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"amyloid plaque"¿¡ ´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
  • mucous patch plaque
    Á¡¸·ÆÇ
  • plaque
    ÆÇ, ÇöóÅ©
  • plaque assay
    ÆÇÃøÁ¤(¹ý), ÇöóÅ©ÃøÁ¤(¹ý)
  • plaque morphology mutation
    ÆÇÇüŵ¹¿¬º¯ÀÌ, ÇöóÅ©Çüŵ¹¿¬º¯ÀÌ
  • plaque technique
    ÇöóÅ©(±â)¹ý
  • plaque-forming unit
    ÇöóÅ©Çü¼º´ÜÀ§
  • yellow plaque
    Ȳ»öÆÇ
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  • ¿µ¹®
    ÇѱÛ
  • mottled plaque
    ¿ë±ÕÆÇ, Åé´Ï¸ð¾çÇöóÅ©
  • mucous patch plaque
    Á¡¸·ÆÇ
  • plaque morphology mutation
    (¢¡plaque-type mutation) ÇöóÅ©Çüµ¹¿¬º¯ÀÌ
  • plaque-type mutation
    ÇöóÅ©Çüµ¹¿¬º¯ÀÌ
  • plaque
    ÆÇ, ÇöóÅ©
  • phage plaque-forming unit
    ÆÄÁö¿ë±ÕÇü¼º´ÜÀ§, ÆÄÁöÇöóÅ©Çü¼º´ÜÀ§
  • plaque technique
    ÇöóÅ©°Ë»ç¹ý
  • plaque-forming unit
    ÇöóÅ©Çü¼º´ÜÀ§
  • yellow plaque
    Ȳ»öÆÇ
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  • ¿µ¹®
    ÇѱÛ
  • Jernes plaque assay
    ¿©´Ï ¿ëÇ÷¹ÝÃøÁ¤¹ý, ¿©´Ï ÇöóÅ©ÃøÁ¤¹ý
  • PFU (plaque forming unit)
    ÇöóÅ© Çü¼º´ÜÀ§
  • artherosclerosis,atheromatous plaque
    Á×»ó ÆÇ
  • gelatinoid plaque =dental p., bacterial p.
    Ä¡¾Æ¼¼±Õ¸·(öÍä³á¬Ð¶Ø¯).
  • haemolytic plaque
    ¿ëÇ÷(éÁúì)ÇöóÅ©, ¿ëÇ÷¹Ý(éÁúìÚè).
  • haemolytic plaque
    ¿ëÇ÷(ËíÌ´)ÇöóÅ©, ¿ëÇ÷¹Ý(ËíÌ´ËÑ).
  • haemolytic plaque techinique
    ¿ëÇ÷ÇöóÅ©¼ö±â(¹ý)(¡­â¢ÐüÛö).
  • haemolytic plaque test
    ¿ëÇ÷ÇöóÅ©½ÃÇè.
  • hemolytic plaque assay
    ¿ëÇ÷¹Ý ÃøÁ¤¹ý, ¿ëÇ÷ÇöóÅ© ÃøÁ¤¹ý
  • hemolytic plaque test
    ¿ëÇ÷ÇöóÅ©Å×½ºÆ®.
  • hemolytic plaque-forming cell
    ¿ëÇ÷¹Ý Çü¼º¼¼Æ÷, ¿ëÇ÷ÇöóÅ© Çü¼º¼¼Æ÷
  • hybridization, plaque
    ÇöóÅ©ºÎÇÕ¹ý(ݬùêÛö)
  • phage plaque-forming unit
    ÆÄÁö¿ë±Õ Çü¼º´ÜÀ§, ÆÄÁöÇöóÅ© Çü¼º´ÜÀ§
  • plague pneumonia ³ª p. plaque
    Æä½ºÆ®Æó·Å(¡­øËæú).
  • plague pneumonia ³ª p. plaque
    Æä½ºÆ®Æó·Å(¡­øËæú).
