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Frequency of mutation of genes
Mutation frequency and mutation rates are highly correlated to each other. Tests for mutation frequency are cost effective in laboratories however; these
Mutation_frequency
Alteration in the nucleotide sequence of a genome
cell populations, cells with mutations will increase or decrease in frequency according to the effects of the mutations on the ability of the cell to
Mutation
Biological term for all non-reproductive bodily cells
of the body. The frequency of mutations in mouse somatic tissue (brain, liver, Sertoli cells) was compared to the mutation frequency in male germline
Somatic_(biology)
Rate at which mutations occur during some unit of time
In genetics, the mutation rate is the frequency of new mutations in a single gene, nucleotide sequence, or organism over time. Mutation rates are not constant
Mutation_rate
Type of mutation on somatic cell
are differences in the types of mutation seen in the germ and in the soma. There is variation in mutation frequency between different somatic tissues
Somatic_mutation
Gamete-producing cell
cells, that is 5 to 10-fold lower than the mutation frequency in somatic cells Thus low mutation frequency is a feature of germline cells in both sexes
Germ_cell
Malignancy that develops from epithelial cells
Whole genome sequencing has established the mutation frequency for whole human genomes. The mutation frequency in the whole genome between generations for
Carcinoma
Sequencing all the DNA of an individual at once
Furthermore, mutation frequency can vary between cancer types: in germline cells, mutation rates occur at approximately 0.023 mutations per megabase,
Whole_genome_sequencing
Tumor or other abnormal growth of tissue
higher exome mutation frequency) the total number of DNA sequence mutations is about 80,000. This compares to the very low mutation frequency of about 70
Neoplasm
Mutation Frequency Decline (mfd) is the gene which encodes the protein Mfd (also known as Transcription Repair Coupling Factor, TRCF). Mfd functions in
Mutation_Frequency_Decline
Mutation that shifts codon alignment
A frameshift mutation (also called a framing error or a reading frame shift) is a genetic mutation caused by indels (insertions or deletions) of a number
Frameshift_mutation
Allele equilibrium in a population when creation equals elimination by negative selection
deleterious (very small s {\displaystyle s} ) and the mutation rate is not very high, the equilibrium frequency of the deleterious allele will be small. In a
Mutation–selection_balance
Cells found in human testes which help produce sperm
Sertoli cells have a higher mutation frequency than spermatogenic cells. Compared to spermatocytes, the mutation frequency is about 5 to 10-fold higher
Sertoli_cell
System for fixing base errors of DNA replication
spontaneous mutation rate (mutator phenotype). In comparison to other cancer types, MMR-deficient (MSI) cancer has a very high frequency of mutations, close
DNA_mismatch_repair
Hypothesis that aging is caused by accumulated DNA damage
cells, mutant cells will increase or decrease in frequency according to the effects of the mutation on the ability of the cell to survive and reproduce
DNA_damage_theory_of_aging
Any biological cell forming the body of an organism
cell types from the same individual. Female germ cells also show a mutation frequency that is lower than that in corresponding somatic cells and similar
Somatic_cell
Concept in genetics
loss through genetic drift as are neutral mutations. Not until the allele frequency for the advantageous mutation reaches a certain threshold will genetic
Genetic_drift
Congenital extreme form of developmental delay and neoteny
patients analyzed, researchers identified missense de novo mutations in a set of genes. Mutations in three of these genes (DDX3X, TLK2 and HDAC8) were shared
Neotenic_complex_syndrome
Biological process
chromosome and causing mutation. Transposon mutagenesis is much more effective than chemical mutagenesis, with a higher mutation frequency and a lower chance
Transposon_mutagenesis
Main model used in radioprotection to minimize radiation exposures
in 1946, asserted in his Nobel lecture, The Production of Mutation, that mutation frequency is "directly and simply proportional to the dose of irradiation
Linear_no-threshold_model
Cells of a multicellular organism that pass on genetic material to progeny
