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Subgroup of tumors
The positive replication error phenotype (RER+) defines a subgroup of tumors that have been documented well in Hereditary nonpolyposis colorectal cancer
Replication_error_phenotype
Observed inability to reproduce scientific studies
category, replication, involves repeating an experiment or study with new, independent data to verify the original conclusions. Replication has been called
Replication_crisis
Type of behavior of a dynamical system
separate categories, including: (1) Replication Control, (2) Replication Information, (3) Replication Substrate, (4) Replicator Structure, (5) Passive Parts
Self-replication
Self-replicating cellular automaton
requirements for machine self-replication. However, it is clear that far simpler machines can achieve self-replication. Examples include trivial crystal-like
Von Neumann universal constructor
Von_Neumann_universal_constructor
Science of genes, heredity and variation
DNA replication, errors occasionally occur in the polymerization of the second strand. These errors, called mutations, can affect the phenotype of an
Genetics
Alteration in the nucleotide sequence of a genome
from errors during replication, mitosis, meiosis, or damage to DNA, which then may trigger error-prone repair or cause an error during replication (translesion
Mutation
Simulation of biological behavior
is the cloning machine implemented for self-replication by Alvarez-Rodriguez et al. The self-replication process clearly only requires interactions between
Quantum_artificial_life
Correction of DNA replication errors
genetics to refer to the error-correcting processes, first proposed by John Hopfield and Jacques Ninio, involved in DNA replication, immune system specificity
Proofreading_(biology)
Physical or chemical agent that increases the rate of genetic mutation
"spontaneous mutations" occur due to spontaneous hydrolysis, errors in DNA replication, repair and recombination. The first mutagens to be identified
Mutagen
Infectious agent that replicates in cells
the viral genomic nucleic acid. Replication of viruses involves primarily multiplication of the genome. Replication involves the synthesis of viral messenger
Virus
Individual living life form
balancing between conceptual and practical considerations, and between phenotype and phylogenomics". Fungal Diversity. 109 (1): 99–154. doi:10.1007/s13225-021-00477-7
Organism
Protein-coding gene in the species Homo sapiens
function in proofreading to ensure replication accuracy during DNA synthesis, and in a number of types of replication-linked DNA repair following DNA damage
POLD1
Genetic mutation not inherited from a parent
spontaneously during DNA replication or repair, particularly in regions of the genome that are repetitive or prone to errors. When an indel occurs in
De_novo_mutation
Cultural idea that spreads through imitation
(from parent to child, via replication of genes) and horizontally (through viruses and other means). Memes can replicate vertically or horizontally within
Meme
Evolutionary algorithm
discover the DNA double helix and propose a mechanism for its replication. But the replication of strings is trivial in artificial evolutionary systems, where
Gene_expression_programming
Population structure of viruses with a large number of variant genomes
concepts are described by two fundamental equations: replication with production of error copies, and the error threshold relationship. They capture two major
Viral_quasispecies
Phenotypically-different organism resulting from a mutation
in pre-existing genomes as a result of errors of DNA replication or errors of DNA repair. Errors of replication often involve translesion synthesis by
Mutant
Theory of the "selfish gene"
of high-fidelity replication through many generations. So, a particular gene coded in a nucleobase sequence of a lineage of replicated DNA molecules can
Gene-centered view of evolution
Gene-centered_view_of_evolution
Mammalian protein found in Homo sapiens
and ubiquitinates it for degradation. Under replication stress, for example a DNA polymerase mismatch error, USP20 disassociates from HERC2 and deubiquitinates
HERC2
Scientific study of genes at the molecular level
gene or induce mutations in a gene to link a gene sequence to a specific phenotype. Therefore molecular genetics is a powerful methodology for linking mutations
Molecular_genetics
Virus of the herpes family
