|
Uridylation by TUT4 and TUT7 marks mRNA for degradation |
136.62 |
|
RUNX1 contributes to higher-order chromatin organization and gene regulation in breast cancer cells. |
113.69 |
|
Genome-wide MAF1-dependent regulation of RNA polymerase III transcription [RNA-Seq] |
104.0 |
|
Genome-wide MAF1-dependent regulation of RNA polymerase III transcription |
104.0 |
|
ncRNA (non-coding RNA) signature in endothelial cells during hypoxia |
97.57 |
|
ncRNA (non-coding RNA) signature in endothelial cells during hypoxia [RNA-seq] |
97.57 |
|
ARID1A and PI3-Kinase pathway mutations in the endometrium drive epithelial transdifferentiation and collective invasion |
95.11 |
|
Studying the selectivity of a small molecule Synucleozid on transcriptome |
94.67 |
|
Gene expression profiles of primary human NK cells before and after expansion on CSTX002 feeder cells, with and without IL-21 stimulation |
93.37 |
|
Impact of dieldrin on transcription in Jurkat T cells |
92.31 |
|
Targeted inhibition of STAT/TET1 axis as a potent therapeutic strategy for acute myeloid leukemia |
92.19 |
|
Triplet nucleotide repeat-based siRNAs are highly toxic to cancer cells |
91.89 |
|
Integrator complex regulates NELF-mediated RNA Polymerase II pause/release and processivity at coding genes. |
79.49 |
|
Integrator complex regulates NELF-mediated RNA Polymerase II pause/release and processivity at coding genes [RNA-seq] |
79.49 |
|
Circular RNAs are super abundant in cervical tumor and plasma detected by high throughput microarray [RNA-Seq] |
78.31 |
|
Circular RNAs are super abundant in cervical tumor and plasma detected by high throughput microarray |
78.31 |
|
Efficient and quantitative high-throughput tRNA sequencing |
77.63 |
|
Gene target specificity of the Super Elongation Complex (SEC) family: How HIV-1 Tat employs selected SEC members to activate viral transcription |
72.44 |
|
Gene expression changes caused by KRAS in MCF-10A |
71.55 |
|
Ribosome profiling of A549 cells depleted of RPLP1 and RPLP2 and infected with DENV. |
67.56 |
|
Zika infected neural stem cells |
67.31 |
|
Transcriptome analysis of Zika infected neural stem cells |
67.31 |
|
Characterizing the contrasting roles of JMJD3 and UTX histone demethylases in T cell acute lymphoblastic leukemia [short_hairpins_RNA-seq] |
65.41 |
|
High-throughput RNA sequencing on circular RNA profiles of human triple-negative breast cancer and adjacent normal tissues |
64.9 |
|
MYCi361 regulates MYC target genes |
64.39 |
|
Human TFIIH kinase CDK7 regulates transcription-associated epigenetic modification |
64.38 |
|
Gene expression data from IMR90 control, IMR90 shRRM2 and shRRM2/shp16 |
63.9 |
|
LMO1 Synergizes with MYCN to Promotes Neuroblastoma Initiation and Metastasis |
62.7 |
|
STVI-120 Induction of differentiation in human epidermal stem cells followed by differential splicing analysis |
59.05 |
|
Single-nucleotide-resolution mapping of HBV promoters using CAGE |
58.43 |
|
Next generation sequencing identifies discrete classes of box C/D snoRNAs featuring different ends and RNA binding protein dependency |
57.82 |
|
Tracking distinct RNA populations using efficient and reversible covalent chemistry |
56.53 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of HIV-1 Latency in Central Memory T Cells |
56.32 |
|
Effect of BCL11B overexpression on transcriptome of T-cell acute lymphoblastic leukemia (T-ALL) cells |
55.64 |
|
Contribution of SRF and Nkx2-5 to androgen-dependent gene expression in prostate cancer |
51.55 |
|
CD95L derived si- and shRNAs and the CD95L mRNA kill cancer cells through an RNAi mechanism by targeting survival genes [siL3.RNAseq.lg] |
50.25 |
|
Expression and functions of long noncoding RNAs during human T helper cell differentiation |
49.53 |
|
Activation of the p53 transcriptional program sensitizes cancer cells to Cdk7 inhibitors |
48.74 |
|
A radiolabeling-free, qPCR-based method for locus-specific pseudouridine detection |
48.25 |
|
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. |
47.51 |
|
Endothelial gene expression analysis |
47.51 |
|
Transcriptome sequencing wide functional analysis of human mesenchymal stem cells with PolyIC treatment |
47.16 |
|
Glioma Stem Cell Specific Super Enhancer Drives Polyunsaturated Fatty Acid Synthesis to Support EGFR Signaling |
46.02 |
|
Circular RNAs in the mammalian brain are highly abundant, conserved, and dynamically expressed |
45.39 |
|
Genome-wide view of the impact of Spt5-Pol II inhibitors (SPIs) on mRNA levels [RNA-Seq 24h] |
44.06 |
|
Global Bidirectional Transcription of the Epstein-Barr Virus Genome During Reactivation |
43.93 |
|
Selective roles of vertebrate PCF11 in premature and full-length transcript termination (chromatin-bound RNA-seq) |
42.61 |
|
RNA-seq of resting and activated CD4+ T cells +-JQ1 |
42.52 |
|
Transcriptome profiling of hnRNP A2/B1 and A1 depleted cells |
39.7 |
|
Global response to chemotherapy-induced apoptosis |
39.69 |
|
Transcriptome sequencing wide functional analysis of human mesenchymal stem cells (Poly(I:C) and LPS) |
39.26 |
|
High-throughput RNA sequencing on circular RNA profiles of human bladder cancer tissues and normal bladder tissues |
38.79 |
|
Transcriptome of iPSC-derived Neural Cells with Heterozygous Knockout in CHD8 |
38.64 |
|
Genome wide transcriptome analysis of palbociclib or GSK3326595 treated A375 cells [Palbociclib_GSK_RNASeq] |
38.6 |
|
The stress granule transcriptome reveals principles of mRNA accumulation in stress granules. |
38.4 |
|
Landscape of H3K4me3 in human CD19 cells |
37.93 |
|
LINE-1 elements are derepressed in senescent cells and elicit a chronic Type-I Interferon response |
37.69 |
|
Differential roles of human PUS10 in miRNA processing and tRNA pseudouridylation |
37.65 |
|
Regulation of PRMT5-MDM4 axis is critical in the response to CDK4/6 inhibitors in melanoma |
37.4 |
|
Mining the stiffness-sensitive transcriptome in human vascular smooth muscle cells identifies long non-coding RNA stiffness regulators |
37.0 |
|
Transcriptomic profiling of HeLa cells infected with Salmonella Typhimurium |
36.91 |
|
Two dimensional and extracellular matrix based three-dimensional cultures of lung and breast cancer cells |
36.7 |
|
Gene expression profiling in two dimensional and extracellular matrix based three-dimensional cultures of lung and breast cancer cells |
36.7 |
|
siRNA-mediated silencing of ORAI3 in MDA-MB-468 breast cancer cells exposed to hypoxia |
36.43 |
|
