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1.
Analysis of MUTYH alternative transcript expression, promoter function, and the effect of human genetic variants.
Hum Mutat
; 40(4): 472-482, 2019 04.
Article
in English
| MEDLINE | ID: mdl-30653782
2.
Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis.
Am J Hum Genet
; 99(2): 337-51, 2016 Aug 04.
Article
in English
| MEDLINE | ID: mdl-27476653
3.
Evaluation of MLH1 variants of unclear significance.
Genes Chromosomes Cancer
; 57(7): 350-358, 2018 Jul.
Article
in English
| MEDLINE | ID: mdl-29520894
4.
DNA mismatch repair activity of MutLα is regulated by CK2-dependent phosphorylation of MLH1 (S477).
Mol Carcinog
; 57(12): 1723-1734, 2018 12.
Article
in English
| MEDLINE | ID: mdl-30136313
5.
Phosphorylation-dependent signaling controls degradation of DNA mismatch repair protein PMS2.
Mol Carcinog
; 56(12): 2663-2668, 2017 Dec.
Article
in English
| MEDLINE | ID: mdl-28767177
6.
Loss of MLH1 sensitizes colon cancer cells to DNA-PKcs inhibitor KU60648.
Mol Carcinog
; 56(7): 1816-1824, 2017 07.
Article
in English
| MEDLINE | ID: mdl-28224663
7.
Functional testing strategy for coding genetic variants of unclear significance in MLH1 in Lynch syndrome diagnosis.
Carcinogenesis
; 36(2): 202-11, 2015 Feb.
Article
in English
| MEDLINE | ID: mdl-25477341
8.
Reduced migration of MLH1 deficient colon cancer cells depends on SPTAN1.
Mol Cancer
; 13: 11, 2014 Jan 24.
Article
in English
| MEDLINE | ID: mdl-24456667
9.
Refining the role of PMS2 in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variants.
J Med Genet
; 50(8): 552-63, 2013 Aug.
Article
in English
| MEDLINE | ID: mdl-23709753
10.
MUTYH gene expression and alternative splicing in controls and polyposis patients.
Hum Mutat
; 33(7): 1067-74, 2012 Jul.
Article
in English
| MEDLINE | ID: mdl-22473953
11.
Comprehensive functional assessment of MLH1 variants of unknown significance.
Hum Mutat
; 33(11): 1576-88, 2012 Nov.
Article
in English
| MEDLINE | ID: mdl-22736432
12.
Identification of Lynch syndrome mutations in the MLH1-PMS2 interface that disturb dimerization and mismatch repair.
Hum Mutat
; 31(8): 975-82, 2010 Aug.
Article
in English
| MEDLINE | ID: mdl-20533529
13.
Validation of an in Vitro Mismatch Repair Assay Used in the Functional Characterization of Mismatch Repair Variants.
J Mol Diagn
; 22(3): 376-385, 2020 03.
Article
in English
| MEDLINE | ID: mdl-31881334
14.
RNA processing in plant mitochondria is independent of transcription.
Plant Mol Biol
; 70(6): 663-8, 2009 Aug.
Article
in English
| MEDLINE | ID: mdl-19412686
15.
Plastid mRNAs are neither spliced nor edited in maize and cauliflower mitochondrial in organello systems.
RNA
; 13(12): 2061-5, 2007 Dec.
Article
in English
| MEDLINE | ID: mdl-17951330
16.
Promoter methylation of MLH1, PMS2, MSH2 and p16 is a phenomenon of advanced-stage HCCs.
PLoS One
; 9(1): e84453, 2014.
Article
in English
| MEDLINE | ID: mdl-24400091
17.
Expression defect size among unclassified MLH1 variants determines pathogenicity in Lynch syndrome diagnosis.
Clin Cancer Res
; 19(9): 2432-41, 2013 May 01.
Article
in English
| MEDLINE | ID: mdl-23403630
18.
C-terminal fluorescent labeling impairs functionality of DNA mismatch repair proteins.
PLoS One
; 7(2): e31863, 2012.
Article
in English
| MEDLINE | ID: mdl-22348133
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