Genetic predisposition to colorectal cancer (Q35930688)

11 August 2017

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title

Genetic predisposition to colorectal cancer (English)

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11 August 2017

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Albert de la Chapelle

series ordinal

1

object named as

Albert de la Chapelle

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language of work or name

English

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publication date

1 October 2004

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11 August 2017

published in

Nature Reviews Cancer

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11 August 2017

volume

4

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11 August 2017

issue

10

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11 August 2017

page(s)

769-780

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Colorectal cancer: molecules and populations

11 August 2017

cites work

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Small changes in expression affect predisposition to tumorigenesis

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Hereditary colorectal cancer

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Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer

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Clues to the pathogenesis of familial colorectal cancer

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A naturally occurring hPMS2 mutation can confer a dominant negative mutator phenotype

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Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer

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Recurrent germline mutation in MSH2 arises frequently de novo

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Reduced Frequency of Extracolonic Cancers in Hereditary Nonpolyposis Colorectal Cancer Families with Monoallelic hMLH1Expression

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A founder MLH1 mutation in families from the districts of Modena and Reggio-Emilia in northern Italy with hereditary non-polyposis colorectal cancer associated with protein elongation and instability.

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MSH2 c.1452-1455delAATG is a founder mutation and an important cause of hereditary nonpolyposis colorectal cancer in the southern Chinese population

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Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases.

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

31 March 2020

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

31 March 2020

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Inherited susceptibility to colorectal adenomas and carcinomas: Evidence for a new predisposition gene on 15q14-q22

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

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31 March 2020

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31 March 2020

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31 March 2020

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31 March 2020

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31 March 2020

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31 March 2020

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Structural alterations of transforming growth factor-beta receptor genes in human cervical carcinoma

31 March 2020

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The MLH1 D132H variant is associated with susceptibility to sporadic colorectal cancer

31 March 2020

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Polymorphisms and colorectal tumor risk

31 March 2020

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Genotype and phenotype in hereditary nonpolyposis colon cancer: a study of families with different vs. shared predisposing mutations

31 March 2020

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A dominant mutation that predisposes to multiple intestinal neoplasia in the mouse

31 March 2020

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Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse

31 March 2020

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Secretory phospholipase Pla2g2a confers resistance to intestinal tumorigenesis

31 March 2020

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Modifier genes in mice and humans

31 March 2020

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Loss of the PLA2G2A gene in a sporadic colorectal tumor of a patient with a PLA2G2A germline mutation and absence of PLA2G2A germline alterations in patients with FAP

31 March 2020

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31 March 2020

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31 March 2020

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31 March 2020

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31 March 2020

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Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutation.

31 March 2020

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Genetic linkage analysis in hereditary non-polyposis colon cancer syndrome.

31 March 2020

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The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population

31 March 2020

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Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene

31 March 2020

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Identification and characterization of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques

31 March 2020

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A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States

31 March 2020

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BLM heterozygosity and the risk of colorectal cancer

31 March 2020

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Association between hemochromatosis (HFE) gene mutation carrier status and the risk of colon cancer

31 March 2020

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Contribution of cyclin d1 (CCND1) and E-cadherin (CDH1) polymorphisms to familial and sporadic colorectal cancer

31 March 2020

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31 March 2020

Identifiers

DOI

10.1038/NRC1453

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Dimensions Publication ID

11 August 2017

1043058854

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