HNPCC mutations in the human DNA mismatch repair gene hMLH1 influence assembly of hMutLalpha and hMLH1-hEXO1 complexes
about
Molecular interactions of human Exo1 with DNACharacterization of human exonuclease 1 in complex with mismatch repair proteins, subcellular localization and association with PCNAEfficiency of Base Excision Repair of Oxidative DNA Damage and Its Impact on the Risk of Colorectal Cancer in the Polish PopulationDirect visualization of asymmetric adenine-nucleotide-induced conformational changes in MutL alpha.Bi-directional routing of DNA mismatch repair protein human exonuclease 1 to replication foci and DNA double strand breaks.ASCIZ regulates lesion-specific Rad51 focus formation and apoptosis after methylating DNA damage.C-terminal fluorescent labeling impairs functionality of DNA mismatch repair proteins.MLH1 mutations differentially affect meiotic functions in Saccharomyces cerevisiaeDimerization of MLH1 and PMS2 limits nuclear localization of MutLalpha.Functional examination of MLH1, MSH2, and MSH6 intronic mutations identified in Danish colorectal cancer patients.Nuclear localization of human DNA mismatch repair protein exonuclease 1 (hEXO1)Human exonuclease 1 (EXO1) activity characterization and its function on flap structures.Exonuclease 1 (Exo1) is required for activating response to S(N)1 DNA methylating agents.Human mismatch repair protein hMutLα is required to repair short slipped-DNAs of trinucleotide repeats.Mismatch repair defects and Lynch syndrome: The role of the basic scientist in the battle against cancerAssociation between three exonuclease 1 polymorphisms and cancer risks: a meta-analysis.Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome familiesCharacterization of a highly conserved binding site of Mlh1 required for exonuclease I-dependent mismatch repair.Assessment of functional effects of unclassified genetic variants.Associations between single-nucleotide polymorphisms of human exonuclease 1 and the risk of hepatocellular carcinoma.Exonuclease 1 and its versatile roles in DNA repair.Determining the functional significance of mismatch repair gene missense variants using biochemical and cellular assays.Functional characterization of MLH1 missense variants identified in Lynch syndrome patients.The significance of Exonuclease 1 K589E polymorphism on hepatocellular carcinoma susceptibility in the Turkish population: a case-control study.Classification of mismatch repair gene missense variants with PON-MMR
P2860
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P2860
HNPCC mutations in the human DNA mismatch repair gene hMLH1 influence assembly of hMutLalpha and hMLH1-hEXO1 complexes
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
HNPCC mutations in the human D ...... lpha and hMLH1-hEXO1 complexes
@ast
HNPCC mutations in the human D ...... lpha and hMLH1-hEXO1 complexes
@en
HNPCC mutations in the human D ...... lpha and hMLH1-hEXO1 complexes
@en-gb
HNPCC mutations in the human D ...... lpha and hMLH1-hEXO1 complexes
@nl
type
label
HNPCC mutations in the human D ...... lpha and hMLH1-hEXO1 complexes
@ast
HNPCC mutations in the human D ...... lpha and hMLH1-hEXO1 complexes
@en
HNPCC mutations in the human D ...... lpha and hMLH1-hEXO1 complexes
@en-gb
HNPCC mutations in the human D ...... lpha and hMLH1-hEXO1 complexes
@nl
prefLabel
HNPCC mutations in the human D ...... lpha and hMLH1-hEXO1 complexes
@ast
HNPCC mutations in the human D ...... lpha and hMLH1-hEXO1 complexes
@en
HNPCC mutations in the human D ...... lpha and hMLH1-hEXO1 complexes
@en-gb
HNPCC mutations in the human D ...... lpha and hMLH1-hEXO1 complexes
@nl
P2093
P2860
P356
P1433
P1476
HNPCC mutations in the human D ...... lpha and hMLH1-hEXO1 complexes
@en
P2093
H C Bisgaard
L J Rasmussen
M Rasmussen
P2860
P2888
P304
P356
10.1038/SJ.ONC.1204467
P407
P577
2001-06-01T00:00:00Z
P5875
P6179
1048899037