Tumor regionality in the mouse intestine reflects the mechanism of loss of Apc function (Q36448895)

14 August 2017

Tumor regionality in the mouse intestine reflects the mechanism of loss of Apc function (English)

1 reference

14 August 2017

1

Kevin M Haigis

1 reference

14 August 2017

Peter D Hoff

2

1 reference

14 August 2017

Alanna White

3

1 reference

14 August 2017

Alex R Shoemaker

4

1 reference

14 August 2017

Richard B Halberg

5

1 reference

14 August 2017

William F Dove

6

1 reference

14 August 2017

language of work or name

English

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publication date

21 June 2004

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Proceedings of the National Academy of Sciences of the United States of America

14 August 2017

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14 August 2017

101

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14 August 2017

9769-9773

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14 August 2017

26

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Intestinal adenomas can develop with a stable karyotype and stable microsatellites

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

Mlh1 deficiency enhances several phenotypes of Apc(Min)/+ mice

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

Hereditary nonpolyposis colorectal cancer

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

Mechanisms of APC-driven tumorigenesis: lessons from mouse models

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

Targeting genes for self-excision in the germ line

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

Tumorigenesis in Mlh1 and Mlh1/Apc1638N mutant mice

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

A resistant genetic background leading to incomplete penetrance of intestinal neoplasia and reduced loss of heterozygosity in ApcMin/+ mice

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

Tumour susceptibility and spontaneous mutation in mice deficient in Mlh1, Pms1 and Pms2 DNA mismatch repair

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

Mom1 is a semi-dominant modifier of intestinal adenoma size and multiplicity in Min/+ mice

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

A targeted chain-termination mutation in the mouse Apc gene results in multiple intestinal tumors

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

Multiple intestinal neoplasia caused by a mutation in the murine homolog of the APC gene

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

Studies of neoplasia in the Min mouse

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

Loss of Apc and the entire chromosome 18 but absence of mutations at the Ras and Tp53 genes in intestinal tumors from Apc1638N, a mouse model for Apc-driven carcinogenesis.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

Manifestations of hereditary colorectal cancer.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470749

A Robertsonian translocation suppresses a somatic recombination pathway to loss of heterozygosity.

28 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0403338101

Clonal analysis of mouse intestinal epithelial progenitors.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0403338101

Tumor-associated Apc mutations in Mlh1-/- Apc1638N mice reveal a mutational signature of Mlh1 deficiency

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15210940

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Loss of Apc+ in intestinal adenomas from Min mice

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15210940

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Engineering chromosomes in mice through targeted meiotic recombination (TAMERE)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15210940

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0403338101

1 reference

14 August 2017

0 references

1 reference

14 August 2017

1 reference