Gene Query: GALNT16

Dataset Description Geneva Score
Comprehensive analysis of microRNA expression in regionalized human neural progenitor cells reveals microRNA-10 as a caudalizing factor 53.34
RNA sequencing of human fibroblasts after SUPT4H1 siRNA treatment 51.68
RNA-seq of Human neck of femur (NOF) fracture hip and osteoarthritic (OA) cartilage 43.35
Long noncoding RNA ROCR contributes to SOX9 expression and chondrogenic differentiation of human mesenchymal stem cells 43.35
EZHIP constrains Polycomb Repressive Complex 2 activity in germ cells (RNA-Seq) 34.29
EZHIP constrains Polycomb Repressive Complex 2 activity in germ cells 34.29
Single Cell Analysis Reveals Unexpected Transcriptional Heterogeneity of Neural Progenitors in the Developing Human Cortex 33.15
Identifying ASCL1 target genes in primary GBM stem cell cultures [RNA-seq] 32.74
Deletion of DXZ4 on the human inactive X chromosome eliminates superdomains and impairs gene silencing 30.94
Random mono-allelic expression in MECP2-mutated cells 27.38
Combined Experimental and System-Level Analyses Reveal the Complex Regulatory Network of miR-124 during Human Neurogenesis [d7+d14] 23.56
Transcriptomic alterations in fibroblasts from Parkinson's disease patients carrying Parkin mutations 21.67
RNA-Sequencing shows novel transcriptomic signatures in failing and non-failing human heart 21.49
Differentially Expressed Genes for Atrial Fibrillation Identified using RNA Sequencing from Paired Human Left and Right Atrial Appendages. 19.9
Lentiviral CRISPR Epigenome Editing of Inflammatory Receptors as a Gene Therapy Strategy for Disc Degeneration 19.69
The m 6 A-methylase complex recruits TREX and regulates mRNA export. 19.67
Transcriptome profiling of microRNA-mediated neuronal reprogramming with REST repression at day 7 19.63
Chromatin accessibility landscape upon induction of Msgn1, Pax3 and Myf5 in mesodermal cells and identification of conserved Pax3 binding sites and target genes during skeletal myogenesis 18.68
Functional Screening in Human Cardiac Organoids Reveals a Metabolic Mechanism for Cardiomyocyte Maturation 18.65
Rescue of Fragile X syndrome neurons by DNA methylation editing of the FMR1 gene [RNA-seq] 16.75
Rescue of Fragile X syndrome by DNA methylation editing of the FMR1 16.75
Rapid neurogenesis through transcriptional activation in human stem cell (RNA-Seq) 16.19
Single-cell survey of human lymphatics unveils marked endothelial cell heterogeneity and mechanisms of homing for neutrophils 16.17
Parkinson’s Disease Genetic Risk in a Midbrain Neuronal Cell Line 15.67
ZBTB48 is both a vertebrate telomere-binding protein and a transcriptional activator [RNA-seq] 15.26
ZBTB48 is both a vertebrate telomere-binding protein and a transcriptional activator 15.26
Identification of PAX7-induced transcriptional changes and PAX7 genomic binding during skeletal myogenic differentiation of H9 embryonic stem cells 14.56
Induction of human SST and PV neurons by expressing a single transcription factor LHX6 14.44
Gene expression profile in response to HIF-1α inhibition together with PPARα activation and the postnatal factors (T3, IGF-1 and dexamethasone) in hiPSC-CMs 14.0
Early transcriptome profiling of microRNA-mediated neuronal reprogramming [RNA-seq timecourse] 13.47
RNA-seq analysis reveals profound changes in transcript profiles between siCon- and siH19-transfected EVT cells 13.41
DJ-1 is dispensable for human stem cell homeostasis 12.86
Ribosome Incorporation into Somatic Cells Promotes Lineage Transdifferentiation towards Multipotency 12.85
Ribosome Incorporation into Somatic Cells Promotes Lineage Transdifferentiation towards Multipotency [RNA-Seq] 12.85
Three congruent human Schwann cell models of CMT1A reveal a converged phenotype 12.77
The histone H3.3K27M mutation in pediatric glioma reprograms H3K27 methylation and gene expression 11.6
Maturation of human iNSCs 11.55
Paired Related Homeobox Protein 1 Regulates Quiescence in Human Oligodendrocyte Progenitors 10.9
Genes altered in expression by Cisplatin treatment in lung cancer cell lines 10.74
Patient iPSC-derived neural stem cells display progressive enlargement of lysosomes and disruptions of glycosaminoglycan pathway and autophagy in concordance with clinical severity of Mucopolysaccharidosis I 9.9
Global transcriptional changes in U87MG glioblastoma cells upon shRNA-mediated TRIM52 knockdown 9.8
A role for ZNF598 in post-transcriptional gene regulation 9.74
Regionally distinct astrocyte interferon signaling promotes blood-brain barrier integrity and limits immunopathology during neurotropic viral infection 9.32
RNA-seq and flow-cytometry of conventional, scalp, and palmoplantar psoriasis reveal shared and distinct molecular pathways 9.01
Genome wide transcript and miRNAanalysis of invitro and in-vivo generated human cardiac samples 8.78
Impaired DNA damage metabolism promotes autoimmunity in TREX1 deficiency  8.77
Gene expression analysis of human haploid cells (HAP1) depleted of SMARCB1 and SMARCA4 8.63
MARS Seq data from human cortical organoids 8.53
Patient iPSC-Derived Neurons for Disease Modeling of Frontotemporal Dementia with Mutation in CHMP2B 8.43
Joint-specific DNA transcriptome signatures in rheumatoid arthritis [RNA-seq] 8.41
Generation of induced neural stem cells from urine derived cells by synthetic mRNA 8.2
Comprehensive evaluation of differential gene expression analysis methods for RNA-seq data 8.11
RNA-sequencing of epicardial adipose tissue of patients with atrial fibrillation 7.73
Activity-dependent transcriptional changes in human neurons 7.65
PTEN suppresses neoplastic transformation of human neural stem cells by transcriptional repression of Pax7 7.63
Genomic Reorganization of Lamin-Associated Domains in Cardiac Myocytes is Associated with Differential Gene Expression and DNA Methylation in Human Dilated Cardiomyopathy 7.59
Genomic Reorganization of Lamin-Associated Domains in Cardiac Myocytes is Associated with Differential Gene Expression and DNA Methylation in Human Dilated Cardiomyopathy [RNA-Seq] 7.59
RNA-seq and Microarray in Transcriptome Profiling of Anterior Cruciate Ligament Tears: Implications for Prognostic Biomarkers Discovery 7.55
mRNA sequencing of clinical-grade neural stem cells derived from human ES cells 7.48
Function and hormonal regulation of GATA3 in human first trimester placentation 7.02
SETDB1 compacts the inactive X chromosome in part through silencing an enhancer in the IL1RAPL1 gene 6.96
