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Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3484, doi. 10.1093/hmg/ddp297
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- Publication type:
- Article
Unexpected moves: a conformational change in MutSα enables high-affinity DNA mismatch binding.
- Published in:
- Nucleic Acids Research, 2023, v. 51, n. 3, p. 1173, doi. 10.1093/nar/gkad015
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- Publication type:
- Article
Truncation of the MSH2 C-terminal 60 amino acids disrupts effective DNA mismatch repair and is causative for Lynch syndrome.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 221, doi. 10.1007/s10689-016-9945-x
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- Publication type:
- Article
Fancf-deficient mice are prone to develop ovarian tumours.
- Published in:
- Journal of Pathology, 2012, v. 226, n. 1, p. 28, doi. 10.1002/path.2992
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- Publication type:
- Article