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"electron staining"¿¡ ´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® electron microscope ÇÑ±Û ÀüÀÚÇö¹Ì°æ
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  Àü±â ¸¶´ç ¶Ç´Â Àڱ⠸¶´çÀ» ÀÌ¿ëÇÏ¿© ÀüÀÚ·ù¸¦ ÀüÀÚ ·»Áî¿¡ Áý¼Ó½ÃÄÑ, ±× Åë·Î¿¡ ³õÀΠǥº»ÀÇ »óÀ» È®´ëÇϴ ÀåÄ¡. ±¤ÇРÇö¹Ì°æº¸´Ù ÈξÀ ¶Ù¾î³­ ºÐÇØ ´É·ÂÀ» °¡Áø´Ù. 
¿µ¹® acid-fast staining ÇÑ±Û Ç׻꿰»ö
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  Ç׻꼺¼ºÁú(Á»Ã³·³ ¿°»öÀÌ µÇÁö ¾ÊÀ¸³ª Çѹø ¿°»öÀÌ µÇ¸é »ê¼º¿ë¾×¿¡ ÀÇÇØ¼­ Å»»öÀÌ µÇÁö ¾Ê´Â ¼ºÁú)À» °¡Áø ±Õ(¿¹¸¦ µé¸é °áÇÙ±Õ µî)ÀÇ °ËÃâ¿¡ ÀÌ¿ëµÇ´Â ¿°»ö¹æ¹ý. ¹æ¹ý¿¡´Â Ziehl-Neelson¹ý°ú Kinyoun¹ý µîÀÌ ÀÖ´Ù.
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  • ¿µ¹®
    ÇѱÛ
  • bipolar staining
    ½Ö±Ø¿°»ö(¹ý)
  • contrast staining
    ´ëÁ¶¿°»ö(¹ý)
  • differential staining
    °¨º°¿°»ö(¹ý)
  • direct fluorescent antibody staining
    Á÷Á¢Çü±¤Ç×ü¿°»ö(¹ý)
  • double staining
    ÀÌÁß¿°»ö(¹ý)
  • fluorescent staining
    Çü±¤¿°»ö(¹ý)
  • immunohistochemical staining
    ¸é¿ªÁ¶Á÷È­Çп°»ö(¹ý)
  • negative staining
    À½¼º¿°»ö(¹ý)
  • negative staining method
    À½¼º¿°»ö¹ý
  • staining
    1. ¿°»ö(¹ý) 2. Âø»ö
  • vital staining
    »ýü¿°»ö(¹ý)
  • electron
    ÀüÀÚ
  • electron affinity
    ÀüÀÚģȭ·Â
  • electron beam
    ÀüÀÚ¼±, ÀüÀÚºö
  • electron capture
    ÀüÀÚÆ÷ȹ
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • staining
    ¿°»ö(¹ý)
  • Gram staining
    ±×¶÷¿°»ö(¹ý)
  • electron
    ÀüÀÚ
  • electron microscope
    ÀüÀÚÇö¹Ì°æ
  • transmission electron microscope
    Åõ°úÀüÀÚÇö¹Ì°æ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • electron staining
    ÀüÀÚ¿°»ö
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • bipolar staining
    ¾ç±Ø¿°»ö, ½Ö±Ø¿°»ö
  • contrast staining
    ´ëÁ¶¿°»ö
  • differential staining
    °¨º°¿°»ö
  • direct fluorescent antibody staining
    Á÷Á¢Çü±¤Ç×ü¿°»ö
  • double staining
    ÀÌÁß¿°»ö
  • fluorescent staining
    Çü±¤¿°»ö
  • histochemical staining
    Á¶Á÷È­Çп°»ö
  • immunohistochemical staining
    ¸é¿ªÁ¶Á÷È­Çп°»ö
  • intravital staining
    (¢¡vital staining) »ýü¿°»ö
  • metachromatic staining
    ÀÌ»ö¿°»ö, µÐ°©¿°»ö
  • negative staining method
    À½¼º¿°»ö¹ý
  • negative staining
    ´ëÁ¶¿°»ö, À½¼º¿°»ö
  • staining
    ¿°»ö(¹ý)
  • supravital staining
    ÃÊ»ýü¿°»ö
  • vital staining
    »ýü¿°»ö
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  • ¿µ¹®
    ÇѱÛ
  • Gram-staining
    ±×¶÷¿°»ö
  • Heidenhain s hematoxylin staining solution
    ÇÏÀ̵§ÇÏÀÎ Ç츶Åå½Ç¸° ¿°»ö¾×.