transversion mutations. Such mutations occur throughout the mouse chromosomes as well as during different stages of gametogenesis. The mutation frequencies for
Germline
Model of aging as a trade-off between growth, reproduction, and DNA maintenance
premature death. No changes were observed in the spontaneous chromosomal mutation frequency of dietary restricted mice (aged 6 and 12 months) compared to ad libitum
Disposable soma theory of aging
Disposable_soma_theory_of_aging
Mutant allele Mutant screening Mutation Mutation breeding Mutation event Mutation frequency Mutation rate Mutational load Muton Myeloma Myotonic dystrophy
Index_of_genetics_articles
Attempts by males to increase their attractiveness to a female
stability (reduced mutation frequency). This signal is perceived as honest because the neocortex structure is susceptible to mutations and genetic diseases;
Peacocking
Sperm precursor cell that undergoes meiosis
the mutation frequencies of cells at the different stages, including pachytene spermatocytes, are 5 to 10-fold lower than the mutation frequencies in somatic
Spermatocyte
Accumulation of mutations
Somatic evolution is the accumulation of mutations and epimutations in somatic cells (the cells of a body, as opposed to germ plasm and stem cells) during
Somatic_evolution_in_cancer
Genetic disorder affecting mostly the lungs
on 11 August 2010. Wennberg C, Kucinskas V (1994). "Low frequency of the delta F508 mutation in Finno-Ugrian and Baltic populations". Human Heredity.
Cystic_fibrosis
Horse coat color
Oum, Muna; Del Longo, Alessandra; et al. (January 2014). "SLC45A2 mutation frequency in Oculocutaneous Albinism Italian patients doesn't differ from other
White_horse
Codon that marks the end of a protein-coding sequence
colors. Nonsense mutations that created this premature stop codon were later called opal mutations or umber mutations. Nonsense mutations are changes in
Stop_codon
Topics referred to by the same term
display, an interactive system for presenting various information Mutation Frequency Decline, a gene/gene product used in transcription-coupled repair
MFD
High frequency of mutations within the genome of a cellular lineage
genomic instability) refers to a high frequency of mutations within the genome of a cellular lineage. These mutations can include changes in nucleic acid
Genome_instability
Condition in multi-cellular organisms
result of which mutations or small chromosomal rearrangements in somatic cells. Thus the inert region causes an increase in mutation frequency or small chromosomal
Mosaic_(genetics)
Phenomenon in biology
allele frequencies too. Selective sweeps happen when newly appeared (and hence still rare) mutations are advantageous and increase in frequency. Neutral
Genetic_hitchhiking
DNA base variants frequency distribution
are themselves summaries of the allele frequency spectrum, including estimates of the population scaled mutation rate, θ = 2 N μ {\displaystyle \theta
Allele_frequency_spectrum
Formation of cancer
a higher exome mutation frequency),) the total number of DNA sequence mutations is about 80,000. These high frequencies of mutations in the total nucleotide
Carcinogenesis
Fungal plant disease on maize and teosinte
agents is increased. Also, mitotic recombination becomes deficient, mutation frequency increases, and meiosis fails to complete. These observations suggest
Corn_smut
Protein-coding gene in the species Homo sapiens
showed a 7,375-fold greater mutation frequency than wild type Chinese hamster ovary cells, and a 967-fold greater mutation frequency than the cells defective
Mismatch repair endonuclease PMS2
Mismatch_repair_endonuclease_PMS2
Subfield of genetics
to this principle, the frequencies of alleles (variations in a gene) will remain constant in the absence of selection, mutation, migration and genetic
Population_genetics
Type of pluripotent blastocystic stem cell
in order to avoid mutation and progression to cancer. Consistent with this strategy, mouse ES stem cells have a mutation frequency about 100-fold lower
Embryonic_stem_cell
Genetic process
process through which a new beneficial mutation that increases its frequency and becomes fixed (i.e., reaches a frequency of 1) in the population leads to the
Selective_sweep
How an animal develops its sexual-reproduction cells
stages of development in the mouse have a frequency of mutation that is 5 to 10-fold lower than the mutation frequency in somatic cells. In Drosophila, the
