| human | Q5 |
| P496 | ORCID iD | 0000-0002-3906-0321 |
| P6023 | ResearchGate contributions ID | Susan-S-Wallace-38235267 |
| P166 | award received | Fellow of the American Association for the Advancement of Science | Q5442484 |
| P1889 | different from | Susan Wallace | Q29643745 |
| P108 | employer | University of Vermont | Q1048898 |
| New York Medical College | Q4115972 | ||
| P734 | family name | Wallace | Q5261248 |
| Wallace | Q5261248 | ||
| Wallace | Q5261248 | ||
| P735 | given name | Susan | Q14936243 |
| Susan | Q14936243 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | female | Q6581072 |
| Q34878256 | 5-Hydroxypyrimidine deoxynucleoside triphosphates are more efficiently incorporated into DNA by exonuclease-free Klenow fragment than 8-oxopurine deoxynucleoside triphosphates |
| Q27670953 | A Crystallographic Study of the Role of Sequence Context in Thymine Glycol Bypass by a Replicative DNA Polymerase Serendipitously Sheds Light on the Exonuclease Complex |
| Q36063330 | A Role for the Fifth G-Track in G-Quadruplex Forming Oncogene Promoter Sequences during Oxidative Stress: Do These "Spare Tires" Have an Evolved Function? |
| Q46643460 | A new technique for the quantitative assessment of 8-oxoguanine in nuclear DNA as a marker of oxidative stress. Application to dystrophin-deficient DMD skeletal muscles |
| Q37355505 | A novel bicistronic vector for overexpressing Mycobacterium tuberculosis proteins in Escherichia coli |
| Q28201222 | A novel human DNA glycosylase that removes oxidative DNA damage and is homologous to Escherichia coli endonuclease VIII |
| Q34978281 | A novel method for site specific introduction of single model oxidative DNA lesions into oligodeoxyribonucleotides |
| Q33638108 | A novel role for Escherichia coli endonuclease VIII in prevention of spontaneous G-->T transversions. |
| Q54680554 | A novel, sensitive, and specific assay for abasic sites, the most commonly produced DNA lesion. |
| Q27641081 | A structural rationale for stalling of a replicative DNA polymerase at the most common oxidative thymine lesion, thymine glycol |
| Q36309404 | Abortive base-excision repair of radiation-induced clustered DNA lesions in Escherichia coli |
| Q39895804 | Absence of a role for DNA polymerase II in SOS-induced translesion bypass of phi X174. |
| Q62061154 | An Escherichia coli endonuclease which acts on x-irradiated DNA |
| Q47680561 | Antibodies specific for purine and pyrimidine nucleosides: effect on in vitro priming ability of DNA. |
| Q62061156 | Antibodies to nucleic acids. Immunochemical studies on dinucleoside phosphate-protein conjugates |
| Q62061106 | Antibodies to oxidative DNA damage: characterization of antibodies to 8-oxopurines |
| Q62061139 | Apurinic endonuclease activity remains constant during early drosophila development |
| Q36174260 | Apurinic endonucleases from Saccharomyces cerevisiae |
| Q45036068 | Attempted base excision repair of ionizing radiation damage in human lymphoblastoid cells produces lethal and mutagenic double strand breaks |
| Q53185190 | Base Excision Repair Variants in Cancer. |
| Q27025537 | Base excision repair and cancer |
| Q46660124 | Base excision repair by hNTH1 and hOGG1: a two edged sword in the processing of DNA damage in gamma-irradiated human cells |
| Q34475112 | Base excision repair processing of radiation-induced clustered DNA lesions. |
| Q54546244 | Base excision repair: NMR backbone assignments of Escherichia coli formamidopyrimidine-DNA glycosylase. |
| Q33908163 | Base excision repair: a critical player in many games |
| Q34710048 | Biological consequences of free radical-damaged DNA bases. |
| Q36046468 | Bumps in the road: how replicative DNA polymerases see DNA damage |
| Q27647517 | Caught bending the A-rule: crystal structures of translesion DNA synthesis with a non-natural nucleotide |
| Q44175820 | Characterization of a novel metabolic strategy used by drug-resistant tumor cells |
| Q62061126 | Characterization of antibodies to dihydrothymine, a radiolysis product of DNA |
