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"polarized light microscopy"¿¡ ´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® light reflex ÇÑ±Û ºû¹Ý»ç
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  1. ÇÑÂÊ ´«¿¡ ºûÀ» ºñÃ߸é, ÀÌ ºûÀº ½Ã°¢½Å°æ¿¡ ÀÇÇØ ³ú¿¡ Àü´ÞµÇ°í, ÀÌ ÀÚ±ØÀº »ç¶÷ÀÇ ÀÇÁö¿Í ¹«°üÇϰԠ°ð, ´«µ¹¸²½Å°æÀ¸·Î Àü´ÞµÇ¾î ¾çÂÊ ´«ÀÇ µ¿°øÀÌ Ãà¼ÒÇϰԠµÈ´Ù. ÀÌ·± ¸ðµç ÀÏ·ÃÀÇ °úÁ¤À» ºû¹Ý»ç¶ó ºÎ¸£´Âµ¥ À̰ÍÀº »ç¶÷ÀÌ ¾îµÎ¿î °÷¿¡ °¡°Å³ª ¾îµÎ¿î °÷¿¡¼­ °©Àڱ⠹àÀº °÷¿¡ ³ª°¬À» ¶§, µ¿°øÀÌ ¹Ý»çÀûÀ¸·Î ¿òÁ÷À̴ °Í°ú °°Àº °ÍÀÌ´Ù. 2. °í¸·¿¡¼­ ¹Ý»çÇϴ ±¤»ó. 3. ¸Á¸·°æÀÇ °Å¿ï·Î ¸Á¸·¿¡¼­ ¹Ý»çÇϴ °í¸®¸ð¾çÀÇ ¸¹Àº Á¡.
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  • ¿µ¹®
    ÇѱÛ
  • polarized light microscopy
    Æí±¤Çö¹Ì°æ°Ë»ç(¹ý)
´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • dark field microscopy
    ¾Ï½Ã¾ßÇö¹Ì°æ°Ë»ç(¹ý)
  • electron microscopy
    ÀüÀÚÇö¹Ì°æ°Ë»ç(¹ý)
  • fluorescence microscopy
    Çü±¤Çö¹Ì°æ°Ë»ç(¹ý)
  • fluorescent microscopy
    Çü±¤Çö¹Ì°æ¹ý
  • immunofluorescence microscopy
    ¸é¿ªÇü±¤Çö¹Ì°æ°Ë»ç(¹ý)
  • microscopy
    Çö¹Ì°æ°Ë»ç(¹ý)
  • axial light
    Ã౤
  • black light
    Èæ»ö±¤¼±
  • coherent light
    Áý¼ÓÆòÇ౤
  • cone of light
    ±¤Ã߸é
  • consensual light reflex
    °ø°¨ºû¹Ý»ç
  • convergent light
    ¸ðÀÓ±¤¼±, ¼ö·Å±¤¼±
  • divergent light
    ÆÛÁü±¤¼±
  • emergency light reflex
    ÀÀ±Þºû¹Ý»ç
  • fixation light
    Áֽõî
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 4 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • microscopy
    Çö¹Ì°æ°Ë»ç(¹ý)
  • light chain
    °¡º­¿î»ç½½, °æ¼â
  • light
    ºû, ±¤, ±¤¼±
  • reflected light
    ¹Ý»ç±¤
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • polarized light microscopy
    Æí±¤Çö¹Ì°æ°Ë»ç
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • dark field microscopy
    ¾Ï½Ã¾ßÇö¹Ì°æ°Ë»ç
  • electron microscopy
    ÀüÀÚÇö¹Ì°æ°Ë»ç
  • fluorescence microscopy
    Çü±¤Çö¹Ì°æ°Ë»ç
  • immunofluorescence microscopy
    ¸é¿ªÇü±¤Çö¹Ì°æ°Ë»ç¹ý
  • microscopy
    Çö¹Ì°æ°Ë»ç(¹ý)
  • axial light
    Ã౤
  • light adaptation
    ¸í¼øÀÀ
  • light alloy
    °æÇÕ±Ý
  • black light
    Èæ»ö±¤¼±
  • coherent light
    Áý¼ÓÆòÇ౤
  • consensual light reflex
    ¸Âµ¿°øºû¹Ý»ç, °ø°¨´ë±¤¹Ý»ç
  • convergent light
    ¸ðÀÓ±¤¼±, ¼ö·Å±¤¼±
  • light cell
    ¹àÀº¼¼Æ÷
  • light chain
    °¡º­¿î»ç½½, °æ¼â
  • light coagulation
    (¢¡photocoagulation) ±¤ÀÀ°í
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • polarized light microscopy
    Æí±¤Çö¹Ì°æ
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • polarized
    ±Ø¼ºÀ» ³ªÅ¸³½
  • polarized lens
    Æí±¤·»Áî
  • Darkfield microscopy
    ¾Ï½Ã¾ßÇö¹Ì°æ
  • immune electron microscopy
    ¸é¿ªÀüÀÚÇö¹Ì°æ¹ý.
