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  • ¿µ¹®
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  • breath holding time
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  • circulation time
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  • clot retraction time
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  • clotting time
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  • coagulation time
    ÀÀ°í½Ã°£
  • colonic transit time
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  • concentration-time curve
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  • conduction time
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  • dead time
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  • diastolic filling time
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  • diffusion time
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  • expiratory pause time
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  • expiratory phase time
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  • exposure time
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  • fast time constant circuit
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  • ¿µ¹®
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  • bleeding time
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  • bleeding time test
    ÃâÇ÷½Ã°£°Ë»ç
  • breath holding time
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  • lead-time bias
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  • clot retraction time
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  • clotting time
    (¢¡coagulation time) ÀÀ°í½Ã°£
  • coagulation time
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  • concentration-time curve
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  • conduction time
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  • fast time constant circuit
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  • reaction time crossover
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  • time cluster
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  • time cue
    ½Ã°£½ÅÈ£ÀÎÀÚ
  • time compensation curve
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  • time-activity curve
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  • ¿µ¹®
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  • T2 relaxation time
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  • TM scan(Time motion)
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  • TM-scan(Time motion)
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  • TOF (time of flight)
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  • acquisition time
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  • activated clotting time
    Ȱ¼ºÈ­ÀÀ°í½Ã°£
  • activated coagulation time(ACT)
    Ȱ¼º Ç÷¾× ÀÀ°í½Ã°£
  • activated coagulation time=ACT
    Ȱ¼ºÈ­ ÀÀ°í½Ã°£
  • activated partial prothrombin time
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  • activated partial thromboplastin time
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  • activated partial thromboplastin time =aPTT
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  • appearance time
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  • area under the concentration-time curve : AUC
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  • arm to tongue time test
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  • ¿µ¹®
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  • carcinoembryonic antigen assay
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  • cell adhesive matrix assay
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  • clonogenic assay
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  • clonogenic assay
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  • colony formation assay
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  • creatine kinase assay
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  • diagnostic assay
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  • dilution assay technique
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  • enzymatic assay
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  • enzymatic assay
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  • enzyme linked immunosorbent assay ( ELISA)
    È¿¼Ò ¸é¿ªÃøÁ¤¹ý
  • enzyme assay
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  • enzyme linked immunosorbent assay (ELISA)
    È¿¼Ò¸é¿ªÃøÁ¤¹ý
  • enzyme-linked immunosorbent assay
    È¿¼Ò¿¬°ü¸é¿ªÈíÂø¹ý
  • enzyme-linked immunosorbent assay
    È¿¼Ò¸é¿ªÃøÁ¤¹ý
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  • time factor effect
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  • transient time
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  • turnover time
    Àüȯ½Ã°£(ï®üµãÁÊà)
  • zero time binding DNA
    ¿µ½Ã(çÍãÁ) °áÇÕ(Ì¿ùê) DNA
  • zero time control
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  • temporal window(scan time)
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  • time compensation curve
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  • time gain compensation [=T.G.C.]
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  • time gain compenstaion curve
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  • time gain control
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  • time interval
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  • time of flight [=TOF]
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  • time of flight MR angiography
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  • time of flight phenomenon
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  • time sharing
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  • time velocity integral
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  • TM scan(Time motion)
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  • TOF [=time of flight]
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  • transit time
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CRT cadaveric renal transplant; cardiac resuscitation team; cathode-ray tube; certified; Certified Recor...
ET educational therapy; effective temperature; ejection time; embryo transfer; endothelin; endotoxin; e...
MRT magnetic resonance tomography; maximum relaxation time; median range score; median reaction time; me...
PST pancreatic suppression test; paroxysmal supraventricular tachycardia; penicillin, streptomycin, and ...
RT radiologic technologist; radiotelemetry; radiotherapy; radium therapy; rapid tranquilization; reacti...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 4
C-ELISA Competitive enzyme-linked immunosorbent assay
DEIA DNA enzyme immuno assay
DIG-ELISA Diffusion-In-Gel Enzyme Linked Immunosorbent Assay
DFA Direct immunofluorescence assay
Dot-ELISA Dot Enzyme-Linked Immunosorbent Assay
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  • fast time constant circuit
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  • first-time dental patient
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  • hardening time
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  • inversion time
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  • left ventricular ejection time
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  • mixing time
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  • operative time
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  • partial prothrombin time
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  • persistence time
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  • plasma prothrombin time
    Ç÷Àå ÇÁ·ÎÆ®·Òºó ½Ã°£
  • prolonged bleeding time
    ¿¬ÀåµÈ ÃâÇ÷ ½Ã°£
  • real time acquisition
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  • real time image
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  • real time study
    ½Ç½Ã°£ °Ë»ç
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
scintillation proximity assay Assay system in which antibody or receptor molecule is bound to a bead that will emit light when _ emission from an isotope occurs in close proximity, i.e. From a radioactively labelled ligand. Avoids the need for scintillant in order to measure the amount of bound isotope and thus the amount of antigen or ligand present.
