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DNA repair

Index DNA repair

DNA repair is a collection of processes by which a cell identifies and corrects damage to the DNA molecules that encode its genome. [1]

279 relations: Adaptive behavior, Adaptive response, Adenosine diphosphate ribose, Adenosine triphosphate, AGT II, Alkylation, Animal, AP endonuclease, AP site, Apoptosis, Aromaticity, Ataxia telangiectasia and Rad3 related, Ataxia-telangiectasia, ATM serine/threonine kinase, ATP hydrolysis, Aziz Sancar, B-cell receptor, Bacteria, Bacteriophage, Basal metabolic rate, Base excision repair, Base pair, Biomolecular structure, Biomolecule, Bloom syndrome, BRCA1, BRCA2, Breast cancer, C-Jun N-terminal kinases, Caenorhabditis elegans, Calorie restriction, Cancer, Cancer epigenetics, Carbohydrate, Carcinogenesis, Catalysis, Cell (biology), Cell cycle, Cell cycle checkpoint, Cell division, Cell nucleus, Cell signaling, CHD1L, CHD4, CHEK1, Chemotherapy, Chromatid, Chromatin, Chromatin remodeling, Chromosomal crossover, ..., Chromosome, Cockayne syndrome, Colorectal cancer, Conserved sequence, Cosmic ray, CRISPR, Crosslinking of DNA, CUL4A, Cyclic compound, Cyclin, Cyclin-dependent kinase, Cyclin-dependent kinase inhibitor protein, Cytoplasm, D-loop, DDB1, DDB2, Deamination, Deinococcus radiodurans, Depurination, Direct DNA damage, DNA, DNA adduct, DNA damage (naturally occurring), DNA damage theory of aging, DNA glycosylase, DNA ligase, DNA methylation, DNA mismatch repair, DNA oxidation, DNA polymerase, DNA polymerase eta, DNA repair, DNA repair protein XRCC4, DNA repair-deficiency disorder, DNA replication, DNA supercoil, Electromagnetic spectrum, Endogeny (biology), Endonuclease, Epigenetics, ERCC1, ERCC4, Escherichia coli, ETS1, Eukaryote, Evolution, Extremophile, FANCB, FANCF, Fanconi anemia, Flap structure-specific endonuclease 1, Fossil, Fungus, G0 phase, G1 phase, G2 phase, Gamete, Gamma ray, Gene, Gene conversion, Gene dosage, Gene expression, Gene therapy, Genome, Genome instability, Germline, Great Oxygenation Event, H2AFX, Hayflick limit, Helicase, Hereditary nonpolyposis colorectal cancer, Heterochromatin, Histone, Histone-modifying enzymes, HMGA1, HMGA2, Homogeneity and heterogeneity, Homologous chromosome, Homologous recombination, Hoogsteen base pair, Hot spring, Human mitochondrial genetics, Hydrogen peroxide, Hydrolysis, Immune system, Indirect DNA damage, Intercalation (biochemistry), Ionizing radiation, Kinase, Knudson hypothesis, Lesion, Leukemia, Li–Fraumeni syndrome, Life expectancy, Life extension, LIG3, LIG4, Lipid, Lymphoma, Malignancy, Mammal, MDC1, Metabolism, Metaphase, Methylation, Mi-2/NuRD complex, Microhomology-mediated end joining, MicroRNA, MiR-155, Missense mutation, Mitochondrion, Mitosis, MLH1, Molecular lesion, MRE11A, MSH2, MSH4, MTOR, Mutagen, Mutation, Mutation Research (journal), Nanometre, NEIL1, Neoplasm, Nitrogenous base, Nobel Prize, Nobel Prize in Chemistry, Non-coding DNA, Non-homologous end joining, Nucleic acid, Nucleic acid sequence, Nucleic acid thermodynamics, Nucleotide excision repair, Nutrient sensing, O-6-methylguanine-DNA methyltransferase, Olaparib, Operator (biology), Organelle, Oxidative deamination, Oxidative phosphorylation, Oxidative stress, P21, P53, Palindrome, PARP1, Paul L. Modrich, Phosphoinositide 3-kinase, Phosphorylation, Photolyase, Photosynthesis, Plant, Pleiotropy, PMS2, Point mutation, POLI, Polycyclic aromatic hydrocarbon, Polymer, Polymerase, Post-translational modification, Postreplication repair, Precambrian, Processivity, Progeria, Progeroid syndromes, Programmed cell death, Prokaryote, Proliferating cell nuclear antigen, Proofreading (biology), Protease, Protein, Protein dimer, Protein kinase, Purine, Pyrimidine dimer, RAD18, RAD51, Radiation, Radiation therapy, Radical (chemistry), Radioactive decay, Reactive oxygen species, RecA, Repressor, Repressor lexA, RNA, RNF8, S phase, Saccharomyces cerevisiae, Senescence, Shock response spectrum, Short hairpin RNA, SiDNA, Signal transduction, Sirtuin 6, SOS response, Spirochaete, Stoichiometry, Structural motif, Superoxide dismutase, T-cell receptor, Telomere, The New York Times, Thermophile, Tomas Lindahl, Topoisomerase, Toxin, TP53BP1, Transcription (biology), Trichothiodystrophy, Tumor suppressor, Tumour heterogeneity, Ubiquitin ligase, Ultraviolet, UvrABC endonuclease, V(D)J recombination, Vertebrate, Vinyl chloride, Virus, Wavelength, Werner syndrome, Werner syndrome helicase, X-ray, Xeroderma pigmentosum, XRCC1, Yeast, 1,000,000, 6-O-Methylguanine, 7-Methylguanosine, 8-Oxo-2'-deoxyguanosine. Expand index (229 more) »

Adaptive behavior

Adaptive behavior refers to behavior that enables a person (usually used in the context of children) to get along in his or her environment with greatest success and least conflict with others.

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Adaptive response

The adaptive response is a form of direct DNA repair in E. coli that protects DNA from damage by external agents or by errors during replication.

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Adenosine diphosphate ribose

Adenosine diphosphate ribose is an ester molecule formed into chains by the enzyme poly ADP ribose polymerase.

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Adenosine triphosphate

Adenosine triphosphate (ATP) is a complex organic chemical that participates in many processes.

