Analysis of changes in DNA sequence copy number by comparative genomic hybridization in archival paraffin-embedded tumor samples.
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Assignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13.Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25.Assignment of the locus for a new lethal neonatal metabolic syndrome to 2q33-37EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas.Chromosomal alterations in the clonal evolution to the metastatic stage of squamous cell carcinomas of the lungThe diagnosis and management of pre-invasive breast disease: genetic alterations in pre-invasive lesionsChromosomal aberrations in benign and malignant bilharzia-associated bladder lesions analyzed by comparative genomic hybridization.Oestrogen receptor alpha gene haplotype and postmenopausal breast cancer risk: a case control studyCYP17 gene polymorphism in relation to breast cancer risk: a case-control studyThe consequences of chromosomal aneuploidy on the transcriptome of cancer cellsComprehensive analysis of the ATM, CHEK2 and ERBB2 genes in relation to breast tumour characteristics and survival: a population-based case-control and follow-up study.Estrogen receptor alpha gene polymorphism and endometrial cancer risk--a case-control studyGenomic profiling by DNA amplification of laser capture microdissected tissues and array CGHAmplification of whole tumor genomes and gene-by-gene mapping of genomic aberrations from limited sources of fresh-frozen and paraffin-embedded DNA.Linkage disequilibrium mapping of CHEK2: common variation and breast cancer risk.The isolation of nucleic acids from fixed, paraffin-embedded tissues-which methods are useful when?FOXP3 transcription factor: a candidate marker for susceptibility and prognosis in triple negative breast cancerMulti-variant pathway association analysis reveals the importance of genetic determinants of estrogen metabolism in breast and endometrial cancer susceptibility.Comparative genomic hybridization and chromosomal instability in solid tumours.Comparative analysis of four methods to extract DNA from paraffin-embedded tissues: effect on downstream molecular applicationsAssignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individualsRAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability.Copy number changes of target genes in chromosome 3q25.3-qter of esophageal squamous cell carcinoma: TP63 is amplified in early carcinogenesis but down-regulated as disease progressedMolecular cytogenetic characterization of tenosynovial giant cell tumors.Array-CGH and breast cancer.High-resolution physical and genetic mapping of the critical region for Meckel syndrome and Mulibrey Nanism on chromosome 17q22-q23.Altered methylation at microRNA-associated CpG islands in hereditary and sporadic carcinomas: a methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA)-based approach.Identification of subgroup-specific miRNA patterns by epigenetic profiling of sporadic and Lynch syndrome-associated colorectal and endometrial carcinoma.Potential role of a navigator gene NAV3 in colorectal cancer.Patterns of chromosomal imbalances in parathyroid carcinomasGenome-wide appraisal of thyroid cancer progression.Endometrial and colorectal tumors from patients with hereditary nonpolyposis colon cancer display different patterns of microsatellite instabilityGenetic alterations in hormone-refractory recurrent prostate carcinomasTypical and atypical carcinoid tumors of the lung are characterized by 11q deletions as detected by comparative genomic hybridization.Interphase cytogenetics and its role in molecular diagnostics of solid tumors.High-level DNA amplifications are common genetic aberrations in B-cell neoplasms.Genetic changes in intraductal breast cancer detected by comparative genomic hybridization.Accumulation of genetic changes is associated with poor prognosis in grade II astrocytomas.DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies.Comparative genomic hybridisation in malignant deciduoid mesothelioma.
P2860
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P2860
Analysis of changes in DNA sequence copy number by comparative genomic hybridization in archival paraffin-embedded tumor samples.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Analysis of changes in DNA seq ...... raffin-embedded tumor samples.
@ast
Analysis of changes in DNA seq ...... raffin-embedded tumor samples.
@en
type
label
Analysis of changes in DNA seq ...... raffin-embedded tumor samples.
@ast
Analysis of changes in DNA seq ...... raffin-embedded tumor samples.
@en
prefLabel
Analysis of changes in DNA seq ...... raffin-embedded tumor samples.
@ast
Analysis of changes in DNA seq ...... raffin-embedded tumor samples.
@en
P2093
P2860
P1476
Analysis of changes in DNA seq ...... raffin-embedded tumor samples.
@en
P2093
P2860
P304
P407
P577
1994-12-01T00:00:00Z