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    ÇѱÛ
  • assay, hemolytic plaque
    ¿ëÇ÷¹Ý ÃøÁ¤¹ý, ¿ëÇ÷ÇöóÅ© ÃøÁ¤¹ý
  • atrophic large-plaque parapsoriasis
    À§Ã༺ ÆÇ(ê×õêàõ ÷ù) À¯°Ç¼±(ëºËëàÈ)
  • attachment plaque
    ºÎÂøÆÇ
  • bacterial plaque
    ¼¼±Õ¼º ¹ÝÁ¡(¡­ÚèïÇ).
  • bacterial plaque
    ¼¼±Õ¼º ¹ÝÁ¡(¡­ÚèïÇ).
  • bubonic plaque
  • cell, plaque-forming
    ÇöóÅ© Çü¼º¼¼Æ÷
  • dense plaque
    Á¶¹ÐÆÇ
  • dental plaque
    Ä¡¸é¼¼±Õ¸·(öÍØüá¬Ð¶Ø¯), Ä¡ÅÂ(öÍ÷Â).
  • dental plaque
    Ä¡¾Æ ÆÇ(öÍä³÷ù)
  • desmosomal plaque
    ºÎÂø¹ÝÆÇ, °áÇÕ¼ÒüÆÇ(¡­á³ô÷÷ù).
  • digitate dermatosis => parapsoriasis, small plaque
  • fibroptic plaque
  • fibrous plaque
    ¼¶À¯¼º ÇöóÅ©
  • formation, plaque
    ÇöóÅ© Çü¼º
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    ÇѱÛ
  • white plaque
    ÈØ Ç÷¹ÀÌÅ©
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PFU plaque-forming unit; pock-forming unit
PI first meiotic prophase; isoelectric point; pacing impulse; package insert; pancreatic insufficiency;...
PN papillary necrosis; parenteral nutrition; penicillin; perceived noise; percussion note; periarteriti...
PrA-HPA protein A hemolytic plaque assay
PRNT plaque reduction neutralization test
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PI Plaque Index
PII Plaque Index
PLI Plaque Index
PRN Plaque Reduction Neutralization
PRNT Plaque reduction neutralization tests
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    ÇѱÛ
    ¼³¸í
  • plaque control
    ġŠÁ¶Àý
  • plaque formation
    º´¼Ò ¹Ý Çü¼º, ÇöóÅ© Çü¼º
    ȹµæ ÇǸ·ÀÇ Çü¼º, ȹµæ ÇǸ·¿¡ ¼¼±ÕÀÇ ÃʱâºÎÂø, ¼¼±Õ¼º ġŰ¡ ¸î ÃþÀ¸·Î ÃàÀûµÇ¾î µÎ²¨¿öÁö´Â °úÁ¤À» ¸»ÇÑ´Ù.
  • plaque forming unit
    ÇöóÅ© Çü¼º ´ÜÀ§
  • plaque like
    ¹ÝÁ¡ °°Àº
  • plaque like lesion
    ¹ÝÁ¡ °°Àº º´¼Ò
  • plaque-like
    ¹ÝÁ¡Çü, ¹ÝÇü
  • scleroderma in plaque
    ġų» °øÇÇÁõ
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dental plaque <dentistry> A soft, thin film of food debris, mucin and dead epithelial cells deposited on the teeth, providing the medium for the growth of various bacteria.
The main inorganic components are calcium and phosphorus with small amounts of magnesium, potassium and sodium, the organic matrix consists of polysaccharides, proteins, carbohydrates, lipids and other components.
Plaque plays an important aetiological role in the development of dental caries and periodontal and gingival diseases and provides the base for the development of materia alba, calcified plaque forms dental calculus.
(19 Mar 1998)
dental plaque index An index which scores the degree of dental plaque accumulation.
(12 Dec 1998)
fibrous plaque Thickened area of arterial intima with accumulation of smooth muscle cells and fibrous tissue (collagen etc.) produced by the fat laden smooth muscle cells. Below the thickening may be free extracellular lipid and debris that, if much necrosis is also present, is referred to as an atheroma.