Next Generation RNA Sequencing Analysis of AMPK Wild Type, AMPKα-KO and AMPKα1-2A U2OS cell Transcriptomes 6.87
Telomere-Dependent and Telomere-Independent Roles of RAP1 in Regulating Human Stem Cell Homeostasis 6.44
Gene expression changes after LOC550643 silencing 6.44
Dynamic epigenetic remodeling underlies microRNA-mediated transdifferentiation of human adult fibroblasts into neuronal subtypes 6.16
A Brain Penetrant Mutant IDH1 Inhibitor Provides In Vivo Survival Benefit 5.77
RNA splicing alteration on glioblastoma and normal neural stem cells 5.61
Overexpression of Claspin and Timeless protects cancer cells from replication stress in a checkpoint-independent manner 5.57
DNA Methylation Reprograms Metabolic Gene Expression in End-Stage Human Heart Failure 5.52
Self-organization of polarized cerebellar plate neuroepithelium in three-dimensional culture of human pluripotent stem cells 5.52
A SIRT1-centered Circuitry Regulates Breast Cancer Stemness and Metastasis 5.38
RNA-Seq analysis of neurons derived from induced pluripotent stem cells reprogrammed from dental pulp 5.33
RNA-Seq analysis of 4N and 2N RPE1 cells following polyploid induction via cytokinesis failure by siRNA knockdown of Anillin [tpo8] 5.17
Anaylsis of the effect of down-regulation of the EWS-FLI1 fusion protein in Ewing Sarcoma cells by RNA-seq. 5.11
transcriptomic profiling of HEK293 cells upon individual knockdown of the splicing factors RBM17, U2SURP or CHERP 5.02
Transcriptional responses of human insulinoma cells to acute cytokine exposure 5.0
Differentially expressed (DE) genes analysis in synovial fluid mesenchymal stem cells (SF-MSCs), SF-MSC derived iPSCs and iPSC derived MSCs (iPSC-MSCs) 4.99
Splicing and gene expression changes in human MDAM-MB231 breast cancer cells with TRA2B knockdown 4.91
Role of FGFR1 in neuronal devlopment 4.86
Loss of Nuclear TDP-43 Is Associated with Decondensation of LINE Retrotransposons [RNA-Seq] 4.86
Loss of Nuclear TDP-43 Is Associated with Decondensation of LINE Retrotransposons 4.86
NGS based identification of GD2-positive tumor-specific phenotype for cancer diagnostics and therapy 4.81
The impact of pro-inflammatory cytokines on the β-cell regulatory landscape provides insights into the genetics of type 1 diabetes 4.76
Ultracentifugation and nanoscale deterministic lateral displacement (nanoDLD) of samples for exRNA analysis 4.73
Incomplete MyoD-induced transdifferentiation is mediated by chromatin remodeling deficiencies 4.7
Incomplete MyoD-induced transdifferentiation is mediated by chromatin remodeling deficiencies [RNA-Seq] 4.7
Verification and rectification of cell type-specific splicing of a Seckel syndrome-associated ATR mutation using iPS cell model 4.69
Prostaglandin E2 inhibits pro-fibrotic function of human pulmonary fibroblasts by disrupting Ca2+-signaling 4.67
SOX21 ensures rostral forebrain identity by suppression of WNT8B during neural regionalization of human embryonic stem cells 4.61
Myeloid-derived suppressor cells facilitie invasion and metastasis of papillary thyroid cancer cells by repressing miR-486-3p 4.6
RNA-seq of hiPSCs-derived NPCs from 3 pairs of dizygotic discordant twins for Congenital Zika syndrome 4.57
De novo reconstruction of human adipose reveals conserved lncRNAs as regulators of brown adipogenesis 4.56
Neuronal Development And The Onset Of Electrical Activity In The Human Enteric Nervous System 4.49
Next Generation Sequencing (RNA-Sequencing) for the analysis of RUNX3 targets in H460, H460-ERT2-RUNX3 WT and H460-ERT2-RUNX3 MT(K94/171R mutation) 4.48
Total RNA sequencing of APC mutant and wt colonic organoids 4.46
RNA-seq of human aneuploid cell lines with Trisomy 21 4.44
DHX15 regulates CMTR1-dependent gene expression and cell proliferation 4.44
Propargite, an environmental chemical, interacts with GWAS identified diabetes genes to impact human pancreatic β-cell death 4.34
Molecular Signatures Associated with ZIKV Exposure in Human Cortical Neural Progenitors 4.3
ZNF804A transcriptome networks in differentiating human neurons derived from induced pluripotent stem cells 4.3
JMJD3 and UTX Determine Fidelity and Lineage Specification of Human Neural Progenitor Cells [RNA-seq] 4.11
JMJD3 and UTX Determine Fidelity and Lineage Specification of Human Neural Progenitor Cells 4.11
Reprogramming of dermal papilla cell intact gene signature with 3D culture and Lef-1 overexpression 4.03
An integrative analysis of non-coding regulatory DNA variations associated with autism 4.02
Transcriptomic profiling discloses molecular and cellular events related to neuronal differentiation in SH-SY5Y cells 4.02
Discovery of Drug Candidates that Inhibit and Eliminate Zika Virus Infection in Fetal and Adult Brain 3.98
The cohesin complex prevents Myc-induced replication stress 3.95
IDH3a KO RNA-seq 3.93
RNA-sequencing of milk cells extracted from pre-partum secretions and longitudinally from mature human milk across the first year of lactation 3.93
Human SETMAR is a DNA sequence-specific histone-methylase with a broad effect on the transcriptome 3.91
SMN deficiency in spinal muscular atrophy causes widespread intron retention and DNA damage 3.75
Adaptive chromatin remodeling in glioblastoma stem cell plasticity and drug tolerance 3.72
Transcriptome analysis of total RNA in human osteosarcoma cell line U2OS before and after inhibition of zinc finger protein ZNF768 3.68
RNA-seq in neurons derived from iPSCs in controls and patients with schizophrenia and 22q11 del 3.67
RNA-seq of young and quiescent MRC-5 human fibroblasts 3.65
RNA Expression Profile of Calcified Bicuspid, Tricuspid and Normal Human Aortic Valves by RNA Sequencing [TAV] 3.63
H9-hESC derived human neural stem cells with combinations of mutant IDH1-R132H overexpression, P53 shRNA knockdown and/or ATRX shRNA knockdown 3.57
RNA-seq of H9-hESC derived human neural stem cells with combinations of mutant IDH1-R132H overexpression, P53 shRNA knockdown and/or ATRX shRNA knockdown 3.57
NR2F2 study 3.56
Estrogen response in breast cancer cell line MCF-7 is dependent on NR2F2 [RNA-seq] 3.56
Characterization of human mosaic Rett syndrome brain tissue by single-nucleus RNA sequencing 3.55
Subtle asymmetry of gene expression in embryonic and foetal human brains 3.55
Nuclear import of the DSCAM-cytoplasmic domain drives signaling capable of inhibiting synapse formation 3.54
