What's the difference between monogenesis and monogenetic?

Monogenesis


Definition:

  • (n.) Oneness of origin; esp. (Biol.), development of all beings in the universe from a single cell; -- opposed to polygenesis. Called also monism.
  • (n.) That form of reproduction which requires but one parent, as in reproduction by fission or in the formation of buds, etc., which drop off and form new individuals; asexual reproduction.
  • (n.) The direct development of an embryo, without metamorphosis, into an organism similar to the parent organism; -- opposed to metagenesis.

Example Sentences:

Monogenetic


Definition:

  • (a.) One in genesis; resulting from one process of formation; -- used of a mountain range.
  • (a.) Relating to, or involving, monogenesis; as, the monogenetic school of physiologists, who admit but one cell as the source of all beings.

Example Sentences:

  • (1) Phylogenetic analysis of both mini-exon-derived RNA gene and 5S gene sequences show that the free-living B. caudatus is more closely related to the monogenetic Crithidia than the digenetic Trypanosoma.
  • (2) The bifunctional dihydrofolate reductase-thymidylate synthase (DHFR-TS) gene from the monogenetic kinetoplastid protozoan, Crithidia fasciculata, was isolated and characterized.
  • (3) RI findings eliminate the hypothesis of monogenetic correlates for all six parameters investigated, and in conjunction with the F1 analysis demonstrate that each indices have polygenic correlates with at least one different locus for each of the measures of activity.
  • (4) Chromosome-sized DNA molecules from Trypanosoma cruzi clone Dm 28c were analyzed and compared with other T. cruzi strains and monogenetic trypanosomatids by orthogonal field alteration gel electrophoresis.
  • (5) Thus, genital dysmorphology may be part of many syndromes of various etiology, such as monogenetic disorders, autosomal chromosomal abnormalities and non-random malformation syndromes of unknown etiology.
  • (6) The TGR(mREN2)27 is a new monogenetic rat model in hypertension research.
  • (7) Through an examination of the pattern of associated malformations seen in RHPD we argue that RHPD-DW is a distinct monogenetic syndrome, and not an association.
  • (8) Hereditary types of hypogonadism and intersexuality are based on a chromosomal aberration, on a monogenetic defect of androgen synthesis, or on a androgen receptor.
  • (9) The 2-hydroxylation which is the most important step of elimination is mediated via microsomal cytochrome P450 isozyme that exhibit monogenetic polymorphism such that 5-10% of the population have a severely reduced clearance.
  • (10) An investigation of transmission and ecology of the monogenetic trypanosomatids, Blastocrithidia gerridis and Crithidia flexonema, in Gerris is described.
  • (11) The mutants were shown to have monogenetic defects and to fall into 12 complementation groups.
  • (12) Monogenetic insect trypanosomatids of the genera Crithidia, Leptomonas and Herpetomonas, multiplied as in axenic cultures, for many months, in the lumen of the scent glands of the opossum Didelphis marsupialis.
  • (13) In the rooted version of the tree, the monogenetic species Crithidia fasciculata is the most deeply rooted, followed by another monogenetic species, Leptomonas sp.
  • (14) The RI method successfully rejects the hypothesis of a monogenetic correlate for all measures.
  • (15) Phenotype distribution in each family and population was consistent with the hypothesis that debrisoquine 4-OH-hydroxylation activity is under diallelic, monogenetic control, with the PM phenotype inheriting in an autosomal recessive trait.
  • (16) A monogenetic factor determining basic pigmentation in Biomphalaria straminea follows simple.
  • (17) The problems of differentiation and characterisation of monogenetic insect flagellates are discussed in the light of these findings.
  • (18) Six new monogenetic trematodes are described from Nebraska fishes: Gyrodactylus bulbacanthus sp.
  • (19) The histone-like proteins of the monogenetic parasite Crithidia fasciculata were extracted with 0.2 M sulfuric acid either from purified nuclei, or from purified chromatin, in both cases in the presence of 1 mM tosyl lysylchloromethylketone and 2 mM phenyl methyl sulfonyl fluoride as proteinase inhibitors.
  • (20) Ataxia-telangiectasia (A-T) is inherited as an monogenetic autosomal recessive disease.

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