|
Landscape of human mast cell chromatin: a rich resource for identification of novel mediators and genetic drivers of allergic and inflammatory diseases |
49.21 |
|
Transcriptomic profiling of human CD34+ derived mast cells [RNA-Seq] |
49.21 |
|
Transcriptomic profiling of human peripheral blood-derived mast cells |
35.85 |
|
Genome-wide analyses of chromatin state in human mast cells reveal molecular drivers and mediators of allergic and inflammatory diseases |
35.85 |
|
R430: A potent inbibitor of DNA and RNA viruses |
35.82 |
|
RNAseq Analysis in glioblastoma cells treated with Mepazine |
34.41 |
|
SETDB2 links E2A-PBX1 to cell cycle dysregulation in acute leukemia through CDKN2C repression [sequencing] |
30.39 |
|
Differentially expressed genes post knock down of lincDUSP26 |
30.22 |
|
Temporal dynamic reorganization of 3D chromatin in hormone-induced breast cancer and endocrine resistance |
28.52 |
|
Oncogenic MYC induces a dependency on the spliceosome in human cancer |
24.76 |
|
Limiting cholesterol biosynthetic flux engages type I IFN signaling in a STING-dependent manner |
24.69 |
|
RNA Seq analysis of NKX2-5 Null and Het human embryonic stem cells in cardiomyogenesis |
23.8 |
|
Gene activation precedes DNA demethylation in response to infection in human dendritic cells |
21.1 |
|
Gene activation precedes DNA demethylation in response to infection in human dendritic cells |
21.1 |
|
The Notch driven long non-coding RNA repertoire in T-cell acute lymphoblastic leukemia |
20.9 |
|
Transcriptomic of MKD (MUC1 kidney disease) patient compares to normal derived kidney epithelial cells |
20.55 |
|
Low cytosolic folate cycling is a hallmark of U251 glioblastoma cells reprogramming towards pluripotency [RNA-seq] |
20.29 |
|
Low cytosolic folate cycling is a hallmark of U251 glioblastoma cells reprogramming towards pluripotency |
20.29 |
|
Gene expression changes upon drug withdrawal (A375/451Lu cell lines) |
19.71 |
|
A Brain Penetrant Mutant IDH1 Inhibitor Provides In Vivo Survival Benefit |
19.59 |
|
Effects on gene expression of ibrutinib treatment in human stem cells-derived atrial- and ventricular-like cardiomyocytes |
17.32 |
|
Large-Scale Atlas of Mutant IDH1-Dependent Chromatin State Reprogramming, Reversibility, and Persistence [RNA-seq] |
16.45 |
|
Large-Scale Atlas of Mutant IDH1-Dependent Chromatin State Reprogramming, Reversibility, and Persistence |
16.45 |
|
CLIC5: a novel ETV6 target gene in childhood acute lymphoblastic leukemia |
16.21 |
|
ASCL1 mediates neuronal differentiation of primary GBM stem cell cultures upon Notch signalling blockade [RNA-seq] |
15.87 |
|
Distinct Roles of BET Family Members in ERα Enhancer Function and Gene Regulation in Breast Cancer Cells |
15.54 |
|
Distinct Roles of BET Family Members in ERα Enhancer Function and Gene Regulation in Breast Cancer Cells [RNA-seq] |
15.54 |
|
Total RNA-seq in ALL-SIL upon TLX1 knockdown |
15.39 |
|
Major roles of cyclobutane pyrimidine dimers, nucleotide excision repair and ATR in the alternative splicing response to UV irradiation |
15.37 |
|
The RNA binding protein IGF2BP3 promotes hematopoietic progenitor cell proliferation by targeting leukemogenic pathways |
15.28 |
|
Gene expression, methylome and splicing of THP-1 monocytic cells and THP-1-derived macrophage |
15.22 |
|
TRIM28-Regulated Transposon Repression Is Required for Human Germline Competency and Not Primed or Naive Human Pluripotency |
15.13 |
|
The role of CFTR in islet function |
14.42 |
|
Transcriptome analysis of AGS cells infected with Helicobacter pylori P12 |
13.92 |
|
Brain organoids reproducibly generate the cellular diversity of the human cerebral cortex |
13.63 |
|
The Jumonji-domain histone demethylase inhibitor JIB-04 deregulates oncogenic programs and increases DNA damage in Ewing Sarcoma, resulting in impaired cell proliferation and survival, and reduced tumor growth |
13.45 |
|
Maintaining iron homeostasis is the key role of lysosomal acidity for cell proliferation |
12.95 |
|
Neuronal brain region-specific DNA methylation and chromatin accessibility are associated with neuropsychiatric trait heritability [RNA-Seq] |
12.91 |
|
Neuronal brain region-specific DNA methylation and chromatin accessibility are associated with neuropsychiatric trait heritability |
12.91 |
|
Altering cancer transcriptomes using epigenomic inhibitors [RNA-Seq] |
12.7 |
|
Altering cancer transcriptomes using epigenomic inhibitors |
12.7 |
|
Selective suppression of endothelial cytokine production by progesterone receptor [RNA-seq] |
12.53 |
|
Selective suppression of endothelial cytokine production by progesterone receptor |
12.53 |
|
Integration of kinase and calcium signaling at the level of chromatin underlines inducible gene activation in T cells |
12.16 |
|
Receptor tyrosine kinase signaling promotes post-embryonic morphogenesis and survival of glia and neural progenitor cells |
12.11 |
|
ARID1A regulates condensin II distribution and chromosomal partition |
12.07 |
|
ARID1A regulates condensin II distribution and chromosomal partition [RNA-seq] |
12.07 |
|
Toxoplasma gondii infection of human retinal pigment epithelial cells |
11.87 |
|
A549 cell transcriptome responses to infection with H7N9 influenza virus |
11.38 |
|
Gene expression changes caused by KRAS in MCF-10A |
10.97 |
|
RNA sequencing to compare gene expession in control and PF228-treated hepatic stellate cells |
10.87 |
|
Transcriptomic analysis reveals novel long non-coding RNAs critical for vertebrate development |
10.74 |
|
Transcriptomic analysis reveals novel long non-coding RNAs critical for vertebrate development [RNA-Seq] |
10.74 |
|
Effect of OVO-like 1 knockdown on global transcript expression in differentiated BeWo trophoblast cells |
10.74 |
|
Next Generation Sequencing upon siRNA-mediated knockdown of EIF5A in MCF-7 cells. |
10.64 |
|
Global Promotion of Alternative Internal Exon Usage by mRNA 3' End Formation Factors |
10.39 |
|
Global Regulation of Alternative Internal Exon Usage by mRNA 3' End Formation Factors [RNA-Seq] |
10.39 |
|
Identification of global regulators of T-helper cell lineage specification (RNA-Seq) |
9.86 |
|
Identification of global regulators of T-helper cell lineage specification |
9.86 |
|
hiPSCs unravel aberrant TGFβ signaling as an etiology of left ventricular non-compaction |
9.71 |
|
Differentially expressed (DE) genes analysis in synovial fluid mesenchymal stem cells (SF-MSCs), SF-MSC derived iPSCs and iPSC derived MSCs (iPSC-MSCs) |
9.65 |
|
ARID1A is a critical regulator of luminal identity and therapeutic response in oestrogen receptor-positive breast cancer (RNA-Seq) |
9.63 |
|
