Loss of heterozygosity analysis: practically and conceptually flawed?
about
Epigenetic regulation of the tumor suppressor gene TCF21 on 6q23-q24 in lung and head and neck cancer.Studies of Tumor Suppressor Genes via Chromosome EngineeringThe roles of UVB and vitamin D in reducing risk of cancer incidence and mortality: A review of the epidemiology, clinical trials, and mechanisms.Pooled analysis of loss of heterozygosity in breast cancer: a genome scan provides comparative evidence for multiple tumor suppressors and identifies novel candidate regions.Tumor heterogeneity: causes and consequencesSingle nucleotide polymorphism array analysis of microsatellite-stable, diploid/near-diploid colorectal carcinomas without the CpG island methylator phenotype.Phenotypic characterization of disseminated cells with TSC2 loss of heterozygosity in patients with lymphangioleiomyomatosisOncoDB.HCC: an integrated oncogenomic database of hepatocellular carcinoma revealed aberrant cancer target genes and lociLoss of heterozygosity: what is it good for?Genomic losses at 5q13.2 and 8p23.1 in dysplastic hepatocytes are common events in hepatitis B virus-related hepatocellular carcinomaTumor heterogeneity: mechanisms and bases for a reliable application of molecular marker designSuccinate dehydrogenase (SDH) D subunit (SDHD) inactivation in a growth-hormone-producing pituitary tumor: a new association for SDH?Allelotyping for loss of heterozygosity on chromosome 18 in gastric cancer.Embryonic reversions and lineage infidelities in tumour cells: genome-based models and role of genetic instability.Characterisation of p53 status at the gene, chromosomal and protein levels in oesophageal adenocarcinoma.A comprehensive study of chromosome 16q in invasive ductal and lobular breast carcinoma using array CGH.Large-scale genomic analysis of ovarian carcinomasPre-tumour clones, periodic selection and clonal interference in the origin and progression of gastrointestinal cancer: potential for biomarker development.CDKN2A, CDKN2B, and MTAP gene dosage permits precise characterization of mono- and bi-allelic 9p21 deletions in childhood acute lymphoblastic leukemia.Methylation-specific multiplex ligation-dependent probe amplification and its impact on clinical findings in medulloblastoma.Rapid generation of detailed loss of heterozygosity profiles for routine diagnosis of gliomas.Pathology of hereditary breast cancer.
P2860
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P2860
Loss of heterozygosity analysis: practically and conceptually flawed?
description
2002 nî lūn-bûn
@nan
2002 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
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name
Loss of heterozygosity analysis: practically and conceptually flawed?
@ast
Loss of heterozygosity analysis: practically and conceptually flawed?
@en
Loss of heterozygosity analysis: practically and conceptually flawed?
@nl
type
label
Loss of heterozygosity analysis: practically and conceptually flawed?
@ast
Loss of heterozygosity analysis: practically and conceptually flawed?
@en
Loss of heterozygosity analysis: practically and conceptually flawed?
@nl
prefLabel
Loss of heterozygosity analysis: practically and conceptually flawed?
@ast
Loss of heterozygosity analysis: practically and conceptually flawed?
@en
Loss of heterozygosity analysis: practically and conceptually flawed?
@nl
P2093
P2860
P356
P1476
Loss of heterozygosity analysis: practically and conceptually flawed?
@en
P2093
Ian P M Tomlinson
Maryou B K Lambros
Rebecca R Roylance
P2860
P304
P356
10.1002/GCC.10085
P577
2002-08-01T00:00:00Z