List of works - Guo-Min Li

A human MUTYH variant linking colonic polyposis to redox degradation of the [4Fe4S] cluster

scientific article published on 18 June 2018

A special issue on DNA damage response and genome stability ⬇️

scientific article published on February 27, 2012

A special issue on DNA damage responses and genome maintenance

article

ATP-dependent interaction of human mismatch repair proteins and dual role of PCNA in mismatch repair

scientific journal article

Altered 8-oxoguanine glycosylase in mild cognitive impairment and late-stage Alzheimer's disease brain

scientific article published on 11 June 2008

Analysis of DNA mismatch repair in cellular response to DNA damage

scientific article published on January 2006

Arsenic Inhibits DNA Mismatch Repair by Promoting EGFR Expression and PCNA Phosphorylation.

scientific article

Bi-directional Processing of DNA Loops by Mismatch Repair-dependent and -independent Pathways in Human Cells

scientific article published in Journal of Biological Chemistry

Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers.

scientific article

Cancer-driving H3G34V/R/D mutations block H3K36 methylation and H3K36me3-MutSα interaction

article published in the Proceedings of the National Academy of Sciences of the United States of America

Clamping down on mismatches

scientific article published on 12 July 2016

Coordinated processing of 3' slipped (CAG)n/(CTG)n hairpins by DNA polymerases β and δ preferentially induces repeat expansions

scientific article published on 12 April 2013

Correction to: DNA mismatch repair in the context of chromatin

scientific article published on 02 July 2020

DNA Mismatch Repair: Biological Functions and Molecular Mechanisms

DNA instability in replicating Huntington's disease lymphoblasts

scientific article

DNA mismatch repair in the context of chromatin

scientific article published on 03 February 2020

DNA-PKcs-dependent phosphorylation of RECQL4 promotes NHEJ by stabilizing the NHEJ machinery at DNA double-strand breaks

scientific article published on 01 June 2022

Decoding the histone code: Role of H3K36me3 in mismatch repair and implications for cancer susceptibility and therapy

scientific article

Differential requirement for proliferating cell nuclear antigen in 5' and 3' nick-directed excision in human mismatch repair

scientific article published on 9 February 2004

Distinct nucleotide binding/hydrolysis properties and molar ratio of MutSalpha and MutSbeta determine their differential mismatch binding activities

scientific article

Effect of carcinogenic acrolein on DNA repair and mutagenic susceptibility

scientific article

Erratum: Author Correction: Identification of novel genetic variants predisposing to familial oral squamous cell carcinomas

scientific article published on 14 July 2020

Evidence for involvement of HMGB1 protein in human DNA mismatch repair

scientific article

Evidence that nucleosomes inhibit mismatch repair in eukaryotic cells

scientific article published on 05 October 2009

Folate deficiency, mismatch repair-dependent apoptosis, and human disease ⬇️

scientific article published on October 1, 2003

Genetic and epigenetic modification of mismatch repair genes hMSH2 and hMLH1 in sporadic breast cancer with microsatellite instability

article

HDAC3 deacetylates the DNA mismatch repair factor MutSβ to stimulate triplet repeat expansions

scientific article published on 08 September 2020

HDAC6 deacetylates and ubiquitinates MSH2 to maintain proper levels of MutSα.

scientific article

Human MutSα Specifically Binds to DNA Containing Aminofluorene and Acetylaminofluorene Adducts

scientific article published in Journal of Biological Chemistry

Identification and characterization of OGG1 mutations in patients with Alzheimer's disease

scientific article published on 10 April 2007

Identification of novel genetic variants predisposing to familial oral squamous cell carcinomas

scientific article published on 26 November 2019

Identification of regulatory factor X as a novel mismatch repair stimulatory factor

scientific article published on 4 March 2008

In vitro and in vivo modulations of benzo[c]phenanthrene-DNA adducts by DNA mismatch repair system

scientific article

In vitro repair of DNA hairpins containing various numbers of CAG/CTG trinucleotide repeats

scientific article

Incision-dependent and error-free repair of (CAG)(n)/(CTG)(n) hairpins in human cell extracts

scientific article

Involvement of DNA mismatch repair in folate deficiency-induced apoptosis☆

scientific article published on 01 June 2002

Mechanisms and functions of DNA mismatch repair

scientific article

Mismatch recognition protein MutSbeta does not hijack (CAG)n hairpin repair in vitro.

