| ¿µ¹® | thymus(gland) | ÇÑ±Û | °¡½¿»ù |
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| ¼³¸í | °¡½¿ÀÇ ¾Õ À§ÂÊ¿¡ À§Ä¡ÇÑ ¸²ÇÁ¼º Àå±â·Î¼, »çÃá±â¿¡ ÃÖ°íÀÇ ¹«°Ô¿¡ ´ÞÇß´Ù°¡ ÀÌÈÄ¿¡ ÅðÃàÇÑ´Ù. À̰ÍÀº ¼¼Æ÷¸Å°³ ¸é¿ª(cell-mediated immunity: ÁÖ·Î T-¸²ÇÁ±¸¿¡ ÀÇÇØ ÀϾ¸ç, ÀÚ±â¿Í ´Ù¸¥ ¼¼Æ÷¿¡ ´ëÇÑ Àνİú À̽İźιÝÀÀ¿¡ °ü¿©ÇÔ)±â´ÉÀÇ ¹ß´Þ°ú ¼º¼÷¿¡ ÇÊ¿äÇÑ Àå±âÀ̸ç, ȸ¹éÀû»öÀ¸·Î º¸Åë Á¤Á߸鿡¼ °áÇÕÁ¶Á÷¿¡ ÀÇÇØ °áÇÕµÈ µÎ °³ÀÇ ¿±À¸·Î µÇ¾î ÀÖ´Ù. °¡½¿»ùÀº »óÇǼ¼Æ÷, ¸²ÇÁ±¸, °¡½¿»ù¼¼Æ÷·Î ±¸¼ºµÇ¾î ÀÖÀ¸¸ç Àü±¸¼¼Æ÷°¡ °¡½¿»ù¿¡ ÀÌÇàÇÏ¿© ¸²ÇÁ±¸·Î ºÐȵǰí, ±× ´ëºÎºÐÀº ÆÄ±«µÇ³ª ³ª¸ÓÁö´Â T¸²ÇÁ±¸¸¦ Çü¼ºÇÑ´Ù. °¡½¿»ùÀº ¶ÇÇÑ È£¸£¸ó À¯»ç¹°ÁúÀÎ thymine, thymopoietin, thymosin µîÀ» ºÐºñÇÑ´Ù. |
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| ¿µ¹® | thyroid gland | ÇÑ±Û | °©»ó»ù |
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| ¼³¸í | »ç¶÷ÀÇ ¸ö¿¡¼ °¡Àå Å« ³»ºÐºñ»ùÀ¸·Î ¸ñÀÇ ¾ÕÂÊ, ¾Æ·¡ÂÊ¿¡ À§Ä¡Çϰí ÀÖÀ¸¸ç 2¿±À¸·Î ±¸¼ºµÇ¾î ÀÖ´Ù. °¢ ¿±Àº ±â°üÀÇ ¾çÂÊ¿¡ ÀÖÀ¸¸ç Á¼Àº Àß·è¿¡ ÀÇÇØ ¾Õ¿¡¼ ¿¬°áµÇ¾î ÀÖ´Ù. °©»ó»ùÈ£¸£¸óÀΠƼ·Ï½Å(thyroxine)À» ºÐºñÇϰí ÀúÀåÇϸç, Çʿ信 µû¶ó ¹æÃâÇÑ´Ù. ¶ÇÇÑ °©»ó»ùÀº Ƽ·ÎÄ®½ÃÅä´Ñ(thyrocalcitonin)µµ ºÐºñÇÑ´Ù. º´ÀûÀÎ »óÅ¿¡¼ Å©±â°¡ ´ë°³ Áõ°¡Çϰí, ÀϺο¡¼´Â µµ¸®¾î À§ÃàµÇ¸ç, ÅëÁõÀ» ³ªÅ¸³»±âµµ ÇÑ´Ù. |
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| ¿µ¹® | adrenal gland | ÇÑ±Û | ºÎ½Å |
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| ¼³¸í | ÄáÆÏÀ§¿¡ Á¸ÀçÇÏ´Â ÇǶó¹Ô¸ð¾çÀÇ ±¸Á¶¹°. °ÑÁú°ú ¼ÓÁú·Î µÇ¾î ÀÖÀ¸¸ç È£¸£¸óÀÇ ºÐºñ°¡ ÁÖ¿ªÇÒÀÌ´Ù. ![]() |
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| MEN | Multiple Endocrine Neoplasia ; AD Trait 1. MEN Type I(= Wermer Syndro... |
|---|---|
| BCAA | Branched Chain Amino Acid |
| BAA | benzoylarginine amide; branched amino acid |
| BCAA | branched chain amino acid |
| BCKA | branched-chain keto acid |
| BCAA | Branched Chain Amino Acid |
|---|---|
| b-DNA | Branched DNA |
| BCKA | Branched chain alpha-ketoacid |
| BCKAD | Branched chain alpha-ketoacid dehydrogenase |
| BCKDH | Branched chain alpha-ketoacid dehydrogenase |
| tubular gland | A gland composed of one or more tubules ending in a blind extremity. (05 Mar 2000) |
|---|---|
| amino acids, branched-chain | Amino acids which have a branched carbon chain. (12 Dec 1998) |
| branched calculus | A calculus occurring in the renal pelvis, with branches extending into the infundibula and calices. Synonym: branched calculus, coral calculus, dendritic calculus. (05 Mar 2000) |
| branched chain acyl-CoA oxidase | <enzyme> Enzyme from human liver peroxisomes acts on both 2-methyl branched fatty acyl- and bile acid-CoA intermediates, unlike rat liver peroxisomes which have separate enzymes for branched chain fatty acids (pristanoyl-CoA) and bile acid-CoA; involved in beta-oxidation of fatty acids and bil Registry number: EC 1.3.3.- Synonym: 2-methyl-branched chain acyl-CoA oxidase, hbrcacox (26 Jun 1999) |
| branched-chain fatty-acid-kinase | <enzyme> From anaerobic spirochete ma-2 Registry number: EC 2.7.2.14 Synonym: isovalerate kinase, 2-methylbutyrate kinase, isobutyrate kinase (26 Jun 1999) |
