Genome and transcriptome sequencing of lung cancers reveal diverse mutational and splicing events. - Wikidata - wikimedia - TriplyDB

Genome and transcriptome sequencing of lung cancers reveal diverse mutational and splicing events.

Genome and transcriptome sequencing of lung cancers reveal diverse mutational and splicing events.

http://www.wikidata.org/entity/Q36446169

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Regulation of deoxynucleotide metabolism in cancer: novel mechanisms and therapeutic implications Differences in driver genes between smoking-related and non-smoking-related lung cancer in the Chinese population Cancer Cell Line Panels Empower Genomics-Based Discovery of Precision Cancer Medicine Targeted therapies in development for non-small cell lung cancer Structural integrity of centromeric chromatin and faithful chromosome segregation requires Pat1 Inactivating CUX1 mutations promote tumorigenesis RNAi screening with shRNAs against histone methylation-related genes reveals determinants of sorafenib sensitivity in hepatocellular carcinoma cells An integrated inspection of the somatic mutations in a lung squamous cell carcinoma using next-generation sequencing The mutational landscape of chromatin regulatory factors across 4,623 tumor samples.Reliable identification of genomic variants from RNA-seq data Sanguinarine inhibits Rac1b-rendered cell survival enhancement by promoting apoptosis and blocking proliferation.ROS-induced epithelial-mesenchymal transition in mammary epithelial cells is mediated by NF-kB-dependent activation of Snail.Lineage-specific splicing of a brain-enriched alternative exon promotes glioblastoma progression.The role of mRNA splicing in prostate cancer.Mouse knockout models for HIV-1 restriction factors.MBASED: allele-specific expression detection in cancer tissues and cell lines.KMT2D maintains neoplastic cell proliferation and global histone H3 lysine 4 monomethylation.Smoking status impacts microRNA mediated prognosis and lung adenocarcinoma biology MicroRNA-181 contributes to downregulation of SAMHD1 expression in CD4+ T-cells derived from Sèzary syndrome patients.Integrated analysis of whole genome and transcriptome sequencing reveals diverse transcriptomic aberrations driven by somatic genomic changes in liver cancers The landscape of alternative splicing in cervical squamous cell carcinoma.Prognostic impact of alternative splicing-derived hMENA isoforms in resected, node-negative, non-small-cell lung cancer.Comprehensive analysis of transcriptome variation uncovers known and novel driver events in T-cell acute lymphoblastic leukemia Human biosample authentication using the high-throughput, cost-effective SNPtrace(TM) system.Protein domain-level landscape of cancer-type-specific somatic mutations.Bioinformatics analysis of thousands of TCGA tumors to determine the involvement of epigenetic regulators in human cancer.Transcriptome-wide identification and study of cancer-specific splicing events across multiple tumors.Vasohibin-1 suppresses colon cancer.Inconsistency and features of single nucleotide variants detected in whole exome sequencing versus transcriptome sequencing: A case study in lung cancer.Predicting lncRNA-disease associations and constructing lncRNA functional similarity network based on the information of miRNA Transposon Mutagenesis Screen Identifies Potential Lung Cancer Drivers and CUL3 as a Tumor Suppressor.A Novel Pharmacologic Activity of Ketorolac for Therapeutic Benefit in Ovarian Cancer Patients.Two Loops Undergoing Concerted Dynamics Regulate the Activity of the ASH1L Histone Methyltransferase.Tumor cell expression of MMP3 as a prognostic factor for poor survival in pancreatic, pulmonary, and mammary carcinoma Functional divergence and convergence between the transcript network and gene network in lung adenocarcinoma.Alternative Splicing in Adhesion- and Motility-Related Genes in Breast Cancer Ibuprofen inhibits colitis-induced overexpression of tumor-related Rac1b Hepatocellular carcinoma cell lines retain the genomic and transcriptomic landscapes of primary human cancers.Next-generation sequencing of paired tyrosine kinase inhibitor-sensitive and -resistant EGFR mutant lung cancer cell lines identifies spectrum of DNA changes associated with drug resistance Integrative analysis of two cell lines derived from a non-small-lung cancer patient--a panomics approach.

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P2860

Genome and transcriptome sequencing of lung cancers reveal diverse mutational and splicing events.

http://www.wikidata.org/entity/Q36446169

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Genome and transcriptome seque ...... utational and splicing events.

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Genome and transcriptome seque ...... utational and splicing events.

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Genome and transcriptome seque ...... utational and splicing events.

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Genome and transcriptome seque ...... utational and splicing events.

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P2860

U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line

Mapping and quantifying mammalian transcriptomes by RNA-Seq

Structure of the Rb C-terminal domain bound to E2F1-DP1: a mechanism for phosphorylation-induced E2F release

The Rac1 splice form Rac1b promotes K-ras-induced lung tumorigenesis

A small-cell lung cancer genome with complex signatures of tobacco exposure

Covalent histone modifications--miswritten, misinterpreted and mis-erased in human cancers

A decade of exploring the cancer epigenome - biological and translational implications

Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation

A comprehensive catalogue of somatic mutations from a human cancer genome

Matrix metalloproteinase induction of Rac1b, a key effector of lung cancer progression

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