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"optical density method"¿¡ ´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
  • proton density contrast
    ¾ç¼ºÀڹеµ´ëÁ¶
  • proton density weighted image
    ¾ç¼ºÀڹеµ°­Á¶¿µ»ó
  • spin density
    ½ºÇɹеµ
  • spin density weighted image
    ½ºÇɹеµ°­Á¶¿µ»ó
  • shadow density
    ±×¸²ÀÚÀ½¿µ, Åõ¿µÀ½¿µ
  • very low density lipoprotein
    ÃÊÀú¹ÐµµÁöÁú´Ü¹éÁú
  • ascending method
    ¿Ã¸²¹ý, »ó½Â¹ý
  • aspirative irrigation method
    ÈíÀμ¼Ã´¹ý
  • auscultatory method
    ûÁø¹ý
  • acquisition method
    ȹµæ¹æ¹ý
  • activated sludge method
    Ȱ¼ºÇذ¨¸ð·¡¹ý, Ȱ¼º¿À´Ï¹ý
  • actuarial method
    º¸ÇèÅë°è¹ý
  • agar diffusion method
    ¿ì¹«È®»ê¹ý
  • alkali denaturation method
    ¾ËÄ®¸®º¯¼º¹ý
  • allochromatic method
    º¯»ö¹ý
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
  • shadow density
    À½¿µ¹Ðµµ
  • spin density
    ½ºÇɹеµ
  • high-density lipoprotein
    °í¹ÐµµÁöÁú´Ü¹é
  • intermediate density lipoprotein
    Á߹еµÁöÁú´Ü¹é
  • proton density weighted image
    ¾çÀڹеµ°­Á¶¿µ»ó
  • spin density weighted image
    ½ºÇɹеµ°­Á¶¿µ»ó
  • acquisition method
    ȹµæ¹æ¹ý
  • activated sludge method
    Ȱ¼ºÇذ¨¸ð·¡¹ý, Ȱ¼º¿À´Ï¹ý
  • actuarial method
    º¸ÇèÅë°è¹ý
  • agar diffusion method
    ¿ì¹«È®»ê¹ý
  • agar filtration method
    ¿ì¹«°Å¸£±â¹ý, ¿ì¹«¿©°ú¹ý
  • agar layer method
    ¿ì¹«ÁßÃþ¹ý
  • agar streak method
    ¿ì¹«È­¼±¹ý
  • alkali denaturation method
    ¾ËÄ®¸®º¯¼º¹ý
  • allochromatic method
    º¯»ö¹ý
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
  • Octoson scanning method
    ¿ÁÅä¼Õ ½ºÄµ¹ý (Ûö)
  • Proetz displacement method
    ÇÁ·ÚÃ÷ġȯ¹ý
  • Quellung method
    ÆØÃ¢¹ý(ø³óìÛö).
  • Quellung method
    ÆØÃ¢¹ý(ø³óìÛö).
  • Rothera method
    ·ÎÅ×¶ó¹ý
  • Schoenheimer-Sperry method
    ½¨ÇÏÀ̸Ó-½ºÆä¸® ¹æ¹ý
  • Shihabi-Bishop method
    ½ÃÇϺñ-ºñ¼ó ¹æ¹ý
  • Spinner method
    ½ºÇdzÊ(¹æ)¹ý
  • Tietz-Fiereck method
    ƼÂÅ-ÇÇ·º¹æ¹ý
  • Valsalva method
    ¹ß»ì¹Ù¹ý
  • Wintrobe hematocrit method
    À©Æ®·ÎºêÇ츶ÅäÅ©¸®Æ®¹ý
  • Zebra-stripe imaging method
    ¾ó·è¸» ¹«´Ì ¿µ»ó ¹æ¹ý
  • Zeeman correction method
    Áö¸¸±³Á¤¹ý
  • acid hematin method
    »êÇ츶ƾ¹ý(¡­Ûö).
  • acquisition method
    ȹµæ ¹æ¹ý
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
  • density difference
    À½¿µÂ÷
  • density gradient
    ¹Ðµµ(Áõ°¨)À², ¹Ðµµ±¸¹è.