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AGT II

O6-alkylguanine DNA alkyltransferase II (O6 AGT II) previously known as O6 Guanine transferase (ogt) is a bacterial protein that is involved in DNA repair together with Ada (also known as O6 AGT I).

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Alkylation

Alkylation is the transfer of an alkyl group from one molecule to another.

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Animal

Animals are multicellular eukaryotic organisms that form the biological kingdom Animalia.

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AP endonuclease

Apurinic/apyrimidinic (AP) endonuclease is an enzyme that is involved in the DNA base excision repair pathway (BER).

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AP site

In biochemistry and molecular genetics, an AP site (apurinic/apyrimidinic site), also known as an abasic site, is a location in DNA (also in RNA but much less likely) that has neither a purine nor a pyrimidine base, either spontaneously or due to DNA damage.

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Apoptosis

Apoptosis (from Ancient Greek ἀπόπτωσις "falling off") is a process of programmed cell death that occurs in multicellular organisms.

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Aromaticity

In organic chemistry, the term aromaticity is used to describe a cyclic (ring-shaped), planar (flat) molecule with a ring of resonance bonds that exhibits more stability than other geometric or connective arrangements with the same set of atoms.

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Ataxia telangiectasia and Rad3 related

Serine/threonine-protein kinase ATR also known as ataxia telangiectasia and Rad3-related protein (ATR) or FRAP-related protein 1 (FRP1) is an enzyme that, in humans, is encoded by the ATR gene.

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Ataxia-telangiectasia

Ataxia-telangiectasia (AT or A-T), also referred to as ataxia-telangiectasia syndrome or Louis–Bar syndrome, is a rare, neurodegenerative, autosomal recessive disease causing severe disability.

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ATM serine/threonine kinase

ATM serine/threonine kinase, symbol ATM, is a serine/threonine protein kinase that is recruited and activated by DNA double-strand breaks.

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ATP hydrolysis

ATP hydrolysis is the catabolic reaction process by which chemical energy that has been stored in the high-energy phosphoanhydride bonds in adenosine triphosphate (ATP) is released by splitting these bonds, for example in muscles, by producing work in the form of mechanical energy.

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Aziz Sancar

Aziz Sancar (born 8September 1946) is a Turkish-American biochemist and molecular biologist specializing in DNA repair, cell cycle checkpoints, and circadian clock.

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B-cell receptor

The B-cell receptor or BCR is composed of immunoglobulin molecules that form a type 1 transmembrane receptor protein usually located on the outer surface of a lymphocyte type known as B cells.

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Bacteria

Bacteria (common noun bacteria, singular bacterium) is a type of biological cell.

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Bacteriophage

A bacteriophage, also known informally as a phage, is a virus that infects and replicates within Bacteria and Archaea.

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Basal metabolic rate

Basal metabolic rate (BMR) is the rate of energy expenditure per unit time by endothermic animals at rest.

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Base excision repair

In biochemistry and genetics, base excision repair (BER) is a cellular mechanism that repairs damaged DNA throughout the cell cycle.

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Base pair

A base pair (bp) is a unit consisting of two nucleobases bound to each other by hydrogen bonds.

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Biomolecular structure

Biomolecular structure is the intricate folded, three-dimensional shape that is formed by a molecule of protein, DNA, or RNA, and that is important to its function.

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Biomolecule

A biomolecule or biological molecule is a loosely used term for molecules and ions that are present in organisms, essential to some typically biological process such as cell division, morphogenesis, or development.

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Bloom syndrome

Bloom syndrome (often abbreviated as BS in literature), also known as Bloom-Torre-Machacek syndrome, is a rare autosomal recessive disorder characterized by short stature, predisposition to the development of cancer and genomic instability.

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BRCA1

BRCA1 and BRCA1 are a human gene and its protein product, respectively.

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BRCA2

BRCA2 and BRCA2 are a human gene and its protein product, respectively.

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Breast cancer

Breast cancer is cancer that develops from breast tissue.

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C-Jun N-terminal kinases

c-Jun N-terminal kinases (JNKs), were originally identified as kinases that bind and phosphorylate c-Jun on Ser-63 and Ser-73 within its transcriptional activation domain.

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Caenorhabditis elegans

Caenorhabditis elegans is a free-living (not parasitic), transparent nematode (roundworm), about 1 mm in length, that lives in temperate soil environments.

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Calorie restriction

Calorie restriction, or caloric restriction, or energy restriction, is a dietary regimen that reduces calorie intake without incurring malnutrition or a reduction in essential nutrients.

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Cancer

Cancer is a group of diseases involving abnormal cell growth with the potential to invade or spread to other parts of the body.

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Cancer epigenetics

Cancer epigenetics is the study of epigenetic modifications to the DNA of cancer cells that do not involve a change in the nucleotide sequence.

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Carbohydrate

A carbohydrate is a biomolecule consisting of carbon (C), hydrogen (H) and oxygen (O) atoms, usually with a hydrogen–oxygen atom ratio of 2:1 (as in water); in other words, with the empirical formula (where m may be different from n).

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Carcinogenesis

Carcinogenesis, also called oncogenesis or tumorigenesis, is the formation of a cancer, whereby normal cells are transformed into cancer cells.

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Catalysis

Catalysis is the increase in the rate of a chemical reaction due to the participation of an additional substance called a catalysthttp://goldbook.iupac.org/C00876.html, which is not consumed in the catalyzed reaction and can continue to act repeatedly.

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Cell (biology)

The cell (from Latin cella, meaning "small room") is the basic structural, functional, and biological unit of all known living organisms.

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Cell cycle

The cell cycle or cell-division cycle is the series of events that take place in a cell leading to its division and duplication of its DNA (DNA replication) to produce two daughter cells.

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Cell cycle checkpoint

Cell cycle checkpoints are control mechanisms in eukaryotic cells which ensure proper division of the cell.

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Cell division

Cell division is the process by which a parent cell divides into two or more daughter cells.

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Cell nucleus

In cell biology, the nucleus (pl. nuclei; from Latin nucleus or nuculeus, meaning kernel or seed) is a membrane-enclosed organelle found in eukaryotic cells.