  • immune-electron microscopy
    ¸é¿ªÀüÀÚÇö¹Ì°æ¹ý
  • immunofluorescence microscopy
    ¸é¿ªÇü±¤Çö¹Ì°æ(°Ë»ç)¹ý.
  • immunologic electron microscopy
    ¸é¿ªÀüÀÚÇö¹Ì°æ¹ý.
  • phase contrast microscopy
    À§»óÂ÷(êÈßÓó¬)Çö¹Ì°æ°Ë»ç
  • phase-contrast microscopy
    À§»óÂ÷Çö¹Ì°æ
  • LASER (light amplification by stimulated emission of
    radiation) ·¹ÀÌÀú
  • LP=>light perception
    ºû´À³¦, ±¤°¢
  • Light adaptation
    ¸í¼øÀÀ(Ù¥â÷ëë)
  • Light reflex
    ´ë±¤¹Ý»ç(ÓÛÎÃÚãÞÒ)
  • Woods light
    ¿ìµåÁ¶¸í.
  • Woods light
    ¿ìµåÁ¶¸í
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • polarized light microscopy
    Æí±¤Çö¹Ì°æ
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • light microscopy
    ±¤ÇÐ Çö¹Ì°æ
  • light microscopy
    ±¤ÇÐÇö¹Ì°æ°Ë»ç(¹ý)(¡­ËþÞÛÛö).
  • linearly polarized transmit/receive coil
    ¼±Çü ±ØÈ­ ¼Û/¼ö½Å ÄÚÀÏ
  • polarized
    ±Ø¼ºÀ» ³ªÅ¸³½
  • polarized lens
    Æí±¤·»Áî
  • bright field microscopy
    ¸í½Ã¾ß Çö¹Ì°æ¹ý
  • brightfield microscopy
    ¸í½Ã¾ß Çö¹Ì°æ
  • dark field microscopy
    ¾Ï½Ã¾ßÇö¹Ì°æ
  • electron microscopy
    ÀüÀÚÇö¹Ì°æ°Ë»ç(¹ý)
  • electron microscopy
    ÀüÀÚÇö¹Ì°æ°Ë»ç(¹ý)(¡­ËþÞÛÛö).
  • electron microscopy(EM)
    ÀüÀÚÇö¹Ì°æ
  • fluorescence microscopy
    Çü±¤Çö¹Ì°æ
  • immune electron microscopy
    ¸é¿ªÀüÀÚÇö¹Ì°æ¹ý.
  • immune-electron microscopy
    ¸é¿ªÀüÀÚÇö¹Ì°æ¹ý
  • immunofluorescence microscopy
    ¸é¿ªÇü±¤Çö¹Ì°æ(°Ë»ç)¹ý.
´ëÇÑÇØºÎÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 2 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • Light cell
    ¹àÀº¼¼Æ÷
    [¿¾ ¿ë¾î] ¸í¼¼Æ÷
  • Light cell
    ¹àÀº¼¼Æ÷
    [¿¾ ¿ë¾î] ¸íÁÖ¼¼Æ÷
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • circularly polarized light
    ¿øÆí±¤(ê­ø¶ÎÃ)
  • plane polarized light
    Æò¸é Æí±¤(øÁØüø¶ÎÃ)
  • polarized light
    Æí±¤(ø¶ÎÃ)
  • fluorescence microscopy
    Çü±¤ Çö¹Ì°æ¹ý(û«ÎÃúéÚ°ÌðÛö)
  • polarized electrode
    ºÐ±Ø(ÝÂп)µÈ Àü±Ø(ï³Ð¿)
  • light chain
    °æ(Ìî)»ç½½
  • light chopper
    ±¤(ÎÃ)ÃÊÆÛ
  • light compensation point
    ±¤ º¸»óÁ¡(ÎÃÜÍßÁïÃ)
  • light-harvesting Chl a/b protein
    Áý±¤¼º¿±·Ïü(ó¢ÎÃàõç¨Öàô÷) a/b ´Ü¹éÁú(Ó±ÛÜòõ)
  • light-harvesting molecule
    Áý±¤ºÐÀÚ(ó¢ÎÃÝÂí­)
  • light isotope
    °æµ¿À§¿ø¼Ò(ÌîÔÒêÈêªáÈ)
  • light label
    °æÇ¥Áö(Ìîøúò½)
  • light meromyosin
    °æ(Ìî) ¸Þ·Î¸¶ÀÌ¿À½Å
  • light microscope
    ±¤ÇÐÇö¹Ì°æ(ÎÃùÊúéÚ°Ìð)
  • light path
    ±¤·Î(ÎÃÖØ)
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 6 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • linearly polarized transmit/receive coil
    ¼±Çü±ØÈ­ ¼Û/¼ö½ÅÄÚÀÏ
  • infrared light
    Àû¿Ü¼±µî
  • laser [=light amplification by stimulated emission of radiation]
    ·¹ÀÌÀú
  • light adaptation
    ¸í¼øÀÀ
  • light amplification by stimulated emission of radiation [=LASER]
    ·¹ÀÌÀú
  • visible light
    °¡½Ã±¤¼±
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
PLM percent labeled mitoses; periodic leg movement; plasma level monitoring; polarized light microscopy
PL palmaris longus; pancreatic lipase; perception of light; peroneus longus; phospholipase; phospholipi...
LM lactic acid mineral [medium]; lactose malabsorption; laryngeal mask; laryngeal muscle; lateral malle...
LS lateral suspensor; left sacrum; left septum; left side; legally separated; leiomyosarcoma; length of...
LEM lateral eye movement; Leibovitz-Emory medium; leukocyte endogenous mediator; light emission microsco...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
PLM Polarized Light Microscopy
CMTF Confocal Microscopy Through Focusing
cryo-EM Cryo-electron microscopy
Cryo-TEM Cryo-transmission electron microscopy
DFM Dark field microscopy
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • polarized lens
    Æí±¤ ·»Áî
  • immune electron microscopy
    ¸é¿ª ÀüÀÚÇö¹Ì°æ¹ý
  • microscopy
    Çö¹Ì°æ °Ë»ç¹ý
    Çö¹Ì°æÀ» ÀÌ¿ëÇÑ °Ë»ç ¶Ç´Â °üÂû.
  • scanning electron microscopy
    ÁÖ»ç ÀüÀÚÇö¹Ì°æ
    ÀüÀÚ¼±ÀÌ Ç¥º»»óÀÇ Á¡¸¶´Ù ÁÖ»çÇÏ¿© À½±Ø¼±°ü
  • accidental light
    »ç±¤¼±
  • axial light
    Ã༺ ±¤¼±
    ±¤¼± »óÈ£°£ ¶Ç´Â ½ÃÃà¿¡ ÆòÇàÇÑ ±¤¼±.