  • hematoxylin eosin staining
    Ç츶Åå½Ç¸°-¿¡¿À½Å¿°»ö(¡­æøßä).
  • histochemical staining
    Á¶Á÷ È­ÇÐ(Àû) ¿°»ö(¹ý)
  • immunohistochemical staining
    ¸é¿ªÁ¶Á÷È­Çп°»ö
  • free electron
    ÀÚÀ¯ÀüÀÚ(í»ë¦ï³í­).
  • free electron
    ÀÚÀ¯ÀüÀÚ
  • high electron density
    °íÀüÀڹеµ(ÍÔï³í­ÚËöô).
  • immune electron microscopy
    ¸é¿ªÀüÀÚÇö¹Ì°æ¹ý.
  • immune-electron microscopy
    ¸é¿ªÀüÀÚÇö¹Ì°æ¹ý
  • immunologic electron microscopy
    ¸é¿ªÀüÀÚÇö¹Ì°æ¹ý.
  • positive electron
    ¾çÀüÀÚ
  • recoil electron
    ¹ÝµµÀüÀÚ
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  • ¿µ¹®
    ÇѱÛ
  • electron staining
    ÀüÀÚ¿°»ö(¹ý)(¡­æøßäÛö).
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  • ¿µ¹®
    ÇѱÛ
  • odd electron ; unpaired electron
    ºÒ´ëÀüÀÚ, ºñ´ëÀüÀÚ.
  • odd electron ; unpaired electron
    ȦÀüÀÚ.
  • bipolar staining
    ¾ç±Ø¿°»ö, ½Ö±Ø¿°»ö(äªÐ¿æøßä).
  • blood staining of the cornea
    °¢¸·Ç÷¾×Âø»ö
  • capsular staining
    Çù¸·¿°»ö
  • contrast staining
    ´ëÁ¶¿°»ö
  • differential staining
    ºÐº°<°¨º°>¿°»ö¹ý.
  • direct fluorescent antibody staining
    Á÷Á¢Çü±¤Ç×ü¿°»ö
  • discoloration and staining of teeth
    Ä¡¾ÆÀÇ Âø»ö(öÍ䳡­ó·ßä).
  • double staining
    ÀÌÁß¿°»ö¹ý(ì£ñìæøßäÛö).
  • fluorescein staining
    Ç÷緹½Å¿°»ö, Çü±¤¿°»ö
  • hematoxylin eosin staining
    Ç츶Åå½Ç¸°-¿¡¿À½Å¿°»ö(¡­æøßä).
  • histochemical staining
    Á¶Á÷ È­ÇÐ(Àû) ¿°»ö(¹ý)
  • immunohistochemical staining
    ¸é¿ªÁ¶Á÷È­Çп°»ö
  • intravital staining
    »ýü(³»)¿°»ö(¹ý)(ßæô÷Ò®æøßäÛö).