Germline_development
Type of mutation in a DNA sequence
In genetics, a nonsense mutation is a point mutation in a sequence of DNA that results in a nonsense codon, or a premature stop codon in the transcribed
Nonsense_mutation
Case in which having two different versions of a gene provides an advantage
the ebony mutation to a wild-type population. The ebony allele persisted through many generations of flies in the study, at genotype frequencies that varied
Heterozygote_advantage
Experimental Therapeutics and Oncology indicated that Colostrin reduces the mutation frequency in the DNA of cells. Such DNA damage is implicated in the general
Colostrinin
Genetic point mutation that results in an amino acid change in a protein
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. It is
Missense_mutation
Mouse assay for heritable germline mutation
tested whether radiation-induced mutation frequency depended on dose rate. The authors found lower specific-locus mutation rates after chronic gamma irradiation
Specific-locus_test
Variant of SARS-CoV-2 detected late 2020
coverage rate is correlated inversely to the SARS-CoV-2 delta variant mutation frequency in 16 countries (R-squared=0.878). Data strongly indicates that full
SARS-CoV-2_Delta_variant
Group of similar haplotypes
ancestor identified by a particular single-nucleotide polymorphism (SNP) mutation. More specifically, a haplotype is a set of closely linked alleles that
Haplogroup
Genetic neurodegenerative disease with brain iron accumulation
caused by loss of function of the enzyme PANK2, due to bi-allelic genetic mutations. It follows autosomal recessive inheritance. This enzyme is the first
Pantothenate kinase-associated neurodegeneration
Pantothenate_kinase-associated_neurodegeneration
Observation of the diversity of tumour cells
temozolomide and other chemotherapy drugs). Mutational tumor heterogeneity refers to variations in mutation frequency in different genes and samples and can
Tumour_heterogeneity
Organic chemical compound
anemia patients. This repair pathway results in increased mutation frequency and altered mutational spectrum. The second repair pathway requires replication
Acetaldehyde
Genetic changes leading to uncontrolled cell growth and tumor formation
repair pathway. This repair pathway results in increased mutation frequency and altered mutational spectrum. Other mechanisms have been proposed, including
Causes_of_cancer
Medical condition multisystem disorder
greatly elevated induction of mutations in sun-exposed skin of affected individuals. This increased mutation frequency probably accounts for the pigmentation
Xeroderma_pigmentosum
Project to catalogue genetic mutations responsible for cancer
researchers found mutations of the gene TP53 in an overwhelming 96% of the cases analyzed, Recurrent mutations at lower frequency were found in a handful
The_Cancer_Genome_Atlas
Nilotic ethnic group in Kenya, Tanzania and Uganda
Reich's laboratory also noted similar findings. They found that mutation frequencies in the Luo were much more similar to those of the surrounding Bantu
Luo_people
Mammalian protein found in Homo sapiens
et al. (2006). "Geographic and racial/ethnic differences in HFE mutation frequencies in the Hemochromatosis and Iron Overload Screening (HEIRS) Study"
HFE_(gene)
Correction of DNA replication errors
PMID 5254574. Gillin FD, Nossal NG (September 1976). "Control of mutation frequency by bacteriophage T4 DNA polymerase. I. The CB120 antimutator DNA polymerase
Proofreading_(biology)
Genetic mutation not inherited from a parent
A de novo mutation is a newly present mutation in an individual organism. These may occur in gametogenesis due to a germline mutation in a parent, or
De_novo_mutation
Time elapsed since an allele first appeared
Allele age (or mutation age) is the amount of time elapsed since an allele first appeared due to mutation. Estimating the time at which a certain allele
Allele_age
Medication used to treat a viral infection
less than 30 kb, which allow them to sustain a high frequency of mutations. The likelihood of mutations is exacerbated by the speed with which viruses reproduce
Antiviral_drug
Replacement, insertion, or deletion of a single DNA or RNA nucleotide
A point mutation is a genetic mutation where a single nucleotide base is changed, inserted or deleted from a DNA or RNA sequence of an organism's genome