Gene expression by high-throughput sequencing of T47D-MTVL human breast cancer cells upon H1.4 knock-down and multiple H1 variants |
35.17 |
|
Comprehensive comparative analysis of 5’ end RNA sequencing methods |
34.68 |
|
Gene induction by the USP6 oncogene in response to interferon |
33.98 |
|
MPTAC determines APP fragmentation via sensing sulfur amino acid catabolism |
33.94 |
|
A quantitative chemotherapy genetic interaction map identifies new factors associated with PARP inhibitor resistance |
33.63 |
|
Genes significantly down or Up-regulated upon RNF219 knockdown |
33.5 |
|
Spatially Constrained Tandem Bromodomain Inhibition Bolsters Sustained Repression of BRD4 Transcriptional Activity for TNBC Cell Growth |
33.34 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and PVT1 Knockdown by CRISPRi in MDA-MB-231 human breast cancer cell line |
33.31 |
|
Promoter of lncRNA gene *PVT1* is a tumor suppressor DNA element |
33.31 |
|
E2F1 orchestrates transcriptomics and oxidative metabolism in Wharton’s jelly derived mesenchymal stem cells from growth-restricted neonates |
33.28 |
|
Epigenome-wide Effects of Vitamin-D on Bronchial Epithelial Cells using ATAC-Seq and RNA-seq |
32.82 |
|
HDAC inhibition enhances the in vivo efficacy of MEK inhibitor therapy in uveal melanoma |
32.71 |
|
U1 snRNP telescripting regulates size-function stratified human genome |
32.54 |
|
hMTR4 plays a central role in creating balanced nuclear RNA pools for degradation and export |
32.24 |
|
RNASeq of 4SU labelled nascent RNA in MV4;11 cell treated with DMSO, I-BET, SGC0946 and combination of I-BET and SGC0946 |
31.99 |
|
Ex-vivo Human Hematopoietic Stem Cell Expansion Requires Coordination of Cellular Reprogramming with Mitochondrial Remodeling and P53 Activation [bulk] |
31.96 |
|
Impact of HypERrlnc Knockdown on the human pericyte transcriptome |
31.02 |
|
Role of microRNAs in the interaction between Salmonella and the host cell |
30.82 |
|
Chemotherapeutic drugs inhibiting Topoisomerase 1 activity inhibit TNF-induced inflammatory gene expression |
30.78 |
|
Transcriptome profiling identified a 3-lncRNA regulatory network in transthyretin against glucose induced hRECs dysfunction |
30.77 |
|
The metabolome regulates the epigenetic landscape during naïve to primed human embryonic stem cell transition |
30.76 |
|
Therapeutic targeting of KDM1A/LSD1 in Ewing sarcoma engages the ER-stress response II |
30.73 |
|
TT-Seq captures the human transient transcriptome |
30.65 |
|
Transcriptomic analysis reveals novel long non-coding RNAs critical for vertebrate development [RNA-Seq] |
30.06 |
|
Transcriptomic analysis reveals novel long non-coding RNAs critical for vertebrate development |
30.06 |
|
circ-ZNF609 regulates G1-S progression in Rhabdomyosarcoma |
29.51 |
|
RNA-Seq analysis of JIB-04 effects on global cellular transcription and HIV in 2D10 T cells |
28.72 |
|
Role for citron kinase in prostate cancer growth |
28.13 |
|
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 |
28.07 |
|
Effect of BB608 on Gene Expression in HNSCC Cell Line |
27.9 |
|
Transcriptome-profiling (RNA-seq) and Ribosome-profiling (Ribo-seq) of BJ cells treated with Nutlin-3a, an MDM2 inhibitor, which induces p53. |
27.5 |
|
Identification of HOXB13 target genes responsive to BET inhibitors |
26.74 |
|
Widespread Transcription beyond mRNA 3’ Ends Yields Abundant Regulatory RNAs |
26.18 |
|
JQ1 +/- Vemurafenib in BRAF mutant melanoma (A375) |
26.03 |
|
RUNX1-ETO and RUNX1-EVI-1 differentially program the chromatin landscape in t(3;21) and t(8;21) AML but share global C/EBP-alpha dysfunction |
25.95 |
|
RUNX1-ETO and RUNX1-EVI-1 differentially program the chromatin landscape in t(3;21) and t(8;21) AML but share global C/EBP-alpha dysfunction (RNA-Seq) |
25.95 |
|
Modulation of ESRP2 and MBNL2 in normal kidney and clear cell renal cell carcinoma cell lines for analysis of stability programs |
25.85 |
|
The effect of REST and its alternatively spliced transcript, REST-003, on breast cancer invasiveness |
25.68 |
|
NRDE2 negatively regulates nuclear exosome functions |
25.47 |
|
Ex-vivo Human Hematopoietic Stem Cell Expansion Requires Coordination of Cellular Reprogramming with Mitochondrial Remodeling and P53 Activation |
25.06 |
|
Mapping interactions for the TNIP2 hub protein |
24.78 |
|
The Molecular Dissection of the Oncogenic Role of ETS1 in the Mesenchymal Subtypes of Head and Neck Squamous Cell Carcinoma [RNA-seq knock-down] |
24.24 |
|
Mitochondrial unfolded protein response controls matrix pre-RNA processing and translation |
23.51 |
|
Genome models integrating chromatin contacts and nuclear lamin-genome interactions reveal implications of laminopathy-causing lamin mutations on genome architecture |
23.21 |
|
Human embryonic stem cell, chimpanzee induced pluripotent stem cell, orangutan induced pluripotent stem cell, rhesus embryonic stem cell, and their derived cortical organoid RNA-seq |
22.77 |
|
ZBTB48 is both a vertebrate telomere-binding protein and a transcriptional activator |
22.66 |
|
ZBTB48 is both a vertebrate telomere-binding protein and a transcriptional activator [RNA-seq] |
22.66 |
|
Cooperation of Nutlin-3a and a Wip1 inhibitor to induce p53 activity |
22.5 |
|
NET-CAGE Characterizes the Dynamics and Topology of Human Transcribed Cis-regulatory Elements |
22.26 |
|
Long non-coding RNA SMILR regulates genes involved in cytokinesis in human vascular smooth muscle cell |
22.23 |
|
Integrative transcriptome-wide analyses reveal critical HER2-regulated mRNAs and lincRNAs in HER2+ breast cancer |
22.2 |
|
Ribo_seq (aka ribosome profiling) analysis of control and Myc-induced U2OS cells |
22.2 |
|
Bromodomain protein BRD4 is required for estrogen receptor-dependent transcription and enhancer activation [RNA-Seq] |
22.11 |
|
Bromodomain protein BRD4 is required for estrogen receptor-dependent transcription and enhancer activation |
22.11 |
|
DRB/GRO-Seq -/+ UV |
22.09 |
|
A non-canonical role of YAP/TEAD is required for activation of estrogen-regulated enhancers in breast cancer [RNA-seq] |
22.09 |
|
A non-canonical role of YAP/TEAD is required for activation of estrogen-regulated enhancers in breast cancer |
22.09 |
|
Human co-transcriptional splicing kinetics and coordination revealed by direct nascent RNA sequencing |
22.09 |
|
Patient iPSC-Derived Neurons for Disease Modeling of Frontotemporal Dementia with Mutation in CHMP2B |
21.94 |
|
Pan-cancer transcriptomic analysis associates long non-coding RNAs with key mutational driver events |
