|
RNA sequencing analysis of human embryonic stem cells and axial progenitors |
114.49 |
|
RNA-seq analysis of RALD iPSCs after in vitro differentiation |
51.34 |
|
RNA-Seq from early time points in the kidney differentiation protocol |
49.98 |
|
‘Naïve’ ESRRB+ iPSCs with the capacity for rapid neural differentiation |
47.77 |
|
Safeguarding nucleolar homeostasis by CBX4 alleviates senescence and osteoarthritis |
44.79 |
|
RNA-seq of UGP2 mutant human embryonic stem cells and in vitro differentiated neural stem cells |
43.79 |
|
CD95/Fas ligand mRNA is toxic to cells |
41.6 |
|
Global transcriptional analysis of human extended pluripotent stem cells, human primed pluripotent stem cells, mouse extended pluripotent stem cells, and mouse embryonic stem cells by RNA-seq |
40.2 |
|
Global transcriptional analysis and genome-wide analysis of chromatin state in extended pluripotent stem cells, primed pluripotent stem cells, and naïve pluripotent stem cells |
40.2 |
|
Detailed genomic and molecular characterization of Indian induced pluripotent stem cell lines |
39.88 |
|
mRNA sequencing of the global effect of SOX2 on gene expression in hESC and hESC derived NPCs. |
38.03 |
|
A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging |
37.93 |
|
Total RNA sequencing of prospective axial stem cell cultures derived from human pluripotant stem cells |
37.92 |
|
The effect of engineered del(7q) on induced pluripotent stem cells (iPSCs) derived from patients with Shwachman Diamond Syndrome (SDS). |
36.86 |
|
Enriched retinal ganglion cells derived from human embryonic stem cells (RNA-seq) |
36.56 |
|
Prostate Cancer Cell RNA-Seq (PC3E and GS689.Li) |
36.18 |
|
MARS Seq data from human cortical organoids |
35.62 |
|
RNA-Seq profiling of days 0, 7 and 18 kidney organoids differentiated from three separate vials of starting material |
34.74 |
|
Transcription factors OVOL1 and OVOL2 induce the mesenchymal to epithelial transition in human cancer |
33.53 |
|
A myogenic double reporter human pluripotent stem cell line allows prospective isolation of skeletal muscle progenitors |
30.64 |
|
Transcriptional alteration after ionizing radiation exposure in human fibroblasts, iPSCs and NPCs |
30.23 |
|
RNA-seq of YB5 and MCF7 treated with different doses of decitabine |
30.02 |
|
Effector and regulatory T cells roll at high shear stress by inducible tether and sling formation |
28.68 |
|
Genome-wide maps of m6A circRNAs identify widespread and cell-type-specific methylation patterns that are distinct from mRNAs |
28.29 |
|
Transcriptome analysis of human embryonic stem cells (hESCs) and human fibroblasts upon rapamycin |
26.59 |
|
Induced pluripotent stem cell modeling of bone marrow failure and MDS identifies therapeutic targets |
26.23 |
|
Transcriptome variation among human embryonic stem cell lines impacts on their differentiation |
26.18 |
|
Transcriptome analysis of genetically matched human induced pluripotent stem cells disomic or trisomic for chromosome 21 |
25.84 |
|
Differentially expressed (DE) genes analysis in synovial fluid mesenchymal stem cells (SF-MSCs), SF-MSC derived iPSCs and iPSC derived MSCs (iPSC-MSCs) |
25.09 |
|
Transcriptome analysis of H9 hESC derived cerebral organoids |
25.05 |
|
Post-transcriptional manipulation of TERC reverses molecular hallmarks of telomere disease |
24.6 |
|
Reprogramming by de-bookmarking somatic transcriptional program via targeting the BET bromodomains |
24.46 |
|
Lineage specific differentiation is influenced by state of human pluripotency |
24.32 |
|
Lineage specific differentiation is influenced by state of human pluripotency [RNA-seq] |
24.32 |
|
Differentially expressed vascular development genes for iPSC-ECs from CDI |
24.31 |
|
GLIS3 Transcriptionally Activates WNT Genes to Promote Differentiation of Human Embryonic Stem Cells to Posterior Neural Progenitors |
23.72 |
|
RNA-Seq analysis of neurons derived from induced pluripotent stem cells reprogrammed from dental pulp |
23.43 |
|
RNA-seq of YB5 cells treated with Proscillaridin A |
22.34 |
|
Dynamic reorganization of nuclear architecture during human cardiogenesis [RNA-seq] |
21.94 |
|
Dynamic reorganization of nuclear architecture during human cardiogenesis |
21.94 |
|
Gene expression profiling of neural crest progenitor cultures derived from human embryonic stem cells carrying nonsense mutations in the Polycomb gene ASXL1 [HOM] |
21.8 |
|
Progressive motor neuron pathology and the role of astrocytes in a human stem cell model of VCP-related ALS |
21.54 |
|
Cerebellar differentiation in Ataxia-Telangiectasia |
21.32 |
|
Genome-wide transcriptome analysis of NIPBL iPSC and commited cardiomyoctes |
20.99 |
|
High-efficiency RNA-based reprogramming of human primary fibroblasts |
20.81 |
|
Generation of a Panel of Induced Pluripotent Stem Cells From Chimpanzees: a Resource for Comparative Functional Genomics (RNA-Seq) |
20.28 |
|
Generation of a Panel of Induced Pluripotent Stem Cells From Chimpanzees: a Resource for Comparative Functional Genomics |
20.28 |
|
Ectoderm specification of H1 human embryonic stem cells |
20.0 |
|
Grainyhead-like 2 (GRHL2) and epigenetic remodeling in the intermediate states of epithelial-mesenchymal transition |
19.77 |
|
Grainyhead-like 2 (GRHL2) and epigenetic remodeling in the intermediate states of epithelial-mesenchymal transition [RNA-seq] |
19.77 |
|
The RNA hairpin binder TRIM71 modulates alternative splicing by repressing MBNL1 |
19.64 |
|
The RNA hairpin binder TRIM71 modulates alternative splicing by repressing Mbnl1 [RNA-seq & Ribo-seq] |
19.64 |
|
Transcriptome profiling of self-renewing hESCs and multipotent mesoderm progenitor cells as a function of substrate stiffness |
18.8 |
|
RNA-sequencing based transcriptome-wide expression profiling of Cynomolgus monkey and human IPSCs in vitro differentiated into endothelial cells |
18.7 |
|
Folliculin regulates mTORC1/2 and WNT pathways in early human pluripotency |
18.65 |
|
Expression profiles of the four human major ectodermal lineages |
18.46 |
|
Deciphering the ‘m6A code’ via quantitative profiling of m6A at single-nucleotide resolution |
18.14 |
|
Deciphering the ‘m6A code’ via quantitative profiling of m6A at single-nucleotide resolution [III] |
18.14 |
|
Cell Type-Specific Chromatin Signatures Underline Regulatory DNA Elements in Human Induced Pluripotent Stem Cells and Somatic Cells |
18.06 |
|
Poly(A)-specific ribonuclease (PARN) mediates 3' end maturation of the telomerase RNA component |
18.03 |
|
Comprehensive analysis of Long non-coding RNA expression in dorsal root ganglion reveals cell type specificity and dysregulation following nerve injury |
17.94 |
|
Comprehensive analysis of Long non-coding RNA expression in dorsal root ganglion reveals cell type specificity and dysregulation following nerve injury [human iPS] |