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Cell signaling

Cell signaling (cell signalling in British English) is part of any communication process that governs basic activities of cells and coordinates all cell actions.

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CHD1L

Chromodomain-helicase-DNA-binding protein 1-like (ALC1) is an enzyme that in humans is encoded by the CHD1L gene.

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CHD4

Chromodomain-helicase-DNA-binding protein 4 is an enzyme that in humans is encoded by the CHD4 gene.

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CHEK1

Checkpoint kinase 1, commonly referred to as Chk1 is an Serine/threonine-specific protein kinase that in humans, is encoded by the CHEK1 gene.

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Chemotherapy

Chemotherapy (often abbreviated to chemo and sometimes CTX or CTx) is a type of cancer treatment that uses one or more anti-cancer drugs (chemotherapeutic agents) as part of a standardized chemotherapy regimen.

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Chromatid

A chromatid (Greek khrōmat- 'color' + -id) is one copy of a newly copied chromosome which is still joined to the original chromosome by a single centromere.

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Chromatin

Chromatin is a complex of macromolecules found in cells, consisting of DNA, protein, and RNA.

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Chromatin remodeling

Chromatin remodeling is the dynamic modification of chromatin architecture to allow access of condensed genomic DNA to the regulatory transcription machinery proteins, and thereby control gene expression.

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Chromosomal crossover

Chromosomal crossover (or crossing over) is the exchange of genetic material between homologous chromosomes that results in recombinant chromosomes during sexual reproduction.

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Chromosome

A chromosome (from Ancient Greek: χρωμόσωμα, chromosoma, chroma means colour, soma means body) is a DNA molecule with part or all of the genetic material (genome) of an organism.

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Cockayne syndrome

Cockayne syndrome (CS), also called Neill-Dingwall syndrome, is a rare and fatal autosomal recessive neurodegenerative disorder characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight (photosensitivity), eye disorders and premature aging.

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Colorectal cancer

Colorectal cancer (CRC), also known as bowel cancer and colon cancer, is the development of cancer from the colon or rectum (parts of the large intestine).

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Conserved sequence

In evolutionary biology, conserved sequences are similar or identical sequences in nucleic acids (DNA and RNA) or proteins across species (orthologous sequences) or within a genome (paralogous sequences).

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Cosmic ray

Cosmic rays are high-energy radiation, mainly originating outside the Solar System and even from distant galaxies.

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CRISPR

CRISPR is a family of DNA sequences in bacteria and archaea.

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Crosslinking of DNA

In genetics, crosslinking of DNA occurs when various exogenous or endogenous agents react with two nucleotides of DNA, forming a covalent linkage between them.

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CUL4A

Cullin-4A is a protein that in humans is encoded by the CUL4A gene.

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Cyclic compound

A cyclic compound (ring compound) is a term for a compound in the field of chemistry in which one or more series of atoms in the compound is connected to form a ring.

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Cyclin

Cyclin is a family of proteins that control the progression of cells through the cell cycle by activating cyclin-dependent kinase (Cdk) enzymes.

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Cyclin-dependent kinase

Gap phase 2. The duration of mitosis in relation to the other phases has been exaggerated in this diagram Cyclin-dependent kinases (CDKs) are a family of sugar kinases first discovered for their role in regulating the cell cycle.

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Cyclin-dependent kinase inhibitor protein

A cyclin-dependent kinase inhibitor protein is a protein which inhibits cyclin-dependent kinase.

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Cytoplasm

In cell biology, the cytoplasm is the material within a living cell, excluding the cell nucleus.

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D-loop

In molecular biology, a displacement loop or D-loop is a DNA structure where the two strands of a double-stranded DNA molecule are separated for a stretch and held apart by a third strand of DNA.

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DDB1

DNA damage-binding protein 1 is a protein that in humans is encoded by the DDB1 gene.

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DDB2

DNA damage-binding protein 2 is a protein that in humans is encoded by the DDB2 gene.

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Deamination

Deamination is the removal of an amine group from a protein molecule.

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Deinococcus radiodurans

Deinococcus radiodurans is an extremophilic bacterium, one of the most radiation-resistant organisms known.

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Depurination

Depurination is a chemical reaction of purine deoxyribonucleosides, deoxyadenosine and deoxyguanosine, and ribonucleosides, adenosine or guanosine, in which the β-N-glycosidic bond is hydrolytically cleaved releasing a nucleic base, adenine or guanine, respectively.

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Direct DNA damage

Direct DNA damage can occur when DNA directly absorbs a UVB photon, or for numerous other reasons.

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DNA

Deoxyribonucleic acid (DNA) is a thread-like chain of nucleotides carrying the genetic instructions used in the growth, development, functioning and reproduction of all known living organisms and many viruses.

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DNA adduct

In molecular genetics, a DNA adduct is a segment of DNA bound to a cancer-causing chemical.

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DNA damage (naturally occurring)

DNA damage is distinctly different from mutation, although both are types of error in DNA.

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DNA damage theory of aging

The DNA damage theory of aging proposes that aging is a consequence of unrepaired accumulation of naturally occurring DNA damages.

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DNA glycosylase

DNA glycosylases are a family of enzymes involved in base excision repair, classified under EC number EC 3.2.2.

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DNA ligase

DNA ligase is a specific type of enzyme, a ligase, that facilitates the joining of DNA strands together by catalyzing the formation of a phosphodiester bond.

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DNA methylation

DNA methylation is a process by which methyl groups are added to the DNA molecule.

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DNA mismatch repair

DNA mismatch repair (MMR) is a system for recognizing and repairing erroneous insertion, deletion, and mis-incorporation of bases that can arise during DNA replication and recombination, as well as repairing some forms of DNA damage.

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DNA oxidation

DNA oxidation is the process of oxidative damage of deoxyribonucleic acid.

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DNA polymerase

DNA polymerases are enzymes that synthesize DNA molecules from deoxyribonucleotides, the building blocks of DNA.

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DNA polymerase eta

DNA polymerase eta (Pol η), is a protein that in humans is encoded by the POLH gene.

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DNA repair

DNA repair is a collection of processes by which a cell identifies and corrects damage to the DNA molecules that encode its genome.

