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"bright field 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.
À̰ÍÀ» ¿øÇϼ̽À´Ï±î?
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¿µ¹® visual field test ÇÑ±Û ½Ã¾ß°Ë»ç
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  ´«À» ÇѰ÷¿¡ °íÁ¤½ÃŲ Ã¤, °üÂûÇÒ ¼ö Àִ ÁÖº¯°ø°£À» ½Ã¾ß¶ó ÇÑ´Ù. ½Ã¾ß¸¦ °Ë»çÇϴ °¡Àå °£´ÜÇÑ ¹æ¹ýÀº ´ë¸é°Ë»ç(confronting test)ÀÌ´Ù. À̰ÍÀº Çǰ˻çÀÚÀÇ ´«À» °Ë»çÀÚÀÇ ´«¿¡ ¸ÂÃ߾¸µµ·Ï ÇÏ¿© ´«À» °íÁ¤½ÃŲä, °Ë»çÀÚ°¡ ¼Õ°¡¶ô³¡À» À§ÂÊ, ¾Æ·¡ÂÊ, ¿ÞÂÊ, ¿À¸¥ÂÊ, ±×¸®°í ºñ½ºµëÈ÷ °æ»çÁø °÷ µîÀ¸·Î ¿Å°Üº¸¾Æ Çǰ˻çÀÚ°¡ °üÂûÇÒ ¼ö ÀÖ´ÂÁö ¿©ºÎ¸¦ Á¤Çϴ °Ë»ç¹ýÀÌ´Ù. À̺¸´Ù Á¤È®ÇÑ °Ë»ç¹ýÀº ÀÚµ¿½Ä ÄÄÇ»Åͽþ߰˻ç¹ýÀÌ ÀÖ´Ù. ´ë°³, ´«ÀÚüÀÇ ÀÌ»óÀÌ À־ ½Ã¾ß°Ë»ç¿¡¼­ ÀÌ»óÀÌ ³ª¿ÀÁö¸¸, À̿ܠ³úÀÇ ÀÌ»óÀ¸·Î ½Ã°¢ÀÇ Çü¼º°æ·Î¿¡ ÀÌ»óÀÌ À־ ¿ª½Ã ÀÌ»ó¼Ò°ßÀ» º¸ÀδÙ.
´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • dark field microscopy
    ¾Ï½Ã¾ßÇö¹Ì°æ°Ë»ç(¹ý)
  • bright spot
    ¹àÀºÁ¡
  • 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)
  • polarized light microscopy
    Æí±¤Çö¹Ì°æ°Ë»ç(¹ý)
  • auditory field
    û°¢¹üÀ§, û¿ª
  • altitudinal visual field defect
    ¼öÆò½Ã¾ß°á¼Õ
  • abutted field
    ÀÎÁ¢Á¶»ç¸é, Á¢ÃËÁ¶»ç¸é
  • B1 field gradient
    ȸÀüÀÚÀå±â¿ï±â
  • binocular field
    ¾ç¾È½Ã¾ß, µÎ´«½Ã¾ß
  • boost field
    Á¶»ç¿µ¿ª, Á¶»ç¸é
  • complex receptive field
    º¹ÇÕ¼ö¿ë¾ß
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 10 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • microscopy
    Çö¹Ì°æ°Ë»ç(¹ý)
  • visual field defect
    ½Ã¾ß°á¼Õ
  • field
    1. ºÐ¾ß, ¿µ¿ª, ¹üÀ§, 2. ºÎÀ§, 3. ½Ã¾ß, 4. Àü±âÀå
  • boost field
    Á¶»ç¿µ¿ª, Á¶»ç¸é
  • electropmagnetic field
    ÀüÀÚ±âÀå
  • irradiation field
    Á¶»ç¿µ¿ª
  • radiation field
    ¹æ»ç¼±Á¶»ç¿µ¿ª
  • sound field
    À½¿ª
  • static magnetic field
    Á¤ÀÚ±âÀå
  • visual field
    ½Ã¾ß
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • dark field microscopy
    ¾Ï½Ã¾ßÇö¹Ì°æ°Ë»ç
  • bright spot
    ¹àÀºÁ¡
  • 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)
  • polarized light microscopy
    Æí±¤Çö¹Ì°æ°Ë»ç
  • abutted field
    ÀÎÁ¢Á¶»ç¸é, Á¢ÃËÁ¶»ç¸é
  • altitudinal visual field defect
    ¼öÆò½Ã¾ß°á¼Õ
  • auditory field
    û°¢¹üÀ§, û¿ª
  • geometric field distortion artifact
    ±âÇÏÇÐÀûÀÚÀå¿Ö°îÀΰø¹°
  • B1 field gradient
    ȸÀüÀÚÀå±â¿ï±â
  • binocular field
    ¾ç¾È½Ã¾ß, µÎ´«½Ã¾ß
  • boost field
    Á¶»ç¿µ¿ª, Á¶»ç¸é
  • field block
    ºÎÀ§Â÷´Ü¸¶Ãë
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • 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
