Found: 13
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Analysis of MUTYH alternative transcript expression, promoter function, and the effect of human genetic variants.
- Published in:
- Human Mutation, 2019, v. 40, n. 4, p. 472, doi. 10.1002/humu.23709
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- Article
Promoter Methylation of MLH1, PMS2, MSH2 and p16 Is a Phenomenon of Advanced-Stage HCCs.
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- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0084453
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- Article
C-Terminal Fluorescent Labeling Impairs Functionality of DNA Mismatch Repair Proteins.
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- PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0031863
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- Article
DNA mismatch repair activity of MutLα is regulated by CK2-dependent phosphorylation of MLH1 (S477).
- Published in:
- Molecular Carcinogenesis, 2018, v. 57, n. 12, p. 1723, doi. 10.1002/mc.22892
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- Article
Phosphorylation-dependent signaling controls degradation of DNA mismatch repair protein PMS2.
- Published in:
- Molecular Carcinogenesis, 2017, v. 56, n. 12, p. 2663, doi. 10.1002/mc.22709
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- Article
Loss of MLH1 sensitizes colon cancer cells to DNA-PKcs inhibitor KU60648.
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- Molecular Carcinogenesis, 2017, v. 56, n. 7, p. 1816, doi. 10.1002/mc.22640
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- Article
Comprehensive Functional Assessment of MLH1 Variants of Unknown Significance.
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- Human Mutation, 2013, v. 34, n. 1, p. 274, doi. 10.1002/humu.22246
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- Article
Comprehensive functional assessment of MLH1 variants of unknown significance.
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- Human Mutation, 2012, v. 33, n. 11, p. 1576, doi. 10.1002/humu.22142
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- Article
MUTYH gene expression and alternative splicing in controls and polyposis patients.
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- Human Mutation, 2012, v. 33, n. 7, p. 1067, doi. 10.1002/humu.22059
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- Article
Identification of Lynch syndrome mutations in the MLH1-PMS2 interface that disturb dimerization and mismatch repair.
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- Human Mutation, 2010, v. 31, n. 8, p. 975, doi. 10.1002/humu.21301
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- Article
Reduced migration of MLH1 deficient colon cancer cells depends on SPTAN1.
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- Molecular Cancer, 2014, v. 13, n. 1, p. 1, doi. 10.1186/1476-4598-13-11
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- Article
Evaluation of <italic>MLH1</italic> variants of unclear significance.
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- Genes, Chromosomes & Cancer, 2018, v. 57, n. 7, p. 350, doi. 10.1002/gcc.22536
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- Article
Functional testing strategy for coding genetic variants of unclear significance in MLH1 in Lynch syndrome diagnosis.
- Published in:
- Carcinogenesis, 2015, v. 36, n. 2, p. 202, doi. 10.1093/carcin/bgu239
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- Article