17.94 |
|
mRNA and RNC-mRNA deep sequencing of three hepatocellular carcinoma cell lines |
17.27 |
|
A global identification of PUM1 and PUM2 mRNA targets and their protein cofactors in human seminoma TCam-2 cells |
17.18 |
|
Global Transcriptome Analysis and Enhancer Landscape of Human Primary T Follicular Helper and T Effector Lymphocytes |
17.04 |
|
Global Transcriptome Analysis and Enhancer Landscape of Human Primary T Follicular Helper and T Effector Lymphocytes (RNA-Seq) |
17.04 |
|
Acetyl-CoA carboxylase inhibition regulates microtubule dynamics and intracellular transport in cystic fibrosis epithelial cells |
16.84 |
|
RNA sequencing for human induced pluripotent stem cell cardiomyocyte differentiation |
16.72 |
|
Human germ cell formation in xenotransplants of induced pluripotent stem cells carrying X chromosome aneuploidies |
16.6 |
|
Transcriptomic Reprogramming of Prostate Cancer Cells Driven by Stroma-Derived SPINK1 |
16.57 |
|
RUNX2/CBFB modulates the response to MEK inhibitors through activation of receptor tyrosine kinases in KRAS mutant colorectal cancer |
16.2 |
|
Error-free and error-prone DNA repair gene expression through reprogramming and passage in human iPS cells |
15.86 |
|
iPSC-Derived Cholangiocytes |
15.57 |
|
Verification and rectification of cell type-specific splicing of a Seckel syndrome-associated ATR mutation using iPS cell model |
15.57 |
|
Targeted differentiation of regional ventral neuroprogenitors and related neuronal subtypes from human pluripotent stem cells |
15.55 |
|
WRN knockout effects upon gene expression in SW48 and OVK18 |
15.49 |
|
Transcriptome analysis of PRMT6 knock-out in NT2/D1 cells |
15.29 |
|
Genomic location of PRMT6-dependent H3R2 methylation is decisive for the transcriptional outcome of associated genes |
15.29 |
|
Tumor suppressor SMARCB1 suppresses super-enhancers to govern hESC lineage determination |
15.27 |
|
Improved LCL to iPSC reprogramming: RNA Analysis of LCLs, reprogrammed iPSCs, and differentiated NSCs reveal potential regulatory and functional processes involved in these cellular transitions. |
14.8 |
|
AKAP8 inhibits tumor metastasis by antagonizing EMT-associated RNA alternative splicing |
14.73 |
|
Temporal activation of NR5A2 and RARγ induce functional human naïve pluripotent state via modulating TGFβ pathway |
14.53 |
|
yylncT acts as a gatekeeper of the mesodermal transcriptional program by local modulation of DNMT3B [human_2] |
14.4 |
|
m6A level and isoform characterization sequencing (m6A-LAIC-seq) reveal the census and complexity of the m6A epitranscriptome |
14.32 |
|
Laminin-guided highly efficient endothelial commitment from human pluripotent stem cells [Bulk RNA-Seq] |
14.17 |
|
Functional interactions between Mi-2β and AP1 complexes control response and recovery from barrier disruption |
14.04 |
|
RNA Sequencing Facilitates Quantitative Analysis of Transcriptomes of human mesenchymal stem cells differentiation from human embryonic stem cells and adult bone marrow mesenchymal stem cells |
14.03 |
|
Engineering Patient-Specific Tissue Implants |
13.93 |
|
Mechanistic Model-Guided Study of Embryonic Morphogenesis |
13.78 |
|
Transcription-dependent control of stem cell self-renewal and differentiation by the splicing factor U2AF1 |
13.76 |
|
RNA-Seq analysis and comparison of corneal epithelium in keratoconus and myopia patients |
13.52 |
|
Transcripotome analysis of different locations of hair follicles (bulb, bulge) in androgenetic alopecia |
13.49 |
|
RNA-Seq of cKIT+ sorted cells from 16-16.5 week old fetal testes and ovaries and RNA-Seq of TRA-1-60+ H1 hESCs |
13.19 |
|
Identification of transcripts altered upon LIN-41 knockdown in human embryonic stem cells |
13.04 |
|
Differential expression of human parthenogenic stem cells, neural stem cells and DA progenitors. |
12.89 |
|
Non-transmissible measles virus vector with segmented RNA genome establishes different types of iPSCs from hematopoietic cells |
12.87 |
|
Mechanism suppressing H3K9 trimethylation in pluripotent stem cells and its demise by polyQ-expanded huntingtin mutations |
12.84 |
|
Mechanism suppressing H3K9 trimethylation in pluripotent stem cells and its demise by polyQ-expanded huntingtin mutations [RNA-seq] |
12.84 |
|
RNA-seq of naive and primed ES cells (NHSM) |
12.74 |
|
Developing a Novel Two-Dimensional Culture System to Enrich Human Prostate Luminal Progenitors That Can Function as a Cell of Origin for Prostate Cancer |
12.68 |
|
Profiling of gene expression using RNA-Seq in fibroblasts, iPSCs, iPSC-derived neurons and cells overexpressing Onecut transcription factors |
12.28 |
|
Changes in chromatin accessibility and gene expression induced by overexpression of ONECUT transcription factors |
12.28 |
|
The RNA helicase DDX6 regulates self-renewal and differentiation of human and mouse stem cells [RNA-seq2] |
12.0 |
|
The acetyllysine reader BRD3R promotes human nuclear reprogramming and regulates mitosis |
11.95 |
|
Critical role of transient activation of human endogenous retroviruses during reprogramming toward pluripotency |
11.84 |
|
Critical role of transient activation of human endogenous retroviruses during reprogramming toward pluripotency (RNA-Seq) |
11.84 |
|
Nucleotide excision repair capacity increases during differentiation of human embryonic carcinoma cells into neurons and muscle cells |
11.75 |
|
Characterization and therapeautic application of mesenchymal stem cells with neuromesodermal origin from human pluripotent stem cells |
11.58 |
|
Derivation of kidney organoids from human pluripotent stem cells [RNA-Seq: Data Set 2] |
11.34 |
|
Disruption of the TFAP2A regulatory domain causes Branchio-Oculo-Facial Syndrome (BOFS) and illuminates pathomechanisms for other human neurocristopathies [RNA-seq data set 2] |
11.17 |
|
BI Human Reference Epigenome Mapping Project |
11.12 |
|
Temporal dynamic reorganization of 3D chromatin in hormone-induced breast cancer and endocrine resistance |
11.09 |
|
mRNA expression data from human parthenogenetic haploid ESCs (hPGES), normal ESCs (H9) and human fibroblast |
10.94 |
|
Genomic analysis of human parthenogenetic haploid ESCs (hPGES), normal human ESCs(H9) and human forskin fibroblast |
10.94 |
|
Landscape of Hematopoiesis Described in Induced Pluripotent Stem Cells and Human Bone Marrow |
10.92 |
|
Derivation of kidney organoids from human pluripotent stem cells [RNA-Seq: Data Set 1] |
10.92 |
|
DRB/GRO-Seq -/+ UV |
10.74 |
|
Genome-wide CRISPR-Cas9 screen identifies SLC1A3 as a key contributor to L-asparaginase Resistance in Solid tumors |
10.58 |
|
Estrogen response in breast cancer cell line MCF-7 is dependent on NR2F2 [RNA-seq] |
10.51 |
|
NR2F2 study |
