| ¿µ¹® | uric acid | ÇÑ±Û | ¿ä»ê |
|---|---|---|---|
| ¼³¸í | °áÁ¤¼ºÀÇ »ê. 2, 6, 8-trioxypurine. ÈÇнÄÀº C5H4N4O3·Î »ç¶÷°ú µ¿¹°ÀÇ ¿ÀÁÜ¿¡¼ ¾òÀ» ¼ö ÀÖ´Ù. ÇÙÀÇ ´ë»ç»ê¹°ÀÇ Çϳª. ¹°, ¾ËÄÝ, ¿¡Å׸£(ether)¿¡´Â °ÅÀÇ ³ìÁö ¾ÊÀ¸³ª ¾ËÄ®¸®¿°ÀÇ ¿ë¾×¿¡´Â ³ì´Â´Ù. À̰ÍÀÇ ³ªÆ®·ý¿° ÇüÅÂ(sodium urate)°¡ °á¼®ÀÇ ´ëºÎºÐÀ» Â÷ÁöÇÑ´Ù. ±Þ¼º¹éÇ÷º´ Ä¡·á Ãʱâ´Ü°è¿Í Åëdz(Gout)¿¡¼ Ç÷Áß¿ä»êÀÌ ±Þ°ÝÈ÷ ¿À¸¦ ¼ö ÀÖ´Ù. |
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| ¿µ¹® | acid-fast bacillus | ÇÑ±Û | Ç׻긷´ë±Õ, Ç×»ê±Õ |
|---|---|---|---|
| ¼³¸í | ¾Æ´Ò¸° »ö¼Ò¿¡ ¿°»öµÇ±â Èûµå³ª ÀÏ´Ü ¿°»öµÇ¸é °»êÀ¸·Î ó¸®ÇÏ¿©µµ Å»»öµÇÁö ¾Æ´ÏÇÏ´Â ¼¼±ÕÀ» ÅëÆ²¾î À̸£´Â ¸». °áÇØ±Õ, ³ªº´±Õ µûÀ§°¡ ÀÖ´Ù. |
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| ¿µ¹® | acid-fast staining | ÇÑ±Û | Ç׻꿰»ö |
|---|---|---|---|
| ¼³¸í | Ç׻꼺¼ºÁú(Á»Ã³·³ ¿°»öÀÌ µÇÁö ¾ÊÀ¸³ª Çѹø ¿°»öÀÌ µÇ¸é »ê¼º¿ë¾×¿¡ ÀÇÇØ¼ Å»»öÀÌ µÇÁö ¾Ê´Â ¼ºÁú)À» °¡Áø ±Õ(¿¹¸¦ µé¸é °áÇÙ±Õ µî)ÀÇ °ËÃâ¿¡ ÀÌ¿ëµÇ´Â ¿°»ö¹æ¹ý. ¹æ¹ý¿¡´Â Ziehl-Neelson¹ý°ú Kinyoun¹ý µîÀÌ ÀÖ´Ù. |
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| ¿µ¹® | nucleic acid | ÇÑ±Û | ÇÙ»ê |
|---|---|---|---|
| ¼³¸í | ¿°±â, ´ç, ÀλêÀ¸·Î ÀÌ·ç¾îÁø ´ºÅ¬·¹¿ÀƼµå°¡ ±ä »ç½½ ¸ð¾çÀ¸·Î ÁßÇÕµÈ °íºÐÀÚ ¹°Áú. À¯ÀüÀ̳ª ´Ü¹éÁú ÇÕ¼ºÀ» Áö¹èÇÏ´Â Áß¿äÇÑ ¹°Áú·Î, »ý¹°ÀÇ Áõ½ÄÀ» ºñ·ÔÇÑ »ý¸í Ȱµ¿ À¯Áö¿¡ Áß¿äÇÑ ÀÛ¿ëÀ» ÇÑ´Ù. ±¸¼º ´çÀÎ ¿Àź´çÀÌ ¸®º¸¿À½ºÀÎ ¸®º¸ÇÙ»ê°ú µð¿Á½Ã¸®º¸¿À½ºÀÎ µð¿Á½Ã¸®º¸ ÇÙ»êÀ¸·Î ³ª´¶´Ù. ÆæÅ佺·Î¼ ¸®º¸½º³ª µ¥¿Á½Ã¸®º¸½º ¾î´À ÇÑÂʸ¸À» Æ÷ÇÔÇϸç ÀüÀÚ¸¦ ¸®º¸ÇÙ»ê(RNA), ÈÄÀÚ¸¦ µ¥¿Á½Ã¸®º¸ÇÙ»ê(deoxyribonucleic acid, DNA)À̶ó ºÎ¸¥´Ù. ¸ðµÎ 4Á¾·ùÀÇ À¯±â¿°±â¿¡ ÀÇÇØ Ư¡Áö¾îÁö¸ç ¾Æµ¥´Ñ, ±¸¾Æ´Ñ ¹× ½ÃÅä½ÅÀº ¾çÀÚ¿¡ °øÅëÀÌ´Ù. Ƽ¹ÎÀº DNA¿¡, ¿ì¶ó½ÇÀº RNA¿¡ Æ÷ÇԵȴÙ. DNA´Â ÁÖ·Î ÇÙ¿¡ Á¸ÀçÇϸç ÇüÁúÀ¯Àü¿¡ ±×¸®°í RNA´Â ¼¼Æ÷Áú¼Ó¿¡¼ ´Ü¹éÁú ÇÕ¼º¿¡ °ü¿©ÇÑ´Ù. ¼·ÃëµÈ ÇÙ»êÀº ¼ÒȰü¿¡¼ ±¸¼ººÐÀڷαîÁö °¡¼öºÐÇØµÇ¾î Èí¼öµÈ´Ù. |
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| MDM | medical decision making; mid-diastolic murmur; minor determinant mix [penicillin] |
|---|---|
| mix, mixt | mixture |
| PA | panic attack; pantothenic acid; paralysis agitans; paranoia; passive aggressive; pathology; patient'... |
| OCP | octacalcium phosphate; ocular cicatricial pemphigoid; oral case presentation; oral contraceptive pil... |
| OET | oral endotracheal tube; oral esophageal tube |
| glucogenic amino acid | <biochemistry> A type of amino acid with carbon chains that can be broken down into an intermediate of the citric acid cycle such as glycogen and then converted into glucose as a means of entering the normal process of carbohydrate metabolism in the body. Examples include: Glycine, alanine, arginine, and ornithine. (14 Oct 1997) |
|---|---|
| RNA, transfer, amino acid-specific | A group of transfer rnas which are specific for carrying each one of the 20 amino acids to the ribosome in preparation for protein synthesis. (12 Dec 1998) |
| polar amino acid | An alpha-amino acid in which the functional group attached to the alpha-carbon (i.e., R in RCH(NH2)COOH) has hydrophilic properties; e.g., serine, cysteine, homocysteine. (05 Mar 2000) |
| sequence homology, amino acid | The degree of similarity between sequences of amino acids. This information is useful for the understanding of genetic relatedness of certain species. (12 Dec 1998) |
| N-(5-amino-1-ribosyl-4-imidazolylcarbonyl)-L-aspartic acid 5'-phosphate synthetase | <enzyme> 5-amino-1-ribosyl-4-imidazole carboxylic acid 5'-phosphate (carboxy-air), ATP and aspartate yield n(5-amino-4-imidazolylcarbonyl)-l-aspartic acid 5'-phosphate(succino-aicar), ADP and p Registry number: EC 6.3.4.- (26 Jun 1999) |
