Expression analysis of candidate breast tumour suppressor genes on chromosome 16q

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Expression analysis of candidate breast tumour suppressor genes on chromosome 16q is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1012872815
P356DOI10.1186/BCR1337
P932PMC publication ID1410740
P698PubMed publication ID16280054
P5875ResearchGate publication ID7488296

P50authorHans BaeldeQ58870473
Tom Van WezelQ42794317
Anne-Marie Cleton-JansenQ45924326
P2093author name stringAnne-Marie Cleton-Jansen
Karoly Szuhai
Eddy H van Roon
Cees J Cornelisse
Marcel Lombaerts
Katja Philippo
P2860cites workInitial sequencing and analysis of the human genomeQ21045365
Characterization and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancerQ22004026
The Sequence of the Human GenomeQ22065842
Defining regions of loss of heterozygosity of 16q in breast cancer cell linesQ57252279
Genetic predisposition to cancerQ70331187
At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancerQ71621780
Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regionsQ73548870
Different mechanisms of chromosome 16 loss of heterozygosity in well- versus poorly differentiated ductal breast cancerQ80403559
Rap1 affects the length and heterogeneity of human telomeresQ24298023
Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genesQ24534395
E-cadherin is a tumour/invasion suppressor gene mutated in human lobular breast cancersQ24597264
BRAF and FBXW7 (CDC4, FBW7, AGO, SEL10) mutations in distinct subsets of pancreatic cancer: potential therapeutic targetsQ24685106
Primer3 on the WWW for general users and for biologist programmersQ27861030
TRF2 Protects Human Telomeres from End-to-End FusionsQ28111898
Human F-box protein hCdc4 targets cyclin E for proteolysis and is mutated in a breast cancer cell lineQ28188152
The Fanconi anaemia/BRCA pathwayQ28201371
Down-regulation of TRF1, TRF2 and TIN2 genes is important to maintain telomeric DNA for gastric cancersQ28203334
Tumor-associated zinc finger mutations in the CTCF transcription factor selectively alter tts DNA-binding specificityQ28215031
An opposing view on WWOX protein function as a tumor suppressorQ28236046
TIN2 binds TRF1 and TRF2 simultaneously and stabilizes the TRF2 complex on telomeresQ28277505
Biallelic inactivation of BRCA2 in Fanconi anemiaQ29616130
The PISSLRE gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancerQ33852958
Degrees and kinds of selection in spontaneous neoplastic transformation: an operational analysisQ33879054
Specific aneusomies in Chinese hamster cells at different stages of neoplastic transformation, initiated by nitrosomethylureaQ34067466
CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3.Q34144906
Sequencing, transcript identification, and quantitative gene expression profiling in the breast cancer loss of heterozygosity region 16q24.3 reveal three potential tumor-suppressor genesQ34147823
Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1.Q35436601
Exclusion of BBC1 and CMAR as candidate breast tumour-suppressor genesQ36431602
Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3.Q36617573
Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: evidence for solvent-induced bends in DNA heteroduplexesQ36647235
Allelotype of 28 human breast cancer cell lines and xenograftsQ36673552
Mutant E-cadherin breast cancer cells do not display constitutive Wnt signaling.Q40825662
Decreased gene expression for telomeric-repeat binding factors and TIN2 in malignant hematopoietic cells.Q45888429
Fbxw7/Cdc4 is a p53-dependent, haploinsufficient tumour suppressor geneQ46284220
Ever since KnudsonQ53395377
P433issue6
P407language of work or nameEnglishQ1860
P304page(s)R998-1004
P577publication date2005-10-18
P1433published inBreast Cancer ResearchQ2208481
P1476titleExpression analysis of candidate breast tumour suppressor genes on chromosome 16q
P478volume7

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cites work (P2860)
Q33328665ATBF1 and NQO1 as candidate targets for allelic loss at chromosome arm 16q in breast cancer: absence of somatic ATBF1 mutations and no role for the C609T NQO1 polymorphism
Q41056167BRAF mutation-specific promoter methylation of FOX genes in colorectal cancer
Q33240170Breast tumor copy number aberration phenotypes and genomic instability
Q49194380CINdex: A Bioconductor Package for Analysis of Chromosome Instability in DNA Copy Number Data
Q36414632Chromosome 16 tumor-suppressor genes in breast cancer
Q37407277Decreased expression of the CHD5 gene and its clinicopathological significance in breast cancer: Correlation with aberrant DNA methylation
Q34497064E-cadherin transcriptional downregulation by promoter methylation but not mutation is related to epithelial-to-mesenchymal transition in breast cancer cell lines.
Q35690493Expression of the epigenetic factor BORIS (CTCFL) in the human genome
Q39991571Frequent mutations in the 3'-untranslated region of IFNGR1 lack functional impairment in microsatellite-unstable colorectal tumours
Q43791752Genetic alterations of the WWOX gene in breast cancer.
Q35832016Genetic characterization of breast cancer and implications for clinical management
Q28260136Infrequent mutation of ATBF1 in human breast cancer
Q53417262Molecular changes in primary breast tumors and the Nottingham Histologic Score
Q36172476Non-operative breast pathology: lobular neoplasia
Q60529794Role of columnar cell lesions in breast carcinogenesis: analysis of chromosome 16 copy number changes by multiplex ligation-dependent probe amplification
Q36953585The JNK inhibitor SP600129 enhances apoptosis of HCC cells induced by the tumor suppressor WWOX.
Q37288532The homeobox gene MEIS1 is methylated in BRAF (p.V600E) mutated colon tumors
Q34088277The promoter methylation status and mRNA expression levels of CTCF and SIRT6 in sporadic breast cancer

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