent Stem Cells via Second Heart Field Progenitors |
12.48 |
|
Polarized B -cell functions |
12.45 |
|
Glioblastoma stem cells infected by ZIKA virus |
12.44 |
|
Expression by CD133+ cells isolated from the adult human exocrine pancreas |
12.38 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of Health donors and SLE patients' PBMC Transcriptomes |
12.31 |
|
A damaged genome's transcriptional landscape through multilayered expression profiling around in situ-mapped DNA double-strand breaks |
12.3 |
|
RNA sequencing (RNA-SEQ) of Human endothelial cells (HUVEC) in LFS, sFRP2OE, and WT conditioned media |
12.29 |
|
Lung Cancer Cell-Mediated Skeletal Muscle Mitochondrial Dysfunction is Mitigated by 1a,25-Dihydroxyvitamin D3 |
12.26 |
|
Analysis by Whole Transcriptome Sequencing of the Effects of LLC1 conditioned medium, LLC1 conditioned plus Calcitriol, non-conditioned medium, and non-conditioned medium plus Calcitriol on mRNA Expression in Primary Human Skeletal Muscle Cells |
12.26 |
|
tRNA modification landscape selectively controls mitochondrial translation efficiency in MERRF |
12.25 |
|
IgG immunocomplexes sensitize human monocytes for inflammatory hyperactivity via transcriptomic and epigenetic reprogramming in Rheumatoid Arthritis |
12.22 |
|
mRNA Sequencing of Human PromoCells Using 3'-directed Digital Gene Expression (3'-DGE) Technique |
12.19 |
|
ChIP-seq and RNA-seq analysis of KMT2D-silenced metastatic melanoma cells |
12.16 |
|
An RNA-centric dissection of host complexes controlling flavivirus infection |
12.16 |
|
Myeloid-derived suppressor cells facilitie invasion and metastasis of papillary thyroid cancer cells by repressing miR-486-3p |
12.12 |
|
RNA-seq of human aneuploid cell lines with Trisomy 21 |
12.12 |
|
Global transcriptional profiling changes upon knockdown of LKB1 in human glioblastoma cell lines |
12.06 |
|
Transcriptome Profiling of Influenza A Virus-infected Lung Epithelial (A549) Cells with Lariciresinol-4-β-D-glucopyranoside Treatment |
12.04 |
|
Generation of a Panel of Induced Pluripotent Stem Cells From Chimpanzees: a Resource for Comparative Functional Genomics (RNA-Seq) |
12.04 |
|
Generation of a Panel of Induced Pluripotent Stem Cells From Chimpanzees: a Resource for Comparative Functional Genomics |
12.04 |
|
The landscape of alternative splicing in aggressive prostate cancers |
12.03 |
|
The mechanism of HHT in treating acute myeloid leukemia on RNA level. |
11.85 |
|
Super-Enhancers Promote Transcriptional Dysregulation in Nasopharyngeal Carcinoma [RNA-seq] |
11.76 |
|
Super-Enhancers Promote Transcriptional Dysregulation in Nasopharyngeal Carcinoma |
11.76 |
|
RNA-seq analysis of CRISPR/Cas9 generated human BMPR2 deficient endothelial cell lines harboring mutations characteristic for hereditary pulmonary hypertension (HPAH) |
11.7 |
|
Genome-wide RNA-sequencing (RNA-seq) of benign and malignant prostate cell lines without and with androgen (R1881) stimulation. |
11.69 |
|
5hmC and gene expression data in breast cancer cell lines treated with an antioxidant |
11.62 |
|
Molecular mechanism underlying increased ischemic damage in the ALDH2*2 genetic polymorphism using a human iPSC model system |
11.57 |
|
Cranial pericytes derived from neural crest cells reveal an inherent cell type-specific defect in Alzheimer's Disease |
11.49 |
|
Suppression of the FOXM1 transcriptional program via novel small molecule inhibition |
11.44 |
|
Bacterial Infection Remodels the DNA Methylation Landscape of Human Dendritic Cells |
11.43 |
|
