| CA | anterior commissure [Lat. commissura anterior]; calcium antagonist; California [rabbit]; cancer; Can... |
|---|---|
| MMA | mastitis-metritis-agalactia [syndrome]; medical management analysis; medical materials account; meth... |
| cRNA | chromosomal ribonucleic acid |
| ICBR | increased chromosomal breakage rate |
| NHC | National Health Council; neighborhood health center; neonatal hypocalcemia; nonhistone chromosomal [... |
| CA | Chromosomal aberration |
|---|---|
| AB | aberration |
| CA | Chromosome aberration |
| NA | nuclear aberration |
| TCA | transverse chromatic aberration |
| chromosomal aberration | Any abnormality of a chromosome's number or structure. (09 Oct 1997) |
|---|
| 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 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) |
| chromosomal region | That part of a chromosome defined either by anatomical details, notably banding, or by its linkages (linkage group). (05 Mar 2000) |
| chromosomal RNA | RNA associated with the chromosome (not mRNA, tRNA, or rRNA) that may have a role in transcription. (05 Mar 2000) |
| chromosomal syndrome | <syndrome> General designation for syndrome's due to chromosomal aberrations; typically associated with mental retardation and multiple congenital anomalies. (05 Mar 2000) |
| chromosomal trait | A trait dependent on a recurrent chromosomal aberration. (05 Mar 2000) |
| nonhistone chromosomal protein | <molecular biology> Chromatin consists of DNA, histones and a very heterogeneous group of other proteins, that include DNA polymerases, regulator proteins, etc. They are often lumped together terminologically as nonhistone proteins or acidic proteins, to distinguish them from the basic histones. (18 Nov 1997) |
| aberration | 1. <ophthalmology> Any error that results in image degradation. Such errors may be chromatic, spherical, astigmatic chromatic, distortion, or curvature of field: and can result from design or execution, or both. 2. <physics> Failure of an optical or electron-optical lens to produce exact geometrical (and chromatic) correspondence between an object and its image. In a video camera tube or cathode-ray tube, aberrations are when the (electrostatic or electromagnetic) lens does not bring the electron beam to sharply focused points uniformly on the target or screen, or to correct geometrical positions, as the beam is deflected. 3. <zoology> A term which, if used to denote a number of individuals within a species, unequivocally signifies infrasubspecific rank. See: aberration, chromatic, aberration, spherical. (09 Jan 1998) |
| aberration, chromatic | <optics> A defect in a lens or optical system due to the greater refraction of shorter wavelengths over that of loner ones at a lens surface. Hence the focal length of a simple lens is shorter for blue than for red rays. This dispersion of the wave-lengths will cause colour fringes in the image field of a lens with such an aberration. (05 Aug 1998) |
| chromosomal aberration |
any change in the normal structure or number of chromosomes; often results in physical or mental abnormalities
출처: wordnet.princeton.edu/perl/webwn
|
|---|---|
| chromosomal aberration |
Any change in chromosome structure or number. Although it can be a mechanism for enhancing genetic diversity, such alterations are usually fatal or ill-adaptive, especially in animals.
출처: www.fao.org/docrep/003/X3910E/X3910E06.htm
|
| chromosomal aberration |
An irregularity in the number or constitution of chromosomes which may cause abnormalities in a developing embryo.
출처: www.uoguelph.ca/GTI/urbanpst/glossa_e.htm
|
| chromosomal aberration |
Any abnormality of chromosome number or structure may be described as an aberration.
출처: www.bio.hw.ac.uk/edintox/glossall.htm
|
| chromosomal aberration | any change in the normal structure or number of chromosomes |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|