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  • ¿µ¹®
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  • cholinergic agent
    Äݸ°¼º¾à¹°
  • cholinergic blocking agent
    Äݸ°Â÷´ÜÁ¦
  • dehydrating agent
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  • denaturizing agent
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  • depolarizing agent
    Å»ºÐ±ØÁ¦
  • diagnostic agent
    Áø´Ü½Ã¾à
  • diluting agent
    Èñ¼®Á¦
  • etiologic agent
    ¿øÀÎü, º´ÀÎü
  • fibrinolytic agent
    ¼¶À¯¼Ò¿ëÇØÁ¦, ÇǺ기¿ëÇØÁ¦
  • germicidal agent
    »ì±ÕÁ¦
  • ganglionic blocking agent
    ½Å°æÀýÂ÷´ÜÁ¦
  • hyperosmotic agent
    °í»ïÅõ¾ÐÁ¦
  • health care agent
    1. °Ç°­°ü¸®¿ä¿ø 2. °Ç°­°ü¸®±â±¸
  • ischemia-inducing agent
    ÇãÇ÷À¯µµÁ¦
  • induction agent
    À¯µµ¹°Áú, À¯µµÁ¦
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  • ¿µ¹®
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  • dehydrating agent
    Å»¼öÁ¦
  • denaturizing agent
    º¯¼ºÁ¦
  • depolarizing agent
    Å»ºÐ±ØÁ¦
  • diagnostic agent
    Áø´Ü¾à
  • diluting agent
    Èñ¼®Á¦
  • etiologic agent
    ¿øÀÎü, º´ÀÎü
  • fibrinolytic agent
    ¼¶À¯¼Ò¿ëÇØ¹°Áú
  • ganglionic blocking agent
    ½Å°æÀýÂ÷´ÜÁ¦
  • germicidal agent
    »ì±ÕÁ¦
  • health care agent
    °Ç°­°ü¸®¿ä¿ø, °Ç°­°ü¸®±â±¸
  • induction agent
    À¯µµ¹°Áú
  • infectious agent
    °¨¿°Ã¼, °¨¿°¿ø
  • ischemia-inducing agent
    ÇãÇæÀ¯µµÁ¦
  • lipotropic agent
    Ä£Áö¹æ¾à
  • masking agent
    Â÷ÆóÁ¦
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  • ¿µ¹®
    ÇѱÛ
  • psychedelic agent
    ȯ°¢Á¦.
  • psychotropic agent =psychotrotropic
    Á¤½ÅÀÛ¿ë¾à(¡­íÂéÄå·).
  • radioopaque agent
    ¹æ»ç¼± ºñÅõ°ú¼º Á¦Àç
  • radioprotective agent
    ¹æ»ç¼±¹æÈ£Á¦
  • radiosensitive agent
    ¹æ»ç¼±°¨ÀÛ¹°Áú, -¹Î°¨Á¦
  • receptor blocking agent
    ¼ö¿ëüÂ÷´Ü<ºÀ¼â>Á¦.
  • reducing agent
    ȯ¿øÁ¦(ü½êªð¥), ȯ¿ø½Ã¾à.
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  • low forceps
    ÀúÀ§°âÀÚ(î¸êÈÌÆí­).
  • low forceps operation
    (žư¡ ±Ø»óµ¹±â ¾Æ·¡¿¡ ÀÖÀ» °æ¿ìÀÇ), Àú À§°âÀÚ¼ö¼ú(î¸êÈÌÆí­â¢âú).
  • low frequency
    ÀúÁÖÆÄ
  • low frequency deafness
    ÀúÁ֯ijó, ÀúÁÖÆÄ±Í¸ÔÀ½
  • low frequency therapeutic apparatus
    ÀúÁÖÆÄÄ¡·á±â
  • low frequency therapeutic apparatus
    ÀúÁÖÆÄÄ¡·á±â(î¸ñ²÷îö½èþÐï).
  • low frequency transduction
    Àúºóµµ ÇüÁúµµÀÔ
  • low fusing porcelain
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  • low heat
    Àú¿­.
  • low intensity void in proton flow
    ¾ç¼ºÀÚ È帧ÀÇ Àú°­µµ ¼Ò½Ç
  • low ionic strenglh salt solution
    ÀúÀ̿°­µµ¿°¿ë¾×
  • low molecular weight
    ÀúºÐÀÚ·®(î¸ÝÂí­åÖ).
  • low output heart failure
    Àú¹ÚÃ⼺ ½ÉºÎÀü.
  • low output syndrome
    Àú¹ÚÃâ·®ÁõÈıº.
  • low oxalate diet
    Àú¼ö»ê¿°½Ä.
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MTS Medicare transaction system; magnetization transfer contrast; methotrexate; multicellular tumor sphe...
NCE negative contrast echocardiography; new chemical entity; nonconvulsive epilepsy
PC avoirdupois weight [Lat. pondus civile]; packed cells; paper chromatography; paracortex; parent cell...