  • polarized light microscopy
    Æí±¤Çö¹Ì°æ
  • B1 field gradient
    ȸÀü ÀÚÀå Àڱ⠰æ»ç
  • FFE, fast field echo
    ±Þ¼Ó ÀÚÀå ¿¡ÄÚ
  • FOV(field of view)
    ¿µ»ó ¿µ¿ª, ¿µ»ó ¹üÀ§
  • Goldman constant-field equation
    °ñµå¸¸ Á¤Àü·ù(ïÒï³×µ) ½Ä
  • abutted field
    ÀÎÁ¢Á¶»ç¸é, -¿µ¿ª, Á¢ÃËÁ¶»ç¸é
  • altitudinal visual field defect
    ¼öÆò½Ã¾ß°á¼Õ
  • fringe field
    ÁÖº¯ ¾ß
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • bright field microscopy
    ¸í½Ã¾ß Çö¹Ì°æ¹ý
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • dark field microscopy
    ¾Ï½Ã¾ßÇö¹Ì°æ
  • bright blood imaging
    ¸íÇ÷·ù ¿µ»ó
  • bright liver
    ¹àÀº °£
  • bright spot
    ¹àÀº Á¡
  • field within a field technique
    Áߺ¹Á¶»ç¿µ¿ª¹ý
  • brightfield microscopy
    ¸í½Ã¾ß Çö¹Ì°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.
  • immunologic electron microscopy
    ¸é¿ªÀüÀÚÇö¹Ì°æ¹ý.
  • light microscopy
    ±¤ÇÐ Çö¹Ì°æ
´ëÇÑÇØºÎÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 2 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • Nail field
    ¹ßÅ鱸¿ª
    [¿¾ ¿ë¾î] Á¶¾ß
  • Nail field
    ¼ÕÅ鱸¿ª
    [¿¾ ¿ë¾î] Á¶¾ß
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • fluorescence microscopy
    Çü±¤ Çö¹Ì°æ¹ý(û«ÎÃúéÚ°ÌðÛö)
  • centrifugal field
    ¿ø½É·Â Àå(êÀãýÕôíÞ)
  • crystal field splitting
    °áÁ¤ ÀåºÐÇÒ(Ì¿ïÜíÞÝÂùÜ)
  • crystal field theory
    °áÁ¤ Àå·Ð(Ì¿ïÜíÞÖå)
  • electric field
    ÀüÀå(ï³íÞ) °ãÃþ(öµ)
  • field desorption mass spectrometry
    ÀåÅ»Âø Áú·®ºÐ±¤ÃøÁ¤¹ý (íÞ÷­ó·òõÕáÝÂÎÃö´ïÒÛö)
  • field effect
    ÀåÈ¿°ú(íÞüùÍý)
  • field flow fractionation
    Àå(íÞ)È帧 ºÐȹ¹ý(ÝÂüñÛö)
  • field inversion gel electrophoresis
    ÀåÀüµµ(íÞï´Óî) Á© Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ)
  • field ionization mass spectrometry
    Àå(íÞ) ÀÌ¿ÂÈ­(ûù) Áú·®ºÐ±¤ÃøÁ¤¹ý(òõÕáÝÂÎÃö´ïÒÛö)
  • field ion microscope
    Àå(íÞ) À̿ Çö¹Ì°æ(úéÚ°Ìð)
  • ligand field theory
    ¸®°£µåÀå(íÞ) ÀÌ·Ð(ìµÖå)
  • linear electric field effect
    ¼±Çü Àü±âÀåÈ¿°ú(àÊû¡ï³Ñ¨íÞüùÍý)
  • magnetic field
    ÀÚÀå(í¸íÞ)
  • pulsed-field gel electrophoresis
    ÆÞ½ºÀå(íÞ) Á© Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ)
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • bright blood imaging
    ¸íÇ÷·ù¿µ»ó
  • bright liver
    ¹àÀº°£
  • bright spot
    ¹àÀºÁ¡
  • B1 field gradient
    ȸÀüÀÚÀå°æ»ç
  • constant field gradient spin echo method
    °íÁ¤°æ»çÀ彺ÇÉ¿¡ÄÚ¹ý
  • demagnetizing field
    ¹ÝÀÚÀå
  • electromagnetic field
    ÀüÀÚ(±â)Àå