21.91 |
|
Comprehensive analysis of Long non-coding RNA expression in dorsal root ganglion reveals cell type specificity and dysregulation following nerve injury [human iPS] |
21.61 |
|
Comprehensive analysis of Long non-coding RNA expression in dorsal root ganglion reveals cell type specificity and dysregulation following nerve injury |
21.61 |
|
RNA-sequencing transcriptome profiling of normal human keratinocytes differentiation |
21.57 |
|
An Argonaute phosphorylation cycle promotes microRNA-mediated silencing [whole transcriptome RNA-seq] |
21.52 |
|
EWS-Fli and LNC regulated genes in comparison to GFP samples |
21.36 |
|
Retinoic acid suppresses MYB in adenoid cystic carcinoma |
21.29 |
|
Retinoic acid suppresses MYB in adenoid cystic carcinoma [RNA-seq] |
21.29 |
|
RNA-sequencing of isogenic primary, pre-malignant immortalized, and Ras-transformed human mammary epithelial cells |
20.81 |
|
Transcriptomic analysis of healthy donor and Sickle Cell Disease (SCD) hematopoietic stem/progenitor cells |
20.53 |
|
An RNA-centric dissection of host complexes controlling flavivirus infection [RNA-Seq] |
20.5 |
|
An RNA-centric dissection of host complexes controlling flavivirus infection |
20.5 |
|
Selectively targeting bromodomain and extraterminal proteins for degradation as a novel anti-glioblastoma strategy [RNA-seq] |
20.38 |
|
p63 controls the enhancer landscape during keratinocyte differentiation |
20.33 |
|
shRNA-mediated knockdown of ETV4 and MED25 in the prostate cell line PC3 reveals set of genes potentially coregulated by MED25 and ETV4 |
20.26 |
|
Genome-wide occupancy of FLAG-MED25 and ETV4 and expression profiling of shRNA-mediated knockdown of ETV4 and MED25 in the prostate cell line PC3 |
20.26 |
|
mRNA destabilization is the dominant effect of mammalian microRNAs by the time substantial repression ensues (sequencing) |
20.13 |
|
mRNA destabilization is the dominant effect of mammalian microRNAs by the time substantial repression ensues |
20.13 |
|
Cellular gene expression during Hepatitis C Virus replication revealed by Ribosome profiling |
19.78 |
|
High-throughput RNA sequencing on circular RNA profiles of human pancreatic cancer cell lines and gemcitabine resistant pancreatic cancer cell lines. |
19.69 |
|
High-throughput sequencing of pluripotent cells |
19.52 |
|
RNA-dependent RNA polymerase sequence specificities of capsnatching viruses are tailored to aid viral replication |
19.25 |
|
BAF controls genome accessibility |
19.22 |
|
RBPJ Maintains Brain Tumor Initiating Cells through CDK9-mediated Transcriptional Elongation |
19.11 |
|
RNA-seq Profiles in RBPJ Maintains Brain Tumor Initiating Cells through CDK9-mediated Transcriptional Elongation |
19.11 |
|
Inducible three-factor direct reprogramming to nephron progenitors using piggyBac transposons |
19.06 |
|
A code of mono-phosphorylation modulates the function of RB. |
19.05 |
|
Histone H3 lysine 4 acetylation-methylation dynamics define breast cancer subtypes [RNA-seq] |
18.98 |
|
Histone H3 Lysine4 Acetylation-Methylation Dynamics Define Breast Cancer Subtypes |
18.98 |
|
Role of BET proteins in YAP/TAZ-dependent transcription [RNA-seq 1] |
18.84 |
|
circRNA profile in hypopharyngeal cancer |
18.83 |
|
RNA-sequencing of formalin fixed human primary melanoma tissue |
18.78 |
|
Human iPSC derived glomeruli facilitate accurate modelling of podocytopathy |
18.44 |
|
RNA Sequencing of three pairs of gastric cancer |
18.41 |
|
LncPRESS1 is a p53-regulated lncRNA that safeguards pluripotency by disrupting SIRT6 mediated de-acetylation of histone H3K56 |
18.26 |
|
RNA sequencing for lncRNA, miRNA and mRNA expression analysis in human laryngeal cancer |
18.13 |
|
Mutation independent activation of the Notch pathway is associated with Lapatinib resistance in Her2+ breast cancer cell lines |
17.99 |
|
RNA-seq of MLLT3-overexpressing cultued HSPC, compared to non-overexpressing and uncutured FL-HSPC [RNAseq_MLLT3_OE] |
17.83 |
|
Mllt3 Governs Self-Renewal And Engraftment Of Human Hematopoietic Stem Cells |
17.83 |
|
Activation of PARP-1 by snoRNAs Controls Ribosome Biogenesis and Cell Growth via the RNA Helicase DDX21 (RNA-Seq) |
17.8 |
|
Activation of PARP-1 by snoRNAs Controls Ribosome Biogenesis and Cell Growth via the RNA Helicase DDX21 |
17.8 |
|
Short and long-term effects of CDK4/6 inhibition on early stage breast cancer |
17.68 |
|
Sequencing of matched pair samples (diagnosis and relapse) in human B-cell acute lymphoblastic leukemia cells (ALL) |
17.63 |
|
Genomic deletion of malic enzyme 2 confers collateral lethality in pancreas cancer |
17.61 |
|
Generation of induced neural stem cells from urine derived cells by synthetic mRNA |
17.54 |
|
Epigenetic Lanscape and BRD4 Transcriptional Dependency of PAX3-FOXO1 Driven Rhabdomyosarcoma |
17.29 |
|
PAX3-FOXO1 requires BRD4 to drive oncogene addiction in RMS cells [RNA-seq] |
17.29 |
|
Transcriptomic but not genomic variability confers phenotype of breast cancer stem cells |
17.21 |
|
The RNA exosome nuclease complex regulates human embryonic stem cell differentiation [RNA-Seq SS] |
17.05 |
|
Campylobacter concisus pathotypes induce distinct global responses in intestinal epithelial cells |
16.91 |
|
Genome-wide DNA accessibility maps and differential gene expression using ChIP-seq, ATAC-seq and RNA-seq for the human secondary fibroblast cell line hiF-T and whole worms with and without knockdown of FACT complex |
16.86 |
|
HEK293 Heat-shock experiment |
16.72 |
|
High-Throughput Screening of Human Induced Pluripotent Stem Cell Cardiomyocytes Predicts Tyrosine Kinase Inhibitor Cardiotoxicity |
16.66 |
|
Tyrosine Kinase Inhibitor Cardiotoxicity |
16.66 |
|
RNA-Seq with and without RNase treatment in PCa cell lines |
16.45 |
|
Reassessment of Exosome Composition |
16.15 |
|
LncRNA-dependent mechanisms of androgen receptor-regulated gene activation programs [GRO-seq II] |
16.0 |
|
The ribonuclease activity of SAMHD1 is required for HIV-1 restriction |
16.0 |
|
A zebrafish melanoma model reveals emergence of neural crest identity during melanoma initiation [human cell line RNA-seq] |
15.88 |
|
A zebrafish melanoma model reveals emergence of neural crest identity during melanoma initiation |
15.88 |
|
Splicing and epigenetic factors jointly regulate epidermal differentiation |
15.79 |
|
Genome-wide identification of cancer-specific alternative splicing in circRNA |
15.77 |
|
Metabolic reprogramming of Kaposi’s sarcoma associated herpes virus infected B-cells in hypoxia |
