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  • ¿µ¹®
    ÇѱÛ
  • plaque morphology mutation
    ÆÇÇüŵ¹¿¬º¯ÀÌ, ÇöóÅ©Çüŵ¹¿¬º¯ÀÌ
  • plaque technique
    ÇöóÅ©(±â)¹ý
  • plaque-forming unit
    ÇöóÅ©Çü¼º´ÜÀ§
  • yellow plaque
    Ȳ»öÆÇ
  • antibody capture enzyme-linked immunosorbent assay
    Ç×üÆ÷ȹȿ¼Ò¸é¿ªÃøÁ¤(¹ý)
  • antigen capture assay
    Ç׿øÆ÷È¹ÃøÁ¤
  • assay
    1. ÃøÁ¤ 2. ÃøÁ¤¹ý 3. °Ë»ç, ºÐ¼®
  • biological assay
    »ý¹°ÇÐÀû°ËÁ¤
  • competitive binding assay
    °æÀïÀû°áÇպм®
  • dilution assay technique
    Èñ¼®ºÐ¼®¹ý
  • double-sandwich enzyme-linked immunosorbent assay
    °ãÈ¿¼Ò¸é¿ªÃøÁ¤(¹ý)
  • enzyme assay
    È¿¼ÒÃøÁ¤
  • enzyme-linked immunosorbent assay
    È¿¼Ò°áÇո鿪ÈíÂøÃøÁ¤(¹ý)
  • foam stability assay
    °Åǰ¾ÈÁ¤ÃøÁ¤
  • hemagglutination assay
    Ç÷±¸ÀÀÁý°Ë»ç
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  • ¿µ¹®
    ÇѱÛ
  • plaque morphology mutation
    (¢¡plaque-type mutation) ÇöóÅ©Çüµ¹¿¬º¯ÀÌ
  • plaque-type mutation
    ÇöóÅ©Çüµ¹¿¬º¯ÀÌ
  • plaque
    ÆÇ, ÇöóÅ©
  • phage plaque-forming unit
    ÆÄÁö¿ë±ÕÇü¼º´ÜÀ§, ÆÄÁöÇöóÅ©Çü¼º´ÜÀ§
  • plaque technique
    ÇöóÅ©°Ë»ç¹ý
  • plaque-forming unit
    ÇöóÅ©Çü¼º´ÜÀ§
  • yellow plaque
    Ȳ»öÆÇ
  • assay
    ºÐ¼®, ÃøÁ¤
  • antibody capture enzyme-linked immunosorbent assay
    Ç×üÆ÷ȹȿ¼Ò¸é¿ªÃøÁ¤¹ý
  • antigen capture assay
    Ç׿øÆ÷È¹ÃøÁ¤
  • biological assay
    »ý¹°ÇÐÀû°ËÁ¤
  • direct fluorescent assay
    Á÷Á¢Çü±¤ºÐ¼®
  • double-sandwich enzyme-linked immunosorbent assay
    °ãÈ¿¼Ò¸é¿ªÃøÁ¤¹ý
  • enzyme assay
    È¿¼ÒÃøÁ¤
  • enzyme-linked immunosorbent assay
    È¿¼Ò¸é¿ªÃøÁ¤¹ý
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • acid phosphatase assay
    »ê¼ºÆ÷½ºÆÄŸÁ¦ ÃøÁ¤
  • ames assay
    ¿¡ÀÓ½ººÐ¼®
  • antibiotic assay
    Ç×»ý¹°Áú ¹ÙÀÌ¿ÀÆò°¡.