  • density gradient
    ¹Ðµµ(Áõ°¨)À², ¹Ðµµ±¸¹è(ÚËÓøÏ£ÛÕ).
  • density gradient centrifugation
    ¹Ðµµ±¸¹è¿ø½ÉºÐ¸®.
  • density, epitope
    Ç׿ø°áÁ¤±â¹Ðµµ
  • electron density
    ÀüÀڹеµ
  • electron density
    ÀüÀڹеµ(¡­ÚËöô).
  • energy flux density
    ¿¡³ÊÁö¼Ó¹Ðµµ
  • epitope density
    Ç׿ø°áÁ¤±â¹Ðµµ
  • equilibrium density gradient centrifugation
    ÆòÇü¹Ðµµ±¸¹è¿ø½É¹ý(¡­ÚËöôÎþÛÕêÀãýÛö).
  • familial high density lipoprotein def
    °¡Á·¼º °íºñÁ߸®Æ÷´Ü¹éÁú°áÇÌ Áõ.
  • flux density
    À¯µ¿ ¹Ðµµ
  • flux density
    ¼Ó¹Ðµµ
  • grain density
    ÀÔÀÚ<±×·¡ÀÎ>¹Ðµµ.
  • high electron density
    °íÀüÀڹеµ(ÍÔï³í­ÚËöô).
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  • ¿µ¹®
    ÇѱÛ
  • Bradford method
    ºê·¡µåÆ÷µå ¹ý(Ûö)
  • catalytic exchange method
    Ã˸ű³È¯¹ý(õºØÚÎßüµÛö)
  • catalytic reduction method
    Ã˸Åȯ¿ø¹ý(õºØÚü½êªÛö)
  • chain terminator method
    »ç½½Çü¼º(û¡à÷) Á¾·áÀÚ¹ý(ðûÖõí­Ûö)
  • channels ratio method
    ä³Î ºñÀ²¹ý(Ýï×ËÛö)
  • chronometric method
    ½Ã°£ ÃøÁ¤¹ý(ãÁÊàö´ïÒÛö)
  • Coon's method
    Äï ¹ý(Ûö) (ÔÒ) indirect fluorescent antibody technique
  • crossover method
    ±³Â÷¹ý(Îßó©Ûö)
  • cryoscopic method
    ºùÁ¡ÃøÁ¤¹ý(Þ¼ïÇö´ïÒÛö)
  • Dean and Webb method
    µò°ú¿þºê ¹ý(Ûö)
  • deletion method
    °á¼Õ¹ý(ÌÀáßÛö)
  • differential method
    °¨º°¹ý(ÊüܬÛö)
  • DNAase protection method
    DNAase º¸È£¹ý(ÜÁûÞÛö)
  • double-label method
    ÀÌÁß Ç¥Áö¹ý(ì£ñìøöò½Ûö) (ÔÒ) handle method
  • end-point method
    Á¾¸»Á¡¹ý(ðûØÇïÇÛö)
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 1 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
  • spin density weighted image
    ½ºÇɹеµ°­Á¶¿µ»ó
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 4
OPS operations; optical position sensor; osteoporosis-pseudolipoma syndrome; outpatient service; outpati...
OpScan optical scanning
ORD optical rotatory dispersion; oral radiation death
OSA obstructive sleep apnea; Office of Services to the Aging; Optical Society of America; ovarian sectio...
LTH Low Temperature Holding Method of Pasteurization; Àú¿ÂÀ¯Áö½Ä»ì±Õ¹ý(¿ìÀ¯¼Òµ¶¹ý)
  ; 62 - 63 ¡É, 30 mi...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 4
NSOM Near-field scanning optical microscopy
OCT Optical Coherence Tomography
OD's Optical Densities
od Optical densisty
OIA Optical ImmunoAssay
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • column diffusion method
    ±âµÕ È®»ê ¹æ¹ý
  • combination method
    ¿¬ÇÕ¹ý
    Àη¹À̳ª Ä¡°ü º¸Ã¶ Á¦ÀÛ¿¡¼­ ¸ðÇü»ó¿¡ ³³ÇüÀ» ÀÏÂ÷·Î ¿Ï¼ºÇÏ¿© ±¸°­³»¿¡ ½ÃÀûÇÏ¿© ½Ã°øÇÏ°í ¸Å¸ôÇÏ¿© ÁÖÁ¶ÇÏ¿© ¾ò´Â °£Á¢¹ý°ú Á÷Á¢¹ýÀ» °â¿ëÇÏ´Â ¹æ¹ýÀÌ´Ù.
