Qiagen drug

External links

DrugBank · PubChem

Related entities (3)

Mentioned in (74)

Papers in which this entity is mentioned.

• Whole-genome landscapes of 1,364 breast cancers. (2026)
• Rapid brain tumor classification from sparse epigenomic data. (2025)
• Functional analysis of cancer-associated germline risk variants. (2025)
• Sequence modeling and design from molecular to genome scale with Evo. (2024)
• ESPRESSO: Robust discovery and quantification of transcript isoforms from error-prone long-read RNA-seq data. (2023)
• Validation of the new EPIC DNA methylation microarray (900K EPIC v2) for high-throughput profiling of the human DNA methylome. (2023)
• Massively parallel reporter perturbation assays uncover temporal regulatory architecture during neural differentiation. (2022)
• Single-cell genomic variation induced by mutational processes in cancer. (2022)
• Inferring gene expression from cell-free DNA fragmentation profiles. (2022)
• Feasibility of whole genome and transcriptome profiling in pediatric and young adult cancers. (2022)
• Integrated analysis of multimodal single-cell data. (2021)
• Prenatal Adversity Alters the Epigenetic Profile of the Prefrontal Cortex: Sexually Dimorphic Effects of Prenatal Alcohol Exposure and Food-Related Stress. (2021)
• Micro-RNA-125a mediates the effects of hypomethylating agents in chronic myelomonocytic leukemia. (2021)
• B cells and tertiary lymphoid structures promote immunotherapy response. (2020)
• Immuno-genomic landscape of osteosarcoma. (2020)
• Folding Keratin Gene Clusters during Skin Regional Specification. (2020)
• ASEP: Gene-based detection of allele-specific expression across individuals in a population by RNA sequencing. (2020)
• Hypermethylation of Proopiomelanocortin and Period 2 Genes in Blood Are Associated with Greater Subjective and Behavioral Motivation for Alcohol in Humans. (2019)
• Genetic compensation triggered by mutant mRNA degradation. (2019)
• Comparison of DNA methylation measured by Illumina 450K and EPIC BeadChips in blood of newborns and 14-year-old children. (2018)
• Mutational processes shape the landscape of TP53 mutations in human cancer. (2018)
• DNA methylation as a predictor of fetal alcohol spectrum disorder. (2018)
• Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome. (2018)
• Accurate Recycling of Parental Histones Reproduces the Histone Modification Landscape during DNA Replication. (2018)
• Picky comprehensively detects high-resolution structural variants in nanopore long reads. (2018)
• Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine Glioma. (2017)
• Assembly of functionally integrated human forebrain spheroids. (2017)
• The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. (2017)
• Benchmark Dose Modeling Estimates of the Concentrations of Inorganic Arsenic That Induce Changes to the Neonatal Transcriptome, Proteome, and Epigenome in a Pregnancy Cohort. (2017)
• Sexual Dimorphism of miRNAs Secreted by Bovine -produced Embryos. (2017)
• Sex differences in DNA methylation of the cord blood are related to sex-bias psychiatric diseases. (2017)
• A method to reduce ancestry related germline false positives in tumor only somatic variant calling. (2017)
• An open access pilot freely sharing cancer genomic data from participants in Texas. (2016)
• DNA Methylation Analysis: Choosing the Right Method. (2016)
• Fragment Length of Circulating Tumor DNA. (2016)
• Alteration of Gene Expression, DNA Methylation, and Histone Methylation in Free Radical Scavenging Networks in Adult Mouse Hippocampus following Fetal Alcohol Exposure. (2016)
• DNA methylation signature of human fetal alcohol spectrum disorder. (2016)
• Establishment of human iPSC-based models for the study and targeting of glioma initiating cells. (2016)
• The National Birth Defects Prevention Study: A review of the methods. (2015)
• Pioglitazone blocks ethanol induction of microglial activation and immune responses in the hippocampus, cerebellum, and cerebral cortex in a mouse model of fetal alcohol spectrum disorders. (2015)
• Integrative clinical genomics of advanced prostate cancer. (2015)
• ENVE: a novel computational framework characterizes copy-number mutational landscapes in colorectal cancers from African American patients. (2015)
• Clinical exome performance for reporting secondary genetic findings. (2015)
• Robust enumeration of cell subsets from tissue expression profiles. (2015)
• A germline polymorphism of thymine DNA glycosylase induces genomic instability and cellular transformation. (2014)
• An atlas of active enhancers across human cell types and tissues. (2014)
• Distribution, recognition and regulation of non-CpG methylation in the adult mammalian brain. (2014)
• Heritability and genomics of gene expression in peripheral blood. (2014)
• Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways. (2014)
• The genomic landscape of the Ewing Sarcoma family of tumors reveals recurrent STAG2 mutation. (2014)
• Alcohol modulates expression of DNA methyltranferases and methyl CpG-/CpG domain-binding proteins in murine embryonic fibroblasts. (2013)
• A simple consensus approach improves somatic mutation prediction accuracy. (2013)
• Intragenic DNA methylation modulates alternative splicing by recruiting MeCP2 to promote exon recognition. (2013)
• Identification and characterization of the miRNA transcriptome of Ovis aries. (2013)
• Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas. (2013)
• The Genotype-Tissue Expression (GTEx) project. (2013)
• Aberrant expression of long noncoding RNAs in autistic brain. (2013)
• Associations between maternal genotypes and metabolites implicated in congenital heart defects. (2012)
• Population-specificity of human DNA methylation. (2012)
• Chronic shift-lag alters the circadian clock of NK cells and promotes lung cancer growth in rats. (2012)
• miR-34s inhibit osteoblast proliferation and differentiation in the mouse by targeting SATB2. (2012)
• Functional analysis of APOE locus genetic variation implicates regional enhancers in the regulation of both TOMM40 and APOE. (2012)
• Mutations in Hedgehog acyltransferase (Hhat) perturb Hedgehog signaling, resulting in severe acrania-holoprosencephaly-agnathia craniofacial defects. (2012)
• Cdon mutation and fetal ethanol exposure synergize to produce midline signaling defects and holoprosencephaly spectrum disorders in mice. (2012)
• Alcohol alters DNA methylation patterns and inhibits neural stem cell differentiation. (2011)
• Postmortem interval effect on RNA and gene expression in human brain tissue. (2011)
• Spatial organization of RYRs and BK channels underlying the activation of STOCs by Ca(2+) sparks in airway myocytes. (2011)
• Alteration of gene expression by alcohol exposure at early neurulation. (2011)
• Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort. (2010)
• Rapid, low-input, low-bias construction of shotgun fragment libraries by high-density in vitro transposition. (2010)
• Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcripts. (2009)
• Rapid SNP discovery and genetic mapping using sequenced RAD markers. (2008)
• Fetal alcohol spectrum disorder-associated depression: evidence for reductions in the levels of brain-derived neurotrophic factor in a mouse model. (2008)
• Genome-wide maps of chromatin state in pluripotent and lineage-committed cells. (2007)

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