Arginine citrullination at the C-terminal domain controls RNA Polymerase II transcription 3.53
T47D RNA-seq and ChrRNA-seq data 3.53
Capturing the biology of mild versus severe disease in a pluripotent stem cell-based model of Familial Dysautonomia 3.49
The histone variant H3.3 G34W substitution in giant cell tumor of the bone link chromatin and RNA processing [RNA-seq] 3.48
NEUROD1 dependent gene regulation in murine pancreatic endocrine cells and human stem cell derived insulin producing cells 3.47
Rna-seq transcriptome data for insulin-GFP+ cells differentiated from NEUROD1 knock out and NEUROD1+/+ control human embryonic stem cells. 3.47
Neuronal brain region-specific DNA methylation and chromatin accessibility are associated with neuropsychiatric trait heritability [RNA-Seq] 3.47
Neuronal brain region-specific DNA methylation and chromatin accessibility are associated with neuropsychiatric trait heritability 3.47
Transcriptomic profiling of O-GlcNAcylated mRNA-protein complexes by using OG-CLAP in HeLa cells. 3.47
Differential gene expression analysis between proliferating and quiescent human dermal fibroblasts 3.46
Induction of human hemogenesis in adult fibroblasts by defined factors and hematopoietic co-culture 3.43
CUREfast: Accelerating research with families 3.43
Lysine benzoylation is a novel histone mark [RNA-seq] 3.41
Lysine benzoylation is a novel histone mark 3.41
Deletions in the ATAD3 gene cluster cause cerebellar developmental defects with mitochondrial DNA abnormalities owing to local cholesterol insufficiency 3.41
RNA-seq analysis of CRISPR/Cas9 generated human BMPR2 deficient endothelial cell lines harboring mutations characteristic for hereditary pulmonary hypertension (HPAH) 3.37
Functional role of CPPED1 in trophoblasts. 3.35
The RNA helicase DDX6 regulates self-renewal and differentiation of human and mouse stem cells [RNA-Seq] 3.35
Mechanism suppressing H3K9 trimethylation in pluripotent stem cells and its demise by polyQ-expanded huntingtin mutations 3.32
Mechanism suppressing H3K9 trimethylation in pluripotent stem cells and its demise by polyQ-expanded huntingtin mutations [RNA-seq] 3.32
Transcriptional profiling at the DLK1/MEG3 domain explains clinical overlap between imprinting disorders 3.27
A genomic study of the contribution of DNA methylation to regulatory evolution in primates 3.26
RNA-Guided Human Gene Activation by Cas9/CRISPR-Based Engineered Transcription Factors 3.26
Transcriptome analysis of eosinophilic and noneosinophilic chronic rhinosinusitis with nasal polyps reveals distinct lncRNA expression profiles 3.25
TGFβ-induced fibroblast activation requires persistent and targeted HDAC-mediated gene repression 3.24
Transcriptome-wide discovery of microRNA binding sites in human brain by Ago2 HITS-CLIP [Ago2-miRNA-target mRNA complexes] 3.22
FGF2 regulation of gene expression in stable inducible Neurons 3.2
Genome-wide transcriptional response to random aneuploidy in human cells 3.15
RNA-Seq analysis of 4N and 2N RPE1 cells following polyploid induction via cytokinesis failure or Aurora kinase inhibition [tpo3] 3.11
Differential expression of human parthenogenic stem cells, neural stem cells and DA progenitors. 3.1
mRNA-sequencing of breast cancer subtypes and normal tissue 3.08
ELP1 splicing correction reverses proprioceptive sensory loss in familial dysautonomia 3.08
Human Cactin interacts with DHX8 and SRRM2 to assure efficient pre-mRNA splicing and sister chromatid cohesion. 3.06
Analysis of the Clustered Protocadherin (cPcdh) Locus in Human Pluripotent Stem and Derived Cells [RNA-seq II our of II] 3.02
RNA-seq analysis of control and Myc-induced U2OS cells 3.01
Differential gene expressions in the heart of hypertrophic cardiomyopathy patients 2.97
Real-time observation of light-controlled transcription in living cells 2.92
Transcriptome analysis of genetically matched human induced pluripotent stem cells disomic or trisomic for chromosome 21 2.92
Examining serotonergic neuron differentiation from human iPSCs 2.89
RNA-seq of SOX5 overexpressing primary human neuronal progenitors 2.87
PolyA-sequencing in Kelly and Kelly E9R neuroblastoma cells treated with THZ531 or DMSO 2.87
Ribo_seq (aka ribosome profiling) analysis of control and Myc-induced U2OS cells 2.87
Novel Targeting of Transcription and Metabolism in Glioblastoma 2.85
BioProject PRJNA381064: Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage (Gene expression profiling in several tetrapod species, bulk tissue RNA-seq) 2.79
A practical evaluation of alignment algorithms for RNA variant calling analysis 2.78
The SS18-SSX fusion oncoprotein hijacks BAF complex targeting and function to drive synovial sarcoma [RNA-Seq Tumor] 2.78
Global Promotion of Alternative Internal Exon Usage by mRNA 3' End Formation Factors 2.75
Global Regulation of Alternative Internal Exon Usage by mRNA 3' End Formation Factors [RNA-Seq] 2.75
RNA sequencing for PDX1, NGN3 and MAFA transduced iPSCs cell 2.74
DHX36 resolves G-rich structures in mRNA untranslated region to allow their translation [ChrRNA-seq] 2.72
Dilated cardiomyopathy vs Myocarditis 2.7
Transcriptomic profiles of nonpregnant and term pregnant human myometrial tissues 2.7
Nonpregnant and term pregnant human myometrial tissues 2.7
Combined Experimental and System-Level Analyses Reveal the Complex Regulatory Network of miR-124 during Human Neurogenesis [ZNF787] 2.66
Transcriptome analysis reveals determinant stages controlling human embryonic stem cell commitment to neuronal cells 2.61
Morphological and molecular characterization of human dermal lymphatic collectors 2.6
FOXP1 orchestration of ASD-relevant signaling pathways. 2.6
Intrinsic histone acetyltransferase activity of BRD4 is responsible for nucleosome eviction and transcriptional activation 2.59
FMRP facilitates the nuclear export of N6-methyladenosine-containing mRNAs 2.57
Cockayne syndrome A and B proteins regulate the transcription arrest upon genotoxic stress through a ubiquitin/proteasome degradation process (RNA-seq) 2.57
Cockayne syndrome A and B proteins regulate the transcription arrest upon genotoxic stress through a ubiquitin/proteasome degradation process 2.57
Zika infected neural stem cells 2.48
Transcriptome analysis of Zika infected neural stem cells 2.48
Transcriptomics profiling of Alzheimer’s disease reveal novel molecular targets 2.46
Valproic acid attenuates hyperglycemia induced complement and coagulation cascade gene expression 2.45