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DNA repair protein XRCC4

DNA repair protein XRCC4 also known as X-ray repair cross-complementing protein 4 or XRCC4 is a protein that in humans is encoded by the XRCC4 gene.

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DNA repair-deficiency disorder

A DNA repair-deficiency disorder is a medical condition due to reduced functionality of DNA repair.

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DNA replication

In molecular biology, DNA replication is the biological process of producing two identical replicas of DNA from one original DNA molecule.

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DNA supercoil

DNA supercoiling refers to the over- or under-winding of a DNA strand, and is an expression of the strain on that strand.

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Electromagnetic spectrum

The electromagnetic spectrum is the range of frequencies (the spectrum) of electromagnetic radiation and their respective wavelengths and photon energies.

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Endogeny (biology)

Endogenous substances and processes are those that originate from within an organism, tissue, or cell.

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Endonuclease

Endonucleases are enzymes that cleave the phosphodiester bond within a polynucleotide chain.

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Epigenetics

Epigenetics is the study of heritable changes in gene function that do not involve changes in the DNA sequence.

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ERCC1

DNA excision repair protein ERCC-1 is a protein that in humans is encoded by the ERCC1 gene.

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ERCC4

ERCC4 is a protein designated as DNA repair endonuclease XPF that in humans is encoded by the ERCC4 gene.

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Escherichia coli

Escherichia coli (also known as E. coli) is a Gram-negative, facultatively anaerobic, rod-shaped, coliform bacterium of the genus Escherichia that is commonly found in the lower intestine of warm-blooded organisms (endotherms).

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ETS1

Protein C-ets-1 is a protein that in humans is encoded by the ETS1 gene.

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Eukaryote

Eukaryotes are organisms whose cells have a nucleus enclosed within membranes, unlike Prokaryotes (Bacteria and other Archaea).

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Evolution

Evolution is change in the heritable characteristics of biological populations over successive generations.

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Extremophile

An extremophile (from Latin extremus meaning "extreme" and Greek philiā (φιλία) meaning "love") is an organism that thrives in physically or geochemically extreme conditions that are detrimental to most life on Earth.

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FANCB

Fanconi anemia group B protein is a protein that in humans is encoded by the FANCB gene.

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FANCF

Fanconi anemia group F protein is a protein that in humans is encoded by the FANCF gene.

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Fanconi anemia

Fanconi anaemia (FA) is a rare genetic disease resulting in impaired response to DNA damage.

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Flap structure-specific endonuclease 1

Flap endonuclease 1 is an enzyme that in humans is encoded by the FEN1 gene.

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Fossil

A fossil (from Classical Latin fossilis; literally, "obtained by digging") is any preserved remains, impression, or trace of any once-living thing from a past geological age.

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Fungus

A fungus (plural: fungi or funguses) is any member of the group of eukaryotic organisms that includes microorganisms such as yeasts and molds, as well as the more familiar mushrooms.

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G0 phase

The G0 phase describes a cellular state outside of the replicative cell cycle.

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G1 phase

The g1 phase, or Gap 1 phase, is the first of four phases of the cell cycle that takes place in eukaryotic cell division.

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G2 phase

G2 phase, or Gap 2 phase, is the second subphase of Interphase in the cell cycle directly preceding mitosis.

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Gamete

A gamete (from Ancient Greek γαμετή gamete from gamein "to marry") is a haploid cell that fuses with another haploid cell during fertilization (conception) in organisms that sexually reproduce.

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Gamma ray

A gamma ray or gamma radiation (symbol γ or \gamma), is penetrating electromagnetic radiation arising from the radioactive decay of atomic nuclei.

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Gene

In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.

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Gene conversion

Gene conversion is the process by which one DNA sequence replaces a homologous sequence such that the sequences become identical after the conversion event.

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Gene dosage

Gene dosage is the number of copies of a particular gene present in a genome.

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Gene expression

Gene expression is the process by which information from a gene is used in the synthesis of a functional gene product.

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Gene therapy

In the medicine field, gene therapy (also called human gene transfer) is the therapeutic delivery of nucleic acid into a patient's cells as a drug to treat disease.

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Genome

In the fields of molecular biology and genetics, a genome is the genetic material of an organism.

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Genome instability

Genome instability (also genetic instability or genomic instability) refers to a high frequency of mutations within the genome of a cellular lineage.

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Germline

In biology and genetics, the germline in a multicellular organism is the population of its bodily cells that are so differentiated or segregated that in the usual processes of reproduction they may pass on their genetic material to the progeny.

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Great Oxygenation Event

The Great Oxygenation Event, the beginning of which is commonly known in scientific media as the Great Oxidation Event (GOE, also called the Oxygen Catastrophe, Oxygen Crisis, Oxygen Holocaust, Oxygen Revolution, or Great Oxidation) was the biologically induced appearance of dioxygen (O2) in Earth's atmosphere.

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H2AFX

H2AFX (H2A histone family, member X) is one of several genes coding for histone H2A.

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Hayflick limit

The Hayflick limit or Hayflick phenomenon is the number of times a normal human cell population will divide before cell division stops.

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Helicase

Helicases are a class of enzymes vital to all living organisms.

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Hereditary nonpolyposis colorectal cancer

Hereditary nonpolyposis colorectal cancer (HNPCC) or Lynch syndrome is an autosomal dominant genetic condition that has a high risk of colon cancer as well as other cancers including endometrial cancer (second most common), ovary, stomach, small intestine, hepatobiliary tract, upper urinary tract, brain, and skin.

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Heterochromatin

Heterochromatin is a tightly packed form of DNA or condensed DNA, which comes in multiple varieties.

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Histone

In biology, histones are highly alkaline proteins found in eukaryotic cell nuclei that package and order the DNA into structural units called nucleosomes.

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Histone-modifying enzymes

The packaging of the eukaryotic genome into highly condensed chromatin makes it inaccessible to the factors required for gene transcription, DNA replication, recombination and repair.

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HMGA1

High-mobility group protein HMG-I/HMG-Y is a protein that in humans is encoded by the HMGA1 gene.

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HMGA2

High-mobility group AT-hook 2, also known as HMGA2, is a protein that, in humans, is encoded by the HMGA2 gene.

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Homogeneity and heterogeneity

Homogeneity and heterogeneity are concepts often used in the sciences and statistics relating to the uniformity in a substance or organism.