ELF1 expression in prostate cells reduces oncogenic ETS functions and promotes senescence and sensitivity to chemotherapy through distinct gene expression programs |
11.4 |
|
ELF1 expression in prostate cells reduces oncogenic ETS functions and promotes senescence and sensitivity to chemotherapy through distinct gene expression programs [RNA-seq] |
11.4 |
|
Pluripotent stem cell model of Nakajo-Nishimura syndrome untangles proinflammatory pathways mediated by oxidative stress |
11.35 |
|
CXCR4 regulates extra-medullary myeloma through epithelial-mesenchymal transition-like transcriptional activation |
11.34 |
|
Nuclear HNRNPA2B1 HITS-CLIP and RNA-seq |
11.32 |
|
Lyophilized human cells stored at room temperature preserve multiple RNA species at excellent quality for RNA sequencing |
11.25 |
|
Transcriptional profiling of MDA-MB-231 and its ρ0 cells (lacking mtDNA) after 48h arginine depletion by arginine deiminase (ADI). |
11.25 |
|
Regulation of DNA methylation landscape in human somatic cell reprogramming by miR-29 family (RNA-seq) |
11.22 |
|
Regulation of DNA methylation landscape in human somatic cell reprogramming by miR-29 family |
11.22 |
|
Transcriptomic analysis to functionally map the intrinsically disordered domain of EWS/FLI [Experiment 1] |
11.1 |
|
RNA-seq analysis of hPSC-derived brain pericyte-like cells, hPSC-derived neural crest stem cells, and primary human brain pericytes |
11.08 |
|
Coding mutations and loss-of-imprinting in human pluripotent cells derived by nuclear transfer and defined factors |
11.06 |
|
Coding mutations and loss-of-imprinting in human pluripotent cells derived by nuclear transfer and defined factors [RNA-Seq] |
11.06 |
|
Stable oxidative cytosine modifications accumulate in cardiac mesenchymal cells from Type2 diabetes patients: rescue by alpha-ketoglutarate and TET-TDG |
10.94 |
|
Stable oxidative cytosine modifications accumulate in cardiac mesenchymal cells from Type2 diabetes patients: rescue by alpha-ketoglutarate and TET-TDG functional reactivation [human cells RNA-seq] |
10.94 |
|
The role of the Calcium-Sensing receptor in colorectal cancer |
10.89 |
|
Transcriptomic profile of human embryonic renal corpuscles |
10.87 |
|
Gene expression profiling by RNA-seq in hTert-HME1 cell line treated with control or BRCA2 siRNAs and grown with or without EGF (epithelial growth factor) II |
10.84 |
|
ER proteostasis and temperature differentially impact the mutational tolerance of influenza hemagglutinin |
10.83 |
|
High-resolution liver cancer genomic profiling links etiology, epigenetic and mutation signatures [RNA-Seq] |
10.8 |
|
High-resolution liver cancer genomic profiling links etiology, epigenetic and mutation signatures |
10.8 |
|
Multidimensional Assessment of the Host Response in Mechanically Ventilated Patients with Suspected Pneumonia |
10.74 |
|
ETS1 acts as a tumor suppressor in breast cancer by inhibiting growth-related factors |
10.71 |
|
A NIK-SIX signaling axis controls inflammation by targeted silencing of noncanonical NF-κB |
10.61 |
|
Next-generation sequencing reveals a novel role of lysine-specific demethylase 1 in adhesion of rhabdomyosarcoma cells [RNA-seq] |
10.54 |
|
Next-generation sequencing reveals a novel role of lysine-specific demethylase 1 in adhesion of rhabdomyosarcoma cells |
10.54 |
|
Transcriptional responses of melanoma cells to BRAF inhibition |
10.46 |
|
Expression data for HT29 cells treated with 5-aza-deoxy-cytidine [RNA-Seq] |
10.38 |
|
Expression data for HT29 cells treated with 5-aza-deoxy-cytidine |
10.38 |
|