| Q43860794 | Characterization of the Escherichia coli X-ray endonuclease, endonuclease III. |
| Q62061105 | Characterization ofEscherichia coliEndonuclease VIII |
| Q54045119 | Chemically altered apurinic sites in phi X174 DNA give increased mutagenesis in SOS-induced E. coli. |
| Q36952320 | Clostridium acetobutylicum 8-oxoguanine DNA glycosylase (Ogg) differs from eukaryotic Oggs with respect to opposite base discrimination |
| Q37424412 | Contribution of DNA unwrapping from histone octamers to the repair of oxidatively damaged DNA in nucleosomes |
| Q92933230 | Cooperation of the NEIL3 and Fanconi anemia/BRCA pathways in interstrand crosslink repair |
| Q27659914 | Crystal Structure of a Replicative DNA Polymerase Bound to the Oxidized Guanine Lesion Guanidinohydantoin , |
| Q27655490 | Crystal Structures of Two Archaeal 8-Oxoguanine DNA Glycosylases Provide Structural Insight into Guanine/8-Oxoguanine Distinction |
| Q37543875 | Crystallographic snapshots of a replicative DNA polymerase encountering an abasic site |
| Q37719258 | DNA glycosylases search for and remove oxidized DNA bases |
| Q35038055 | DNA polymerases provide a canon of strategies for translesion synthesis past oxidatively generated lesions |
| Q44454284 | Decline of nuclear and mitochondrial oxidative base excision repair activity in late passage human diploid fibroblasts |
| Q37395818 | Deficiency of base excision repair enzyme NEIL3 drives increased predisposition to autoimmunity. |
| Q33558133 | Destabilization of the PCNA trimer mediated by its interaction with the NEIL1 DNA glycosylase |
| Q62061142 | Detection and repair of DNA base damages produced by ionizing radiation |
| Q62061157 | Effect of X-Irradiation on Gene Function in Bacteriophage T4 |
| Q67908976 | Effects of base damages on DNA replication |
| Q35080156 | Endonucleolytic incision of x-irradiated deoxyribonucleic acid by extracts of Escherichia coli |
| Q46646764 | Engineering functional changes in Escherichia coli endonuclease III based on phylogenetic and structural analyses |
| Q62061102 | Enzymatic Processing of Uracil Glycol, a Major Oxidative Product of DNA Cytosine |
| Q62061101 | Enzymatic processing of radiation-induced free radical damage in DNA |
| Q35624116 | Escherichia coli endonuclease VIII: cloning, sequencing, and overexpression of the nei structural gene and characterization of nei and nei nth mutants |
| Q62061089 | Estimation of DNA Sequence Context-dependent Mutation Rates Using Primate Genomic Sequences |
| Q36044239 | Expression and purification of active mouse and human NEIL3 proteins. |
| Q36907669 | Expression of cloned bacteriophage T4 uvsW and uvsY genes in rec+ and rec- Escherichia coli |
| Q40574949 | Expression of the oxidative base excision repair enzymes is not induced in TK6 human lymphoblastoid cells after low doses of ionizing radiation. |
| Q31424354 | Fabs specific for 8-oxoguanine: control of DNA binding |
| Q30868826 | Fluorescence detection of 8-oxoguanine in nuclear and mitochondrial DNA of cultured cells using a recombinant Fab and confocal scanning laser microscopy. |
| Q27681153 | Genome and cancer single nucleotide polymorphisms of the human NEIL1 DNA glycosylase: Activity, structure, and the effect of editing |
| Q37143498 | Germ-line variant of human NTH1 DNA glycosylase induces genomic instability and cellular transformation |
| Q40637201 | Host- and phage-mediated repair of radiation damage in bacteriophage T4. |
| Q34141563 | Human DNA polymerase kappa bypasses and extends beyond thymine glycols during translesion synthesis in vitro, preferentially incorporating correct nucleotides |
| Q36174152 | Human endonuclease VIII-like (NEIL) proteins in the giant DNA Mimivirus |
| Q42692838 | In vitro selection of sequence contexts which enhance bypass of abasic sites and tetrahydrofuran by T4 DNA polymerase holoenzyme. |
| Q41563460 | Incorporation of thymine-containing DNA precursors in plasmolysed cells infected by the T4 non-lethal recombination defective mutants. |