15.76 |
|
Enhancement of direct reprogramming from fibroblasts to epithelial lineages by OVOL2-induced mesenchymal-to-epithelial transition |
15.67 |
|
Enhancement of direct reprogramming from fibroblasts to epithelial lineages by OVOL2-induced mesenchymal-to-epithelial transition [CAGE] |
15.67 |
|
UBR7 is a novel E3 ubiquitin ligase for H2BK120 and acts as a tumor-suppressor in breast cancer [RNA-Seq] |
15.67 |
|
UBR7 is a novel E3 ubiquitin ligase for H2BK120 and acts as a tumor-suppressor in breast cancer |
15.67 |
|
RNA-sequencing in irradiated and normal A549 cells. |
15.41 |
|
circRNA-sequencing |
15.38 |
|
RNA-seq of YB5 cells treated with Proscillaridin A |
15.32 |
|
mTORC1 balances cellular amino acid supply with demand for protein synthesis through post-transcriptional control of ATF4 |
15.03 |
|
Genome-wide maps of WT and over-expressing CenH3/CENP-A in Human HeLa S3 cells |
14.92 |
|
Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia [shRNA] |
14.82 |
|
Dynamic 3D chromosomal landscapes in acute leukemia |
14.81 |
|
Dynamic 3D chromosomal landscapes in acute leukemia [RNA-Seq] |
14.81 |
|
Short and Long RNA sequencing of human mature erythrocytes |
14.72 |
|
A role for ZNF598 in post-transcriptional gene regulation |
14.71 |
|
Solid phase chemistry to covalently and reversibly capture thiolated RNA |
14.67 |
|
Post-transcriptional manipulation of TERC reverses molecular hallmarks of telomere disease |
14.55 |
|
Biochemical fractionation of HEK293 nuclei and RNA-seq of chromatin-associated and soluble-nuclear RNA |
14.43 |
|
Recapitulation of Human Neural Microenvironment Signatures in iPSC-Derived NPC 3D Differentiation |
14.3 |
|
Genome-wide search for differentially expressed RNAs responsible for the effects induced by Ebola virus replication and transcription |
14.17 |
|
BRG1 governs Glucocorticoid Receptor interactions with chromatin and pioneer factors across the genome |
14.1 |
|
Differential Gene Expression between MCF10A and MCF7 cells |
13.84 |
|
Differential responses of human fetal brain neural stem cells to Zika virus infection |
13.78 |
|
Selective expression of long non-coding RNAs in a breast cancer cell progression model |
13.78 |
|
SnapShot-Seq: a method for extracting genome-wide, in vivo mRNA dynamics from a single total RNA sample |
13.75 |
|
RNA G-quadruplexes cause eIF4A-dependent oncogene translation in cancer |
13.65 |
|
RNA polymerase in pre-B-ALL cell lines |
13.54 |
|
Base-resolution mapping reveals distinct classes of N1-methyladenosine methylome in nuclear- and mitochondrial-encoded transcripts |
13.53 |
|
Three congruent human Schwann cell models of CMT1A reveal a converged phenotype |
13.52 |
|
R430: A potent inbibitor of DNA and RNA viruses |
13.37 |
|
Next Generation Sequencing Facilitated Differential Transcriptome Study of melanoma cells transduced with Notch 1 Intracellular Domain (NICD) |
13.36 |
|
Differentiation enhances Zika virus infection in neuronal brain cells |
13.29 |
|
Strand-specific Dual RNA-seq of Bronchial Epithelial cells Infected with Influenza A/H3N2 Viruses Reveals Splicing of Gene Segment 6 and Novel Host-Virus Interactions |
12.6 |
|
C9orf72 Intermediate Repeats are Associated with Corticobasal Degeneration, Increased C9orf72 Expression and Disruption of Autophagy |
12.6 |
|
Poly(A)-specific ribonuclease (PARN) mediates 3' end maturation of the telomerase RNA component |
12.56 |
|
Catalogue of differentially expressed long non-coding RNAs following activation of human and mouse innate immunity |
12.36 |
|
LINC00520 is Induced by Src, STAT3, and PI3K and Plays a Functional Role in Breast Cancer |
12.28 |
|
SPOP mutation confers intrinsic BET inhibitor resistance in prostate cancer |
12.12 |
|
BCL11B |
11.79 |
|
Profiling and bioinformatics analyses reveal differential expression of circular RNA in tongue cancer revealed by high-throughput sequencing |
11.73 |
|
Gene expression profiles in NORAD knockout and PUMILIO overexpressing cells |
11.66 |
|
Identification of ADAR1 adenosine deaminase dependency in a subset of cancer cells |
11.64 |
|
DHX9 suppresses spurious RNA processing defects originating from the Alu invasion of the human genome [uvCLAP CLIP-seq] |
11.58 |
|
BI Human Reference Epigenome Mapping Project |
11.58 |
|
Comparison of microRNA Profiling Platforms (HTS) |
11.53 |
|
Comparison of microRNA Profiling Platforms |
11.53 |
|
miR-191 regulates human cell proliferation and directly targets multiple oncogenes [seq] |
11.52 |
|
Genome wide miR-191 target profile determined by RIP and gene expression profiling |
11.52 |
|
Effect of circPTPRM on the biological behaviors of hepatocellular carcinoma cells in vitro and its clinical significance. |
11.5 |
|
The immediate impact of exoribonucleolysis on nuclear RNA processing, turnover and transcriptional control revealed by rapid depletion of DIS3, EXOSC10 or XRN2 from human cells |
11.46 |
|
Epigenome regulation during epidermal lineage commitment [ATAC-seq, RNA-seq] |
11.38 |
|
Gene expression and 4sUDRB-seq for NF90/NF110 of human scramble and KD HeLa cells. |
11.38 |
|
The effects of U1 snRNA mutation in chronic lymphocytic leukemia cell lines |
11.2 |
|
Landscape and variation of RNA secondary structure across the human transcriptome |
11.13 |
|
Cooperation of GRSF1 and the mitochondrial degradosome (hSuv3-PNPase complex) in degradation of mitochondrial RNA |
11.13 |
|
Transcriptional dependencies in diffuse intrinsic pontine glioma |
11.08 |
|
Comparative transcriptomic analysis of human and Drosophila extracellular vesicles reveals extensive conservation |
10.95 |
|
TUT-DIS3L2 is a mammalian surveillance pathway for aberrant structured non-coding RNAs. |
10.91 |
|
Uridylation-mediated RNA quality control pathway in mammalian cytoplasm [RNA-Seq] |
10.91 |
|
MicroRNAs reinforce repression of PRC2 transcriptional targets independently and through a feed-forward regulatory network with PRC2 [RNA-seq] |
10.61 |
|
MicroRNAs reinforce repression of PRC2 transcriptional targets independently and through a feed-forward regulatory network |
10.61 |
|
An epigenetic mark of polycomb response elements implemented by Trx/MLL/COMPASS |
10.56 |
|
The pause-initiation limit restricts transcription activation in human cells |
10.46 |
|
Presence of NAD+-capped RNA in human cells: function and removal by the DXO deNADing Protein |
10.4 |
|
Genome-wide maps of m6A circRNAs identify widespread and cell-type-specific methylation patterns that are distinct from mRNAs |