Gene activation precedes DNA demethylation in response to infection in human dendritic cells |
10.37 |
|
Gene activation precedes DNA demethylation in response to infection in human dendritic cells |
10.37 |
|
The interplay between SOX4 and SMAD3 in the context of breast cancer |
10.37 |
|
EHMT1 and EHMT2 inhibition induce fetal hemoglobin expression |
10.36 |
|
EHMT1 and EHMT2 inhibition induce fetal hemoglobin expression [RNA-seq] |
10.36 |
|
Comparative whole-transcriptomic analysis between normal and AKAP-Lbc-depleted human embryonic stem cells |
10.29 |
|
RelA mutants 'reconstituted' and cell cycle synchronized HCT116 Colorectal Cancer Cells |
10.26 |
|
Recapitulating and Deciphering Tumor-stroma Microenvironment by Using a “LEGO” like 3D printed microfluidic device |
10.21 |
|
SAM68 is required for regulation of Pumilio by the NORAD long noncoding RNA |
10.19 |
|
Gene expression in TAL1-driven T-cell ALL in response to TAL1-KD, UTX-KD, and GSKJ4 treatment |
10.02 |
|
T-cell ALL in response to TAL1-KD, UTX-KD, and GSKJ4 treatment |
10.02 |
|
Knock-down of Ror1 in MDA-MB-231 cell line decreases cell invasiveness |
9.94 |
|
CD161+ Tconv and Treg share transcriptome and display a migratory phenotype which is modified at the inflamed site |
9.94 |
|
Overexpression of PHF8 promotes an EMT-related gene signature in MCF10A cells |
9.74 |
|
The LRF/ZBTB7A transcription factor is a BCL11A-independent repressor of fetal hemoglobin |
9.72 |
|
Nucleotide excision repair capacity increases during differentiation of human embryonic carcinoma cells into neurons and muscle cells |
9.63 |
|
RNA seq with AML (NB4) cells upon FTO inhibition |
9.54 |
|
Differential responses by human respiratory epithelial cell lines to respiratory syncytial virus reflect distinct patterns of infection control |
9.52 |
|
Transcriptome analyses of human pancreatic islets and pseudoislets |
9.46 |
|
Human Treg NaCl stimulation |
9.36 |
|
Prediction of bacterial infection outcome using single cell RNA-seq analysis of human immune cells [sorted population Bulk RNA-seq] |
9.17 |
|
CD1c+ dendritic cell activation by Plasmodium falciparum-infected red blood cells |
9.16 |
|
X-Ray induced DNA-Hydroxymethylation changes |
9.15 |
|
Transcriptome profile of ATP7B KO cells and WT cells treated with Copper (Cu) to study Autophagy as a pro-survival mechanism in Wilson disease |
9.13 |
|
ARID1A and ARID1B loss in HCT116 and TOV21G cells |
8.92 |
|
Expression profiles of long non-coding RNAs located in autoimmune disease-associated regions reveal immune cell type specificity |
8.8 |
|
Transcriptomic changes mediated by β-amyloid in human aortic endothelial cells (HAOEC) |
8.62 |
|
RNA sequencing analysis of selumetinib-resistant CRC cells lines |
8.59 |
|
HMGA1 and FOXM1 synergistically regulate a common gene network modulating angiogenesis in breast cancer |
8.57 |
|
Major hnRNP proteins act as general TDP-43 functional modifiers both in Drosophila and human neuronal cells. |
8.55 |
|
Characterization and therapeautic application of mesenchymal stem cells with neuromesodermal origin from human pluripotent stem cells |
8.55 |
|
Cell responses to dysregulated VZV-induced cell-cell fusion |
8.35 |
|
BRD9 defines a novel SWI/SNF sub-complex and constitutes a specific vulnerability in malignant rhabdoid tumors [RNA-seq 2] |
8.25 |
|
Gene expression profiling of human iPS cell-derived podocytes and sorted human adult podocytes |
8.23 |
|
RNA-sequencing of mRNAs from control and CAP-D3 deficient Salmonella infected HT-29 cells |
8.19 |
|
RNA-seq analysis and shRNA screen of breast cancer |