| Q62061145 | Incorporation of thymine-containing DNA precursors in wild-type and mutant T4-infected plasmolysed cells |
| Q62061107 | Influence of .alpha.-Deoxyadenosine on the Stability and Structure of DNA. Thermodynamic and Molecular Mechanics Studies |
| Q43569931 | Inhibition of oxidative DNA repair in cadmium-adapted alveolar epithelial cells and the potential involvement of metallothionein |
| Q41886603 | Initiation of base excision repair of oxidative lesions in nucleosomes by the human, bifunctional DNA glycosylase NTH1. |
| Q30585004 | Insights into the glycosylase search for damage from single-molecule fluorescence microscopy |
| Q54640652 | Isolation and characterization of endonuclease VIII from Escherichia coli. |
| Q27659910 | Kinetics of Mismatch Formation opposite Lesions by the Replicative DNA Polymerase from Bacteriophage RB69 |
| Q34600540 | Kinetics of error generation in homologous B-family DNA polymerases. |
| Q34514909 | Lesion bypass activity of DNA polymerase θ (POLQ) is an intrinsic property of the pol domain and depends on unique sequence inserts. |
| Q40398133 | Major oxidative products of cytosine, 5-hydroxycytosine and 5-hydroxyuracil, exhibit sequence context-dependent mispairing in vitro. |
| Q62061131 | Mechanism of action of Escherichia coli endonuclease III |
| Q62061132 | Mechanism of action of Micrococcus luteus .gamma.-endonuclease |
| Q46672488 | Methylperoxyl radicals as intermediates in the damage to DNA irradiated in aqueous dimethyl sulfoxide with gamma rays |
| Q34656380 | Multiply damaged sites in DNA: interactions with Escherichia coli endonucleases III and VIII |
| Q33787450 | Multiprobe RNase protection assay analysis of mRNA levels for the Escherichia coli oxidative DNA glycosylase genes under conditions of oxidative stress |
| Q41712614 | NEIL3 Repairs Telomere Damage during S Phase to Secure Chromosome Segregation at Mitosis |
| Q34362594 | Neil3 and NEIL1 DNA glycosylases remove oxidative damages from quadruplex DNA and exhibit preferences for lesions in the telomeric sequence context |
| Q36853206 | Neil3, the final frontier for the DNA glycosylases that recognize oxidative damage. |
| Q42283571 | New substrates for old enzymes. 5-Hydroxy-2'-deoxycytidine and 5-hydroxy-2'-deoxyuridine are substrates for Escherichia coli endonuclease III and formamidopyrimidine DNA N-glycosylase, while 5-hydroxy-2'-deoxyuridine is a substrate for uracil DNA N- |
| Q33693773 | Non-specific DNA binding interferes with the efficient excision of oxidative lesions from chromatin by the human DNA glycosylase, NEIL1. |
| Q28248511 | Nucleosome disruption by DNA ligase III-XRCC1 promotes efficient base excision repair |
| Q33931095 | Nucleosomes suppress the formation of double-strand DNA breaks during attempted base excision repair of clustered oxidative damages |
| Q28263121 | Overproduction, crystallization and preliminary crystallographic analysis of a novel human DNA-repair enzyme that recognizes oxidative DNA damage |
| Q62061093 | Oxidative DNA Glycosylases: Recipes from Cloning to Characterization |
| Q54748389 | Oxidative damage in DNA. Lack of mutagenicity by thymine glycol lesions. |
| Q43720975 | Personal reflections of a woman scientist growing up in a man’s world |
| Q62061149 | Phenotypic differences among the alleles of the T4 recombination defective mutants |
| Q37315825 | Plant and fungal Fpg homologs are formamidopyrimidine DNA glycosylases but not 8-oxoguanine DNA glycosylases. |
| Q51099354 | Probing the activity of NTHL1 orthologs by targeting conserved amino acid residues. |
| Q28334662 | Processing of DNA base damage by DNA polymerases. Dihydrothymine and beta-ureidoisobutyric acid as models for instructive and noninstructive lesions |
| Q54386327 | Processing of model single-strand breaks in phi X-174 RF transfecting DNA by Escherichia coli. |
| Q54116415 | Processing of ring saturation and fragmentation products of DNA thymine in Escherichia coli. |
