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"Agents primarily affecting the cardiovascular system"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • ¿µ¹®
    ÇѱÛ
  • remote afterloading system
    ¿ø°ÝÁ¶ÀÛÈÄÀåÁø¹ý
  • reproductive system
    »ý½Ä°èÅë
  • respiratory system
    È£Èí°èÅë
  • reticuloendothelial system
    ±×¹°³»ÇǰèÅë, ¼¼¸Á³»ÇǰèÅë
  • Rh blood group system
    ¾Ë¿¡ÃëÇ÷¾×Çü±º
  • self-system
    ÀÚ±âü°è
  • system
    °èÅë, ÀåÄ¡, Á¦µµ
  • scavenging system
    ¸¶Ãë°¡½ºÁ¦°Åü°è
  • skeletal system
    »À´ë°èÅë
  • social security system
    »çȸº¸ÀåÁ¦µµ
  • somatosensory system
    ¸ö°¨°¢°èÅë
  • sound conduction system
    ¼Ò¸®Àü´Þ°èÅë, ÀüÀ½°è
  • static system
    Á¤Áö°è
  • stereotactic system
    Á¤À§°íÁ¤±â
  • subcortical descending system
    °ÑÁú¹ØÇÏÇà°è, °ÑÁú¹Ø³»¸²°èÅë
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  • ¿µ¹®
    ÇѱÛ
  • pituitary adrenal system
    ÇϼöüºÎ½ÅÇÇÁú°è(¡­Üùãìù«òõͧ).
  • pituitary portal system
    ³úÇϼöü¹®¸Æ°è(¡­Ú¦ØæÍ§).
  • pneumatic tube system
    ±â¼Û°üÀåÄ¡(ѨáêηíûöÇ)
  • portal system
    ¹®¸Æ°è(Ú¦ØæÍ§).
  • pressoreceptor nervous system
    ¾Ð·Â¼ö¿ë½Å°æ°è(¡­ãêÌèͧ).
  • pride system
    ÀÚ±àü°è£¨í»Ðèô÷ͧ£©
  • primary signal system
    ÀÏÂ÷½ÅÈ£°è(ìéó­ãáûÜ Í§).
  • primary signalling system
    ÀÏÂ÷Àû¡¡½Åȣü°è
  • primitive duct system
    ¿ø½Ã°ü°èÅë
  • projective system
    Åõ»çü°è
  • real time system
    ½Ç½Ã°£ ü°è
  • reciprocal system
    »ó¹Ý°è(ßÓÚãͧ).
  • recirculating system
    Àç¼øÈ¯(¹æ)½Ä .
  • redox system
    »êȭȯ¿ø°è(ß«ûùü»êªÍ§).
  • registration system
    ½Å°íÁ¦µµ(Ëà˭̡̬).
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  • distric health system
    Áö¿ªº¸°Çü°è
  • dorsolateral system(brain stem)
    ¹èÃø°è(³ú°£)
  • drug delivery system
    ¾à¹°Àü´Þü°è.
  • dual foil system
    ÀÌÁß¹Ú¸·±¸Á¶
  • dynamic system
    µ¿Àû°èÅë(ÔÑîÜͧ÷Ö).
  • ecological system
    »ýÅÂ(ÇÐ)°è.
  • electro-optical system
    Àü±â±¤Çкм®°è
  • electron system
    ÀüÀÚÀü´Þ°è.
  • electron transfer system
    ÀüÀÚ¿î¹Ýü.
  • electron transfer system
    ÀüÀÚÀü´Þ°è(¡­ì¹ÔÑ), ÀüÀÚ¿î¹Ýü(¡­ê¡Úæô÷).
  • electronically steered system
    ÀüÀÚ Á¶Çâ ÀåÄ¡
  • endocrine system
    ³»ºÐºñ°è(¡­Í§)
  • endocrine system
    ³»ºÐºñ°èÅë
  • endogenous analsegic system
    ³»ÀμºÁøÅë°è(Ò®ì×àõòæ÷Ôͧ)
  • endometrial system
    ÀڱüӸ·°èÅë, Àڱ󻸷°è(¡­Í§).
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CVRR cardiovascular recovery room
CVT cardiovascular technologist; central venous temperature; congenital vertical talus
HASCVD hypertensive arteriosclerotic cardiovascular disease
HCVD hypertensive cardiovascular disease
HTCVD hypertensive cardiovascular disease
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CDSS Clinical Decision Support System
CIS Clinical Information System
CRS Compliance of the respiratory system
CELSS Controlled Ecological Life Support System
CNCPS Cornell Net Carbohydrate and Protein System
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  • primary signalling system
    ÀÏÂ÷Àû¡¡½Åȣü°è Á¤½Å
  • psychological modulation system
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  • Q : Àü±â·®ÀÇ coulombÀÇ ±âÈ£.

    Q blood group system

    Å¥½Ä Ç÷¾×Çü
    Ç÷¾×ÇüÀÇ Çϳª. µÅÁö Ç÷ûÀÇ ¾î¶² °Í¿¡ Á¸ÀçÇÏ´Â Ç× Q ÀÀÁý¼Ò¸¦ °¡ÇßÀ» ¶§ ÀÀÁýÇϴ°¡ ÇÏÁö ¾Ê´Â°¡¿¡ µû¶ó Ç÷¾×À» ºÐ·ùÇÏ´Â °ÍÀÌ´Ù. Ç× QÀÀÁý¼Ò´Â P½Ä Ç÷¾×ÇüÀÇ Ç× P ÀÀÁý¼Ò¿Í µ¿ÀÏÇÑ °ÍÀ̶ó´Â Çм³µµ ÀÖ´Ù.