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Homologous chromosome

A couple of homologous chromosomes, or homologs, are a set of one maternal and one paternal chromosome that pair up with each other inside a cell during meiosis.

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Homologous recombination

Homologous recombination is a type of genetic recombination in which nucleotide sequences are exchanged between two similar or identical molecules of DNA.

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Hoogsteen base pair

A Hoogsteen base pair is a variation of base-pairing in nucleic acids such as the A•T pair.

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Hot spring

A hot spring is a spring produced by the emergence of geothermally heated groundwater that rises from the Earth's crust.

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Human mitochondrial genetics

Human mitochondrial genetics is the study of the genetics of human mitochondrial DNA (the DNA contained in human mitochondria).

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Hydrogen peroxide

Hydrogen peroxide is a chemical compound with the formula.

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Hydrolysis

Hydrolysis is a term used for both an electro-chemical process and a biological one.

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Immune system

The immune system is a host defense system comprising many biological structures and processes within an organism that protects against disease.

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Indirect DNA damage

Indirect DNA damage occurs when a UV-photon is absorbed in the human skin by a chromophore that does not have the ability to convert the energy into harmless heat very quickly.

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Intercalation (biochemistry)

In biochemistry, intercalation is the insertion of molecules between the planar bases of deoxyribonucleic acid (DNA).

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Ionizing radiation

Ionizing radiation (ionising radiation) is radiation that carries enough energy to liberate electrons from atoms or molecules, thereby ionizing them.

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Kinase

In biochemistry, a kinase is an enzyme that catalyzes the transfer of phosphate groups from high-energy, phosphate-donating molecules to specific substrates.

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Knudson hypothesis

The Knudson hypothesis, also known as the two-hit hypothesis or multiple-hit hypothesis, is the hypothesis that cancer is the result of accumulated mutations to a cell's DNA.

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Lesion

A lesion is any abnormal damage or change in the tissue of an organism, usually caused by disease or trauma.

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Leukemia

Leukemia, also spelled leukaemia, is a group of cancers that usually begin in the bone marrow and result in high numbers of abnormal white blood cells.

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Li–Fraumeni syndrome

Li–Fraumeni syndrome is a rare, autosomal dominant, hereditary disorder that pre-disposes carriers to cancer development.

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Life expectancy

Life expectancy is a statistical measure of the average time an organism is expected to live, based on the year of its birth, its current age and other demographic factors including gender.

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Life extension

Life extension science, also known as anti-aging medicine, indefinite life extension, experimental gerontology, and biomedical gerontology, is the study of slowing down or reversing the processes of aging to extend both the maximum and average lifespan.

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LIG3

DNA ligase 3 is an enzyme that, in humans, is encoded by the LIG3 gene.

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LIG4

DNA ligase 4 is an enzyme that in humans is encoded by the LIG4 gene.

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Lipid

In biology and biochemistry, a lipid is a biomolecule that is soluble in nonpolar solvents.

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Lymphoma

Lymphoma is a group of blood cancers that develop from lymphocytes (a type of white blood cell).

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Malignancy

Malignancy is the tendency of a medical condition to become progressively worse.

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Mammal

Mammals are the vertebrates within the class Mammalia (from Latin mamma "breast"), a clade of endothermic amniotes distinguished from reptiles (including birds) by the possession of a neocortex (a region of the brain), hair, three middle ear bones, and mammary glands.

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MDC1

Mediator of DNA damage checkpoint protein 1 is a 2080 amino acid long protein that in humans is encoded by the MDC1 gene located on the short arm (p) of chromosome 6.

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Metabolism

Metabolism (from μεταβολή metabolē, "change") is the set of life-sustaining chemical transformations within the cells of organisms.

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Metaphase

Metaphase (from the Greek μετά, "adjacent" and φάσις, "stage") is a stage of mitosis in the eukaryotic cell cycle in which chromosomes are at their second-most condensed and coiled stage (they are at their most condensed in anaphase).

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Methylation

In the chemical sciences, methylation denotes the addition of a methyl group on a substrate, or the substitution of an atom (or group) by a methyl group.

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Mi-2/NuRD complex

In the field of molecular biology, the Mi-2/NuRD (Nucleosome Remodeling Deacetylase) complex, is a group of associated proteins with both ATP-dependent chromatin remodeling and histone deacetylase activities.

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Microhomology-mediated end joining

Microhomology-mediated end joining (MMEJ), also known as alternative nonhomologous end-joining (Alt-NHEJ) is one of the pathways for repairing double-strand breaks in DNA.

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MicroRNA

A microRNA (abbreviated miRNA) is a small non-coding RNA molecule (containing about 22 nucleotides) found in plants, animals and some viruses, that functions in RNA silencing and post-transcriptional regulation of gene expression.

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MiR-155

MiR-155 is a microRNA that in humans is encoded by the MIR155 host gene or MIR155HG.

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Missense mutation

In genetics, a missense mutation is a point mutation in which a single nucleotide change results in a codon that codes for a different amino acid.

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Mitochondrion

The mitochondrion (plural mitochondria) is a double-membrane-bound organelle found in most eukaryotic organisms.

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Mitosis

In cell biology, mitosis is a part of the cell cycle when replicated chromosomes are separated into two new nuclei.

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MLH1

MutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli) is a protein that in humans is encoded by the MLH1 gene located on Chromosome 3.

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Molecular lesion

A molecular lesion or point lesion is damage to the structure of a biological molecule such as DNA, enzymes, or proteins that results in reduction or absence of normal function or, in rare cases, the gain of a new function.

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MRE11A

Double-strand break repair protein MRE11A is a protein that in humans is encoded by the MRE11A gene.

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MSH2

DNA mismatch repair protein Msh2 also known as MutS protein homolog 2 or MSH2 is a protein that in humans is encoded by the MSH2 gene, which is located on chromosome 2.

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MSH4

MutS protein homolog 4 is a protein that in humans is encoded by the MSH4 gene.

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MTOR

The mammalian target of rapamycin (mTOR), also known as the mechanistic target of rapamycin and FK506-binding protein 12-rapamycin-associated protein 1 (FRAP1), is a kinase that in humans is encoded by the MTOR gene.

