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A monogenic function is a complex function with a single finite derivative. More precisely, a function f ( z ) {\displaystyle f(z)} defined on A ⊆ C {\displaystyle
Monogenic_function
Topics referred to by the same term
Monogenic obesity Monogenic field, in mathematics, an algebraic number field K Monogenic function, a function in an algebra over a field Monogenic polynomial
Monogenic
Provides integral formulas for all derivatives of a holomorphic function
f ( r ) {\displaystyle f(r)} is called a monogenic function, the generalization of holomorphic functions to higher-dimensional spaces – indeed, it can
Cauchy's_integral_formula
the euclidean Dirac equation Df = 0 are called (left) monogenic functions. Monogenic functions are special cases of harmonic spinors on a spin manifold
Clifford_analysis
Russian mathematician
Kronrod, A. S. (1945), "On a direct proof of the analyticity of a monogenic function", Doklady Akademii Nauk SSSR, New Series, 50: 7–9, MR 0051912. Adel'son-Vel'skiĭ
Georgy_Adelson-Velsky
French mathematician (1871–1956)
some physical theories (1914) A course on complex variable uniform monogenic functions (1917) On the method in sciences (1919) Space and time (1921) Game
Émile_Borel
Obesity caused by a mutation in a single gene
Monogenic obesity is excess weight caused by a mutation in a single gene. It differs from syndromic obesity, which involves additional clinical phenotypes
Monogenic_obesity
Medical condition
Along with neonatal diabetes, MODY is a form of the conditions known as monogenic diabetes. While the more common types of diabetes (especially type 1 and
Maturity-onset diabetes of the young
Maturity-onset_diabetes_of_the_young
Polynomial with 1 as leading coefficient
simpler in the case of monic polynomials: The kth elementary symmetric function of the roots of a monic polynomial of degree n equals ( − 1 ) k c n − k
Monic_polynomial
Type of system in classical mechanics
generalized scalar potential is a function of generalized coordinates, generalized velocities, or time, then, this system is a monogenic system. Expressed using
Monogenic_system
Particular representation of a signal
two elements of the vector-valued monogenic signal, as it is defined for one-variable signals. However, the monogenic signal can be extended to arbitrary
Analytic_signal
Romanian mathematician
multi-dimensional extension of Pompeiu's areolar derivative, and studied monogenic functions of one hypercomplex variable with applications to mechanics. Moisil
Grigore_Moisil
Italian mathematician (1924–2018)
main result is the extension of Cauchy's integral theorem to every monogenic function F on a general complex algebra A, ∫ Γ 1 F ( X ) d X = 0 {\displaystyle
Giovanni_Battista_Rizza
Expulsion of feces from the digestive tract
bowel function, symptom recurrence, disability, etc. Patients can be children or adults. Recent research shows that immunodeficiency and monogenic disorders
Defecation
Rare neurodegenerative disease
ALS is thought to account for 10–15% of cases overall and can include monogenic, oligogenic, and polygenic modes of inheritance. There is considerable
ALS
Group of neurodegenerative conditions
disorders, that present symptoms before the age of 18. They are typically monogenic (caused by mutations of a single gene). Their main characteristics are
Childhood_dementia
Transmembrane protein
multi-organ epithelial inflammation was found to have a homozygous loss-of-function mutation in the EGFR gene. The pathogenicity of the EGFR mutation was supported
Epidermal growth factor receptor
Epidermal_growth_factor_receptor
Mammalian protein found in humans
growth velocity (MC4R monogenic diabetes).[citation needed] There is limited treatment options for the most common form of monogenic obesity, MC4R mutations
Melanocortin_4_receptor
Progressive neurodegenerative disease
genetic disease, as rare inherited gene variants have been firmly linked to monogenic PD, and most cases carry variants that increase PD risk. PD heritability
Parkinson's_disease
that occurred early in vertebrate evolution may be the reason that human monogenic disease genes often contain a high number of redundant genes. Chen et
Gene_redundancy
Protein-coding gene in the species Homo sapiens
genetic locus conferring susceptibility was identified (juvenile audiogenic monogenic seizures1, jams1) on chromosome 10. A positional cloning approach aimed
GIPC3
Genetic diversity in human populations
incidence of some monogenic diseases, and they may contribute to differences in the incidence of some common diseases. For the monogenic diseases, the frequency
Human_genetic_variation
Transcription factor gene of the forkhead box family