  • antigen capture assay
    Ç׿øÆ÷È¹ÃøÁ¤
  • antigenic assay
    Ç׿ø¼ººÐ¼®
  • antimicobial assay
    Ç×±ÕÁ¦ÃøÁ¤
  • growth hormone assay
    ¼ºÀåÈ£¸£¸óÃøÁ¤
  • hemizona assay (index)
    ¹ÝÅõ¸í´ë ÃøÁ¤(ÁöÇ¥)
  • human zona binding assay
    »ç¶÷Á¤ÀÚ Åõ¸í´ëºÎÂø°Ë»ç
  • immunoconcentration assay
    ¸é¿ª³óÃàÃøÁ¤<--Á¤·®
  • immunoenzymometric assay
    ¸é¿ªÈ¿¼Ò°èÃø<--°è·®>ºÐ¼®
  • immunofluorescence assay
    ¸é¿ªÇü±¤°Ë»ç
  • immunometric assay
    ¸é¿ª°è·®<--°èÃø>°Ë»ç
  • immunoradiometric assay
    ¸é¿ª¹æ»çÃøÁ¤(¹ý)
  • predictive assay
    È¿°ú¿¹Ãø½ÃÇè
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • bacterial killing assay
    ¼¼±Õ»ìÇØÃøÁ¤
  • biological assay
    Àθí [¸é¿ª,°£È£,À¯Àü,¹Ì»ý,±â»ý,¹ÙÀÌ]»ý¹°ÇÐÀû °ËÁ¤(¡­ËþïÒ).
  • biological assay
    Àθí[¸é¿ª,°£È£,À¯Àü,¹Ì»ý,±â»ý,¹ÙÀÌ] »ý¹°ÇÐÀû ¾Æ¼¼ÀÌ(¡­ËþïÒ).
  • biological assay
    »ý¹°ÇÐÀû °ËÁ¤(¡­ËþïÒ)
  • biological assay
    Àθí [¸é¿ª,°£È£,À¯Àü,¹Ì»ý,±â»ý,¹ÙÀÌ]»ý¹°ÇÐÀû °ËÁ¤(¡­ËþïÒ).
  • biological assay
    Àθí [¸é¿ª,°£È£,À¯Àü,¹Ì»ý,±â»ý,¹ÙÀÌ]»ý¹°ÇÐÀû °ËÁ¤(¡­ËþïÒ).
  • calcitonin assay
    Ä®½ÃÅä´ÑÃøÁ¤
  • carcinoembryonic antigen assay
    ¾Ï(¼º)¹è¾Æ¼º Ç׿øÃøÁ¤
  • cell adhesive matrix assay
    ¼¼Æ÷Á¡Âø±âÁúºÐ¼®
  • clonogenic assay
    Ŭ·Ð¿ø¼º ºÐ¼®
  • clonogenic assay
    Ŭ·Ð¿ø¼ººÐ¼®
  • colony formation assay
    Áý¶ôÇü¼º´ÉÃøÁ¤
  • creatine kinase assay
    Å©·¹¾ÆÆ¾Å°³ªÁ¦ÃøÁ¤
  • diagnostic assay
    Áø´ÜÀûºÐ¼®
  • dilution assay technique
    Èñ¼®ºÐ¼®¹ý
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  • ¿µ¹®
    ÇѱÛ
  • assay
    ¾Æ½êÀÌ
  • binding assay
    °áÇÕ(Ì¿ùê)¾Æ½êÀÌ
  • biological assay
    »ý¹°ÇÐÀû(ßæÚªùÊîÜ) ¾Æ½êÀÌ
  • competitive radioligand assay
    °æÇÕÀû(ÌæùêîÜ ¹æ»ç´É(Û¯ÞÒÒö)¸®°£µå ¾Æ½êÀÌ
  • continuous assay
    ¿¬¼Ó(Ö§áÙ)¾Æ½êÀÌ
  • coupled assay
    °ø¿ª(Íìæµ) ¾Æ¼¼ÀÌ (ÔÒ) auxiliary enzyme
  • d-assay
    d-¾Æ½êÀÌ
  • discontinuous assay
    ºÒ¿¬¼Ó(ÝÕææáÙ) ¾Æ½êÀÌ
  • dot blot assay
    Á¡(ïÃ)ºí·Ô ¾Æ¼¼ÀÌ
  • enzyme assay
    È¿¼Ò(ý£áÈ)¾Æ½êÀÌ
  • enzyme-linked immunosorbent assay
    È¿¼Ò¿¬°ü ¸é¿ªÈíÂø (ý£áÈ֤μØóæ¹ýåó·) ¾Æ½êÀÌ
  • fixed time assay
    ÀÏÁ¤½Ã°£(ìéïÒãÁÊà) ¾Æ½êÀÌ
  • i-assay
    i-¾Æ½êÀÌ
  • immunoenzymometric assay
    ¸é¿ªÈ¿¼ÒÃøÁ¤(Øóæ¹ý£áÈö´ïÒ) ¾Æ½êÀÌ
  • immunofluorometric assay
    ¸é¿ªÇü±¤ÃøÁ¤(Øóæ¹û«ÎÃö´ïÒ) ¾Æ½êÀÌ
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
AP accessory pathway; accounts payable; acid phosphatase; acinar parenchyma; action potential; active p...
