| ¿µ¹® | mutation | ÇÑ±Û | µ¹¿¬º¯ÀÌ |
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| ¼³¸í | ¼¼Æ÷ÀÇ dna ÀÚüÀÇ º¯ÀÌ¿¡ ÀÇÇØ ÀϾ´Â ¼¼Æ÷º¯À̸¦ ¸»ÇÑ´Ù. ÀÌ·¯ÇÑ °æ¿ì µ¹¿¬º¯ÀÌ·Î ÀÏ¾î³ ¼¼Æ÷´Â ±× ÀÌÈÄ µþ¼¼Æ÷(daughter cell)¿¡¼µµ ±× º¯À̰¡ ¿©ÀüÈ÷ À¯ÁöµÇ¹Ç·Î Á¾(species)ÀÇ º¯È³ª, ȤÀº ¼¼Æ÷ÀÇ ¾Ç¼ºº¯È¯(malignant transformation)¿¡ °ü¿©ÇÑ´Ù. |
||
| SMI | Self-Motivation Inventory; senior medical investigator; severe mental impairment; silent myocardial ... |
|---|---|
| SP | sacroposterior; sacrum to pubis; salivary progesterone; schizotypal personality; semi-private [room]... |
| ARMS | adverse reaction monitoring system; amplification refractory mutation system |
| MF | magnetic field; meat free; medium frequency; megafarad; membrane filler; merthiolate-formaldehyde [s... |
| TFM | testicular feminization male; testicular feminization mutation; total fluid movement; transmission e... |
| SMI | Silent myocardial ischemia |
|---|---|
| SIR | Silent Information Regulator |
| SP | Silent Period |
| SCI | Silent cerebral infarction |
| SI | Silent myocardial ischaemia |
| silent mutation | Mutations that have no effect on phenotype because they do not affect the activity of the product of the gene, usually because of codon ambiguity. (18 Nov 1997) |
|---|
| masticatory silent period | A pause in electromyographic patterns associated with tooth contacts during chewing and biting; a part of the complex feedback mechanism of mandibular control involving receptors in the periodontal ligament and muscles. (05 Mar 2000) |
|---|---|
| silent | Producing no detectable signs or symptoms, said of certain diseases or morbid processes. (05 Mar 2000) |
| silent allele | 1. <genetics> A gene which is inactive. Thus, an amorphic gene. 2. <cell biology> Something that lacks a discernible shape and thus can be describes as amorphous. (05 Feb 1998) |
| silent area | Any area of the cerebrum or cerebellum in which lesions cause no definite sensory or motor symptoms. (05 Mar 2000) |
| silent electrode | In unipolar electrocardiography, a remote electrode placed either upon a single limb or connected with the central terminal and paired with an exploring electrode; the indifferent electrode is supposed to contribute little or nothing to the resulting record. Synonym: dispersing electrode, silent electrode. (05 Mar 2000) |
| silent gap | The period during which Korotkoff sounds indicating true systolic pressure fade away and reappear at a lower pressure point; responsible for errors made in recording falsely low systolic blood pressure, especially in hypertensive patients, of up to 25 mm Hg, and avoided by pumping the cuff 30 mm Hg beyond palpable systolic pressure. Synonym: silent gap. (05 Mar 2000) |
| silent ischemia | Myocardial ischemia without accompanying signs or symptoms of angina pectoris; can be detected by EKG and other lab techniques. See: silent myocardial infarction. (05 Mar 2000) |
| silent mutant | A mutant that is not phenotypically manifest. Synonym: silent mutant. (05 Mar 2000) |
| silent myocardial infarction | Infarction that produces none of the characteristic symptoms and signs of myocardial infarction. (05 Mar 2000) |
| silent period | The time during which there is no electrical activity in a muscle following its rapid unloading, any pause in an otherwise continuous series of electrophysiologic events. (05 Mar 2000) |
| acquired mutation | A change in a gene or chromosome that occurs in a single cell after the conception of the individual. That change is then passed along to all cells descended from that cell. Acquired mutations are involved in the development of cancer. (12 Dec 1998) |
| 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) |
| addition 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) |
| amber mutation | <molecular biology> A mutation from a codon which codes for an amino acid into the amber codon UAG, which normally signals that the translation of mRNA into an amino acid chain should stop. The mutation causes the amino acid chain to stop forming before it is actually completed. (09 Oct 1997) |
| back mutation | <molecular biology> A mutation that causes a mutant gene to revert to its original wild-type base sequence. Compare: forward mutation. (09 Oct 1997) |
| silent mutation |
A mutation in a codon that does not cause a change in the amino acid sequence of the translation product.
Ãâó: www.genpromag.com/Glossary~LETTER~S.html
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|---|---|
| silent mutation |
Mutation that results in an unchanged amino acid sequence and thus in a protein with normal function.
Ãâó: science.education.nih.gov/supplements/nih1/genetic...
|
| silent mutation |
a change in the genetic sequence that does not alter the protein sequence.
Ãâó: www.uvm.edu/~cgep/Education/Glossary.html
|
| silent mutation |
Mutation in which the function of the protein product of the gene is unaltered.
Ãâó: depts.washington.edu/~genetics/courses/genet372/w2...
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