Molecular basis and diagnostics of hereditary colorectal cancers (Q35915251)

11 August 2017

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title

Molecular basis and diagnostics of hereditary colorectal cancers (English)

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11 August 2017

Wael M Abdel-Rahman

1

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Päivi Peltomäki

object named as

Päivi Peltomäki

series ordinal

2

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language of work or name

English

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publication date

1 January 2004

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11 August 2017

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11 August 2017

36

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11 August 2017

5

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11 August 2017

379-388

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11 August 2017

Colon cancer screening

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Family history of colorectal cancer as a marker of potential malignancy within a screening program.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Family history and colorectal cancer: predictors of risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Mutation of a mutL homolog in hereditary colon cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Mutations of GTBP in genetically unstable cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

A role for MLH3 in hereditary nonpolyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

The molecular basis of Turcot's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Identification of FAP locus genes from chromosome 5q21

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Germ-line and somatic mutations of the APC gene in patients with Turcot syndrome and analysis of APC mutations in brain tumors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Mutations in the SMAD4/DPC4 gene in juvenile polyposis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Germline mutations of the gene encoding bone morphogenetic protein receptor 1A in juvenile polyposis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Role of DNA mismatch repair defects in the pathogenesis of human cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Variable mutation frequencies in coding repeats of TCF-4 and other target genes in colon, gastric and endometrial carcinoma showing microsatellite instability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Caught up in a Wnt storm: Wnt signaling in cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Biology of the adenomatous polyposis coli tumor suppressor

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Molecular diagnosis of familial adenomatous polyposis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Genetic and clinical characterisation of familial adenomatous polyposis: a population based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Chromosomal instability and p53 inactivation are required for genesis of glioblastoma but not for colorectal cancer in patients with germline mismatch repair gene mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Gastric fundic gland polyps

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

A juvenile polyposis tumor suppressor locus at 10q22 is deleted from nonepithelial cells in the lamina propria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Very high risk of cancer in familial Peutz-Jeghers syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Will the real Cowden syndrome please stand up: revised diagnostic criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

PTEN hamartoma tumour syndrome: variability of an entity

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2-31.2

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Contribution of the CHEK2 1100delC variant to risk of multiple colorectal adenoma and carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

The I1307K polymorphism of the APC gene in colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

ONCOGENESIS: Landscaping the Cancer Terrain

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

Frequency of Microsatellite Instability in Unselected Sebaceous Gland Neoplasias and Hyperplasias

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890410018222

10.1080/07853890410018222

21 January 2018

Identifiers

DOI

1 reference

11 August 2017

1 reference

PubMed ID

15478312