(Q47604676)

4 February 2018

title

Unusual tumors associated with the hereditary nonpolyposis colorectal cancer syndrome (English)

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4 February 2018

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3

Karen H Lu

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4 February 2018

author name string

Russell R Broaddus

1

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4 February 2018

Patrick M Lynch

2

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4 February 2018

Raja Luthra

4

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4 February 2018

Sara J Michelson

5

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4 February 2018

publication date

1 August 2004

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4 February 2018

published in

Modern Pathology

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4 February 2018

volume

17

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4 February 2018

issue

8

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4 February 2018

page(s)

981-989

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4 February 2018

https://scigraph.springernature.com/pub.10.1038/modpathol.3800150

exact match

0 references

cites work

Life-time risk of different cancers in hereditary non-polyposis colorectal cancer (HNPCC) syndrome.

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Cancer risk associated with germline DNA mismatch repair gene mutations

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Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindreds

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https://api.crossref.org/works/10.1038%2FMODPATHOL.3800150

Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma

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https://api.crossref.org/works/10.1038%2FMODPATHOL.3800150

Endometrial and colorectal tumors from patients with hereditary nonpolyposis colon cancer display different patterns of microsatellite instability

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https://api.crossref.org/works/10.1038%2FMODPATHOL.3800150

Fourteen and counting: unraveling trinucleotide repeat diseases

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https://api.crossref.org/works/10.1038%2FMODPATHOL.3800150

Somatic instability of CTG repeat in myotonic dystrophy

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https://api.crossref.org/works/10.1038%2FMODPATHOL.3800150

Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes.

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.3800150

Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.3800150

Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.3800150

Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

21 January 2018

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Familial endometrial cancer in female carriers of MSH6 germline mutations

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Adrenocortical adenocarcinoma in an MSH2 carrier: Coincidence or causal relation?

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Mouse tissue culture models of unstable triplet repeats: in vitro selection for larger alleles, mutational expansion bias and tissue specificity, but no association with cell division rates

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Tumor spectrum in cancer family syndrome (hereditary nonpolyposis colorectal cancer)

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Extracolonic cancer in hereditary nonpolyposis colorectal cancer

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https://api.crossref.org/works/10.1038%2FMODPATHOL.3800150

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Molecular genetic evidence of the occurrence of breast cancer as an integral tumor in patients with the hereditary nonpolyposis colorectal carcinoma syndrome

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https://api.crossref.org/works/10.1038%2FMODPATHOL.3800150

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Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer

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Prostate cancer is part of the hereditary non-polyposis colorectal cancer (HNPCC) tumor spectrum

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https://api.crossref.org/works/10.1038%2FMODPATHOL.3800150

7 January 2021

Inclusion of malignant fibrous histiocytoma in the tumour spectrum associated with hereditary non-polyposis colorectal cancer

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https://api.crossref.org/works/10.1038%2FMODPATHOL.3800150

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Male breast cancer in the hereditary nonpolyposis colorectal cancer syndrome

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Adrenal cortical carcinoma. A study of 77 cases.

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Mutations associated with microsatellite unstable colorectal carcinomas exhibit widespread intratumoral heterogeneity

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https://api.crossref.org/works/10.1038%2FMODPATHOL.3800150

7 January 2021

Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy

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7 January 2021

10.1038/MODPATHOL.3800150

Identifiers

DOI

1 reference

4 February 2018

PubMed ID

15143336

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4 February 2018