HDAC and NFκB antagonists synergistically inhibit growth and metastatic dissemination of MYC-driven medulloblastoma 2.44
Identification of metabolically distinct adipocyte progenitor cells in human adipose tissues 2.43
Analysis of human, chimpanzee, macaque and mouse tissue transcriptomes using Next Generation Sequencing 2.43
RNA sequencing for lncRNA, miRNA and mRNA expression analysis in human laryngeal cancer 2.41
In vivo genome editing restores dystrophin expression in Duchenne muscular dystrophy patient muscle fibers 2.41
Next Generation Sequencing Study of Circadian Changes in Transcriptome of Human Pineal Gland 2.4
Next generation sequencing of human hepatic stellate cell line, LX-2 treated with recombinant human TGF-β1, with DMSO or ML290 (5 µM) for 72h. 2.38
Recapitulation of Human Neural Microenvironment Signatures in iPSC-Derived NPC 3D Differentiation 2.34
Role of miR-146a in neural stem cell differentiation and neural lineage determination: relevance for neurodevelopmental disorders 2.33
Integrated Profiling of mRNAs and microRNAs to Identify Potential Biomarkers for Oral Malignant Transformation [mRNA-Seq] 2.3
Integrated Profiling of mRNAs and microRNAs to Identify Potential Biomarkers for Oral Malignant Transformation 2.3
Multiple mechanisms disrupt let-7 miRNA biogenesis and function in neuroblastoma [longRNA] 2.3
RNA-seq of exosomes identifies lncRNA profiles that distinguish early-stage esophageal squamous cell carcinoma (ESCC) from non-malignant esophagitis 2.27
Dissecting cell composition and cell-cell interaction network of normal human heart tissue by single-cell sequencing 2.27
Gene expression in GBM with Cav3.2 inhibition 2.26
FUS mutant human motoneurons transcriptome analysis reveals altered pathways and impairment of microRNA function 2.25
Reversible LSD1 Inhibition with HCI-2509 induces the p53 gene expression signature in high-risk neuroblastoma cells 2.24
Profile of gene expression in U87-MG xenografts expressing control vector (V0), the ubiquitin ligase KPC1 or the p50 subunit of the NF-kB transcription factor, using RNASeq analysis of transcripts mapped independently to the human and murine genomes 2.23
The mSWI/SNF ATPase module mediates subcomplex identity and non-catalytic targeting in SCCOHT [RNA-seq] 2.22
The ATPase module of mammalian SWI/SNF family complexes mediates subcomplex identity and catalytic activity-independent genomic targeting 2.22
Open chromatin mapping identifies transcriptional networks regulating human epididymis epithelial function [Rnase-Seq] 2.21
Open chromatin mapping identifies transcriptional networks regulating human epididymis epithelial function 2.21
Arginine methylation controls cell proliferation by integrating E2F activity with the splicing machinery 2.21
Arginine methylation controls cell proliferation by integrating E2F activity with the splicing machinery (RNA-seq data set) 2.21
SETBP1-WT and SETBP1-G870S epigenetic landscapes 2.2
SETBP1-WT and SETBP1-G870S transcriptional profiles [RNA-Seq] 2.2
Gene Expression Signature in Adipose Tissue of Acromegaly Patients 2.18
Tricyclic Antidepressants Induce Inactivation of Hepatic Stellate Cell (HSC) Myofibroblasts 2.17
Comparing effects of perfusion and hydrostatic pressure on human chondrocytes using gene profiles 2.17
RNA-seq data of small cell carcinoma of the bladder (SCCB) /urothelial carcinoma (Non-SCCB) clinical samples, and bladder-PARCB cell lines 2.12
Gene expression profiling associated with knockdown of RNF20 in human normal and malignant lung epithelial cell lines 2.12
Brain organoids reproducibly generate the cellular diversity of the human cerebral cortex 2.11
RNA-Seq characterization of human H1-derived NPC differentiation timecourse 2.06
Gene expression profile of calcified and normal tricuspid aortic valves by RNA sequencing. 2.05
Generation of Brain Region-specific Organoids using a Miniaturized Spinning Bioreactor and Modelling ZIKV Exposure 2.04
RNA-sequencing of human peripheral blood mononuclear cells (PB MNCs) and induced neural progenitor cells derived from PB MNCs 2.03
Human iPSC-derived microglia assume a primary microglia-like state after transplantation into the neonatal mouse brain [Single Cell RNAseq] 2.01
Transcriptome analysis of diverse cell types infected with human cytomegalovirus [RNA-Seq] 2.0
RNA sequencing and pathway analysis identify important pathways involved in hypertrichosis and intellectual disability in patients with Wiedemann-Steiner syndrome 2.0
Identification of a LIF-responsive replication-competent human β cell 1.98
HNF1A deficiency impairs β-cell fate, granule maturation and function 1.97
Chemical Modulation of Glycolysis Regulates the KEAP1-NRF2 Pathway Through a Metabolite-Induced Posttranslational Modification 1.97
Targeted differentiation of regional ventral neuroprogenitors and related neuronal subtypes from human pluripotent stem cells 1.97
Expression profiles of the four human major ectodermal lineages 1.96
SQSTM1/p62-directed metabolic reprogramming is essential for normal neurodifferentiation 1.95
The Cushing's disease adipose gene expression profile reveals effects of long term glucocorticoids on adipose tissue lipid, protein and glucose metabolism 1.94
Single-cell analysis reveals stochastic regulation of type I IFN production by plasmacytoid dendritic cells and identifies host-derived environmental cues as amplifier of type I IFN production 1.93
Expression profiling of lncRNAs, miRNAs and mRNAs and their differential expression in leiomyoma using next generation RNA sequencing 1.93
Gene expression profiles of rescue with wild type or SUMO double mutant TRIM24 1.91
Transcriptome sequencing reveals aberrant alternative splicing in Huntington's disease 1.87
Distinct and shared functions of ALS-associated TDP-43, FUS, and TAF15 revealed by comprehensive multi-system integrative analyses [RNA-Seq_human] 1.86
3’ Uridylation Expands miRNA Target Repertoire 1.85
Cerebral Organoids Recapitulate Epigenomic Signatures of the Human Fetal Brain 1.84
Nuclear HNRNPA2B1 HITS-CLIP and RNA-seq 1.84
Next Generation Sequencing Facilitates Quantitative Analysis of Retinoblastoma Transcriptomes 1.82
RNA Expression Profile of Calcified Bicuspid, Tricuspid and Normal Human Aortic Valves by RNA Sequencing [BAV] 1.82
H3.3K27M cooperates with p53 loss and Pdgfra gain in mouse embryonic neural progenitor cells to induce invasive high-grade gliomas [Human RNA-Seq] 1.81
