scholarly article | Q13442814 |
review article | Q7318358 |
P50 | author | Alexander C Drohat | Q47503014 |
P2093 | author name string | Christopher T Coey | |
P2860 | cites work | MED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1 | Q22009114 |
DNA methylation patterns and epigenetic memory | Q22065780 | ||
Instability and decay of the primary structure of DNA | Q22122361 | ||
Definitive identification of mammalian 5-hydroxymethyluracil DNA N-glycosylase activity as SMUG1 | Q24291615 | ||
Hydroxylation of 5-methylcytosine by TET1 promotes active DNA demethylation in the adult brain | Q24299862 | ||
Mammalian 5-Formyluracil−DNA Glycosylase. 2. Role of SMUG1 Uracil−DNA Glycosylase in Repair of 5-Formyluracil and Other Oxidized and Deaminated Base Lesions | Q24300667 | ||
Thymine DNA glycosylase specifically recognizes 5-carboxylcytosine-modified DNA | Q24305161 | ||
Thymine DNA glycosylase is essential for active DNA demethylation by linked deamination-base excision repair | Q24309357 | ||
Crystal structure of TET2-DNA complex: insight into TET-mediated 5mC oxidation | Q24311603 | ||
Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1 | Q24316558 | ||
Genome demethylation and imprinting in the endosperm | Q34856775 | ||
Role of the Arabidopsis DNA glycosylase/lyase ROS1 in active DNA demethylation | Q34984573 | ||
DNA demethylation in hormone-induced transcriptional derepression | Q35008010 | ||
Differential stabilities and sequence-dependent base pair opening dynamics of Watson-Crick base pairs with 5-hydroxymethylcytosine, 5-formylcytosine, or 5-carboxylcytosine | Q35076369 | ||
A mechanistic perspective on the chemistry of DNA repair glycosylases | Q35171800 | ||
Chemistry and biology of DNA repair | Q35173709 | ||
Gadd45a promotes DNA demethylation through TDG. | Q35562151 | ||
GADD45A protein plays an essential role in active DNA demethylation during terminal osteogenic differentiation of adipose-derived mesenchymal stem cells | Q35562615 | ||
Reading the unique DNA methylation landscape of the brain: Non-CpG methylation, hydroxymethylation, and MeCP2. | Q35699206 | ||
DNA demethylation in the Arabidopsis genome. | Q35741567 | ||
Characterization of the Catalytic Domain of Human APOBEC3B and the Critical Structural Role for a Conserved Methionine | Q35747955 | ||
DNA charge transport as a first step in coordinating the detection of lesions by repair proteins | Q35751064 | ||
A DNA 3' phosphatase functions in active DNA demethylation in Arabidopsis | Q35754674 | ||
The mammalian de novo DNA methyltransferases DNMT3A and DNMT3B are also DNA 5-hydroxymethylcytosine dehydroxymethylases | Q36286073 | ||
Methylcytosine and normal cytosine deamination by the foreign DNA restriction enzyme APOBEC3A | Q36298528 | ||
Efficient deamination of 5-methylcytosines in DNA by human APOBEC3A, but not by AID or APOBEC3G. | Q36305701 | ||
Structure of Naegleria Tet-like dioxygenase (NgTet1) in complexes with a reaction intermediate 5-hydroxymethylcytosine DNA. | Q36370892 | ||
Toward a detailed understanding of base excision repair enzymes: transition state and mechanistic analyses of N-glycoside hydrolysis and N-glycoside transfer | Q36389665 | ||
Uracil-DNA Glycosylase UNG Promotes Tet-mediated DNA Demethylation | Q36442386 | ||
Nucleic acid modifications with epigenetic significance | Q36456771 | ||
Lesion processing by a repair enzyme is severely curtailed by residues needed to prevent aberrant activity on undamaged DNA | Q24319667 | ||
Thymine DNA glycosylase can rapidly excise 5-formylcytosine and 5-carboxylcytosine: potential implications for active demethylation of CpG sites | Q24328865 | ||
Modification of the human thymine-DNA glycosylase by ubiquitin-like proteins facilitates enzymatic turnover | Q24534803 | ||
Identification of 5-formyluracil DNA glycosylase activity of human hNTH1 protein | Q24537479 | ||
Excision of cytosine and thymine from DNA by mutants of human uracil-DNA glycosylase | Q24562354 | ||
Mutational analysis of the damage-recognition and catalytic mechanism of human SMUG1 DNA glycosylase | Q24563901 | ||