Point_mutation
Relative frequency of a variant of a gene at a particular locus in a population
mechanism), gene flow, and mutation combine to change allele frequencies across generations. Genetic drift causes changes in allele frequency from random sampling
Allele_frequency
Physical or chemical agent that increases the rate of genetic mutation
in an organism and thus increases the frequency of mutations above the natural background level. As many mutations can cause cancer in animals, such mutagens
Mutagen
Enzymes that catalyze DNA formation
PMID 4554914. Gillin FD, Nossal NG (September 1976). "Control of mutation frequency by bacteriophage T4 DNA polymerase. I. The CB120 antimutator DNA polymerase
DNA_polymerase
Change in the heritable traits of populations
Mechanisms that can lead to changes in allele frequencies include natural selection, genetic drift, and mutation bias. Evolution by natural selection is the
Evolution
Measure in population genetics
the accumulation of mutation load, culminating in extinction via mutational meltdown. The accumulation of deleterious mutations in humans has been of
Genetic_load
Process inducing mutations in seeds
roughly two minutes. Mutation frequencies are notably higher for ion beam radiation compared to electron radiation, and the mutation spectrum is broader
Mutation_breeding
Mexican colloquialism
slow, castrated bulls. Over time, the initial /b/ underwent a consonant mutation to a /g/, often elided, resulting in the modern pronunciation "wey". The
Güey
Chemical compound
that the mutation frequency improved to be 12 times that of X-rays, 36 times that of procarbazine and over 200 times that of spontaneous mutations. When
ENU
Medical condition
will show a mutation on gene PIK3R1 (5q13.1), which codifies the regulating alpha subunit of phosphatidylinositol 3-kinase. This mutation can alter the
SHORT_syndrome
Medical condition
Limb region 1 protein homolog. The mutation that this gene contains varies among families, most of the point mutations that have been reported have either
Familial opposable triphalangeal thumbs duplication
Familial_opposable_triphalangeal_thumbs_duplication
population expansion rather than positive selection explained the mutation frequency spectrum during the early pandemic. Cagliani et al. wrote that the
Zoonotic_origins_of_COVID-19
Human disease
deafness is relatively slow and initially influences high-frequency sounds. Patients with WFS1 mutation have degenerative impairment in the central nervous
Wolfram_syndrome
sieve. Therefore, male-specific deleterious mtDNA mutations could be maintained and reach a high frequency in populations, decreasing males' fitness and population
Mother's_curse
Gene variant
unexpectedly high frequency, and distinct geographic distribution, which together suggest that (a) it arose from a single mutation, and (b) it was historically
CCR5-Δ32
Medical condition
kinds of seizures, but partial seizures are often the most common. The frequency of seizures can vary greatly from person-to-person. Variants in the LGI1
Autosomal dominant partial epilepsy with auditory features
Autosomal_dominant_partial_epilepsy_with_auditory_features
of identification is genetic testing for this particular mutation, the identification frequency is lower in underrepresented population. African descendants
Cystic_fibrosis_and_race
Science of genes, heredity and variation
Mendel published. In his third law, he developed the basic principles of mutation (he can be considered a forerunner of Hugo de Vries). Festetics argued
Genetics
DNA mutation involving an increase in number of trinucleotide repeats
repeat expansion, also known as a triplet repeat expansion, is the DNA mutation responsible for causing any type of disorder categorized as a trinucleotide
Trinucleotide repeat expansion
Trinucleotide_repeat_expansion
Species of bacterium
of blunt DNA ends within a functional gene sequence occurs with a mutation frequency of about 50%. NHEJ is the preferred pathway during stationary phase
Mycobacterium_smegmatis
Medical condition
endometrial endometrioid carcinomas (28%). This difference in CTNNB1 mutation frequency may be reflective of the distinct tumoral microenvironments; the epithelial
Endometrioid_tumor
2nd episode of the 10th season of The X-Files
"Founder's Mutation" is the second episode of the tenth season of The X-Files. It was written and directed by James Wong, and aired on January 25, 2016