infectious virions. EBV can undergo lytic replication in both B cells and epithelial cells. In B cells, lytic replication normally only takes place after reactivation
Epstein–Barr_virus
Immune cells found in lymph nodes
or with blocked TNF-a and lymphotoxin (LT) production, cells with FDC phenotype are missing. In normal lymphoid tissue, recirculating resting B cells
Follicular_dendritic_cells
Sequence of DNA that determines traits in an organism
cell division: replication origins, telomeres, and the centromere. Replication origins are the sequence regions where DNA replication is initiated to
Gene
Conversion of DNA single-stranded gaps
takes place after replication. Some example genes in humans include: BRCA2 and BRCA1 BLM NBS1 Accurate and efficient DNA replication is crucial for the
Postreplication_repair
System for fixing base errors of DNA replication
deletion, and mis-incorporation of bases that can arise during DNA replication and recombination, as well as repairing some forms of DNA damage. Mismatch
DNA_mismatch_repair
Study of the human mitochondrial genome
of replication, it replicates in a D-loop mode. One strand begins to replicate first, displacing the other strand. This continues until replication reaches
Human_mitochondrial_genetics
Condition of genetic hypermutability
that MMR is not functioning normally. MMR corrects errors that spontaneously occur during DNA replication, such as single base mismatches or short insertions
Microsatellite_instability
Genetic point mutation that results in an amino acid change in a protein
spontaneously from mutagens like UV radiation, tobacco smoke, an error in DNA replication, and other factors. Screening for missense mutations can be done
Missense_mutation
Possible earliest ancestor of the LUCA ancestral cell
biological systems that would have used RNA for their genome and self-replication. By comparison, LUCA would have had a complex metabolism and a DNA genome
First universal common ancestor
First_universal_common_ancestor
the time spent copying instructions during replication. Some individuals even started executing the replication code in other organisms, allowing those "cheaters"
Evolving digital ecological network
Evolving_digital_ecological_network
Aspect of population genetics
linkage) several fold. The increase in recombination may be due to replication errors by the defective DNA polymerase that are themselves recombination
Genetic_linkage
Repeating sequences of 2–13 base pairs of DNA
cause of such length changes is replication slippage, caused by mismatches between DNA strands while being replicated during meiosis. DNA polymerase,
Microsatellite
Gene that inhibits tumorigenic phenotype
anti-oncogene, is a gene that regulates a cell during cell division and replication. When a tumor suppressor gene is mutated, it results in a loss or reduction
Tumor_suppressor_gene
Molecule that carries genetic information
DNA adducts that induce errors in replication. Nevertheless, due to their ability to inhibit DNA transcription and replication, other similar toxins are
DNA
DNA mutation involving an increase in number of trinucleotide repeats
Triplet expansion is caused by slippage during DNA replication, also known as "copy choice" DNA replication. Due to the repetitive nature of the DNA sequence
Trinucleotide repeat expansion
Trinucleotide_repeat_expansion
American scientist (1923–2026)
"A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication". Proceedings of the National
Stanley_Michael_Gartler
Austrian biologist and friar (1822–1884)
the pea): the wrinkled phenotype of peas (wild-type round) is caused by an insertion in the PsSBE1 gene. The yellow phenotype (wild-type: green) is caused
Gregor_Mendel
Change in allele frequencies that occurs over time within a population
as well as errors that occur during meiosis or DNA replication. Errors are introduced particularly often in the process of DNA replication, in the polymerization
Microevolution
Human retrovirus, cause of AIDS
and released from the cell as new virus particles that will begin the replication cycle anew. Two types of HIV have been characterized: HIV-1 and HIV-2
HIV
Genetic disorder
molecule. DNA helicases function in DNA replication and DNA repair. BLM very likely functions in DNA replication, as cells from persons with Bloom syndrome
Bloom_syndrome
Chinese-American physician-scientist
Advisor), a comprehensive public database linking genotype-phenotype information for inborn errors of immunity. Peng received her Bachelor of Science degree
