High resolution genomic analysis of sporadic breast cancer using array-based comparative genomic hybridization
about
Genomic subtypes of breast cancer identified by array-comparative genomic hybridization display distinct molecular and clinical characteristicsMTDH activation by 8q22 genomic gain promotes chemoresistance and metastasis of poor-prognosis breast cancerIL-32: A Novel Pluripotent Inflammatory Interleukin, towards Gastric Inflammation, Gastric Cancer, and Chronic Rhino SinusitisThe Potential Role of Hedgehog Signaling in the Luminal/Basal Phenotype of Breast Epithelia and in Breast Cancer Invasion and MetastasisCooperative integration between HEDGEHOG-GLI signalling and other oncogenic pathways: implications for cancer therapyNUCKS1 is a novel RAD51AP1 paralog important for homologous recombination and genome stabilityAberrant overexpression of the cell polarity module scribble in human cancerClinical validation of an array CGH test for HER2 status in breast cancer reveals that polysomy 17 is a rare eventDistinct lymphocyte antigens 6 (Ly6) family members Ly6D, Ly6E, Ly6K and Ly6H drive tumorigenesis and clinical outcomeIntegration of transcript expression, copy number and LOH analysis of infiltrating ductal carcinoma of the breastA systematic comparison of copy number alterations in four types of female cancerAmplified loci on chromosomes 8 and 17 predict early relapse in ER-positive breast cancersShank-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 dataAdvances 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 tissuesAn 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 cellsGenome 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 cellsQuantitative high-resolution genomic analysis of single cancer cells.Copy number analysis identifies novel interactions between genomic loci in ovarian cancerInositol polyphosphate 4-phosphatase II regulates PI3K/Akt signaling and is lost in human basal-like breast cancersA genomewide screen for suppressors of Alu-mediated rearrangements reveals a role for PIF1Molecular 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 signalingThe risk allele of SNP rs3803662 and the mRNA level of its closest genes TOX3 and LOC643714 predict adverse outcome for breast cancer patientsComparative 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.
P2860
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P2860
High resolution genomic analysis of sporadic breast cancer using array-based comparative genomic hybridization
description
2005 nî lūn-bûn
@nan
2005 թուականին հրատարակուած գիտական յօդուած
@hyw
2005 թվականին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
High resolution genomic analys ...... parative genomic hybridization
@ast
High resolution genomic analys ...... parative genomic hybridization
@en
High resolution genomic analys ...... parative genomic hybridization
@nl
type
label
High resolution genomic analys ...... parative genomic hybridization
@ast
High resolution genomic analys ...... parative genomic hybridization
@en
High resolution genomic analys ...... parative genomic hybridization
@nl
prefLabel
High resolution genomic analys ...... parative genomic hybridization
@ast
High resolution genomic analys ...... parative genomic hybridization
@en
High resolution genomic analys ...... parative genomic hybridization
@nl
P2093
P2860
P3181
P356
P1476
High resolution genomic analys ...... parative genomic hybridization
@en
P2093
Barbara L Weber
Joel Greshock
Tal Z Zaks
Tara L Naylor
Theresa Colligon
Virginia Clemmer
P2860
P2888
P304
P3181
P356
10.1186/BCR1356
P407
P577
2005-01-01T00:00:00Z
P5875
P6179
1045823176