H3.3K27M cooperates with p53 loss and Pdgfra gain in mouse embryonic neural progenitor cells to induce invasive high-grade gliomas 1.81
Microsatellite expansion RNA visualization, elimination, and reversal of molecular pathology by RNA-targeting Cas9 1.8
Defective transcription elongation in a subset of cancers confers immunotherapy resistance (BGI12 RNA-Seq) 1.8
RNA isoform screens reveal the essentiality and tumor suppressor activity of ultraconserved poison exons 1.79
Transcriptome-wide analysis links the short-term expression of the b isoforms of T-cell intracellular antigens to protective proteostasis-mediated survival and quiescence 1.79
Genome-Wide DNA Methylation Encodes Cardiac Transcriptional Reprogramming in Human Ischemic Heart Failure [DNA Methylation] 1.78
Genome-Wide DNA Methylation Encodes Cardiac Transcriptional Reprogramming in Human Ischemic Heart Failure [RNA-Seq] 1.78
Identification of differentially expressed circRNA in gallbladder cancer compared with matched normal tissue 1.77
RNA expression following TMPRSS11B overexpression or depletion 1.76
High-throughput RNA sequencing on circular RNA profiles of human triple-negative breast cancer and adjacent normal tissues 1.75
Over expression of Receptor Activity Modifying Protein 2 in HEK293T cells 1.74
CRISPR activation of long non-coding RNAs transiently expressed during cortical neuron differentiation associated with Field, et al, Stem Cell Reports 2018 1.73
A SRp55-regulated alternative splicing network controls pancreatic beta cell survival and function 1.72
An aspartyl protease defines a novel pathway for export of Toxoplasma proteins into the host cell 1.72
RNA-seq analysis of gene expression patterns during hESC neural differentiation 1.72
hESC neural differentiation 1.72
Effects of transcription on genome - nuclear lamina interactions 1.71
Effects of transcription on genome - nuclear lamina interactions: RNA-seq data 1.71
RNA-sequencing WT vs SOCS3 knockout Glioblastoma stem-cells 1.71
Transcript abundance in A-T-derived iPSC: Comparing isogenic cells to unrelated individual 1.71
Defining a microRNA-mRNA targetome for calcineurin inhibitor induced nephrotoxicity 1.7
Epigenomic landscape during organ formation in human early embryos 1.7
Effect of SHP2 inhibition on hepatic stellate cell transcriptome. 1.68
mRNA destabilization is the dominant effect of mammalian microRNAs by the time substantial repression ensues (sequencing) 1.67
mRNA destabilization is the dominant effect of mammalian microRNAs by the time substantial repression ensues 1.67
The effect of Abl kinases on non-small cell carcinoma global transcriptome 1.66
Distinct Pathological Signatures in Human Cellular Models of Myotonic Dystrophy Subtypes 1.66
The expression of genes encoding palmitoylated proteins in axonal and synaptic compartments is affected in CLN1/PPT1 transfected neuronal cells 1.65
Gata6 potently initiates reprogramming of pluripotent and differentiated cells to extraembryonic endoderm stem cells [ChIP-Seq & RNA-Seq] 1.65
Gata6 potently initiates reprogramming of pluripotent and differentiated cells to extraembryonic endoderm stem cells 1.65
RNA-seq analysis of hPSC-derived brain pericyte-like cells, hPSC-derived neural crest stem cells, and primary human brain pericytes 1.62
Aneuploidy-induced cellular stresses limit autophagic degradation. 1.61
Serotonin-induced hyperactivity in SSRI-resistant major depressive disorder patient-derived neurons 1.61
Gene expression profiling study by RNA-seq for identifying genes associated with epithelial-mesenchymal transition and acquired resistance to ALK inhibitors 1.6
Epithelial-mesenchymal transition and acquired resistance to ALK inhibitors 1.6
UTX and 53BP1 co-regulate genetic programs for neural differentiation of human embryonic stem cells [RNA-seq] 1.59
UTX and 53BP1 co-regulate genetic programs for neural differentiation of human embryonic stem cells 1.59
Fibroblasts in cholesteatoma activate osteoclasts. 1.59
Reversing Abnormal Neural Development by Inhibiting OLIG2 in Down Syndrome Human iPSC Brain Organoids and Neuronal Mouse Chimeras 1.56
Stably-paused genes revealed through inhibition of transcription initiation by the TFIIH inhibitor Triptolide 1.55
Effect of estrogen (E2) treatment on the C4-12 relative to the MCF7 cells 1.54
Changes in chromatin accessibility and gene expression induced by overexpression of ONECUT transcription factors 1.54
Profiling of gene expression using RNA-Seq in fibroblasts, iPSCs, iPSC-derived neurons and cells overexpressing Onecut transcription factors 1.54
Long-term expandable SOX9+ chondrogenic ectomesenchymal cells from human pluripotent stem cells 1.53
Networks of cultured iPSC-derived neurons reveal the human synaptic activity-regulated adaptive gene program 1.53
C9orf72 Intermediate Repeats are Associated with Corticobasal Degeneration, Increased C9orf72 Expression and Disruption of Autophagy 1.52
Engineered human pluripotent stem cell-derived intestinal tissues with a functional enteric nervous system 1.52
Modelling and rescuing neurodevelopmental defect of Down syndrome using induced pluripotent stem cells from monozygotic twins discordant for trisomy 21 1.52
Modelling and rescuing neurodevelopmental defect of Down syndrome using induced pluripotent stem cells from monozygotic twins discordant for trisomy 21 [RNA-seq] 1.52
Reassessment of Exosome Composition 1.52
A global identification of PUM1 and PUM2 mRNA targets and their protein cofactors in human seminoma TCam-2 cells 1.51
LEDGF and HDGF2, histone H3K36 methyl-binding proteins that assist RNA polymerase II transcription through nucleosomes 1.5
Differetially expressed genes after hTR overexpression in U2OS cells 1.49
LMO1 Synergizes with MYCN to Promotes Neuroblastoma Initiation and Metastasis 1.49
Transcriptome Sequencing of Adipose-Derived Mesechymal Stromal Cells 1.48
Human Airway Smooth Muscle Transcriptome Changes in Response to Asthma Medications 1.47
Replicative senescence is associated with nuclear reorganization and DNA methylation at specific transcription factor binding sites (RNA-seq) 1.46
Replicative senescence is associated with nuclear reorganization and DNA methylation at specific transcription factor binding sites 1.46
RNA-Seq analysis of proliferating 4N and 2N RPE1 cells derived from single cell clones following inhibition of Aurora B to induce polyploidization [tpo10] 1.46
