(Q44463232)

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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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scholarly article

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Europe PubMed Central

3 December 2017

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 (English)

1 reference

Europe PubMed Central

3 December 2017

familial adenomatous polyposis

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7

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object named as

I Tomlinson

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author name string

H Lamlum

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M Ilyas

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A Rowan

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S Clark

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V Johnson

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J Bell

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J Efstathiou

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K Pack

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S Payne

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R Roylance

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P Gorman

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D Sheer

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K Neale

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R Phillips

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I Talbot

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language of work or name

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publication date

1 September 1999

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3 December 2017

Nature Medicine

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5

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1071-1075

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3 December 2017

https://scigraph.springernature.com/pub.10.1038/12511

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Familial polyposis: recent advances

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https://api.crossref.org/works/10.1038%2F12511

7 January 2021

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Alleles of the APC gene: an attenuated form of familial polyposis.

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https://api.crossref.org/works/10.1038%2F12511

7 January 2021

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Attenuated familial adenomatous polyposis due to a mutation in the 3' part of the APC gene. A clue for understanding the function of the APC protein

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https://api.crossref.org/works/10.1038%2F12511

7 January 2021

based on heuristic

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Two cases of 5q deletions in patients with familial adenomatous polyposis: possible link with Caroli's disease

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https://api.crossref.org/works/10.1038%2F12511

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1038%2F12511

7 January 2021

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The APC variants I1307K and E1317Q are associated with colorectal tumors, but not always with a family history.

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https://api.crossref.org/works/10.1038%2F12511

7 January 2021

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Somatic mutations of the APC gene in colorectal tumors: mutation cluster region in the APC gene

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https://api.crossref.org/works/10.1038%2F12511

7 January 2021

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Alleles of APC modulate the frequency and classes of mutations that lead to colon polyps

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https://api.crossref.org/works/10.1038%2F12511

7 January 2021

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Selection, the mutation rate and cancer: Ensuring that the tail does not wag the dog

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https://api.crossref.org/works/10.1038%2F12511

7 January 2021

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Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis

1 reference

https://api.crossref.org/works/10.1038%2F12511

7 January 2021

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Dysregulation of the E-cadherin/catenin complex by irreversible mutations in human carcinomas.

1 reference

https://api.crossref.org/works/10.1038%2F12511

7 January 2021

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Phenotypic expression in familial adenomatous polyposis: partial prediction by mutation analysis

1 reference

https://api.crossref.org/works/10.1038%2F12511

7 January 2021

based on heuristic

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Rapid detection of translation-terminating mutations at the adenomatous polyposis coli (APC) gene by direct protein truncation test.

1 reference

https://api.crossref.org/works/10.1038%2F12511

7 January 2021

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Germline mutations of the APC gene in Korean familial adenomatous polyposis patients

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https://api.crossref.org/works/10.1038%2F12511

7 January 2021

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APC mutations occur early during colorectal tumorigenesis

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https://api.crossref.org/works/10.1038%2F12511

7 January 2021

based on heuristic

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Polyclonal origin of colonic adenomas in an XO/XY patient with FAP.

1 reference

https://api.crossref.org/works/10.1038%2F12511

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F12511

7 January 2021

based on heuristic

inferred from DOI database lookup

Detailed chromosomal and molecular genetic analysis of single cells by whole genome amplification and comparative genomic hybridisation

1 reference

https://api.crossref.org/works/10.1038%2F12511

7 January 2021

based on heuristic

inferred from DOI database lookup

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Europe PubMed Central

3 December 2017

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1 reference

Europe PubMed Central

3 December 2017

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