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"primary protein derivative"¿¡ ´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
  • primary epilepsy
    ¿ø¹ß(¼º) °£Áú(ê«Û¡(àõ) ÊÖòð)
  • primary epilepsy
    ¿ø¹ß(¼º) °£Áú(ê«Û¡àõ ÊÖòð).
  • primary eye vesicle
    ÀÏÂ÷¾ÈÆ÷(¡­äÑøà).
  • primary facilitation
    ÀÏÂ÷¼ÒÅë(ìéó­áÂ÷×).
  • primary failure
    ÀÏÂ÷Àû ¹«È¿(ì£ó­îÜÙíüù).
  • primary fissure
    ù°ƴ»õ
  • primary focal point
    Á¦ÀÏÃÊÁ¡
  • primary focus
    ¿ø¹ß¼Ò(ê«Û¡áµ).
  • primary focus
    ¿øº´¼Ò
  • primary follicle
    ÀÏÂ÷³­Æ÷, ¿ø½Ã³­Æ÷(ê«ã·Õ°øà), ¿ø½Ã¿©Æ÷(¡­æ¤øà).
  • primary follicle
    ÀÏÂ÷³­Æ÷
  • primary gain
    ÀÏÂ÷(Àû) À̵æ(ìéó­îÜì¦Ôð).
  • primary germ layer
    ÀÏÂ÷¹è¿±(¡­ÛÏç¨).
  • primary glaucoma
    ¿ø¹ß³ì³»Àå(ê«Û¡ÖàÒ®î¡).
  • primary glaucoma ³ª g. primarium
    ¿ø¹ß³ì³»Àå(ê«Û¡ÖàÒ®î¡)
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  • ¿µ¹®
    ÇѱÛ
  • protein therapy
    ´Ü¹é(Áú)¿ä¹ý(¡­èþÛö).
  • protein,actin-binding
    ¾×ƾ-°áÇÕ(´Ü¹é)
  • protein,al
    AL(´Ü¹é)
  • protein,bence jones
    º¥½º-Á¸½º(´Ü¹é)
  • protein-calorie deficiency
    ´Ü¹é(Áú)¿­·®°áÇÌ(Ó±ÛÜ(òõ)æðÕáÌÀù¹)
  • protein-calorie malnutrition
    ´Ü¹é(Áú)¿­·®¿µ¾ç½ÇÁ¶(Áõ)(Ó±ÛÜ(òõ)æðÕáç½å×ã÷ðà(ñø))
  • protein-energy malnutrition
    ´Ü¹é(Áú)¿¡³ÊÁö¿µ¾ç½ÇÁ¶(Áõ)(¡­ç½å×ã÷ðà(ñø))
  • protein-losing
    ´Ü¹é»ó½Ç¼º.
  • protein-losing enteropathy
    ´Ü¹é»ó½Ç¼º À庴Áõ(íóÜ»ñø)
  • protein-losing enteropathy
    ´Ü¹é»ó½ÇÀ庴Áõ(Ó±ÛÜßÃã÷íóÜ»ñø)
  • racemized protein
    ¶ó¼¼¹ÌÈ­´Ü¹éÁú(¡­ûùÓ±ÛÜòõ).
  • ras protein
    ras ´Ü¹é(¡­Ó±ÛÜ)
  • reserve protein
    ÀúÀå´Ü¹éÁú.
