CiiiDER: A tool for predicting and analysing transcription factor binding sites.
PMID:31483836
Allele specific chromatin signals, 3D interactions, and motif predictions for immune and B cell related diseases.
PMID:30804403
Myocyte enhancer factor-2 and p300 interact to regulate the expression of homeostatic regulator Pumilio in Drosophila.
PMID:30687963
Dempster-Shafer Theory for the Prediction of Auxin-Response Elements (AuxREs) in Plant Genomes.
PMID:30515394
p53 positively regulates the expression of cancer stem cell marker CD133 in HCT116 colon cancer cells.
PMID:29928431
Drosophila Model for the Analysis of Genesis of LIM-kinase 1-Dependent Williams-Beuren Syndrome Cognitive Phenotypes: INDELs, Transposable Elements of the Tc1/Mariner Superfamily and MicroRNAs.
PMID:28979292
1,25D3 differentially suppresses bladder cancer cell migration and invasion through the induction of miR-101-3p.
PMID:28947955
A microRNA signature of response to erlotinib is descriptive of TGFβ behaviour in NSCLC.
PMID:28646226
SNPs in microRNA target sites and their potential role in human disease.
PMID:28381629
The pseudokinase MLKL mediates programmed hepatocellular necrosis independently of RIPK3 during hepatitis.
PMID:27756058
CLOCK gene variation is associated with incidence of type-2 diabetes and cardiovascular diseases in type-2 diabetic subjects: dietary modulation in the PREDIMED randomized trial.
PMID:26739996
Inhibition of ERRα suppresses epithelial mesenchymal transition of triple negative breast cancer cells by directly targeting fibronectin.
PMID:26160845
Nuclear respiratory factor 2 induces SIRT3 expression.
PMID:26109058
Chronic morphine-induced microRNA-124 promotes microglial immunosuppression by modulating P65 and TRAF6.
PMID:25539811
Enhanced transgene expression from recombinant single-stranded D-sequence-substituted adeno-associated virus vectors in human cell lines in vitro and in murine hepatocytes in vivo.
PMID:25355884
Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25.
PMID:25327703
Congenital methemoglobinemia in a dog with a promoter deletion and a nonsynonymous coding variant in the gene encoding cytochrome b₅.
PMID:25145387
Sox17 inhibits hepatocellular carcinoma progression by downregulation of KIF14 expression.
PMID:25106407
Mechanisms of interferon-γ production by neutrophils and its function during Streptococcus pneumoniae pneumonia.
PMID:25100610
Epigenetic silencing of EYA2 in pancreatic adenocarcinomas promotes tumor growth.
PMID:24810906
A genetic variant in the LDLR promoter is responsible for part of the LDL-cholesterol variability in primary hypercholesterolemia.
PMID:24708769
c-Myc-mediated repression of miR-15-16 in hypoxia is induced by increased HIF-2α and promotes tumor angiogenesis and metastasis by upregulating FGF2.
PMID:24704828
Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation.
PMID:24430186
Plant promoters: an approach of structure and function.
PMID:24122284
The next generation of transcription factor binding site prediction.
PMID:24039567
Expression profiling of Aldh1l1-precursors in the developing spinal cord reveals glial lineage-specific genes and direct Sox9-Nfe2l1 interactions.
PMID:23840004
D-Light on promoters: a client-server system for the analysis and visualization of cis-regulatory elements.
PMID:23617301
Multi-species comparative analysis of the equine ACE gene identifies a highly conserved potential transcription factor binding site in intron 16.
PMID:23408978
Tethering of the conserved piggyBac transposase fusion protein CSB-PGBD3 to chromosomal AP-1 proteins regulates expression of nearby genes in humans.
PMID:23028371
Genetic variants and haplotypes of the UGT1A9, 1A7 and 1A1 genes in Chinese Han.
PMID:22888291
Large-scale computational identification of regulatory SNPs with rSNP-MAPPER.
PMID:22759655
An information transmission model for transcription factor binding at regulatory DNA sites.
PMID:22672438
ANKRD7 and CYTL1 are novel risk genes for alcohol drinking behavior.
PMID:22613542
Cataloguing functionally relevant polymorphisms in gene DNA ligase I: a computational approach.
PMID:22558535
Genetic variation at a Yin-Yang 1 response site regulates the transcription of cyclin-dependent kinase inhibitor p18INK4C transcript in lupus-prone mice.