Xiao_P._Peng
Significance of the peppered moth in evolutionary biology
frequency is scarce. Much more is known about the subsequent fall in phenotype frequency, as it has been measured by lepidopterists using moth traps
Peppered_moth_evolution
Repeated DNA variation between individuals
types of short repeats are often thought to be due to errors in polymerase activity during replication including polymerase slippage, template switching,
Copy_number_variation
Medical condition
needed for DNA replication to prepare for cell division and for mending damaged DNA. The RECQL4 protein is involved in DNA replication and repair as well
RAPADILINO_syndrome
American scientist and cancer researcher
“mutator phenotype” hypothesis of cancers. This hypothesis posits that, because malignant cells exhibit defects in the fidelity of DNA replication, large
Lawrence_A._Loeb
enhance misincorporation of nucleotides (error-prone PCR), for example by reducing the fidelity of replication or using nucleotide analogues. A variation
Mutagenesis (molecular biology technique)
Mutagenesis_(molecular_biology_technique)
Pathogenic small single-stranded circular RNA
small size, imposed by error-prone replication. Their high guanine and cytosine content, which increases stability and replication fidelity. Their circular
Viroid
Synthesis of complex molecules from simple precursors
RNA polymerase, and it can add a primer to an existing strand awaiting replication. DNA polymerase cannot add primers, and therefore, needs primase to add
De_novo_synthesis
Hypothesis that aging is caused by accumulated DNA damage
DNA damages that do not kill the cell by blocking replication will tend to cause replication errors and thus mutation. The great majority of mutations
DNA_damage_theory_of_aging
Statistical phenomenon
offspring will have an intermediate phenotype with some trending towards the dominant phenotype or the recessive phenotype. The population-genetic phenomenon
Regression_toward_the_mean
Statistical method for handling multiple comparisons
family-wise error rate criterion. For example, if inspecting 100 hypotheses (say, 100 genetic mutations or SNPs for association with some phenotype in some
False_discovery_rate
DNA ligase DNA marker DNA polymerase DNA probe DNA repair genes DNA replication DNA sequence DNA sequencing Docking protein Domain Dominant Dominant
Index_of_genetics_articles
Inherited genetic variation
undergoes continuous replication throughout his lifetime, resulting in many small point mutations that result from errors in replication. These mutations
Germline_mutation
replicates from a single origin of replication. replisome The entire complex of molecular machinery that carries out the process of DNA replication,
Glossary of cellular and molecular biology (M–Z)
Glossary_of_cellular_and_molecular_biology_(M–Z)
Application of statistical techniques to biological systems
the three basic principles of experimental statistics: randomization, replication, and local control. The research question will define the objective of
Biostatistics
Medical condition
normal and abnormal cells in the developing embryo. Reduced or improved replication rates of the trisomic cells could affect the number of abnormal cells
Confined_placental_mosaicism
Replacement, insertion, or deletion of a single DNA or RNA nucleotide
and function. Point mutations usually take place during DNA replication. DNA replication occurs when one double-stranded DNA molecule creates two single
Point_mutation
changes in DNA. Incidental, or natural, mutations occur following errors during replication and repair, either spontaneously or due to environmental stressors
Modifications_(genetics)
Medical condition
associated with an aging phenotype, such as cystic fibrosis and sickle cell anemia. It is further argued that segmental aging phenotype is a natural part of
DNA repair-deficiency disorder
DNA_repair-deficiency_disorder
Theory in the domain of evolutionary biology
phenotype using a genotype–phenotype map. A given phenotype identifies a network in genotype-space including all of the genotypes with that phenotype
Bias in the introduction of variation
Bias_in_the_introduction_of_variation
Response to the same environmental variation differently by different genotypes
and thus gene–environment interactions can result in different disease phenotypes. For example, sunlight exposure has a stronger influence on skin cancer