| Q62061121 | Properties of a monoclonal antibody for the detection of abasic sites, a common DNA lesion |
| Q62061147 | Properties of the nonlethal recombinational repair deficient mutants of bacteriophage T4 |
| Q37506970 | Properties of the nonlethal recombinational repair x and y mutants of bacteriophage T4. II. DNA synthesis. |
| Q54639966 | Pyrimidine ring fragmentation products. Effects of lesion structure and sequence context on mutagenesis. |
| Q62061100 | Radiation-induced DNA base damage detected in individual aerobic and hypoxic cells with endonuclease III and formamidopyrimidine-glycosylase |
| Q52455861 | Radiation-induced and transposon-induced chromosome damage in Drosophila: translocations and transmission distortion. |
| Q35781828 | Rapid determination of the active fraction of DNA repair glycosylases: a novel fluorescence assay for trapped intermediates. |
| Q56897217 | Recombinant Phabs reactive with 7,8-dihydro-8-oxoguanine, a major oxidative DNA lesion |
| Q41137791 | Repair of psoralen plus near ultraviolet light damage in bacteriophage T4 |
| Q36297388 | Repair-defective mutants of Alteromonas espejiana, the host for bacteriophage PM2. |
| Q62061146 | Reversion of bacteriophage T4rIImutants by high levels of pyrimidine deoxyribonucleosides |
| Q36309928 | Rules of engagement for base excision repair in chromatin |
| Q62061128 | SOS processing of unique oxidative DNA damages in Escherichia coli |
| Q27930744 | Saccharomyces cerevisiae Ntg1p and Ntg2p: broad specificity N-glycosylases for the repair of oxidative DNA damage in the nucleus and mitochondria |
| Q39811802 | Selective inhibition of in vitro DNA synthesis dependent on phiX174 compared with fd DNA. I. Protein requirements for selective inhibition |
| Q35224383 | Single Qdot-labeled glycosylase molecules use a wedge amino acid to probe for lesions while scanning along DNA |
| Q64226584 | Single molecule glycosylase studies with engineered 8-oxoguanine DNA damage sites show functional defects of a MUTYH polyposis variant |
| Q34300281 | Single-stranded breaks in DNA but not oxidative DNA base damages block transcriptional elongation by RNA polymerase II in HeLa cell nuclear extracts. |
| Q45231846 | Solution-state NMR investigation of DNA binding interactions in Escherichia coli formamidopyrimidine-DNA glycosylase (Fpg): a dynamic description of the DNA/protein interface. |
| Q50509102 | Spectroscopic studies of zinc(II)- and cobalt(II)-associated Escherichia coli formamidopyrimidine-DNA glycosylase: extended X-ray absorption fine structure evidence for a metal-binding domain. |
| Q27654633 | Structural Characterization of Clostridium acetobutylicum 8-Oxoguanine DNA Glycosylase in Its Apo Form and in Complex with 8-Oxodeoxyguanosine |
| Q27676196 | Structural Characterization of Viral Ortholog of Human DNA Glycosylase NEIL1 Bound to Thymine Glycol or 5-Hydroxyuracil-containing DNA |
| Q27675877 | Structural Characterization of a Mouse Ortholog of Human NEIL3 with a Marked Preference for Single-Stranded DNA |
| Q27656645 | Structural Characterization of a Viral NEIL1 Ortholog Unliganded and Bound to Abasic Site-containing DNA |
| Q28273546 | Structural and biochemical investigation of the role in proofreading of a beta hairpin loop found in the exonuclease domain of a replicative DNA polymerase of the B family |
| Q27670719 | Structural and biochemical studies of a plant formamidopyrimidine-DNA glycosylase reveal why eukaryotic Fpg glycosylases do not excise 8-oxoguanine |
| Q27657403 | Structural basis for the lack of opposite base specificity of Clostridium acetobutylicum 8-oxoguanine DNA glycosylase |
| Q27680235 | Structural investigation of a viral ortholog of human NEIL2/3 DNA glycosylases |
| Q40753003 | Studies on Escherichia coli X-Ray Endonuclease Specificity: Roles of Hydroxyl and Reducing Radicals in the Production of DNA Lesions |
| Q54767366 | Synthesis of dihydrothymidine and thymidine glycol 5'-triphosphates and their ability to serve as substrates for Escherichia coli DNA polymerase I. |