Reprogramming towards pluripotency requires AID-dependent DNA demethylation | Q24607262 | ||
A decade of exploring the cancer epigenome - biological and translational implications | Q24614467 | ||
Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine | Q24614582 | ||
Tet-mediated formation of 5-carboxylcytosine and its excision by TDG in mammalian DNA | Q24632387 | ||
Early steps in the DNA base excision/single-strand interruption repair pathway in mammalian cells | Q24650179 | ||
5-halogenated pyrimidine lesions within a CpG sequence context mimic 5-methylcytosine by enhancing the binding of the methyl-CpG-binding domain of methyl-CpG-binding protein 2 (MeCP2). | Q24794741 | ||
Kinetics of substrate recognition and cleavage by human 8-oxoguanine-DNA glycosylase | Q24812802 | ||
Mechanism and function of oxidative reversal of DNA and RNA methylation | Q27002361 | ||
Overview of base excision repair biochemistry | Q27021659 | ||
The Fpg/Nei family of DNA glycosylases: substrates, structures, and search for damage | Q27021912 | ||
Heteronuclear NMR and crystallographic studies of wild-type and H187Q Escherichia coli uracil DNA glycosylase: electrophilic catalysis of uracil expulsion by a neutral histidine 187 | Q27619846 | ||
Structural basis for recognition and repair of the endogenous mutagen 8-oxoguanine in DNA | Q27621681 | ||
Structural and biochemical exploration of a critical amino acid in human 8-oxoguanine glycosylase | Q27640474 | ||
Structural basis for removal of adenine mispaired with 8-oxoguanine by MutY adenine DNA glycosylase | Q27643123 | ||
Atomic substitution reveals the structural basis for substrate adenine recognition and removal by adenine DNA glycosylase | Q27657850 | ||
Separation-of-function mutants unravel the dual-reaction mode of human 8-oxoguanine DNA glycosylase | Q27666499 | ||
Excision of thymine and 5-hydroxymethyluracil by the MBD4 DNA glycosylase domain: structural basis and implications for active DNA demethylation | Q27670542 | ||
Biochemical and structural characterization of the glycosylase domain of MBD4 bound to thymine and 5-hydroxymethyuracil-containing DNA | Q27670999 | ||
Excision of 5-hydroxymethyluracil and 5-carboxylcytosine by the thymine DNA glycosylase domain: its structural basis and implications for active DNA demethylation | Q27672864 | ||
Crystal Structure of Human Methyl-Binding Domain IV Glycosylase Bound to Abasic DNA | Q27678915 | ||
Crystal structures of isoorotate decarboxylases reveal a novel catalytic mechanism of 5-carboxyl-uracil decarboxylation and shed light on the search for DNA decarboxylase | Q27679377 | ||
Structure of a Naegleria Tet-like dioxygenase in complex with 5-methylcytosine DNA | Q27681187 | ||
Postreplicative mismatch repair | Q27690911 | ||
Structural insight into substrate preference for TET-mediated oxidation | Q27702550 | ||
A nucleotide-flipping mechanism from the structure of human uracil-DNA glycosylase bound to DNA | Q27733802 | ||
MutY catalytic core, mutant and bound adenine structures define specificity for DNA repair enzyme superfamily | Q27766319 | ||
Mismatch-specific thymine DNA glycosylase and DNA polymerase beta mediate the correction of G.T mispairs in nuclear extracts from human cells | Q33721136 | ||
A mammalian protein with specific demethylase activity for mCpG DNA. | Q33853552 | ||
An invariant aspartic acid in the DNA glycosylase domain of DEMETER is necessary for transcriptional activation of the imprinted MEDEA gene | Q33906087 | ||
Base excision repair: a critical player in many games | Q33908163 | ||
DEMETER DNA glycosylase establishes MEDEA polycomb gene self-imprinting by allele-specific demethylation. | Q33931372 | ||
X inactivation, differentiation, and DNA methylation | Q33999850 | ||
Methylation-independent DNA binding modulates specificity of Repressor of Silencing 1 (ROS1) and facilitates demethylation in long substrates | Q34003906 | ||
The discovery of 5-formylcytosine in embryonic stem cell DNA. | Q34027511 | ||