  • retinol-binding protein
    ·¹Æ¼³î°áÇմܹé(Áú)(·¹Æ¼³î Ì¿ùêÓ±ÛÜòõ)
  • serum protein
    Ç÷û´Ü¹é
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    ÇѱÛ
  • multiheaded protein
    ´ÙµÎ´Ü¹éÁú(ÒýÔéÓ±ÛÜòõ)
  • mutant protein
    º¯À̴ܹéÁú(ܨì¶Ó±ÛÜòõ)
  • myelin basic protein
    ¼öÃÊ¿°±â¼º(âËÃÊç¤Ðñàõ) ´Ü¹éÁú(Ó±ÛÜòõ)
  • myelin protein A1
    ¼öÃʴܹéÁú(âËÃÊÓ±ÛÜòõ) A1
  • myeloma protein
    °ñ¼öÁ¾´Ü¹éÁú(ÍéâÐðþÓ±ÛÜòõ)
  • nonheme-iron protein
    ºñ(Þª)Èû-ö(ôÑ) ´Ü¹éÁú(Ó±ÛÜòõ)
  • omega protein
    ¿À¸Þ°¡ ´Ü¹éÁú(Ó±ÛÜòõ)
  • peripheral protein
    ÁÖº¯´Ü¹éÁú(ñ²Ü«Ó±ÛÜòõ)
  • polycephalic protein
    º¹ÇÕ±â´É ´Ü¹éÁú(ÜÜùêѦÒöÓ±ÛÜòõ)
  • polyfunctional protein
    ´Ù±â´É ´Ü¹éÁú(ÒýѦÒöÓ±ÛÜòõ)
  • P protein
    P ´Ü¹éÁú(Ó±ÛÜòõ)
  • prepriming protein
    ÇÁ·¹ÇÁ¶óÀÌ¹Ö ´Ü¹éÁú(Ó±ÛÜòõ)
  • protein
    ´Ü¹éÁú(Ó±ÛÜòõ)
  • protein A
    ´Ü¹éÁú(Ó±ÛÜòõ) A
  • protein biosynthesis
    ´Ü¹éÁú »ýÇÕ¼º(Ó±ÛÜòõßæùêà÷)
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HSP Health Systems Plan; heat shock protein; hemostatic screening profile; Henoch-Schonlein purpura; her...
IAP immunosuppressive acidic protein; inosinic acid pyrophosphorylase; Institute of Animal Physiology; i...
IBP insulin-like growth factor binding protein; International Biological Program; intra-aortic balloon p...
LP labile peptide; labile protein; laboratory procedure; lactic peroxidase; lamina propria; laryngophar...
LSP left sacroposterior [fetal position]; linguistic string project; liver-specific protein; lymphocyte-...
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PSC Primary Sclerosing Cholangitis
PSS Primary Sjogren Syndrome
PAM Primary acquired melanosis
PAD Primary afferent depolarization
PA Primary aldosteronism
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primary visual cortex See: visual cortex.
(05 Mar 2000)
primary vitreous The vitreous first formed in the embryo between the optic cup and the lens vesicle, and later vascularised by the hyaloid artery and its branches.
(05 Mar 2000)
hyperoxaluria, primary Either of two genetic disorders characterised by urinary excretion of large amounts of oxalate, with nephrolithiasis, nephrocalcinosis, early onset of renal failure, and often a generalised deposit of calcium oxalate, resulting from a defect in glyoxalate metabolism.
(12 Dec 1998)
neoplasms, multiple primary Two or more abnormal growths of tissue occurring simultaneously. The neoplasms are histologically different and may be found in the same or different sites.
(12 Dec 1998)
neoplasms, second primary Abnormal growths of tissue that follow a previous neoplasm but are not metastases of the latter. The second neoplasm may have the same or different histological type and can occur in the same or different organs as the previous neoplasm but in all cases arises from an independent oncogenic event. The development of the second neoplasm may or may not be related to the treatment for the previous neoplasm since genetic risk or predisposing factors may actually be the cause.
(12 Dec 1998)
neoplasms, unknown primary Metastases in which the tissue of origin is unknown.
(12 Dec 1998)
dentition, primary The teeth first in order or time of development that will be replaced by permanent dentition upon their loss.