mRNA-sequencing of 293T-no dice transfected with miR-16, miR-214, or KSHV-miR-K6-5p 1.45
Heterogeneous nuclear ribonucleoprotein C1/C2 links transcriptional and splicing actions of 1,25-dihydroxyvitamin D 1.44
Altered expression of signaling pathways regulating neuronal excitability in hippocampal tissue of temporal lobe epilepsy patients with low and high seizure frequency 1.43
Total RNA sequencing of WT intestinal orgaonids. 1.42
Large-Scale Atlas of Mutant IDH1-Dependent Chromatin State Reprogramming, Reversibility, and Persistence 1.41
Large-Scale Atlas of Mutant IDH1-Dependent Chromatin State Reprogramming, Reversibility, and Persistence [RNA-seq] 1.41
Gene expression changes in human melanoma cell lines compared to primary melanocytes 1.41
PML2‐mediated thread‐like nuclear bodies mark late senescence in Hutchinson–Gilford progeria syndrome [RNA-seq] 1.39
PML2-mediated thread-like nuclear bodies mark late senescence in Hutchinson–Gilford progeria syndrome 1.39
Necroptosis inhibition protects from dopaminergic neuronal cell death in OPA1 mutant Parkinson’s disease patient neurons and MPTP treated mice 1.37
RNA-seq in endometrial stromal tumors 1.36
Small-molecule-based Human Genome G4 Profiling Reveals Potential Gene Regulation Activity 1.36
RNA-Seq Analysis in hES/ iPS cell-derived neuronal samples 1.36
Protein kinase A-mediated phosphorylation regulates STAT3 activation and oncogenic EZH2 activity 1.36
Genome-wide transcriptome profiles in Control and Schizophrenia hiPSC-dervied NPC [RNA-seq] 1.36
Next-generation sequencing of control and schizophrenia hiPSC derived NPC 1.36
Transcriptional dependencies in diffuse intrinsic pontine glioma 1.36
Human optic chiasm from healthy controls and multiple sclerosis patients 1.35
Multiple sclerosis and EAE 1.35
The serine hydroxymethyltransferase-2 (SHMT2) initiates lymphoma development through epigenetic tumor suppressor silencing. 1.31
Gene expression profiling in follicular lymphoma (FL) samples and paired transformed follicular lymphoma (tFL) (n=6 samples) 1.31
RNA-Seq profiling of iPSC-derived ventricular and atrial cardiomyocytes 1.31
N6-methyladenosine (m6A) profiling of EndoC-bH1 cell line and RNA seq of Mettl14 knockout mice beta cell 1.31
Increased Neanderthal ancestry in genomic regions associated with lipid catabolism in contemporary Europeans 1.29
Normal stroma suppresses cancer cell proliferation via mechanosensitive regulation of JMJD1a-mediated transcription 1.29
Normal stroma suppresses cancer cell proliferation via mechanosensitive regulation of JMJD1a-mediated transcription [RNA-Seq] 1.29
PNET animal model: new insights (II) 1.28
Cis-SAGe fusion RNAs in transcription splicing factors knocking-down 293T cells 1.28
RNA sequencing of ESC/iPSC-derived purified PAX6-GFP neural progenitors form control and Phelan-Mcdermid patients 1.28
Selective expansion of myeloid and NK cells in humanized mice yields human-like vaccine responses (Experiment 2: scRNA-seq) 1.28
Identification of miRNA-mRNA regulatory network for Human Atrial Aging [mRNA] 1.27
Identification of miRNA-mRNA regulatory network for Human Atrial Aging 1.27
BI Human Reference Epigenome Mapping Project 1.25
Chronophin regulates metabolic and transcriptomic features of glioblastoma stem-like cells 1.24
Mucosal Profiling of Pediatric-Onset Colitis and IBD Reveals Common Pathogenics and Therapeutic Pathways 1.24
Progressive motor neuron pathology and the role of astrocytes in a human stem cell model of VCP-related ALS 1.23
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 1.22
RNA-Seq in PWS iPSC-derived neurons 1.22
Molecular Signature of CAID Syndrome: Noncanonical Roles of SGO1 in Regulation of TGF-β Signaling and Epigenomics. 1.19
Molecular Signature of CAID Syndrome: Noncanonical Roles of SGO1 in Regulation of TGF-β Signaling and Epigenomics. [RNA-seq] 1.19
SAM68 is required for regulation of Pumilio by the NORAD long noncoding RNA 1.19
Global reduction in H3K27me3 and DNA hypomethylation define poorly prognostic pediatric posterior fossa ependymomas 1.18
Epigenetic Control of Skeletal Development by the Histone Methyltransferase Ezh2 1.17
Characterization of sperm lncRNA and its differently expression in the sperm of asthenozoospermic patients 1.16
The Glioma-Infiltrating T Cell Receptor Repertoire 1.15
Engineering Patient-Specific Tissue Implants 1.14
SHANK2 mutations associated with autism spectrum disorder cause hyperconnectivity of human neurons 1.14
RNA-seq characterization of downstream effects of upregulating SMN2 via down-regulating PRC2 or blocking the PRC2:SMN-AS1 interaction with a mixmer oligonucleotide 1.13
Effect of FGF13 depletion on the H460 cell line 1.12
An intramolecular salt bridge linking TDP43’s RNA recognition motifs dictates RNA binding, protein stability and TDP43-dependent neurodegeneration 1.11
Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioural and myelin alterations rescuable by a remyelinating drug [human] 1.08
Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioural and myelin alterations rescuable by a remyelinating drug 1.08
Molecular Pathology of adverse local tissue reaction caused by metal-on-metal implants 1.08
RNA-seq of synchronized S phase or G2 phase cells treated with an ATR inhibitor 1.08
Modulation of nonsense-mediated decay by rapamycin 1.07
Spatial proximity to fibroblasts impacts molecular features and therapeutic sensitivity of breast cancer cells influencing clinical outcomes 1.07
Low MITF/AXL ratio predicts early resistance to multiple targeted drugs in melanoma 1.06
Mapping cis-regulatory chromatin contacts in neural cells links neuropsychiatric disorder risk variants to target genes 1.05
Mapping cis-regulatory chromatin contacts in neural cells links neuropsychiatric disorder risk variants to target genes [RNA-Seq] 1.05
Single cell analysis of smooth muscle cell phenotypic modulation in vivo during disease in mice and humans [human scRNA-seq] 1.0
Single cell analysis of smooth muscle cell phenotypic modulation in vivo during disease in mice and humans 1.0
RNA-seq analysis of melanoma and carcinoma cells expressing FOXQ1 0.98
mRNA sequencing of the global effect of SOX2 on gene expression in hESC and hESC derived NPCs. 0.97
Dissecting the single-cell transcriptome network underlying gastric premalignant lesions and early gastric cancer [10x genomics] 0.97
RNAseq in Alzheimer's Disease patients 0.97