(18 Nov 1997)
amyloid Glycoprotein deposited extracellularly in tissues in amyloidosis. The glycoprotein may either derive from light chain of immunoglobulin (AIO (amyloid of immune origin): 5-18 kD glycoprotein, product of a single clone of plasma cells, the N terminal part of lambda or kappa light chain) or, in what used to be referred to as AUO, amyloid of unknown origin, from serum amyloid A (SAA), one of the acute phase proteins that increases many fold in inflammation. The polypeptides are organised as a _ pleated sheet making the material rather inert and insoluble. Minor protein components are also found. Should be distinguished from _ amyloid deposited in the brain and that is derived from amyloid precursor protein (see amyloidogenic glycoprotein.
(18 Nov 1997)
amyloid A-degrading serine protease <enzyme> Reduced in amyloidosis associated with rheumatoid arthritis
Registry number: EC 3.4.21.-
Synonym: amyloid a-degrading activity, aad-protease
(26 Jun 1999)
amyloid angiopathy Deposition of acellular hyaline material in small arteries and arterioles of the leptomeninges and cerebral cortex in the elderly with resulting predilection for recurrent lobar intraparenchymal haematomas.
(05 Mar 2000)
amyloid beta-protein A 4 kD protein, 39-43 amino acids long, expressed by a gene located on chromosome 21. It is the major protein subunit of the vascular and plaque amyloid filaments in individuals with alzheimer's disease and in aged individuals with trisomy 21 (down syndrome). The protein is found predominantly in the nervous system, but there have been reports of its presence in non-neural tissue.
(12 Dec 1998)
amyloid beta-protein precursor A precursor to the amyloid-beta protein (beta/a4). Alterations in the expression of the amyloid beta-protein precursor (abpp) gene, located on chromosome 21, plays a role in the development of the neuropathology common to both alzheimer disease and down syndrome. Abpp is associated with the extensive extracellular matrix secreted by neuronal cells. Upon cleavage, this precursor produces three proteins of varying amino acid lengths: 695, 751, and 770. The beta/a4 (695 amino acids) or beta-amyloid protein is the principal component of the extracellular amyloid in senile plaques found in alzheimer disease, down syndrome and, to a limited extent, in normal aging.
(12 Dec 1998)
amyloid bodies of the prostate An obsolete term for small masses of colloid material often present in the tubules of the gland.
See: corpus amylaceum.
(05 Mar 2000)
amyloid corpuscle One of a number of small ovoid or rounded, sometimes laminated, bodies resembling a grain of starch and found in nervous tissue, in the prostate, and in pulmonary alveoli; of little pathological significance, and apparently derived from degenerated cells or proteinaceous secretions.
Synonym: amniotic corpuscle, amylaceous corpuscle, amyloid corpuscle, colloid corpuscle.
(05 Mar 2000)
amyloid degeneration Infiltration of amyloid between cells and fibres of tissues and organs.
Synonym: waxy degeneration.
(05 Mar 2000)
amyloid kidney A kidney in which amyloidosis has occurred, usually in association with some chronic illness such as multiple myeloma, tuberculosis, osteomyelitis, or other chronic suppurative inflammation; such kidney's are moderately enlarged and grossly manifest a waxy appearance, with amyloid deposited beneath the endothelium in the glomerular loops and in the arterioles, apparently beginning as foci of thickening of the basement membranes.
Synonym: waxy kidney.
(05 Mar 2000)
amyloid nephrosis The nephrotic syndrome due to deposition of amyloid in the kidney.
See: renal amyloidosis.
(05 Mar 2000)
amyloid neuropathies Disorders of the peripheral nervous system associated with deposition of amyloid. Amyloid neuropathies may result from non-hereditary or hereditary amyloidosis. Several different forms of familial amyloid neuropathies have been described, most of which have specific mutations in the prealbumin gene.
(12 Dec 1998)
amyloid p component Amyloid p component is a small, non-fibrillar glycoprotein found in normal serum and in all amyloid deposits. It has a pentagonal (pentaxin) structure. It acts as an acute phase protein in the mouse, modulates immunologic responses in man, inhibits elastase, and has been suggested as an indicator of liver disease.
(12 Dec 1998)
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