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  • ¿µ¹®
    ÇѱÛ
  • competence factor
    1. ¸é¿ª°¡´ÉÀÎÀÚ 2. ¹ÝÀÀ°¡´ÉÀÎÀÚ
  • competence inducing factor
    ¸é¿ª°¡´ÉÀ¯¹ßÀÎÀÚ
  • complementary factor
    º¸ÃæÀÎÀÚ
  • conglutinogen activating factor
    ±³Âø¿øÈ°¼ºÀÎÀÚ
  • conversion factor
    º¯È¯ÀÎÀÚ, º¯È¯°è¼ö
  • carcinogenic factor
    ¹ß¾ÏÀÎÀÚ
  • corticotropin-releasing factor
    ºÎ½Å°ÑÁúÀÚ±ØÈ£¸£¸ó¹æÃâÀÎÀÚ
  • chemotactic factor
    È­Çнò¸²ÀÎÀÚ
  • drug resistance factor
    ¾àÁ¦ÀúÇ×ÀÎÀÚ
  • dermonecrotic factor
    ÇǺα«»çÀÎÀÚ
  • diabetogenic factor
    ´ç´¢º´À¯¹ßÀÎÀÚ
  • decay accelerating factor
    ºØ±«ÃËÁøÀÎÀÚ
  • dilution factor
    Èñ¼®ÀÎÀÚ
  • exclusion of confounding factor
    ±³¶õ¹èÁ¦ÀÎÀÚ
  • exogenous factor
    ¿ÜÀοä¼Ò
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  • ¿µ¹®
    ÇѱÛ
  • atrial natriuretic factor
    ½É¹æ³ªÆ®·ýÀÌ´¢ÀÎÀÚ
  • colonizing factor antigen
    Áý¶ôÇü¼ºÀÎÀÚÇ׿ø
  • behavioral risk factor
    ÇൿÀ§Çè¿äÀÎ
  • carcinogenic factor
    ¹ß¾ÏÀÎÀÚ
  • chemotactic factor
    È­ÇÐÁÖ¼ºÀÎÀÚ, È­Çнò¸²ÀÎÀÚ
  • coagulation factor
    ÀÀ°íÀÎÀÚ
  • coagulation factor inhibitor
    ÀÀ°íÀÎÀÚ¾ïÁ¦Á¦
  • colony-stimulating factor
    Áý¶ôÀÚ±ØÀÎÀÚ
  • common factor
    °øÅëÀÎÀÚ
  • competence factor
    Àû°ÝÀÎÀÚ
  • competence inducing factor
    Àû°ÝÀ¯¹ßÀÎÀÚ
  • complementary factor
    º¸ÃæÀÎÀÚ, º¸Ã¼ÀÎÀÚ
  • conglutinogen activating factor
    ±³Âø¿øÈ°¼ºÀÎÀÚ
  • conversion factor
    º¯È¯ÀÎÀÚ, º¯È¯°è¼ö
  • corticotropin releasing factor
    ºÎ½Å°ÑÁúÀÚ±ØÈ£¸£¸ó¹æÃâÀÎÀÚ
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  • ¿µ¹®
    ÇѱÛ
  • B cell stimulating factor (BSF)
    B¼¼Æ÷ ÀÚ±ØÀÎÀÚ
  • Castles extrinsic factor
    Ĺ½½¿ÜÀÎÀÚ.
  • Castles intrinsic factor
    Ĺ½½³»ÀÎÀÚ.
  • Christmas factor
    Å©¸®½º¸¶½º ÀÎÀÚ(ì×í­)
  • Christmas factor.
    Å©¸®½º¸¶½ºÀÎÀÚ
  • D factor
    DÀÎÀÚ
  • Decay accelerating factor
    ºØ±«°¡¼Ó¿ä¼Ò(¿äÀÎ)
  • EDCF (endothlium-derived contracting factor)
    ³»ÇǼ¼Æ÷¼º(Ò®ù«á¬øààõ) ¼öÃàÀÎÀÚ(â¥õêì×í­)
  • EDRF (endothlium-derived relaxing factor)
    ³»ÇǼ¼Æ÷¼º(Ò®ù«á¬øààõ) ÀÌ¿ÏÀÎÀÚ(ì¬èÐì×í­)
  • EDRF=£¾endothelium derived relaxing factor
    ³»ÇǼ¼Æ÷¼ºÀÌ¿ÏÀÎÀÚ.