dominant fashion. This is one of the few known examples of Mendelian (monogenic) inheritance for a disorder affecting speech and language skills, which
FOXP2
Study of role of genetics in the nervous system
multi-gene conditions influenced by environmental factors. Major Categories: Monogenic Neurogenic Disorders - These are mutations in a single gene and closely
Neurogenetics
Group of innate immune system disorders
diseases is historically called MAS, and in the context of the familial monogenic defects resulting in impaired NK (natural killer cells) or CD8+ T cell
Autoinflammatory_diseases
Group of endocrine diseases characterized by high blood sugar levels
diabetes can result from other specific causes, such as genetic conditions (monogenic diabetes syndromes like neonatal diabetes and maturity-onset diabetes
Diabetes
Relation between obesity and genetic factors
challenges associated with detecting gene-gene interactions for obesity. Monogenic obesity results from single-gene mutations that disrupt the body's ability
Genetics_of_obesity
Medical condition
Deficiency of Adenosine deaminase 2 (DADA2) is a monogenic disease associated with systemic inflammation and vasculopathy that affects a wide variety
Adenosine deaminase 2 deficiency
Adenosine_deaminase_2_deficiency
Finite extension of the rationals
the field K {\displaystyle K} is called a monogenic field. An example of a number field that is not monogenic was first given by Dedekind. His example
Algebraic_number_field
Branch of mathematics
Clifford valued functions that are annihilated by Dirac or Dirac-like operators, termed in general as monogenic or Clifford analytic functions. p-adic analysis
Mathematical_analysis
Abnormally elevated levels of lipids or lipoproteins in the blood
Hazzard W. R.; Albers J. J.; Cooper M. N.; Motulsky A. G. "Frequency of monogenic forms of hyperlipidemia in a normal population." A19. In: "Program and
Hyperlipidemia
Protein-coding gene in the species Homo sapiens
YX (2016). "Ghrelin Receptor Mutations and Human Obesity". Genetics of Monogenic and Syndromic Obesity. Vol. 140. pp. 131–50. doi:10.1016/bs.pmbts.2016
Growth hormone secretagogue receptor
Growth_hormone_secretagogue_receptor
Medical condition
Silva, Jorge Diogo (2023-09-01). "An SPG7 mutation as a novel cause of monogenic progressive muscular atrophy". Neurological Sciences. 44 (9): 3303–3305
Progressive_muscular_atrophy
Branch of philosophy
most powerful is the etiogically defined approach as can be found in the monogenic conception of disease which covers not only infectious agents (bacteria
Philosophy_of_medicine
Belgian researcher and physician
research interest is pancreatic beta cell failure in type 2 diabetes and monogenic forms of diabetes. She contributed to show that lipotoxicity, the deleterious
Miriam_Cnop
Protein-coding gene in the species Homo sapiens
successful conclusion to the long search for TRPV5 pathogenic variants in monogenic hypercalciuria". European Journal of Human Genetics. 32 (11): 1345–46
TRPV5
Medical condition
S2CID 195676310. Garovic VD, Hilliard AA, Turner ST (November 2006). "Monogenic forms of low-renin hypertension". Nature Clinical Practice. Nephrology
Pseudohypoaldosteronism
Numerical score aimed at predicting a trait based on variation in multiple genetic loci
it is important to realize that polygenic traits are different from monogenic traits; the latter stem from fewer genetic loci and can be detected more
Polygenic_score
Medical condition
1126/science.2448879. PMID 2448879. Fleisher TA; Oliveira JB (2012). "Monogenic defects in lymphocyte apoptosis". Current Opinion in Allergy and Clinical
RAS-associated autoimmune leukoproliferative disorder
RAS-associated_autoimmune_leukoproliferative_disorder
Genetic profiling of embryos prior to implantation
and the severity of the disease. PGD is available for a large number of monogenic disorders—that is, disorders due to a single gene only (autosomal recessive
Preimplantation genetic diagnosis
Preimplantation_genetic_diagnosis
Potassium channel
Burton PR, Samani NJ (June 2008). "Common variants in genes underlying monogenic hypertension and hypotension and blood pressure in the general population"
ROMK
Fact of an action or object originating externally
Gumus Balikcioglu, Pinar (September 10, 2014). "Screening for Hormonal, Monogenic, and Syndromic Disorders in Obese Infants and Children". Pediatric Annals
Exogeny
Medical condition
select unaffected embryos to implant. This process call be applied to any monogenic disease.[citation needed] While choroideremia is an ideal candidate for
Choroideremia
Enzyme in humans
Weinshilboum RM, Sladek SL (1980). "Mercaptopurine pharmacogenetics: Monogenic inheritance of erythrocyte thiopurine methyltransferase activity". American