PMID:22504641
A flexible integrative approach based on random forest improves prediction of transcription factor binding sites.
PMID:22492513
DNA-protein interactions: methods for detection and analysis.
PMID:22399265
SIRT1 activates MAO-A in the brain to mediate anxiety and exploratory drive.
PMID:22169038
Isoform diversity and its importance for axon regeneration.
PMID:22151581
The MAPPER2 Database: a multi-genome catalog of putative transcription factor binding sites.
PMID:22121218
Genetic variation within a metabolic motif in the chromogranin a promoter: pleiotropic influence on cardiometabolic risk traits in twins.
PMID:21918574
Tree-based position weight matrix approach to model transcription factor binding site profiles.
PMID:21912677
Inflammatory gene regulatory networks in amnion cells following cytokine stimulation: translational systems approach to modeling human parturition.
PMID:21655103
Discovery and assessment of conserved Pax6 target genes and enhancers.
PMID:21617155
Cyclin-dependent kinase inhibitor Cdkn2c regulates B cell homeostasis and function in the NZM2410-derived murine lupus susceptibility locus Sle2c1.
PMID:21543644
The PLIN4 variant rs8887 modulates obesity related phenotypes in humans through creation of a novel miR-522 seed site.
PMID:21533135
Elevated levels of hypoxia-inducible microRNA-210 in pre-eclampsia: new insights into molecular mechanisms for the disease.
PMID:21388517
Estrogen-related receptor gamma promotes mesenchymal-to-epithelial transition and suppresses breast tumor growth.
PMID:21339306
SOX5 is a candidate gene for chronic obstructive pulmonary disease susceptibility and is necessary for lung development.
PMID:21330457
A Bayesian search for transcriptional motifs.
PMID:21124986
miR-301a as an NF-κB activator in pancreatic cancer cells.
PMID:21113131
Down-regulation of microRNAs 222/221 in acute myelogenous leukemia with deranged core-binding factor subunits.
PMID:21076613
Use of structural DNA properties for the prediction of transcription-factor binding sites in Escherichia coli.
PMID:21051340
Genomic repertoires of DNA-binding transcription factors across the tree of life.
PMID:20675356
Tissue-specific regulatory regions of the PTH gene localized by novel chromosome 11 rearrangement breakpoints in a parathyroid adenoma.
PMID:20641034
miR-29 modulates Wnt signaling in human osteoblasts through a positive feedback loop.
PMID:20551325
Intron-1 rs3761548 is related to the defective transcription of Foxp3 in psoriasis through abrogating E47/c-Myb binding.
PMID:20414968
AML1 is overexpressed in patients with myeloproliferative neoplasms and mediates JAK2V617F-independent overexpression of NF-E2.
PMID:20339092
Regulation of FGF21 expression and secretion by retinoic acid receptor-related orphan receptor alpha.
PMID:20332535
Genetic variations at ABCG5/G8 genes modulate plasma lipids concentrations in patients with familial hypercholesterolemia.
PMID:20172523
CLOCK gene is implicated in weight reduction in obese patients participating in a dietary programme based on the Mediterranean diet.
PMID:20065968
Nuclear respiratory factor 2 induces the expression of many but not all human proteins acting in mitochondrial DNA transcription and replication.
PMID:19951946
Genetic variants in human CLOCK associate with total energy intake and cytokine sleep factors in overweight subjects (GOLDN population).
PMID:19888304
CLOCK genetic variation and metabolic syndrome risk: modulation by monounsaturated fatty acids.
PMID:19846548
Transcriptional downregulation of p27KIP1 through regulation of E2F function during LMP1-mediated transformation.
PMID:19828622
Identification of functionally related genes using data mining and data integration: a breast cancer case study.
PMID:19828084
ADAM17_i33708A>G polymorphism interacts with dietary n-6 polyunsaturated fatty acids to modulate obesity risk in the Genetics of Lipid Lowering Drugs and Diet Network study.
PMID:19819120
Analysis of human CYP1A1 and CYP1A2 genes and their shared bidirectional promoter in eight world populations.
PMID:19802894
Repression of the miR-17-92 cluster by p53 has an important function in hypoxia-induced apoptosis.