  • F factor
    FÀÎÀÚ
  • Factor IX
    IX ÀÀ°íÀÎÀÚ(ëêͳì×í­)
  • Factor V
    V ÀÀ°íÀÎÀÚ(ëêͳì×í­)
  • Factor VII
    VII ÀÀ°íÀÎÀÚ(ëêͳì×í­)
  • Factor VIII
    VIII ÀÀ°íÀÎÀÚ(ëêͳì×í­)
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  • ¿µ¹®
    ÇѱÛ
  • amplification factor
    ÁõÆøÀÎÀÚ
  • anisotropy factor
    ºñµî¹æ¼º°è¼ö
  • antigen, colonization factor
    Áý¶ôÇü¼ºÀÎÀÚÇ׿ø, ¼¼Æ÷±ºÇü¼ºÀÎÀÚÇ׿ø
  • antihemophilic A factor =AHA
    Ç×Ç÷¿ìº´ AÀÎÀÚ(?ËöËö).
  • antihemophilic factor =AHF
    Ç×Ç÷¿ìº´ÀÎÀÚ(¡­ì×í­)
  • antihemophilic factor =AHF
    Ç×Ç÷¿ìº´ÀÎÀÚ(?ËöËö).
  • antihemophllic factor
    Ç×Ç÷¿ìº´ÀÎÀÚ
  • antiinsulin factor
    Ç×Àν¶¸°ÀÎÀÚ.
  • antineuritic factor
    Ç׽Ű濰ÀÎÀÚ(ù÷ãêÌèæúì×í­).
  • antinuclear factor =ANF
    Ç×ÇÙÀÎÀÚ.
  • antipellagra factor
    Çׯç¶ó±×¶óÀÎÀÚ.
  • antiphagocytic factor
    Ç׎½ÄÀÎÀÚ, Ç׽ıÕÀÎÀÚ
  • antirachitic factor
    Ç×±¸·çº´ÀÎÀÚ(¡­ì×í­).
  • antiscorbutic factor
    Ç×±«Ç÷º´ÀÎÀÚ.
  • antisterility factor
    Ç׺ÒÀÓÀÎÀÚ(ù÷ÝÕìôì×í­).
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  • ¿µ¹®
    ÇѱÛ
  • instability factor
    ºÒ¾ÈÁ¤ÀÎÀÚ(ÝÕäÌïÒì×í­)
  • integration host factor
    ÅëÇÕ ¼÷ÁÖÀÎÀÚ(÷ÖùêâÖñ«ì×í­)
  • intrinsic factor
    ³»ÀÎÀÎÀÚ(Ò®ì×ì×í­)
  • labile factor
    ºÒ¾ÈÁ¤ÀÎÀÚ(ÝÕäÌïÒì×í­)
  • Laki-Lorand factor
    ¶óŰ-·Î¶õµå ÀÎÀÚ(ì×í­)
  • Lande G factor
    ¶õµ¥ G ÀÎÀÚ(ì×í­)
  • lard factor
    µ·Áö(ÔÊò·) ÀÎÀÚ(ì×í­)
  • leukocyte inhibitory factor
    ¹éÇ÷±¸ÀúÇØÀÎÀÚ(ÛÜúìϹîÁúªì×í­)
  • Lewis factor
    ·çÀ̽ºÀÎÀÚ(ì×í­)
  • lipoprotein tissue factor
    ÁöÁú´Ü¹éÁú(ò·òõÓ±ÛÜòõ) Á¶Á÷ÀÎÀÚ(ðÚòÄì×í­)
  • liver filtrate factor
    °£ ¿©°ú ÀÎÀÚ(ÊÜÕëΦì×í­)
  • LLD factor
    LLD ÀÎÀÚ(ì×í­)
  • L-L factor
    "L-L ÀÎÀÚ(ì×í­), (å²) Laki-Lorand ÀÎÀÚ(ì×í­)"
  • lymph node permeability factor
    ¸²ÇÁÀý(ï½)Åõ°úÀÎÀÚ(÷âΦì×í­)
  • lymphocyte-derived chemotactic factor
    ¸²ÇÁ±¸-À¯µµ(ë¯Óô) È­ÇÐÁÖ¼ºÀÎÀÚ(ûùùÊñËà÷ì×í­)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 8
TAF albumose-free tuberculin [Ger. Tuberculin Albumose frei]; tissue angiogenesis factor; toxin-antitoxi...
TDF testis-determining factor; thoracic duct fistula; thoracic duct flow; time-dose fractionation; tissu...