Gene–environment_interaction
Type of genomic instability
radiation. Radiation is known to cause DNA damage, which can cause errors in cell replication, which may result in chromosomal instability. Chromosomal instability
Chromosome_instability
Rate at which mutations occur during some unit of time
quinolones in Salmonella enterica serovar Enteritidis with a mutator phenotype". Antimicrobial Agents and Chemotherapy. 48 (7): 2355–2363. doi:10.1128/AAC
Mutation_rate
Difference in DNA among individuals or populations
cause of most spontaneous mutations, either because of error-prone replication past damages or error-prone repair of damages. Evolutionary biologists are
Genetic_variation
Genetic characteristic
Inheriting these mutations impairs the body's ability to correct DNA replication errors, significantly increasing the risk of developing colorectal and other
Genetic_predisposition
Specialized DNA sequence of a chromosome that links a pair of sister chromatids
(the two copies of each chromosomal DNA molecule resulting from DNA replication in chromatin form) are linked along their length by the action of the
Centromere
Mammalian protein found in Homo sapiens
absence of PARP1, when these breaks are encountered during DNA replication, the replication fork stalls, and double-strand DNA (dsDNA) breaks accumulate
PARP1
Medical condition
carriers of Nijmegen Breakage Syndrome have a distinct gene expression phenotype". Genome Research (Free full text). 16 (8): 973–979. doi:10.1101/gr.5320706
Nijmegen_breakage_syndrome
Protein-coding gene in the species Homo sapiens
POLG activity is coordinated with mitochondrial SSB activity during DNA replication. Deoxynucleoside triphosphate + DNA(n) = diphosphate + DNA(n+1). Mutations
POLG
Portion of gene's sequence which codes for protein
include proofreading by some DNA Polymerases during replication, mismatch repair following replication, and the 'Wobble Hypothesis' which describes the degeneracy
Coding_region
Evolutionary process
is complex. Adaptation is not always a simple matter where the ideal phenotype evolves for a given environment. An organism must be viable at all stages
Adaptation
Mammalian protein found in Homo sapiens
O6-methylguanine back to guanine and prevents mismatch and errors during DNA replication and transcription. Accordingly, loss of MGMT increases the carcinogenic
Methylated-DNA–protein-cysteine methyltransferase
Methylated-DNA–protein-cysteine_methyltransferase
Genetic form of macular degeneration
variants (STGD1). However, there are Stargardt-like diseases with mimicking phenotypes that are referred to as STGD3 and STGD4, and have an autosomal dominant
Stargardt_disease
Biological entity within the hierarchy of biological organization
cause phenotypes and a gene is 'judged' by its phenotypic effects. Dawkins distinguishes entities which survive or fail to survive ("replicators") from
Unit_of_selection
Statistical method in genetic epidemiology
the expression of parental genotype in the parental phenotype directly affects the offspring phenotype).[citation needed] Mendelian randomization is currently
Mendelian_randomization
Japanese scientist (born 1933)
is a Japanese pioneer of molecular biology known for her work on DNA replication and specifically for discovering Okazaki fragments, along with her late
Tsuneko_Okazaki
Respiratory disease of chickens
relevant if a different amino acid (non-synonymous) is encoded, and the new phenotype has different biological properties (strain). Amino acid changes located
Avian_infectious_bronchitis
Large chromosome with thousands of DNA strands
rounds of DNA replication without cell division forms a giant chromosome. Thus polytene chromosomes form when multiple rounds of replication produce many
Polytene_chromosome
Cell response to DNA damage
response was articulated by Evelyn Witkin. Later, by characterizing the phenotypes of mutagenised E. coli, she and post doctoral student Miroslav Radman
SOS_response
Theory in neurology
neurophysiologist William Calvin had proposed true replication in the brain, whereas Edelman opposed the idea of true replicators in the brain. Stephen Smoliar published
Neural_Darwinism
X-linked dominant genetic disorder
developmental delays. Female carriers often show little to no physical phenotype, but have an increased risks for premature ovarian failure (FXPOI) and
Fragile_X_syndrome
Genetic disease causing anemia, birth defects, and cancers
