about
Evidence for involvement of HMGB1 protein in human DNA mismatch repairThe histone mark H3K36me3 regulates human DNA mismatch repair through its interaction with MutSαNew insights and challenges in mismatch repair: getting over the chromatin hurdleMechanisms and functions of DNA mismatch repairArsenic Inhibits DNA Mismatch Repair by Promoting EGFR Expression and PCNA Phosphorylation.Partial reconstitution of human DNA mismatch repair in vitro: characterization of the role of human replication protein AATP-dependent interaction of human mismatch repair proteins and dual role of PCNA in mismatch repairIncision-dependent and error-free repair of (CAG)(n)/(CTG)(n) hairpins in human cell extractsReconstitution of 5'-directed human mismatch repair in a purified system.Regulation of replication protein A functions in DNA mismatch repair by phosphorylation.Decoding the histone code: Role of H3K36me3 in mismatch repair and implications for cancer susceptibility and therapy.DNA instability in replicating Huntington's disease lymphoblastsMolecular cooperation between the Werner syndrome protein and replication protein A in relation to replication fork blockage.Effect of carcinogenic acrolein on DNA repair and mutagenic susceptibility.hMRE11 deficiency leads to microsatellite instability and defective DNA mismatch repair.HDAC6 deacetylates and ubiquitinates MSH2 to maintain proper levels of MutSα.Prereplicative repair of oxidized bases in the human genome is mediated by NEIL1 DNA glycosylase together with replication proteins.Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologsMismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approachesThe Role of XPG in Processing (CAG)n/(CTG)n DNA HairpinsPhosphorylation of PCNA by EGFR inhibits mismatch repair and promotes misincorporation during DNA synthesis.Identification and characterization of OGG1 mutations in patients with Alzheimer's disease.A special issue on DNA damage response and genome stability.Okazaki fragment maturation involves α-segment error editing by the mammalian FEN1/MutSα functional complex.Truncating mutation in the autophagy gene UVRAG confers oncogenic properties and chemosensitivity in colorectal cancersIn vitro repair of DNA hairpins containing various numbers of CAG/CTG trinucleotide repeats.The C-terminal Domain (CTD) of Human DNA Glycosylase NEIL1 Is Required for Forming BERosome Repair Complex with DNA Replication Proteins at the Replicating Genome: DOMINANT NEGATIVE FUNCTION OF THE CTD.Modulation of microRNA processing by mismatch repair protein MutLα.Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers.The Werner syndrome protein promotes CAG/CTG repeat stability by resolving large (CAG)(n)/(CTG)(n) hairpinsThe hMSH2(M688R) Lynch syndrome mutation may function as a dominant negative.Trinucleotide repeat expansions catalyzed by human cell-free extractsIdentification of regulatory factor X as a novel mismatch repair stimulatory factorCoordinated processing of 3' slipped (CAG)n/(CTG)n hairpins by DNA polymerases β and δ preferentially induces repeat expansions.Ubiquitin-specific Peptidase 10 (USP10) Deubiquitinates and Stabilizes MutS Homolog 2 (MSH2) to Regulate Cellular Sensitivity to DNA Damage.Mismatch recognition protein MutSbeta does not hijack (CAG)n hairpin repair in vitro.Altered 8-oxoguanine glycosylase in mild cognitive impairment and late-stage Alzheimer's disease brain.Proteomic analysis of mismatch repair-mediated alkylating agent-induced DNA damage response.In vitro and in vivo modulations of benzo[c]phenanthrene-DNA adducts by DNA mismatch repair system.Evidence that nucleosomes inhibit mismatch repair in eukaryotic cells
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P50
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onderzoeker
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researcher
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հետազոտող
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Guo-Min Li
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Guo-Min Li
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Guo-Min Li
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Guo-Min Li
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Guo-Min Li
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Guo-Min Li
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Guo-Min Li
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Guo-Min Li
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Guo-Min Li
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Guo-Min Li
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Guo-Min Li
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Guo-Min Li
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Guo-Min Li
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Guo-Min Li
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Guo-Min Li
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P214
P244
P106
P1153
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P214
P244
n2008180834
P31
P496
0000-0002-9842-4578
P7859
lccn-n2008180834