RNA expression following TMPRSS11B overexpression or depletion |
9.61 |
|
Endometrial epithelial cell transcriptome response to co-culture with adipose stromal cells |
9.47 |
|
Epigenetic reprogramming at estrogen-receptor binding sites alters 3D chromatin landscape in endocrine resistant breast cancer |
9.42 |
|
Epigenetic reprogramming at estrogen-receptor binding sites alters the 3D chromatin landscape in endocrine resistant breast cancer [RNA-seq] |
9.42 |
|
Dual inhibition of HDMX and HDM2 as a Therapeutic Strategy in Leukemia |
9.38 |
|
The Short Isoform of BRD4 Promotes HIV-1 Latency by Engaging Repressive SWI/SNF Chromatin Remodeling Complexes |
9.19 |
|
DHX9 suppresses spurious RNA processing defects originating from the Alu invasion of the human genome [uvCLAP CLIP-seq] |
8.84 |
|
Effect of BET bromodomain inhibition with JQ1 in stressed human derived iPS cardiomyocytes |
8.79 |
|
BET bromodomain inhibition |
8.79 |
|
Deciphering the ‘m6A code’ via quantitative profiling of m6A at single-nucleotide resolution |
8.78 |
|
Deciphering the ‘m6A code’ via quantitative profiling of m6A at single-nucleotide resolution [III] |
8.78 |
|
Loss of Nuclear TDP-43 Is Associated with Decondensation of LINE Retrotransposons [RNA-Seq] |
8.75 |
|
Loss of Nuclear TDP-43 Is Associated with Decondensation of LINE Retrotransposons |
8.75 |
|
A novel Menin-MLL inhibitor induces specific chromatin changes and eradicates disease in models of MLL-rearranged leukemia [RNA-Seq II] |
8.7 |
|
Transcriptome analysis of total RNA in human osteosarcoma cell line U2OS before and after inhibition of zinc finger protein ZNF768 |
8.69 |
|
AMPK signaling for naïve pluripotency [Hs] |
8.67 |
|
AMPK signaling for naïve pluripotency |
8.67 |
|
Prostaglandin E2 inhibits pro-fibrotic function of human pulmonary fibroblasts by disrupting Ca2+-signaling |
8.57 |
|
IL-33 activates tumor stroma to promote intestinal polyposis |
8.49 |
|
Oligogenic inheritance of congenital heart disease involving a NKX2-5 modifier |
8.37 |
|
Oligogenic inheritance of congenital heart disease involving a NKX2-5 modifier [human] |
8.37 |
|
Analyzing the interactions of mRNAs, miRNAs, lncRNAs and circRNAs to predict competing endogenous RNA networks in glioblastoma |
8.3 |
|
Ribosome profiling and RNA sequencing of MCF10A-ER-Src and fibroblast cell transformation |
8.23 |
|
Smad5 acts as an intracellular pH messenger and maintains bioenergetic homoeostasis |
8.22 |
|
Identification of mRNAs with reduced ribosomal loading upon knock-down of translation factor DAP5 from hESCs. |
8.2 |
|
Analysis of regulatory element evolution between human and mouse reveals a lack of cis-trans compensation |
8.19 |
|
A quantitative chemotherapy genetic interaction map identifies new factors associated with PARP inhibitor resistance |
8.15 |
|
The RNA hairpin binder TRIM71 modulates alternative splicing by repressing MBNL1 |
8.05 |
|
The RNA hairpin binder TRIM71 modulates alternative splicing by repressing Mbnl1 [RNA-seq & Ribo-seq] |
8.05 |
|
Single-cell transcription profiling in KS1 patient iPSCs and NPCs |
8.03 |
|
Expression data for KDM1B knockdown in Glioma-Initiating Cells (GICs) |
8.0 |
|
Knockdown of ADNP in HCT116 colon cancer cells |
7.97 |
|
Effect of Toxoplasma gondii efector TgIST on global transcriptome of human foreskin fibroblasts (HFFs) upon type I IFN activation |
7.92 |
|
Identification of IL-27 as potent regulator of inflammatory osteolysis associated with vitamin E-blended ultra-high molecular weight polyethylene debris of orthopedic implants |
7.91 |
|
TFPa/HADHA is required for fatty acid beta-oxidation and cardiolipin re-modeling in human cardiomyocytes |
7.88 |
|
IMP3 regulated gene expression in breast cancer cells |
7.77 |
|
Human iPSC-derived microglia assume a primary microglia-like state after transplantation into the neonatal mouse brain [Single Cell RNAseq] |
7.75 |
|
Transcriptomic characterization of a human in vitro model of arrhythmogenic cardiomyopathy under topological and mechanical stimuli |
7.73 |
|
RNA Sequencing Facilitates Quantitative Analysis of Transcriptomes of H1, H1 derived APLNR+ cells, CD31+CD34+ cells and CD43+ cells during human early hematopoietic differentiation |
7.68 |
|
mRNA sequencing of the global effect of SOX2 on gene expression in hESC and hESC derived NPCs. |
7.64 |
|
The histone H3.3K27M mutation in pediatric glioma reprograms H3K27 methylation and gene expression |
7.64 |
|
Impact of dieldrin on transcription in Jurkat T cells |
7.56 |
|
Transcriptomic analysis of the effect of trastuzumab in human iPSC-CMs |
7.55 |
|
mRNA and miRNA expression in primary human muscle cells treated with 1,25(OH)2D3 or vehicle |
7.5 |
|
RNA expression in primary huamn muscle cells treated with 1,25(OH)2D3 or vehicle |
7.5 |
|
Activation of a SOX2-dependent transcriptional regulatory circuit drives glioblastoma. |
7.48 |
|
RNA-Seq profiling of days 0, 7 and 18 kidney organoids differentiated from three separate vials of starting material |
7.37 |
|
RNA-Seq analysis of human lung fibroblasts exposed to TGF-β |
7.37 |
|
The DNM3OS lncRNA is a reservoir of fibromiRs with major functions in fibroblast response to TGF-beta and fibrogenesis |
7.37 |
|
Deciphering H3K4me3 Broad Domains Associated With Gene Regulatory Networks and Conserved Epigenomic Landscapes in the Human Brain [RNA-Seq] |
7.32 |
|
Deciphering H3K4me3 Broad Domains Associated With Gene Regulatory Networks and Conserved Epigenomic Landscapes in the Human Brain |
7.32 |
|
Transcriptome analysis of H9 hESC derived cerebral organoids |
7.27 |
|
RNA-Sequencing experiment for effects of PKF115-584 treatment on four T-ALL cell lines (RPMI8402, HPB-ALL, Jurkat, CCRF-CEM). |
7.25 |
|
Differential gene expression of static and intermittent compressive force treated human periodontal ligament cells |
7.23 |
|
Cerebellar differentiation in Ataxia-Telangiectasia |
7.17 |
|
Modeling the ESR1 tyrosine 537 mutation with CRISPR-Cas9 for mechanistic studies and evaluation of therapeutic approaches for metastatic breast cancer |
7.14 |
|
Modeling the ESR1 tyrosine 537 mutation with CRISPR-Cas9 for mechanistic studies and evaluation of therapeutic approaches for metastatic breast cancer [RNA-Seq] |
7.14 |
|
Small RNA-seq of human granulosa cells reveals miRNAs in FSHR and aromatase genes |
7.11 |
|
High-throughput RNA sequencing of human preovulatory cumulus and mural granulosa cells (mRNA) |
7.11 |
|
Dynamics of Proteo-Transcriptomic Response to HIV-1 Infection |
7.03 |
|
Transcriptional profiling of LS1034 cells treated with tepoxalin |
6.93 |
|
Genome-wide maps of m6A circRNAs identify widespread and cell-type-specific methylation patterns that are distinct from mRNAs |
