1,284 results on '"van IJcken, Wilfred"'
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2. Runx1+ vascular smooth muscle cells are essential for hematopoietic stem and progenitor cell development in vivo
3. Bulk and single-cell transcriptomics identify gene signatures of stem cell-derived NK cell donors with superior cytolytic activity
4. Retrospective analysis of enhancer activity and transcriptome history
5. Machine learning-based somatic variant calling in cell-free DNA of metastatic breast cancer patients using large NGS panels
6. Genome-wide analysis toward the epigenetic aetiology of myelodysplastic syndrome disease progression and pharmacoepigenomic basis of hypomethylating agents drug treatment response
7. NOXA expression drives synthetic lethality to RUNX1 inhibition in pancreatic cancer
8. CABA-V7: a prospective biomarker selected trial of cabazitaxel treatment in AR-V7 positive prostate cancer patients
9. Dominant-acting CSF1R variants cause microglial depletion and altered astrocytic phenotype in zebrafish and adult-onset leukodystrophy
10. PDGFRβ+ cells play a dual role as hematopoietic precursors and niche cells during mouse ontogeny
11. A three-dimensional vessel-on-chip model to study Puumala orthohantavirus pathogenesis.
12. Genome-wide methylation analysis in patients with proximal hypospadias – a pilot study and review of the literature.
13. The tumor suppressor MIR139 is silenced by POLR2M to promote AML oncogenesis
14. Effect of bovine milk fat-based infant formulae on microbiota, metabolites and stool parameters in healthy term infants in a randomized, crossover, placebo-controlled trial
15. Identification of candidate enhancers controlling the transcriptome during the formation of interphalangeal joints
16. JMJD3 intrinsically disordered region links the 3D-genome structure to TGFβ-dependent transcription activation
17. CRISPRs in the human genome are differentially expressed between malignant and normal adjacent to tumor tissue
18. Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblasts
19. Genome-wide aberrant methylation in primary metastatic UM and their matched metastases
20. Epigenetic and Genomic Hallmarks of PARP-Inhibitor Resistance in Ovarian Cancer Patients
21. Unraveling the impact of AXIN1 mutations on HCC development: Insights from CRISPR/Cas9 repaired AXIN1-mutant liver cancer cell lines
22. RMplex: An efficient method for analyzing 30 Y-STRs with high mutation rates
23. Targeted Apoptosis of Senescent Cells Restores Tissue Homeostasis in Response to Chemotoxicity and Aging
24. Molecular analysis of the erythroid phenotype of a patient with BCL11A haploinsufficiency
25. Combined Analysis of Transcriptome and T-Cell Receptor Alpha and Beta (TRA/TRB) Repertoire in Paucicellular Samples at the Single-Cell Level
26. CTCF chromatin residence time controls three-dimensional genome organization, gene expression and DNA methylation in pluripotent cells
27. Orphan CpG islands amplify poised enhancer regulatory activity and determine target gene responsiveness
28. BMP4 and Temozolomide Synergize in the Majority of Patient-Derived Glioblastoma Cultures.
29. Human Pluripotent Stem Cell-Derived Astrocyte Functionality Compares Favorably with Primary Rat Astrocytes.
30. MAU2 and NIPBL Variants Impair the Heterodimerization of the Cohesin Loader Subunits and Cause Cornelia de Lange Syndrome
31. Distinctive cell‐free DNA methylation characterizes presymptomatic genetic frontotemporal dementia
32. Pathogen-induced activation of disease-suppressive functions in the endophytic root microbiome
33. Notch signaling licenses allergic airway inflammation by promoting Th2 cell lymph node egress
34. Genome-wide methylation analysis in patients with proximal hypospadias–a pilot study and review of the literature
35. Epigenomic partitioning of a polygenic risk score for asthma reveals distinct genetically driven disease pathways
36. Species-specific responses during Seoul orthohantavirus infection in human and rat lung microvascular endothelial cells
37. Distinctive cell-free DNA methylation characterizes presymptomatic genetic frontotemporal dementia
38. Runx1+ vascular smooth muscle cells are essential for hematopoietic stem and progenitor cell development in vivo
39. In vitro capture and characterization of embryonic rosette-stage pluripotency between naive and primed states
40. Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases
41. Enhancer-associated H3K4 methylation safeguards in vitro germline competence
42. Genome wide DNA methylation analysis of alveolar capillary dysplasia lung tissue reveals aberrant methylation of genes involved in development including the FOXF1 locus
43. SPEN is required for Xist upregulation during initiation of X chromosome inactivation
44. Selective cell death in HIV-1-infected cells by DDX3 inhibitors leads to depletion of the inducible reservoir
45. High-throughput and affordable genome-wide methylation profiling of circulating cell-free DNA by methylated DNA sequencing (MeD-seq) of LpnPI digested fragments
46. Modeling the Pathological Long-Range Regulatory Effects of Human Structural Variation with Patient-Specific hiPSCs
47. A cellular reporter system to evaluate endogenous fetal hemoglobin induction and screen for therapeutic compounds.
48. MaterniCode: New Bioinformatic Pipeline to Detect Fetal Aneuploidies and Rearrangements Using Next‐Generation Sequencing.
49. Low Input Targeted Chromatin Capture (Low-T2C)
50. Epigenome analysis links gene regulatory elements in group 2 innate lymphocytes to asthma susceptibility
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