about
Imputation and subset based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer typesGeneralizations of Markov model to characterize biological sequencesA genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancerMeta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian womenGenome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in AsiaNdPASA: a pairwise sequence alignment server for distantly related proteins.DDGni: dynamic delay gene-network inference from high-temporal data using gapped local alignment.Inferring gene regulatory networks by integrating ChIP-seq/chip and transcriptome data via LASSO-type regularization methods.FaSD-somatic: a fast and accurate somatic SNV detection algorithm for cancer genome sequencing data.Basonuclin regulates a subset of ribosomal RNA genes in HaCaT cellsMetaProm: a neural network based meta-predictor for alternative human promoter prediction.Mouse ribosomal RNA genes contain multiple differentially regulated variantsFastPval: a fast and memory efficient program to calculate very low P-values from empirical distribution.Robust and rapid algorithms facilitate large-scale whole genome sequencing downstream analysis in an integrative frameworkInhibition of KAP1 enhances hypoxia-induced Kaposi's sarcoma-associated herpesvirus reactivation through RBP-Jκ.ChIP-Array: combinatory analysis of ChIP-seq/chip and microarray gene expression data to discover direct/indirect targets of a transcription factorEpiRegNet: constructing epigenetic regulatory network from high throughput gene expression data for humans.Rare SNP rs12731181 in the miR-590-3p Target Site of the Prostaglandin F2α Receptor Gene Confers Risk for Essential Hypertension in the Han Chinese Population.Inference of gene-phenotype associations via protein-protein interaction and orthology.GWASdb: a database for human genetic variants identified by genome-wide association studies.The support of human genetic evidence for approved drug indications.Potent Paracrine Effects of human induced Pluripotent Stem Cell-derived Mesenchymal Stem Cells Attenuate Doxorubicin-induced CardiomyopathyAdvanced Computational Approaches for Medical Genetics and Genomics.GWASdb v2: an update database for human genetic variants identified by genome-wide association studies.Five endometrial cancer risk loci identified through genome-wide association analysis.Hyperglycemia-induced protein kinase C β2 activation induces diastolic cardiac dysfunction in diabetic rats by impairing caveolin-3 expression and Akt/eNOS signaling.Dataset of TWIST1-regulated genes in the cranial mesoderm and a transcriptome comparison of cranial mesoderm and cranial neural crestSusceptibility to myocardial ischemia reperfusion injury at early stage of type 1 diabetes in rats.DLX1 acts as a crucial target of FOXM1 to promote ovarian cancer aggressiveness by enhancing TGF-β/SMAD4 signaling.Exploring the function of genetic variants in the non-coding genomic regions: approaches for identifying human regulatory variants affecting gene expression.Current trend of annotating single nucleotide variation in humans--A case study on SNVrap.Transcriptional targets of TWIST1 in the cranial mesoderm regulate cell-matrix interactions and mesenchyme maintenance.Search for basonuclin target genes.Lung cancer tumorigenicity and drug resistance are maintained through ALDH(hi)CD44(hi) tumor initiating cells.Next generation sequencing has lower sequence coverage and poorer SNP-detection capability in the regulatory regions.Improved cell survival and paracrine capacity of human embryonic stem cell-derived mesenchymal stem cells promote therapeutic potential for pulmonary arterial hypertension.Proteomic profiling identifies the SIM-associated complex of KSHV-encoded LANA.PU.1 can recruit BCL6 to DNA to repress gene expression in germinal center B cells.Genetic variant representation, annotation and prioritization in the post-GWAS era.
P50
Q23924183-5026EEDC-9042-4B04-9849-24C5BB64584BQ24170413-AF81DE25-91FD-4C59-9FA2-0847A78D6690Q24816544-EBA20158-D45D-42DD-915F-60D49C25CD3AQ28303909-0EC9F7A1-3BDD-4B88-87F1-6CEE3B13D45AQ28385292-EB7C0F43-8D62-4B4B-8851-588DB13BFE71Q28943345-89C2B791-EF07-4528-AF19-2559A944A98DQ30351257-5AA2EE61-BE58-489C-BD2A-AC635B96C825Q30703235-4FFF28C7-F868-4E33-9D51-0CB116BBEE86Q30781627-ECA26BFA-D72A-4EE3-85A0-84ED35722849Q30822013-A0832993-1752-4DEC-8E6A-B51E7B4502CCQ33299466-78FD16B7-42E8-472D-AE3C-FDCDB1D3CA26Q33302977-ECAA1DCA-07EF-4981-A8F4-B5DC3921BF32Q33325468-1C0C85A6-BFCB-425E-AB52-D9AB527AF4F8Q33699527-5B95CE1A-E379-471F-BB9D-44D79BBECCC0Q33701488-8FCAA722-7F7B-4806-B426-68C249A3647AQ33743831-0BE1F169-8F21-407C-BFD9-BF1E466EF922Q33903683-7D2C5EE9-59D1-4F90-BB8D-2A848FE18CDBQ34090490-E12D0DC0-729C-4326-9234-F96A2B660428Q34476529-518FA33B-6AE7-4DA1-8CF7-020234132933Q35032445-9C72EA5E-9F4C-4503-BD6C-1DA787B22BFCQ35630781-67E77E4F-EDEB-4F04-9530-0CAEA9E02B89Q35677036-845A158F-96A2-41CE-BE82-BA8ACCCAB63AQ35702033-D59CEBC4-DF74-4F72-81AD-65BF9A2C27A7Q35947263-6055D778-045A-49EB-9637-FD1438825954Q36435017-5551A635-B7F4-47B6-A4F9-E3C2E66A1881Q37002930-6FC44689-1081-4A53-BB7B-1D585AAE5493Q37015027-89760616-2F99-4A67-853C-B60FE04EB86AQ37280435-A52494B2-EA78-4305-A1B9-0E6579EDD9B9Q37357405-4EECAA79-A83B-4F60-9434-31D0C374EEB9Q37697488-370326AE-6881-4E7C-A108-336B6F7132A7Q38219266-0AC5B72B-7EF0-4336-96BA-DDFB0E90F5AEQ38259526-240D9E44-004E-46AE-96AC-221FFABA41B6Q38750827-3D358DEE-DBAC-42DC-98B1-1E9439D54A76Q38981690-B84B52D9-D5EC-463C-A28B-620BA20E0E48Q39088028-A3B4C942-59FA-4AA8-9805-07E94D8E54B3Q39120229-408C1E26-8E3B-4F04-8548-BF5DBE70BFE6Q39317535-468A134C-6666-4176-AFC7-B2045D59FA28Q41306617-2889368B-D39E-4FA5-811C-29E211EF9552Q41824952-EDF3C8BE-19D8-4BA3-96BC-08C44E2026F3Q42532351-ABED4F3F-D831-4F7F-9E77-874DE76E2F43
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Junwen Wang
@ast
Junwen Wang
@en
Junwen Wang
@es
Junwen Wang
@sl
type
label
Junwen Wang
@ast
Junwen Wang
@en
Junwen Wang
@es
Junwen Wang
@sl
altLabel
Junwen John Wang
@en
prefLabel
Junwen Wang
@ast
Junwen Wang
@en
Junwen Wang
@es
Junwen Wang
@sl
P1053
D-3700-2011
P106
P1153
8950599500
P31
P3829
P496
0000-0002-4432-4707
P569
2000-01-01T00:00:00Z