6.89 |
|
Gene-Edited Human Kidney Organoids Reveal Mechanisms of Disease in Podocyte Development |
6.88 |
|
NAD+ Analog-sensitive PARPs Reveal a Role for PARP-1 in Transcription Elongation |
6.87 |
|
Tamoxifen Resistance in Breast Cancer is Regulated by the EZH2-ERa-GREB1 Transcriptional Axis |
6.86 |
|
Enriched retinal ganglion cells derived from human embryonic stem cells (RNA-seq) |
6.84 |
|
Global mRNA expression profile in cardiac progenitor cells generated by ISX-9 |
6.82 |
|
Global expression profiles in cardiac progenitor cells generated by ISX-9 |
6.82 |
|
RNA-seq analysis of activated plasmacytoid dendritic cell subsets after viral infection |
6.81 |
|
Codon usage optimization in pluripotent embryonic stem cells [RNA-seq] |
6.8 |
|
Increased Serine and One Carbon Pathway Metabolism by PKCl/i Deficiency Promotes Neuroendocrine Prostate Cancer [RNA-seq] |
6.78 |
|
Increased Serine and One Carbon Pathway Metabolism by PKCl/i Deficiency Promotes Neuroendocrine Prostate Cancer |
6.78 |
|
Global transcript structure resolution of high gene density genomes through multi-platform data integration: Illumina RNA-Seq |
6.77 |
|
Reduced CYFIP1 in human neural progenitors as 15q11.2 deletion model: donor specific dysregulation of schizophrenia/epilepsy genes |
6.69 |
|
Cell Type-Specific Chromatin Signatures Underline Regulatory DNA Elements in Human Induced Pluripotent Stem Cells and Somatic Cells |
6.68 |
|
Estrogen Receptor Beta Impacts Hormone-Induced Alternative mRNA Splicing in Breast Cancer Cells |
6.61 |
|
Effect of ROQUIN2(Y691F) expression on mRNA levels upon BCR stimulation |
6.57 |
|
PNET animal model: new insights (II) |
6.56 |
|
Transcripotome analysis of different locations of hair follicles (bulb, bulge) in androgenetic alopecia |
6.56 |
|
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) |
6.53 |
|
Transcriptional regulation in pluripotent stem cells by Methyl CpG binding protein 2 (MeCP2) |
6.41 |
|
Peptidomimetic blockade of MYB in acute myeloid leukemia |
6.37 |
|
Peptidomimetic blockade of MYB in acute myeloid leukemia [RNA-seq] |
6.37 |
|
ChIP-seq of ER and RUNX2 in MCF7 breast cancer cell lines |
6.37 |
|
Toxoplasma gondii remodels the cis-regulatory landscape of infected human host cells |
6.37 |
|
Toxoplasma gondii remodels the cis-regulatory landscape of infected human host cells [RNA-seq] |
6.37 |
|
Evolved Labels of Placental Invasion in Human and Bovine Endometrial Stroma |
6.35 |
|
The RNA exosome nuclease complex regulates human embryonic stem cell differentiation [RNA-Seq rescue_SS] |
6.3 |
|
RNA-seq analysis of RALD iPSCs after in vitro differentiation |
6.29 |
|
Histone deacetylase inhibition enhances antimicrobial peptide but not inflammatory cytokine expression upon bacterial challenge |
6.19 |
|
Open chromatin mapping identifies transcriptional networks regulating human epididymis epithelial function |
6.15 |
|
Open chromatin mapping identifies transcriptional networks regulating human epididymis epithelial function [Rnase-Seq] |
6.15 |
|
The pause-initiation limit restricts transcription activation in human cells |
6.12 |
|
Reprogramming by de-bookmarking somatic transcriptional program via targeting the BET bromodomains |
6.09 |
|
Networks of cultured iPSC-derived neurons reveal the human synaptic activity-regulated adaptive gene program |
6.07 |
|
Genetic and pharmacological restoration of TET2 function blocks stem cell self-renewal and progression of leukemia |
6.05 |
|
RNA-sequencing of human leukemia cells and mouse hematopoietic progenitors |
6.05 |
|
Vitamin C Promotes Apoptosis in Breast Cancer Cells by Increasing TRAIL Expression |
6.04 |
|
Global Mapping of Human RNA-RNA Interactions |
6.0 |
|
High-efficiency RNA-based reprogramming of human primary fibroblasts |
5.88 |
|
ILF2 Regulates RNA Splicing of DNA Damage Response Genes to Confer Poor Prognosis in 1q21-Amplified Multiple Myeloma |
5.87 |
|
The Promyelocytic Leukemia Zinc Finger Dependent Transcriptome during Human Endometrial Stromal Cell Decidualization |
5.84 |
|
The Molecular Dissection of the Oncogenic Role of ETS1 in the Mesenchymal Subtypes of Head and Neck Squamous Cell Carcinoma [RNA-seq knock-down] |
5.83 |
|
The LRF/ZBTB7A transcription factor is a BCL11A-independent repressor of fetal hemoglobin |
5.82 |
|
A transcriptome-wide divergence in protein translation scales with LIN28B expression |
5.76 |
|
N6-methyladenosine Recruits HNRNPG for Alternative Splicing Regulation |
5.75 |
|
Profiling of gene expression using RNA-Seq in fibroblasts, iPSCs, iPSC-derived neurons and cells overexpressing Onecut transcription factors |
5.75 |
|
Changes in chromatin accessibility and gene expression induced by overexpression of ONECUT transcription factors |
5.75 |
|
Determination of a comprehensive alternative splicing regulatory network and the combinatorial regulation by key factors during Epithelial-to-Mesenchymal Transition [ESRP KD] |
5.73 |
|
Discovery of naturally occurring ESR1 mutations during acquisition of resistance to endocrine therapy in widely used estrogen receptor positive breast cancer cell lines |
5.69 |
|
Discovery of naturally occurring ESR1 mutations during acquisition of resistance to endocrine therapy in widely used estrogen receptor positive breast cancer cell lines [RNA-Seq] |
5.69 |
|
The effect of insulin on mRNA transcription of human pluripotent stem cells |
5.69 |
|
Exercise-induced transcriptome changes in skeletal muscle adapted to aerobic training |
5.65 |
|
The stress granule transcriptome reveals principles of mRNA accumulation in stress granules. |
5.62 |
|
Cancerous inhibitor of PP2A (CIP2A) Constrains Th17 Differentiation by Modulating STAT3 Signaling |
5.62 |
|
The cohesin complex prevents Myc-induced replication stress |
5.61 |
|
Transcriptome profiling of a mouse model of alveolar soft part sarcoma |
5.58 |
|
Global Long Terminal Repeat activation participates in establishing the unique gene expression program of classical Hodgkin Lymphoma [RNA-Seq] |
5.58 |
|
Non-transmissible measles virus vector with segmented RNA genome establishes different types of iPSCs from hematopoietic cells |
5.55 |
|
EZH2 and BCL6 cooperate to assemble CBX8-BCOR Polycomb complex to repress bivalent promoters, mediate germinal center formation and promote lymphomagenesis [RNA-seq] |
5.54 |
|
EZH2 and BCL6 cooperate to assemble CBX8-BCOR Polycomb complex to repress bivalent promoters, mediate germinal center formation and promote lymphomagenesis |
5.54 |
|
Post-transcriptional manipulation of TERC reverses molecular hallmarks of telomere disease |
5.53 |
|
