| ¿µ¹® | recognition, perception | ÇÑ±Û | ÀÎÁö, ÀνÄ, ÀçÀÎ½Ä |
|---|---|---|---|
| ¼³¸í | »ýü°¡ Àڱ⠶Ǵ Àڱ⿡°Ô ÀûÇÕÇÑ °ÍÀ¸·Î ºñÀڱ⸦ ½Äº°ÇÏ´Â °Í. »ýü°¡ ¾î¶°ÇÑ ÀÚ±ØÀ» ¼ö¿ëü µîÀ¸·Î ¼ö¿ëÇÏ¿© ½Äº°ÇÑ °á°ú ÀÏ¾î³ º¯È, ¹ÝÀÀ ¶Ç´Â Çൿ±îÁö¸¦ Æ÷ÇÔÇØ¼ ¸»ÇÏ´Â °æ¿ìµµ ÀÖ´Ù. Ç׿øÀÚ±ØÀ» ¹ÞÀº ¸é¿ª´ã´ç¼¼Æ÷¿¡ ÀϾ´Â º¯È¿Í °°Àº ¹°Áú¼öÁØÀÇ Çö»óÀ¸·ÎºÎÅÍ °íµîµ¿¹°¿¡¼ °³Ã¼ÀÇ ÀÎÁö µîÀÌ ÀÖ´Ù. ¶ÇÇÑ º¸´Ù °íÂ÷ÀÇ Ãß»óÀûÀÎ °³³äÀ¸·Î¼ °¨°¢¿¡ ÀÖ¾î¼ÀÇ ÀÎÁö³ª ÁßÃ߽ŰæÀÇ ´É·Â¿¡ °ü¿©ÇÏ´Â ÆÐÅÏÀÎ½Ä µîÀÌ ÀÖ´Ù. |
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| ¿µ¹® | carcinoembryonic antigen | ÇÑ±Û | ¾Ï¹è¾ÆÇ׿ø |
|---|---|---|---|
| ¼³¸í | ¿ø·¡ žÆÀÇ ÀåÁ¶Á÷¿¡¼ Á¤»óÀûÀ¸·Î Á¸ÀçÇÏ´Â ¹°Áú·Î žƱâ ÀÌÈÄ¿¡´Â Á¸ÀçÇÏÁö ¾Ê´Â ¹°ÁúÀÌ´Ù. ±×·¯³ª À§, °£, ÇãÆÄ µîÀÇ ¾ÏÀÌ ÀÖ´Â °æ¿ì¿¡ ¼ºÀο¡¼µµ Á¸ÀçÇÑ´Ù. À̸¦ ÀÌ¿ëÇØ¼ ¾ÏÀÇ Ä¡·áÈ¿°ú ÆÇÁ¤À̳ª Àç¹ß¿©ºÎÀÇ Á¶»ç¿¡ ÀÌ¿ëÇÑ´Ù. |
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| ¿µ¹® | antigen | ÇÑ±Û | Ç׿ø |
|---|---|---|---|
| ¼³¸í | ƯÀÌÇÑ ¸é¿ª¹ÝÀÀÀ» ÀÏÀ¸Å³ ¼ö ÀÖ´Â ¾î¶°ÇÑ ¹°Áú. ¿©±â¿¡¼ ¸»Çϴ ƯÀÌÇÑ ¸é¿ª¹ÝÀÀÀ̶õ ºñƯÀÌÀûÀÎ ¸é¿ª¹ÝÀÀ°ú´Â ¹Ý´ëµÇ´Â Àǹ̷Π±× ¹°Áú¿¡ ´ëÇØ¼ ƯÀÌÇÏ°Ô ¹ÝÀÀÇÒ ¼ö ÀÖ´Â Ç×ü³ª ±× ¹°Áú¿¡ ´ëÇØ¼ ƯÀÌÇÏ°Ô ¹ÝÀÀÇÒ ¼ö ÀÖ´Â ¼¼Æ÷¸¦ ¸¸µå´Â °ÍÀ» ¸»ÇÑ´Ù. |
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| HLA | histocompatibility leukocyte antigen; histocompatibility locus antigen; homologous leukocyte antibod... |
|---|---|
| ARAM | antigen recognition activation motif |
| TSA | technical surgical assistance; toluene sulfonic acid; total shoulder arthroplasty; total solute abso... |
| TSTA | toxoplasmin skin test antigen; tumor-specific tissue antigen; tumor-specific transplantation antigen... |
| CEARP | Continuing Education Approval and Recognition Program |
| ARS | antigen recognition site |
|---|---|
| CRD | Carbohydrate recognition domain |
| FRT | FLP recognition target |
| MARE | Maf recognition element |
| ORC | Origin Recognition Complex |
| recognition factors | Factors which effect "recognition" of target antigens by polymorphonuclear leukocytes; apparently the Fc portion of antibody molecules and the activated third component of complement (C3), for both of which phagocytes have receptor sites. (05 Mar 2000) |
|---|---|
| recognition sequence | A nucleotide sequence --typically composed of 4, 6, or 8nucleotides -- that is recognised by a restriction endonuclease. Type II enzymes cut (and theircorresponding modification enzymes methylate) within or very near the recognition sequence. (09 Oct 1997) |
| recognition time | The interval between the application of a stimulus and the recognition of its nature. (05 Mar 2000) |
| pattern recognition | In information retrieval, machine-sensing or identification of visible patterns (shapes, forms, and configurations). (harrod's librarians' glossary, 7th ed) (12 Dec 1998) |
| pattern recognition, visual | Visually perceived characters, shapes, displays, or designs. (12 Dec 1998) |
| cell recognition | <cell biology> Interaction between cells that is possibly dependent upon specific adhesion. Since the mechanism is not entirely clear in most cases, the term should be used with caution. (26 Mar 1998) |
