High resolution genomic analysis of sporadic breast cancer using array-based comparative genomic hybridization - Wikidata - awgldk - TriplyDB

High resolution genomic analysis of sporadic breast cancer using array-based comparative genomic hybridization

High resolution genomic analysis of sporadic breast cancer using array-based comparative genomic hybridization

http://www.wikidata.org/entity/Q25257525

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Genomic subtypes of breast cancer identified by array-comparative genomic hybridization display distinct molecular and clinical characteristics MTDH activation by 8q22 genomic gain promotes chemoresistance and metastasis of poor-prognosis breast cancer IL-32: A Novel Pluripotent Inflammatory Interleukin, towards Gastric Inflammation, Gastric Cancer, and Chronic Rhino Sinusitis The Potential Role of Hedgehog Signaling in the Luminal/Basal Phenotype of Breast Epithelia and in Breast Cancer Invasion and Metastasis Cooperative integration between HEDGEHOG-GLI signalling and other oncogenic pathways: implications for cancer therapy NUCKS1 is a novel RAD51AP1 paralog important for homologous recombination and genome stability Aberrant overexpression of the cell polarity module scribble in human cancer Clinical validation of an array CGH test for HER2 status in breast cancer reveals that polysomy 17 is a rare event Distinct lymphocyte antigens 6 (Ly6) family members Ly6D, Ly6E, Ly6K and Ly6H drive tumorigenesis and clinical outcome Integration of transcript expression, copy number and LOH analysis of infiltrating ductal carcinoma of the breast A systematic comparison of copy number alterations in four types of female cancer Amplified loci on chromosomes 8 and 17 predict early relapse in ER-positive breast cancers Shank-interacting protein-like 1 promotes tumorigenesis via PTEN inhibition in human tumor cells.Identifying in-trans process associated genes in breast cancer by integrated analysis of copy number and expression data Advances in network-based metabolic pathway analysis and gene expression data integration.STAC: A method for testing the significance of DNA copy number aberrations across multiple array-CGH experiments.Identification of cancer genes using a statistical framework for multiexperiment analysis of nondiscretized array CGH data.Whole-genome cartography of estrogen receptor alpha binding sites.Assessing the significance of conserved genomic aberrations using high resolution genomic microarrays.SIRAC: Supervised Identification of Regions of Aberration in aCGH datasets.Comparison of the Agilent, ROMA/NimbleGen and Illumina platforms for classification of copy number alterations in human breast tumors.Alterations in candidate genes PHF2, FANCC, PTCH1 and XPA at chromosomal 9q22.3 region: pathological significance in early- and late-onset breast carcinoma.Breast cancer cell lines carry cell line-specific genomic alterations that are distinct from aberrations in breast cancer tissues: comparison of the CGH profiles between cancer cell lines and primary cancer tissues An integrative multi-dimensional genetic and epigenetic strategy to identify aberrant genes and pathways in cancer.Proteomic changes resulting from gene copy number variations in cancer cells Genome profiling of ERBB2-amplified breast cancers.Expanding the genetic basis of copy number variation in familial breast cancer.Detecting cancer gene networks characterized by recurrent genomic alterations in a population.Hedgehog signaling in the normal and neoplastic mammary gland.Fine scale mapping of the breast cancer 16q12 locus.EphB6 receptor modulates micro RNA profile of breast carcinoma cells Quantitative high-resolution genomic analysis of single cancer cells.Copy number analysis identifies novel interactions between genomic loci in ovarian cancer Inositol polyphosphate 4-phosphatase II regulates PI3K/Akt signaling and is lost in human basal-like breast cancers A genomewide screen for suppressors of Alu-mediated rearrangements reveals a role for PIF1 Molecular homology and difference between spontaneous canine mammary cancer and human breast cancer.Evidence that inositol polyphosphate 4-phosphatase type II is a tumor suppressor that inhibits PI3K signaling The risk allele of SNP rs3803662 and the mRNA level of its closest genes TOX3 and LOC643714 predict adverse outcome for breast cancer patients Comparative analysis of methods for identifying recurrent copy number alterations in cancer.Genome wide analysis of chromosomal alterations in oral squamous cell carcinomas revealed over expression of MGAM and ADAM9.

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P2860

High resolution genomic analysis of sporadic breast cancer using array-based comparative genomic hybridization

http://www.wikidata.org/entity/Q25257525

description

2005 nî lūn-bûn

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2005 թվականին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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High resolution genomic analys ...... parative genomic hybridization

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High resolution genomic analys ...... parative genomic hybridization

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High resolution genomic analys ...... parative genomic hybridization

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type

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High resolution genomic analys ...... parative genomic hybridization

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High resolution genomic analys ...... parative genomic hybridization

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High resolution genomic analys ...... parative genomic hybridization

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prefLabel

High resolution genomic analys ...... parative genomic hybridization

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High resolution genomic analys ...... parative genomic hybridization

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High resolution genomic analys ...... parative genomic hybridization

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Breast Cancer Research

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High resolution genomic analys ...... parative genomic hybridization

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Barbara L Weber

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Joel Greshock

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Q C Yu

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Tal Z Zaks

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Tara L Naylor

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Virginia Clemmer

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Yan Wang

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P2860

The protein kinase complement of the human genome

Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization

1-Mb resolution array-based comparative genomic hybridization using a BAC clone set optimized for cancer gene analysis

A census of human cancer genes

Identification and confirmation of a module of coexpressed genes

EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy.

Gene expression profiling predicts clinical outcome of breast cancer

Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib

GenMAPP, a new tool for viewing and analyzing microarray data on biological pathways

Genome-wide analysis of DNA copy-number changes using cDNA microarrays

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R1186-98

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2445027

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10.1186/BCR1356

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6

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1410746

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