High-resolution chromosome 3p allelotyping of breast carcinomas and precursor lesions demonstrates frequent loss of heterozygosity and a discontinuous pattern of allele loss
about
The RASSF1A tumor suppressor blocks cell cycle progression and inhibits cyclin D1 accumulation.Molecular cloning and characterization of CIDE-3, a novel member of the cell-death-inducing DNA-fragmentation-factor (DFF45)-like effector familyIncreased copy number at 3p14 in breast cancerEvidence of epigenetic regulation of the tumor suppressor gene cluster flanking RASSF1 in breast cancer cell linesExpression of several genes in the human chromosome 3p21.3 homozygous deletion region by an adenovirus vector results in tumor suppressor activities in vitro and in vivoGenetic alteration and gene expression modulation during cancer progressionGenomic Changes in Normal Breast Tissue in Women at Normal Risk or at High Risk for Breast CancerMicroRNA Regulation of Brain Tumour Initiating Cells in Central Nervous System TumoursActivation of the DNA damage checkpoint and genomic instability in human precancerous lesionsPooled analysis of loss of heterozygosity in breast cancer: a genome scan provides comparative evidence for multiple tumor suppressors and identifies novel candidate regions.High-resolution 19p13.2-13.3 allelotyping of breast carcinomas demonstrates frequent loss of heterozygosity.Endometrial glandular dysplasia: a putative precursor lesion of uterine papillary serous carcinoma. Part II: molecular features.RASSF1A promoter methylation is frequently detected in both pre-malignant and non-malignant microdissected prostatic epithelial tissues.The ubiquitin specific protease 4 (USP4) is a new player in the Wnt signalling pathway.Identification of 5 novel genes methylated in breast and other epithelial cancers.Cripto haploinsufficiency affects in vivo colon tumor developmentDown regulation of 3p genes, LTF, SLC38A3 and DRR1, upon growth of human chromosome 3-mouse fibrosarcoma hybrids in severe combined immunodeficiency mice.Regulation of the human telomerase reverse transcriptase gene.Real-time quantitative PCR analysis of pediatric ependymomas identifies novel candidate genes including TPR at 1q25 and CHIBBY at 22q12-q13.Negative Regulation of Receptor Tyrosine Kinase (RTK) Signaling: A Developing FieldCoincidence of synteny breakpoints with malignancy-related deletions on human chromosome 3.Search for unknown tumor-antagonizing genes.Loss of heterozygosity of the BRCA1 and FHIT genes in patients with sporadic breast cancer from Southern Brazil.Microsatellite analysis in multistage carcinogenesis of esophageal squamous cell carcinoma from Chongqing in Southern China.Identification of a core member of the SWI/SNF complex, BAF155/SMARCC1, as a human tumor suppressor gene.Fragile histidine triad gene abnormalities in the pathogenesis of gallbladder carcinoma.Tumor suppressor FUS1 signaling pathway.Loss of heterozygosity analysis of microsatellites on multiple chromosome regions in dysplasia and squamous cell carcinoma of the esophagusIdentification of novel gene expression targets for the Ras association domain family 1 (RASSF1A) tumor suppressor gene in non-small cell lung cancer and neuroblastoma.3p21.3 tumor suppressor cluster: prospects for translational applications.Mouse chromosome engineering for modeling human disease.ErbB receptor negative regulatory mechanisms: implications in cancer.The expression of FHIT, PCNA and EGFR in benign and malignant breast lesionsThe clinical significance of SWI/SNF complex in pancreatic cancer.High resolution chromosome 3p, 8p, 9q and 22q allelotyping analysis in the pathogenesis of gallbladder carcinoma.The role of ErbB3 and its binding partners in breast cancer progression and resistance to hormone and tyrosine kinase directed therapies.An update on apocrine lesions of the breast.Allelic losses on chromosome 3p are accumulated in relation to morphological changes of lung adenocarcinoma.Hijacking the chromatin remodeling machinery: impact of SWI/SNF perturbations in cancer.A preliminary study of the relationship between breast cancer metastasis and loss of heterozygosity by using exome sequencing.
P2860
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P2860
High-resolution chromosome 3p allelotyping of breast carcinomas and precursor lesions demonstrates frequent loss of heterozygosity and a discontinuous pattern of allele loss
description
2001 nî lūn-bûn
@nan
2001 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
High-resolution chromosome 3p ...... tinuous pattern of allele loss
@ast
High-resolution chromosome 3p ...... tinuous pattern of allele loss
@en
High-resolution chromosome 3p ...... tinuous pattern of allele loss
@nl
type
label
High-resolution chromosome 3p ...... tinuous pattern of allele loss
@ast
High-resolution chromosome 3p ...... tinuous pattern of allele loss
@en
High-resolution chromosome 3p ...... tinuous pattern of allele loss
@nl
prefLabel
High-resolution chromosome 3p ...... tinuous pattern of allele loss
@ast
High-resolution chromosome 3p ...... tinuous pattern of allele loss
@en
High-resolution chromosome 3p ...... tinuous pattern of allele loss
@nl
P2093
P2860
P3181
P1476
High-resolution chromosome 3p ...... tinuous pattern of allele loss
@en
P2093
A F Gazdar
A K Virmani
C Washington
I I Wistuba
S Milchgrub
P2860
P304
P3181
P356
10.1016/S0002-9440(10)61679-3
P407
P577
2001-07-01T00:00:00Z