(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

0 references

publication date

21 June 2004

1 reference

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

14 August 2017

1 reference

14 August 2017

101

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14 August 2017

26

1 reference

14 August 2017

9769-9773

1 reference

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

PubMed publication ID

15210940

1 reference