| ¿µ¹® | mutation | ÇÑ±Û | µ¹¿¬º¯ÀÌ |
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||
| DSST | Digit Symbol Substitution Task |
|---|---|
| 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... |
| DSS | Digit Symbol Substitution |
|---|---|
| D.S. | degree of substitution |
| FS | freeze substitution |
| ARMS | Amplification Refractory Mutation System |
| MFD | Mutation frequency decline |
| substitution mutation | A mutation caused by a nucleotide base being replaced by a different one. (09 Oct 1997) |
|---|
| amino acid substitution | The naturally occurring or experimentally induced replacement of one or more amino acids in a protein with another. If a functionally equivalent amino acid is substituted, the protein may retain wild-type activity. Substitution may also diminish or eliminate protein function. Experimentally induced substitution is often used to study enzyme activities and binding site properties. (12 Dec 1998) |
|---|---|
| base substitution | <molecular biology> One nucleotide base is replaced by another in a DNA molecule. This is also called a point mutation. (09 Oct 1997) |
| conservative substitution | In a gene product, a substitution of one amino acid with another with generally similar properties (size, hydrophobicity, etc), such that the overall functioning is likely not to be seriously affected. (18 Nov 1997) |
| stimulus substitution | <psychology> Learning that takes place when a conditioned stimulus is paired with an unconditioned stimulus. (12 Dec 1998) |
| substitution | 1. The act of putting one thing in the place of another, especially the chemical replacement of one element or radical by some other. 2. A defense mechanism, operating unconsciously, in which an unattainable or unacceptable goal, emotion or object is replaced by one that is attainable or acceptable. Origin: L. Substitutio, from statuere = to place (18 Nov 1997) |
| substitution product | A product obtained by replacing one atom or group in a molecule with another atom or group. (05 Mar 2000) |
| substitution therapy | Replacement therapy, particularly when replacement is not physiological but entails administration of a substitute. (05 Mar 2000) |
| substitution transfusion | Removal of most of a patient's blood followed by introduction of an equal amount from donors. Synonym: exsanguination transfusion, substitution transfusion, total transfusion. (05 Mar 2000) |
| symptom substitution | An unconscious psychological process by which a repressed impulse is indirectly manifested through a particular symptom, e.g., anxiety, compulsion, depression, hallucination, obsession. Synonym: symptom formation. (05 Mar 2000) |
| freeze substitution | A modification of the freeze-drying method in which the ice within the frozen tissue is replaced by alcohol or other solvent at a very low temperature. (12 Dec 1998) |
| 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) |
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