8.13 |
|
RNA-seq analysis of breast cancer |
8.13 |
|
Transcriptome sequencing wide functional analysis of human mesenchymal stem cells |
8.09 |
|
A Suv39H1-low chromatin state drives migratory cell populations in cervical cancer [RNA-Seq] |
7.98 |
|
A Suv39H1-low chromatin state drives migratory cell populations in cervical cancer |
7.98 |
|
Thyroid State Regulates Gene Expression in Human Whole Blood Cells |
7.95 |
|
Differential effects of estrogen receptor beta isoforms on glioblastoma progression |
7.9 |
|
The regulation of ferroptosis by TAZ in epithelial ovarian cancer |
7.84 |
|
Structural basis for human respiratory syncytial virus NS1-mediated modulation of host responses |
7.76 |
|
The dynamic landscape of coding and non-coding RNAs in the innate immune response to microbial pathogens |
7.66 |
|
Global transcriptome analysis in the MYCN-amplified neuroblastoma cell line IMR5-75 upon inducible MYCN-knockdown |
7.57 |
|
Stochastic genome - nuclear lamina contacts are linked to histone H3K9 dimethylation |
7.2 |
|
Stochastic genome - nuclear lamina contacts are linked to histone H3K9 dimethylation (RNA-seq data) |
7.2 |
|
RNA seq analysis of human Fetal and adult derived Enterospheres |
7.14 |
|
Identification of metabolically distinct adipocyte progenitor cells in human adipose tissues |
7.13 |
|
Stage-specific human induced pluripotent stem cells map the progression of myeloid transformation to transplantable leukemia |
7.11 |
|
Identification of a Cell-of-Origin for Fibroblasts Comprising the Fibrotic Reticulum in Idiopathic Pulmonary Fibrosis |
6.99 |
|
Decoding breast cancer tissue-stroma interactions using species-specific sequencing |
6.96 |
|
Ewing sarcoma resistance to SP-2509 is not mediated through KDM1A/LSD1 mutation I |
6.9 |
|
Selective expression of long non-coding RNAs in a breast cancer cell progression model |
6.85 |
|
RNA-seq analysis of human KMT2A rearranged MV4;11 AML cell line treated with DOT1L and/or EZH2 inhibitor |
6.81 |
|
U2AF1 mutations alter splice site recognition in hematological malignancies |
6.76 |
|
ETS1 induction by the omental microenvironment promotes ovarian cancer metastasis |
6.71 |
|
ETS1 induction by the omental microenvironment promotes ovarian cancer metastasis [RNA-Seq] |
6.71 |
|
Epigenome regulation during epidermal lineage commitment |
6.63 |
|
Next Generation Sequencing for Quantitative Analysis of transcriptome of follicular compared to non-follicular CD8 T cells from HIV+ Lymph nodes |
6.57 |
|
Integrative Analysis of Tamoxifen-resistant Cell Line Models Based on Sequencing Genomes, Transcriptomes and Epigenomes |
6.47 |
|
Integrative Analysis of Tamoxifen-resistant Cell Line Models Based on Sequencing Genomes, Transcriptomes and Epigenomes [seq] |
6.47 |
|
Transcriptional profiling of PBMC from patients with aGvHD and patients without aGvHD after alloHSCT |
6.44 |
|
ATXN7L3 And ENY2 Coordinate Activity Of Multiple H2B Deubiquitinases Important For Cellular Proliferation And Tumor Growth [RNA-Seq] |
6.35 |
|
ATXN7L3 And ENY2 Coordinate Activity Of Multiple H2B Deubiquitinases Important For Cellular Proliferation And Tumor Growth |
6.35 |
|
Transcriptome of activated human and mouse MAIT cells |
6.29 |
|
Physiologic expression of Sf3b1K700E causes impaired erythropoieses, aberrant splicing, and sensitivity to pharmacologic spliceosome modulation |
6.22 |
|
β-Caryophyllene Enhances the Transcriptional Upregulation of SREBP-dependent Lipid Biosynthesis in Breast Cancer Cells |
6.11 |
|
CD74 role in transcription regulation |
