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Key role of phosphorylation sites in ATPase domain and Linker region of MLH1 for DNA binding and functionality of MutLα

Scientific reports, 2023-08, Vol.13 (1), p.12503-12503, Article 12503

2023

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Investigation of the Wilson gene ATP7B transcriptional start site and the effect of core promoter alterations

Scientific reports, 2021-04, Vol.11 (1), p.7674-7674, Article 7674

2021

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Functional characterization of MLH1 missense variants unveils mechanisms of pathogenicity and clarifies role in cancer

PloS one, 2022-12, Vol.17 (12)

2022

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Functional characterization of MLH1 missense variants unveils mechanisms of pathogenicity and clarifies role in cancer

PloS one, 2022-12, Vol.17 (12), p.e0278283-e0278283

2022

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Functional analysis of hMLH1 variants and HNPCC-related mutations using a human expression system

Gastroenterology (New York, N.Y. 1943), 2002-01, Vol.122 (1), p.211-219

2002

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An Interstitial Deletion at 3p21.3 Results in the Genetic Fusion of MLH1 and ITGA9 in a Lynch Syndrome Family

Clinical cancer research, 2009-02, Vol.15 (3), p.762-769

2009

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Expression and secretion of the pro-inflammatory cytokine IL-8 is increased in colorectal cancer cells following the knockdown of non-erythroid spectrin [alpha]ll

International journal of oncology, 2020-06, Vol.56 (6), p.1551

2020

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Phosphorylation meets DNA mismatch repair

DNA repair, 2018-12, Vol.72, p.107-114

2018

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A conserved motif in the disordered linker of human MLH1 is vital for DNA mismatch repair and its function is diminished by a cancer family mutation

Nucleic acids research, 2023-07, Vol.51 (12), p.6307-6320

2023

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Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis

American journal of human genetics, 2016-08, Vol.99 (2), p.337-351

2016

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Analysis of MUTYH alternative transcript expression, promoter function, and the effect of human genetic variants

Human mutation, 2019-04, Vol.40 (4), p.472-482

2019

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Expression Defect Size among Unclassified MLH1 Variants Determines Pathogenicity in Lynch Syndrome Diagnosis

Clinical cancer research, 2013-05, Vol.19 (9), p.2432-2441

2013

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Pathogenetic mechanisms and therapeutic approaches of acute-to-chronic liver failure

American Journal of Physiology: Cell Physiology, 2023-07, Vol.325 (1), p.C129-C140

2023

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Loss of MLH1 sensitizes colon cancer cells to DNA‐PKcs inhibitor KU60648

Molecular carcinogenesis, 2017-07, Vol.56 (7), p.1816-1824

2017

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Phosphorylation‐dependent signaling controls degradation of DNA mismatch repair protein PMS2

Molecular carcinogenesis, 2017-12, Vol.56 (12), p.2663-2668

2017

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DNA mismatch repair activity of MutLα is regulated by CK2‐dependent phosphorylation of MLH1 (S477)

Molecular carcinogenesis, 2018-12, Vol.57 (12), p.1723-1734

2018

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Upon Drug-Induced Apoptosis in Lymphoma Cells X-linked Inhibitor of Apoptosis (XIAP) Translocates from the Cytosol to the Nucleus

Leukemia & lymphoma, 2004-07, Vol.45 (7), p.1429-1436

2004

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MUTYH gene expression and alternative splicing in controls and polyposis patients

Human mutation, 2012-07, Vol.33 (7), p.1067-1074

2012

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Thymosin beta 4 expression and nuclear transport are regulated by hMLH1

Biochemical and biophysical research communications, 2007-12, Vol.364 (4), p.731-736

2007

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Functional testing strategy for coding genetic variants of unclear significance in MLH1 in Lynch syndrome diagnosis

Carcinogenesis (New York), 2015-02, Vol.36 (2), p.202-211

2015

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Comprehensive functional assessment of MLH1 variants of unknown significance

Human mutation, 2012-11, Vol.33 (11), p.1576-1588

2012

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A CRM1-dependent nuclear export pathway is involved in the regulation of MutLα subcellular localization

Genes chromosomes & cancer, 2011-02, Vol.50 (2), p.59-70

2011

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Malignant fibrous histiocytoma is a rare Lynch syndrome-associated tumor in two German families

Familial cancer, 2011-09, Vol.10 (3), p.591-595

2011

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Comprehensive Functional Assessment of MLH1 Variants of Unknown Significance

Human mutation, 2013-01, Vol.34 (1), p.274-274

2013

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Bethesda guidelines: relation to microsatellite instability and MLH1 promoter methylation in patients with colorectal cancer

Annals of internal medicine, 2001-10, Vol.135 (8 Pt 1), p.566

2001

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Key role of phosphorylation sites in ATPase domain and Linker region of MLH1 for DNA binding and functionality of MutLα

Investigation of the Wilson gene ATP7B transcriptional start site and the effect of core promoter alterations

Functional characterization of MLH1 missense variants unveils mechanisms of pathogenicity and clarifies role in cancer

Functional characterization of MLH1 missense variants unveils mechanisms of pathogenicity and clarifies role in cancer

Functional analysis of hMLH1 variants and HNPCC-related mutations using a human expression system

An Interstitial Deletion at 3p21.3 Results in the Genetic Fusion of MLH1 and ITGA9 in a Lynch Syndrome Family

Expression and secretion of the pro-inflammatory cytokine IL-8 is increased in colorectal cancer cells following the knockdown of non-erythroid spectrin [alpha]ll

Phosphorylation meets DNA mismatch repair

A conserved motif in the disordered linker of human MLH1 is vital for DNA mismatch repair and its function is diminished by a cancer family mutation

Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis

Analysis of MUTYH alternative transcript expression, promoter function, and the effect of human genetic variants

Expression Defect Size among Unclassified MLH1 Variants Determines Pathogenicity in Lynch Syndrome Diagnosis

Pathogenetic mechanisms and therapeutic approaches of acute-to-chronic liver failure

Loss of MLH1 sensitizes colon cancer cells to DNA‐PKcs inhibitor KU60648

Phosphorylation‐dependent signaling controls degradation of DNA mismatch repair protein PMS2

DNA mismatch repair activity of MutLα is regulated by CK2‐dependent phosphorylation of MLH1 (S477)

Upon Drug-Induced Apoptosis in Lymphoma Cells X-linked Inhibitor of Apoptosis (XIAP) Translocates from the Cytosol to the Nucleus

MUTYH gene expression and alternative splicing in controls and polyposis patients

Thymosin beta 4 expression and nuclear transport are regulated by hMLH1

Functional testing strategy for coding genetic variants of unclear significance in MLH1 in Lynch syndrome diagnosis

Comprehensive functional assessment of MLH1 variants of unknown significance

A CRM1-dependent nuclear export pathway is involved in the regulation of MutLα subcellular localization

Malignant fibrous histiocytoma is a rare Lynch syndrome-associated tumor in two German families

Comprehensive Functional Assessment of MLH1 Variants of Unknown Significance

Bethesda guidelines: relation to microsatellite instability and MLH1 promoter methylation in patients with colorectal cancer

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