Repression of stress-induced LINE-1 expression protects cancer cell populations from lethal drug-exposures 0.96
Repression of stress-induced LINE-1 expression protects cancer cell populations from lethal drug-exposures [RNA-Seq] 0.96
High throughput characterization of the m6A demethylase FTO by CLIP and RNAseq 0.95
Transcriptome of human white and brown adipose tissue biopsies 0.92
Repurposing of promoters and enhancers during mammalian evolution 0.91
Functional astrocytes differentiated from hiPSCs 0.91
Primate-specific gene TMEM14B promotes cortical expansion and folding 0.91
RNA helicase A is necessary for KIF1Bβ tumor suppression in neuroblastoma 0.89
Comparison of 7 small cell lung cancer PDX models, cultured ex vivo, for response to LSD1 inhibitor RG6016/ORY1001 0.89
Single-cell RNA Sequencing Resolves Spatiotemporal Development of Pre-thymic Lymphoid Progenitors and Thymus Organogenesis in Human Embryos 0.87
YAP and MRTF-A, transcriptional co-activators of RhoA- mediated gene expression, are critical for glioblastoma tumorigenicity 0.85
Systems-level analyses reveal a convergent pathway for progression of diffuse astrocytoma and potential role for resveratrol in delaying high-grade transformation 0.84
Studying iPSCs from a hibernating mammal reveals molecular mechanisms of cold resistance in neural tissues 0.84
ELAVL2-regulated transcriptional networks in human neurons link atlernative splicing, autism and human neocortical evolution 0.84
Transcriptomic analysis of human neural progenitor cells differentiation into astrocytes 0.82
Transcriptome analysis of PC9 cells with gefitinib or/and hypoxia treatment and comparison with gefitinib resistant PC9 cells and ALDH positive PC9 cells 0.82
RNA profiling Analysis of the Serum Exosomes Derived from Active and Latent M.tuberculosis infectious Patients 0.82
Integrated Multi-omic Analysis of Esthesioneuroblastomas Identifies Two Subgroups Linked to Cell Ontogeny 0.8
Gene expression profiling via RNA sequencing of patient brain tumors cultured in 3D bioengineered cultures 0.8
Aortic Valve Tissue: Stenosis vs. Sclerosis 0.78
Multiple mechanisms disrupt let-7 miRNA biogenesis and function in neuroblastoma 0.77
Transcriptome data of temporal and cingulate cortex in the Rett syndrome brain 0.76
Functional Importance of eRNAs for Estrogen-dependent Gene Transcriptional Activation 0.76
Transcriptomic analysis of the effect of histone H4 K31R mutation in U2OS cells 0.75
ARID1A is a critical regulator of luminal identity and therapeutic response in oestrogen receptor-positive breast cancer (RNA-Seq) 0.75
Restoration of Progranulin Expression Rescues Cortical Neuron Generation in Induced Pluripotent Stem Cell Model of Frontotemporal Dementia 0.75
HEK293 Heat-shock experiment 0.74
Developmental origins define epigenomic differences between subcutaneous and visceral adipocytes [RNA_seq_Whole] 0.73
ALS implicated protein TDP-43 sustains levels of STMN2 a mediator of motor neuron growth and repair 0.73
The Developmental Heterogeneity of Human Natural Killer Cells Defined by Single-cell Transcriptome 0.73
Transcriptomes of iPSC-derived and post-mortum Hypothalamus Neurons from obese and control donors 0.72
miR-155 plays a crucial role in ALS and is an immune therapeutic target [RNA-Seq] 0.71
Targeting miR-155 restores abnormal microglia and attenuates disease in SOD1 mice 0.71
Analysis of MGE Transcriptomes with or without Ctnnb1 knockout in human through RNA Sequencing 0.71
An Alternative Splicing Event Amplifies Evolutionary Differences Between Vertebrates 0.68
Integrative Genomic and Transcriptomic Analysis Identified Candidate Genes Implicated in the Pathogenesis of Hepatosplenic T-cell Lymphoma 0.67
Hepatosplenic T cell lymphoma 0.67
Genome wide association study of bone size yields eleven loci that also affect height, bone density, osteoarthritis and fractures 0.67
CSL 0.66
CSL RNA-Seq on HKC and SCC cell lines 0.66
Robust generation of honemogeneous midbrain organoids with in vivo–like cellular composition facilitates neurotoxin-based Parkinson’s disease modeling 0.66
Analysis of an artificial zinc finger epigenetic modulator: widespread binding but limited regulation 0.63
A stably self-renewing adult blood-derived induced neural stem cell exhibiting patternability and epigenetic rejuvenation 0.62
A transcriptional regulatory network connects mitochondrial biogenesis and metabolic shift with stem cell commitment to hepatic differentiation 0.6
Transcriptome of EBV-infected gastric cancer cell lines 0.6
Identification of microRNA-dependent gene regulatory networks driving human pancreatic endocrine cell differentiation [H1 RNA-seq] 0.59
Enhancer Activation Requires Trans-Recruitment of a Mega Transcription Factor Complex (Gro-seq) 0.59
Enhancer Activation Requires Trans-Recruitment of a Mega Transcription Factor Complex 0.59
RNA-seq of SCLC PDX models treated with EP 0.58
Sodium butyrate ameliorates aSyn-induced transcription deregulation and DNA damage 0.58
Identification of novel recurrent ETV6-IGH fusions in primary central nervous system lymphoma using high throughput RNA sequencing 0.58
A damaged genome's transcriptional landscape through multilayered expression profiling around in situ-mapped DNA double-strand breaks 0.57
Exercise-induced transcriptome changes in skeletal muscle adapted to aerobic training 0.57
Meta-organization of Translation Centers Revealed by Proximity Mapping of Endoplasmic Reticulum Ribosome Interactors 0.57
A single-cell atlas of the human cortex reveals drivers of transcriptional changes in Alzheimer’s disease in specific cell subpopulations 0.56
Disease modelling of core pre-mRNA splicing factor haploinsufficiency 0.55
Epigenetic activation and memory at a TGFB2 enhancer in systemic sclerosis 0.54
mRNAseq of Huntington's disease and control patient iPSC-derived neural cells 0.52
Transcriptomic and Epigenomic analysis of Huntington's disease and control patient iPSC-derived neural cells 0.52
ENCODE Cold Spring Harbor Labs Long RNA-seq 0.51
Molecular analysis of renal cell carcinoma with unclassfied histology [gene expression] 0.51
Molecular analysis of renal cell carcinoma with unclassfied histology 0.51
Transcriptome-wide discovery of microRNA binding sites in human brain by Ago2 HITS-CLIP 0.5
Discovery of a Drug Candidate for GLIS3-Associated Diabetes 0.49
Recurrent alterations of TNFAIP3 (A20) in T-cell large granular lymphocytic leukemia 0.48