Founder's_Mutation
Medical condition
from deep vein thrombosis, and of pulmonary embolism. One copy of the mutation increases the risk of a blood clot from 1 in 1,000 per year to 2.5 in 1
Prothrombin_G20210A
Changes to DNA with no overall impact
genetics, mutations in which natural selection does not affect the spread of the mutation in a species are termed neutral mutations. Neutral mutations that
Neutral_mutation
Theory in the domain of evolutionary biology
("origination") is a technical term for events that shift an allele frequency upward from zero (mutation is the genetic process that converts one allele to another
Bias in the introduction of variation
Bias_in_the_introduction_of_variation
Aspect of population genetics
spermatogenesis. Mutations in genes that encode proteins involved in the processing of DNA often affect recombination frequency. In bacteriophage T4, mutations that
Genetic_linkage
Process whereby cells acquire the properties of cancer
melanoma (where melanomas have a higher exome mutation frequency) the total number of DNA sequence mutations is about 80,000. A second underlying commonality
Malignant_transformation
Measure of divergence between populations
ecological factors), mutations that occur after the split will be present only in the isolated population. Random fluctuation of allele frequencies also produces
Genetic_distance
Genetic disorder caused by a mutation of chromosome 15
syndrome. In 1997, Dr. Arthur Beaudet discovered the cause of AS was the mutation of the UBE3A gene. 100% of AS diagnoses have the following symptoms: developmental
Angelman_syndrome
Change in a gene pool
arises by mutation and undergoes fixation by spreading through the population by random genetic drift or positive selection. Once the frequency of the allele
Fixation (population genetics)
Fixation_(population_genetics)
Field of study in cancer research
of thousands of mutations in their whole genomes. (Also see Mutation frequencies in cancers.) By comparison, the mutation frequency in the whole genome
Cancer_epigenetics
A behaviour mutation is a genetic mutation that alters genes that control the way in which an organism behaves, causing their behavioural patterns to change
Behavior_mutation
Prokaryotic protein
needed] Rho factor has not been found in Archaea. Termination factor Mutation Frequency Decline (Mfd) protein is also capable of dissociating RNA polymerase
Rho_factor
Cellular mechanism
usual level and these excess damages cause increased frequencies of mutation or epimutation. Mutation rates increase substantially in cells defective in
DNA_repair
American geneticist (1921–2023)
describe the processes of mutation frequency decline (MFD). She observed a decrease in damage-induced suppressor mutations when protein synthesis was
Evelyn_M._Witkin
Effect in population genetics
gene flow and mutation all contribute to this divergence. This potential for relatively rapid changes in the colony's gene frequency led most scientists
Founder_effect
Range of frequencies or wavelengths of electromagnetic radiation
spectrum is the full range of electromagnetic radiation, organized by frequency or wavelength. The spectrum is divided into separate bands, with different
Electromagnetic_spectrum
2013–2016 major disease outbreak
Griffiths, A. (16 December 2015). "Determination of the Spontaneous Mutation Frequency of Ebola virus and Exploitation of this Therapeutically". Journal
Western African Ebola epidemic
Western_African_Ebola_epidemic
Genetic neurodegenerative disease with brain iron accumulation
caused by individuals having two mutations to the gene C19orf12, but autosomal dominant disease caused by a single mutation in the same gene has also been
Mitochondrial membrane protein-associated neurodegeneration
Mitochondrial_membrane_protein-associated_neurodegeneration
Migrations of Indo-Aryans into the Indian subcontinent
plotting a decreasing North West to South East Indian cline for the mutations frequency. Kumar et al. 2015 harvnb error: no target: CITEREFKumar_et_al.2015
Indo-Aryan_migrations
MUTATION FREQUENCY
MUTATION FREQUENCY
Boy/Male
Hindu, Indian, Sanskrit
A Sort of Sound Imitation; Like a River Flow
Female
English
English unisex form of Hebrew Terach, TERAH means "delay" and "station." In the bible, this is the name of a place in the wilderness where the Israelites stopped on their Exodus. It is also the name of the father of Abraham.
