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Pms2 cre Apc fx conditional knockout mice
eagle-i ID
http://ohsu.eagle-i.net/i/0000012b-eab3-cd0b-db67-de4080000000
Resource Type
Properties
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Resource Description
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DNA mismatch repair (MMR) leads to an increased mutation frequency and a predisposition to neoplasia. Knockout mice deficient in the MMR proteins PMS2 crossed with mutation detection reporter (supF) transgenic mice have been used to facilitate a comparison of the changes in mutation frequency and spectra. PMS2 -deficient mice accumulate transition mutations as the predominant mutation.
Both male and female mice are available.
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Related Disease
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colon cancer
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Related Publication or Documentation
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Enhanced intestinal adenomatous polyp formation in Pms2-/-;Min mice.
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Related Publication or Documentation
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Different Phenotypic Consequences of Simultaneous Versus Stepwise Apc Loss
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Parental Strain Name
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C57BL/6
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Genetic Alteration(s)
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Pms2 knockout
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Genetic Alteration(s)
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supF insertion
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Phenotype Findings
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Severe cancer phenotype
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Location
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Michael Liskay Laboratory