10.51 |
|
Cerebral Organoids Recapitulate Epigenomic Signatures of the Human Fetal Brain |
10.51 |
|
RNA Sequencing Facilitates Quantitative Analysis of Transcriptomes of H1, H1 derived APLNR+ cells, CD31+CD34+ cells and CD43+ cells during human early hematopoietic differentiation |
10.37 |
|
Transcriptome analysis reveals determinant stages controlling human embryonic stem cell commitment to neuronal cells |
10.32 |
|
Modelling and rescuing neurodevelopmental defect of Down syndrome using induced pluripotent stem cells from monozygotic twins discordant for trisomy 21 |
10.29 |
|
Modelling and rescuing neurodevelopmental defect of Down syndrome using induced pluripotent stem cells from monozygotic twins discordant for trisomy 21 [RNA-seq] |
10.29 |
|
Identification of PRMT5-dependent genes in ESA+CD24lowCD44+ MCF7 cells |
10.08 |
|
BAF controls genome accessibility |
10.03 |
|
Expression profiles of long non-coding RNAs located in autoimmune disease-associated regions reveal immune cell type specificity |
9.88 |
|
Self-organized amniogenesis by human pluripotent stem cells in a biomimetic implantation-like niche |
9.86 |
|
Rapid neurogenesis through transcriptional activation in human stem cell (RNA-Seq) |
9.74 |
|
Integrative analysis of mRNA and lncRNA profiles identified pathogenetic lncRNAs in esophageal squamous cell carcinoma |
9.46 |
|
Heterozygous and homozygous knock-in of PIK3CA-H1047R into human iPSCs |
9.35 |
|
hESC neural differentiation |
9.32 |
|
RNA-seq analysis of gene expression patterns during hESC neural differentiation |
9.32 |
|
ARID1A is a critical regulator of luminal identity and therapeutic response in oestrogen receptor-positive breast cancer (RNA-Seq) |
9.27 |
|
Analysis of human ES cell differentiation establishes that the dominant isoforms of the lncRNAs RMST and FIRRE are circular |
9.2 |
|
Acquisition of a hybrid E/M state is essential for tumorigenicity of basal breast cancer cells |
9.18 |
|
Effect of circPTPRM on the biological behaviors of hepatocellular carcinoma cells in vitro and its clinical significance. |
9.1 |
|
Transcriptome analysis in HT29 and SW480 cells depleted of Prdx2 |
8.91 |
|
In vivo generation of post-infarct human cardiac muscle by laminin-promoted cardiovascular progenitors [LN-521 or LN-521+LN-221] |
8.88 |
|
Culture-induced recurrent epigenetic aberrations in human pluripotent stem cells |
8.84 |
|
Culture-induced recurrent epigenetic aberrations in human pluripotent stem cells [RNA-seq] |
8.84 |
|
Evidence for HOXC6 as a potential molecular marker for non-small cell lung cancer |
8.82 |
|
Deep sequencing of transcript levels in pluripotent stem cells and their differentiated derivatives in all three germ layers |
8.77 |
|
RNA-seq of naive and primed ES cells |
8.75 |
|
UTX and 53BP1 co-regulate genetic programs for neural differentiation of human embryonic stem cells [RNA-seq] |
8.72 |
|
UTX and 53BP1 co-regulate genetic programs for neural differentiation of human embryonic stem cells |
8.72 |
|
Transcriptional Regulationand Chromatin Dynamics inHuman Epithelial Cell Differentiation |
8.6 |
|
Transcriptional Regulationand Chromatin Dynamics inHuman Epithelial Cell Differentiation (RNA-seq) |
8.6 |
|
RNA-Seq analysis of cSCC cells after siRNA-induced gene knockdown of lncRNA PRECSIT |
8.55 |
|
Genome-scale screens identify JNK/JUN signaling as a barrier for pluripotency exit and endoderm differentiation |
8.49 |
|
Estrogen deprivation triggers and immunosuppressive phenotype in breast cancer cells |
8.47 |
|
Reprogramming postnatal human epidermal keratinocytes toward functional neural crest fates |
8.44 |
|
Hypertonic saline attenuates the cytokine-induced pro-inflammatory signature in primary human lung epithelia |
8.24 |
|
Examining serotonergic neuron differentiation from human iPSCs |
8.16 |
|
CD161+ Tconv and Treg share transcriptome and display a migratory phenotype which is modified at the inflamed site |
8.08 |
|
The RNA helicase DDX6 regulates self-renewal and differentiation of human and mouse stem cells [RNA-seq] |
8.08 |
|
Multiple roles for Grainyheadlike transcription factors in the establishment and maintenance of human mucociliary airway epithelium |
8.01 |
|
Polycomb complexes associate with enhancers to promote oncogenic transcriptional programs in cancer |
7.99 |
|
Next Generation Sequencing Analysis of human embryonic stem cells derived MESP1-mTomato reporter cells |
7.92 |
|
Derivation and differentiation of haploid human embryonic stem cells |
7.62 |
|
Characterization of sperm lncRNA and its differently expression in the sperm of asthenozoospermic patients |
7.59 |
|
Coding mutations and loss-of-imprinting in human pluripotent cells derived by nuclear transfer and defined factors |
7.55 |
|
Coding mutations and loss-of-imprinting in human pluripotent cells derived by nuclear transfer and defined factors [RNA-Seq] |
7.55 |
|
Expansion, in vivo-ex vivo cycling and genetic manipulation of primary human hepatocytes |
7.52 |
|
Transcriptional changes after overexpression of proliferation drivers in human mammary epithelial cells. |
7.52 |
|
Endothelial Cells Control Pancreatic Cell Fate at Defined Stages through EGFL7 Signaling |
7.51 |
|
Modeling Trilateral Retinoblastoma using Human Embryonic Stem Cells |
7.42 |
|
SIX4 acts as a master regulator of genes associated with the malignant phenotype of non-small cell lung cancer cells |
7.36 |
|
Human naïve pluripotent stem cells exhibit X chromosome dampening and X-inactivation (RNA-Seq) |
7.31 |
|
The E3 ubiquitin ligase HectD1 suppresses EMT and metastasis by targeting the +TIP protein ACF7 for degradation |
7.31 |
|
LSD1 mediates AKT activity in PIK3CA mutant colorectal cancer |
7.31 |
|
LSD1 mediates AKT activity in PIK3CA mutant colorectal cancer [RNA-Seq] |
7.31 |
|
Characterization and transplantation of enteric neural crest cells from human induced pluripotent stem cells |
7.24 |
|
Analysis of chromosomal aberrations and recombination by allelic bias in RNA-Seq |
7.11 |
|
AMPK signaling for naïve pluripotency |
7.04 |
|
AMPK signaling for naïve pluripotency [Hs] |
7.04 |
|
miRNA-1343 attenuates pathways of fibrosis by targeting the TGF-beta receptors [RNA-seq] |
6.98 |
|
Proliferation-correlated expression |
6.96 |
|
Tamoxifen Resistance in Breast Cancer is Regulated by the EZH2-ERa-GREB1 Transcriptional Axis |
6.87 |
|
Transcriptomic insights into human decidual and peripheral blood CD8 T cells |
6.73 |
|
Dermal fibroblasts play a central role in skin model protection against C. albicans invasion |
6.69 |
|
FGF2 regulation of gene expression in stable inducible Neurons |
6.69 |
|
RNA sequence analysis of stable versus reversible EMT events and the resultant metastases |
6.69 |
|