Surname or Lastname
English
English : topographic name for someone who lived by a hill used as a lookout station, from an unattested Old English tÅt hyll ‘lookout hill’, or a habitational name from some place named with this word, for example Tootle Heights in Lancashire, Tothill in Lincolnshire, or Tuttle Hill in Warwickshire. This surname became established in Ireland in the 17th century, and is now more common in Ireland than England.
Surname or Lastname
English and Scottish
English and Scottish : habitational name, in part possibly from Lapley in Staffordshire, so named from Old English læppa ‘end of a parish’ + lēah ‘woodland clearing’, although the frequency of the surname in Scotland suggests another, unidentified source may also be involved.
Boy/Male
Arabic
Duration; Endurance
Male
Hebrew
(תֶּרַח) Hebrew name TERACH means "delay" and "station." In the bible, this is the name of a place in the wilderness where the Israelites stopped on their Exodus. It is also the name of the father of Abraham.
Biblical
station;
Boy/Male
Arabic, Muslim
One who Entrusts his Affairs to the Management of Another
Female
English
(תֶּרַח) English feminine form of Hebrew Terach, TARAH means "delay" and "station." In the bible, this is the name of a place in the wilderness where the Israelites stopped on their Exodus. Variant spelling of English Tara, meaning "hill."Â
Male
English
Anglicized form of Hebrew Terach, TAHATH means "delay" and "station." In the bible, this is the name of a place in the wilderness where the Israelites stopped on their Exodus.Â
Surname or Lastname
English
English : variant of Mutton.
Surname or Lastname
English
English : Reaney identifies this as a habitational name from Roselands Farm in Ulcombe, Kent. However, he gives only one (late) citation, and the surname, if it exists at all in the United Kingdom, is now very rare.Americanized form of Norwegian Røys(e)land, a habitational name from about 30 farmsteads, many in Agder, named from Old Norse reysi ‘heap of stones’ + land ‘land’, ‘farmstead’.
Male
English
Anglicized unisex form of Hebrew Terach, TERAH means "delay" and "station." In the bible, this is the name of a place in the wilderness where the Israelites stopped on their Exodus. It is also the name of the father of Abraham.
Surname or Lastname
English (chiefly Devon)
English (chiefly Devon) : nickname for someone thought to resemble a sheep (e.g. a gentle but unimaginative person), or metonymic occupational name for a shepherd, from Anglo-Norman French muto(u)n ‘sheep’ (Old French mouton, probably of Gaulish origin; compare Breton maout ‘sheep’).
Surname or Lastname
English (chiefly Northamptonshire)
English (chiefly Northamptonshire) : probably from the obsolete slang term facer, denoting a braggart or bully. The earliest citation for this term in OED is c. 1515.Americanized spelling of German Feeser.
Male
Greek
(ΠαÏαμονιμος) Ancient Greek name possibly derived from the word paramone, PARAMONIMOS means "constant, enduring," or composed of para "beside, beyond" and the name Monimos "to be favorable, pleasing." In ancient Greece there was a slave contract known as the paramone; though of limited duration, it was the most restrictive type of slavery, giving the master absolute rights.
Surname or Lastname
English
English : from Old English Englisc. The word had originally distinguished Angles (see Engel) from Saxons and other Germanic peoples in the British Isles, but by the time surnames were being acquired it no longer had this meaning. Its frequency as an English surname is somewhat surprising. It may have been commonly used in the early Middle Ages as a distinguishing epithet for an Anglo-Saxon in areas where the culture was not predominantly English--for example the Danelaw area, Scotland, and parts of Wales--or as a distinguishing name after 1066 for a non-Norman in the regions of most intensive Norman settlement. However, explicit evidence for these assumptions is lacking, and at the present day the surname is fairly evenly distributed throughout the country.Irish : see Golightly.