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Mutagen

In genetics, a mutagen is a physical or chemical agent that changes the genetic material, usually DNA, of an organism and thus increases the frequency of mutations above the natural background level.

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Mutation

In biology, a mutation is the permanent alteration of the nucleotide sequence of the genome of an organism, virus, or extrachromosomal DNA or other genetic elements.

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Mutation Research (journal)

Mutation Research is a peer-reviewed scientific journal that publishes research papers in the area of mutation research which focus on fundamental mechanisms underlying the phenotypic and genotypic expression of genetic damage.

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Nanometre

The nanometre (International spelling as used by the International Bureau of Weights and Measures; SI symbol: nm) or nanometer (American spelling) is a unit of length in the metric system, equal to one billionth (short scale) of a metre (m).

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NEIL1

Endonuclease VIII-like 1 is an enzyme that in humans is encoded by the NEIL1 gene.

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Neoplasm

Neoplasia is a type of abnormal and excessive growth of tissue.

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Nitrogenous base

A nitrogenous base, or nitrogen-containing base, is an organic molecule with a nitrogen atom that has the chemical properties of a base.

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Nobel Prize

The Nobel Prize (Swedish definite form, singular: Nobelpriset; Nobelprisen) is a set of six annual international awards bestowed in several categories by Swedish and Norwegian institutions in recognition of academic, cultural, or scientific advances.

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Nobel Prize in Chemistry

The Nobel Prize in Chemistry (Nobelpriset i kemi) is awarded annually by the Royal Swedish Academy of Sciences to scientists in the various fields of chemistry.

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Non-coding DNA

In genomics and related disciplines, noncoding DNA sequences are components of an organism's DNA that do not encode protein sequences.

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Non-homologous end joining

Non-homologous end joining (NHEJ) is a pathway that repairs double-strand breaks in DNA.

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Nucleic acid

Nucleic acids are biopolymers, or small biomolecules, essential to all known forms of life.

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Nucleic acid sequence

A nucleic acid sequence is a succession of letters that indicate the order of nucleotides forming alleles within a DNA (using GACT) or RNA (GACU) molecule.

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Nucleic acid thermodynamics

Nucleic acid thermodynamics is the study of how temperature affects the nucleic acid structure of double-stranded DNA (dsDNA).

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Nucleotide excision repair

Nucleotide excision repair is a DNA repair mechanism.

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Nutrient sensing

Nutrient sensing is a cell's ability to recognize and respond to fuel substrates such as glucose.

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O-6-methylguanine-DNA methyltransferase

O6-alkylguanine DNA alkyltransferase (also known as AGT, MGMT or AGAT) is a protein that in humans is encoded by the O6-methylguanine DNA methyltransferase (MGMT) gene.

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Olaparib

Olaparib (AZD-2281, trade name Lynparza) is an FDA-approved targeted therapy for cancer, developed by scientists at the University of Cambridge, including Steve Jackson, KuDOS Pharmaceuticals, and later by AstraZeneca.

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Operator (biology)

In genetics, an operator is a segment of DNA to which a transcription factor binds to regulate gene expression by repressing it.

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Organelle

In cell biology, an organelle is a specialized subunit within a cell that has a specific function, in which their function is vital for the cell to live.

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Oxidative deamination

Oxidative deamination is a form of deamination that generates α-keto acids and other oxidized products from amine-containing compounds, and occurs largely in the liver and kidney.

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Oxidative phosphorylation

Oxidative phosphorylation (or OXPHOS in short) (UK, US) is the metabolic pathway in which cells use enzymes to oxidize nutrients, thereby releasing energy which is used to produce adenosine triphosphate (ATP).

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Oxidative stress

Oxidative stress reflects an imbalance between the systemic manifestation of reactive oxygen species and a biological system's ability to readily detoxify the reactive intermediates or to repair the resulting damage.

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P21

p21Cip1 (alternatively p21Waf1), also known as cyclin-dependent kinase inhibitor 1 or CDK-interacting protein 1, is a cyclin-dependent kinase inhibitor (CKI) that is capable of inhibiting all cyclin/CDK complexes, though is primarily associated with inhibition of CDK2.

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P53

Tumor protein p53, also known as p53, cellular tumor antigen p53 (UniProt name), phosphoprotein p53, tumor suppressor p53, antigen NY-CO-13, or transformation-related protein 53 (TRP53), is any isoform of a protein encoded by homologous genes in various organisms, such as TP53 (humans) and Trp53 (mice).

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Palindrome

A palindrome is a word, number, or other sequence of characters which reads the same backward as forward, such as madam or racecar.

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PARP1

Poly polymerase 1 (PARP-1) also known as NAD+ ADP-ribosyltransferase 1 or poly synthase 1 is an enzyme that in humans is encoded by the PARP1 gene.

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Paul L. Modrich

Paul Lawrence Modrich (born June 13, 1946) is an American biochemist, James B. Duke Professor of Biochemistry at Duke University and Investigator at the Howard Hughes Medical Institute.

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Phosphoinositide 3-kinase

Phosphatidylinositol-4,5-bisphosphate 3-kinase (also called phosphatidylinositide 3-kinases, phosphatidylinositol-3-kinases, PI 3-kinases, PI(3)Ks, PI-3Ks or by the HUGO official stem symbol for the gene family, PI3K(s)) are a family of enzymes involved in cellular functions such as cell growth, proliferation, differentiation, motility, survival and intracellular trafficking, which in turn are involved in cancer.

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Phosphorylation

In chemistry, phosphorylation of a molecule is the attachment of a phosphoryl group.

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Photolyase

Photolyases (EC 4.1.99.3) are DNA repair enzymes that repair damage caused by exposure to ultraviolet light.

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Photosynthesis

Photosynthesis is a process used by plants and other organisms to convert light energy into chemical energy that can later be released to fuel the organisms' activities (energy transformation).

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Plant

Plants are mainly multicellular, predominantly photosynthetic eukaryotes of the kingdom Plantae.

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Pleiotropy

Pleiotropy (from Greek πλείων pleion, "more", and τρόπος tropos, "way") occurs when one gene influences two or more seemingly unrelated phenotypic traits.