Therapeutic targeting of GCB- and ABC-DLBCLs by rationally designed BCL6 inhibitors |
5.51 |
|
Endogenous interaction profiling identifies DDX5 as an oncogenic coactivator of transcription factor Fra-1 |
5.42 |
|
Endogenous interaction profiling identifies DDX5 as an oncogenic coactivator of transcription factor Fra-1 [RNA-seq] |
5.42 |
|
mRNA-sequencing of breast cancer subtypes and normal tissue |
5.42 |
|
Transcriptome analysis of human embryonic stem cells (hESCs) and human fibroblasts upon rapamycin |
5.35 |
|
Profiling of circular RNAs in gastric cancer tissues and adjacent normal tissues |
5.32 |
|
Differentially expressed vascular development genes for iPSC-ECs from CDI |
5.27 |
|
Distinct roles of cohesin-SA1 and cohesin-SA2 in 3D chromosome organization |
5.25 |
|
Alternative classification of glioblastoma based on BUB1B-inhibition sensitivity |
5.25 |
|
Gene expression analysis in response to hypoxic pathway inhibition |
5.22 |
|
Laminin-guided highly efficient endothelial commitment from human pluripotent stem cells [Bulk RNA-Seq] |
5.21 |
|
Gene expression analysis of the impact of TDP-43 knockout in human cells. |
5.2 |
|
Transcriptomic analysis of inter- and intra-patient variation in human iPSC cardiomyocytes: Platform for precision medicine to predict drug toxicity |
5.17 |
|
RNA-seq analysis reveals profound changes in transcript profiles between siCon- and siH19-transfected EVT cells |
5.16 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of SW480 cells and HPSE-knockdown SW480 cells Transcriptomes |
5.16 |
|
Oncogenic Notch promotes long-range regulatory interactions within hyperconnected 3D cliques [HCC1599_RNA-seq] |
5.16 |
|
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 |
5.15 |
|
Gene expression profiling of iPSC-derived cardiomyocytes with BAG3 mutations |
5.12 |
|
‘Naïve’ ESRRB+ iPSCs with the capacity for rapid neural differentiation |
5.12 |
|
SMN2 splicing modifiers improve motor function and longevity in mice with spinal muscular atrophy |
5.08 |
|
FMRP facilitates the nuclear export of N6-methyladenosine-containing mRNAs |
5.08 |
|
RNA sequencing of heart samples of myotonic dystrophic (DM1) patients |
5.06 |
|
RNA-seq data from human lymphoma cell lines |
5.03 |
|
ChIP-seq and RNA-seq from human lymphoma cell lines |
5.03 |
|
Transcriptome data of temporal and cingulate cortex in the Rett syndrome brain |
5.02 |
|
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] |
4.94 |
|
H3.3K27M cooperates with p53 loss and Pdgfra gain in mouse embryonic neural progenitor cells to induce invasive high-grade gliomas [Human RNA-Seq] |
4.93 |
|
H3.3K27M cooperates with p53 loss and Pdgfra gain in mouse embryonic neural progenitor cells to induce invasive high-grade gliomas |
4.93 |
|
RNA-seq analysis of FET cells treated with RSPO1 or TGFβ1 |
4.9 |
|
MYCL and EP400 are required for Max and MCPyV mediated gene activation |
4.88 |
|
Human cell line and subcutaneous tumor |
4.87 |
|
CD90 Identifies Adventitial Mesenchymal Progenitor Cells in Adult Humans |
4.84 |
|
RNA-seq of UGP2 mutant human embryonic stem cells and in vitro differentiated neural stem cells |
4.84 |
|
Time-course expression data from HEK293∆RAF1:ER cells stimulated with 4OHT and labelled with 4SU |
4.84 |
|
Time-course expression data from HEK293∆RAF1:ER cells stimulated with 4OHT, U0126, CYHX, ActD, EGF, FGF, or IGF and labelled with 4SU |
4.84 |
|
iPSC-Derived Cholangiocytes |
4.83 |
|
SOX21 ensures rostral forebrain identity by suppression of WNT8B during neural regionalization of human embryonic stem cells |
4.81 |
|
RNA-seq of naive and primed ES cells (NHSM) |
4.81 |
|
TGFβ-induced fibroblast activation requires persistent and targeted HDAC-mediated gene repression |
4.78 |
|
Transcriptomic analysis of frontal fibrosing alopecia |
4.77 |
|
Integrated high-throughput screen to identify novel treatment leads for pediatric acute myeloid leukemia (AML) |
4.73 |
|
Transcriptional alteration after ionizing radiation exposure in human fibroblasts, iPSCs and NPCs |
4.73 |
|
circRNA-sequencing |
4.7 |
|
RNAseq of T-ALL upon long non coding rna purturbation |
4.7 |
|
Cooperation between TLX1 and the NUP214-ABL1/STAT5 signaling in T-cell acute lymphoblastic leukemia |
4.68 |
|
Metabolic reprogramming of Kaposi’s sarcoma associated herpes virus infected B-cells in hypoxia |
4.65 |
|
Poly(A)-specific ribonuclease (PARN) mediates 3' end maturation of the telomerase RNA component |
4.64 |
|
Total RNAseq of human putamen and caudate nucleus tissues in healthy control and Bipolar Disorder individuals |
4.64 |
|
RNA expression analysis upon JMJD1C depletion |
4.63 |
|
JMJD1C is required for the survival of acute myeloid leukemia by functioning as a co-activator for key transcription factors |
4.63 |
|
The landscape of alternative splicing in aggressive prostate cancers |
4.61 |
|
SNHG5 siRNA knock down in HCT116 cells |
4.61 |
|
Transcriptomic analysis to functionally map the intrinsically disordered domain of EWS/FLI [Experiment 1] |
4.6 |
|
Gene expression in control and DOCK8 CRISPR KHYG1 NK cells |
4.59 |
|
Transcription factor p63 bookmarks genomic loci in epithelial cells and regulates a subset of target genes during epidermal differentiation through dynamic enhancers (RNA-Seq) |
4.57 |
|
Transcription factor p63 bookmarks genomic loci in epithelial cells and regulates a subset of target genes during epidermal differentiation through dynamic enhancers |
4.57 |
|
The Human Testis Cell Atlas via Single-cell RNA-seq |
4.56 |
|
Characterization of human CDK12 and CDK13 in the regulation of RNA processing |
4.56 |
|
MYOD Gene Expression Regulation during Myogenic Conversion of Fibroblasts |
4.55 |
|
Messenger RNA expression after silencing or inhibition of MEN1in MCF-7 breast cancer cells |
4.51 |
|
TT-seq captures simultaneous activation of eRNAs and promoters during T cell activation |
4.48 |
|
Gene expression in skeletal muscle in older individuals subject to ten days of complete bed rest. |
4.48 |
|
The transition from proliferation to quiescence in glioblastoma stem-like cells requires Ca2+ signaling and mitochondria remodeling |
4.47 |
|
ChIP-seq and RNA-Seq analyses of epithelial and mesenchymal cells - HMLE, N8, N8-CTx |
4.45 |
|
RNA-Seq comparisons of gene expression profiles of epithelial and mesenchymal cells - HMLE, N8, N8-CTx |
4.45 |
|
Trisomy of a ‘Down syndrome critical region’ globally amplifies transcription via HMGN1 overexpression |
4.43 |
|
EWS-Fli and LNC regulated genes in comparison to GFP samples |
4.41 |
|
Zika virus infection reprograms global transcription of host cells to allow sustained infection |
4.41 |
|