10.34 |
|
Oncogenic MYC induces a dependency on the spliceosome in human cancer |
10.31 |
|
Laminin-guided highly efficient endothelial commitment from human pluripotent stem cells [Bulk RNA-Seq] |
10.31 |
|
|
10.21 |
|
Insights into snoRNA biogenesis and processing from PAR-CLIP of snoRNA core proteins and small RNA sequencing |
10.2 |
|
Expanding the Nucleoside Recoding Toolkit: Revealing RNA Population Dynamics with 6-thioguanisine |
10.08 |
|
The RNA helicase DDX6 regulates self-renewal and differentiation of human and mouse stem cells [RNA-seq] |
10.03 |
|
Uridilation by TUT4/7 restricts retrotransposition of human Line-1s |
10.03 |
|
Integrative classification of human coding and non-coding genes based on RNA metabolism profiles |
10.01 |
|
CNOT1 and Transcriptomic Landscape of a HeLa Cell Line |
9.97 |
|
Evolving Spindlin1 Small Molecule Inhibitors Using Protein Microarrays |
9.94 |
|
Mitochondrial dsRNA triggers antiviral signalling in humans |
9.9 |
|
Global Transcriptional analysis of human spinal cord and neocortical neuroepithelial stem (NES) cells |
9.84 |
|
The NFkB subunit RELA is a master transcriptional regulator of the committed epithelial-mesenchymal transition in airway epithelial cells |
9.68 |
|
MYCi975 regulates MYC target genes |
9.65 |
|
RNA-Seq profiling of day 7 and day 18 kidney organoids differentiated in two batches |
9.59 |
|
Gene expression profiling of human and murine in vitro muscle differentiation |
9.5 |
|
The long non-coding RNA MALAT1 contributes to the pathogenesis of multiple sclerosis through alternative splicing and backsplicing regulation |
9.43 |
|
Epigenome-wide analysis of DNA methylation in lung tissue shows concordance with blood studies and identifies tobacco smoke-inducible enhancers |
9.38 |
|
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) |
9.37 |
|
Global analysis of pre-mRNA subcellular localization upon splicing inhibition by spliceostatin A |
9.37 |
|
The WNT target SP5 negatively regulates WNT transcriptional programs in human pluripotent stem cells |
9.33 |
|
Prolyl hydroxylation regulates protein degradation, synthesis, and splicing in human induced pluripotent stem cell-derived cardiomyocytes |
9.24 |
|
MLL-AF4 binds directly to a BCL-2 specific enhancer and impacts H3K27 acetylation |
9.22 |
|
Analyzing the interactions of mRNAs, miRNAs, lncRNAs and circRNAs to predict competing endogenous RNA networks in glioblastoma |
9.0 |
|
Identification of transcription start sites for human A549 cell line using ReCappable-seq |
8.92 |
|
UMI-count modeling and differential expression analysis for single-cell RNA sequencing |
8.9 |
|
Sequencing of freshly produced RNA following exposure of cells to DNA damage-inducing UV mimetic 4-hydroxyaminoquinolone (4-NQO) |
8.87 |
|
Genes regulated by soluble guanylyl cyclase in VCaP prostate cancer cells |
8.86 |
|
Determination of tRNA aminoacylation levels by high throughput sequencing |
8.85 |
|
REST and Neural Gene Network Dysregulation in iPS Cell Models of Alzheimer’s Disease |
8.81 |
|
REST and Neural Gene Network Dysregulation in iPS Cell Models of Alzheimer’s Disease (RNA-seq data set) |
8.81 |
|
Retroviral Replicating Vectors Deliver Cytosine Deaminase Leading to Targeted 5-FU-Mediated Cytotoxicity in Multiple Human Cancer Types |
8.8 |
|
Quantitative analysis of bi-modal binding of BET proteins at promoters predicts I-BET sensitivity |
8.7 |
|
Transcriptomic profiling of mRNA and miRNA from nasopharyngeal carcinoma (NPC) and normal control samples |
8.69 |
|
Transcriptomic profiling of nasopharyngeal carcinoma (NPC) and normal control samples |
8.69 |
|
A systematic analysis of the time series gene expression in TGF-beta induced EMT by Next-generation sequencing |
8.69 |
|
RNA editing in nascent RNA affects pre-mRNA splicing |
8.66 |
|
Enhancer activation during EGF response |
8.65 |
|
RNA-Seq analysis of cSCC cells after siRNA-induced gene knockdown of lncRNA PRECSIT |
8.64 |
|
Comparative total RNA and mRNA sequencing and systems analysis reveals nascent transcriptional response to early HIV-1 infection in a CD4+ T cell line |
8.63 |
|
Proteinase-Activated Receptor 4 (PAR4) mediates cell membrane blebbing in a Gaq/11, Gai independent, RhoA and ß-arrestin-dependent manner. |
8.49 |
|
The RNA exosome nuclease complex regulates human embryonic stem cell differentiation [RNA-Seq rescue_SS] |
8.47 |
|
HDAC and NFκB antagonists synergistically inhibit growth and metastatic dissemination of MYC-driven medulloblastoma |
8.42 |
|
Specific labeling of stem cell activity in human colorectal organoids using an ASCL2-responsive minigene |
8.4 |
|
Che-1 is targeted by c-Myc to sustain proliferation in pre-B-cell acute lymphoblastic leukemia [RNA-seq] |
8.4 |
|
Che-1 is targeted by c-Myc to sustain proliferation in pre-B-cell acute lymphoblastic leukemia |
8.4 |
|
Epigenome regulation during epidermal lineage commitment |
8.35 |
|
Expression profile of wild type (WT) vs miR-155-/- in FLT3-ITD+ AML (MV4-11) cell lines |
8.3 |
|
Genome-wide CRISPR-Cas9 screen identifies functionally relevant microRNAs in AML |
8.3 |
|
Bromodomain protein BRD4 is a transcriptional repressor of autophagy and lysosomal function |
8.26 |
|
Human Cactin interacts with DHX8 and SRRM2 to assure efficient pre-mRNA splicing and sister chromatid cohesion. |
8.19 |
|
Ribosomal footprinting of CN34-Parental and CN34-LM1a |
8.13 |
|
CHD1 loss sensitizes prostate cancer to DNA damaging therapy by promoting error-prone double-strand break repair |
8.05 |
|
ChIPseq and RNAseq analysis of T47D cells with/without silencing TRPS1/CHD4 |
8.05 |
|
The interplay between SOX4 and SMAD3 in the context of breast cancer |
7.96 |
|
Structure and degradation of circular RNAs regulate PKR activation in innate immunity |
7.96 |
|
An improved method for circular RNA purification that efficiently removes linear RNAs containing G-quadruplexes or structured 3’ ends |
7.94 |
|
Human cells contain natural double-stranded RNAs with potential regulatory capacity |
7.91 |
|
Transcription elongation regulates genome 3D structure |
7.82 |
|
Programmable RNA N6-methyladenosine editing by CRISPR-Cas9 conjugates |
7.76 |
|
ILF2 Regulates RNA Splicing of DNA Damage Response Genes to Confer Poor Prognosis in 1q21-Amplified Multiple Myeloma |
7.69 |
|
Overexpression of PHF8 promotes an EMT-related gene signature in MCF10A cells |
7.66 |
|
Genome-wide analysis of the Integrator complex (HTS) |
