| del | deletion; delivery; delusion |
|---|---|
| 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 [... |
| D | Deletion |
|---|---|
| I/D | Insertion-deletion |
| D-I | deletion-insertion |
| CA | Chromosomal aberration |
| CISS | Chromosomal in situ suppression |
| chromosomal deletion | A microscopically evident loss of part of a chromosome. See: monosomy. (05 Mar 2000) |
|---|
| addition-deletion mutation | <molecular biology> A type of mutation that results from insertion or deletion of a single nucleotide into, or from, an open reading frame in the normal DNA sequence. Normally, the genetic code is read in the wrong frame, three nucleotides at a time, and the entire sequence downstream of the mutation, is translated into a polypeptide with a garbled amino acid sequence from the mutated codon onwards. These mutations may be induced by certain types of mutagens or may occur spontaneously and usually result in the generation, downstream, of nonsense, chain termination codons. Synonym: addition mutation, addition-deletion mutation, deletion mutation, reading-frameshift mutation. (21 Jun 2000) |
|---|---|
| gene deletion | The total loss (or absence) of a gene. Gene deletion plays a role in birth defects and in the development of cancer. (12 Dec 1998) |
| chromosome deletion | Actual loss of a portion of the chromosome. (12 Dec 1998) |
| clonal deletion | The removal of B-cell and T-cell varieties which recognise parts of the organisms body as targets of the immune system. This process naturally occurs early in the organisms development so that the organism will not be autoimmune (having an immune reaction against one's own body tissues) later in life. (09 Oct 1997) |
| clonal deletion theory | The elimination of certain T-cell populations in the thymus that have receptors for self-antigens. See: immunologic tolerance. (05 Mar 2000) |
| point deletion | Deletion involving a submicroscopic loss of genetic material too small to be resolved by linkage analysis. Synonym: nucleotide deletion. (05 Mar 2000) |
| sequence deletion | Deletion of sequences of bases or amino acids from the genetic material of an individual. Evidence for these deletions may be obtained by cytological methods. (12 Dec 1998) |
| nucleotide deletion | Deletion of a single nucleotide, which in a transcribed gene will lead to a frameshift mutation. Synonym: point deletion. (05 Mar 2000) |
| deletion | <genetics> A chromosome abnormality in which part of a single chromosome has been lost. (13 Nov 1997) |
| deletion mutation | <molecular biology> A mutation in which one or more (sequential) nucleotides is lost by the genome. If the number lost is not divisible by 3 and is in a coding region, the result is a frameshift mutation. (18 Nov 1997) |
| interstitial deletion | Deletion that does not involve the terminal parts of a chromosome. (05 Mar 2000) |
| terminal deletion | Deletion involving the terminal part of a chromosome and leading to a adhesive terminus. (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) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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