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PMS2

Mismatch repair endonuclease PMS2 is an enzyme that in humans is encoded by the PMS2 gene.

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Point mutation

A point mutation is a genetic mutation where a single nucleotide base is changed, inserted or deleted from a sequence of DNA or RNA.

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POLI

DNA polymerase iota is an enzyme that in humans is encoded by the POLI gene.

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Polycyclic aromatic hydrocarbon

Polycyclic aromatic hydrocarbons (PAHs, also polyaromatic hydrocarbons or polynuclear aromatic hydrocarbons) are hydrocarbons—organic compounds containing only carbon and hydrogen—that are composed of multiple aromatic rings (organic rings in which the electrons are delocalized).

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Polymer

A polymer (Greek poly-, "many" + -mer, "part") is a large molecule, or macromolecule, composed of many repeated subunits.

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Polymerase

A polymerase is an enzyme (EC 2.7.7.6/7/19/48/49) that synthesizes long chains of polymers or nucleic acids.

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Post-translational modification

Post-translational modification (PTM) refers to the covalent and generally enzymatic modification of proteins following protein biosynthesis.

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Postreplication repair

Postreplication repair is the repair of damage to the DNA that takes place after replication.

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Precambrian

The Precambrian (or Pre-Cambrian, sometimes abbreviated pЄ, or Cryptozoic) is the earliest part of Earth's history, set before the current Phanerozoic Eon.

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Processivity

In molecular biology and biochemistry, processivity is an enzyme's ability to catalyze "consecutive reactions without releasing its substrate".

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Progeria

Progeria is an extremely rare autosomal dominant genetic disorder in which symptoms resembling aspects of aging are manifested at a very early age.

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Progeroid syndromes

Progeroid syndromes (PS) are a group of rare genetic disorders which mimic physiological aging, making affected individuals appear to be older than they are.

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Programmed cell death

Programmed cell death (or PCD) is the death of a cell in any form, mediated by an intracellular program.

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Prokaryote

A prokaryote is a unicellular organism that lacks a membrane-bound nucleus, mitochondria, or any other membrane-bound organelle.

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Proliferating cell nuclear antigen

Proliferating cell nuclear antigen (PCNA) is a DNA clamp that acts as a processivity factor for DNA polymerase δ in eukaryotic cells and is essential for replication.

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Proofreading (biology)

The term proofreading is used in genetics to refer to the error-correcting processes, first proposed by John Hopfield and Jacques Ninio, involved in DNA replication, immune system specificity, enzyme-substrate recognition among many other processes that require enhanced specificity.

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Protease

A protease (also called a peptidase or proteinase) is an enzyme that performs proteolysis: protein catabolism by hydrolysis of peptide bonds.

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Protein

Proteins are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues.

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Protein dimer

In biochemistry, a protein dimer is a macromolecular complex formed by two protein monomers, or single proteins, which are usually non-covalently bound.

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Protein kinase

A protein kinase is a kinase enzyme that modifies other proteins by chemically adding phosphate groups to them (phosphorylation).

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Purine

A purine is a heterocyclic aromatic organic compound that consists of a pyrimidine ring fused to an imidazole ring.

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Pyrimidine dimer

Pyrimidine dimers are molecular lesions formed from thymine or cytosine bases in DNA via photochemical reactions.

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RAD18

E3 ubiquitin-protein ligase RAD18 is an enzyme that in humans is encoded by the RAD18 gene.

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RAD51

RAD51 is a eukaryotic gene.

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Radiation

In physics, radiation is the emission or transmission of energy in the form of waves or particles through space or through a material medium.

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Radiation therapy

Radiation therapy or radiotherapy, often abbreviated RT, RTx, or XRT, is therapy using ionizing radiation, generally as part of cancer treatment to control or kill malignant cells and normally delivered by a linear accelerator.

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Radical (chemistry)

In chemistry, a radical (more precisely, a free radical) is an atom, molecule, or ion that has an unpaired valence electron.

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Radioactive decay

Radioactive decay (also known as nuclear decay or radioactivity) is the process by which an unstable atomic nucleus loses energy (in terms of mass in its rest frame) by emitting radiation, such as an alpha particle, beta particle with neutrino or only a neutrino in the case of electron capture, gamma ray, or electron in the case of internal conversion.

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Reactive oxygen species

Reactive oxygen species (ROS) are chemically reactive chemical species containing oxygen.

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RecA

RecA is a 38 kilodalton protein essential for the repair and maintenance of DNA.

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Repressor

In molecular genetics, a repressor is a DNA- or RNA-binding protein that inhibits the expression of one or more genes by binding to the operator or associated silencers.

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Repressor lexA

Repressor LexA or LexA is a transcriptional repressor that represses SOS response genes coding primarily for error-prone DNA polymerases, DNA repair enzymes and cell division inhibitors.

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RNA

Ribonucleic acid (RNA) is a polymeric molecule essential in various biological roles in coding, decoding, regulation, and expression of genes.

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RNF8

E3 ubiquitin-protein ligase RNF8 is an enzyme that in humans is encoded by the RNF8 gene.

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S phase

S phase (synthesis phase) is the part of the cell cycle in which DNA is replicated, occurring between G1 phase and G2 phase.

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Saccharomyces cerevisiae

Saccharomyces cerevisiae is a species of yeast.

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Senescence

Senescence or biological ageing is the gradual deterioration of function characteristic of most complex lifeforms, arguably found in all biological kingdoms, that on the level of the organism increases mortality after maturation.

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Shock response spectrum

A Shock Response Spectrum (SRS) is a graphical representation of a shock, or any other transient acceleration input, in terms of how a Single Degree Of Freedom (SDOF) system (like a mass on a spring) would respond to that input.

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Short hairpin RNA

A short hairpin RNA or small hairpin RNA (shRNA/Hairpin Vector) is an artificial RNA molecule with a tight hairpin turn that can be used to silence target gene expression via RNA interference (RNAi).

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SiDNA

Signal interfering DNA (siDNA) is a class of short modified double stranded DNA molecules, 8–64 base pairs in length.

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Signal transduction

Signal transduction is the process by which a chemical or physical signal is transmitted through a cell as a series of molecular events, most commonly protein phosphorylation catalyzed by protein kinases, which ultimately results in a cellular response.