Targeted degradation of BRD9 reverses oncogenic gene expression in synovial sarcoma |
4.41 |
|
Targeted degradation of BRD9 reverses oncogenic gene expression in synovial sarcoma [RNA-seq] |
4.41 |
|
Dissecting the dynamics of signaling events in the BMP,WNT and NODAL cascade during self-organized fate patterning in human gastruloids |
4.41 |
|
Epithelial-mesenchymal transition and acquired resistance to ALK inhibitors |
4.4 |
|
Gene expression profiling study by RNA-seq for identifying genes associated with epithelial-mesenchymal transition and acquired resistance to ALK inhibitors |
4.4 |
|
MYC interacts with the G9a histone methyltransferase to drive transcriptional repression and tumorigenesis |
4.39 |
|
Comparison of single-cell transcriptomics quality between unfixed cells and cells that were fixed and mock stained according to the RAID procedure |
4.35 |
|
cKIT+ sorted cells from 57-137 day old fetal testes and ovaries |
4.28 |
|
RNA-Seq of cKIT+ sorted cells from 53-137 day old fetal testes and ovaries and RNA-Seq of TRA-1-81+ H1 and UCLA1 hESCs. |
4.28 |
|
ICE1 promotes the link between splicing and nonsense-mediated mRNA decay |
4.26 |
|
Selective roles of vertebrate PCF11 in premature and full-length transcript termination (chromatin-bound RNA-seq) |
4.25 |
|
The age and genomic integrity of neurons after cortical stroke in humans |
4.22 |
|
RNA-sequencing analysis for gene expression profiles affected by CASC9 knockdown |
4.15 |
|
COMBINING BET AND MEK INHIBITORS SYNERGISTICALLY TARGETS NRAS MUTANT MELANOMA |
4.13 |
|
MYOD Remodeling of the Genome Architecture during Myogenic Conversion of Somatic Cells |
4.12 |
|
Chromatin Topology Reorganization and Transcription Repression by PML/RARα in Acute Promyeloid Leukemia (RNA-seq) |
4.12 |
|
Chromatin Topology Reorganization and Transcription Repression by PML/RARα in Acute Promyeloid Leukemia |
4.12 |
|
Distinct and shared functions of ALS-associated TDP-43, FUS, and TAF15 revealed by comprehensive multi-system integrative analyses [RNA-Seq_human] |
4.1 |
|
Global analysis of alternative splicing regulated by RBM10 |
4.09 |
|
Gene expression in GBM with Cav3.2 inhibition |
4.06 |
|
The RNA helicase DDX6 regulates self-renewal and differentiation of human and mouse stem cells [RNA-seq2] |
4.05 |
|
Critical role of transient activation of human endogenous retroviruses during reprogramming toward pluripotency |
4.05 |
|
Critical role of transient activation of human endogenous retroviruses during reprogramming toward pluripotency (RNA-Seq) |
4.05 |
|
Whole-transcriptome profilings between a pair of HCA7-derived KRAS-wildtype cetuximab sensitive and resistant colon cancer cells from 3D culture |
4.03 |
|
The translation termination factor GSPT1 is a phenotypically relevant off-target of heterobifunctional phthalimide degraders |
4.03 |
|
RNA-seq of YB5 cells treated with Proscillaridin A |
4.03 |
|
Conserved roles for murine mDUX and human DUX4 in activating cleavage stage genes and MERVL/HERVL retrotransposons [RNA-Seq Human] |
3.98 |
|
RNA-Seq from early time points in the kidney differentiation protocol |
3.97 |
|
Assessing the effect of SUPT4H1 RNAi on the transcription of a repeat-containing reporter construct |
3.96 |
|
Cap-specific terminal N6-methylation of RNA by an RNA polymerase II-associated methyltransferase. |
3.95 |
|
Next Generation Sequencing Study of Circadian Changes in Transcriptome of Human Pineal Gland |
3.94 |
|
POU2AF1 Functions in the Human Airway Epithelium to Regulate Expression of Host Defense Genes |
3.93 |
|
POU2AF1 Functions in the Human Airway Epithelium to Regulate Expression of Host Defense Genes [RNA-Seq] |
3.93 |
|
Derivation of kidney organoids from human pluripotent stem cells [RNA-Seq: Data Set 2] |
3.86 |
|
Small molecule targets TMED9, promotes lysosomal degradation to reverse proteinopathy |
3.78 |
|
AKAP8 inhibits tumor metastasis by antagonizing EMT-associated RNA alternative splicing |
3.77 |
|
Effect of disulfiram treatment on pediatric high grade glioma |
3.73 |
|
Role of BET proteins in YAP/TAZ-dependent transcription [RNA-seq 1] |
3.72 |
|
circRNA profile in hypopharyngeal cancer |
3.68 |
|
SREBP1 drives Keratin 80-dependent cytoskeletal changes and invasive behavior in endocrine resistant ERα breast cancer |
3.68 |
|
mTORC1 balances cellular amino acid supply with demand for protein synthesis through post-transcriptional control of ATF4 |
3.62 |
|
Functional studies of missense TREM2 mutations in human stem cell-derived microglia |
3.62 |
|
PGE2 mediated gene expression changes in human cervical stromal cells |
3.61 |
|
Transcriptomic Profiling of Posterior Polymorphous Corneal Dystrophy |
3.59 |
|
Expression data for hiPSC-derived RPE treated with 10mM Nicotinamide or vehicle |
3.59 |
|
Disease Model of GATA4 Mutation Reveals Transcription Factor Cooperativity in Human Cardiogenesis [RNA-Seq] |
3.55 |
|
Disease Model of GATA4 Mutation Reveals Transcription Factor Cooperativity in Human Cardiogenesis |
3.55 |
|
RNA-sequencing of the brain transcriptome implicates dysregulation of neuroplasticity, circadian rhythms, and GTPase binding in bipolar disorder |
3.54 |
|
Stimulation of isolated plasmacytoid dendritic cells (pDCs) with TLR9 agonist CpG C (CpG) and TLR7 agonist imiquimod (IMQ) |
3.51 |
|
MPTAC determines APP fragmentation via sensing sulfur amino acid catabolism |
3.48 |
|
Characterization of human mosaic Rett syndrome brain tissue by single-nucleus RNA sequencing (Total RNA sequencing) |
3.48 |
|
Circular RNAs are super abundant in cervical tumor and plasma detected by high throughput microarray |
3.45 |
|
Circular RNAs are super abundant in cervical tumor and plasma detected by high throughput microarray [RNA-Seq] |
3.45 |
|
Transcriptome profile of HepG2-expressing ATP7B-H1069Q (liver hepatocellular cells) exposed to JNK or p38 Inhibitor |
3.45 |
|
JAK2 is dispensable for maintenance of JAK2 mutant B-cell acute lymphoblastic leukemias |
3.38 |
|
Comparative gene expression profiling of MHH-CALL4 cells subject to pharmacological JAK2 inhibitor treatment (ruxolitinib or CHZ868) or shRNA-mediated JAK2 depletion in vitro |
3.38 |
|
Lentiviral CRISPR Epigenome Editing of Inflammatory Receptors as a Gene Therapy Strategy for Disc Degeneration |
3.38 |
|
Conserved roles for murine mDUX and human DUX4 in activating cleavage stage genes and MERVL/HERVL retrotransposons [RNA-Seq] |
3.36 |
|
Functional Cardiac Fibroblasts Derived from Human Pluripotent Stem Cells via Second Heart Field Progenitors |
3.33 |
|
Noncoding regions are the main source of targetable tumor-specific antigens |
3.32 |
|
Improved genome-wide mapping of uncapped and cleaved transcripts in eukaryotes—GMUCT 2.0 |
