Cancer Genet. Cytogenet
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Int. J. Oncol.
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Am. J. Pathol.
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Genes Chromosomes Cancer
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Am. J. Hum. Genet.
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Int.J.Oncol.
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Nat.Genet.
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Nat. Genet.
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Science
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J. Pathology
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Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation
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Med. Hypotheses.
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Science
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Methods Enzymol.
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Mamm. Genome.
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Genome Res.
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Am. J. Med. Genet. A.
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High-resolution mapping of molecular events associated with immortalization, transformation, and progression to breast cancer in the MCF10 model.
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Clin. Genet.
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Curr. Op. Chem. Biol.
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Mass Spec. Rev.
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Nature
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Specific expression of the annexin VIII gene in acute promyelocytic leukemia
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Y4 receptor knockout rescues fertility in ob/ob mice
| [0176]
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Identification of high risk breast-cancer patients by gene expression profiling
| [0178]
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Prognostic relevance of gene amplifications and coamplifications in breast cancer
| [0178]
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Profiling breast cancer by array CGH
| [0178]
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The genetics and genomics of cancer
| [0178]
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Association between RB-1 gene alterations and factors of favourable prognosis in human breast cancer, without effect on survival
| [0178]
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Analysis of different deleted regions in chromosome 11 and their interrelations in early- and late-onset breast tumors: association with cyclin D1 amplification and survival
| [0178]
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Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons
| [0178]
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A versatile statistical analysis algorithm to detect genome copy number variation
| [0178]
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Cancer chromosomes in crisis
| [0178]
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Good Old'' clinical markers have similar power in breast cancer prognosis as microarray gene expression profilers
| [0178]
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Near tetraploid prostate carcinoma. Methodologic and prognostic aspects
| [0178]
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Ploidy level determinations in high-grade and low-grade malignant variants of prostatic carcinoma
| [0178]
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A 1 Mb minimal amplicon at 8p11-12 in breast cancer identifies new candidate oncogenes
| [0178]
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Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
| [0178]
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A role for common fragile site induction in amplification of human oncogenes
| [0178]
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HER-2/neu and topoisomerase IIalpha in breast cancer
| [0178]
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Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization
| [0178]
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Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
| [0178]
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Detection of retinoblastoma gene copy number in metaphase chromosomes and interphase nuclei by fluorescence in situ hybridization
| [0178]
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ERBB2 amplification in breast cancer analyzed by fluorescence in situ hybridization
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Retrospective analysis of topoisomerase IIa amplifications and deletions as predictive markers in primary breast cancer patients randomly assigned to cyclophosphamide, methotrexate, and fluorouracil or cyclophosphamide, epirubicin, and fluorouracil: Danish Breast Cancer Cooperative Group
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Improved grading of breast adenocarcinomas based on genomic instability
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Whole genome analysis of genetic alterations in small DNA samples using hyperbranched strand displacement amplification and array-CGH
| [0178]
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Array comparative genomic hybridization analysis of genomic alterations in breast cancer subtypes
| [0178]
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Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation
| [0178]
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Total loss of MHC class I is an independent indicator of good prognosis in breast cancer
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The production of homozygous deficient tissues with mutant characteristics by means of the aberrant mitotic behavior of ring-shaped chromosomes
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The stability of broken ends of chromosomes in Zea Mays
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HER2 as a prognostic factor in breast cancer
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PROBER : oligonucleotide FISH probe design software
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Candidate genes in breast cancer revealed by microarray-based comparative genomic hybridization of archived tissue
| [0178]
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Circular binary segmentation for the analysis of array-based DNA copy number data
| [0178]
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Cyclin D1, EMS1 and 11q13 amplification in breast cancer
| [0178]
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A multigene assay to predict recurrence of tamoxifen-treated, node-negative breast cancer
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Molecular portraits of human breast tumours
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Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors
| [0178]
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Comparative genomic hybridization of formalin-fixed, paraffin-enbedded breast tumors reveals different patterns of chromosomal gains and losses in fibroadenomas and diploid and aneuploid carcinomas
| [0178]
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Tumor cytogenetics revisited: comparative genomic hybridization and spectral karyotyping
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Large-scale copy number polymorphism in the human genome
| [0178]
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A consistent pattern of RIN1 rearrangements in oral squamous cell carcinoma cell lines supports a breakage-fusion-bridge cycle model for 11q13 amplification
| [0178]
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Studies of the HER-2/neu proto-oncogene in human breast and ovarian cancer
| [0178]
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Gene expression patterns of carcinomas distinguish tumor subclasses with clinical implications
| [0178]
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Breast cancer classification and prognosis based on gene expression profiles from a population-based study
| [0178]
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Widespread and nonrandom distribution of DNA palindromes in cancer cells provides a structural platform for subsequent gene amplification
| [0178]
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Molecular cytogenetics of primary breast cancer by CGH
| [0178]
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Gene expression profiling predicts clinical outcome of breast cancer
| [0178]
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Amplification of the neu (c-erbB-2) oncogene in human mammmary tumors is relatively frequent and is often accompanied by amplification of the linked c-erbA oncogene
| [0178]
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Detection of isolated tumor cells in bone marrow is an independent prognostic factor in breast cancer
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