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Two glycosylase families diffusively scan DNA using a wedge residue to probe for and identify oxidatively damaged bases

Proceedings of the National Academy of Sciences - PNAS, 2014-05, Vol.111 (20), p.E2091-E2099

2014

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Detection of OG:A Lesion Mispairs by MutY Relies on a Single His Residue and the 2‑Amino Group of 8‑Oxoguanine

Journal of the American Chemical Society, 2020-08, Vol.142 (31), p.13283-13287

2020

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Mouse Embryonic Fibroblasts Isolated From Nthl1 D227Y Knockin Mice Exhibit Defective DNA Repair and Increased Genome Instability

DNA repair, 2022-01, Vol.109, p.103247-103247, Article 103247

2022

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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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Single molecule glycosylase studies with engineered 8-oxoguanine DNA damage sites show functional defects of a MUTYH polyposis variant

Nucleic acids research, 2019-04, Vol.47 (6), p.3058

2019

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Single-Stranded Breaks in DNA but Not Oxidative DNA Base Damages Block Transcriptional Elongation by RNA Polymerase II in HeLa Cell Nuclear Extracts

The Journal of biological chemistry, 2004-04, Vol.279 (18), p.18511-18520

2004

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Germ-line variant of human NTH1 DNA glycosylase induces genomic instability and cellular transformation

Proceedings of the National Academy of Sciences - PNAS, 2013-08, Vol.110 (35), p.14314-14319

2013

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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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Plant and fungal Fpg homologs are formamidopyrimidine DNA glycosylases but not 8-oxoguanine DNA glycosylases

DNA repair, 2009-05, Vol.8 (5), p.643-653

2009

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The enigma of endonuclease VIII

DNA Repair, 2003-05, Vol.2 (5), p.441-453

2003

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Unhooking of an interstrand cross-link at DNA fork structures by the DNA glycosylase NEIL3

DNA repair, 2020-02, Vol.86, p.102752-102752, Article 102752

2020

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Bacterial origin of a chloroplast intron: conserved self-splicing group I introns in cyanobacteria

Science (American Association for the Advancement of Science), 1990-12, Vol.250 (4987), p.1566-1570

1990

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Origin and evolution of group I introns in cyanobacterial tRNA genes

Journal of Bacteriology, 1997-11, Vol.179 (21), p.6798-6806

1997

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Detection of OG:A lesion mispairs by MutY relies on interactions of a single His residue with the 2-amino group of 8-oxoguanine

Journal of the American Chemical Society, 2020-07, Vol.142 (31), p.13283-13287

2020

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Abstract 3590: A Neil1 DNA glycosylase germline variant induces genomic instability and cellular transformation

Cancer research (Chicago, Ill.), 2016-07, Vol.76 (14_Supplement), p.3590-3590

2016

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Direct Observation of MUTYH and the Cancer-Associated Y150C Variant Binding to OG: A Mismatches at the Single Molecule Level

Biophysical journal, 2018-02, Vol.114 (3), p.82a-83a

2018

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Two glycosylase families diffusively scan DNA using a wedge residue to probe for and identify oxidatively damaged bases

Proceedings of the National Academy of Sciences - PNAS, 2014-05, Vol.111 (20), p.7174-7174

2014

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The NEIL1 G83D germline DNA glycosylase variant induces genomic instability and cellular transformation

Oncotarget, 2017-10, Vol.8 (49), p.85883-85895

2017

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Single-stranded breaks in DNA but not oxidative DNA base damages block transcriptional elongation by RNA polymerase II in HeLa cell nuclear extracts. Vol. 279 (2004) 18511-18520

The Journal of biological chemistry, 2004-06, Vol.279 (26), p.27830-27830

2004

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Group I self -splicing introns in cyanobacteria

Kathe, Scott David

1999

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ProQuest

Neuroprosthetic baroreflex controls haemodynamics after spinal cord injury

Nature (London), 2021-02, Vol.590 (7845), p.308-314

2021

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Trial Participation and Outcomes Among English-Speaking and Spanish-Speaking Patients With Appendicitis Randomized to Antibiotics: A Secondary Analysis of the CODA Randomized Clinical Trial

JAMA surgery, 2023-09, Vol.158 (9), p.901

2023

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Rapid identification of a novel phosphodiesterase 7B tracer for receptor occupancy studies using LC─MS/MS

Neurochemistry international, 2020-07, Vol.137, p.104735-104735, Article 104735

2020

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LC-MS/MS Rapid identification of a novel tracer for a subtype specific phosphodiesterase (PDE) with no known ligand

Drug metabolism and pharmacokinetics, 2019-01, Vol.34 (1), p.S67-S67

2019

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Identification of a recurrent germline PAX5 mutation and susceptibility to pre-B cell acute lymphoblastic leukemia

Nature genetics, 2013-09, Vol.45 (10), p.1226-1231

2013

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Two glycosylase families diffusively scan DNA using a wedge residue to probe for and identify oxidatively damaged bases

Detection of OG:A Lesion Mispairs by MutY Relies on a Single His Residue and the 2‑Amino Group of 8‑Oxoguanine

Mouse Embryonic Fibroblasts Isolated From Nthl1 D227Y Knockin Mice Exhibit Defective DNA Repair and Increased Genome Instability

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

Single molecule glycosylase studies with engineered 8-oxoguanine DNA damage sites show functional defects of a MUTYH polyposis variant

Single-Stranded Breaks in DNA but Not Oxidative DNA Base Damages Block Transcriptional Elongation by RNA Polymerase II in HeLa Cell Nuclear Extracts

Germ-line variant of human NTH1 DNA glycosylase induces genomic instability and cellular transformation

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

Plant and fungal Fpg homologs are formamidopyrimidine DNA glycosylases but not 8-oxoguanine DNA glycosylases

The enigma of endonuclease VIII

Unhooking of an interstrand cross-link at DNA fork structures by the DNA glycosylase NEIL3

Bacterial origin of a chloroplast intron: conserved self-splicing group I introns in cyanobacteria

Origin and evolution of group I introns in cyanobacterial tRNA genes

Detection of OG:A lesion mispairs by MutY relies on interactions of a single His residue with the 2-amino group of 8-oxoguanine

Abstract 3590: A Neil1 DNA glycosylase germline variant induces genomic instability and cellular transformation

Direct Observation of MUTYH and the Cancer-Associated Y150C Variant Binding to OG: A Mismatches at the Single Molecule Level

Two glycosylase families diffusively scan DNA using a wedge residue to probe for and identify oxidatively damaged bases

The NEIL1 G83D germline DNA glycosylase variant induces genomic instability and cellular transformation

Single-stranded breaks in DNA but not oxidative DNA base damages block transcriptional elongation by RNA polymerase II in HeLa cell nuclear extracts. Vol. 279 (2004) 18511-18520

Group I self -splicing introns in cyanobacteria

Neuroprosthetic baroreflex controls haemodynamics after spinal cord injury

Trial Participation and Outcomes Among English-Speaking and Spanish-Speaking Patients With Appendicitis Randomized to Antibiotics: A Secondary Analysis of the CODA Randomized Clinical Trial

Rapid identification of a novel phosphodiesterase 7B tracer for receptor occupancy studies using LC─MS/MS

LC-MS/MS Rapid identification of a novel tracer for a subtype specific phosphodiesterase (PDE) with no known ligand

Identification of a recurrent germline PAX5 mutation and susceptibility to pre-B cell acute lymphoblastic leukemia

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