  • black light
    Èæ»ö ±¤¼±
  • central light
    Á᫐ ±¤
  • coherent light
    °£¼· ±¤¼±
    °¨ÁöµÉ ¼ö ÀÖ´Â ºÐ»ê±¤ÀÌ ¾ø´Â °­·ÂÇÏ°í °ÅÀÇ ¿ÏÀüÇÑ ÆòÇà ±¤¼±.
  • cold light
    ³Ã±¤
    ¿­À» ¼Ò»ê½Ã۱â À§ÇØ ¼®¿µ ¶Ç´Â ÇÃ¶ó½ºÆ½ ±¸Á¶¸¦ Åë°ú½ÃŲ ±¤¼±.
  • collimated light
    ½ÃÁر¤
  • diffused light
    È®»ê±¤
    ¹Ý»ç¿Í ±¼Àý¿¡ ÀÇÇØ »ê¶õµÈ ±¤¼±.
  • Finsen light
    Çɼ¾ ±¤¼±
    Çɼ¾ µî¿¡¼­ ¹ß»êµÇ´Â ÁÖ·Î ÀÚ±¤¼± ¹× Àڿܼ±À¸·Î ÀÌ·ç¾îÁø ±¤¼±À¸·Î ·çǪ½º Ä¡·á¿¡ ÀÌ¿ëµÈ´Ù.
  • idioretinal light
    ¸Á¸· °íÀ¯±¤
    ÀϹÝÀûÀ¸·Î °¨°¢À» ÀÚ±ØÇÏ´Â ÀüÀ򮀡¡ ¿ÏÀüÈ÷ °á¿©µÈ »óÅ¿¡¼­ ÀϾ´Â ±¤ÀÇ °¨°¢.
  • infrared light
    Àû¿Ü¼±
    º¹»ç¼± Áß ÆÄÀåÀÌ °¡½Ã ±¤¼±º¸´Ù ±æ¸ç ±ØÃÊ´ÜÆÄº¸´Ù ªÀº, 750m? - 1mmÀÇ ÀüÀÚÆÄ. ¿­¼±.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
plane-polarized light <chemistry> Light which is passed through a filter which blocks out all the light except that which ocillates in one plane.
(09 Jan 1998)
polarized light <microscopy> Light that is vibrating in one plane (plane-polarized light), light with a rotary vibration (circular polarized light), or light that is vibrating elliptically (elliptically polarized light). Moonlight and skylight are polarized, as is much reflected light, cloud light is polarized under certain conditions. However, naturally polarized light is, on the whole, rather imperfectly polarized.
(05 Aug 1998)
polarized light microscope <instrument, microscopy> A microscopical polarizcope, i.e., a compound microscope which is equipped with two polars and a Bertrand lens, chemists and mineralogists are the principal users.
(05 Aug 1998)
light microscopy <procedure> In contrast to electron microscopy.
See: bright field, phase contrast, interference, interference contrast, interference reflection, dark field, confocal and fluorescence microscopy.
(18 Nov 1997)
spin-polarized fusion <radiobiology> A method to enhance nuclear fusion reaction rates in some fusion fuels by polarizing the nuclear spins.
(09 Oct 1997)
aperture for electron microscopy <technique> Anode aperture: The opening in the accelerating voltage anode shield of the electron gun through which the electrons must pass to irradiate the specimen. Condenser aperture: An opening in the condenser lens controlling the number of electrons entering the lens and the angular aperture of the electron beam.
The angular aperture can also be controlled by the condenser lens current. Physical objective aperture: A metallic diaphragm, with a small central hole, used to limit the cone of electrons accepted by the objective lens. This improves image-contrast since highly scattered electrons are prevented from arriving at the Gaussian image plane and therefore cannot contribute to background fog. Aplanatic. Free from spherical aberration and coma.
(05 Aug 1998)
bright field microscopy <technique> Optical microscopy, in which absorption to a great extent and diffraction to a minor extent give rise to the image, as opposed to phase contrast or interference methods of microscopy.
