Fate mapping of human glioblastoma reveals an invariant stem cell hierarchy. - Wikidata - awgldk - TriplyDB

Fate mapping of human glioblastoma reveals an invariant stem cell hierarchy.

Fate mapping of human glioblastoma reveals an invariant stem cell hierarchy.

http://www.wikidata.org/entity/Q48134470

about

Order in Chaos: Understanding Intratumoral Heterogeneity in Gliomas by Tracking Tumor Cell Fate.Left or right? Directions to stem cell engraftment.Utility of Glioblastoma Patient-Derived Orthotopic Xenografts in Drug Discovery and Personalized Therapy.Reconstructing the molecular life history of gliomas.Cellular origin of glioblastoma and its implication in precision therapy.Cancer: Division hierarchy leads to cell heterogeneity.The developmental origin of brain tumours: a cellular and molecular framework.RESTRICTION OF γ34.5-DELETED ONCOLYTIC HERPES SIMPLEX VIRUS REPLICATION IN GLIOBLASTOMA STEM-LIKE CELLS.Next-Generation Modeling of Human Cancers

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P2860

Fate mapping of human glioblastoma reveals an invariant stem cell hierarchy.

http://www.wikidata.org/entity/Q48134470

description

2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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name

Fate mapping of human glioblastoma reveals an invariant stem cell hierarchy.

@en

Fate mapping of human glioblastoma reveals an invariant stem cell hierarchy.

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type

label

Fate mapping of human glioblastoma reveals an invariant stem cell hierarchy.

@en

Fate mapping of human glioblastoma reveals an invariant stem cell hierarchy.

@nl

prefLabel

Fate mapping of human glioblastoma reveals an invariant stem cell hierarchy.

@en

Fate mapping of human glioblastoma reveals an invariant stem cell hierarchy.

@nl

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Fate mapping of human glioblastoma reveals an invariant stem cell hierarchy

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Annaick Carles

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Betty Luu

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Clare Che

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Connie J Eaves

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Davide Pellacani

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Fiona J Coutinho

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Florence M G Cavalli

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Hayden J Selvadurai

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Heather Whetstone

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Laura M Richards

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P2860

Model-based analysis of ChIP-Seq (MACS)

An integrated map of genetic variation from 1,092 human genomes

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

dbSNP: the NCBI database of genetic variation

VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing

Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1

A global reference for human genetic variation

Analysis of protein-coding genetic variation in 60,706 humans

Molecular identity of human outer radial glia during cortical development

Fast gapped-read alignment with Bowtie 2

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10.1038/NATURE23666

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Benjamin D. Simons

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2017-08-30T00:00:00Z

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