| N(6)-(6-carbamoylhexyl)-FAD-D-amino acid oxidase | <enzyme> A semi-synthetic oxidase; prepared by reacting the succinimido ester of n(6)-(6-carboxyhexyl)-fad with apo-d-amino acid oxidase from pig kidney in the presence of the benzoate Registry number: EC 1.4.3.- Synonym: nch-fad-daao (26 Jun 1999) |
| N-carbamoyl-D-amino acid amidohydrolase | <enzyme> From comamonas sp.e222c; mw 120 kD; hydrolyzes d-enantiomers of various n-carbamoyl-d-amino acids to d-amino acids, ammonia and co2; sensitive to thiol reagents; does not require metal ions Registry number: EC 3.5.1.- Synonym: caa-amidohydrolase, carbamoyl d-aa amidohyrolase (26 Jun 1999) |
| nonessential amino acid | <biochemistry> The amino acid's that can be synthesised by an organism and are thus not required in the diet. (05 Mar 2000) |
| nonpolar amino acid | An alpha-amino acid in which the functional group attached to the alpha-carbon (i.e., R in RCH(NH2)COOH) has hydrophobic properties; e.g., valine, leucine, alpha-aminobutyrate. (05 Mar 2000) |
| D-amino acid malonyltransferase | <enzyme> From mung beans Registry number: EC 2.3.1.- Synonym: 1-aminocyclopropanecarboxylate malonyltransferase, d-acc-malonyltransferase, acc n-malonyltransferase (26 Jun 1999) |
| d-amino-acid oxidase | <enzyme> Chemical name: D-Amino-acid:oxygen oxidoreductase (deaminating) Registry number: EC 1.4.3.3 (12 Dec 1998) |
| D-amino acid transaminase | <enzyme> Catalyses the alpha,beta elimination of the (d)-isomer of beta-chloroalanine or other amino acids to yield pyruvate, chloride and ammonia Registry number: EC 2.6.1.- (26 Jun 1999) |
| D-amino acid transferase | <enzyme> Mw 41 kD; catalyses d-amino acid transfer; d-configuration specific; recognises aromatic d-amino acid esters to form oligo d-amino acid esters Registry number: EC 2.3.2.- (26 Jun 1999) |
| dibasic amino acid | An amino acid containing a second basic group (usually an amino group); e.g., lysine, arginine, ornithine. Synonym: dibasic amino acid. (05 Mar 2000) |
| excitatory amino acid | <biochemistry> The naturally occurring amino acids L glutamate and L aspartate and their synthetic analogues, notably kainate, quisqualate and NMDA. They have the properties of excitatory neurotransmitters in the CNS, may be involved in long-term potentiation and can act as excitotoxins. at least three classes of EAA receptor have been identified, the agonists of the N type receptor are L aspartate, NMDA and ibotenate, the agonists of the Q type receptor are L glutamate and quisqualate, agonists of the K type are L glutamate and kainate. All three receptor types are found widely in the CNS and particularly the telencephalon, N and Q type receptors tend to occur together and may interact, their distribution is complementary to the K type receptors. The ion fluxes through the Q and K receptors are relatively brief, whereas the flux through the N type is longer and carries a significant amount of calcium. Additionally the N type receptor is blockaded by magnesium near the resting potential and thus shows voltage gated ion channel properties, leading to a regenerative response, this is why N type receptors have been linked to long-term potentiation. Invertebrate glutamate receptors may not have the same properties as those described above. (18 Nov 1997) |
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