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • positive staining
    ¾ç¼º¿°»ö(åÕàõæøßä)
  • supravital staining
    ÃÊ»ýü ¿°»ö(õ±ßæô÷æøßä)
  • conversion electron
    ÀüȯÀüÀÚ(ï®üµï³í­)
  • cyclic electron flow
    ¼øÈ¯(âàü») ÀüÀÚ(ï³í­) È帧
  • electron
    ÀüÀÚ(ï³í­)
  • electron acceptor
    ÀüÀÚ ¼ö³³Ã¼(ï³í­ áôÒ¡ô÷)
  • electron affinity
    "ÀüÀÚ Ä£È­¼º(ï³í­öÑûúàõ)(µµ,Óø)"
  • electron capture
    ÀüÀÚ Æ÷ȹ(ï³í­øÚüò)
  • electron carrier
    ÀüÀÚ¿î¹ÝÀÚ(ï³í­ê¡Úæí­)
  • electron diffraction
    ÀüÀÚȸÀý(ï³í­üÞï¹)
  • electron donor
    ÀüÀÚ°ø¿©Ã¼(ï³í­Íêæ¨ô÷)
  • electron-exchange resin
    ÀüÀÚ±³È¯ ¼öÁö(ï³í­Îßüµâ§ò·)
  • electron ionization mass spectrometry
    ÀüÀÚ(ï³í­)ÀÌ¿ÂÈ­(ûù) Áú·® ºÐ¼®¹ý(òõÕáÝÂà°Ûö)
  • electron magnetic resonance
    ÀüÀÚ ÀÚ±â°ø¸í(ï³í­í¸Ñ¨ÍìÙ°)
  • electron microscope
    ÀüÀÚÇö¹Ì°æ(ï³í­úéÚ°Ìð)
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • hematoxilylin-eosin staining
    Ç츶Åå½Ã¸°-¿¡¿ÀÁø¿°»ö
  • staining
    ¿°»ö(¹ý)
  • electron
    ÀüÀÚ
  • electron beam
    ÀüÀÚ¼±
  • electron capture
    ÀüÀÚÆ÷Âø
  • electron density
    ÀüÀڹеµ
  • electron emission
    ÀüÀÚ¹æÃâ
  • electron microscope
    ÀüÀÚÇö¹Ì°æ
  • electron pair
    ÀüÀÚ½Ö
  • electron ray
    ÀüÀÚ¼±
  • electron volt
    ÀüÀÚº¼Æ®
  • electron wave
    ÀüÀÚÆÄ
  • free electron
    ÀÚÀ¯ ÀüÀÚ
  • proton electron dipole dipole interaction
    ¾çÀÚÀüÀÚ½Ö±ØÀÚ½Ö±ØÀÚ»óÈ£¹ÝÀÀ
  • recoil electron
    ¹ÝµµÀüÀÚ
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
EM early memory; ejection murmur; electromagnetic; electron micrograph; electron microscopy, electron m...
A [band] the dark-staining zone of a striated muscle
AgNOR silver-staining nucleolar organizer region
FAST flow-assisted, short-term [balloon catheter]; fluorescent antibody staining technique; fluoro-allerg...
HSR Harleco synthetic resin; heated serum reagin; homogeneously staining region
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
DiSC Differential Staining Cytotoxicity
hsr Homogeneous staining region
HSR Homogeneously staining region
IGSS Immuno-Gold-Silver staining
IGS Immunogold staining
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • acid fast staining
    Ç×»ê ¿°»ö
  • double staining
    ÀÌÁß ¿°»ö¹ý
  • hematoxylin-eosin staining
    Ç츶Åå½Ç¸° ¿¡¿À½Å ¿°»ö
    µÎ °¡Áö ¿°·á·Î Áߺ¹ ¿°»öÇÏ´Â °Í. Á¶Á÷ ¿°»ö Áß °¡Àå ÈçÇÏ´Ù.
  • pale(o) °í ¶Ç´Â ±¸¸¦ ¶æÇÏ´Â Á¢µÎ¾î.