7.64 |
|
Genome-wide analysis of the Integrator complex |
7.64 |
|
Patient-iPSC-derived kidney organoids show functional validation of a ciliopathic renal phenotype |
7.64 |
|
Joint-specific DNA transcriptome signatures in rheumatoid arthritis [RNA-seq] |
7.55 |
|
Medial Ganglionic Eminence and Cortical Organoids Model Human Brain Development and Interneuron Migration |
7.54 |
|
Bromodomain inhibition of the transcriptional coactivators CBP/EP300 as a therapeutic strategy to target the IRF4 network in multiple myeloma |
7.54 |
|
Bromodomain inhibition of the transcriptional coactivators CBP/EP300 as a therapeutic strategy to target the IRF4 network in multiple myeloma (RNA-Seq) |
7.54 |
|
Epigenome regulation during epidermal lineage commitment [RNA-seq] |
7.52 |
|
m6A-dependent regulation of messenger RNA stability |
7.4 |
|
RNA deep sequencing analysis of glioma stem cells(GSCs) and non-GSCs |
7.38 |
|
Transcriptomic profile of T cell acute lymphoblastic leukemia (T-ALL) cell from patients in CHCQMU |
7.38 |
|
Non-transmissible measles virus vector with segmented RNA genome establishes different types of iPSCs from hematopoietic cells |
7.33 |
|
Circular RNAs are down-regulated in KRAS mutant colon cancer cells and can be transferred to exosomes |
7.32 |
|
Toxoplasma gondii remodels the cis-regulatory landscape of infected human host cells |
7.27 |
|
Toxoplasma gondii remodels the cis-regulatory landscape of infected human host cells [RNA-seq] |
7.27 |
|
RNA expression analysis of neuroblastoma cell lines treated with epigenetic drugs |
7.16 |
|
β-catenin/Tcf7l2 dependent transcriptional regulation of GLUT1 gene expression by Zic family proteins in colon cancer |
7.15 |
|
Total RNA was extracted from three samples of CD33 CAR or control T cells from three different donors |
7.12 |
|
Gene expression profile of human iPSC-derived nephron progenitor cells |
7.09 |
|
RNA seq analysis of human macrophages after treatment of glimepiride versus empagliflozin. |
7.05 |
|
Study functions of ADAR proteins using next generation sequencing of genome and transcriptome |
7.04 |
|
Androgen receptor functions as transcriptional repressor of Cancer Associated Fibroblast (CAF) activation |
6.89 |
|
Androgen receptor functions as transcriptional repressor of Cancer Associated Fibroblast (CAF) activation [RNA-seq] |
6.89 |
|
In vivo generation of post-infarct human cardiac muscle by laminin-promoted cardiovascular progenitors [LN-521 or LN-521+LN-221] |
6.86 |
|
Genome-scale identification of transcription factors that mediate an inflammatory network during breast cellular transformation |
6.77 |
|
RNA-seq during MCF10A-ER-Src cell transformation and upon factor knockdowns |
6.77 |
|
Methylation DNA mediated KLF4 binding activity in glioblastoma cells |
6.72 |
|
LncRNA-dependent mechanisms of androgen receptor-regulated gene activation programs |
6.7 |
|
Ewing sarcoma resistance to SP-2509 is not mediated through KDM1A/LSD1 mutation I |
6.6 |
|
C/EBPα overexpression overrides epigenetic reprogramming by RUNX1-ETO and RUNX1-EVI1 [RNA-seq] |
6.58 |
|
C/EBPα overexpression overrides epigenetic reprogramming by RUNX1-ETO and RUNX1-EVI1 |
6.58 |
|
Genome-wide RNA-sequencing (RNA-seq) of benign and malignant prostate cell lines without and with androgen (R1881) stimulation. |
6.49 |
|
RB tumor suppressor promotes cancer immunity through downregulating PD-L1 expression |
6.44 |
|
Hyper-activation of HUSH complex function by Charcot-Marie-Tooth disease mutation in MORC2 |
6.39 |
|
Subcellular RNA fractions of HSV-1 infected primary human fibroblasts |
6.38 |
|
Global transcriptional changes in the JJN3 myeloma cell line that occur as a result of treatment with 2 pyrrolobenzodiazepine (PBD) monomers |
6.36 |
|
T-bet recruits P-TEFb to super-enhancers to regulate T helper cell differentiation (RNA-Seq) |
6.32 |
|
T-bet recruits P-TEFb to super-enhancers to regulate T helper cell differentiation |
6.32 |
|
6mer seed toxicity in tumour suppressive microRNAs |
6.2 |
|
Conservative alteration of chromosomal expression pattern across human solid tumor types |
6.15 |
|
Genome-wide discovery of human splicing branchpoints |
6.11 |
|
RNA-seq in LNCaP cell line overexpressing WT or mutant FOXA1 |
5.96 |
|
Forkhead domain mutations in FOXA1 drive prostate cancer cell progression |
5.96 |
|
The expression profiles of GBC liver metastasis |
5.93 |
|
Effects of human adipose tissue-derived and umbilical cord tissue-derived mesenchymal stem cells in a dextran sulfate sodium-induced mouse model |
5.86 |
|
ATXN7L3 And ENY2 Coordinate Activity Of Multiple H2B Deubiquitinases Important For Cellular Proliferation And Tumor Growth |
5.85 |
|
ATXN7L3 And ENY2 Coordinate Activity Of Multiple H2B Deubiquitinases Important For Cellular Proliferation And Tumor Growth [RNA-Seq] |
5.85 |
|
A Druggable TCF4- and BRD4-dependent Transcriptional Network Sustains Malignancy in Blastic Plasmacytoid Dendritic Cell Neoplasm (RNA-Seq) |
5.69 |
|
MLL-AF4 Spreading Identifies Binding Sites that Are Distinct from Super-Enhancers and that Govern Sensitivity to DOT1L Inhibition in Leukemia. |
5.57 |
|
Elongation Factor TFIIS Prevents Transcription Stress and R-Loop Accumulation to Maintain Genome Stability |
5.53 |
|
Elongation Factor TFIIS Prevents Transcription Stress and R-Loop Accumulation to Maintain Genome Stability [ RNA-seq] |
5.53 |
|
Global transcriptome analysis of WT versus HEB-/- hESCs |
5.39 |
|
p53 activity results in DNA replication fork processivity |
5.28 |
|
RNA-seq of SCLC PDX models treated with EP |
5.23 |
|
Precise Gene Editing Preserves Hematopoietic Stem Cell Function Following Transient p53-Mediate DNA Damage Response [bulk RNA-seq] |
5.1 |
|
circNFIB suppresses lymphatic metastasis of pancreatic cancer |
5.09 |
|
RNA-seq of cells with TET1 knockout |
5.07 |
|
Transcriptome analysis-identified long noncoding RNA CRNDE in maintaining endothelial cell proliferation, migration, and tube formation |
5.03 |
|
ARID1A regulates condensin II distribution and chromosomal partition |
4.99 |
|
ARID1A regulates condensin II distribution and chromosomal partition [RNA-seq] |
4.99 |
|
RNA transcriptome analysis during HSV-1 infection |
4.92 |
|
Regulation of poly(A) tail and translation during the somatic cell cycle |
4.72 |
|
Mitochondrial unfolded protein response controls matrix pre-RNA processing and translation |
4.65 |
|
SRSF1 role in cellular gene expression and splicing |
4.62 |
|