Thiopurine_methyltransferase
Medical condition
1155/2017/6279460. PMC 5370477. PMID 28396810. Ingelfinger, Julie R (2018). "Monogenic and Polygenic Contribution to Hypertension". In Flynn, JT (ed.). Pediatric
Liddle's_syndrome
Protein-coding gene in the species Homo sapiens
(2014). "Roles of HNF1α and HNF4α in pancreatic β-cells: lessons from a monogenic form of diabetes (MODY)". Vitamins and Hormones. 95: 407–23. doi:10
Hepatocyte nuclear factor 4 alpha
Hepatocyte_nuclear_factor_4_alpha
System involved in the regulation of weight and peripheral tissue such as hair and skin
to result in morbid obesity, and is the most commonly known cause of monogenic morbid obesity. Mutation in an allele of the melanocortin-4 receptor causes
Central_melanocortin_system
Form of diabetes mellitus
pancreatic beta cell functions. There are a number of rare cases of diabetes that arise due to an abnormality in a single gene (known as monogenic forms of diabetes
Type_2_diabetes
Medical condition where fat accumulates in the liver
Alcohol-associated liver disease (ALD) Specific aetiology SLD (including drug-induced, monogenic diseases and others) Often there are no or few symptoms. Occasionally
Fatty_liver_disease
Biological molecules constituting nucleic acids
limitations of antisense oligonucleotide therapies for the treatment of monogenic disorders". Communications Medicine. 4 (1) 6. doi:10.1038/s43856-023-00419-1
Nucleotide
Medical condition
of diabetes that, along with maturity onset diabetes of the young is monogenic (regulated by a single gene) and arises in the first 6 months of life
Neonatal_diabetes
Genetic disorder characterized by high cholesterol levels
multiple names: authors list (link) Rader DJ, Cohen J, Hobbs HH (2003). "Monogenic hypercholesterolemia: new insights in pathogenesis and treatment". J.
Familial_hypercholesterolemia
Abnormally low levels of albumin in the blood
0916. ISSN 1665-2681. PMID 29893696. Cil, Onur; Perwad, Farzana (2018). "Monogenic Causes of Proteinuria in Children". Frontiers in Medicine. 5: 55. doi:10
Hypoalbuminemia
Protein-coding gene in the species Homo sapiens
Moreews M, Rieux-Laucat F, Soulas-Sprauel P, et al. (October 2019). "Monogenic lupus: Dissecting heterogeneity". Autoimmunity Reviews. 18 (10) 102361
Deoxyribonuclease_gamma
Algebraic structure
A semigroup generated by a single element is said to be monogenic (or cyclic). If a monogenic semigroup is infinite then it is isomorphic to the semigroup
Semigroup
Rare genetic syndrome
unbalanced chromosomal translocation). Although early researchers sought a monogenic (single gene genetic disorder) explanation, recent studies have not supported
22q13_deletion_syndrome
Excessive fat buildup in the liver with other metabolic disease
(etiologies) such as cryptogenic SLD, drug-induced liver injury (DILI), and monogenic diseases. By various mechanisms and possible insults to the liver, SLD
Metabolic dysfunction–associated steatotic liver disease
Metabolic_dysfunction–associated_steatotic_liver_disease
Enzyme known as Human Protective Protein
Della-Ripa B, Davagnanam I, et al. (December 2022). "A rare cause of monogenic cerebral small vessel disease and stroke: Cathepsin A-related arteriopathy
Cathepsin_A
Medication
S2CID 40097592. Oddi D, Crusio WE, D'Amato FR, Pietropaolo S (August 2013). "Monogenic mouse models of social dysfunction: implications for autism". Behav Brain
Naltrexone
the GKRP gene (GCKR) in humans have been sought as possible causes of monogenic diabetes (MODY), but no examples have yet been discovered. However, variant
Glucokinase regulatory protein
Glucokinase_regulatory_protein
Theory of plural human origins
an increased understanding of speciation in a human context, with the monogenic "Out of Africa" hypothesis and its variants being the most widely accepted
Polygenism
Protein-coding gene in the species Homo sapiens
variants in the NFKB2 gene have been identified as one of the possible monogenic causes of the disease. The frequency of NFKB2 mutation in CVID population
NFKB2
Medical condition
Leu C, et al. (April 2020). "A catalogue of new incidence estimates of monogenic neurodevelopmental disorders caused by de novo variants". Brain. 143 (4):
SYNGAP1-related intellectual disability
SYNGAP1-related_intellectual_disability
Protein-coding gene in the species Homo sapiens
Phosphorylation of RELA plays a key role in regulating NF-κB activation and function. Subsequent to NF-κB nuclear translocation, RELA undergoes site-specific
RELA
Edible berry
Tomato Genetics Resource Center maintains a gene bank of wild relatives, monogenic mutants and genetic stocks. Research on processing tomatoes is also conducted
Tomato
Diagnosis, treatment, and prevention of illness