    pale-staining zone

    ¿¯Àº ¿°»öÃþ
  • pappenheim's staining
    ÆÄÆæÇÏÀÓ ¿°»ö¹ý
  • silver impregnation staining
    µµÀº ¿°»ö, µµÀº ¿°»ö¹ý
  • electron
    ÀüÀÚ
    À½ Àü±âÀÇ ÃÖ¼Ò ´ÜÀ§ ¶Ç´Â ÀÚ±â ÀÔÀÚ. Àý´ë Á¤Àü±â ´ÜÀ§. 4.77*10-10 ¶Ç´Â Àý´ë ÀüÀڱ⠴ÜÀ§ 1.59*10-20 ¿¡ »ó´çÇϸç, ±×ÀÇ Áú·®Àº Àû´çÇÑ ¼Óµµ·Î À̵¿Çϰí ÀÖÀ» ¶§¿¡ ¼ö¼Ò ¿øÀÚÀÇ 1/1845, Áï 9*10-28 ±×·¥ÀÌ´Ù. µµÃ¼ Áß¿¡ È帣´Â ÀüÀÚ´Â Àü·ù·Î¼­, ¹æ»ç¼± ¹°Áú·ÎºÎÅÍ´Â ¥â¼±À¸·Î ¹æÃâµÇ¾î ¿øÀÚÇÙ ÁÖÀ§ÀÇ ±Ëµµ¸¦ ȸÀüÇÏ¿© ±× ¿øÀÚÀÇ Áú·®°ú ¹æ»ç´É ÀÌ¿ÜÀÇ ÀÌÈ­ÇÐÀû ¼º»óÀ» Á¿ìÇÑ´Ù.
  • electron affinity
    ÀüÀÚ Ä£È­·Â
    ¿øÀÚ°¡ ÀüÀÚ 1°³¿Í °áÇÕÇÒ ¶§¿¡ ¹æÃâÇÏ´Â ¿¡³ÊÁö.
  • electron bath
    ÀüÇØÁ¶
  • electron beam microporbe analysis
    ÀüÀÚ±¤ ¹Ì¼¼ Žħ ¿ä¼Ò ºÐ¼®, ÀüÀÚ±¤ ¹Ì¼¼ Žħ ºÐ¼®
  • electron beam therapy
    ÀüÀÚ¼± Ä¡·á
  • electron carrier
    ÀüÀÚ ¿î¹Ýü
  • electron configuration
    ÀüÀÚ ¹èÄ¡
  • electron density
    ÀüÀÚ ¹Ðµµ
    ÀüÀÚÇö¹Ì°æ¿¡¼­ ÀüÀÚÀÇ Åõ°ú¸¦ ¸·À» ¼ö ÀÖ´Â µÎ²² ¶Ç´Â ¹Ðµµ.
  • electron emission
    ÀüÀÚ ¹æÃâ
    ¿øÀÚ¿¡ ¹æ»ç´ÉÀ» ÁÖ´Â ÀüÀÚÀÇ Çϳª.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
regressive staining A type of staining in which tissues are overstained and the excess dye is then removed selectively until the desired intensity is obtained.
(05 Mar 2000)
progressive staining A procedure in which staining is continued until the desired intensity of colouring of tissue elements is attained.
(05 Mar 2000)
homogeneously staining region <molecular biology> A region on a chromosome which, when stained, is uniform in appearance. (Normally, a stained chromosome shows a banding pattern.) Homogeneously staining regions contain multiple copies of a single gene.
(09 Oct 1997)
silver staining The use of silver, usually silver nitrate, as a reagent for producing contrast or colouration in tissue specimens.
(12 Dec 1998)
staining The use of a dye, reagent, or other material for producing colouration in tissues or microorganisms for microscopic examination.
(12 Dec 1998)
negative staining Microscopic technique in which the object stands out against a dark background of stain. For electron microscopy the sample is suspended in a solution of an electron dense stain such as sodium phosphotungstate and then sprayed onto a support grid. The stain dries as structureless solid and fills all crevices in the sample. When examined in the electron microscope the sample appears as a light object against a dark background. Quite fine structural detail can be observed using negative staining and it has been used extensively to study the structure of viruses and other particulate samples.
(18 Nov 1997)
dispersion staining <microscopy> A procedure involving central or annular stops in the objective back focal plane to induce coloured images of transparent particles mounted in liquids with indices matching the particle at a wavelength in the visible. The particle and liquid should possess very different dispersion curves for best colours.
(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)
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)
Auger electron An electron ejected from a lower energy orbital after a photoelectric interaction of an X-ray photon with a K-shell electron by the characteristic radiation photon; the Auger electron recoils with energy equal to the characteristic radiation less the difference in shell binding energies.