| branched-chain fatty acid synthetase | <enzyme> Analogous to fatty acid synthetase complex but starting with a branched chain keto acid; from bacillis subtilis Registry number: EC 2.3.1.- Synonym: bcfa synthetase (26 Jun 1999) |
| branched chain ketoaciduria | Hereditary disease due to deficiency of an enzyme involved in amino acid metabolism, characterised by urine that smells like maple syrup. (12 Dec 1998) |
| branched chain ketonuria | Hereditary disease due to deficiency of an enzyme involved in amino acid metabolism, characterised by urine that smells like maple syrup. (12 Dec 1998) |
| 2-methyl branched-chain enoyl-CoA reductase | <enzyme> Important in the reversal of beta-oxidation under anaerobic conditions in ascaris suum Registry number: EC 1.3.1.52 Synonym: 2-methyl bce-CoA reductase (26 Jun 1999) |
| acute tubular necrosis | <nephrology> A kidney disorder that results in damage to the renal tubule cells leading to acute renal failure. Acute tubular necrosis can result from any condition which deprives the kidney of oxygen (ischaemia). Acute tubular necrosis may occur as a complication of shock, trauma or sepsis. Conditions such as diabetes or liver disease can predispose people to the development of acute tubular necrosis. Certain medications (for example aminoglycosides, amphotericin B, cyclosporine) are known to cause acute tubular necrosis as a toxic side effect. Radiopaque contrast dyes, used in some radiologic procedures, may also result in acute tubular necrosis as a rare complication from contrast dye use. Acronym: ATN (13 Nov 1997) |
| renal tubular acidosis | <nephrology> A rare sometimes familial disorder of the renal tubule characterised by the inability to excrete urine of normal acidity. This leads to a hyperchloraemic acidosis which is often associated with one or more secondary complications such as hypercalcinuria with nephrolithiasis and nephrocalcinosis, rickets, or osteomalacia and severe potassium depletion. (25 Jun 1999) |
| renal tubular transport, inborn errors | Genetically determined disorders of the reabsorptive functions of the kidney with regard to specific nephron segments responsible for specific transport functions, classifiable by proximal nephron function, loop of henle function, and distal nephron function. The transport defects can be selective or nonselective. (12 Dec 1998) |
| Pick's tubular adenoma | A neoplasm of the ovary, arising from the ovarian stroma, mimicking to a greater or lesser extent derivatives of the sex cord mesenchyme of the testis, and sometimes causing defeminization and virilization. (12 Dec 1998) |
| primary renal tubular acidosis | A metabolic defect in the mechanism of urinary acidification that may be either the transient type, with onset in infancy, or the persistent type, with onset in childhood or adult years; both types are familial. (05 Mar 2000) |
| secondary renal tubular acidosis | Renal tubular acidosis that may occur as a complication of hypercalcaemic states, hyperglobulinaemic disorders, and in some other chronic renal conditions; a regular component of De Toni-Fanconi syndrome. (05 Mar 2000) |
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