| Q27659026 | The C-terminal Lysine of Ogg2 DNA Glycosylases is a Major Molecular Determinant for Guanine/8-Oxoguanine Distinction |
| Q27021912 | The Fpg/Nei family of DNA glycosylases: substrates, structures, and search for damage |
| Q46420229 | The Human Ligase IIIα-XRCC1 Protein Complex Performs DNA Nick Repair after Transient Unwrapping of Nucleosomal DNA. |
| Q27675214 | The Miscoding Potential of 5-Hydroxycytosine Arises Due to Template Instability in the Replicative Polymerase Active Site |
| Q35562087 | The NEIL glycosylases remove oxidized guanine lesions from telomeric and promoter quadruplex DNA structures |
| Q42552953 | The NEIL glycosylases remove oxidized guanine lesions from telomeric and promoter quadruplex DNA structures |
| Q47100233 | The NEIL1 G83D germline DNA glycosylase variant induces genomic instability and cellular transformation. |
| Q39264183 | The Production of Alkali-labile Lesions in X-irradiated PM2 DNA |
| Q62061110 | The Sequence Context-Dependent Mispairing of 5-Hydroxycytosine and 5-Hydroxyuridine in Vitro |
| Q28553470 | The Tumor-Associated Variant RAD51 G151D Induces a Hyper-Recombination Phenotype |
| Q24564283 | The crystal structure of human endonuclease VIII-like 1 (NEIL1) reveals a zincless finger motif required for glycosylase activity |
| Q40671181 | The effect of exogenous deoxyribonucleosides on thymidine incorporation in T4-infected cells |
| Q35114231 | The enigma of endonuclease VIII. |
| Q33613798 | The genes encoding endonuclease VIII and endonuclease III in Escherichia coli are transcribed as the terminal genes in operons. |
| Q33992543 | The genes encoding formamidopyrimidine and MutY DNA glycosylases in Escherichia coli are transcribed as part of complex operons. |
| Q52453510 | The interaction between X-rays and transposon mobility in Drosophila: hybrid sterility and chromosome loss. |
| Q64226572 | The lyase activity of bifunctional DNA glycosylases and the 3'-diesterase activity of APE1 contribute to the repair of oxidized bases in nucleosomes |
| Q28586574 | The mouse ortholog of NEIL3 is a functional DNA glycosylase in vitro and in vivo |
| Q28487547 | The oxidative DNA glycosylases of Mycobacterium tuberculosis exhibit different substrate preferences from their Escherichia coli counterparts |
| Q38350341 | The phosphodiester bond 3' to a deoxyuridine residue is crucial for substrate binding for uracil DNA N-glycosylase. |
| Q52457702 | The relationship between radiation-induced and transposon-induced genetic damage during Drosophila oogenesis. |
| Q52457988 | The relationship between radiation-induced and transposon-induced genetic damage during Drosophila spermatogenesis. |
| Q35564216 | Thymine glycols and urea residues in M13 DNA constitute replicative blocks in vitro. |
| Q54658619 | Thymine ring saturation and fragmentation products: lesion bypass, misinsertion and implications for mutagenesis. |
| Q33665271 | Two glycosylase families diffusively scan DNA using a wedge residue to probe for and identify oxidatively damaged bases |
| Q92557366 | Unhooking of an interstrand cross-link at DNA fork structures by the DNA glycosylase NEIL3 |
| Q54627595 | Uracil DNA N-glycosylase distributively interacts with duplex polynucleotides containing repeating units of either TGGCCAAGCU or TGGCCAAGCTTGGCCAAGCU. |
| Q62061104 | Uracil Glycol Deoxynucleoside Triphosphate Is a Better Substrate for DNA Polymerase I Klenow Fragment Than Thymine Glycol Deoxynucleoside Triphosphate† |
| Q31036870 | Using shifts in amino acid frequency and substitution rate to identify latent structural characters in base-excision repair enzymes |
| Q44198891 | UvrABC nuclease complex repairs thymine glycol, an oxidative DNA base damage |
| Q21558646 | Variant base excision repair proteins: contributors to genomic instability |
| Q29643745 | Susan Wallace | different from | P1889 |
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