(12 Dec 1998)
dorsal primary ramus of spinal nerve <anatomy, nerve> The smaller, posteriorly-directed major terminal branch (with the ventral primary ramus) of all 31 pairs of mixed spinal nerves, formed at the intervertebral foramen and turning abruptly posteriorly to divide into lateral and medial branches, both of which will supply the deep (true) muscles of the back. The medial branch (rami medialis ) of the dorsal primary ramus also supplies articular branches to the zygopophyseal joints and the periosteum of the vertebral arch. In the neck and upper back, the medial branch continues through the deep and superficial back muscles to supply overlying skin; in the lower back, the lateral branch does this. Nomina Anatomica lists dorsal primary rami as "rami dorsales" for each group of spinal nerves: 1) cervical (nervorum cervicalium ), 2) thoracic (nervorum thoracicorum ), 3) lumbar (nervorum lumbalium ), 4) sacral (nervorum sacralium ), and 5) coccygeal (nervi coccygei ).
Synonym: ramus dorsalis nervorum spinalium, ramus dorsalis, rami posteriores nervorum spinalium, dorsal branch, posterior primary division.
(05 Mar 2000)
International Classification of Health Problems in Primary Care A classification of diseases, conditions and problems arranged for use in primary care where diagnostic precision is seldom possible.
(05 Mar 2000)
osteoarthropathy, primary hypertrophic A conditioned chiefly characterised by thickening of the skin of the head and distal extremities, deep folds and furrows of the skin of the forehead, cheeks, and scalp, seborrhoea, hyperhidrosis, periostosis of the long bones, digital clubbing, and spadelike enlargement of the hands and feet. It is more prevalent in the male, and is usually first evident during adolescence. It is believed to be inherited as an autosomal dominant trait.
(12 Dec 1998)
lateral cutaneous branches of ventral primary ramus of thoracic spinal nerves Branches arising in approximately the anterior axillary line at the level of the second through sixth intercostal spaces.
Synonym: rami mammarii laterales nervorum intercostalium, lateral cutaneous branches of intercostal nerves.
(05 Mar 2000)
acetoacetyl-acyl carrier protein synthase <enzyme> E coli enzyme, that catalyses condensation of malonyl-acyl carrier protein plus acetyl-acyl carrier protein; not inhibited by cerulenin
Registry number: EC 2.3.1.-
Synonym: acetoacetyl-acp synthase
(26 Jun 1999)
acid soluble spore protein <molecular biology> A DNA binding protein in the spores of some bacteria, thought to stabilise the DNA in an A configuration, so protecting it from cleavage by enzymes or UV light.
(18 Nov 1997)
acute-phase protein <haematology> These plasma proteins (in addition to fibrinogen) increase 25% or more in response to inflammation and injury are under direct control of interleukin-6 (IL-6) (hepatocyte-stimulating factor).
Other proteins which increase are ceruloplasmin, C3 and C4 which increase 50% or more; alpha-1 acid glycoprotein, alpha-1 antitrypsin, haptoglobin and fibrinogen (the major determinant of viscosity 1 ) which increase two- to fourfold; C-reactive protein (CRP) and serum amyloid A which increase several hundred-fold.
Despite long-held clinical opinion to the contrary, available data indicate that neither ESR nor measurement of specific acute-phase reactants are useful in excluding underlying infection or inflammation regardless of the pretest probability.
These proteins are secreted into the blood in increased or decreased quantities by hepatocytes in response to trauma, inflammation, or disease. They can serve as inhibitors or mediators of the inflammatory processes. Certain acute-phase proteins have been used to diagnose and follow the course of diseases or as tumour markers.
See also: amyloid, c-reactive protein, erythrocyte sedimentation rate, viscosity.
(25 Jun 1999)
acyl-(acyl-carrier-protein)-phospholipid acyltransferase <enzyme> Catalyses the formation of phosphatidylethanolamine from acyl-acyl carrier protein and 2-acyl-sn-glycero-3-phosphoethanolamine
Registry number: EC 2.3.1.40
Synonym: 2-acyl-gpe acyltransferase, 2-acylglycerophosphoethanolamine acyltransferase
(26 Jun 1999)
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