LPF leukocytosis-promoting factor; leukopenia factor; lipopolysaccharide factor; localized plaque format...
PFC pair-fed control [mice]; patient-focused care; pelvic flexion contracture; perfluorocarbon; pericard...
PFU plaque-forming unit; pock-forming unit
PI first meiotic prophase; isoelectric point; pacing impulse; package insert; pancreatic insufficiency;...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
P1I Plaque Index
PI Plaque Index
PII Plaque Index
PLI Plaque Index
PRN Plaque Reduction Neutralization
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • micrologica assay
    ¹Ì»ý¹°ÇÐÀû Á¤·®¹ý
  • radioreceptor assay
    ¹æ»ç¼± ¼ö¿ëü ÃøÁ¤¹ý
    ÀÏÁ¾ÀÇ ¹æ»ç Ç¥Áö °ËÁ¤¹ýÀ¸·Î¼­, Á¶Á÷ Ç¥º» ³»¿¡ Àִ ȣ¸£¸ó¿¡ ´ëÇØ Ư¼öÇÑ ¼¼Æ÷ ¼ö¿ëüÀÇ ³óµµ¸¦ ¹æ»ç Ç¥ÁöÇÑ È£¸£¸óÀ» ÀÌ¿ëÇÏ¿© ÃøÁ¤ÇÏ´Â °Í.
  • atrophic large-plaque parapsoriasis
    À§Ã༺ ÆÇ
  • clear plaque mutation
    Åõ¸í ÇöóÅ© µ¹¿¬º¯ÀÌ
  • dental microbial plaque
    Ä¡¸é ±ÕÅÂ
    Ä¡¾Æ Ç¥¸é¿¡ ȹµæ ÇǸ·ÀÇ ¼®È¸È­·Î ÀÎÇØ ¾ß±âµÈ
  • dental plaque
    Ä¡ÅÂ
    ´Ù¾çÇÑ ¹ÚÅ׸®¾ÆÀÇ ¼ºÀåÀ» À§ÇÑ È¯°æÀÇ Á¦°øÀÌ µÇ´Â Ä¡¾Æ Ç¥¸é¿¡ Ä§ÂøµÇ¾îÁø Á×Àº »óÇǼ¼Æ÷¿Í ¹Â½Å, À½½Ä¹° Â±âÀÇ ¾ã°í ºÎµå·¯¿î ¸·. ÁÖ¿äÇÑ ¹«±â ¼ººÐÀº Ä®½·°ú ÀÎ ±×¸®°í ¼Ò·®ÀÇ ¸¶±×³×½·, œþ·ý, ³ªÆ®·ýÀÌ´Ù. À¯±â ±âÁúÀº ´Ù´çÁú, ´Ü¹éÁú, ź¼öÈ­¹°, ÁöÁú ±×¸®°í ´Ù¸¥ ¼ººÐÀÌ´Ù. Çöó±×
  • fibrous plaque
    ¼¶À¯¹Ý
  • flat plaque
    ÆíÆò ¹Ý
  • flat skin plaque
    ÆíÆò ÇǺΠ¹Ý
  • moist plaque
    ÃàÃàÇÑ Ä¡ÅÂ
  • mottled plaque
    ¿ë±Õ ¹Ý
  • opaline plaque
    ´Ü¹é¼®¾ç ¹Ý
  • plaque control
    ġŠÁ¶Àý
  • plaque formation
    º´¼Ò ¹Ý Çü¼º, ÇöóÅ© Çü¼º
    ȹµæ ÇǸ·ÀÇ Çü¼º, ȹµæ ÇǸ·¿¡ ¼¼±ÕÀÇ ÃʱâºÎÂø, ¼¼±Õ¼º ġŰ¡ ¸î ÃþÀ¸·Î ÃàÀûµÇ¾î µÎ²¨¿öÁö´Â °úÁ¤À» ¸»ÇÑ´Ù.