An N -Glycosidase from Escherichia coli That Releases Free Uracil from DNA Containing Deaminated Cytosine Residues | Q34052545 | ||
E2-mediated small ubiquitin-like modifier (SUMO) modification of thymine DNA glycosylase is efficient but not selective for the enzyme-product complex | Q34076047 | ||
Genome-wide erasure of DNA methylation in mouse primordial germ cells is affected by AID deficiency. | Q34249450 | ||
Atomic structure of the DNA repair [4Fe-4S] enzyme endonuclease III | Q34256473 | ||
Mechanism of stimulation of the DNA glycosylase activity of hOGG1 by the major human AP endonuclease: bypass of the AP lyase activity step | Q34286685 | ||
Recent advances in the structural mechanisms of DNA glycosylases | Q34306735 | ||
AP endonucleases process 5-methylcytosine excision intermediates during active DNA demethylation in Arabidopsis | Q34313038 | ||
Domain structure of the DEMETER 5-methylcytosine DNA glycosylase | Q34320211 | ||
Mammalian base excision repair: the forgotten archangel | Q34327812 | ||
AID enzymatic activity is inversely proportional to the size of cytosine C5 orbital cloud | Q34391465 | ||
Genome-wide high-resolution mapping and functional analysis of DNA methylation in arabidopsis | Q34562910 | ||
DEMETER and REPRESSOR OF SILENCING 1 encode 5-methylcytosine DNA glycosylases. | Q34598249 | ||
CpG-rich islands and the function of DNA methylation | Q28131800 | ||
The thymine glycosylase MBD4 can bind to the product of deamination at methylated CpG sites | Q28145111 | ||
Uracil-DNA glycosylase acts by substrate autocatalysis | Q28199337 | ||
Role of base excision repair in maintaining the genetic and epigenetic integrity of CpG sites | Q28262535 | ||
DNA Methylation and Gene Function | Q28263722 | ||
The purification of a mismatch-specific thymine-DNA glycosylase from HeLa cells | Q28264721 | ||
Purification and characterization of human NTH1, a homolog of Escherichia coli endonuclease III. Direct identification of Lys-212 as the active nucleophilic residue | Q28279728 | ||
Activation-induced cytidine deaminase deaminates 5-methylcytosine in DNA and is expressed in pluripotent tissues: implications for epigenetic reprogramming | Q28284694 | ||
Base excision repair | Q28288115 | ||
DNA mismatch repair: functions and mechanisms | Q28296096 | ||
CpG islands and the regulation of transcription | Q28315762 | ||
Role of Tet proteins in 5mC to 5hmC conversion, ES-cell self-renewal and inner cell mass specification | Q28504641 | ||
Embryonic lethal phenotype reveals a function of TDG in maintaining epigenetic stability | Q28508931 | ||
Mammalian 5-formyluracil-DNA glycosylase. 1. Identification and characterization of a novel activity that releases 5-formyluracil from DNA | Q28577035 | ||
Quality control by DNA repair | Q28608962 | ||
Stimulation of human 8-oxoguanine-DNA glycosylase by AP-endonuclease: potential coordination of the initial steps in base excision repair | Q28645611 | ||
Dependence of substrate binding and catalysis on pH, ionic strength, and temperature for thymine DNA glycosylase: Insights into recognition and processing of G·T mispairs | Q28740645 | ||
Crystal structure of thymine DNA glycosylase conjugated to SUMO-1 | Q28910402 | ||
Base-excision repair of oxidative DNA damage | Q29615373 | ||
Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning | Q29615977 | ||
Cancer epigenetics comes of age | Q29617275 | ||
The DNA methyltransferases of mammals | Q29617317 | ||
The role of DNA methylation in mammalian epigenetics | Q29617979 | ||
Distribution, recognition and regulation of non-CpG methylation in the adult mammalian brain | Q30433875 | ||
Role of electrophilic and general base catalysis in the mechanism of Escherichia coli uracil DNA glycosylase. | Q30582190 | ||
Conformation and proton configuration of pyrimidine deoxynucleoside oxidation damage products in water | Q30597717 | ||
Escherichia coli uracil DNA glycosylase: NMR characterization of the short hydrogen bond from His187 to uracil O2. | Q30614512 | ||