increasingly significant influence on medicine, as the causative genes of most monogenic genetic disorders have now been identified, and the development of techniques
Medicine
Series of interconnected biochemical reactions
PMC 6405412. PMID 30137266. Baranowski ES, Arlt W, Idkowiak J (2018). "Monogenic Disorders of Adrenal Steroidogenesis". Horm Res Paediatr. 89 (5): 292–310
Androgen_backdoor_pathway
Congenital excess of melanin in an organism resulting in dark pigment
in the cat family. Melanism in leopards is inherited as a Mendelian, monogenic recessive trait relative to the spotted form. Pairings of black animals
Melanism
Chemical compound
Natale V, et al. (September 2019). "46,XX DSD due to Androgen Excess in Monogenic Disorders of Steroidogenesis: Genetic, Biochemical, and Clinical Features"
5α-Pregnane-3α,17α-diol-20-one
5α-Pregnane-3α,17α-diol-20-one
Protein-coding gene in the species Homo sapiens
this syndrome is new. However, they also overlap with several recognized monogenic conditions that are neurological in nature including Troyer syndrome,
FITM2
X-linked dominant genetic disorder
Protein and Genome Function". Molecular Neurobiology. 56 (1): 711–721. doi:10.1007/s12035-018-1122-9. PMID 29796988. S2CID 44159474. "Monogenic diseases". Human
Fragile_X_syndrome
Range of genetic disorders which cause a person to appear to grow older faster
aging.[citation needed] All disorders within this group are thought to be monogenic, meaning they arise from mutations of a single gene. Most known PS are
Progeroid_syndromes
Genetic process
supporting monoallelic expression of V1rb2mv and V1rb2vg alleles and monogenic expression of the V1rb2 locus. Monoallelic expression was also found in
Allelic_exclusion
Medical conditions more common in autistic people
with autism. Symptoms are likely affected by age, level of cognitive functioning, degree of social impairment, and autism-specific difficulties. Many
Conditions_comorbid_to_autism
Medical condition
Kornvalee (April 2023). "Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome". Journal of Allergy
STAT3_GOF
Disease category
polygenic diseases; clues to their understanding are coming from the rarer monogenic forms of common symptoms such as seizures, ataxia, and migraine. Gargus
Calciumopathy
All Latin and Greek roots beginning with G
homogeneous, hydrogen, hypogene, hypogenesis, hypogenic, hypogenous, monogenic, oogenesis, paragenesis, pathogen, polygenous, progenesis, pseudogene
List of Greek and Latin roots in English/A–G
List_of_Greek_and_Latin_roots_in_English/A–G
Degree to which a phenotype is expressed
spectrum. Sickle Cell Anemia is an autosomal recessive, prototypical monogenic Mendelian disease, meaning that the disease follows Mendelian inheritance
Expressivity_(genetics)
Genetically modified human embryo
identification of specific genes. The process is often used when screening for monogenic disorders, such as cystic fibrosis. Another screening technique, fluorescent
Designer_baby
Medical condition
Adult polyglucosan body disease (APBD) is a rare monogenic glycogen storage disorder (GSD type IV) caused by an inborn error of metabolism. Symptoms can
Adult polyglucosan body disease
Adult_polyglucosan_body_disease
Mammalian protein found in Homo sapiens
causes a number of different autoinflammatory syndromes, most notably the monogenic conditions referred to as Cryopyrin-Associated Periodic Syndromes (CAPS)
Interleukin_1_beta
Mental disorder with psychotic symptoms
affect this axis. Response to stress can cause lasting changes in the function of the HPA axis possibly disrupting the negative feedback mechanism, homeostasis
Schizophrenia
Non-technical introduction to genetics
These may be monogenic (caused by alterations in a single gene), polygenic (caused by alterations in multiple genes). Examples of monogenic gene disorders
Introduction_to_genetics
Range of possible values for any characteristic of human beings
single loci or multiple loci, labeling said biological traits as either monogenic or polygenic, respectively. Concerning polygenic traits it may be essential
Human_variability
Medical condition
myoclonic seizures and/or myoclonic astatic seizures. Some of the common monogenic causes include mutations in the genes SLC6A1 (3p25.3), CHD2 (15q26.1)
Myoclonic_astatic_epilepsy
Human disease
Eichler, Evan E. (2022-11-09). "Estimating the Prevalence of De Novo Monogenic Neurodevelopmental Disorders from Large Cohort Studies". Biomedicines
Okur–Chung neurodevelopmental syndrome
Okur–Chung_neurodevelopmental_syndrome
Medical condition
Yeshwanter; Nair, Nikhil R.; Kusumi, Kirsten (2019-07-01). "Overview of Monogenic or Mendelian Forms of Hypertension". Frontiers in Pediatrics. 7: 263.