  • renal depressor system
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  • renal pressor system
    ½Å ½Â¾Ð°è
  • respiratory system
    È£Èí±â°è, È£ÈíÅë
  • reticular system
    ¸Á»ó°è
  • scavenging system
    ¸¶Ãë °¡½º Á¦°Åü°è, ¹è±â ü°è
  • sensory modulatory system
    °¨°¢ Á¶Àý°è
  • serotonergic endogenous analgesic system
    ¼¼·ÎÅä´Ñ ³»¿ø¼º ÁøÅë°è
  • shift system
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    8½Ã°£ ÀÌ»óÀÇ ³ëµ¿À» ÇÊ¿ä·Î ÇÏ´Â Á÷Àå¿¡¼­ Á¶·Î ³ª´©¾î ÀÏÇÏ´Â Á¦µµ.
  • sodium transport system
    ³ªÆ®·ý ¿î¹Ý°è
  • stomatognathic system
    ±¸°­¾Ç°è, ±¸°­ ÇϾǰè, ¾Ç±¸°­°è
    Ä¡¾Æ, ¾Ç°ñ, ÃøµÎÇϾǰüÀý, ÀúÀÛ±Ù »çÀÌÀÇ ±â´ÉÀû ¹× ÇØºÎÇÐÀû °ü°è.
  • superficial musculoaponeurotic system
    Ç¥Ãþ ±Ù°Ç¸· ü°è
  • supraopticohypophyseal system
    ½Ã°¢ ±³Â÷ À§³úÇÏ ¼öü°è, ½Ã°¢·ÎÀ§ ³úÇÏ ¼öü·Î
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 8
neuromuscular nondepolarising agents Drugs that interrupt transmission at the skeletal neuromuscular junction without causing depolarisation of the motor end plate. They prevent acetylcholine from triggering muscle contraction and are used as muscle relaxants during electroshock treatments, in convulsive states, and as anaesthesia adjuvants.
(12 Dec 1998)
neuroprotective agents Drugs intended to prevent damage to the brain or spinal cord from ischemia, stroke, convulsions, or trauma. Some must be administered before the event, but others may be effective for some time after. They act by a variety of mechanisms, but often directly or indirectly minimise the damage produced by endogenous excitatory amino acids.
(12 Dec 1998)
neurotransmitter agents Substances used for their pharmacological actions on any aspect of neurotransmitter systems. Neurotransmitter agents include agonists, antagonists, degradation inhibitors, uptake inhibitors, depleters, precursors, and modulators of receptor function.
(12 Dec 1998)
neurotransmitters and neurotransmitter agents A collective grouping for neurotransmitters and substances that act on the neurotransmitter system.
(12 Dec 1998)
nootropic agents Drugs used to specifically facilitate learning or memory, particularly to prevent the cognitive deficits associated with dementias. These drugs act by a variety of mechanisms. While no potent nootropic drugs have yet been accepted for general use, several are being actively investigated.
(12 Dec 1998)
sunscreening agents Chemical or physical agents that protect the skin from sunburn and erythema by absorbing or blocking ultraviolet radiation.
(12 Dec 1998)
sweetening agents Substances that sweeten food, beverages, medications, etc., such as sugar, saccharine or other low-calorie synthetic products.
(12 Dec 1998)
dentin-bonding agents Cements that act through infiltration and polymerization within the dentinal matrix and are used for dental restoration. They can be adhesive resins themselves, adhesion-promoting monomers, or polymerization initiators that act in concert with other agents to form a dentin-bonding system.
(12 Dec 1998)
dermatologic agents Drugs used to treat or prevent skin disorders or for the routine care of skin.
(12 Dec 1998)
dopamine agents Any drugs that are used for their effects on dopamine receptors, on the life cycle of dopamine, or on the survival of dopaminergic neurons.
(12 Dec 1998)
imaging agents Proteins developed to act as imaging or contrast agents for use with various types of bodyscanners. The proteins, usually antibodies, bind to specific tissue types, usually tumours, and allow the scanner to distinguish those tissues from the surrounding tissue very easily.
(14 Nov 1997)
immunosuppressive agents Agents that suppress immune function by one of several mechanisms of action. Classical cytotoxic immunosuppressants act by inhibiting DNA synthesis. Others may act through activation of suppressor T-cell populations or by inhibiting the activation of helper cells. While immunosuppression has been brought about in the past primarily to prevent rejection of transplanted organs, new applications involving mediation of the effects of interleukins and other cytokines are emerging.
(12 Dec 1998)
intercalating agents Agents that are capable of inserting themselves between the successive bases in DNA, thus kinking, uncoiling or otherwise deforming it and therefore preventing its proper functioning. They are used in the study of DNA.
(12 Dec 1998)
iron chelating agents Organic chemicals that form two or more coordination links with an iron ion. Once coordination has occurred, the complex formed is called a chelate. The iron-binding porphyrin group of haemoglobin is an example of a metal chelate found in biological systems.
(12 Dec 1998)
tocolytic agents Drugs that prevent preterm labour and immature birth by suppressing uterine contractions. Agents used to delay premature uterine activity include magnesium sulfate, beta-mimetics, oxytocin antagonists, calcium channel inhibitors, and adrenergic beta-receptor agonists. The use of intravenous alcohol as a tocolytic is now obsolete.
(12 Dec 1998)
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