Analysis of the Clustered Protocadherin (cPcdh) Locus in Human Pluripotent Stem and Derived Cells [RNA-seq II our of II] |
6.64 |
|
Analysis and expansion of the eosinophilic esophagitis transcriptome by RNA sequencing |
6.6 |
|
Derivation and differentiation of haploid human embryonic stem cells [RNA-Seq 1] |
6.52 |
|
LncRNA-GAS5 negative regulation of YAP-target genes expression |
6.47 |
|
Campylobacter concisus pathotypes induce distinct global responses in intestinal epithelial cells [Toxin] |
6.37 |
|
Oncogenic Notch promotes long-range regulatory interactions within hyperconnected 3D cliques [MB157_RNA-seq] |
6.28 |
|
Next Generation Sequencing of human SMA and healthy control Motor Neurons |
6.27 |
|
The Notch driven long non-coding RNA repertoire in T-cell acute lymphoblastic leukemia |
6.23 |
|
RNA Sequencing Facilitates Quantitative Analysis of Transcriptomes of H1 and H1 after SNAI1 deletion at Day2 after human early hematopoietic differentiation . |
6.22 |
|
Profiles of Long Noncoding RNAs in Human Naive and Memory T Cells |
6.21 |
|
Helios enhances the preferential differentiation of human fetal CD4+ naïve T cells into regulatory T cells. [RNA-Seq - ex vivo] |
6.15 |
|
Molecular pathogenesis of human prostate basal cell hyperplasia reveals a keratinocyte metaplasia |
6.12 |
|
Oncogenic Serine-Threonine Kinase Receptor Associated Protein Supports Hepatocellular Carcinoma Cell Growth by Enhancing Wnt/β-catenin Signaling |
6.1 |
|
Characterization of EZH2-deficient human embryonic stem cells [ChIP-seq and bulk RNA-seq] |
6.08 |
|
Robust generation of honemogeneous midbrain organoids with in vivo–like cellular composition facilitates neurotoxin-based Parkinson’s disease modeling |
6.03 |
|
Codon usage optimization in pluripotent embryonic stem cells [RNA-seq] |
6.0 |
|
circRNA profile in hypopharyngeal cancer |
5.89 |
|
The metabolome regulates the epigenetic landscape during naïve to primed human embryonic stem cell transition |
5.85 |
|
Poly(ADP-ribosyl)ation dependent changes in CTCF-chromatin binding and gene expression in breast cells |
5.64 |
|
Genome-wide expression profiling of an in vitro model for studying esophageal epithelial differentiation |
5.6 |
|
Generation of targeted homozygosity in the genome of human induced pluripotent stem cells |
5.55 |
|
C9/ALS Human Embryonic Stem Cells and C9/ALS Induced Pluripotent Stem Cells |
5.53 |
|
POU2AF1 Functions in the Human Airway Epithelium to Regulate Expression of Host Defense Genes [RNA-Seq] |
5.49 |
|
POU2AF1 Functions in the Human Airway Epithelium to Regulate Expression of Host Defense Genes |
5.49 |
|
Long Non-coding RNA PICSAR Promotes Growth of Cutaneous Squamous Cell Carcinoma by Regulating ERK1/2 Activity |
5.47 |
|
Determination of a comprehensive alternative splicing regulatory network and the combinatorial regulation by key factors during Epithelial-to-Mesenchymal Transition [ESRP KD] |
5.43 |
|
Bach1 Regulates the Self-renewal and Mesendodermal Differentiation of Human Embryonic Stem Cells |
5.41 |
|
RNA-Seq from human ILC transitional populations |
5.41 |
|
Expression profiling of ILC transitional populations and Aiolos accessability and H3K27ac histone modifications in transfected MNK3 cells |
5.41 |
|
Analysis Of The TGFb-Induced Program In Primary Airway Epithelial Cells Shows Essential Role Of NF-kB/RelA Signaling Network In Type II Epithelial Mesenchymal Transition |
5.36 |
|
Transcriptomic Reprogramming of Prostate Cancer Cells Driven by Stroma-Derived AREG |
5.35 |
|
RNA-Seq comparisons of gene expression profiles of epithelial and mesenchymal cells - HMLE, N8, N8-CTx |
5.3 |
|
ChIP-seq and RNA-Seq analyses of epithelial and mesenchymal cells - HMLE, N8, N8-CTx |
5.3 |
|
Histone Demethylase-Assisted Somatic Cell Nuclear Transfer Facilitates Derivation of Human Pluripotent Stem Cells |
5.28 |
|
Development of an In Vitro Human Liver System for Interrogating Non-Alcoholic Steatohepatitis |
5.19 |
|
Codon usage optimization in pluripotent embryonic stem cells [tRNA sequencing] |
5.19 |
|
Generating Patterned Kidney Organoids for Studying Development and Diseases [bulk RNA-Seq] |
5.17 |
|
Diverse Compounds from Pleuromutilin Lead to a Thioredoxin Inhibitor and Inducer of Ferroptosis |
5.04 |
|
Conserved roles for murine mDUX and human DUX4 in activating cleavage stage genes and MERVL/HERVL retrotransposons [RNA-Seq Human] |
5.04 |
|
Connexin 32-mediated cell-cell communication is essential for hepatic differentiation from human embryonic stem cells |
5.02 |
|
Paxillin regulates genomic networks in prostate cancer [LNCaP] |
5.0 |
|
Generation of KRAS signatures using immortalized isogenic lung cells. |
4.98 |
|
Pharmacological Induction of a Progenitor State for the Efficient Expansion of Primary Human Hepatocytes |
4.89 |
|
Human pluripotent stem cell-derived brain tumor model uncovered embryonic stem cell signature as a key driver in atypical teratoid/rhabdoid tumor (RNA-Seq) |
4.86 |
|
MKL1 augments megakaryocyte maturation by enhancing the SRF regulatory axis |
4.86 |
|
MKL1 augments megakaryocyte maturation by enhancing the SRF regulatory axis [RNA-seq] |
4.86 |
|
Regulation of DNA methylation landscape in human somatic cell reprogramming by miR-29 family |
4.85 |
|
Regulation of DNA methylation landscape in human somatic cell reprogramming by miR-29 family (RNA-seq) |
4.85 |
|
Transcriptomic analysis reveals novel long non-coding RNAs critical for vertebrate development [RNA-Seq] |
4.85 |
|
Transcriptomic analysis reveals novel long non-coding RNAs critical for vertebrate development |
4.85 |
|
Exploring the gene expression profile upon FXR1 knockdown in H358 cells using RNA-seq |
4.84 |
|
Activin/Smad2-induced H3K27me3 reduction is crucial to initiate mesendoderm differentiation of ES Cells |
4.83 |
|
Dynamic developmental signaling logic underlying lineage bifurcations during human endoderm induction and patterning from pluripotent stem cells [Endoderm RNA-seq and ChIP-seq data sets] |
4.8 |
|
Dynamic developmental signaling logic underlying lineage bifurcations during human endoderm induction and patterning from pluripotent stem cells |
4.8 |
|
RNA-sequencing analysis of CD4 T cells following ipilimumab therapy |
4.79 |
|
Patient-derived xenograft models of non-small cell lung cancer for evaluating targeted drug sensitivity and resistance |
4.72 |
|
Gene Expression of Breast Cancer Cell Lines Across Biomaterial Platforms |
4.68 |
|
Genetic disruption of COX-1 inhibits multiple oncogenic pathways |
4.68 |
|
Transcriptomic analysis of human iPS cells derived from fragile X syndrome patients during neural differentiation |
4.67 |
|
CDK12 catalytic activity is rate-limiting for RNAPII processivity on core DNA replication genes and G1/S progression (nuclear RNA) |
4.67 |
|