Pseudohyperaldosteronism
diabetes that arise due to an abnormality in a single gene (known as monogenic forms of diabetes). These include maturity onset diabetes of the young
Genetic causes of type 2 diabetes
Genetic_causes_of_type_2_diabetes
Human gene
PMID 32226026. Liu A, Ying S (October 2023). "Aicardi-Goutières syndrome: A monogenic type I interferonopathy". Scandinavian Journal of Immunology. 98 (4) e13314
IFI44L
Medical condition
deficiency over time. Genetic testing can help distinguish LADA from monogenic forms of diabetes (e.g., MODY), which lack autoimmune markers and do not
Latent autoimmune diabetes in adults
Latent_autoimmune_diabetes_in_adults
French medical doctor
identification of genes and mutations responsible for rare inherited monogenic diseases affecting the nervous system and/or muscles. He has also contributed
Jean-Louis_Mandel
Protein-coding gene in humans
cause maturity onset diabetes of the young type 3, one of the forms of "monogenic diabetes", as well as hepatocellular adenoma. HNF-1 protein is present
HNF1A
Type of constraints for mechanical systems
system. For example, if a physical system is a holonomic system and a monogenic system, then Hamilton's principle is the necessary and sufficient condition
Holonomic_constraints
Medical condition
distinguish between PHA2 and DA3. Ceccato, Filippo; Mantero, Franco (2019). "Monogenic Forms of Hypertension". Endocrinology and Metabolism Clinics of North
Gordon_syndrome
Biological system that determines the development of an organism's sex
your eggs in one basket? Evolutionary perspectives on the origins of monogenic reproduction". Heredity. 131 (2): 87–95. Bibcode:2023Hered.131...87B.
Sex-determination_system
Type of modifier gene
genetic disease. Whereas medical genetics has tended to distinguish between monogenic traits, governed by simple, Mendelian inheritance, and quantitative traits
Human_disease_modifier_gene
Condition involving social and behavioral differences
include defects in synapse structure and function, reduced synaptic plasticity, disrupted neural circuit function, gut–brain axis dyshomeostasis, neuroinflammation
Autism
Medical model that tailors medical practices to the individual patient
scores for common diseases identify individuals with risk equivalent to monogenic mutations". Nat Genet. 50 (9): 1219–1224. doi:10.1038/s41588-018-0183-z
Personalized_medicine
Approach to study autism using non-human species
S2CID 143857251. Oddi D, Crusio WE, d'Amato FR, Pietropaolo S (2013). "Monogenic mouse models of social dysfunction: Implications for autism". Behavioural
Animal_model_of_autism
Dilution gene
Fjord Horse Registry. Retrieved January 20, 2010. Imsland, Freyja (2015). Monogenic Traits Associated with Structural Variants in Chicken and Horse (PDF)
Dun_gene
MONOGENIC FUNCTION
MONOGENIC FUNCTION
Male
Celtic
, great justiciary, or functionary.
Surname or Lastname
English
English : nickname from the animal, Middle English catte ‘cat’. The word is found in similar forms in most European languages from very early times (e.g. Gaelic cath, Slavic kotu). Domestic cats were unknown in Europe in classical times, when weasels fulfilled many of their functions, for example in hunting rodents. They seem to have come from Egypt, where they were regarded as sacred animals.English : from a medieval female personal name, a short form of Catherine.Variant spelling of German and Dutch Katt.
Male
Egyptian
, an Egyptian functionary.
Male
Egyptian
, a high Egyptian functionary.
Male
Egyptian
, an Egyptian functionary.
Boy/Male
Buddhist, Indian, Japanese
Mysterious Function
Male
Egyptian
, the son of the functionary Heknofre.
