U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line
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P1343
Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndromeNCG 4.0: the network of cancer genes in the era of massive mutational screenings of cancer genomesNetwork of Cancer Genes (NCG 3.0): integration and analysis of genetic and network properties of cancer genesIdentification of high-confidence somatic mutations in whole genome sequence of formalin-fixed breast cancer specimensIn vivo models of primary brain tumors: pitfalls and perspectives.Contemporary murine models in preclinical astrocytoma drug developmentSensitive Tumorigenic Potential Evaluation of Adult Human Multipotent Neural Cells Immortalized by hTERT Gene TransductionAnalysis of next-generation genomic data in cancer: accomplishments and challengesExosomes reflect the hypoxic status of glioma cells and mediate hypoxia-dependent activation of vascular cells during tumor developmentEngineered drug resistant γδ T cells kill glioblastoma cell lines during a chemotherapy challenge: a strategy for combining chemo- and immunotherapyHigh-resolution mutational profiling suggests the genetic validity of glioblastoma patient-derived pre-clinical modelsDoxycycline alters metabolism and proliferation of human cell linesDistinct patterns of somatic alterations in a lymphoblastoid and a tumor genome derived from the same individualModulation of HJURP (Holliday Junction-Recognizing Protein) levels is correlated with glioblastoma cells survivalCharacterization of a setup to test the impact of high-amplitude pressure waves on living cells.Cooperativity between MAPK and PI3K signaling activation is required for glioblastoma pathogenesis.ReQON: a Bioconductor package for recalibrating quality scores from next-generation sequencing data.Fastbreak: a tool for analysis and visualization of structural variations in genomic data.Linking proteomic and transcriptional data through the interactome and epigenome reveals a map of oncogene-induced signaling.Secondary Data Analytics of Aquaporin Expression Levels in Glioblastoma Stem-Like CellsChallenges of sequencing human genomes.Local alignment of generalized k-base encoded DNA sequence.The (r)evolution of cancer geneticsImproved variant discovery through local re-alignment of short-read next-generation sequencing data using SRMA.Integrated analysis of recurrent properties of cancer genes to identify novel driversSilencing of protein kinase D2 induces glioma cell senescence via p53-dependent and -independent pathways.SeqWare Query Engine: storing and searching sequence data in the cloud.A murine model of targeted infusion for intracranial tumors.Modulation of the inwardly rectifying potassium channel Kir4.1 by the pro-invasive miR-5096 in glioblastoma cellsComprehensive genomic analysis of a BRCA2 deficient human pancreatic cancerMyc inhibition is effective against glioma and reveals a role for Myc in proficient mitosis.Novel multi-nucleotide polymorphisms in the human genome characterized by whole genome and exome sequencing.Current review of in vivo GBM rodent models: emphasis on the CNS-1 tumour model.Next-generation sequencing of colorectal cancers in chinese: identification of a recurrent frame-shift and gain-of-function Indel mutation in the TFDP1 geneRecurrent somatic mutation of FAT1 in multiple human cancers leads to aberrant Wnt activation.Multiplexed detection and label-free quantitation of microRNAs using arrays of silicon photonic microring resonatorsLong span DNA paired-end-tag (DNA-PET) sequencing strategy for the interrogation of genomic structural mutations and fusion-point-guided reconstruction of amplicons.Next-generation sequencing of endoscopic biopsies identifies ARID1A as a tumor-suppressor gene in Barrett's esophagusOASIS/CREB3L1 is induced by endoplasmic reticulum stress in human glioma cell lines and contributes to the unfolded protein response, extracellular matrix production and cell migrationCMV-independent lysis of glioblastoma by ex vivo expanded/activated Vδ1+ γδ T cells.
P2860
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P2860
U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line
description
2010 nî lūn-bûn
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2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
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2010年論文
@yue
2010年論文
@zh-hant
2010年論文
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2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
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U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line
@ast
U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line
@en
U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line
@en-gb
U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line
@nl
type
label
U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line
@ast
U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line
@en
U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line
@en-gb
U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line
@nl
altLabel
U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line
@en
prefLabel
U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line
@ast
U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line
@en
U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line
@en-gb
U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line
@nl
P2093
P2860
P3181
P1433
P1476
U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line
@en
P2093
Ascia Eskin
Barry Merriman
Brian D O'Connor
Michael James Clark
Nils Homer
Stanley F Nelson
Zugen Chen
P2860
P304
P3181
P356
10.1371/JOURNAL.PGEN.1000832
P407
P4510
P577
2010-01-01T00:00:00Z