scientific article published on 12 June 2009

Mismatch repair deficiency in hematological malignancies with microsatellite instability

scientific article published on August 2002

Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches

scientific article

Modulation of microRNA processing by mismatch repair protein MutLα.

scientific article

Molecular cooperation between the Werner syndrome protein and replication protein A in relation to replication fork blockage

scientific article

New insights and challenges in mismatch repair: getting over the chromatin hurdle

scientific article

Nick-dependent and -independent processing of large DNA loops in human cells

scientific article published on 30 September 2003

Novel molecular insights into the mechanism of GO removal by MutM.

scientific article published in February 2010

Okazaki fragment maturation involves α-segment error editing by the mammalian FEN1/MutSα functional complex

scientific article published on 28 April 2015

Partial reconstitution of human DNA mismatch repair in vitro: characterization of the role of human replication protein A

scientific journal article

Phosphorylation of PCNA by EGFR inhibits mismatch repair and promotes misincorporation during DNA synthesis

scientific article published on 30 March 2015

Phosphorylation of proliferating cell nuclear antigen promotes cancer progression by activating the ATM/Akt/GSK3β/Snail signaling pathway

scientific article published on 11 March 2019

Prereplicative repair of oxidized bases in the human genome is mediated by NEIL1 DNA glycosylase together with replication proteins

scientific article

Proteomic analysis of mismatch repair-mediated alkylating agent-induced DNA damage response ⬇️

scientific article published on 19 September 2013

Reconstitution of 5'-directed human mismatch repair in a purified system

scientific article published in September 2005

Regulation of replication protein A functions in DNA mismatch repair by phosphorylation

scientific article published on 26 May 2006

Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs

scientific article

Roles of mismatch repair proteins hMSH2 and hMLH1 in the development of sporadic breast cancer

scientific article

Specific binding of human MSH2.MSH6 mismatch-repair protein heterodimers to DNA incorporating thymine- or uracil-containing UV light photoproducts opposite mismatched bases.

scientific article

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.

scientific article

The Role of XPG in Processing (CAG)n/(CTG)n DNA Hairpins

scientific article

The Werner syndrome protein promotes CAG/CTG repeat stability by resolving large (CAG)(n)/(CTG)(n) hairpins

scientific article

The hMSH2(M688R) Lynch syndrome mutation may function as a dominant negative

scientific article

The histone mark H3K36me3 regulates human DNA mismatch repair through its interaction with MutSα

scientific article

Trinucleotide repeat expansions catalyzed by human cell-free extracts

scientific article published on 22 January 2013

Truncating mutation in the autophagy gene UVRAG confers oncogenic properties and chemosensitivity in colorectal cancers

scientific article published on 3 August 2015

Ubiquitin-specific Peptidase 10 (USP10) Deubiquitinates and Stabilizes MutS Homolog 2 (MSH2) to Regulate Cellular Sensitivity to DNA Damage

scientific article published on 14 March 2016

hMRE11 deficiency leads to microsatellite instability and defective DNA mismatch repair

scientific article

List of works by Guo-Min Li

A human MUTYH variant linking colonic polyposis to redox degradation of the [4Fe4S] cluster

A special issue on DNA damage response and genome stability ⬇️

A special issue on DNA damage responses and genome maintenance

ATP-dependent interaction of human mismatch repair proteins and dual role of PCNA in mismatch repair

Altered 8-oxoguanine glycosylase in mild cognitive impairment and late-stage Alzheimer's disease brain

Analysis of DNA mismatch repair in cellular response to DNA damage

Arsenic Inhibits DNA Mismatch Repair by Promoting EGFR Expression and PCNA Phosphorylation.

Bi-directional Processing of DNA Loops by Mismatch Repair-dependent and -independent Pathways in Human Cells

Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers.