(18 Nov 1997)
hormone receptor assay A diagnostic test to determine whether a breast cancer's growth is influenced by hormones or if it can be treated with hormones.
(09 Oct 1997)
subrenal capsule assay In vivo method of screening investigative anticancer drugs and biologic response modifiers for individual cancer patients. Fresh tumour tissue is implanted under the kidney capsule of immunocompetent mice or rats; gross and histological assessments follow several days after tumour treatment in situ.
(12 Dec 1998)
nuclear run off assay <investigation, procedure> Technique for determining which genes are being actively transcribed at a given moment in an experiment by extracting nuclear material and allowing transcription to continue, then analysing the resulting RNAs.
(18 Nov 1997)
DNA filter assay <molecular biology> A lab technique used to identify the complementary base sequences of DNA. It involves immobilising the DNA on a filter and putting it in a solution that contains radioactively-labelled probe DNA or RNA molecules.
(09 Oct 1997)
double antibody sandwich assay For antigen; an application of the ELISA method in which material being tested for antigen is added to wells coated with known antibody; the presence of antigen fixed to the antibody coat can be determined either directly, by adding human antibody linked to the enzyme of the indicator system, or indirectly, by first adding unlabelled known antibody, the attachment of which to the antigen can be demonstrated by addition of immunoglobulin-specific antibody linked to the enzyme.
(05 Mar 2000)
immunochemical assay <investigation> A process that measures and identifies a specific biological substance such as an antigen.
(09 Oct 1997)
immunocytochemical assay Involves the computerised assessment of microscopic fields following direct fluorescent antibody, indirect fluorescent antibody or indirect or direct immunoperoxidase analysis of biopsy tissue from the patient. In addition to improved specificity with the removal of operator subjectivity, the quantifiability of results through computer data analysis of colour, intensity and concentration has only begun to be realised.
(05 Mar 2000)
immunoradiometric assay <immunology> A test that measures the concentration of antigens in a specimen throughserological analysis that involves mixing radioactive antibodies with the antigen in question.
(09 Oct 1997)
indirect assay For antibody; an application of the ELISA method in which serum being tested for antibody is added to wells coated with known antigen; presence of antibody bound to the antigen coat can be determined by addition of immunoglobulin-specific antibody to which is linked the enzyme of the indicator system, followed by addition of substrate to the washed aggregate.
(05 Mar 2000)
Ouchterlony assay <investigation> Immunological test for antigen antibody reactions in which diffusion of soluble antigen and antibody in a gel leads to precipitation of an antigen-antibody complex, visible usually as a whitish band. The system has the advantage that, because of radial diffusion of the reagents, a very wide range of ratios of antigen to antibody concentration develop, thus it is likely that precipitation will occur somewhere in the gel even when no care is taken with quantitation of the system.
(18 Nov 1997)
EAC rosette assay <haematology> Rosettes formed from erythrocytes (E) coated with antibody (A) and complement (C).
A test for C3b or C3bi receptors (CR1 or CR3). The rosettes form more easily then E or EA rosettes.
See: E rosettes.
(16 Mar 2000)
enzyme-linked immunoabsorbent assay <investigation> The enzyme-linked immunoabsorbent assay is serologic test used as a general screening tool for the detection of antibodies to the HIV virus. Reported as positive or negative. Since false positive tests due occur (for example recent flu shot), positives will require further evaluation using the western blot. ELISA technology links an a measurable enzyme to either an antigen or antibody. In this way, it can then measure the presence of an antibody or an antigen in the bloodstream.
Acronym: ELISA
(27 Sep 1997)
enzyme-linked immunosorbent assay An immunoassay utilizing an antibody labelled with an enzyme marker such as horseradish peroxidase. While either the enzyme or the antibody is bound to an immunosorbent substrate, they both retain their biologic activity; the change in enzyme activity as a result of the enzyme-antibody-antigen reaction is proportional to the concentration of the antigen and can be measured spectrophotometrically or with the naked eye. Many variations of the method have been developed.
(12 Dec 1998)
tumour stem cell assay <investigation> A cytologic technique for measuring the functional capacity of tumour stem cells by assaying their activity. It is used primarily for the in vitro testing of antineoplastic agent.
(12 Dec 1998)
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