(Q54540294)

31 May 2018

title

Somatic APC inactivation mechanisms in sporadic colorectal cancer cases in Hungary. (English)

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31 May 2018

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Eniko Kámory

1

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31 May 2018

Judit Olasz

series ordinal

2

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31 May 2018

Orsolya Csuka

series ordinal

3

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31 May 2018

publication date

28 March 2008

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31 May 2018

Pathology Oncology Research

published in

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31 May 2018

volume

14

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31 May 2018

issue

1

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31 May 2018

page(s)

51-56

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31 May 2018

https://scigraph.springernature.com/pub.10.1007/s12253-008-9019-y

exact match

0 references

cites work

Identification of an alternative 5' untranslated region of the adenomatous polyposis coli gene.

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https://api.crossref.org/works/10.1007%2FS12253-008-9019-Y

Germ-line mutations of the APC gene in 53 familial adenomatous polyposis patients

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Adenomatous polyposis coli (APC) differentially regulates beta-catenin phosphorylation and ubiquitination in colon cancer cells.

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Colorectal cancer and genetic alterations in the Wnt pathway

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Mutations of the APC Gene in Human Sporadic Colorectal Cancers

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How the I1307K adenomatous polyposis coli gene variant contributes in the assessment of risk of colorectal cancer, but not stomach cancer, in a Turkish population.

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Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC.

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Identification and characterization of the familial adenomatous polyposis coli gene

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Identification of APC gene mutations in Italian adenomatous polyposis coli patients by PCR-SSCP analysis.

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Phenotypes of invasion in sporadic colorectal carcinomas related to aberrations of the adenomatous polyposis coli (APC ) gene.

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Densely methylated MLH1 promoter correlates with decreased mRNA expression in sporadic colorectal cancers

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Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients

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Promoter methylation precedes chromosomal alterations in colorectal cancer development.

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Epigenetic patterns in the progression of esophageal adenocarcinoma

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The 1993-94 Généthon human genetic linkage map

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Genetic and epigenetic changes of components affecting the WNT pathway in colorectal carcinomas stratified by microsatellite instability

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The type of somatic mutation at APC in familial adenomatous polyposis is determined by the site of the germline mutation: a new facet to Knudson's 'two-hit' hypothesis

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Mutations of the APC (adenomatous polyposis coli) gene

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Methylation and colorectal cancer

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APC promoter hypermethylation contributes to the loss of APC expression in colorectal cancers with allelic loss on 5q.

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Demonstration of promoter activity and alternative splicing in the region 5' to exon 1 of the APC gene.

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Novel germline mutations in the APC gene of Cypriot patients with familial and sporadic adenomatous polyposis

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Loss of heterozygosity analysis: practically and conceptually flawed?

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The CpG island methylator phenotype and chromosomal instability are inversely correlated in sporadic colorectal cancer.

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Identical APC exon 15 mutations result in a variable phenotype in familial adenomatous polyposis.

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Prediction of deleterious human alleles

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Molecular analysis of the APC gene in 205 families: extended genotype-phenotype correlations in FAP and evidence for the role of APC amino acid changes in colorectal cancer predisposition

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Genetic analysis of familial colorectal cancer in Israeli Arabs

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SIFT: Predicting amino acid changes that affect protein function

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Adenomatous polyposis coli (APC) plays multiple roles in the intestinal and colorectal epithelia

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Mismatch repair deficiency and CpG island hypermethylation in sporadic colon adenocarcinomas.

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12 December 2020

Molecular analysis of the APC gene in 71 Israeli families: 17 novel mutations

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12 December 2020

10.1007/S12253-008-9019-Y

Identifiers

DOI

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31 May 2018

PubMed ID

18369740

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31 May 2018