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Sirtuin 6

Sirtuin 6 (SIRT6 or Sirt6) is a stress responsive protein deacetylase and mono-ADP ribosyltransferase enzyme encoded by the SIRT6 gene.

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SOS response

The SOS response is a global response to DNA damage in which the cell cycle is arrested and DNA repair and mutagenesis are induced.

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Spirochaete

A spirochaete or spirochete is a member of the phylum Spirochaetes, which contains distinctive diderm (double-membrane) bacteria, most of which have long, helically coiled (corkscrew-shaped or spiraled, hence the name) cells.

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Stoichiometry

Stoichiometry is the calculation of reactants and products in chemical reactions.

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Structural motif

In a chain-like biological molecule, such as a protein or nucleic acid, a structural motif is a supersecondary structure, which also appears in a variety of other molecules.

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Superoxide dismutase

Superoxide dismutase (SOD) is an enzyme that alternately catalyzes the dismutation (or partitioning) of the superoxide (O2&minus) radical into either ordinary molecular oxygen (O2) or hydrogen peroxide (H2O2).

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T-cell receptor

The T-cell receptor, or TCR, is a molecule found on the surface of T cells, or T lymphocytes, that is responsible for recognizing fragments of antigen as peptides bound to major histocompatibility complex (MHC) molecules.

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Telomere

A telomere is a region of repetitive nucleotide sequences at each end of a chromosome, which protects the end of the chromosome from deterioration or from fusion with neighboring chromosomes.

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The New York Times

The New York Times (sometimes abbreviated as The NYT or The Times) is an American newspaper based in New York City with worldwide influence and readership.

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Thermophile

A thermophile is an organism—a type of extremophile—that thrives at relatively high temperatures, between.

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Tomas Lindahl

Tomas Robert Lindahl FRS FMedSci (born 28 January 1938) is a Swedish-born British scientist specialising in cancer research.

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Topoisomerase

Topoisomerases are enzymes that participate in the overwinding or underwinding of DNA.

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Toxin

A toxin (from toxikon) is a poisonous substance produced within living cells or organisms; synthetic toxicants created by artificial processes are thus excluded.

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TP53BP1

Tumor suppressor p53-binding protein 1 also known as p53-binding protein 1 or 53BP1 is a protein that in humans is encoded by the TP53BP1 gene.

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Transcription (biology)

Transcription is the first step of gene expression, in which a particular segment of DNA is copied into RNA (especially mRNA) by the enzyme RNA polymerase.

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Trichothiodystrophy

Trichothiodystrophy (TTD) is an autosomal recessive inherited disorder characterised by brittle hair and intellectual impairment.

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Tumor suppressor

A tumor suppressor gene, or antioncogene, is a gene that protects a cell from one step on the path to cancer.

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Tumour heterogeneity

Tumour heterogeneity describes the observation that different tumour cells can show distinct morphological and phenotypic profiles, including cellular morphology, gene expression, metabolism, motility, proliferation, and metastatic potential.

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Ubiquitin ligase

A ubiquitin ligase (also called an E3 ubiquitin ligase) is a protein that recruits an E2 ubiquitin-conjugating enzyme that has been loaded with ubiquitin, recognizes a protein substrate, and assists or directly catalyzes the transfer of ubiquitin from the E2 to the protein substrate.

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Ultraviolet

Ultraviolet (UV) is electromagnetic radiation with a wavelength from 10 nm to 400 nm, shorter than that of visible light but longer than X-rays.

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UvrABC endonuclease

UvrABC endonuclease is a multienzyme complex in Escherichia coli involved in DNA repair by nucleotide excision repair, and it is, therefore, sometimes called an excinuclease.

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V(D)J recombination

V(D)J recombination is the unique mechanism of genetic recombination that occurs only in developing lymphocytes during the early stages of T and B cell maturation.

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Vertebrate

Vertebrates comprise all species of animals within the subphylum Vertebrata (chordates with backbones).

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Vinyl chloride

Vinyl chloride is an organochloride with the formula H2C.

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Virus

A virus is a small infectious agent that replicates only inside the living cells of other organisms.

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Wavelength

In physics, the wavelength is the spatial period of a periodic wave—the distance over which the wave's shape repeats.

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Werner syndrome

Werner syndrome (WS), also known as "adult progeria",James, William; Berger, Timothy; Elston, Dirk (2005).

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Werner syndrome helicase

"Werner syndrome ATP-dependent helicase" also known as DNA helicase, RecQ-like type 3 is an enzyme that in humans is encoded by the WRN gene.

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X-ray

X-rays make up X-radiation, a form of electromagnetic radiation.

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Xeroderma pigmentosum

Xeroderma pigmentosum (XP) is a genetic disorder in which there is a decreased ability to repair DNA damage such as that caused by ultraviolet (UV) light.

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XRCC1

DNA repair protein XRCC1 also known as X-ray repair cross-complementing protein 1 is a protein that in humans is encoded by the XRCC1 gene.

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Yeast

Yeasts are eukaryotic, single-celled microorganisms classified as members of the fungus kingdom.

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1,000,000

1,000,000 (one million), or one thousand thousand, is the natural number following 999,999 and preceding 1,000,001.

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6-O-Methylguanine

6-O-Methylguanine is a derivative of the nucleobase guanine in which a methyl group is attached to the oxygen atom.

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7-Methylguanosine

7-Methylguanosine (m7G) is a modified purine nucleoside.

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8-Oxo-2'-deoxyguanosine

8-Oxo-2'-deoxyguanosine (8-oxo-dG) is an oxidized derivative of deoxyguanosine.

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Redirects here:

DNA Repair, DNA damage, DNA damage checkpoint, DNA damage checkpoints, DNA lesion, DNA lesions, DNA repair gene, DNA repair genes, DNA-damage response, Dna repair, Dna repair enzymes, Dna repair genes, Dna repair-deficiency disorders, Double strand break, Double strand breaks, Double-strand break, Double-strand breaks, Excision repair, Excision repair mechanism, Self-repair mechanisms, Single strand break, Single-strand break, Translation polymerase, Translesion, Translesion synthesis, Types of DNA lesions.

References

[1] https://en.wikipedia.org/wiki/DNA_repair

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