  • far field
    ¿ø°Å¸®±¸¿ª
  • fast field echo [=FFE]
    ±Þ¼ÓÀÚÀå¿¡ÄÚ
  • FFE [=fast field echo]
    ±Þ¼ÓÀÚÀå¿¡ÄÚ
  • field
    ¾ß, ¿µ¿ª, Çʵå, Ç׸ñ
  • field echo
    ÀÚÀå¿¡ÄÚ
  • field gradient
    ÀÚÀå°æ»ç
  • field inhomogeneity
    ÀÚÀåºÒ±ÕÀÏ(¼º)
  • field of view [=FOV]
    ¿µ»ó¿µ¿ª, ¿µ»ó¹üÀ§
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
FIM field ion microscopy; functional independence measure
BRB bright red blood
BRBPR bright red blood per rectum
UBO unidentified bright object
UBS unidentified bright signal
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
BL bright light
DFM Dark field microscopy
FESEM Field Emission Scanning Electron Microscopy
NSOM Near-field scanning optical microscopy
E-field Electric field
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • bright field photomicrograph
    ?
  • bright signal
    ¹àÀº »ó
  • Bright's blindness
    ºê¶óÀÌÆ® ¸Í
    ¿äµ¶Áõ ȯÀÚ¿¡°Ô ¸Á¸·À̳ª À¯µÎºÎÀÇ º´º¯ÀÌ ¾øÀÌ ÀϾ´Â ½Ã°¢ÀÇ °¨Åð, ¿ÏÀü ¶Ç´Â ºÒ¿ÏÀü ¼Ò½Ç µîÀ» ¶æÇÏ´Â ¿¾ ¸íĪ.
  • 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
  • absolute field
    Àý´ë ºÎ
    ´ë³úÀÇ ÀϺηÎ, ±× º´º¯¿¡ ÀÇÇØ °æ·Ã ¶Ç´Â ¸¶ºñ¸¦ ÀÏÀ¸Å²´Ù.
  • abutted field
    ÀÎÁ¢ Á¶»ç¸é
  • color field
    »ö ½Ã¾ß
  • constant field equation
    Á¤ÀüÀå ¹æÁ¤½Ä
  • cortical field
    ÇÇÁú ¿µ¿ª
  • dark-field microscope
    ¾Ï½Ã¾ß Çö¹Ì°æ
    ¾Ï½Ã¾ß Á¶¸í¹ý¿¡ ÀÇÇØ º¸ÅëÀÇ Çö¹Ì°æÀ¸·Î´Â º¸ÀÌÁö ¾Ê´Â ¹Ì¼¼ÇÑ ÀÔÀÚ¸¦ º¼ ¼ö ÀÖ´Â Çö¹Ì°æ. ÇÑ¿Ü Çö¹Ì°æÀ» ¸»Çϴµ¥, ¾Ï½Ã¾ß Á¶¸í°ú ±× Áý±¤ ·»Á »ç¿ëÇϹǷΠÀÌ¿Í °°ÀÌ ºÒ¸®±âµµ ÇÑ´Ù.
  • depository field
    ÷°¡ ¾ß
  • electromagnetic field
    ÀüÀÚÀå
    1. Àü±âÀå°ú ÀÚ±âÀåÀ» ÅëÆ²¾î ÁöĪÇÏ´Â ¸». 2. Àü±âÀå°ú ÀÚ±âÀåÀÌ ¼­·Î ¿¬°üµÇ¾î °°ÀÌ ³ªÅ¸³¯ ¶§ À̸£´Â ¸».
  • equivalent field
    µî°¡ Á¶»ç ¿µ¿ª
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
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)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
bright field illumination <microscopy> The method of lighting the specimen with a solid cone of rays. Transmitted bright field illumination is performed by a substage condenser. Reflected bright field illumination is performed by a vertical illuminator.
Compare: dark field illumination
(05 Aug 1998)
bright field imaging <microscopy> An imaging mode in a transmission electron microscopy that uses only unscattered Electrons to form the image. Contrast in such an image is due entirely to mass-thickness variations in amorphous samples, and may include diffraction contrast in crystalline samples.
