| 영문 | genome | 한글 | 유전체 |
|---|---|---|---|
| 설명 | 1. 낱낱의 생물체에 들어있는 유전정보 전체를 이르는 말. 진핵세포에서는 염색체 쌍내에, 세균에서는 단일염색체에, 또 바이러스에서는 DNA나 RNA 내에 함유되어 있다. 1920년 H. 윙클러는 단배체의 염색체 한 쌍을 게놈이란 용어로 사용하기를 제창했다. 유전자(gene)와 염색체(chromosome) 두 단어를 합성한 것이 genome으로 우리말로는 유전체로 표준화되었다. 1유전체 속에는 상동염색체가 포함될 수 없으며, 유전체 속의 한개의 염색체 또는 그 일부분만 상실되어도 생활기능에 중대한 영향을 받는다. 유전체를 구성하는 염색체는 각종 생물에 있어서 고유의 기본수로 이루어져 있다. 이와 같이 유전체가 여러 개의 장으로 구성된 교과서라고 한다면 염색체는 개개의 장이라 할 수 있고, 유전자는 장을 구성하는 문장이라 할 것이며, 다시 문장을 구성하는 글자 하나하나가 염기쌍이라고 할 수 있다. 2. 한 개체에 있는 유전자의 완전한 세트. |
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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 |
| CGH | Comparative genome hybridization |
|---|---|
| GGR | Global Genome Repair |
| HGP | Human Genome Project |
| MGD | Mouse Genome Database |
| CA | Chromosomal aberration |
| 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) |
| 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) |
| genome | <genetics, molecular biology> The total set of genes carried by an individual or cell. (18 Nov 1997) |
| genome, bacterial | The complete gene complement contained in a single chromosome in a bacterium. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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