3.31 |
|
Complete deconvolution of cellular mixtures based on linearity of transcriptional signatures |
3.31 |
|
High-throughput RNA sequencing on circular RNA profiles of human triple-negative breast cancer and adjacent normal tissues |
3.3 |
|
Genome-wide maps of chromatin state and mRNA expression patterns in leukemic cell lines |
3.24 |
|
RNA-seq of SOX5 overexpressing primary human neuronal progenitors |
3.23 |
|
RNA seq comparison between scrambled and shGRP78 cells |
3.22 |
|
Investigation about fibroblasts of different origins in culture |
3.21 |
|
Impeding transcription of expanded microsatellite repeats by deactivated Cas9 |
3.2 |
|
PolyA-sequencing in IMR-32 cells treated with THZ531 or DMSO |
3.17 |
|
Epigenome Editing by a CRISPR/Cas9-Based Acetyltransferase Activates Genes from Promoters and Enhancers |
3.15 |
|
A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab [ribosome profiling] |
3.14 |
|
Pseudouridylation of tRNA-derived fragments steers translation control in stem cells [Polysome-Seq] |
3.14 |
|
The oncogenic BRD4-NUT chromatin regulator drives aberrant transcription within large topological domains |
3.14 |
|
Recovery and analysis of nascent RNA |
3.14 |
|
RBM25 is a global splicing factor promoting inclusion of alternatively spliced exons |
3.12 |
|
Transcriptome of human white and brown adipose tissue biopsies |
3.09 |
|
Grainyhead-like 2 is essential for androgen receptor expression and activity in prostate cancer |
3.07 |
|
Grainyhead-like 2 is essential for androgen receptor expression and activity in prostate cancer (RNA-seq) |
3.07 |
|
α Cell Function and Gene Expression Are Compromised in Type 1 Diabetes |
3.06 |
|
ETS family proteins bind glucocorticoid receptor: relevance for treatment of Ewing sarcoma |
3.06 |
|
Analysis of transcriptome changes following SOX2 knockdown in three different Ewing sarcoma cell lines |
3.04 |
|
Mitochondrial phosphoenolpyruvate carboxykinase (PCK2) regulates metabolic adaptation and glucose-independent tumor cell growth |
3.01 |
|
CHD1 loss sensitizes prostate cancer to DNA damaging therapy by promoting error-prone double-strand break repair |
3.01 |
|
RNA sequencing analysis of triple cytokine-captured human CD4 T cells |
3.01 |
|
Single-cell transcriptome of human epithelial cells reveals novel insights into early innate immune responses to influenza virus and viral antagonism |
2.9 |
|
Dioxin and AHR impairs mesoderm gene expression and cardiac differentiation in human embryonic stem cells |
2.88 |
|
Dioxin and AHR impairs mesoderm gene expression and cardiac differentiation in human embryonic stem cells (RNA-Seq) |
2.88 |
|
Expression analysis of PC3 cells treated with scramble AON or AON directed against MBNL1 |
2.87 |
|
Global Bidirectional Transcription of the Epstein-Barr Virus Genome During Reactivation |
2.84 |
|
Priming mobilization of hair follicle stem cells triggers permanent loss of regeneration after alkylating chemotherapy |
2.81 |
|
Dissecting cell composition and cell-cell interaction network of human disease heart tissue by single-cell sequencing |
2.8 |
|
Transcriptional profiling of JEG3 cells with HLA-G ablation via deletion of Enhancer L |
2.73 |
|
Steroid Receptor Coactivator-2 Regulated Transcriptome in Human Endometrial Stromal Cells |
2.71 |
|
RNA Sequencing of Human iPS derived Cardiomyocytes |
2.69 |
|
|
2.66 |
|
C9/ALS Human Embryonic Stem Cells and C9/ALS Induced Pluripotent Stem Cells |
2.65 |
|
Functional Comparison of the HGF/Met and MSP/Ron Systems in a Pancreatic Cancer Model |
2.64 |
|
Effect of venetoclax, tedizolid, and combination treatment on gene expression in a venetoclax-resistant AML cell line |
2.6 |
|
Dilated cardiomyopathy vs Myocarditis |
2.53 |
|
Single-Cell RNA Sequencing Reveals Metallothionein Heterogeneity during hESC Differentiation to Definitive Endoderm [RNA-Seq] |
2.52 |
|
PER2 synchronizes mitotic expansion and decidual transformation of human endometrial stromal cells |
2.47 |
|
Regulation of DNA methylation landscape in human somatic cell reprogramming by miR-29 family (RNA-seq) |
2.45 |
|
Regulation of DNA methylation landscape in human somatic cell reprogramming by miR-29 family |
2.45 |
|
Single Cell RNA-sequencing of cell types isolated by FACS from normal human prostates |
2.45 |
|
PolyA+ RNA-seq in ALL-SIL upon TLX1 knockdown |
2.45 |
|
Elongation Factor TFIIS Prevents Transcription Stress and R-Loop Accumulation to Maintain Genome Stability [ RNA-seq] |
2.45 |
|
Elongation Factor TFIIS Prevents Transcription Stress and R-Loop Accumulation to Maintain Genome Stability |
2.45 |
|
Single Cell RNASeq profiling of stromal vascular fraction from Subcutaneous and visceral adipose tissue |
2.42 |
|
Transcriptome Analysis of CircMRPS35 mediated mRNA expression profiles |
2.41 |
|
An epigenetic mark of polycomb response elements implemented by Trx/MLL/COMPASS |
2.39 |
|
Transcriptome analysis reveals determinant stages controlling human embryonic stem cell commitment to neuronal cells |
2.35 |
|
Identification of expressed and conserved human non-coding RNAs |
2.3 |
|
RNA Missplicing in Fuchs Endothelial Corneal Dystrophy |
2.2 |
|
Gene expression profile of human iPSC-derived nephron progenitor cells |
2.18 |
|
Low H3K27me3 and DNA hypomethylation define poorly prognostic pediatric posterior fossa ependymomas |
2.17 |
|
THZ1 targeting CDK7 suppresses STAT transcriptional activity and sensitizes T-cell lymphomas to BCL2 inhibitors |
2.15 |
|
Transcriptomic analysis of human neural progenitor cells differentiation into astrocytes |
2.15 |
|
Oncogenic roles of ARID5B in T-ALL |
2.15 |
|
RNA-seq analysis in knockdown Jurkat samples for each factor of TAL1 complex |
2.15 |
|
Inactivation of CFTR by CRISPR/Cas9 alters transcriptional regulation of inflammatory pathways and other networks |
2.13 |
|
A single-cell atlas of the human cortex reveals drivers of transcriptional changes in Alzheimer’s disease in specific cell subpopulations |
2.12 |
|
Time series total RNA sequencing of a differentiation of human embryonic stem cells towards trophoblast lineage |
2.08 |
|
Cell cycle positioning drives heterogeneity within the pluripotent stem cell compartment |
2.08 |
|
RNA-Seq of human induced pluripotent stem cell-derived cardiomyocytes from a cardiomyopathy patient and familial control |
2.06 |
|
pSILAC mass spectrometry reveals ZFP91 as novel IMiD dependent substrate of the CRL4CRBN ligase |
2.06 |
|
Next Generation Sequencing upon siRNA-mediated knockdown of DRAIC in MCF-7 cells. |
2.01 |
|
Stage-specific regulation of the WNT/β-catenin pathway enhances differentiation of hESCs into hepatocytes |