5.99 |
|
CD74 role in transcription regulation [RNA-seq] |
5.99 |
|
Alterations of the MEK/ERK, BMP, and Wnt/b-catenin pathways detected in the blood of individuals with lymphatic malformations |
5.85 |
|
RNA-sequencing analysis of 5' capped RNAs identifies novel differentially expressed genes in sessile serrated colon polyps (SSPs) |
5.81 |
|
RNA-seq reveals abundant circRNA, lncRNA and mRNA in blood exosomes of patients with colorectal carcinoma |
5.64 |
|
RNA-seq of healthy CD34+ HSPCs after co-culture with myelodyplastic syndrome patient-derived mesenchymal stromal cells |
5.63 |
|
Sirt6 Oncogene Mediates PI3K/Akt Signaling Activation in Diffuse Large B-Cell Lymphoma |
5.43 |
|
KRASG12C inhibition produces a driver-limited state revealing collateral dependencies |
5.35 |
|
Vitamin C Promotes Apoptosis in Breast Cancer Cells by Increasing TRAIL Expression |
5.34 |
|
Reprogramming of human stem cells towards a rejuvenated and transformation-resisting state by recoding a single nucleotide |
5.33 |
|
AR-independent prostate cancer is sustained through FGF signaling |
5.27 |
|
c-Jun promotes cell migration and drives expression of the motility factor ENPP2 in soft tissue sarcomas [RNA-Seq] |
5.2 |
|
c-Jun promotes cell migration and drives expression of the motility factor ENPP2 in soft tissue sarcomas |
5.2 |
|
Regulators of cellular heterogeneity in basal-like breast cancer influence symmetric versus asymmetric division rates (shRNA targeting) |
5.19 |
|
Epigenomes and Transcriptomes of human monocytes from Hyper IgD Syndrome (HIDS) patients |
5.17 |
|
RNAseq of T-ALL upon long non coding rna purturbation |
5.17 |
|
Domain-focused CRISPR-screen identifies HRI as a fetal hemoglobin regulator in human erythroid cells |
5.16 |
|
Identification of Differentially Expressed Splice Variants by the Proteogenomic Pipeline Splicify |
5.07 |
|
GATA2 is Dispensable for Generation of Hemogenic Endothelium But Required for Endothelial-to-Hematopoietic Transition |
5.01 |
|
Abnormal RNA splicing and genomic instability after induction of DNMT3A mutations by CRISPR/Cas9 gene editing |
4.99 |
|
Abnormal RNA splicing and genomic instability after induction of DNMT3A mutations by CRISPR/Cas9 gene editing [RNA-Seq] |
4.99 |
|
Quantitative Proteomics Reveals a Unique Wiring of Signaling Pathways that Protects Human Regulatory T Cell Identity |
4.98 |
|
IMP3 regulated gene expression in breast cancer cells |
4.93 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of UVB(20mJ/cm2 and 40mJ/cm2) exposed and untreated HaCaT keratinocytes Transcriptomes |
4.88 |
|
Parvovirus B19 NS1 protein induces cell cycle arrest at G2 phase |
4.87 |
|
Characterisation of the EZH2 regulated transcriptome in de novo transformed cells (RNA-Seq) |
4.7 |
|
Next Generation Sequencing (RNA-Sequencing) for the analysis of RUNX3 targets in H460, H460-ERT2-RUNX3 WT and H460-ERT2-RUNX3 MT(K94/171R mutation) |
4.58 |
|
Comparative Analysis of the Transcriptome of Latent Autoimmune Diabetes (LADA) Patients from Eastern China |
4.56 |
|
6mer seed toxicity in tumour suppressive microRNAs |
4.55 |
|
Targeting Chromatin Regulators Inhibits Leukemogenic Gene Expression in NPM1 Mutant Leukemia |
4.48 |
|
Mutational landscape of aggressive natural killer-cell leukemia and drug profiling highlight JAK-STAT signaling as a therapeutic target in NK-cell malignancies |
4.33 |
|
Macrophage Ad5f35 PhenoMap |
4.17 |
|
INO80 governs super-enhancer-mediated oncogenic transcription and tumor growth in melanoma [RNA-seq] |
4.15 |
|