  • Dehn-Clark`s method
    µ§-Ŭ¶óÅ©¹ý
  • Denis-Leche's method
    µ¥´Ï½º-·¹Ä¡¹ý
    Àü Ȳȭ¹°ÀÇ °ËÃâ¹ýÀ¸·Î, »êÀ» °¡ÇØ ºÎÆÐÇÑ ´Ü¹éÁúÀ» Á¦°ÅÇÏ°í ¿°È­ ¹Ù·ý¿¡ ÀÇÇØ ħÀü °ÇÁ¶½ÃŲ ÈÄ Äª·®ÇÑ´Ù.
  • diffusion method
    È®»ê¹ý
  • direct method
    Á÷Á¢¹ý
    ȯÀÚÀÇ ±¸°­³»¿¡¼­ ¿Î½º Á¶°¢ÇÏ¿© ³³ ¿øÇüÀ» ¾ò¾î ¸Å¸ôÇϰí ÁÖÁ¶ÇÏ¿© Àη¹À̳ª Ä¡°ü º¸Ã¶¹°À» ¾ò´Â ¹æ¹ýÀÌ´Ù.
  • discomfort with this imaging method
    ÃÔ¿µ½Ã ºÒÆí°¨
  • double investing method
    ÀÌÁß ¸Å¸ô¹ý
  • draining method
    ¹è³ó¹ý, È긮´Â ¹æ¹ý
    »óó, ±Ë¾ç, °øµ¿¿¡¼­ ¾×ü³ª ¹è¼³¹°À» ü°èÀûÀ¸·Î ¹èÃâ½ÃŰ´Â °Í.
  • dye dilution method
    »ö¼Ò Èñ¼®¹ý
  • electromyogram biofeedback method
    ±ÙÀüµµ ¹ÙÀÌ¿ÀÇǵå¹é¹ý
    ¹ÙÀÌ¿ÀÆÐµå¹éÀÇ ÁöÇ¥·Î ±ÙÀüµµ¸¦ »ç¿ëÇÏ´Â °ÍÀÌ°í ±Ù·Â Áõ°­ ÈÆ·Ã°ú ±Ù ÀÌ¿Ï ÈÆ·Ã°ú´Â ÀüÇô ¹Ý´ëÀÇ Ä¡·á¹ýÀ¸·Î ÇÔ²² ÀÌ¿ëµÈ´Ù. ±Ù·Â Áõ°­ ÈÆ·ÃÀ¸·Î¼­´Â ¸»ÃÊ½Å°æ ¸¶ºñ, ³úÁ¹Áß, ³ú¼º ¸¶ºñ µî¿¡ »ç¿ëµÇ°í ±ÙÀÌ¿Ï ÈÆ·ÃÀ¸·Î¼­´Â »ç°æ µî¿¡ »ç¿ëµÈ´Ù.
  • expansion method
    ÆØÃ¢ ¹æ¹ý
    ¸Å¸ôÀçÀÇ °æÈ­ ÆØÃ¢, °¡¿­ ÆØÃ¢À» ÀÌ¿ëÇϰųª ¸ðÇü Àç·áÀÇ °æÈ­ ÆØÃ¢À» ÀÌ¿ëÇÏ´Â ¹æ¹ýÀÌ´Ù.