Identifying markers predicting successful graft outcome for clinical translation of hESC-based cell therapy for Parkinson’s disease 0.48
5hmC dynamically correlated with enhancer's activities during hES-to-Pancreatic endoderm cell differentiation (RNA-Seq) 0.48
5hmC dynamically correlated with enhancer's activities during hES-to-Pancreatic endoderm cell differentiation 0.48
IL-21/type I interferon interplay regulates neutrophil-dependent innate immune responses to Staphylococcus aureus 0.47
iPSC derived motor neuron cultures from C9ORF72 carriers 0.46
RNA-Seq of the corpus callosum from 12 individuals 0.46
Dissecting cell composition and cell-cell interaction network of human disease heart tissue by single-cell sequencing 0.43
A single cell reference map for human blood and tissue T cell activation 0.42
Genome wide impact of loss of mechanoluminal stimulation on neonatal intestine 0.41
Genome-wide DNA hypomethylation and RNA:DNA hybrid accumulation in Aicardi-Goutières syndrome 0.4
Influenza Vaccination Primes Human Myeloid Cell Cytokine Secretion and Natural Killer Cell Function 0.4
Short-term effect of Boost versus Radical doses of Intraoperative electron Radiotherapy in breast cancer tumor bed using high-throughput approaches 0.4
RNA-Seq Analysis in purified iPS cell-derived neuronal samples 0.4
High-resolution comparative analysis of great ape genomes 0.39
Self-organized cerebral organoids with human specific features predict effective drugs to combat Zika virus infection [RNA-seq] 0.39
Self-organized cerebral organoids with human specific features predict effective drugs to combat Zika virus infection 0.39
RNA-sequencing of pediatric idiopathic dilated cardiomyopathy patients and healthy controls 0.36
Gene expression profiles of active and restricted R/G-HIV+ primary human fetal astrocytes 0.36
Next Generation Sequencing Facilitates Comparisons of Control and Schizophrenia-Patient derived hiPSC-derived neurons 0.35
Transcriptional profiling of microglia; current state of the art and future perspectives 0.33
Transcriptome analysis of diverse cell types infected with human cytomegalovirus 0.32
Dissecting neural differentiation regulatory networks through epigenetic footprinting 0.32
Low H3K27me3 and DNA hypomethylation define poorly prognostic pediatric posterior fossa ependymomas 0.32
Profiling of circular RNAs in gastric cancer tissues and adjacent normal tissues 0.32
Single cell RNA-seq resolves lineage-specific activation dynamics of human blood and tissue T cells 0.31
Single-cell transcription profiling in KS1 patient iPSCs and NPCs 0.31
Comparative Analysis of Cas9 Activators Across Multiple Species 0.3
Defective transcription elongation in a subset of cancers confers immunotherapy resistance 0.3
Single cell transcriptome of peritoneal cells 0.29
Vitamin d receptor-mediated stromal reprogramming suppresses pancreatitis and enhances pancreatic cancer therapy 0.29
Profiling gene expression changes in ovarian cancer cells seeded on 3D organotypic culture of omentum 0.29
Next Generation Sequencing Facilitates Comparisons of Control and Schizophrenia-Patient derived hiPSC-derived NPCs 0.28
RNA sequencing of hiPSC derived neural crest populations from Familial Dysautonomia patients 0.27
Epigenomic conservation of transposable element silencing [RNA-seq] 0.25
Epigenomic conservation of transposable element silencing 0.25
RUNX2/CBFB modulates the response to MEK inhibitors through activation of receptor tyrosine kinases in KRAS mutant colorectal cancer 0.24
RNA-Seq of Kaposi’s sarcoma reveal alterations in glucose and lipid metabolism 0.23
polyA RNA Sequencing Analysis of HTR-8/SVneo cells after lnc-SLC4A1-1 overexpression 0.22
Gene expression analysis upon mtDNA depletion 0.21
Gene expression analysis upon mtDNA depletion [RNA-seq] 0.21
Analysis of gene expression, motif and pattern of m6A modified region and m6A enrichment level in Ocular melanoma and Melanocyte cell lines. Gene expressin analysis of METTL3 knock down in PIG1, ALKBH5 knock down and HINT2 over expression in OCM1. 0.18
hNSCs siRNA NOVA2 0.17
single cell RNA-seq from Purkinje cell (ENCSR888LYA) 0.16
Differential gene expression of static and intermittent compressive force treated human periodontal ligament cells 0.16
Biomarkers of Cavernous Angioma with Symptomatic Hemorrhage (CASH) [RNA-seq] 0.15
Biomarkers of Cavernous Angioma with Symptomatic Hemorrhage (CASH) 0.15
RNA sequencing of prostate cancer and normal tissue from African Americans and European Americans 0.12
RNAseq analysis of ruxolitinib treated breast cancers 0.11
Genome-wide search for differentially expressed RNAs responsible for the effects induced by Ebola virus replication and transcription 0.1
The control of rRNA synthesis during the directed differentiation of human embryonic stem cells precedes heterochromatin formation. 0.09
Transcriptomic analysis of human iPS cells derived from fragile X syndrome patients during neural differentiation 0.08
The MEF2B Regulatory Network - RNA-seq data 0.08
The MEF2B Regulatory Network 0.08
RNA sequencing of lesional and nonlesional skin from patients with atopic dermatitis 0.07
Analysis of transcrptomes of Danon patient derived hiPSC-cardiomyocytes by RNA-deep Sequencing 0.07
Widespread regulated alternative splicing of single codons accelerates proteome evolution 0.05
Defective removal of ribonucleotides from DNA promotes systemic autoimmunity 0.04
Gene expression profiling of patient's DCIS-IDC tandem lesions by RNA sequencing analysis 0.03
Enhancer divergence and cis-regulatory evolution in the human and chimpanzee neural crest 0.02
Identification of microRNA-dependent gene regulatory networks driving human pancreatic endocrine cell differentiation [RNA-Seq III] 0.01
BMS-470539 on human synovial fibroblasts 0.01
RNAseq of Breast cancer PDX samples 0.01
Unlocking the transcriptomic potential of formalin-fixed paraffin embedded clinical tissues: Comparison of gene expression profiling approaches 0.01
Unlocking the transcriptomic potential of formalin-fixed paraffin embedded clinical tissues: Comparison of gene expression profiling approaches [RNA-Seq] 0.01
A transcriptome-wide divergence in protein translation scales with LIN28B expression 0.01
RNA sequencing quantitative analysis of RNA editing levels in ADAR1, ADAR2, AIMP2 overexpression and wild type HEK293 cells 0.0


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