Male
Egyptian
, a great functionary.
Male
Egyptian
, Functionary of the Interior.
Surname or Lastname
English
English : occupational name for a dresser of cloth, Old English fullere (from Latin fullo, with the addition of the English agent suffix). The Middle English successor of this word had also been reinforced by Old French fouleor, foleur, of similar origin. The work of the fuller was to scour and thicken the raw cloth by beating and trampling it in water. This surname is found mostly in southeast England and East Anglia. See also Tucker and Walker.In a few cases the name may be of German origin with the same form and meaning as 1 (from Latin fullare).Americanized version of French Fournier.Samuel Fuller (1589–1633), born in Redenhall, Norfolk, England, was among the Pilgrim Fathers who sailed on the Mayflower in 1620. He was a deacon of the church and until his death functioned as Plymouth Colony’s physician.
Surname or Lastname
English (chiefly Kent and Sussex)
English (chiefly Kent and Sussex) : occupational name for a designer or engineer, from a Middle English reduced form of Old French engineor ‘contriver’ (a derivative of engaigne ‘cunning’, ‘ingenuity’, ‘stratagem’, ‘device’). Engineers in the Middle Ages were primarily designers and builders of military machines, although in peacetime they might turn their hands to architecture and other more pacific functions.German : from the Latin personal name Januarius (see January 1). Jänner is a South German word for ‘January’, and so it is possible that this is one of the surnames acquired from words denoting months of the year, for example by converts who had been baptized in that month, people who were born or baptized in that month, or people whose taxes were due in January.
Biblical
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Surname or Lastname
English
English : topographic name for someone who lived by the gates of a medieval walled town. The Middle English singular gate is from the Old English plural, gatu, of geat ‘gate’ (see Yates). Since medieval gates were normally arranged in pairs, fastened in the center, the Old English plural came to function as a singular, and a new Middle English plural ending in -s was formed. In some cases the name may refer specifically to the Sussex place Eastergate (i.e. ‘eastern gate’), known also as Gates in the 13th and 14th centuries, when surnames were being acquired.Americanized spelling of German Götz (see Goetz).Translated form of French Barrière (see Barriere).In New England, Gates was the preferred English version of the name of an extensive French family, called Barrière dit Langevin.
MONOGENIC FUNCTION
MONOGENIC FUNCTION
Girl/Female
Arabic, Australian, German, Hebrew, Indian, Muslim
Goddess; Good Luck; Pious
Boy/Male
Arabic, Muslim
Shadow of Allah
Girl/Female
Tamil
Chandrani | சஂதà¯à®°à®¾à®¨à¯€
Wife of the Moon (Wife of the Moon)
Boy/Male
Hindu, Indian
Name of God
Surname or Lastname
English and Irish
English and Irish : variant of Mullins.
Girl/Female
Spanish
Guardtower.
Male
Irish
Diminutive form of Irish Gaelic Cian, CIANÃN means "little ancient one."
Boy/Male
Hindu, Indian, Tamil
Lord Shiva
Boy/Male
Hindu, Indian, Traditional
Righteous; Virtuous Man
Girl/Female
American, British, Chinese, English, Irish
Clever; Curly-haired
MONOGENIC FUNCTION
MONOGENIC FUNCTION
MONOGENIC FUNCTION
MONOGENIC FUNCTION
MONOGENIC FUNCTION
a.
Relating to, or involving, monogenesis; as, the monogenetic school of physiologists, who admit but one cell as the source of all beings.
a.
Belonging to, or affecting, a single organ, or set of organs.
a.
Pertaining to the Monogynia; monogynous.
a.
One in genesis; resulting from one process of formation; -- used of a mountain range.
n.
One of the Monogynia.
a.
Alt. of Monogamic
a.
Alt. of Monotonical
a.
Of or pertaining to the Monogamia; having a simple flower with united anthers.
n.
Monogenesis.
a.
Of or pertaining to monogenesis.
a.
Ontogenetic.
a.
Monogenic.
a.
Pertaining to, or involving, monogamy.
a.
Of or pertaining to zoogeny, animal production.
n.
One who maintains that the human races are all of one species; -- opposed to polygenist.
n.
One of the Monogynia.
n.
The doctrine that the members of the human race have all a common origin.
n.
The theory or doctrine that the human races have a common origin, or constitute a single species.
n. pl.
A Linnaean order of plants, including those which have only one style or stigma.
a.
Producing only one kind of germs, or young; developing only in one way.