INO80 governs super-enhancer-mediated oncogenic transcription and tumor growth in melanoma |
4.15 |
|
Aneuploidy-induced cellular stresses limit autophagic degradation. |
4.13 |
|
Impact on erythroid progenitor type on erythroid differntiation |
4.07 |
|
Zika Virus Has Oncolytic Activity against Glioblastoma Stem Cells |
3.91 |
|
SF3B1 Degron knockdown RNA-seq |
3.85 |
|
Reconstitution of the human pancreatic niche stimulates differentiation of hESCs into beta cells and reveals new signals for pancreatic endocrine cell maturation |
3.76 |
|
Organelle-based therapy for immune mediated disease: mitochondrial transfer elicits Tregs reprogramming |
3.47 |
|
Single Cell Sequencing Reveals Gene Expression Signatures Associated with Bone Marrow Stromal Cell Subpopulations and Time in Culture [NGS_bulk cell RNA-seq] |
3.32 |
|
COMBINING BET AND MEK INHIBITORS SYNERGISTICALLY TARGETS NRAS MUTANT MELANOMA |
3.14 |
|
MALT1 Inhibition Is Efficacious in Both Naïve and Ibrutinib-Resistant Chronic Lymphocytic Leukemia. |
3.09 |
|
Identification of long noncoding RNAs regulated by p53 |
2.99 |
|
RNA-Seq analysis of prostate cancer cell line LNCaP treated with vehicle, androgen, androgen and IMTPPE, androgen and JJ-(+)-450, androgen and JJ-(-)450, androgen and enzalutamide |
2.98 |
|
Dynamic developmental signaling logic underlying lineage bifurcations during human endoderm induction and patterning from pluripotent stem cells |
2.79 |
|
Dynamic developmental signaling logic underlying lineage bifurcations during human endoderm induction and patterning from pluripotent stem cells [Endoderm RNA-seq and ChIP-seq data sets] |
2.79 |
|
A stably self-renewing adult blood-derived induced neural stem cell exhibiting patternability and epigenetic rejuvenation |
2.73 |
|
The RNA-binding protein RBM47 suppresses metastatic breast cancer progression |
2.71 |
|
Analysis of an artificial zinc finger epigenetic modulator: widespread binding but limited regulation |
2.68 |
|
Hepatocyte maturation |
2.55 |
|
Gene expression analysis of CD4+ and CD4- ILC1 subsets by RNAseq |
2.52 |
|
Combined MEKi (GDC-0973) and WNT (G007-LK) treatment in APC and KRAS mutant HCT-15 cell line |
2.39 |
|
ATRX is necessary for cellular senescence and represses HRAS to drive cells from quiescence into senescence |
2.38 |
|
ATRX is necessary for cellular senescence and represses HRAS to drive cells from quiescence into senescence [RNA-Seq] |
2.38 |
|
RNA-seq of CD33 KO and control HSPCs |
2.38 |
|
Transcriptional Profiling of Werner Syndrome (WS) iPSC-derived MSC and the isogenic gene-edited controls |
2.27 |
|
High-throughput RNAi cell viability screen to identify selective targets for EWS-FLI1 positive Ewing sarcoma |
2.19 |
|
Genome-wide RNA deep sequencing of CAL-101 or AKTi primed human T cells in comparison to traditionally expanded T cells |
2.11 |
|
RNA-Seq of SHEP TET21N cells upon Doxorubicin treatment |
2.08 |
|
Gene expression profiling of KSHV-infected periodontal ligament cells |
2.06 |
|
Bromodomain protein BRD4 is required for estrogen receptor-dependent transcription and enhancer activation [RNA-Seq] |
1.93 |
|
Bromodomain protein BRD4 is required for estrogen receptor-dependent transcription and enhancer activation |
1.93 |
|
The mRNA expression analysis of psoriasis skin lesion mesenchymal stem cell |
1.93 |
|
nELAVL HITS-CLIP in Alzheimer's Disease patients |
1.92 |
|
RNA sequencing quantitative analysis of RNA editing levels in ADAR1, ADAR2, AIMP2 overexpression and wild type HEK293 cells |
1.89 |
|
mRNA-sequencing of 293T-no dice transfected with miR-16, miR-214, or KSHV-miR-K6-5p |