Transcriptional regulation in pluripotent stem cells by Methyl CpG binding protein 2 (MeCP2) |
4.62 |
|
RNA-seq of human aneuploid cell lines with Trisomy 21 |
4.6 |
|
The RNA exosome nuclease complex regulates human embryonic stem cell differentiation [RNA-Seq SS] |
4.52 |
|
PRC2 specifies ectoderm lineages and maintains pluripotency in primed but not naïve ESCs |
4.48 |
|
High-throughput sequencing of pluripotent cells |
4.43 |
|
The Molecular Dissection of the Oncogenic Role of ETS1 in the Mesenchymal Subtypes of Head and Neck Squamous Cell Carcinoma [RNA-seq knock-down] |
4.39 |
|
|
4.38 |
|
The phosphatidylinositol 3-kinase pathway as a potential therapeutic target in bladder cancer |
4.37 |
|
A high-throughput screening strategy identifies regulators of alternative splicing via interaction with RNA G-quadruplexes |
4.34 |
|
Nickel induced transcriptional changes persist post exposure through epigenetic reprograming |
4.31 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of SW480 cells and HPSE-knockdown SW480 cells Transcriptomes |
4.28 |
|
Single-cell transcription profiling in KS1 patient iPSCs and NPCs |
4.27 |
|
Gata6 potently initiates reprogramming of pluripotent and differentiated cells to extraembryonic endoderm stem cells [ChIP-Seq & RNA-Seq] |
4.26 |
|
Gata6 potently initiates reprogramming of pluripotent and differentiated cells to extraembryonic endoderm stem cells |
4.26 |
|
RNAseq of ribosomal fractionation to assess the effect of CBFB on translation regulation |
4.26 |
|
Functional Haploid Human Oocytes Generated from Polar Body Genomes (RNA-Seq) |
4.21 |
|
Functional Haploid Human Oocytes Generated from Polar Body Genomes |
4.21 |
|
Profiling of lung tumor-infiltrating CD8 T cells according to their expression status of CD39 |
4.2 |
|
Transcriptional differences between skin from patients with atopic dermatitis and control skin obtained from the healthy margins of Mohs surgery patients |
4.2 |
|
Repression of stress-induced LINE-1 expression protects cancer cell populations from lethal drug-exposures [RNA-Seq] |
4.13 |
|
Repression of stress-induced LINE-1 expression protects cancer cell populations from lethal drug-exposures |
4.13 |
|
Postnatal lipids drive hepatocyte maturation |
4.1 |
|
Directed differentiation of human embryonic stem cells to corneal endothelial cell-like cells: A transcriptomic analysis |
4.1 |
|
Comparative principles of DNA methylation reprogramming during human and mouse in vitro primordial germ cell specification |
4.09 |
|
Comparative principles of DNA methylation reprogramming during human and mouse in vitro primordial germ cell specification [Mouse and Human RNA-seq and BS-seq] |
4.09 |
|
RNA-seq analysis of HT-29, MCF10A, and MDA-MB-436 cells |
4.07 |
|
RNA-seq Analysis of Castration-Resistant Prostate Cancer With Knock-down of E2F1 |
4.05 |
|
A peninsular structure coordinates asynchronous differentiation with morphogenesis to generate pancreatic islets [bulk vs buds] |
4.05 |
|
Targeted reactivation of FMR1 transcription in FXS embryonic stem cells |
4.02 |
|
RNA sequencing of lesional and nonlesional skin from patients with atopic dermatitis |
4.02 |
|
Bladder cancer associated mutations in RXRA activate peroxisome proliferator-activated receptors |
4.01 |
|
Bladder-cancer-associated mutations in RXRA activate peroxisome proliferator-activated receptors to drive urothelial proliferation |
4.01 |
|
Transcriptomic and gene ontology profiling of the human corneal cell types |
3.99 |
|
A specific missense mutation in GTF2I occurs at high frequency in thymic epithelial tumors |
3.88 |
|
The RNA exosome nuclease complex regulates human embryonic stem cell differentiation [RNA-Seq rescue_SS] |
3.84 |
|
Nickel induced transcriptional changes persist post exposure through epigenetic reprograming (ChIP-seq & RNA-seq datasets) |
3.77 |
|
The flightless I protein is involved in the genome-wide mRNA post-transcriptional regulation in lung carcinoma cells |
3.77 |
|
Stem and effector CD8 T-cells from human cancers |
3.76 |
|
RNA-Seq expression profiling of hepatocellular carcinoma and adjacent non-tumor liver tissues |
3.75 |
|
Identifying the molecular mode of action of itraconazole in colorectal cancer |
3.75 |
|
Transcriptome of EBV-infected gastric cancer cell lines |
3.71 |
|
TRPS1 shapes YAP/TEAD-dependent transcription in breast cancer cells |
3.67 |
|
TRPS1 shapes YAP/TEAD-dependent transcription in breast cancer cells [RNA-seq] |
3.67 |
|
RNA Seq of Alagille liver biopsies |
3.65 |
|
Alagille_Nodder |
3.65 |
|
Modulation of Indoleamine 2, 3-dioxygenase 1 Expression by Activated Human T cells in Breast Cancer Cells is Controlled by DNA Promoter Methylation |
3.65 |
|
RNA-seq differential expression studies: more sequence, or more replication? |
3.63 |
|
Large-scale epigenetic reprogramming is punctuated late during the evolution of pancreatic cancer progression |
3.62 |
|
LncPRESS1 is a p53-regulated lncRNA that safeguards pluripotency by disrupting SIRT6 mediated de-acetylation of histone H3K56 |
3.61 |
|
Cell-to-cell variation in defective virus expression and effect on host response during influenza virus infection |
3.57 |
|
Transcriptome of human keratinocytes with or without HPV16 oncogene expression |
3.56 |
|
G9a-Mediated Methylation of ERα Links the PHF20/MOF Histone Acetyltransferase Complex to Hormonal Gene Expression |
3.55 |
|
Transcriptome of activated human and mouse MAIT cells |
3.54 |
|
MEIS1 regulates hematopoiesis in hPSCs |
3.51 |
|
Selective modulation of inflammatory Natural Killer (NK) cell phenotypes following histone H3K27 demethylase inhibition [RNA-Seq] |
3.48 |
|
Selective modulation of inflammatory Natural Killer (NK) cell phenotypes following histone H3K27 demethylase inhibition |
3.48 |
|
KMT2C medaites the estrogen dependence of breast cancer through regulation of ERα enhancer function |
3.47 |
|
Disruption of the TFAP2A regulatory domain causes Branchio-Oculo-Facial Syndrome (BOFS) and illuminates pathomechanisms for other human neurocristopathies |
3.45 |
|
T-bet recruits P-TEFb to super-enhancers to regulate T helper cell differentiation (RNA-Seq) |
3.43 |
|
T-bet recruits P-TEFb to super-enhancers to regulate T helper cell differentiation |
3.43 |
|
RNA-Seq analysis of cSCC cells followed by siRNA-induced gene knockdown of AIM2. |
3.42 |
|
Growth factor-free, chemically-defined culture system for expansion and derivation of human pluripotent stem cells |
3.39 |
|
Human embryonic stem cells in E8 and AKIT culture medium |
3.39 |
|
Super-enhancer-driven CCAT1 is co-activated by SOX2 and TP63 and promotes squamous cancer from esophagus, head and neck and lung [RNA-seq] |
3.39 |
|
Super-enhancer-driven CCAT1 is co-activated by SOX2 and TP63 and promotes squamous cancer from esophagus, head and neck and lung |