Transcriptional Down-regulation of CCR5 in a Subset of HIV+ Controllers |
4.59 |
|
Transcriptional Down-regulation of CCR5 in a Subset of HIV+ Controllers (RNA-Seq) |
4.59 |
|
MYC interacts with the G9a histone methyltransferase to drive transcriptional repression and tumorigenesis |
4.57 |
|
Role of BET proteins in YAP/TAZ-dependent transcription [RNA-seq 2] |
4.55 |
|
hnRNP L protects mRNAs from nonsense-mediated mRNA decay |
4.48 |
|
Wide-spread disruption of transcription termination in HSV-1 infection: Next-generation sequencing of translational activityd by ribosome profiling |
4.44 |
|
Transcriptome-wide analysis of the role of HTLV-1 Tax PBM in T-Cells from infected humanized-mice (hu-Mice) |
4.36 |
|
Histone variant H2A.Bbd is associated with active transcription and mRNA processing in human cells |
4.35 |
|
Histone variant H2A.Bbd is associated with active transcription and mRNA processing in human cells [RNA-Seq] |
4.35 |
|
Genome-wide profiling of cervical RNA-binding proteins identified HPV regulation of RNASEH2A expression by viral E7 and E2F1 |
4.22 |
|
Transcriptome landscape of HeLa response upon triamcinolone acetonide |
4.09 |
|
A cytoplasmic COMPASS is necessary for cell survival and triple-negative breast cancer pathogenesis by regulating metabolism |
4.01 |
|
Allosteric Antagonist Modulation of TRPV2 by Piperlongumine Impairs Glioblastoma Progression |
3.93 |
|
RNA:DNA hybrids in the human genome have distinctive nucleotide characteristics, chromatin composition, and transcriptional relationships |
3.89 |
|
RNA:DNA hybrids in the human genome have distinctive nucleotide characteristics, chromatin composition, and transcriptional relationships (RNA-seq) |
3.89 |
|
Estrogen Receptor Beta Impacts Hormone-Induced Alternative mRNA Splicing in Breast Cancer Cells |
3.8 |
|
UBE3A-mediated regulation of imprinted genes and epigenome-wide marks in human neurons |
3.73 |
|
Interphase condensins regulate ligand-depedent enhancer activation |
3.71 |
|
Interphase condensins regulate ligand-depedent enhancer activation (GRO-seq) |
3.71 |
|
Enhancer Activation Requires Trans-Recruitment of a Mega Transcription Factor Complex (Gro-seq) |
3.51 |
|
Enhancer Activation Requires Trans-Recruitment of a Mega Transcription Factor Complex |
3.51 |
|
Critical role of transient activation of human endogenous retroviruses during reprogramming toward pluripotency |
3.49 |
|
Critical role of transient activation of human endogenous retroviruses during reprogramming toward pluripotency (RNA-Seq) |
3.49 |
|
An siRNA screen identifies CHD4 as a target for epigenetic therapy |
3.49 |
|
Re-programing chromatin with a bifunctional LSD1/HDAC inhibitor induces therapeutic differentiation in DIPG [RNA-seq] |
3.38 |
|
Re-programing chromatin with a bifunctional LSD1/HDAC inhibitor induces therapeutic differentiation in DIPG |
3.38 |
|
UV_24h_GRO-Seq |
3.36 |
|
TAF1 is critical for AE driven leukemogenesis [RNA-seq] |
3.35 |
|
TAF1 is critical for AE driven leukemogenesis |
3.35 |
|
Derivation of kidney organoids from human pluripotent stem cells [RNA-Seq: Data Set 1] |
3.18 |
|
RNA sequencing of lesional and nonlesional skin from patients with atopic dermatitis |
3.14 |
|
The RNA exosome nuclease complex regulates human embryonic stem cell differentiation |
3.11 |
|
Zika virus infection reprograms global transcription of host cells to allow sustained infection |
3.1 |
|
Newly defined ABCB5+ dermal mesenchymal stem cells promote healing of chronic iron overload wounds via secretion of interleukin-1 receptor antagonist |
3.08 |
|
Characterisation of the EZH2 regulated transcriptome in de novo transformed cells (RNA-Seq) |
3.04 |
|
4sUDRB-seq: measuring transcription elongation and initiation genomewide |
3.04 |
|
Transcriptomic Alterations in Lung Adenocarcinoma Unveil New Mechanisms Targeted by the TBX2 Subfamily of Tumor Suppressor Genes |
3.02 |
|
Expression Analysis of dic(1;7)(q10;p10) in Myelodysplastic Syndromes (MDS) compared to control cohort and therapy-related Myeloid Neoplasms (t-MN) |
2.99 |
|
A Distinct Epigenetic Program Underlies the 1;7 Translocation in Myelodysplastic Syndromes (MDS) |
2.99 |
|
Entrectinib Resistance in a Neuroblastoma Xenograft Model |
2.97 |
|
Developing a Novel Two-Dimensional Culture System to Enrich Human Prostate Luminal Progenitors That Can Function as a Cell of Origin for Prostate Cancer |
2.92 |
|
Studying the selectivity of a targeted small molecule degrading a hypoxia-associated non-coding RNA |
2.92 |
|
iPSCs Reveal Protective Modifiers of the BMPR2 mutation in Pulmonary Arterial Hypertension |
2.81 |
|
Dynamic reorganization of nuclear architecture during human cardiogenesis [RNA-seq] |
2.76 |
|
Dynamic reorganization of nuclear architecture during human cardiogenesis |
2.76 |
|
Transcriptome of melanoma cell lines resistant to inhibition of the MAPK pathway. |
2.71 |
|
Human Bone Marrow Assessment by Single Cell RNA Sequencing, Mass Cytometry and Flow Cytometry [bulk] |
2.64 |
|
Circular RNA profiling reveals the different distribution/characteristic and possible transport mechanism among the subcellular fractions |
2.6 |
|
Transcriptome-analysis of patient-derived normal and ulcerative colitis intestinal epithelial organoids |
2.53 |
|
Positively selected enhancer elements endow tumor cells with metastatic competence |
2.52 |
|
Long non-coding RNA TYKRIL controls pericyte function and survival in the cardiovascular and central nervous system through regulation of p53 activity and PDGFRß expression |
2.47 |
|
Effects of plasticizers (bisphenol A, bisphenol AF) and an herbicide in MCF7 human breast cancer cells |
2.41 |
|
Montelukast counteracts the influenza virus-induced block in unfolded protein stress response and reduces virus multiplication |
2.39 |
|
CD8+ T cells regulate tumor ferroptosis during cancer immunotherapy |
2.32 |
|
Functional Significance of U2AF1 S34F Mutation in Lung Adenocarcinomas |
2.29 |
|
Genome-wide modelling of transcription kinetics reveals patterns of RNA processing delays |
2.27 |
|
Targeting EZH2 in MYCN-amplified Neuroblastoma [RNA-seq] |
2.24 |
|
Comprehensive comparative analysis of RNA sequencing methods for degraded or low input samples |
2.23 |
|
Role for the Transcriptional Activator ZRF1 in Breast Cancer Progression and Endocrine Resistance |
2.22 |
|
RNAseq analysis of ruxolitinib treated breast cancers |
2.1 |
|
A next generation sequencing based approach to identify extracellular vesicle mediated mRNA transfers between cells |
