Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma - Wikidata - thesis-toulmin - TriplyDB

Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma

Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma

http://www.wikidata.org/entity/Q30014823

about

Paired tumor and normal whole genome sequencing of metastatic olfactory neuroblastoma U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line Mutational profiling of kinases in glioblastoma.Estrogen receptor alpha gene amplification in breast cancer: 25 years of debate NIRF constitutes a nodal point in the cell cycle network and is a candidate tumor suppressor Genomic subtypes of breast cancer identified by array-comparative genomic hybridization display distinct molecular and clinical characteristics A landscape of driver mutations in melanoma Targeting the hepatocyte growth factor-cMET axis in cancer therapy CaSNP: a database for interrogating copy number alterations of cancer genome from SNP array data The histone methyltransferase SETDB1 is recurrently amplified in melanoma and accelerates its onset Comprehensive molecular characterization of human colon and rectal cancer Recent advances in the molecular understanding of glioblastoma Convergent structural alterations define SWItch/Sucrose NonFermentable (SWI/SNF) chromatin remodeler as a central tumor suppressive complex in pancreatic cancer Characterizing the cancer genome in lung adenocarcinoma.Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1 Co-amplified genes at 8p12 and 11q13 in breast tumors cooperate with two major pathways in oncogenesis Comprehensive genomic characterization defines human glioblastoma genes and core pathways Targeting RTK Signaling Pathways in Cancer Molecular characterizations of glioblastoma, targeted therapy, and clinical results to date Cancer stem cell division: when the rules of asymmetry are broken Role of SOX family of transcription factors in central nervous system tumors Computational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challenges Bioinformatics for cancer immunology and immunotherapy The consequences of chromosomal aneuploidy on the transcriptome of cancer cells Synthetic lethal screens as a means to understand and treat MYC-driven cancers Will kinase inhibitors make it as glioblastoma drugs?Connexin 30 expression inhibits growth of human malignant gliomas but protects them against radiation therapy.Frequent and focal FGFR1 amplification associates with therapeutically tractable FGFR1 dependency in squamous cell lung cancer.Inhibitor-sensitive FGFR1 amplification in human non-small cell lung cancer.Adverse outcomes in clear cell renal cell carcinoma with mutations of 3p21 epigenetic regulators BAP1 and SETD2: a report by MSKCC and the KIRC TCGA research network Integrated genomic analyses of ovarian carcinoma Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma Comprehensive molecular profiling of lung adenocarcinoma.PAK1 is a breast cancer oncogene that coordinately activates MAPK and MET signaling Proportional upregulation of CD97 isoforms in glioblastoma and glioblastoma-derived brain tumor initiating cells CDK8 is a colorectal cancer oncogene that regulates beta-catenin activity Integrative genomic analysis of medulloblastoma identifies a molecular subgroup that drives poor clinical outcome piRNA involvement in genome stability and human cancer A systematic comparison of copy number alterations in four types of female cancer Integrated DNA Copy Number and Gene Expression Regulatory Network Analysis of Non-small Cell Lung Cancer Metastasis

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Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma

http://www.wikidata.org/entity/Q30014823

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2007 nî lūn-bûn

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2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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Linda Liau

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Inferring loss-of-heterozygosity from unpaired tumors using high-density oligonucleotide SNP arrays

High-resolution genomic profiles of human lung cancer

Amplification of MET may identify a subset of cancers with extreme sensitivity to the selective tyrosine kinase inhibitor PHA-665752

A census of human cancer genes

Characterizing the cancer genome in lung adenocarcinoma.

Oncogenic transformation by inhibitor-sensitive and -resistant EGFR mutants

Molecular determinants of the response of glioblastomas to EGFR kinase inhibitors.

Model-based analysis of oligonucleotide arrays: expression index computation and outlier detection

The consensus coding sequences of human breast and colorectal cancers

Exploration, normalization, and summaries of high density oligonucleotide array probe level data

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