3.39 |
|
Generation of mature lung alveolar epithelial cells from human pluripotent stem cells |
3.37 |
|
Campylobacter concisus pathotypes induce distinct global responses in intestinal epithelial cells [UNSWCD] |
3.35 |
|
RNA-seq analysis of melanoma and carcinoma cells expressing FOXQ1 |
3.26 |
|
Transcription factor p63 bookmarks genomic loci in epithelial cells and regulates a subset of target genes during epidermal differentiation through dynamic enhancers (RNA-Seq) |
3.24 |
|
Transcription factor p63 bookmarks genomic loci in epithelial cells and regulates a subset of target genes during epidermal differentiation through dynamic enhancers |
3.24 |
|
RNA-seq of resting and activated CD4+ T cells +-JQ1 |
3.24 |
|
Alternative splicing regulated by QKI and RBFOX1 promotes the mesenchymal cell state in breast cancer |
3.15 |
|
RNA-sequencing in immortalized human mammary epithelial cells |
3.15 |
|
RNA-seq analysis reveals endogenous aryl hydrocarbon receptor regulation is highly associated with eicosanoid synthesis and tumor necrosis factor activity in MCF-7 cancer cells |
3.12 |
|
Recovery and analysis of nascent RNA |
3.11 |
|
The oncogenic BRD4-NUT chromatin regulator drives aberrant transcription within large topological domains |
3.11 |
|
RNA sequencing for lncRNA, miRNA and mRNA expression analysis in human laryngeal cancer |
3.11 |
|
GCTM-5 positive and negative cells in pancreatic adenocarcinoma cell lines |
3.1 |
|
LncRNA DEANR1 facilitates human endoderm differentiation by activating FOXA2 expression |
3.09 |
|
Next generation sequencing identifies discrete classes of box C/D snoRNAs featuring different ends and RNA binding protein dependency |
3.09 |
|
RNA seq data of Hep3B-control, Hep3B-sertraline, Hep3B-XL413, Hep3B-XL413-sertraline, Huh7-control, Huh7-sertraline, Huh7-XL413, Huh7-XL413-sertraline cells |
3.07 |
|
Global expression profiles in cardiac progenitor cells generated by ISX-9 |
3.05 |
|
Global mRNA expression profile in cardiac progenitor cells generated by ISX-9 |
3.05 |
|
RNA sequencing of CACO-2 cells incubated with bifidobacteria grown on human milk oligosaccharides. |
3.04 |
|
The NORAD lncRNA assembles a topoisomerase complex critical for genome stability |
3.03 |
|
The NORAD lncRNA assembles a topoisomerase complex critical for genome stability [RNA-seq] |
3.03 |
|
Epigenome regulation during epidermal lineage commitment |
3.02 |
|
An epigenetic mark of polycomb response elements implemented by Trx/MLL/COMPASS |
2.99 |
|
Single-cell RNA sequencing-based CRISPRi screening resolves molecular drivers of early human endoderm development |
2.98 |
|
Analysis of Th17 gene signature in the presence of CD28 costimulation in human CD4 naïve T cells |
2.97 |
|
4sU-seq of HFF exposed to salt and heat stress |
2.97 |
|
Identifying a novel candidate diagnostic and prognostic biomarker SPRR3 for oral squamous cell carcinoma via mRNA Sequencing and Bioinformatics |
2.96 |
|
Isogenic patient-derived human iPSCs, wild-type or heterozygous for PIK3CA-E418K |
2.86 |
|
Distinct roles of cohesin-SA1 and cohesin-SA2 in 3D chromosome organization |
2.84 |
|
Noncoding regions are the main source of targetable tumor-specific antigens |
2.83 |
|
Evaluating pre-clinical models for studying NASH driven HCC. |
2.82 |
|
Epigenome regulation during epidermal lineage commitment [RNA-seq] |
2.81 |
|
POLR3G Dependent PolyA+ and smallRNA Transcriptomes in Human Pluripotent Stem Cells |
2.7 |
|
RNA-Seq Analysis in hES/ iPS cell-derived neuronal samples |
2.69 |
|
Single-Cell RNA Sequencing Reveals Metallothionein Heterogeneity during hESC Differentiation to Definitive Endoderm [RNA-Seq] |
2.69 |
|
Single-Cell reconstruction of differentiation trajectory reveals essential dynamics in human cardiac lineage commitment |
2.69 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of mesoderm posterior bHLH transcription factor 1(MESP1)+ and MESP1- cells' Transcriptomes |
2.69 |
|
Human induced pluripotent stem cell-derived vocal fold mucosa mimics development and responses to smoke exposure |
2.69 |
|
Pancreatic cancer-derived exosomes induce apoptosis of T lymphocytes through the p38 MAPK signal transduction pathway |
2.68 |
|
The RNA exosome nuclease complex regulates human embryonic stem cell differentiation |
2.63 |
|
TCR and inflammatory signals tune human MAIT cells to exert specific tissue repair and effector functions |
2.59 |
|
SOX17 Is a Critical Specifier of Human Primordial Germ Cell Fate |
2.58 |
|
Transcriptomic analysis of primary human T cells and murine RAW 264.7 macrophages 3D cultured in different collagen densities |
2.57 |
|
Paxillin regulates genomic networks in prostate cancer [PC3] |
2.54 |
|
mRNAseq of Huntington's disease and control patient iPSC-derived brain microvascular endothelial cells |
2.54 |
|
Engineered human pluripotent stem cell-derived intestinal tissues with a functional enteric nervous system |
2.52 |
|
Gene expression profiling of neural crest progenitor cultures derived from human embryonic stem cells carrying nonsense mutations in the Polycomb gene ASXL1 |
2.52 |
|
Hsa-miR-371a-5p and hsa-miR-518a-3p regulated genes in choriocarcinoma cells |
2.51 |
|
Epigenetic reprogramming at estrogen-receptor binding sites alters the 3D chromatin landscape in endocrine resistant breast cancer [RNA-seq] |
2.49 |
|
Epigenetic reprogramming at estrogen-receptor binding sites alters 3D chromatin landscape in endocrine resistant breast cancer |
2.49 |
|
Insights into snoRNA biogenesis and processing from PAR-CLIP of snoRNA core proteins and small RNA sequencing |
2.46 |
|
Chromatin remodeling mediated by ARID1A is indispensable for normal hematopoiesis in mice (human RNA-Seq) |
2.46 |
|
Analysis of transcriptomes of healthy donor and CD46 deficient CD8 T cells |
2.33 |
|
Transcriptome analysis of CD8+ T cells from healthy controls and patients wth CD46 deficiency |
2.33 |
|
DIGIT regulates endoderm differentiation of human embryonic stem cells |
2.27 |
|
Single-cell RNA sequencing-based CRISPRi screening resolves molecular drivers of early human endoderm development [set 1] |
2.27 |
|
Microglia innatly develop within cerebral organoids |
2.25 |
|
Transcriptome analysis of PC9 cells with gefitinib or/and hypoxia treatment and comparison with gefitinib resistant PC9 cells and ALDH positive PC9 cells |
2.25 |
|
Investigate A2M treatment on human prostate cancer xenograft in mice |
2.21 |
|
Investigate A2M treatment on human prostate cancer and mouse liver |
2.21 |
|
Genome-wide effect of inhibition of glutamine transporter ASCT2 in PC-3 cells by BenSer or GPNA |
2.2 |
|
Analysis of HPV16 E2 host gene expression using TERT immortalized keratinocytes (NOKs) cell lines and RNA-sequencing |