  • fast gradient recalled echo method
    °í¼Ó °æ»ç ȸº¹ ¿¡ÄÚ ±â¹ý
  • flash method
    ¿ìÀ¯ ¼Òµ¶¹ý
    ¿ìÀ¯¸¦ 80¡É±îÁö ±Þ¼ÓÈ÷ °¡¿­ÇÑ ÈÄ¿¡ ±Þ¼ÓÈ÷ 5¡É·Î ³»¸®´Â ¸ê±Õ¹ý.
  • functional jaw orthopedic method
    ±â´ÉÀû ¾Ç±³Á¤¹ý
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
optical keratoplasty Transplantation of transparent corneal tissue to replace a leukoma or scar that impairs vision.
(05 Mar 2000)
optical microscope <instrument, microscopy> A very ambiguous term since all microscopes involve optics, better to specify light, acoustic, X-ray or electron microscope, etc.
(05 Aug 1998)
optical noise <microscopy> Image defects that become especially conspicuous when the image is enhanced. In video microscopy, includes hot spots, mottle, uneven illumination, etc.
(05 Aug 1998)
optical pachymeter A lens and/or mirror used to measure corneal thickness.
(05 Mar 2000)
optical righting reflexes Visual stimuli that enable an animal to maintain the correct position of the head in space, by bringing about movements of the muscles of the neck and limbs.
(05 Mar 2000)
optical rotatory dispersion The method of measuring the dispersion of an optically active molecule to determine the relative magnitude of right- or left-handed components and sometimes structural features of the molecule.
(12 Dec 1998)
optical scrambler <microscopy> An optical device for scrambling the image of a non-uniform light source so that it now fills the condenser aperture uniformly without appreciable loss of total luminous flux through the microscope. The scrambler can be a simple loop of a single optical fibre with its ends appropriately polished
(05 Aug 1998)
optical sectioning <microscopy> The use of high numerical aperture objective and condenser lenses on a microscope to achieve a shallow depth of field. With a very shallow depth of field, objects above and below focus contribute little to the in-focus image, so that a clean optical section is obtained.
See: depth of field.
(05 Aug 1998)
optical staining <microscopy> Producing colour in the microscopical image so as to differentiate one part of the object from another. One way is by use of Rheinberg filters. Another is to use polarized light on an anisotropic specimen. Another important method is by dispersion staining.
(05 Aug 1998)
optical storage devices A computer disk read by a laser beam, containing data prerecorded by a vendor. The buyer cannot enter or modify data in any way but the advantages lie in the speed of accessibility, relative immunity to damage, and relatively low cost of purchase.
(12 Dec 1998)
optical transfer function <microscopy> The relationship between the image produced by an optical instrument and the amplitude and phase of a periodic specimen, measured at various spatial frequencies.
The optical transfer function curve, which shows how well contrast is maintained for finer specimen details, is a complex function, of which the real term gives the ratio of amplitudes, and the imaginary term the phase relationships.
When the brightness of the periodic specimen varies as a sine wave, the modulus or absolute value of the optical transfer function becomes the modulation transfer function, when the brightness varies as a square wave, the modulation transfer function is known as a contrast transfer function.
Acronym: OTF
(26 Mar 1998)
optical tubelength <microscopy> The distance from the second principal focal plane of the objective to the front focal plane of the ocular. This distance is about 180 mm for high-power objectives, less for those of low power.
(05 Aug 1998)
electron optical axis <physics> The path of an electron through an electron optical system along which it suffers no deflection due to lens fields. This axis does not necessarily coincide with the mechanical axis of the system.
(05 Aug 1998)
electron optical system <apparatus> A combination of parts capable of producing and controlling a beam of electrons to produce an image of an object.
(05 Aug 1998)
tubelength optical <microscopy> This distance is measured from the upper focal plane of the objective to the image formed by the objective alone upon removal of the eyepiece. A light microscope so arranged that the specimen, usually a solid-liquid colloid or suspension, is illuminated by a strong pencil of light at right angles to the microscope axis. The visibility is limited by the intensity of the light source. A laser can be used as the source. It is used to detect the presence of light-ultramicroscopic particles within the range of about 0.005,um to 0.2 ~m. Not to be confused with an electron microscope.
(05 Aug 1998)
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