| ¿µ¹® | nomenclature | ÇÑ±Û | ¸í¸í¹ý |
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| CA | anterior commissure [Lat. commissura anterior]; calcium antagonist; California [rabbit]; cancer; Can... |
|---|---|
| cRNA | chromosomal ribonucleic acid |
| ICBR | increased chromosomal breakage rate |
| NHC | National Health Council; neighborhood health center; neonatal hypocalcemia; nonhistone chromosomal [... |
| NHCP | nonhistone chromosomal protein |
| SNOMED | Systematized Nomenclature of Medicine |
|---|---|
| CA | Chromosomal aberration |
| CISS | Chromosomal in situ suppression |
| NHCP | Nonhistone chromosomal proteins |
| CIN | chromosomal instability |
| binary nomenclature | The system of nomenclature in which the names of species are composed of two parts, a generic name and a specific epithet (species name, in botany). Synonym: binary nomenclature, binomial nomenclature. Origin: Carl von Linne (05 Mar 2000) |
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| binomial nomenclature | <biology, ecology> The system of having two names (genus and specific epithet, also called Latin binomial) for each organism. (09 Oct 1997) |
| Cleland nomenclature | A nomenclature for representing the binding mechanisms of enzyme-catalyzed reactions; in this nomenclature, substrates are represented by the letters A, B, C, etc., while products are represented by P, Q, R, etc., enzyme by E, and modified forms of the enzyme by F, G, etc.; in addition, the number of substrates or products is represented by uni, bi, ter, etc.; thus, an aminotransferase reaction (e.g., alanine transaminase) has a ping-pong bi bi mechanism; glutamine synthetase has been reported to have a random ter ter mechanism.subentries under mechanism. (05 Mar 2000) |
| nomenclature | <zoology> The description of new taxa or alterations to the concept of previously described taxa which involve changes in the names of taxa. (09 Jan 1998) |
| International Code of Zoological Nomenclature | <zoology> An Authoritative document containing a system of rules and recommendations to be followed in giving a scientific name to an animal or animal group. Adopted by the International Congresses of Zoology and Administered by the International Commission on Zoological Nomenclature. The most recent version of the Code, adopted in principle by the 20th General Assembly of the International Union of Biological Sciences at Helsinki in 1979, was approved by the ICZN late in 1983. With minor exceptions it retains the same format as the first two editions. Minor amendments for immediate incorporation are published in Bulletin Zoological Nomenclature as Declarations to remain in force until ratified or rejected by future congresses. (09 Jan 1998) |
| linnaean system of nomenclature | The system of nomenclature in which the names of species are composed of two parts, a generic name and a specific epithet (species name, in botany). Synonym: binary nomenclature, binomial nomenclature. Origin: Carl von Linne (05 Mar 2000) |
| genome, chromosomal | All of the genetic information in the chromosomes of an organism. For humans, that is all of the DNA contained in our normal complement of 46 rod-like chromosomes in virtually every cell in the body. (Mature red blood cells, for one exception, have no nucleus and therefore no chromosomes). The chromosomal genome is synonymous with the nuclear genome. Together with the mitochondrial genome, it constitutes the genome of the human being. (12 Dec 1998) |
| chromosomal | Pertaining to chromosomes. (18 Nov 1997) |
| chromosomal aberration | Any abnormality of a chromosome's number or structure. (09 Oct 1997) |
| chromosomal deletion | A microscopically evident loss of part of a chromosome. See: monosomy. (05 Mar 2000) |
| chromosomal gap | A localised area of thinning in a chromatid which may simulate a complete break. (05 Mar 2000) |
| chromosomal instability syndromes | A group of mendelian conditions associated with chromosomal instability and breakage in vitro, they often manifest an increased tendency to certain types of malignancies. See: Bloom's syndrome, fragile X syndrome, xeroderma pigmentosum. (05 Mar 2000) |
| chromosomal map | A formal, stylised representation of the karyotype and of the positioning and ordering on it of those loci that have been localised by any of several mapping methods. (05 Mar 2000) |
| chromosomal mutation | Can refer to any of a number of DNA mutations which results in a change in the protein encoded by the mutated gene, such as point mutations, insertion or deletion mutations (frameshift mutations), or nonsense mutations. More often this refers to mutations involving chromosomes, such as the inversion of part of one chromosome such that the inverted part no longer matches with its homologous pair, a translocation of one part of a chromosome to a different chromosome, deletions of parts of chromosomes, or accidents which happen during the division of the nucleus like the unequal portioning of chromosomes between the daughter cells. (09 Oct 1997) |
| chromosomal proteins, non-histone | Nucleoproteins which in contrast to histones are acid insoluble. They are involved in chromosomal functions; e.g. They bind selectively to DNA, stimulate transcription resulting in tissue-specific RNA synthesis and undergo specific changes in response to various hormones or phytomitogens. (12 Dec 1998) |
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