2.19 |
|
Campylobacter concisus pathotypes induce distinct global responses in intestinal epithelial cells [BAA] |
2.18 |
|
Antiviral innate immunity of hepatitis C virus-infected stem cell-derived hepatocytes |
2.15 |
|
Homolog-selective degradation as a strategy to probe the function of CDK6 in AML |
2.15 |
|
RNA profiling Analysis of the Serum Exosomes Derived from Active and Latent M.tuberculosis infectious Patients |
2.14 |
|
An siRNA screen identifies CHD4 as a target for epigenetic therapy |
2.12 |
|
Neuronal Development And The Onset Of Electrical Activity In The Human Enteric Nervous System |
2.12 |
|
Gene expression profiling by RNA-seq of SW480 TGM2 knockdown cells |
2.11 |
|
The control of rRNA synthesis during the directed differentiation of human embryonic stem cells precedes heterochromatin formation. |
2.05 |
|
Transcriptomic analysis of iPSC and ESC challenged with atmospheric or physiological oxygen |
2.05 |
|
ETS1 is a genome-wide effector of RAS/ERK signaling in epithelial cells (RNA-Seq) |
2.05 |
|
ETS1 is a genome-wide effector of RAS/ERK signaling in epithelial cells |
2.05 |
|
Generating Patterned Kidney Organoids for Studying Development and Diseases |
2.03 |
|
Genome-wide maps of chromatin state and Gene Expression Profiling in HCT116 cells |
2.03 |
|
Gene Expression Profiling of WT and KDM3A Knocked out Cell |
2.03 |
|
Bioreactor-engineered cancer tissues mimic phenotypes, gene expression profiles and drug resistance mechanisms detectable in xenografts and clinical specimens. |
1.99 |
|
Gene expression profiling study by RNA-seq in PDX model based diffuse type gastric cancers. |
1.96 |
|
CSL |
1.96 |
|
CSL RNA-Seq on HKC and SCC cell lines |
1.96 |
|
RNA-sequencing |
1.96 |
|
Human antimicrobial cytotoxic T lymphocytes, defined by NK receptors and antimicrobial proteins, kill intracellular bacteria |
1.91 |
|
Gene expression analysis of human adenomas. |
1.91 |
|
RNA-seq analysis of hPSC-derived brain pericyte-like cells, hPSC-derived neural crest stem cells, and primary human brain pericytes |
1.91 |
|
Time series total RNA sequencing of a differentiation of human embryonic stem cells towards trophoblast lineage |
1.86 |
|
Spontaneous single-copy loss of TP53 in human embryonic stem cells markedly increases cell proliferation and survival |
1.86 |
|
Spontaneous single-copy loss of TP53 in human embryonic stem cells markedly increases cell proliferation and survival [RNA-Seq] |
1.86 |
|
Treatment of prostate cancer cells with S-adenosylmethionine leads to genomewide alterations of transcription profiles |
1.83 |
|
KRASG12C inhibition produces a driver-limited state revealing collateral dependencies |
1.83 |
|
Analysis of gene expression in primary human foreskin keratinocytes +/- HPV16 E7 or PTPN14 knockout |
1.82 |
|
Medial Ganglionic Eminence and Cortical Organoids Model Human Brain Development and Interneuron Migration |
1.76 |
|
The lipodystrophic hotspot lamin A p.R482W mutation deregulates the mesodermal inducer T/Brachyury and early vascular differentiation gene networks |
1.75 |
|
Identification of a core p53 transcriptional program with highly fractionated tumor suppressive activity |
1.68 |
|
GRO-seq from HCT116, MCF7 and SJSA cell lines treated with DMSO and Nutlin |
1.68 |
|
Germline NLRP1 mutations cause skin inflammatory and cancer susceptibility syndromes via inflammasome activation |
1.65 |
|
RNA-Seq of human PDA cell lines transfected with control siRNA or Pdx1 siRNA |
1.58 |
|
Gene expression profile in endometrial organoids cultured in normal follicular phase vs PCOS-like hormone profile |
1.56 |
|
Transcriptome-wide analysis of IL2RA enhancer activation by CRISPRa |
1.53 |
|
Campylobacter concisus pathotypes induce distinct global responses in intestinal epithelial cells |
1.52 |
|
Transcriptome analysis of human embryonic stem cells (hESCs) upon siRNA-mediated knockdown of hESC-essential genes |
1.46 |
|
The circadian transcriptional landscape in primary human mammary epithelial cells |
1.41 |
|
RNA sequencing of human pancreatic cancer cell lines |
1.4 |
|
APOBEC mutation drives early-onset squamous cell carcinomas in recessive dystrophic epidermolysis bullosa |
1.34 |
|
Gene expression profiles of primary human NK cells before and after expansion on CSTX002 feeder cells, with and without IL-21 stimulation |
1.33 |
|
A MAFG-lncRNA axis links systemic nutrient abundance to hepatic glucose metabolism. |
1.32 |
|
A MAFG-lncRNA axis links systemic nutrient abundance to hepatic glucose metabolism: Liver RNA profiles of lean non-diabetic, obese non-diabetic as well as obese diabetic humans. |
1.32 |
|
LIN28A modulates splicing and gene expression programs in breast cancer cells [RNA-Seq] |
1.29 |
|
LIN28A modulates splicing and gene expression programs in breast cancer cells |
1.29 |
|
Functional Comparison of the HGF/Met and MSP/Ron Systems in a Pancreatic Cancer Model |
1.27 |
|
RNA-Seq analysis of human colorectal cancer with liver metastasis |
1.21 |
|
Molecular Criteria for Defining the Naive Human Pluripotent State |
1.19 |
|
IL-1β induces the rapid secretion of the antimicrobial protein IL-26 from Th17 cells |
1.18 |
|
Next Generation Sequencing for Quantitative Analysis of transcriptome of follicular compared to non-follicular CD8 T cells from HIV+ Lymph nodes |
1.14 |
|
Genomic profiling of biliary tract cancer cell lines reveals molecular subtypes and actionable drug targets |
1.12 |
|
DLX3-dependent p53 signaling network controls keratinocyte cell cycle and squamous tumor growth |
1.1 |
|
DLX3 alters transcriptomic profile of adhesion, cell cycle, and cell death in Squamous Cell Carcinoma Cells |
1.1 |
|
Xeno-free and Chemically Defined Human System for Culturing Human Epidermal Keratinocytes |
1.1 |
|
Expression data for HT29 cells treated with 5-aza-deoxy-cytidine |
1.1 |
|
Expression data for HT29 cells treated with 5-aza-deoxy-cytidine [RNA-Seq] |
1.1 |
|
Mutant p63 disrupts the key specification switch from the multipotent cell state to stratified epithelia during epithelial differentiation/in ectodermal dysplasia disorders |
1.08 |
|
Widespread Transcription beyond mRNA 3’ Ends Yields Abundant Regulatory RNAs |
1.06 |
|
Dissecting neural differentiation regulatory networks through epigenetic footprinting |
1.04 |
|
RB tumor suppressor promotes cancer immunity through downregulating PD-L1 expression |
1.03 |
|
KLF4 as a rheostat of osteolysis and osteogenesis in prostate tumors in the bone |
1.0 |
|
SAMHD1 is recurrently mutated in T-cell prolymphocytic leukemia [RNA-seq] |
1.0 |
|
UV-Irradiation Induces a Noncoding RNA that Functionally Opposes the Protein Encoded by the Same Gene |
1.0 |
|
Transcriptomic Dynamics during Differentiation Process of Human Pluripotent Cells into Hepatocyte-like Cells |
