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  • lethal mutation
    Ä¡»ç µ¹¿¬º¯ÀÌ
  • loss mutation
    »ó½Çµ¹¿¬º¯ÀÌ(ßÃã÷ÔÍæÔܨì¶).
  • missense mutation
    °ú¿Àµ¹¿¬º¯ÀÌ(Φè¦ÔÍæÔܨì¶).
  • multiple allelic mutation
    º¹´ë¸³ÇüÁúº¯ÀÌ(ÜÜÓßí¡û¡òõܨì¶).
  • mutation
    (µ¹¿¬)º¯ÀÌ(ÔÍæÔܨì¶)
  • mutation detection
    (µ¹¿¬)º¯À̰ËÃâ
  • mutation disturbance
    º¯¼ºÀå¾Ö(ܨàõî¡äô).
  • mutation genetics
    º¯ÀÌÀ¯ÀüÇÐ(ܨì¶ë¶îîùÊ).
  • mutation rate
    (µ¹¿¬)º¯ÀÌÀ².
  • mutation, back
    ¿ªµ¹¿¬º¯ÀÌ, º¹±Íµ¹¿¬º¯ÀÌ
  • mutation, chromosomal
    ¿°»öüµ¹¿¬º¯ÀÌ
  • mutation, dominant
    ¿ì¼ºµ¹¿¬º¯ÀÌ
  • mutation, forward
    ÀüÇâ µ¹¿¬º¯ÀÌ
  • mutation, frame-shift
    ÇØµ¶Æ² µ¹¿¬º¯ÀÌ, ÇÁ·¹ÀÓ½¬ÇÁÆ® µ¹¿¬º¯ÀÌ
  • mutation, missense
    °ú¿À µ¹¿¬º¯ÀÌ, ¹Ì¼¾½º µ¹¿¬º¯ÀÌ
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  • promoter-up mutation
    ÇÁ·Î¸ðÅÍ ±â´É»ó½Âº¯ÀÌ(ѦÒöß¾ã°Ü¨ì¶)
  • Quaking mutation
    ÄùÀÌÅ· º¯ÀÌ(ܨì¶).
  • samesense mutation
    µ¿ÀÇ º¯ÀÌ(ÔÒëòܨì¶)
  • second-site mutation
    µÑ° ÀÚ¸® º¯ÀÌ(ܨì¶)
  • semilethal mutation
    ÁØÄ¡»ç º¯ÀÌ(ñÞöÈÞÝܨì¶)
  • sign mutation
    ½ÅÈ£º¯ÀÌ(ãáûÜܨì¶)
  • silent mutation
    ħ¹¬ º¯ÀÌ(öØÙùܨì¶)
  • single-site mutation
    ¿ÜÀÚ¸® º¯ÀÌ(ܨì¶)
  • somatic mutation
    ü¼¼Æ÷ º¯ÀÌ(ô÷á¬øàܨì¶)
  • somatic mutation theory
    ü¼¼Æ÷ º¯ÀÌÀÌ·Ð(ô÷á¬øàܨì¶×âÖå)
  • spontaneous mutation
    "ÀÚ¿¬º¯ÀÌ(í»æÔܨì¶), ÀúÀý·Îº¯ÀÌ(ܨì¶)"
  • subvital mutation
    ¾ÆÄ¡¸í º¯ÀÌ(ä¬öÈ٤ܨì¶)
  • transverse mutation
    ¿°±âº¯È¯º¯ÀÌ(ç¤ÐñܨüµÜ¨ì¶)
  • umber mutation
    ¾Ï¹ö º¯ÀÌ
  • unstable mutation
    ºÒ¾ÈÁ¤(ÝÕäÌïÒ) º¯ÀÌ(ܨì¶)
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TS Takayasu syndrome; Tay-Sachs; temperature sensitivity; temperature, skin; temporal stem; tensile str...
Ts T-cell suppressor
TVSS transient voltage surge suppressor
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SF Suppressor Factors
SCA Suppressor cell activity
SC Suppressor cells
Socs Suppressor of Cytokine Signaling
SOCS-1 suppressor of cytokine signalling-1
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new mutation Redundant term for a heritable trait present in the offspring but in neither parent, i.e., not a pre-existing mutant form inherited.
(05 Mar 2000)
substitution mutation A mutation caused by a nucleotide base being replaced by a different one.
(09 Oct 1997)
nonsense mutation <molecular biology> A mutation that causes a polypeptide chain to be ended prematurely.
(13 Nov 1997)
null mutation Change in a gene that leads to nothing, for example to no enzyme or to a nonfunctioning enzyme.
(12 Dec 1998)
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)
down promoter mutation <molecular biology> A mutation (a change in base pair sequence) in a promoter region, this results in lower gene expression (less transcription of the gene occurs).
(09 Oct 1997)
induced mutation A mutation caused by exposure to a mutagen.
(05 Mar 2000)
insertion mutation A mutation caused by the insertion of at least one extra nucleotide basein a DNA sequence.
(09 Oct 1997)
ochre mutation Mutation that changes any codon to the termination codon UAA.
(18 Nov 1997)
opal mutation <molecular biology> Mutation that changes any codon to the termination codon UGA.
(18 Nov 1997)
temperature sensitive mutation <genetics, molecular biology> A type of conditional mutation in organism, somatic cell or virus that makes it possible to study genes whose total inactivation would be lethal. Such ts mutations can also make possible studies of the effect of reversible switching by temperature changes) in expression of the mutated gene. The usual mechanism of temperature sensitivity is that the mutated gene codes for a protein with a temperature dependent conformational instability, so that it possesses normal activity at one temperature (the permissive temperature), but is inactive at a second (nonpermissive) temperature.
(18 Nov 1997)
transition mutation A point mutation involving substitution of one base-pair for another, i.e., replacement of one purine for another and of one pyrimidine for another pyrimidine without change in the purine-pyrimidine orientation.
(05 Mar 2000)
transversion mutation A point mutation involving base substitution in which the orientation of purine and pyrimidine is reversed, in contradistinction to transition mutation.
(05 Mar 2000)
umber mutation A mutation yielding the termination codon UGA, resulting in premature termination of a polypeptide chain.
Compare: suppressor mutation.
Synonym: opal mutation.
(05 Mar 2000)
unstable mutation <molecular biology> A mutation that has a high likelihood of reverting to its original form.
(13 Nov 1997)
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