2.01 |
|
Tissue-resident memory T cells mediate immune homeostasis in the human pancreas through the PD-1/PD-L1 pathway |
2.01 |
|
Differential effects of estrogen receptor beta isoforms on glioblastoma progression |
1.95 |
|
Gene expression profiles of ibrutinib-responsive and ibrutinib non-responsive cells in ERBB4 expressing cancer cell lines |
1.95 |
|
Regulation of Cell Cycle to Stimulate Adult Cardiomyocyte Proliferation and Cardiac Regeneration |
1.93 |
|
Induction of Cardiomyocyte Proliferation [pz-822_human] |
1.93 |
|
Global transcriptome analysis in the MYCN-amplified neuroblastoma cell line IMR5-75 upon inducible MYCN-knockdown |
1.93 |
|
Transcriptome-wide analysis links the short-term expression of the b isoforms of T-cell intracellular antigens to protective proteostasis-mediated survival and quiescence |
1.92 |
|
Disease modelling of core pre-mRNA splicing factor haploinsufficiency |
1.89 |
|
SEUSS: A scalable screening platform to assess transcriptomic and fitness effects of transcription factor overexpression |
1.89 |
|
UTX and 53BP1 co-regulate genetic programs for neural differentiation of human embryonic stem cells [RNA-seq] |
1.88 |
|
UTX and 53BP1 co-regulate genetic programs for neural differentiation of human embryonic stem cells |
1.88 |
|
RNA-seq of HEK293T cells overexpressing TET1-FL or TET1-ALT |
1.87 |
|
Small molecule inhibition of ERK dimerization prevents tumorigenesis by Ras-ERK pathway oncogenes |
1.85 |
|
MHC Transcriptomic landscape at haplotype-specific resolution |
1.85 |
|
Profiles of ribosome-associated mRNAs regulated by expression of wild-type (WT) or R534H variant of DDX3 with or without Sodium Arsenite treatment |
1.82 |
|
Total RNA profiles associated with DDX3 wild-type (WT) or R534H variant expression with or without sodium arsenite treatment [RNA-seq] |
1.82 |
|
hESC neural differentiation |
1.81 |
|
RNA-seq analysis of gene expression patterns during hESC neural differentiation |
1.81 |
|
Direct interaction of MYCN and p53 regulate transcriptional responses in neuroblastoma [RNA-Seq] |
1.75 |
|
Direct interaction of MYCN and p53 regulate transcriptional responses in neuroblastoma |
1.75 |
|
Single cell transcriptome of peritoneal cells |
1.75 |
|
The transcriptome of Kawasaki Disease arteritis |
1.75 |
|
Effect of ILF3 depletion in HeLa cells on RNA steady state levels |
1.73 |
|
Transcriptional changes after overexpression of proliferation drivers in human mammary epithelial cells. |
1.72 |
|
Real-time observation of light-controlled transcription in living cells |
1.72 |
|
Dissecting cell composition and cell-cell interaction network of normal human heart tissue by single-cell sequencing |
1.71 |
|
RNAseq in Alzheimer's Disease patients |
1.7 |
|
Global gene expression analysis of human monocyte-derived dendritic cells (DCs) treated with HMGN1 (N1) and R848 alone or in combination. |
1.7 |
|
SOX11 knockdown in B-ALL cell lines |
1.69 |
|
BI Human Reference Epigenome Mapping Project |
1.65 |
|
Early transcriptome profiling of microRNA-mediated neuronal reprogramming [RNA-seq timecourse] |
1.65 |
|
Co-Stimulation–Induced AP-1 Activity is Required for Chromatin Opening During T Cell Activation. |
1.61 |
|
Co-Stimulation–Induced AP-1 Activity is Required for Chromatin Opening During T Cell Activation [RNA-seq] |
1.61 |
|
RNA-seq analysis of control and Myc-induced U2OS cells |
1.59 |
|
Transcriptional profiling identifies differential expression of long non-coding RNAs in Jo-1 associated and inclusion body myositis |
1.58 |
|
Alarmin S100A11 initiates a chemokine response to the human pathogen Toxoplasma gondii |
1.57 |
|
Distinct Pathological Signatures in Human Cellular Models of Myotonic Dystrophy Subtypes |
1.57 |
|
SLAM-seq for K562 endogenous mRNA decay |
1.56 |
|
The dynamic landscape of coding and non-coding RNAs in the innate immune response to microbial pathogens |
1.52 |
|
DECIDUALIZATION INDUCES A SECRETOME SWITCH IN THE PERIVASCULAR NICHE CELLS OF THE HUMAN ENDOMETRIUM |
1.52 |
|
Genome-scale screens identify JNK/JUN signaling as a barrier for pluripotency exit and endoderm differentiation |
1.5 |
|
Germline NLRP1 mutations cause skin inflammatory and cancer susceptibility syndromes via inflammasome activation |
1.49 |
|
Uridylation-mediated RNA quality control pathway in mammalian cytoplasm [RNA-Seq] |
1.46 |
|
TUT-DIS3L2 is a mammalian surveillance pathway for aberrant structured non-coding RNAs. |
1.46 |
|
Re-Wiring 3D Nuclear Architecture by a Single Transcription Factor during Somatic Cell Reprogramming |
1.43 |
|
Stranded RNA-seq were performed on total RNA following ribosomal RNAs depletion (Ribo-zero removal kit, illumina) for 3 brain , 8 IDHwt and 5 IDHmut glioma samples. |
1.43 |
|
Self-associated molecular patterns mediate cancer immune evasion by engagement of Siglec receptors |
1.4 |
|
Activity-dependent transcriptional changes in human neurons |
1.39 |
|
Tunable protein synthesis by transcript isoforms in human cells (Transcript Isoforms in Polysomes sequencing: TrIP-seq) |
1.34 |
|
Characterizing the contrasting roles of JMJD3 and UTX histone demethylases in T cell acute lymphoblastic leukemia [GSKJ4_RNA-seq] |
1.27 |
|
Global unleashing of transcription elongation waves in response to genotoxic stress restricts somatic mutation rate |
1.22 |
|
The antineoplastic drug, trastuzumab, dysregulates metabolism in iPSC derived cardiomyocytes. |
1.2 |
|
Sodium butyrate ameliorates aSyn-induced transcription deregulation and DNA damage |
1.14 |
|
Effect of hyper-and hypoactivation of Notch signaling in IL-4-stimulate THP-1 |
1.12 |
|
Transcriptome analysis of human cumulus cells reveals hypoxia as the main determinant of follicular senescence. |
1.08 |
|
The human cellular nucleic acid binding protien binds G-rich elements close to translation initiation sires and promotes translation. [RNA-Seq] |
1.06 |
|
The human cellular nucleic acid binding protien binds G-rich elements close to translation initiation sires and promotes translation. |
1.06 |
|
Ex vivo Dynamics of Human Glioblastoma Cells in a Microvasculature-on-a-Chip System Correlates with Tumor Heterogeneity and Subtypes |
1.04 |
|
Muscle transcriptome analysis following Total Knee Arthroplasty with Tourniquet |
1.03 |
|
Dynamic 3D chromosomal landscapes in acute leukemia |
0.98 |
|
Dynamic 3D chromosomal landscapes in acute leukemia [RNA-Seq] |
0.98 |
|
RNA sequencing to study transcriptomic changes in DLD-1 (colorectal adenocarcinoma) cells exposed to soft polyacrylamide matrices (~2 kPa and ~55 kPa) for short time scale of 90 minutes |
0.96 |
|
Dissecting neural differentiation regulatory networks through epigenetic footprinting |
