Mlh1 deficiency enhances several phenotypes of Apc(Min)/+ mice (Q28588324)

31 January 2017

title

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

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31 January 2017

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GOA release 2020-03-11

author name string

A. R. Shoemaker

1

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31 January 2017

K. M. Haigis

2

1 reference

31 January 2017

S. M. Baker

3

1 reference

31 January 2017

S. Dudley

4

1 reference

31 January 2017

R. M. Liskay

5

1 reference

31 January 2017

W. F. Dove

6

1 reference

31 January 2017

language of work or name

English

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publication date

25 May 2000

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31 January 2017

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31 January 2017

volume

19

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31 January 2017

issue

23

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31 January 2017

page(s)

2774–2779

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Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis

31 January 2017

cites work

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

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

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Secretory phospholipase Pla2g2a confers resistance to intestinal tumorigenesis

21 January 2018

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Mouse MutS-like protein Msh5 is required for proper chromosome synapsis in male and female meiosis

21 January 2018

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

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

21 January 2018

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Meiotic pachytene arrest in MLH1-deficient mice

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Mutation in the mismatch repair gene Msh6 causes cancer susceptibility

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

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The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations

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The tyrosine kinase c-Abl regulates p73 in apoptotic response to cisplatin-induced DNA damage

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Identification and characterization of the familial adenomatous polyposis coli gene

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APC mutations in colorectal tumors with mismatch repair deficiency

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Identification of FAP locus genes from chromosome 5q21

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21 January 2018

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

21 January 2018

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MSH2 deficient mice are viable and susceptible to lymphoid tumours

21 January 2018

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

21 January 2018

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Apc1638T: a mouse model delineating critical domains of the adenomatous polyposis coli protein involved in tumorigenesis and development

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Intestinal tumorigenesis in compound mutant mice of both Dpc4 (Smad4) and Apc genes

21 January 2018

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Msh2 status modulates both apoptosis and mutation frequency in the murine small intestine

21 January 2018

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Intestinal tumorigenesis is suppressed in mice lacking the metalloproteinase matrilysin

21 January 2018

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Different mutator phenotypes in Mlh1- versus Pms2-deficient mice

21 January 2018

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Somatic genetic events linked to the Apc locus in intestinal adenomas of the Min mouse

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

The adenomatous polyposis coli (APC) tumor suppressor

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inferred from DOI database lookup

7 January 2021

based on heuristic

Studies of neoplasia in the Min mouse

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1203574