(05 Aug 1998)
dark field microscopy <procedure> A system of microscopy in which particles are illuminated at a very low angle from the side so that the background appears dark and the objects are seen by diffracted and reflected patches of light against a dark background.
(18 Nov 1997)
bright 1. Radiating or reflecting light; shedding or having much light; shining; luminous; not dark. "The sun was bright o'erhead." (Longfellow) "The earth was dark, but the heavens were bright." (Drake) "The public places were as bright as at noonday." (Macaulay)
2. Transmitting light; clear; transparent. "From the brightest wines He 'd turn abhorrent." (Thomson)
3. Having qualities that render conspicuous or attractive, or that affect the mind as light does the eye; resplendent with charms; as, bright beauty. "Bright as an angel new-dropped from the sky." (Parnell)
4. Having a clear, quick intellect; intelligent.
5. Sparkling with wit; lively; vivacious; shedding cheerfulness and joy around; cheerful; cheery. "Be bright and jovial among your guests." (Shak)
6. Illustrious; glorious. "In the brightest annals of a female reign." (Cotton)
7. Manifest to the mind, as light is to the eyes; clear; evident; plain. "That he may with more ease, with brighter evidence, and with surer success, draw the bearner on." (I. Watts)
8. Of brilliant colour; of lively hue or appearance. "Here the bright crocus and blue violet grew." (Pope)
Bright is used in composition in the sense of brilliant, clear, sunny, etc.; as, bright-eyed, bright-haired, bright-hued.
Synonym: Shining, splending, luminous, lustrous, brilliant, resplendent, effulgent, refulgent, radiant, sparkling, glittering, lucid, beamy, clear, transparent, illustrious, witty, clear, vivacious, sunny.
Origin: OE. Briht, AS. Beorht, briht; akin to OS. Berht, OHG. Beraht, Icel. Bjartr, Goth. Bairhts.
Source: Websters Dictionary
(01 Mar 1998)
Bright, Richard <person> English internist and pathologist, 1789-1858.
See: Bright's disease.
(05 Mar 2000)
bright's disease <medicine> An affection of the kidneys, usually inflammatory in character, and distinguished by the occurrence of albumin and renal casts in the urine. Several varieties of Bright's disease are now recognised, differing in the part of the kidney involved, and in the intensity and course of the morbid process.
Origin: From Dr. Bright of London, who first described it.
Source: Websters Dictionary
(01 Mar 1998)
bright t1 lesion <radiology> (short T1), fat (lipoma, dermoid), sub-acute haemorrhage (metHb), paramagnetic agent (Gd, ? posterior pituitary), proteinaceous fluid (colloid cyst) most abnormalities cause long T1 and T2 (dark/bright) see also: dark T2 lesion
(12 Dec 1998)
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)
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)
ÇÑ¿µ/¿µÇÑ »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • microscopy
    Çö¹Ì°æ °Ë»ç(»ç¿ë¹ý)
  • bright
    ¹àÀº,ÄèûÇÑ,ÄèȰÇÑ,¿µ¸®ÇÑ
  • bright
    ȯÇÑ;¸Ó¸®°¡ÁÁÀº;¹à°Ôºû³ª´Â;ȭâÇÑ;ÄèȰÇÑ;À¯¸ÁÇÑ
  • bright'sdisease
    ºê¶óÀÌÆ®¾¾º´
  • field
    ÀüÅõ,ÅõÁö,½Î¿ì´Ù,´ÙÅõ´Ù
  • Field Marshal
    À°±º ¿ø¼ö
  • Field prize
    Çʵå»ó
  • brick field
    º®µ¹°øÀå
  • center field
    ¼¾ÅÍ(ÀÇ ¼öºñÀ§Ä¡)
  • dark field
    (Çö¹Ì°æÀÇ) ¾Ï½Ã¾ß
  • dark field illumination
    ¾Ï½Ã¾ß Á¶¸í¹ý(Çö¹Ì°æ ½Ã·áÀÇ)
  • dark field microscope
    (±¤)ÇÑ¿Ü Çö¹Ì°æ;¾Ï½Ã¾ß Çö¹Ì°æ
  • electric field
    Àü°è
  • field
    µé;¹úÆÇ;¹ç;±¤Àå;Ç¥¸é;»êÁö;½Î¿òÅÍ;°æ±âÀå;³»(¿Ü)¾ß;ºÐ¾ß;¹ÙÅÁ;¿µ»ó¸é(coal field źÀü)
  • field allowance
    ÃâÁ¤ ¼ö´ç
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
KMLE ¾àǰ/ÀǾàǰ ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
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