depletion of the neural stem cell pool with aging. Much of the Fanconi anemia phenotype might be interpreted as a reflection of premature aging of stem cells
Fanconi_anemia
Study of the inheritance of continuously variable traits
of quantitative traits, which are phenotypes that vary continuously—such as height or mass—as opposed to phenotypes and gene-products that are discretely
Quantitative_genetics
Concept in genetics
must determine the minimal set of genes required for metabolism and replication, which can be achieved by experimental and computational analysis of
Minimal_genome
Process of fatty acid breakdown
Intermediate Phenotype: characterized by hypoketotic hypoglycemia and is triggered by infection or fasting during infancy Mild (Late-Onset) Phenotype: presents
Beta_oxidation
Condition in multi-cellular organisms
chromosome from some trisomic cells. Generally, this leads to a milder phenotype than in nonmosaic patients with the same disorder. In rare cases, intersex
Mosaic_(genetics)
occurrence is integral to the process of evolution. They can result from errors in replication, chemical damage, exposure to high-energy radiation, or manipulations
Glossary of genetics and evolutionary biology
Glossary_of_genetics_and_evolutionary_biology
Study of health and disease within a population
JG, Weijenberg MP, van Engeland M (2012). "The CpG island methylator phenotype in colorectal cancer: Progress and problems". Biochim Biophys Acta. 1825
Epidemiology
strain that requires multiple mutations before reverting to a virulent phenotype. Andino described this approach as "putting the virus in an evolutionary
Raul_Andino
Rules by which information encoded within genetic material is translated into proteins
DNA replication, errors occasionally occur in the polymerization of the second strand. These errors, mutations, can affect an organism's phenotype, especially
Genetic_code
values of the phenotype y Negative gene set — lower expression of most genes in the gene set correlates with higher values of the phenotype y Data from
Microarray analysis techniques
Microarray_analysis_techniques
Causes of death outside the individual's control
normal, chronologic aging, such as, for example, mutations due to DNA replication errors, and which determined species maximum lifespan. Extrinsic mortality
Extrinsic_mortality
membrane or in peroxisomes. bidirectional replication A common mechanism of DNA replication in which two replication forks move in opposite directions away
Glossary of cellular and molecular biology (0–L)
Glossary_of_cellular_and_molecular_biology_(0–L)
presence of fermentable carbon sources (such as glucose). The petite phenotype can be caused by the absence of, or mutations in, mitochondrial DNA (termed
Petite_mutation
Cell division producing haploid gametes
frequent genetic cause of developmental disabilities. In meiosis, DNA replication is followed by two rounds of cell division to produce four daughter cells
Meiosis
Enzyme family
such as HIV and are required for viral replication. In eukaryotes, ribonuclease H1 is involved in DNA replication of the mitochondrial genome. Both H1 and
Ribonuclease_H
American theoretical biologist
the matter it is made of roughly every 8 weeks, through metabolism, replication and repair. Yet, you're still you --with all your memories, your personality
Robert_Rosen_(biologist)
on the other chromosome. Non-homologous duplications result from replication errors that shift the gene of interest into a new position. A tandem duplication
Gene_redundancy
Biological process
methylation after every cellular DNA replication cycle. Without the DNA methyltransferase (DNMT), the replication machinery itself would produce daughter
DNA_methylation
Correlation between human biology and political tendencies
achieved a partial replication of Kanai et al, using a larger sample size of 928 subjects, making it the largest preregistered replication study in political
Biology and political orientation
Biology_and_political_orientation
REPLICATION ERROR-PHENOTYPE
REPLICATION ERROR-PHENOTYPE
Boy/Male
Tamil
King of terror
Girl/Female
Hindu, Indian
Without Error
Male
English
Scottish surname transferred to forename use, from a place name possibly ERROL means "to wander."Â
Girl/Female
Tamil
Prachiti | பà¯à®°à®šà¯€à®¤à¯€
Experience & realization
Prachiti | பà¯à®°à®šà¯€à®¤à¯€
Boy/Male
Christian & English(British/American/Australian)
Wanderering Noble
Boy/Male
Anglo Saxon
Terror.
