fetal bovine serum drug

Aliases

10% FBS, 15% FBS, FBS, dialysed fetal calf serum

External links

DrugBank · PubChem

No related entities found.

Mentioned in (45)

Papers in which this entity is mentioned.

• Investigation of a global mouse methylome atlas reveals subtype-specific copy number alterations in pediatric cancer models. (2026)
• Single-cell exon deletion profiling reveals splicing events that shape gene expression and cell state dynamics. (2026)
• Tumour-wide RNA splicing aberrations generate actionable public neoantigens. (2025)
• Multi-omic quantitative trait loci link tandem repeat size variation to gene regulation in human brain. (2025)
• MYC ecDNA promotes intratumour heterogeneity and plasticity in PDAC. (2025)
• Reduction of APOE accounts for neurobehavioral deficits in fetal alcohol spectrum disorders. (2024)
• Global impact of unproductive splicing on human gene expression. (2024)
• Single-molecule methylation profiles of cell-free DNA in cancer with nanopore sequencing. (2023)
• Most non-canonical proteins uniquely populate the proteome or immunopeptidome. (2021)
• Integrated Genomic Analysis Identifies Driver Genes and Cisplatin-Resistant Progenitor Phenotype in Pediatric Liver Cancer. (2021)
• Joint single-cell measurements of nuclear proteins and RNA in vivo. (2021)
• Simultaneous single cell measurements of intranuclear proteins and gene expression (2021)
• Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X. (2020)
• B cells and tertiary lymphoid structures promote immunotherapy response. (2020)
• Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes. (2020)
• Diverse noncoding mutations contribute to deregulation of cis-regulatory landscape in pediatric cancers. (2020)
• Effects of chronic intermittent ethanol exposure and withdrawal on neuroblastoma cell transcriptome. (2020)
• Reciprocal monoallelic expression of ASAR lncRNA genes controls replication timing of human chromosome 6. (2020)
• Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing. (2020)
• Genetic compensation triggered by mutant mRNA degradation. (2019)
• Alternative Lengthening of Telomeres through Two Distinct Break-Induced Replication Pathways. (2019)
• Maternal circulating miRNAs that predict infant FASD outcomes influence placental maturation. (2019)
• Rapid and reversible suppression of ALT by DAXX in osteosarcoma cells. (2019)
• Ethanol activates immune response in lymphoblastoid cells. (2019)
• RNA-Seq Signatures Normalized by mRNA Abundance Allow Absolute Deconvolution of Human Immune Cell Types. (2019)
• The role and robustness of the Gini coefficient as an unbiased tool for the selection of Gini genes for normalising expression profiling data. (2019)
• Orthotopic patient-derived xenografts of paediatric solid tumours. (2017)
• Cancer-Specific Retargeting of BAF Complexes by a Prion-like Domain. (2017)
• Interaction of glycosphingolipids GD3 and GD2 with growth factor receptors maintains breast cancer stem cell phenotype. (2017)
• PGBD5 promotes site-specific oncogenic mutations in human tumors. (2017)
• A role for human homologous recombination factors in suppressing microhomology-mediated end joining. (2016)
• Fragment Length of Circulating Tumor DNA. (2016)
• Estimating the population abundance of tissue-infiltrating immune and stromal cell populations using gene expression. (2016)
• EWS and FUS bind a subset of transcribed genes encoding proteins enriched in RNA regulatory functions. (2015)
• Position-specific binding of FUS to nascent RNA regulates mRNA length. (2015)
• The landscape of long noncoding RNAs in the human transcriptome. (2015)
• The use of exome capture RNA-seq for highly degraded RNA with application to clinical cancer sequencing. (2015)
• A germline polymorphism of thymine DNA glycosylase induces genomic instability and cellular transformation. (2014)
• Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants. (2014)
• Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine. (2014)
• PVT1 dependence in cancer with MYC copy-number increase. (2014)
• Commonality in Down and fetal alcohol syndromes. (2013)
• Cleft lip and palate results from Hedgehog signaling antagonism in the mouse: Phenotypic characterization and clinical implications. (2010)
• Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcripts. (2009)
• Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. (2009)

Merged raw entities (5)

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