Surname or Lastname
English
English : variant of Joslin.English : nickname from Middle English gosling ‘young goose’ (from Old English gÅs + the Germanic suffix -ling, partly in imitation of Old Norse gæslingr from gás).German : from a short form of a Germanic personal name formed with god, got ‘god’ or gÅd ‘good’.
Boy/Male
Hindu, Indian, Kannada, Marathi, Sanskrit, Telugu
Never Ending; Persistence; Continuity; Perpetuity; Eternity; Uninterrupted Duration; Diligence; Conscientiousness; Truthful; Straightforward; Honest
Boy/Male
Indian, Sanskrit
Long Life; Age; Duration of Life; Lineage
MUTATION FREQUENCY
MUTATION FREQUENCY
Girl/Female
Arabic, Muslim, Sindhi
Narrator of Hadith; Daughter of Anas Bin Malik
Male
Croatian
, work rule.
Boy/Male
American, Australian, British, English, German
Valiant Fighter; Dusty Area
Boy/Male
Muslim
Kind, Willing and wiseman
Surname or Lastname
Scandinavian (especially Norwegian), Scottish, and northern English
Scandinavian (especially Norwegian), Scottish, and northern English : topographic name for someone who lived on a headland or promontory, Old Norse nes, or a habitational name from any of the numerous places named with this word; there are over a hundred farms in Norway and many settlements in Scotland and northern England so namedEnglish : according to Reaney and Wilson, a variant of Nash.German : habitational name from places called Nesse in Oldenburg and Friesland.German : from a short form of the female personal name Agnes (see Agnes 1).
Boy/Male
Australian, Celtic, French
God is Gracious; Oak-hearted; Form of Shane
Boy/Male
Tamil
Lover, Lovable, Trustable
Male
African
obstinate, persistent.
Girl/Female
Hindu, Indian, Kannada, Malayalam, Marathi, Telugu
Radha
Girl/Female
Bengali, Indian
Prayer of God
MUTATION FREQUENCY
MUTATION FREQUENCY
MUTATION FREQUENCY
MUTATION FREQUENCY
MUTATION FREQUENCY
n.
Change; alteration, either in form or qualities.
a.
Pertaining to, or resulting from, rotation; of the nature of, or characterized by, rotation; as, rotational velocity.
n.
Irregular change; revolution; mutation.
n.
A table showing the notation, length, or duration of the several notes.
v. t.
To place; to set; to appoint or assign to the occupation of a post, place, or office; as, to station troops on the right of an army; to station a sentinel on a rampart; to station ships on the coasts of Africa.
n.
The act of turning, as a wheel or a solid body on its axis, as distinguished from the progressive motion of a revolving round another body or a distant point; thus, the daily turning of the earth on its axis is a rotation; its annual motion round the sun is a revolution.
n.
Duration.
n.
The act or method of luting vessels.
n.
The act of citing a passage from a book, or from another person, in his own words; also, the passage or words quoted; quotation.
n.
One of the places at which ecclesiastical processions pause for the performance of an act of devotion; formerly, the tomb of a martyr, or some similarly consecrated spot; now, especially, one of those representations of the successive stages of our Lord's passion which are often placed round the naves of large churches and by the side of the way leading to sacred edifices or shrines, and which are visited in rotation, stated services being performed at each; -- called also Station of the cross.
n.
A portion of a book or document, separately transcribed; a citation; a quotation.
n.
The spot or place where anything stands, especially where a person or thing habitually stands, or is appointed to remain for a time; as, the station of a sentinel.
n.
The motion of a flower in following the apparent movement of the sun, from the east in the morning to the west in the evening.
n.
Change; alteration; mutation.
n.
Citation; quotation
n.
Enumeration; mention; as, a citation of facts.
n.
The act of nodding.
n.
A very small libratory motion of the earth's axis, by which its inclination to the plane of the ecliptic is constantly varying by a small amount.
n.
Circumnutation.