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DNA mismatch repair: from biophysics to bedside

DNA repair, 2016-02, Vol.38, p.1-2

2016

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Contribution of mRNA Splicing to Mismatch Repair Gene Sequence Variant Interpretation

Frontiers in genetics, 2020-07, Vol.11, p.798-798

2020

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A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants

Human mutation, 2012-03, Vol.33 (3), p.488-494

2012

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Genetic screens to identify pathogenic gene variants in the common cancer predisposition Lynch syndrome

Proceedings of the National Academy of Sciences - PNAS, 2013-06, Vol.110 (23), p.9403-9408

2013

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Induction of mismatch repair deficiency, compromised DNA damage signaling and compound hypermutagenesis by a dietary mutagen in a cell-based model for Lynch syndrome

Carcinogenesis (New York), 2022-03, Vol.43 (2), p.160-169

2022

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Inactivation of DNA Mismatch Repair by Variants of Uncertain Significance in the PMS2 Gene

Human mutation, 2013-11, Vol.34 (11), p.1477-1480

2013

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Predictive functional assay‐based classification of PMS2 variants in Lynch syndrome

Human mutation, 2022-09, Vol.43 (9), p.1249-1258

2022

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Adjuvant Treatment for POLE Proofreading Domain-Mutant Cancers: Sensitivity to Radiotherapy, Chemotherapy, and Nucleoside Analogues

Clinical cancer research, 2018-07, Vol.24 (13), p.3197-3203

2018

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Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein

Molecular genetics & genomic medicine, 2014-07, Vol.2 (4), p.352-355

2014

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A functional assay–based procedure to classify mismatch repair gene variants in Lynch syndrome

Genetics in medicine, 2019-07, Vol.21 (7), p.1486-1496

2019

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Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer

Genes chromosomes & cancer, 2020-12, Vol.59 (12), p.697-701

2020

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Pathological assessment of mismatch repair gene variants in Lynch syndrome: Past, present, and future

Human mutation, 2012-12, Vol.33 (12), p.1617-1625

2012

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Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndrome

Genetics in medicine, 2020-05, Vol.22 (5), p.847-856

2020

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Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity

Molecular carcinogenesis, 2015-07, Vol.54 (7), p.513-522

2015

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A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1

Human mutation, 2010-03, Vol.31 (3), p.247-253

2010

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Functional characterization of MLH1 missense variants identified in lynch syndrome patients

Human mutation, 2012-12, Vol.33 (12), p.1647-1655

2012

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Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2 : Use of potential alternative start sites and implications for predicting variant pathogenicity: VARIANTS DISRUPTING TRANSLATION INITIATION

Molecular carcinogenesis, 2015-07, Vol.54 (7), p.513-522

2015

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Response to: Design of a Core Classification Process for DNA Mismatch Repair Variations of A Priori Unknown Functional Significance

Human mutation, 2013-06, Vol.34 (6), p.923-924

2013

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In the Realm of the Senses: Saint Thomas Aquinas on Sensory Love, Desire, and Delight

The Thomist, 1995, Vol.59 (1), p.47-58

Drost, Mark P

1995

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Husserl and Goodman on the Role of Resemblance in Pictorial Representation

International studies in philosophy, 1994, Vol.26 (4), p.17-27

Drost, Mark P.

1994

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Intentionality in Aquinas’s Theory of Emotions

International philosophical quarterly, 1991-12, Vol.31 (4), p.449-460

Drost, Mark P.

1991

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The Primacy of Perception in Husserl's Theory of Imagining

Philosophy and phenomenological research, 1990-03, Vol.50 (3), p.569-582

Drost, Mark P.

1990

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Nietzsche and Mimesis

Philosophy and literature, 1986-10, Vol.10 (2), p.309-317

Drost, Mark P

1986

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DNA mismatch repair: from biophysics to bedside

Contribution of mRNA Splicing to Mismatch Repair Gene Sequence Variant Interpretation

A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants

Genetic screens to identify pathogenic gene variants in the common cancer predisposition Lynch syndrome

Induction of mismatch repair deficiency, compromised DNA damage signaling and compound hypermutagenesis by a dietary mutagen in a cell-based model for Lynch syndrome

Inactivation of DNA Mismatch Repair by Variants of Uncertain Significance in the PMS2 Gene

Predictive functional assay‐based classification of PMS2 variants in Lynch syndrome

Adjuvant Treatment for POLE Proofreading Domain-Mutant Cancers: Sensitivity to Radiotherapy, Chemotherapy, and Nucleoside Analogues

Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein

A functional assay–based procedure to classify mismatch repair gene variants in Lynch syndrome

The High Diagnostic Yield of Prenatal Exome Sequencing Followed by 3400 Gene Panel Analysis in 629 Ongoing Pregnancies With Ultrasound Anomalies

Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer

Pathological assessment of mismatch repair gene variants in Lynch syndrome: Past, present, and future

Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndrome

Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome

Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity

A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1

Functional characterization of MLH1 missense variants identified in lynch syndrome patients

Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2 : Use of potential alternative start sites and implications for predicting variant pathogenicity: VARIANTS DISRUPTING TRANSLATION INITIATION

Response to: Design of a Core Classification Process for DNA Mismatch Repair Variations of A Priori Unknown Functional Significance

In the Realm of the Senses: Saint Thomas Aquinas on Sensory Love, Desire, and Delight

Husserl and Goodman on the Role of Resemblance in Pictorial Representation

Intentionality in Aquinas’s Theory of Emotions

The Primacy of Perception in Husserl's Theory of Imagining

Nietzsche and Mimesis

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