| signal recognition particle | A complex between a 7S RNA and six proteins. SRP binds to the nascent polypeptide chain of eukaryotic proteins with a signal sequence and halts further translation until the ribosome becomes associated with the rough endoplasmic reticulum. One of the SRP proteins (srp54) binds GTP and in association with 7SRNA and srp19 has GTPase activity. (18 Nov 1997) |
| signal recognition particle receptor | Receptor for the signal recognition particle (SRP) found in the membrane of the endoplasmic reticulum. Also called docking protein. Heterodimeric, both protomers having GTP binding capacity, though dissimilar binding sites. Not until the complex of SRP, ribosome, message and nascent polypeptide chain binds to the SRP receptor is the block to further chain elongation released and concurrently the SRP is released, leaving the ribosome attached to the endoplasmic reticulum membrane. Cotranslational transport of the polypeptide delivers it into the lumen of the ER. (18 Nov 1997) |
| dual recognition hypothesis | An outmoded hypothesis that is known to be incorrect now that the structure of the T-cell receptor is known. The proposal was that viral (and some chemical) antigens were recognised in association with histocompatibility antigens by separate receptors on the T-cell. The generation of cytotoxic T-cells was by association with Class I MHC antigens, of T helper cells by association with Class II MHC antigens. See: altered self hypothesis. (18 Nov 1997) |
| acetone-insoluble antigen | A diphosphatidyl glycerol that is found in the membrane of Treponema pallidum and is the antigen detected by the Wasserman test for syphilis. (18 Nov 1997) |
| allogeneic antigen | Genetic variations of the same antigens within a given species. (05 Mar 2000) |
| antigen | Virus coded cell surface antigens that appear soon after the infection of a cell by virus, but before virus replication has begun. See: early gene. (18 Nov 1997) |
| antigen-antibody complex | The complex formed by the binding of antigen and antibody molecules. The deposition of large antigen-antibody complexes leading to tissue damage causes immune complex diseases. If the antigen is polyvalent the complex may be insoluble. Immune complexes activate complement through the classical pathway. See: glomerulonephritis, Arthus reaction, type III hypersensitivity. (12 Dec 1998) |
| antigen-antibody reaction | The phenomenon, occurring in vitro or in vivo, of antibody combining with antigen of the type that stimulated the formation of the antibody, thereby resulting in agglutination, precipitation, complement fixation, greater susceptibility to ingestion and destruction by phagocytes, or neutralization of exotoxin. See: skin test. (05 Mar 2000) |
| antigen-binding site | <immunology> In immune network theory, an idiotope, an antigenic site of an antibody that is responsible for that antibody binding to an antigenic determinant (epitope). Also used of the site on a ligand molecule to which a cell surface receptor binds. (18 Nov 1997) |
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