Thymine DNA glycosylase exhibits negligible affinity for nucleobases that it removes from DNA | Q30992958 | ||
Transition-state analysis of the DNA repair enzyme MutY. | Q31151684 | ||
5-methylcytosine-DNA glycosylase activity is present in a cloned G/T mismatch DNA glycosylase associated with the chicken embryo DNA demethylation complex | Q33180228 | ||
Genes of the thymidine salvage pathway: thymine-7-hydroxylase from a Rhodotorula glutinis cDNA library and iso-orotate decarboxylase from Neurospora crassa | Q33213312 | ||
GADD45A does not promote DNA demethylation | Q33325901 | ||
Base excision repair of tandem modifications in a methylated CpG dinucleotide. | Q33619413 | ||
Active DNA demethylation in plant companion cells reinforces transposon methylation in gametes | Q33668697 | ||
TET enzymes, TDG and the dynamics of DNA demethylation. | Q33715010 | ||
Effects of cytosine modifications on DNA flexibility and nucleosome mechanical stability | Q36627544 | ||
Biochemical reconstitution of TET1-TDG-BER-dependent active DNA demethylation reveals a highly coordinated mechanism | Q36651017 | ||
The mechanics of base excision repair, and its relationship to aging and disease | Q36656724 | ||
Weakened N3 Hydrogen Bonding by 5-Formylcytosine and 5-Carboxylcytosine Reduces Their Base-Pairing Stability | Q36662987 | ||
Selective excision of 5-carboxylcytosine by a thymine DNA glycosylase mutant. | Q36674636 | ||
DNA-mediated charge transport for DNA repair | Q36689389 | ||
Genome-wide profiling of 5-formylcytosine reveals its roles in epigenetic priming | Q36853522 | ||
Active DNA demethylation in plants and animals. | Q36854300 | ||
Characterizing Requirements for Small Ubiquitin-like Modifier (SUMO) Modification and Binding on Base Excision Repair Activity of Thymine-DNA Glycosylase in Vivo | Q36884795 | ||
Reprogramming of DNA methylation in pollen guides epigenetic inheritance via small RNA | Q36970371 | ||
The DNA glycosylase AlkD uses a non-base-flipping mechanism to excise bulky lesions | Q36977957 | ||
DNA demethylation in zebrafish involves the coupling of a deaminase, a glycosylase, and gadd45. | Q37068711 | ||
Stochastic properties of processive cytidine DNA deaminases AID and APOBEC3G. | Q37140478 | ||
The AID/APOBEC family of nucleic acid mutators. | Q37206307 | ||
Mechanisms of base selection by human single-stranded selective monofunctional uracil-DNA glycosylase | Q37257364 | ||
ROS1 5-methylcytosine DNA glycosylase is a slow-turnover catalyst that initiates DNA demethylation in a distributive fashion | Q37273644 | ||
Redox signaling between DNA repair proteins for efficient lesion detection | Q37340789 | ||
Role of two strictly conserved residues in nucleotide flipping and N-glycosylic bond cleavage by human thymine DNA glycosylase | Q37479458 | ||
Divergent mechanisms for enzymatic excision of 5-formylcytosine and 5-carboxylcytosine from DNA. | Q37595036 | ||
A TET homologue protein from Coprinopsis cinerea (CcTET) that biochemically converts 5-methylcytosine to 5-hydroxymethylcytosine, 5-formylcytosine, and 5-carboxylcytosine | Q37701368 | ||
5-methylcytosine recognition by Arabidopsis thaliana DNA glycosylases DEMETER and DML3 | Q37731556 | ||
Detection of damaged DNA bases by DNA glycosylase enzymes | Q37752315 | ||
The curious chemical biology of cytosine: deamination, methylation, and oxidation as modulators of genomic potential. | Q37946460 | ||
Advances in understanding the coupling of DNA base modifying enzymes to processes involving base excision repair. | Q38122803 | ||
Mechanisms for enzymatic cleavage of the N-glycosidic bond in DNA. | Q38245504 | ||
Probing the limits of electrostatic catalysis by uracil DNA glycosylase using transition state mimicry and mutagenesis. | Q38291765 | ||
5-Methylcytosine DNA glycosylase activity is also present in the human MBD4 (G/T mismatch glycosylase) and in a related avian sequence | Q38307104 | ||
Substrate specificity and reaction mechanism of murine 8-oxoguanine-DNA glycosylase | Q38310719 | ||