CPA tumor Cerebello-Pontine Angle(¼Ò³ú±³°¢ºÎ) tumor
IDEM tumor Intra-Dural Extra-Medullary tumor
MEN Multiple Endocrine Neoplasia
  ; AD Trait
  1. MEN Type I(= Wermer Syndro...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 8
CB1 cannabinoid 1 receptors
ER, PR Estrogen and progesterone receptors
FcR Fc gamma Receptors
GRPR Gastrin-releasing peptide receptors
hPR Human progesterone receptors
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • primary tumor
    ¿ø¹ß Á¾¾ç
  • pulmonary sulcus tumor
    Æó±¸ Á¾¾ç
  • recurrent tumor
    Àç¹ß¼º Á¾¾ç
  • red-blue tumor
    Àûû»ö Á¾¾ç
  • renal pelvic tumor
    ½Å¿ì Á¾¾ç
  • renal tumor
    ½Å Á¾¾ç
  • sand tumor
    ¸ð·¡Á¾
  • skin tumor
    ÇǺΠÁ¾¾ç
    ÇǺΠÁ¶Á÷¿¡ ¹ß»ýÇÑ Á¾¾ç.
  • soft tumor
    ¿¬¼º Á¾¾ç
  • suprasellar tumor
    ¾È»ó Á¾¾ç
  • tensa-elastic tumor
    ±äÀå-ź¼º Á¾¾ç
  • teratodermoid tumor
    ±âÇü À¯ÇÇÁ¾
  • testicular tumor
    °íȯ Á¾¾ç
    °íȯ¿¡ ¹ß»ýÇÏ´Â ¾Ç¼º Á¾¾ç. °íȯ ¾ÏÀ̶ó°íµµ ÇÑ´Ù. °íȯÀÇ Á¾¾çÀº Àü¹®ÀûÀ¸·Î´Â ¿©·¯ °¡Áö Á¾·ù·Î ±¸ºÐµÇÁö¸¸ ´ëü·Î ¾Ç¼ºÀÌ´Ù. 20~30´ë¿¡¼­ °¡Àå ¸¹°í À¯¾Æ¿¡°Ôµµ ¹ß»ýÇÑ´Ù. °íȯ Á¤Ã¼Áõ¿¡¼­ ¹ß»ýµÇ±â ½±´Ù. À½³¶ Àüü°¡ Ä¿Áö°í ´Ü´ÜÇØÁú »Ó, ÅëÁõÀ» ´À³¢´Â ÀÏÀÌ °ÅÀÇ ¾ø±â ¶§¹®¿¡ ¹æÄ¡µÇ±â°¡ ½±´Ù. ¹ßÀ°ÀÌ ½Å¼ÓÇÏ¿© ºü¸¥ ¼Óµµ·Î Èĺ¹°­ÀÇ ´ëµ¿¸Æ ÁÖº¯ ¸²ÇÁÀý¿¡ ÀüÀ̵DZ⠽±´Ù. À¶¸ð¼º ¾ÏÀº Ç÷Ç༺À¸·Î ÀüÀÌÇÏ¿© ºü¸¥ ¼Óµµ·Î °£ µîÀÇ Àå±â·Î °£´Ù. À¯¾ÆÀÇ °íȯ Á¾¾çÀº À¯¾ÆÀÇ µ¶Æ¯ÇÑ Áõ¼¼·Î¼­ Ãâ»ý Á÷ÈÄ¿¡ ¹ß°ßµÇ´Â °æ¿ìµµ µå¹°Áö ¾Ê´Ù. °íȯÀÇ ÇÑÂÊÀÌ Ä¿Áö¸ç ´Ü´ÜÇÑ Á¾·ù°¡ »ý±â´Â °ÍÀ¸·Î, ¿ª½Ã º¹ºÎ·Î ÀüÀÌÇÏ¸ç °£À¸·Îµµ ÀüÀÌÇÑ´Ù. À¯¾ÆÀÇ À½³¶ÀÌ Ä¿Áö´Â º´¿¡´Â °íȯ Á¾¾ç ¿Ü¿¡µµ À½³¶ ¼öÁ¾, À½³¶ Ç츣´Ï¾Æ µîÀÌ ÀÖÀ¸³ª, ±×·± Áúº´¿¡¼­´Â ´Ü´ÜÇÑ Á¾·ù´Â ¸¸Á®ÁöÁö ¾Ê´Â´Ù. °íȯ Á¾¾çÀº ÀüÀ̰¡ ºü¸£±â ¶§¹®¿¡ ¼ö¼ú¿¡ À־´Â ¼­ÇýºÎ³ª º¹ºÎÀÇ ¸²ÇÁÀýÀ» µ¿½Ã¿¡ ÀýÁ¦ÇÑ´Ù. ±×¹Û¿¡ Ä¡·á¹ýÀ¸·Î´Â Ç×¾ÏÁ¦ÀÇ »ç¿ëÀ̳ª ¹æ»ç¼± ¿ä¹ý µî ÀϹÝÀûÀÎ ¾Ï Ä¡·á¹ý°ú °°´Ù.