(18 Nov 1997)
ratio imaging fluorescence microscopy <procedure> A method of measurement of intracellular pH or intracellular calcium levels, using a fluorescent probe molecule (see fura-2), in which the two different excitation wavelengths are used and the emitted light levels compared.
If emission at one wavelength is sensitive to the intracellular ion level and emission at the other wavelength is not, then standardisation for intracellular probe concentration, efficiency of light collection, inactivation of probe and thickness of cytoplasm can all be performed automatically.
(17 Dec 1997)
reflection X-ray microscopy <technique> A method of producing enlarged images by means of X rays. In this method the radiation is totally reflected at glancing incidence from polished concave mirrors or from the curved surfaces of single crystals by Bragg reflection. The problem of aberration corrections still limits the resolution obtainable.
(05 Aug 1998)
video microscopy <technique> Microscopy that takes advantage of video as an imaging, image processing, analysing, or controlling device.
(05 Aug 1998)
phase contrast microscopy <investigation> A simple nonquantitative form of interference micoscopy of great utility in visualising live cells. Small differences in optical path length due to differences in refractive index and thickness of structures are visualised as differences in light intensity.
(18 Nov 1997)
microscopy <technique> The science of the interpretive use, and applications of microscopes.
(05 Aug 1998)
microscopy, atomic force Microscopy in which a probe systematically rides across the surface of a sample being scanned in a raster pattern. The vertical position is recorded as a spring attached to the probe rises and falls in response to peaks and valleys on the surface. A microcomputer keeps track of the vertical excursions as a function of the position of the probe in the horizontal plane and presents the sample's image.
(12 Dec 1998)
microscopy, confocal A light microscopic technique in which only a small spot is illuminated and observed at a time. An image is constructed through point-by-point scanning of the field in this manner. Light sources may be conventional or laser, and fluorescence or transmitted observations are possible.
(12 Dec 1998)
microscopy, electron Visual and photographic microscopy in which electron beams with wavelengths thousands of times shorter than visible light are used in place of light, thereby allowing much greater magnification.
(12 Dec 1998)
ÇÑ¿µ/¿µÇÑ »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • microscopy
    Çö¹Ì°æ °Ë»ç(»ç¿ë¹ý)
  • in the light of
    -¿¡ ºñÃß¾î º¼ ¶§
  • light
    ºû,¹àÀº,°¡º­¿î,Á¡È­ÇÏ´Ù,°¡º±°Ô
  • light-handed
    ¼Ø¾¾°¡ ÁÁÀº
  • light-headed
    ¸ù·ÕÇÑ
  • light-heartedness
    ³«ÃµÀûÀÓ
  • light-minded
    °æ¼ÖÇÑ
  • make light of
    °æ½ÃÇÏ´Ù
  • shed light on
    ÀÇ ¼³¸í¿¡ µµ¿òÀ» ÁÖ´Ù
  • throw light on
    ¿¡ ÇØ°áÀÇ ±¤¸íÀ» ÁÖ´Ù
  • Finsen light
    Çɼ¾±¤(·¥ÇÁ)
  • Inner Light
    ³»ÀûÀÎ ºû(ÄùÀÌÄ¿ ±³µµ°¡ ¸¶À½ ¼Ó¿¡ ´À³¢´Â ±×¸®½ºµµÀÇ ºû ?,
  • calcium light
    Ä®½·±¤(limelight)
  • ceiling light
    »ï°¢Ãø·®À¸·Î ¿îÀú °íµµ¸¦ Àç´Â ŽÁ¶µî
  • clear light
    =LSD(ȯ°¢Á¦)
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
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  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
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  • ¿µ¹®
    ÇѱÛ
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  • ¿µ¹®
    ÇѱÛ
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  • ¿µ¹®
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    ÇÑÀÚ
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  • ¿µ¹®
    ÇѱÛ
    ÇÑÀÚ
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    ÇѱÛ
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