0.95 |
|
Transcriptomic analysis to underly the heterogeneity between 4 cellular models derived from patients diagnosed with pediatric high-grade gliomas under controlled atmosphere (modulation of oxygen level). |
0.92 |
|
Single-cell analysis of adult human ovary using 10X genomics |
0.86 |
|
GLIS3 Transcriptionally Activates WNT Genes to Promote Differentiation of Human Embryonic Stem Cells to Posterior Neural Progenitors |
0.77 |
|
Single-cell survey of human lymphatics unveils marked endothelial cell heterogeneity and mechanisms of homing for neutrophils |
0.76 |
|
Increased Neanderthal ancestry in genomic regions associated with lipid catabolism in contemporary Europeans |
0.73 |
|
The WNT target SP5 negatively regulates WNT transcriptional programs in human pluripotent stem cells |
0.7 |
|
Expanding the Nucleoside Recoding Toolkit: Revealing RNA Population Dynamics with 6-thioguanisine |
0.69 |
|
Gene expression profiling of neural crest progenitor cultures derived from human embryonic stem cells carrying nonsense mutations in the Polycomb gene ASXL1 |
0.68 |
|
Transcriptome sequencing reveals aberrant alternative splicing in Huntington's disease |
0.66 |
|
Azithromycin induces epidermal differentiation and multivesicular bodies in airway epithelia |
0.66 |
|
KANK1 inhibits cell growth by inducing apoptosis though regulating CXXC5 in human malignant peripheral nerve sheath tumors |
0.65 |
|
Modeling Human Cancer-induced Cachexia (Human) |
0.64 |
|
Neurotrophic Tyrosine Kinase Receptor 1 is Epigenetically Regulated by IL-13 and Contributes to Allergic Inflammation |
0.61 |
|
The contribution of Alu exons to the human proteome |
0.6 |
|
High-throughput RNAi cell viability screen to identify selective targets for EWS-FLI1 positive Ewing sarcoma |
0.59 |
|
Splicing towards noncoding isoforms in colorectal carcinoma is associated with tumor hypoxia and the DNA damage response |
0.59 |
|
Patient-derived xenograft platform for metastatic melanoma: a model for studying resistance to targeted therapy. |
0.56 |
|
C19ORF66 broadly escapes viral-induced endonuclease cleavage and restricts Kaposi’s Sarcoma Associated Herpesvirus (KSHV) |
0.55 |
|
RNA-seq of three Ewing sarcoma cell lines (A673, SK-N-MC, RDES), transfected with either siControl or siMYBL2. |
0.55 |
|
Cooperation of dominant oncogenes with regulatory variants shapes clinical outcomes in pediatric cancer |
0.55 |
|
Mapping interactions for the TNIP2 hub protein |
0.55 |
|
Genome-wide maps of H3K36me3 in ccRCC and RNA-seq of matched nephrectomy samples |
0.51 |
|
RNA sequencing of matched nephrectomy samples [RNA-seq] |
0.51 |
|
Human ovarian granulosa cell transcriptome |
0.51 |
|
Altered expression of signaling pathways regulating neuronal excitability in hippocampal tissue of temporal lobe epilepsy patients with low and high seizure frequency |
0.51 |
|
Effects of a nutritional supplement in older individuals subject to ten days of complete bed rest. |
0.5 |
|
Effect of Ro 08-2750 treatment on gene expression of human leukemia cell lines MOLM13 and K562 |
0.47 |
|
Unbiased identification of trans regulators of ADAR and A-to-I RNA editing |
0.47 |
|
Identification of trans regulators of ADAR and A-to-I RNA editing using RNA-seq |
0.47 |
|
Transcriptome profiling of H1-iCas9 cells grown on laminin and on MEFs |
0.42 |
|
An electrical pulse stimulation protocol to study acute epigenetic response to muscle cell contraction uncovers acute hydroxymethylation of the exercise-responsive gene Nr4a3 |
0.42 |
|
An electrical pulse stimulation protocol to study acute epigenetic response to muscle cell contraction uncovers acute hydroxymethylation of the exercise-responsive gene Nr4a3 [RNA-Seq] |
0.42 |
|
Identification of long noncoding RNAs in T-ALL cell lines |
0.38 |
|
Functional genomic analysis of the haploinsufficient tumor suppressor, CUX1 |
0.37 |
|
Novel kinase fusion oncogenes in post-Chernobyl radiation-induced pediatric thyroid cancers |
0.36 |
|
Arnica montana stimulates extracellular matrix gene expression in human macrophages differentiated to wound-healing phenotype. |
0.35 |
|
DNA Methylation Reprograms Metabolic Gene Expression in End-Stage Human Heart Failure |
0.35 |
|
WNT signaling memory is required for ACTIVIN to function as a morphogen |
0.34 |
|
FTSEC cells (FT190 and FT194 cell lines) transduced with shRNA to knockdown RNF20 or with control shRNA |
0.23 |
|
Gene expression profile in FTSEC cells (FT190 and FT194 cell lines) transduced with shRNA to knockdown RNF20 or with control shRNA using RNA-seq. |
0.23 |
|
Transcriptional landscape changes during human embryonic stem cell derivation |
0.22 |
|
LncPRESS1 is a p53-regulated lncRNA that safeguards pluripotency by disrupting SIRT6 mediated de-acetylation of histone H3K56 |
0.19 |
|
Human Embryoid Body Transcriptomes Reveal Maturation Differences Influenced by Size and Formation in Custom Microarrays |
0.18 |
|
Genome-wide search for differentially expressed RNAs responsible for the effects induced by Ebola virus replication and transcription |
0.16 |
|
RNAseq of CCRF-CEM, a T-cell acute lymphoblastic leukemia cell line, after knockdown with 2 control hairpins and 6 hairpins targeting the PRC2 complex. |
0.12 |
|
RNA-sequencing of pediatric idiopathic dilated cardiomyopathy patients and healthy controls |
0.11 |
|
Preclinical model of obesity and ER-positive breast cancer |
0.1 |
|
RNA-Seq identifies condition-specific biological signatures of ischemia-reperfusion injury in the human kidney |
0.1 |
|
CD133hi, Notchhi, DP (double positive) and DN (double negative) in GBML8 and GBML20, both patient-derived glioblastoma tumorsphere cultures |
0.09 |
|
Molecular mechanism underlying increased ischemic damage in the ALDH2*2 genetic polymorphism using a human iPSC model system |
0.09 |
|
KSDM1b Role in Ewing Sarcoma |
0.06 |
|
NSD2 overexpression links drives clustered chromatin and transcriptional changes in a subset of insulated domains of insulated domains |
0.05 |
|
The Small Molecule ISRIB Reverses the Effects of eIF2α Phosphorylation on Translation and Stress Granule Assembly |
0.04 |
|
The multiple myeloma risk allele at 5q15 lowers ELL2 expression and increases ribosomal gene expression [ELL2 rescue] |
0.03 |
|
Differential gene expressions in the heart of hypertrophic cardiomyopathy patients |
0.03 |
|
LINE-2 transposable elements are a source of functional human microRNAs and target sites |
0.02 |
|
Modulation of nonsense-mediated decay by rapamycin |
0.01 |
|
Whole transcriptome sequencing of the human thyroid primary cells with knock-down of the NRG1 gene |
0.01 |