  • tough tumor border
    ´Ü´ÜÇÑ Á¾¾ç º¯¿¬
  • trophoblastic tumor
    ¿µ¾ç¸· Á¾¾ç
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 8
receptors, corticotropin Cell surface receptors that bind corticotropin (acth, adrenocorticotropic hormone) with high affinity and trigger intracellular changes. Pharmacology suggests there may be multiple acth receptors. An acth receptor has been cloned and belongs to a subfamily of g-protein-coupled receptors. In addition to the adrenal cortex, acth receptors are found in the brain and immune systems.
(12 Dec 1998)
receptors, corticotropin-releasing hormone Cell surface proteins that bind corticotropin-releasing hormone with high affinity and trigger intracellular changes which influence the behaviour of cells. The corticotropin releasing-hormone receptors on anterior pituitary cells mediate the stimulation of corticotropin release by hypothalamic corticotropin releasing factor. The physiological consequence of activating corticotropin-releasing hormone receptors on central neurons is not well understood.
(12 Dec 1998)
receptors, cxcr4 Seven-transmembrane G-protein-coupled receptors for alpha-chemokines. They also function as fusion cofactors for T-cell-tropic HIV-1 strains.
(12 Dec 1998)
receptors, cyclic AMP Cell surface proteins that bind cyclic AMP with high affinity and trigger intracellular changes which influence the behaviour of cells. The best characterised cyclic AMP receptors are those of the slime mold dictyostelium discoideum. The transcription regulator cyclic AMP receptor protein of prokaryotes is not included nor are the eukaryotic cytoplasmic cyclic AMP receptor proteins which are the regulatory subunits of cyclic AMP-dependent protein kinases.
(12 Dec 1998)
receptors, cytoadhesin A group of integrins that includes the platelet outer membrane glycoprotein gpiib-iiia (platelet glycoprotein gpiib-iiia complex) and the vitronectin receptor (receptors, vitronectin). They play a major role in cell adhesion and serve as receptors for fibronectin, von willebrand factor, and vitronectin.
(12 Dec 1998)
receptors, cytokine Cell surface proteins that bind cytokines and trigger intracellular changes influencing the behaviour of cells.
(12 Dec 1998)
receptors, cytoplasmic and nuclear Proteins in the cytoplasm or nucleus that specifically bind signalling molecules and trigger changes which influence the behaviour of cells. The major groups are the steroid hormone receptors, which usually are found in the cytoplasm, and the thyroid hormone receptors, which usually are found in the nucleus. Receptors, unlike enzymes, generally do not catalyze chemical changes in their ligands.
(12 Dec 1998)
receptors, dopamine Cell-surface proteins that bind dopamine with high affinity and trigger intracellular changes influencing the behaviour of cells.
(12 Dec 1998)
receptors, dopamine d1 A class of dopamine receptors identified by their binding profiles for synthetic ligands, their molecular biology, and, perhaps, by their mode of action.
(12 Dec 1998)
receptors, dopamine d2 A class of dopamine receptors identified by their binding profiles for synthetic ligands, their molecular biology, and, perhaps, their mode of action.
(12 Dec 1998)
receptors, drug Proteins that bind specific drugs with high affinity and trigger intracellular changes influencing the behaviour of cells. Drug receptors are generally thought to be receptors for some endogenous substance not otherwise specified.
(12 Dec 1998)
receptors, eicosanoid Cell surface proteins that bind eicosanoids with high affinity and trigger intracellular changes influencing the behaviour of cells. Among the eicosanoid receptors are receptors for the prostaglandins, thromboxanes, and leukotrienes.
(12 Dec 1998)
receptors, endothelin Cell surface proteins that bind endothelin with high affinity and trigger intracellular changes which influence the behaviour of cells.
(12 Dec 1998)
receptors, erythropoietin Cell surface proteins that bind erythropoietin with high affinity and trigger intracellular changes influencing the behaviour of cells.
(12 Dec 1998)
receptors, estradiol Cytoplasmic proteins that bind estradiol, migrate to the nucleus, and regulate DNA transcription.
(12 Dec 1998)
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