Functionality of human thymine DNA glycosylase requires SUMO-regulated changes in protein conformation | Q38328146 | ||
Human thymine DNA glycosylase binds to apurinic sites in DNA but is displaced by human apurinic endonuclease 1. | Q38330113 | ||
A mammalian DNA repair enzyme that excises oxidatively damaged guanines maps to a locus frequently lost in lung cancer | Q38345459 | ||
Repair of the mutagenic DNA oxidation product, 5-formyluracil | Q38358598 | ||
Tet2 Catalyzes Stepwise 5-Methylcytosine Oxidation by an Iterative and de novo Mechanism. | Q38587746 | ||
Neil DNA glycosylases promote substrate turnover by Tdg during DNA demethylation. | Q38804981 | ||
An ONIOM and MD Investigation of Possible Monofunctional Activity of Human 8-Oxoguanine-DNA Glycosylase (hOgg1). | Q39001898 | ||
DNA-mediated signaling by proteins with 4Fe-4S clusters is necessary for genomic integrity | Q39494713 | ||
Cyclical DNA methylation of a transcriptionally active promoter | Q40005351 | ||
The DNA N-glycosylase MED1 exhibits preference for halogenated pyrimidines and is involved in the cytotoxicity of 5-iododeoxyuridine. | Q40248506 | ||
GADD45a physically and functionally interacts with TET1 | Q40347085 | ||
Counteracting the mutagenic effect of hydrolytic deamination of DNA 5-methylcytosine residues at high temperature: DNA mismatch N-glycosylase Mig.Mth of the thermophilic archaeon Methanobacterium thermoautotrophicum THF | Q41077567 | ||
DNA charge transport for sensing and signaling | Q41233751 | ||
Transition state analysis of thymidine hydrolysis by human thymidine phosphorylase | Q41906991 | ||
AID/APOBEC deaminases disfavor modified cytosines implicated in DNA demethylation. | Q41917830 | ||
Coordinating the initial steps of base excision repair. Apurinic/apyrimidinic endonuclease 1 actively stimulates thymine DNA glycosylase by disrupting the product complex | Q41952309 | ||
Specificity of human thymine DNA glycosylase depends on N-glycosidic bond stability | Q42161686 | ||
The DNA repair protein XRCC1 functions in the plant DNA demethylation pathway by stimulating cytosine methylation (5-meC) excision, gap tailoring, and DNA ligation | Q42182040 | ||
Mechanisms of base selection by the Escherichia coli mispaired uracil glycosylase | Q42182897 | ||
A discontinuous DNA glycosylase domain in a family of enzymes that excise 5-methylcytosine | Q42567554 | ||
Fe(II)/alpha-ketoglutarate hydroxylases involved in nucleobase, nucleoside, nucleotide, and chromatin metabolism | Q42719732 | ||
Base-resolution maps of 5-formylcytosine and 5-carboxylcytosine reveal genome-wide DNA demethylation dynamics | Q42738710 | ||
TET-mediated oxidation of methylcytosine causes TDG or NEIL glycosylase dependent gene reactivation | Q42761123 | ||
5-Formylcytosine alters the structure of the DNA double helix | Q43096431 | ||
Genome-wide analysis reveals TET- and TDG-dependent 5-methylcytosine oxidation dynamics. | Q43121080 | ||
Uracil and thymine reactivity in the gas phase: the S(N)2 reaction and implications for electron delocalization in leaving groups | Q43237888 | ||
Kinetics and binding of the thymine-DNA mismatch glycosylase, Mig-Mth, with mismatch-containing DNA substrates | Q44267635 | ||
ROS1, a repressor of transcriptional gene silencing in Arabidopsis, encodes a DNA glycosylase/lyase | Q44277312 | ||
Rational Engineering of a DNA Glycosylase Specific for an Unnatural Cytosine:Pyrene Base Pair | Q44426214 | ||
Product inhibition and magnesium modulate the dual reaction mode of hOgg1. | Q45231852 | ||
Genetic interactions between DNA demethylation and methylation in Arabidopsis. | Q45962529 | ||
DEMETER, a DNA glycosylase domain protein, is required for endosperm gene imprinting and seed viability in arabidopsis. | Q45981966 | ||
Cytosine-5-methyltransferases add aldehydes to DNA. | Q46017177 | ||
Synthesis and characterization of isotopically enriched pyrimidine deoxynucleoside oxidation damage products | Q46082221 | ||
Arabidopsis DEMETER-LIKE proteins DML2 and DML3 are required for appropriate distribution of DNA methylation marks. | Q46584490 | ||