Cancer-driving H3G34V/R/D mutations block H3K36 methylation and H3K36me3-MutSα interaction

Clamping down on mismatches

Coordinated processing of 3' slipped (CAG)n/(CTG)n hairpins by DNA polymerases β and δ preferentially induces repeat expansions

Correction to: DNA mismatch repair in the context of chromatin

DNA Mismatch Repair: Biological Functions and Molecular Mechanisms

DNA instability in replicating Huntington's disease lymphoblasts

DNA mismatch repair in the context of chromatin

DNA-PKcs-dependent phosphorylation of RECQL4 promotes NHEJ by stabilizing the NHEJ machinery at DNA double-strand breaks

Decoding the histone code: Role of H3K36me3 in mismatch repair and implications for cancer susceptibility and therapy

Differential requirement for proliferating cell nuclear antigen in 5' and 3' nick-directed excision in human mismatch repair

Distinct nucleotide binding/hydrolysis properties and molar ratio of MutSalpha and MutSbeta determine their differential mismatch binding activities

Effect of carcinogenic acrolein on DNA repair and mutagenic susceptibility

Erratum: Author Correction: Identification of novel genetic variants predisposing to familial oral squamous cell carcinomas

Evidence for involvement of HMGB1 protein in human DNA mismatch repair

Evidence that nucleosomes inhibit mismatch repair in eukaryotic cells

Folate deficiency, mismatch repair-dependent apoptosis, and human disease ⬇️

Genetic and epigenetic modification of mismatch repair genes hMSH2 and hMLH1 in sporadic breast cancer with microsatellite instability

HDAC3 deacetylates the DNA mismatch repair factor MutSβ to stimulate triplet repeat expansions

HDAC6 deacetylates and ubiquitinates MSH2 to maintain proper levels of MutSα.

Human MutSα Specifically Binds to DNA Containing Aminofluorene and Acetylaminofluorene Adducts

Identification and characterization of OGG1 mutations in patients with Alzheimer's disease

Identification of novel genetic variants predisposing to familial oral squamous cell carcinomas

Identification of regulatory factor X as a novel mismatch repair stimulatory factor

In vitro and in vivo modulations of benzo[c]phenanthrene-DNA adducts by DNA mismatch repair system

In vitro repair of DNA hairpins containing various numbers of CAG/CTG trinucleotide repeats

Incision-dependent and error-free repair of (CAG)(n)/(CTG)(n) hairpins in human cell extracts

Involvement of DNA mismatch repair in folate deficiency-induced apoptosis☆

Mechanisms and functions of DNA mismatch repair

Mismatch recognition protein MutSbeta does not hijack (CAG)n hairpin repair in vitro.

Mismatch repair deficiency in hematological malignancies with microsatellite instability

Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches

Modulation of microRNA processing by mismatch repair protein MutLα.

Molecular cooperation between the Werner syndrome protein and replication protein A in relation to replication fork blockage

New insights and challenges in mismatch repair: getting over the chromatin hurdle

Nick-dependent and -independent processing of large DNA loops in human cells

Novel molecular insights into the mechanism of GO removal by MutM.

Okazaki fragment maturation involves α-segment error editing by the mammalian FEN1/MutSα functional complex

Partial reconstitution of human DNA mismatch repair in vitro: characterization of the role of human replication protein A

Phosphorylation of PCNA by EGFR inhibits mismatch repair and promotes misincorporation during DNA synthesis

Phosphorylation of proliferating cell nuclear antigen promotes cancer progression by activating the ATM/Akt/GSK3β/Snail signaling pathway

Prereplicative repair of oxidized bases in the human genome is mediated by NEIL1 DNA glycosylase together with replication proteins

Proteomic analysis of mismatch repair-mediated alkylating agent-induced DNA damage response ⬇️

Reconstitution of 5'-directed human mismatch repair in a purified system

Regulation of replication protein A functions in DNA mismatch repair by phosphorylation

Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs

Roles of mismatch repair proteins hMSH2 and hMLH1 in the development of sporadic breast cancer

Specific binding of human MSH2.MSH6 mismatch-repair protein heterodimers to DNA incorporating thymine- or uracil-containing UV light photoproducts opposite mismatched bases.

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.

The Role of XPG in Processing (CAG)n/(CTG)n DNA Hairpins

The Werner syndrome protein promotes CAG/CTG repeat stability by resolving large (CAG)(n)/(CTG)(n) hairpins

The hMSH2(M688R) Lynch syndrome mutation may function as a dominant negative

The histone mark H3K36me3 regulates human DNA mismatch repair through its interaction with MutSα

Trinucleotide repeat expansions catalyzed by human cell-free extracts

Truncating mutation in the autophagy gene UVRAG confers oncogenic properties and chemosensitivity in colorectal cancers

Ubiquitin-specific Peptidase 10 (USP10) Deubiquitinates and Stabilizes MutS Homolog 2 (MSH2) to Regulate Cellular Sensitivity to DNA Damage

hMRE11 deficiency leads to microsatellite instability and defective DNA mismatch repair