RCIRF radiologic contrast-induced renal failure
RCM radial contour model; radiographic contrast medium; red cell mass; reinforced clostridial medium; re...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 7
MCE Myocardial contrast echocardiography
PC Phase Contrast
PCM Phase contrast microscopy
RCM Radiographic contrast media
RCM Reflection contrast microscopy
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    ¼³¸í
  • dehydrating agent
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  • developing agent
    Çö»ó ÁÖ¾à
  • douching : a jet or current of water, sometimes a dissolved medicating or cleansing agent, applied to a body part, organ or cavity for medicinal or hygienic purposes.

    dough

    ¹ÝÁ×ÇÑ °Í, ³¯ ºÐ
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  • fixing agent
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  • flavoring agent
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  • human parvovirus-like agent
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  • immunosupressive agent
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  • immuuppressive agent
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    °¨¿° ÀÎÀÚ
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  • intercalating agent
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  • miscellaneous agent
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  • neuromuscular blocking agent
    ½Å°æ±Ù Â÷´ÜÁ¦, ½Å°æ±Ù Â÷´Ü ¾à
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 7
Agent Orange An herbicide and defoliant, consisting of (2,4,5-trichlorophenoxy)acetic acid, (2,4-dichlorophenoxy)acetic acid, and dioxin, that was widely used in the Vietnam War; it has been shown to possess residual post-exposure carcinogenic and teratogenic properties in humans.
(05 Mar 2000)
agent, tocolytic A medication that can inhibit labour, slow down or halt the contractions of the uterus. Tocolytic agents are widely used today to treat premature labour and permit pregnancy to procede and so let the foetus gain in size and maturity before being born.
(12 Dec 1998)
alkylating agent <oncology, pharmacology> A reagent that places an alkyl group, for example propyl in place of a nucleophilic group in a molecule. Alkylating reagents include a number of cytotoxic drugs some of which react fairly specifically with N7 of the purine ring and lead to depurination of DNA, for example the agent ethyl ethanesulphonic acid and thus to mutagenesis. The drugs interaction with DNAand prevents the division of the cells.
Examples of drugs include: busulphan, chlorambucil, cyclophosphamide, melphalan.
(29 Sep 1997)
alpha-adrenergic blocking agent An agent that competitively blocks alpha-adrenergic receptors; used in the treatment of hypertension.
Synonym: alpha-blocker.
(05 Mar 2000)
antianxiety agent A functional category of drugs useful in the treatment of anxiety and able to reduce anxiety at doses which do not cause excessive sedation (e.g., diazepam).
Synonym: anxiolytic, minor tranquilliser.
(05 Mar 2000)
antidiabetic agent A substance that helps a person with diabetes control the level of glucose (sugar) in the blood so that the body works as it should. See: insulin.
(09 Oct 1997)
antifibrinolytic agent Agents that prevent fibrinolysis or lysis of a blood clot or thrombus. Several endogenous antiplasmins are known. The drugs are used to control massive haemorrhage and in other coagulation disorders.
(12 Dec 1998)
antifoam agent A chemical that reduces the surface tension of foams that form on thesurface of broths in fermentors because of aeration or agitation. Stearyldecanol, octal decanol, vegetable oils, silicones, sulphonates, andpolypropylene glycol are typically used, though they can cause problems inrefining the broth later on.
(09 Oct 1997)
anti-inflammatory agent Agents that counteract or suppress the inflammatory process. An antirheumatic agent or inflammation mediator, both endogenous and exogenous substances used to counteract the inflammatory process or alleviate or prevent rheumatic diseases, and the compounds that mediate the inflammation process.
(12 Dec 1998)
anti-inflammatory agent, non-steroidal Anti-inflammatory agents that are not steroids. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They are used primarily in the treatment of chronic arthritic conditions and certain soft tissue disorders associated with pain and inflammation. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. Certain nsaids also may inhibit lipoxygenase enzymes or phospholipase c or may modulate T-cell function. (ama drug evaluations annual, 1994, p 1814-5)
(12 Dec 1998)
anti-inflammatory agent, steroidal Steroidal agents capable of suppressing or counteracting the inflammatory process by acting on body mechanisms, without directly antagonizing the causative agents.
(12 Dec 1998)
anti-inflammatory agent, topical Anti-inflammatory agent that are applied to the skin and whose pharmacological effect only occurs at the area of application.
(12 Dec 1998)
antinematodal agent Substances used in the treatment or control of nematode infestations. They are used also in veterinary practice.
(12 Dec 1998)
antineoplastic agent Agents inhibiting or preventing the growth of neoplasms, checking the maturation and proliferation of malignant cells.
(12 Dec 1998)
antineoplastic agent, alkylating A class of drugs that differs from other alkylating agents used clinically in that they are monofunctional and thus unable to cross-link cellular macromolecules. Among their common properties are a requirement for metabolic activation to intermediates with antitumour efficacy and the presence in their chemical structures of n-methyl groups, that after metabolism, can covalently modify cellular DNA. The precise mechanisms by which each of these drugs acts to kill tumour cells are not completely understood.
(12 Dec 1998)
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