Synthesis and properties of oligodeoxynucleotides containing 5-carboxy-2'-deoxycytidines. | Q46893221 | ||
Deamination, oxidation, and C-C bond cleavage reactivity of 5-hydroxymethylcytosine, 5-formylcytosine, and 5-carboxycytosine | Q47691191 | ||
Establishment of methylation patterns in ES cells. | Q50703085 | ||
Genome-wide analysis of Arabidopsis thaliana DNA methylation uncovers an interdependence between methylation and transcription. | Q53013759 | ||
Direct decarboxylation of 5-carboxylcytosine by DNA C5-methyltransferases. | Q53058810 | ||
Transition state analysis of acid-catalyzed dAMP hydrolysis. | Q53553616 | ||
Crystallization and crystallographic characterization of the iron-sulfur-containing DNA-repair enzyme endonuclease III from Escherichia coli. | Q54673167 | ||
Mechanism and Stem-Cell Activity of 5-Carboxycytosine Decarboxylation Determined by Isotope Tracing | Q57376743 | ||
Improved Synthesis and Mutagenicity of Oligonucleotides Containing 5-Hydroxymethylcytosine, 5-Formylcytosine and 5-Carboxylcytosine | Q57376757 | ||
Acidic hydrolysis of deoxycytidine and deoxyuridine derivatives. The general mechanism of deoxyribonucleoside hydrolysis | Q67278441 | ||
Aromatic substituent constants for structure-activity correlations | Q69600149 | ||
Kinetic isotope effect studies of the reaction catalyzed by uracil DNA glycosylase: evidence for an oxocarbenium ion-uracil anion intermediate | Q73212716 | ||
The critical active-site amine of the human 8-oxoguanine DNA glycosylase, hOgg1: direct identification, ablation and chemical reconstitution | Q73790587 | ||
PYRIMIDINES. I. THE SYNTHESIS OF 6-FLUOROCYTOSINE AND RELATED COMPOUNDS | Q76892774 | ||
Single-Base Resolution Analysis of 5-Formyl and 5-Carboxyl Cytosine Reveals Promoter DNA Methylation Dynamics | Q86688630 | ||
P433 | issue | 20 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 12711-12729 | |
P577 | publication date | 2016-08-08 | |
P1433 | published in | Chemical Reviews | Q900502 |
P1476 | title | Role of Base Excision "Repair" Enzymes in Erasing Epigenetic Marks from DNA | |
P478 | volume | 116 |
Q41510570 | APOBEC3A efficiently deaminates methylated, but not TET-oxidized, cytosine bases in DNA. |
Q58716914 | APURINIC/APYRIMIDINIC ENDONUCLEASE2 and ZINC FINGER DNA 3'-PHOSPHOESTERASE Play Overlapping Roles in the Maintenance of Epigenome and Genome Stability |
Q55321915 | Base-flipping dynamics from an intrahelical to an extrahelical state exerted by thymine DNA glycosylase during DNA repair process. |
Q90350691 | Comparison of DNA and RNA substrate effects on TET2 structure |
Q92174412 | Defining the Role of Nucleotide Flipping in Enzyme Specificity Using 19F NMR |
Q55446744 | Defining the impact of sumoylation on substrate binding and catalysis by thymine DNA glycosylase. |
Q49170182 | Dynamics of the excised base release in thymine DNA glycosylase during DNA repair process |
Q49917892 | Harnessing natural DNA modifying activities for editing of the genome and epigenome. |
Q64255145 | High-resolution DNA methylome reveals that demethylation enhances adaptability to continuous cropping comprehensive stress in soybean |
Q92122417 | Mitochondrial DNA: Epigenetics and environment |
Q92809345 | Oxidative DNA Damage Modulates DNA Methylation Pattern in Human Breast Cancer 1 (BRCA1) Gene via the Crosstalk between DNA Polymerase β and a de novo DNA Methyltransferase |
Q39200289 | Repair of oxidatively induced DNA damage by DNA glycosylases: Mechanisms of action, substrate specificities and excision kinetics |
Q52720777 | Simultaneous sensitive detection of multiple DNA glycosylases from lung cancer cells at the single-molecule level. |
Q38290315 | Structural Basis for Excision of 5-Formylcytosine by Thymine DNA Glycosylase |
Q58760147 | The effect of dietary level of two inulin types differing in chain length on biogenic amine concentration, oxidant-antioxidant balance and DNA repair in the colon of piglets |
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