1.88 |
|
Pluripotent stem cell models of Blau syndrome reveal an IFN-<gamma>-dependent inflammatory response in macrophages |
1.83 |
|
RNA deep sequencing analysis of human brain microvascular endothelial cells (ECs) treated with glioma-conditioned medium (glioma-CM) |
1.81 |
|
The Regulation of IFN Type I Pathway Related Genes RSAD2 and ETV7 Specifically Indicate Antibody-Mediated Rejection After Kidney Transplantation |
1.81 |
|
Aging-associated patterns in the expression of human endogenous retroviruses |
1.8 |
|
Probing the Global Cellular Responses to Lipotoxicity Caused by Saturated Fatty Acids |
1.77 |
|
6mer seed toxicity in viral microRNAs |
1.77 |
|
A transcriptional regulatory network connects mitochondrial biogenesis and metabolic shift with stem cell commitment to hepatic differentiation |
1.73 |
|
Effect of low-dose sorafenib and alkylating agents in inflammation and angiogenesis in breast cancer |
1.7 |
|
Transcriptome analysis of the HepG2 cells expressing hepatic transcription factors |
1.43 |
|
Transcriptomic analysis of human macrophages in 3D |
1.41 |
|
IL-6 augments IL-4-induced polarization of primary human macrophages through synergy of STAT3, STAT6 and BATF transcription factors |
1.41 |
|
Mutant p63 disrupts the key specification switch from the multipotent cell state to stratified epithelia during epithelial differentiation/in ectodermal dysplasia disorders |
1.31 |
|
Differentiation of Induced Pluripotent Stem Cells towards Mesenchymal Stromal Cells is Hampered by Culture in 3D Hydrogels [RNA-Seq] |
1.27 |
|
Differentiation of Induced Pluripotent Stem Cells towards Mesenchymal Stromal Cells is Hampered by Culture in 3D Hydrogels |
1.27 |
|
Alarmin S100A11 initiates a chemokine response to the human pathogen Toxoplasma gondii |
0.9 |
|
Long noncoding RNA signatures induced by TLR7 and type I IFN signaling in activated human plasmacytoid dendritic cells |
0.84 |
|
lncRNA expression analysis in patients with eosinophilic and neutrophilic asthma |
0.76 |
|
Vammin induces a highly efficient angiogenic response through VEGFR-2/NRP-1 and bypasses the regulatory function of VEGFR-1 |
0.63 |
|
Loss of ANCO1 repression of AIB1/YAP drives breast cancer progression |
0.6 |
|
Gene expression profile of calcified and normal tricuspid aortic valves by RNA sequencing. |
0.54 |
|
Antibiotics induce polarization of pleural macrophages to M2-like phenotype in patients with tuberculous pleuritis |
0.53 |
|
Gene expression profiling of human MSC-educated macrophages vs. classical macrophages from bone marrow and blood |
0.49 |
|
Sex-specific gene expression differences are evident in human embryonic stem cells and during in vitro differentiation of human placental progenitor cells |
0.44 |
|
CRISPR/Cas9 Screens Reveal Epstein-Barr virus Synthetic Lethal Targets |
0.4 |
|
RNA Expression Profile of Calcified Bicuspid, Tricuspid and Normal Human Aortic Valves by RNA Sequencing [TAV] |
0.35 |
|
mRNA sequencing of highly and lowly metastatic human colorectal cancer PDXs |
0.21 |
|
Human pulmonary artery endothelial cells (hPAECs) with downregulated BMPR2 signaling demonstrate a unique gene expression signature after exposure to overexpression of AdAlox5 |
0.14 |
|
The impact of oil spill to lung health – insights from an RNA-seq study of human airway epithelial cells |
0.1 |
|
Cell cycle positioning drives heterogeneity within the pluripotent stem cell compartment |
0.08 |
|
Immunophenotyping and Transcriptomic Outcomes in PDX-Derived TNBC Tissue |
0.04 |