  • plaque forming unit
    ÇöóÅ© Çü¼º ´ÜÀ§
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
dental plaque <dentistry> A soft, thin film of food debris, mucin and dead epithelial cells deposited on the teeth, providing the medium for the growth of various bacteria.
The main inorganic components are calcium and phosphorus with small amounts of magnesium, potassium and sodium, the organic matrix consists of polysaccharides, proteins, carbohydrates, lipids and other components.
Plaque plays an important aetiological role in the development of dental caries and periodontal and gingival diseases and provides the base for the development of materia alba, calcified plaque forms dental calculus.
(19 Mar 1998)
dental plaque index An index which scores the degree of dental plaque accumulation.
(12 Dec 1998)
fibrous plaque Thickened area of arterial intima with accumulation of smooth muscle cells and fibrous tissue (collagen etc.) produced by the fat laden smooth muscle cells. Below the thickening may be free extracellular lipid and debris that, if much necrosis is also present, is referred to as an atheroma.
(18 Nov 1997)
acetyl reduction assay <investigation> A technique for measuring the nitrogen fixation activity in photosynthetic organisms. It uses a flame ionisation detector and a gas chromatography apparatus to determine the reduction of acetylene to ethylene by the enzyme nitrogenase.
(06 May 1997)
Ames assay <procedure> One of a number of procedures used to test substances for likely ability to cause cancer that combines the use of animal tissue to generate active metabolites of the substance with a test for mutagenicity in bacteria.
(18 Nov 1997)
antibiotic assay <investigation> A test to determine how sensitive a bacterial or fungal strain is to arange of antibiotics bymeasuring the microbes' ability to grow in astandard dilution of each chemical.
(09 Oct 1997)
assay <procedure> The determination of the amount of a particular constituent of a mixture or of the biological or pharmacological potency of a drug.
(10 May 1997)
bandshift assay <investigation> An assay for proteins, such as transcription factors, that bind specific DNA sequences.
A labelled oligonucleotide corresponding to the recognition sequence is incubated with an appropriate nuclear protein extract and run on a nondenaturing acrylamide gel. Oligonucleotides that have been bound by proteins are retarded relative to those that are unbound.
(18 Nov 1997)
biological assay <technique> Once a pharmaceutical protein is isolated from the cells in which it was grown, researchers perform tests to measure the protein's biological activity.
It must maintain a certain minimal level of biological activity to be used for animal or clinical testing or, later, for market. Researchers also test to confirm that the isolated protein is identical to the desired protein.
(21 Mar 1998)
radioimmunoprecipitation assay Sensitive assay using radiolabelled antigens to detect specific antibodies in serum. The antigens are allowed to react with the serum and then precipitated using a special reagent such as protein a sepharose beads. The bound radiolabelled immunoprecipitate is then commonly analyzed by gel electrophoresis. Radioimmunoprecipitation assay (ripa) is often used as a confirmatory test for diagnosing the presence of HIV antibodies.
(12 Dec 1998)
radioligand assay <radiobiology> Quantitative determination of receptor (binding) proteins in body fluids or tissue using radioactively labelled binding reagents (e.g., antibodies, intracellular receptors, plasma binders).
(12 Dec 1998)
radioreceptor assay A competitive binding assay in which the binder is a membrane or tissue receptor rather than an antibody.
(05 Mar 2000)
Raji cell radioimmune assay For immune complexes; a procedure by which immune complexes adsorbed from a test serum by a standard preparation of lymphoblastoid (Raji) cells are assayed by the capacity to bind 125I-labelled antibody to immunoglobulin.
(05 Mar 2000)
gel retardation assay A lab technique used to find out if there are proteins binding a fragment of DNA (in a DNA-protein complex) by watching how fast the DNA fragment moves through an electric field and seeing whether it moves slower when a particular protein is also present.
(09 Oct 1997)
checkerboard assay <procedure> Variant of the Boyden chamber assay for leucocyte chemotaxis introduced by Zigmond. By testing different concentrations of putative chemotactic factor in nongradient conditions, it is possible to calculate the enhancement of movement expected due simply to chemokinesis and to compare this with the distances moved in positive and negative gradients. Good experimental design thus allows chemotaxis to be distinguished from chemokinesis.
(21 May 1997)
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