1.97 |
|
YTHDF1 Amplifies Wnt/β-Catenin Signaling to Promote Intestinal Stemness |
1.8 |
|
Microprocessor mediates transcription termination in long noncoding microRNA genes |
1.8 |
|
hsa-miR-503, hsa-miR-103, and hsa-miR-494 genome wide target profiles [RNA-Seq and RIP-Seq] |
1.8 |
|
Genome-wide hsa-miR-503, hsa-miR-103, and hsa-miR-494 target profiles |
1.8 |
|
Genetic analysis of Ikaros target genes and tumor suppressor function in BCR-ABL1+ pre-B ALL |
1.77 |
|
Genetic analysis of Ikaros target genes and tumor suppressor function in BCR-ABL1+ pre-B ALL [RNA-seq] |
1.77 |
|
RNA-seq of MDA-MB-231 cells with TET1 knockout |
1.74 |
|
Mutant p63 disrupts the key specification switch from the multipotent cell state to stratified epithelia during epithelial differentiation/in ectodermal dysplasia disorders |
1.74 |
|
Ewing sarcoma resistance to SP-2509 is not mediated through KDM1A/LSD1 mutation II |
1.73 |
|
SNHG12 knockdown in Human Umbilical Vein Cells under ROS conditions. |
1.72 |
|
Analysis of human ES cell differentiation establishes that the dominant isoforms of the lncRNAs RMST and FIRRE are circular |
1.7 |
|
Gene expression profiling of neural crest progenitor cultures derived from human embryonic stem cells carrying nonsense mutations in the Polycomb gene ASXL1 |
1.55 |
|
System-wide profiling of RNA-binding proteins uncovers key regulators of virus infection |
1.48 |
|
Targetting super enhancer associated oncogenes in esophageal squamous cell carcinoma [RNA-seq] |
1.36 |
|
Targetting super enhancer associated oncogenes in esophageal squamous cell carcinoma |
1.36 |
|
Ribosome profiling upon inhibition of eIF4A |
1.34 |
|
Uridylation by TUT4 and TUT7 marks mRNA for degradation [RNA-Seq] |
1.32 |
|
Regulatory network controlling tumor-promoting inflammation in human cancers [RNA-seq] |
1.27 |
|
Regulatory network controlling tumor-promoting inflammation in human cancers |
1.27 |
|
ATF7IP-mediated stabilization of the histone methyltransferase SETDB1 is essential for heterochromatin formation by the HUSH complex |
1.25 |
|
Assessing the impact of loss of ATF7IP and SETDB1 on the transcriptome |
1.25 |
|
pSILAC mass spectrometry reveals ZFP91 as novel IMiD dependent substrate of the CRL4CRBN ligase |
1.19 |
|
Identification of long noncoding RNAs in T-ALL cell lines |
1.13 |
|
Transcriptome profiling of A2M treated A549 Cell Line Samples |
1.09 |
|
Therapy-induced hypoxia contributes to AML drug-resistance through BMX Kinase upregulation |
1.0 |
|
Enhancer Sequence Variants and Transcription Factor Deregulation Synergize to Construct Pathogenic Regulatory Circuits in B Cell Lymphoma (RNA-Seq) |
0.98 |
|
Enhancer Sequence Variants and Transcription Factor Deregulation Synergize to Construct Pathogenic Regulatory Circuits in B Cell Lymphoma |
0.98 |
|
Comparing oestrogen-responsive genes in endometrial and breast cancer cell lines |
0.95 |
|
Genome-wide expression from the esophageal biopsies of subjects with and without eosinophilic esophagitis |
0.92 |
|
Xrn2 accelerates termination by RNA polymerase II, which is underpinned by CPSF73 activity |
0.84 |
|
Mutually Exclusive CBC-Containing Complexes Contribute to RNA Fate. |
0.82 |
|
UV-Irradiation Induces a Noncoding RNA that Functionally Opposes the Protein Encoded by the Same Gene |
0.79 |
|
Xeno-free and Chemically Defined Human System for Culturing Human Epidermal Keratinocytes |
0.77 |
|
mRNA expression levels in splenic human mononuclear cells of mock- and HIV-1-infected humanized mice |
0.73 |
|
Mesothelioma xenografts in nude mice: PBS treated versus pirfenidone treated |
0.71 |
|
TimeLapse-seq: adding a temporal dimension to RNA sequencing through nucleoside recoding |
0.67 |
|
RUNX1 mutations lead to a myeloid differentiation block by altering the RUNX1 transcriptional program |
0.67 |
|
RUNX1 mutations lead to a myeloid differentiation block by altering the RUNX1 transcriptional program (RNA-Seq) |
0.67 |
|
RNA expression profiles comparing primary and omental ovarian carcinoma samples |
0.66 |
|
RNA-Seq of SHEP TET21N cells upon Doxorubicin treatment |
0.64 |
|
Pre-clinical evaluation of cysteamine bitartrate as a therapeutic agent for mitochondrial respiratory chain disease |
0.61 |
|
Pre-clinical evaluation of cysteamine bitartrate as a therapeutic agent for mitochondrial respiratory chain disease (human) |
0.61 |
|
CBFβ-MYH11 fusion blocks hematopoietic differentiation via repression of a GATA2 gene program |
0.59 |
|
Myc activation coordinates gene transcription and protein translation responses |
0.56 |
|
Targeting Spt5-Pol II small-molecule inhibitors uncouple distinct activities and reveal additional regulatory roles |
0.54 |
|
Multi-platform assessment of transcriptional profiling technologies utilizing a precise probe mapping methodology |
0.52 |
|
Compare of gene expression between p16INK4A positive and negative regions of colon cancer from five patients |
0.5 |
|
The RNA hairpin binder TRIM71 modulates alternative splicing by repressing Mbnl1 [RNA-seq & Ribo-seq] |
0.48 |
|
The RNA hairpin binder TRIM71 modulates alternative splicing by repressing MBNL1 |
0.48 |
|
CLIC5: a novel ETV6 target gene in childhood acute lymphoblastic leukemia |
0.46 |
|
MHC Transcriptomic landscape at haplotype-specific resolution |
0.46 |
|
Splicing function of mitotic regulators links R-loop mediated DNA damage to tumor cell killing |
0.38 |
|
Acetylation-Dependent Control of Global Poly(A) RNA Degradation by CBP/p300 and HDAC1/2 |
0.36 |
|
Transcriptome-profiling (RNA-seq) and Ribosome-profiling (Ribo-seq) in proliferation, quiescence, senescence and transformed states. |
0.25 |
|
DHX36 resolves G-rich structures in mRNA untranslated region to allow their translation |
0.24 |
|
Inheritable Silencing of Endogenous Genes by Hit-and-Run Targeted Epigenetic Editing |
0.2 |
|
ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing (RNA-seq) |
0.19 |
|
ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing |
0.19 |
|
The effect of slow and rapid H2S production on the levels of LPS-induced proinflammatory mediators and transcription in different human cell cultures |
0.14 |
|
YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction. |
0.11 |
|
YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction [RNA-seq] |
0.11 |
|
Expression profile of MM.1S tumors folloiwing treatment with bortezomib |
0.1 |
|
Mouse Dux is myotoxic and shares partial functional homology with its human paralog DUX4 |
0.1 |