0.97 |
|
Aberrant expression profile of lncRNA and mRNA in dilated cardiomyopathy by RNA-sequence |
0.97 |
|
Integrating the Epigenome to Identify Novel Drivers of Hepatocellular Carcinoma |
0.96 |
|
Profiling gene expression changes in ovarian cancer cells seeded on 3D organotypic culture of omentum |
0.93 |
|
RNA-sequencing transcriptome profiling of normal human keratinocytes differentiation |
0.92 |
|
The global transcriptome analysis in the time course of hESC-derived cardiac differentiation |
0.9 |
|
Characterizing the Chemoresistant Ovarian Cancer Population using the Heterogeneous PDX |
0.9 |
|
HSB-2 cells stably expressing LDB1 or mutant LDB1 proteins |
0.86 |
|
Smad5 acts as an intracellular pH messenger and maintains bioenergetic homoeostasis |
0.84 |
|
The Wnt/β-catenin and RAS-ERK Pathways were Activated in Tissues of Chemotherapy-Resistant Gastric Cancer PDX Tumor |
0.82 |
|
Gene-Edited Human Kidney Organoids Reveal Mechanisms of Disease in Podocyte Development |
0.81 |
|
The expression profiles of GBC liver metastasis |
0.8 |
|
Total RNA sequencing of APC mutant and wt colonic organoids |
0.79 |
|
Altered Hydroxymethylation is seen at regulatory regions in pancreatic cancer and regulates oncogenic pathways [RNA-seq] |
0.78 |
|
Altered Hydroxymethylation is seen at regulatory regions in pancreatic cancer and regulates oncogenic pathways |
0.78 |
|
MRTF activates TEAD-YAP target gene expression |
0.77 |
|
Identification of long noncoding RNAs regulated by p53 |
0.74 |
|
SEUSS: A scalable screening platform to assess transcriptomic and fitness effects of transcription factor overexpression |
0.73 |
|
Evaluation of the effectiveness of semen collection and sperm purification methods for spermatozoa transcript profiling |
0.71 |
|
Dynamics of MBD2 deposition across methylated DNA regions during malignant transformation of human mammary epithelial cells |
0.71 |
|
Dynamics of MBD2 deposition across methylated DNA regions during malignant transformation of human mammary epithelial cells (2) |
0.71 |
|
Differential LINE-1 retrotransposition in induced pluripotent stem cells between humans and great apes |
0.69 |
|
RNAseq transcriptome analysis of White Blood Cells (WBCs) from individuals with and without trisomy 21 [stranded] |
0.66 |
|
Rapid Irreversible Transcriptional Reprogramming in Human Stem Cells Accompanied by Discordance between Replication Timing and Chromatin Compartment |
0.61 |
|
Rapid Irreversible Transcriptional Reprogramming in Human Stem Cells Accompanied by Discordance between Replication Timing and Chromatin Compartment [RNA-Seq] |
0.61 |
|
TALEN-based knockout of mir-141 and mir-200c in SK-BR-3 cells |
0.58 |
|
Genome-wide transcriptome analysis of organotypic rafts derived from human papillomavirus type 16 infected primary keratinocytes [3D raft] |
0.56 |
|
Low carbohydrate diet study for non-alcoholic fatty liver disease patients |
0.54 |
|
The WNT target SP5 negatively regulates WNT transcriptional programs in human pluripotent stem cells |
0.53 |
|
Human MAIT cells exit peripheral tissues and re-circulate via lymph in steady state conditions |
0.52 |
|
Epigenetic changes induced by Bacteroides fragilis toxin (BFT) |
0.5 |
|
Epigenetic changes induced by Bacteroides fragilis toxin (BFT) [RNA-seq] |
0.5 |
|
Discovery and verification of liver cancer marker genes and variable scission based on second-generation sequencing data analysis |
0.48 |
|
Next generation sequencing of the transcriptome in MCF-7 cells with/without SRA knockdown |
0.43 |
|
Dexamethasone inhibits respiratory syncytial virus-driven mucus production while increasing viral replication without altering antiviral interferon signaling |
0.42 |
|
Transcriptome-analysis of patient-derived normal and ulcerative colitis intestinal epithelial organoids |
0.41 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and SMAD4 Y95 Mutation Transcriptomes |
0.41 |
|
RNA sequencing of CACO-2 cells incubated with Bifidobacteria breve grown on human milk oligosaccharides. |
0.39 |
|
Role of OSGIN1 in Mediating Smoking-induced Autophagy in the Human Airway Epithelium [RNA-Seq] |
0.36 |
|
Role of OSGIN1 in Mediating Smoking-induced Autophagy in the Human Airway Epithelium |
0.36 |
|
Smoking Dysregulates the Human Airway Basal Cell Transcriptome at COPD-linked Risk Locus 19q13.2 |
0.35 |
|
Epigenetic reprogramming of immune cells in women with PCOS impact genes controlling reproductive function |
0.33 |
|
Epigenetic reprogramming of immune cells in women with PCOS impact genes controlling reproductive function [RNAseq] |
0.33 |
|
Gene expression analysis of breast cancer cell-lines |
0.33 |
|
Gene expression and genome-wide location analysis of breast cancer cell-lines |
0.33 |
|
Super-Enhancers Promote Transcriptional Dysregulation in Nasopharyngeal Carcinoma [RNA-seq] |
0.32 |
|
Super-Enhancers Promote Transcriptional Dysregulation in Nasopharyngeal Carcinoma |
0.32 |
|
RNA-seq in HT-29 colorectal cancer cells after F. nucleatum treatment |
0.29 |
|
BASP1 modifies the Tamoxifen response |
0.29 |
|
ERK signaling regulates opposing functions of JUN family transcription factors in prostate cancer cell migration |
0.28 |
|
mRNA expression data from ESCs derived by polar body transfer reconstructed embryos (PBTESCs) |
0.28 |
|
RNA sequencing of hiPSC derived neural crest populations from Familial Dysautonomia patients |
0.27 |
|
ML29755 RNA-seq data |
0.26 |
|
Macrophages redirect phagocytosis by non-professional phagocytes and influence inflammation |
0.24 |
|
Next Generation Sequencing Facilitates Quantitative Analysis of UVB(20mJ/cm2 and 40mJ/cm2) exposed and untreated HaCaT keratinocytes Transcriptomes |
0.23 |
|
Maturing an Enteric Nervous System in Human Intestinal Organoid-derived Tissue-Engineered Small Intestine |
0.22 |
|
HIV Reprograms Human Airway Basal Stem/Progenitor Cells to Acquire a Tissue Destructive Phenotype |
0.18 |
|
Cell cycle dynamics of human pluripotent stem cells primed for differentiation |
0.17 |
|
Inactivation of CFTR by CRISPR/Cas9 alters transcriptional regulation of inflammatory pathways and other networks |
0.16 |
|
p63 controls the enhancer landscape during keratinocyte differentiation |
0.1 |
|
A compendium of promoter-centered long-range chromatin interactions in diverse human tissues and cell types |
0.09 |
|
Human ES Cell-derived Hepatoblasts are an Optimal Lineage Stage for HCV Infection |
0.08 |
|
Sex-specific gene expression differences are evident in human embryonic stem cells and during in vitro differentiation of human placental progenitor cells |
0.05 |
|
UV_24h_GRO-Seq |
0.0 |
|
Transcriptomic Analysis Of circRNAs/miRNAs/mRNAs upon Middle East Respiratory Syndrome Coronavirus (MERS-CoV) infection |
0.0 |