Boy/Male
Hindu, Indian
Application
Boy/Male
English American German Latin Scottish
Army commander. Army, weald power. Also can be a, meaning nobleman. Famous bearer: Australian...
Boy/Male
Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi
Error-less
Girl/Female
Australian, British, English, Gaelic, Irish
Terror; Lovers
Boy/Male
Anglo Saxon
Terror.
Boy/Male
Indian
Realisation
Boy/Male
Anglo Saxon
Terror.
Female
Arthurian
, error for Nineve (q.v.).
Girl/Female
Hindu
Experience & realization
Boy/Male
Hindu, Indian
Self Realization
Boy/Male
Anglo Saxon
Terror.
Boy/Male
Hindu
King of terror
Boy/Male
American, Anglo, British, Christian, Danish, English, German, Jamaican, Latin, Scottish
To Wander; Nobleman; Leader; Earl; Wanderer
Girl/Female
Hindu, Indian
Realization
REPLICATION ERROR-PHENOTYPE
REPLICATION ERROR-PHENOTYPE
Boy/Male
Hindu
Knowledge
Girl/Female
Tamil
Grace of God
Girl/Female
Hindu
The sign of the zodiac, Collection
Boy/Male
Tamil
Sentence
Girl/Female
British, Indian, Modern, Romanian, Sikh
Sunlight; Meadow; Combination of Names Lee and Ann
Boy/Male
Muslim Arabic
Determined. Resolved.
Girl/Female
Tamil
Aritrika | அரீதà¯à®°à®¿à®•à®¾Â
Dusk lamp beneath Tulsi plant (Basil)
Girl/Female
Australian, Celtic, Irish, Latin
Royal
Boy/Male
Hindi
Moon king.
Male
African
born when the sun shines.
REPLICATION ERROR-PHENOTYPE
REPLICATION ERROR-PHENOTYPE
REPLICATION ERROR-PHENOTYPE
REPLICATION ERROR-PHENOTYPE
REPLICATION ERROR-PHENOTYPE
n.
The reply of the plaintiff, in matters of fact, to the defendant's plea.
n.
An answer; a reply.
n.
The difference between the observed value of a quantity and that which is taken or computed to be the true value; -- sometimes called residual error.
n.
Misguidance; error.
n.
Return or repercussion, as of sound; echo.
n.
A wandering or deviation from the right course or standard; irregularity; mistake; inaccuracy; something made wrong or left wrong; as, an error in writing or in printing; a clerical error.
n.
The act of applying or laying on, in a literal sense; as, the application of emollients to a diseased limb.
n.
A request; a document containing a request; as, his application was placed on file.
n.
The act of making request of soliciting; as, an application for an office; he made application to a court of chancery.
n.
Hence, in specific uses: (a) That part of a sermon or discourse in which the principles before laid down and illustrated are applied to practical uses; the "moral" of a fable. (b) The use of the principles of one science for the purpose of enlarging or perfecting another; as, the application of algebra to geometry.
n.
Exemption from error.
n.
A repetition; a copy.
n.
A mistake in the proceedings of a court of record in matters of law or of fact.
n.
The act or process of dividing by natural growth or spontaneous action; as, the duplication of cartilage cells.
n.
Liability to error.
n.
Mistake; error; fault.
n.
The act of directing or referring something to a particular case, to discover or illustrate agreement or disagreement, fitness, or correspondence; as, I make the remark, and leave you to make the application; the application of a theory.
n.
The capacity of being practically applied or used; relevancy; as, a rule of general application.
n.
The act of fixing the mind or closely applying one's self; assiduous effort; close attention; as, to injure the health by application to study.
n.
A fault of a player of the side in the field which results in failure to put out a player on the other side, or gives him an unearned base.