PMID:19696742
The effects of ABCG5/G8 polymorphisms on HDL-cholesterol concentrations depend on ABCA1 genetic variants in the Boston Puerto Rican Health Study.
PMID:19692220
Gene expression patterns in heterozygous Plk4 murine embryonic fibroblasts.
PMID:19607708
Novel variants at KCTD10, MVK, and MMAB genes interact with dietary carbohydrates to modulate HDL-cholesterol concentrations in the Genetics of Lipid Lowering Drugs and Diet Network Study.
PMID:19605566
Gene expression profiling in monocytes and SNP association suggest the importance of the STAT1 gene for osteoporosis in both Chinese and Caucasians.
PMID:19594299
Effects of variations in the APOA1/C3/A4/A5 gene cluster on different parameters of postprandial lipid metabolism in healthy young men.
PMID:19592705
The p53HMM algorithm: using profile hidden markov models to detect p53-responsive genes.
PMID:19379484
Genetic variants at the PDZ-interacting domain of the scavenger receptor class B type I interact with diet to influence the risk of metabolic syndrome in obese men and women.
PMID:19321583
New scoring schema for finding motifs in DNA Sequences.
PMID:19302709
COTRASIF: conservation-aided transcription-factor-binding site finder.
PMID:19264796
ADIPOQ polymorphisms, monounsaturated fatty acids, and obesity risk: the GOLDN study.
PMID:19238139
Novel promoter and exon mutations of the BMPR2 gene in Chinese patients with pulmonary arterial hypertension.
PMID:19223935
Lamin B1 controls oxidative stress responses via Oct-1.
PMID:19139261
Identification of neuronal target genes for CCAAT/enhancer binding proteins.
PMID:19103292
Hair follicle stem cell-specific PPARgamma deletion causes scarring alopecia.
PMID:19052558
Network integration and graph analysis in mammalian molecular systems biology.
PMID:19045817
A 19-base pair deletion polymorphism in dihydrofolate reductase is associated with increased unmetabolized folic acid in plasma and decreased red blood cell folate.
PMID:19022952
The effects of ABCG5/G8 polymorphisms on plasma HDL cholesterol concentrations depend on smoking habit in the Boston Puerto Rican Health Study.
PMID:19005228
Associations between single nucleotide polymorphisms in folate uptake and metabolizing genes with blood folate, homocysteine, and DNA uracil concentrations.
PMID:18842806
Upstream stimulatory factor is required for human angiotensinogen expression and differential regulation by the A-20C polymorphism.
PMID:18802024
Association analysis of Rgs7 variants with panic disorder.
PMID:18762858
ReXSpecies--a tool for the analysis of the evolution of gene regulation across species.
PMID:18410675
Probabilistic inference of transcription factor binding from multiple data sources.
PMID:18364997
Evolutionary and transcriptional analysis of karyopherin beta superfamily proteins.
PMID:18353765
Association study of the oestrogen signalling pathway genes in relation to age at natural menopause.
PMID:18305346
Association of common C-reactive protein (CRP) gene polymorphisms with baseline plasma CRP levels and fenofibrate response: the GOLDN study.
PMID:18285551
Transcription factors CTCF and Pax6 are segregated to different cell types during retinal cell differentiation.
PMID:18224715
The interplay between the master transcription factor PU.1 and miR-424 regulates human monocyte/macrophage differentiation.
PMID:18056638
Age-related subproteomic analysis of mouse liver and kidney peroxisomes.
PMID:18042274
JASPAR, the open access database of transcription factor-binding profiles: new content and tools in the 2008 update.
PMID:18006571
Comparative analysis of regulatory motif discovery tools for transcription factor binding sites.
PMID:17893078
A candidate gene approach identifies the TRAF1/C5 region as a risk factor for rheumatoid arthritis.
PMID:17880261
Xenobiotic metabolizing enzyme gene polymorphisms predict response to lung volume reduction surgery.
PMID:17686149
Olig2-regulated lineage-restricted pathway controls replication competence in neural stem cells and malignant glioma.
PMID:17296553
In silico modelling of hormone response elements.
PMID:17217520
Stubb: a program for discovery and analysis of cis-regulatory modules.
PMID:16845069
Djinn Lite: a tool for customised gene transcript modelling, annotation-data enrichment and exploration.
PMID:16426464
A new generation of JASPAR, the open-access repository for transcription factor binding site profiles.
PMID:16381983