See: photoelectric effect.
(05 Mar 2000)
backscattered electron <microscopy> Produced by an incident electron colliding with the nucleus of an atom in the specimen. The incident electron is then scattered backward about 180 degrees with no appreciable loss of energy, an elastic collision.
(05 Aug 1998)
backscattered electron imaging <microscopy> The production of backscattered electrons from a sample varies directly with the specimen's average atomic number, higher atomic number elements produce more backscattered electrons than lower atomic number ones. Detection of Backscattered Electrons is achieved by using a donut shaped solid state saemiconductor device mounted on the bottom of the objective lens. When Backscattered Electrons strike the detector electron-hole pairs are created which are then counted. This quantity is translated into a pixel intensity and displayed on the CRT, forming the image. By splitting the detector into halves (or quadrants) differences in the signal level on the individual detector segments provide surface topography information.
(05 Aug 1998)
valence electron One of the electron's that take part in chemical reactions of an atom.
(05 Mar 2000)
Parallel Electron Energy Loss Spectroscopy <technique> Electron energy loss spectroscopy analyses the inelastically scattered electrons present in the beam after it has been transmitted through the sample. An electron energy loss spectrum typically consists of a monatomic decreasing background on which are superimposed a number of peaks. Each peak is characteristic of the scattering process that has occurred in the sample. The peaks can be used to obtain information about the chemical composition and electronic structure of the sample. Electron energy loss spectra are acquired typically in a magnetic sector spectrometer located under the camera chamber of the transmission electron microscope. Spatial resolution is typically limited by the minimum probe diameter of the microscope. Electron energy loss spectroscopy tends to be complimentary to EDS in that it can be used to analyse very thin samples of low Z materials.
Acronym: PEELS
(05 Aug 1998)
reverse electron transport <chemistry> The energy-dependent movement of electrons against the thermodynamic gradient to form a strong reductant from a weaker electron donor.
(11 Jan 1998)
ÇÑ¿µ/¿µÇÑ »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • staining
    ´õ·¯¿öÁö´Ù
  • electron
    ÀüÀÚ
  • electron
    ÀüÀÚ
  • electron affinity
    (¹°)ÀüÀÚ Ä£È­·Â
  • electron beam
    (¹°)ÀüÀÚ ºö(Àü°è,ÀÚ°è¿¡¼­ ÇÑ ¹æÇâÀ¸·Î ¸ð¾ÆÁ® È帣´Â ÀüÀÚÀÇ È帧)
  • electron beam melting
    (±Ý¼Ó)ÀüÀÚºö ¿ëÇØ¹ý Àå
  • electron bomb
    ÀÏ·ºÆ®·Ð ¼ÒÀÌź
  • electron gas
    (¹°)ÀüÀÚ ±âü(°¡½º)
  • electron gun
    ÀüÀÚÃÑ(ºê¶ó¿î°üÀÇ ÀÜÀÚ·ù ÁýÁß°ü) )
  • electron lens
    ÀüÀÚ ·»Áî
  • electron microseope
    ÀüÀÚ Çö¹Ì°æ
  • electron optics
    ÀüÀÚ °øÇÐ
  • electron spin resonance
    (¹°)ÀüÀÚ ½ºÇÉ °ø¸í
  • electron telescope
    ÀüÀÚ ¸Á¿ø°æ
  • electron tube
    ÀüÀÚ°ü(X¼±°ü µûÀ§)
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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    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
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  • ¿µ¹®
    ÇѱÛ
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  • ¿µ¹®
    ÇѱÛ
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  • ¿µ¹®
    ÇѱÛ
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  • ¿µ¹®
    ÇѱÛ
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    ÇѱÛ
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  • ¿µ¹®
    ÇѱÛ
    ÇÑÀÚ
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  • ¿µ¹®
    ÇѱÛ
    ÇÑÀÚ
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  • ¿µ¹®
    ÇѱÛ
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  • ¿µ¹®
    ÇѱÛ
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