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¿µ¹® amyloidosis ÇÑ±Û ¾Æ¹Ð·ÎÀ̵åÁõ
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  º»·¡ »ýü¿¡´Â ¾ø´Â ´ç´Ü¹éÁúÀÇ ÀÏÁ¾À¸·Î ºñÁ¤»óÀûÀ¸·Î ¾Æ¹Ð·ÎÀ̵å´Ü¹éÀÌ Á¶Á÷À̳ª Àå±â¿¡ Ä§ÂøµÇ´Â º´. ¹ßÇöºÎÀ§°¡ Àü½Å¼ºÀΠ°æ¿ìÀÇ ¾Æ¹Ð·ÎÀ̵åÁõ(Àü½Å¼º ¾Æ¹Ð·ÎÀ̵åÁõ)¿¡´Â ¸í¹éÇÑ ¿øÀξøÀÌ ÀϾ´Â ¿ø¹ß¼º ¾Æ¹Ð·ÎµåÁõ°ú ¸¸¼ºÈ­³ó¼º ¿°ÁõÀ̳ª °áÇÙ µî ¼Ò¸ð¼º Áúȯ¿¡¼­ Ã£¾Æº¼ ¼ö Àִ ¼Ó¹ß¼º ¾Æ¹Ð·ÎÀ̵åÁõÀÌ ÀÖ´Ù. ¹ßÇöºÎÀ§°¡ ±¹¼Ò¼ºÀΠ°æ¿ìÀÇ ±¹¼Ò¼º ¾Æ¹Ð·ÎÀ̵åÁõÀ¸·Î¼­´Â ³úÀÇ ³ëÀιÝÀÌ ±× ¿¹À̸ç, Æ¯È÷ ÀԾȿ¡¼­´Â Çô³ª ÀÕ¸ö¿¡ ´ëÇÑ Ä§ÂøÀÌ ÇöÀúÇÏ°í ¿©·¯ °¡Áö ±â´ÉÀå¾Ö¸¦ ³ªÅ¸³½´Ù. Á¶Á÷ÇÐÀûÀ¸·Î´Â Ç츶Åå½Ç¸° ¿¡¿ÀÁø¿°»ö¿¡¼­´Â ¿¡¿ÀÁø¼º ¹«±¸Á¶ÀΠÀ¯¸®È­¸¦ ³ªÅ¸³»¸ç Äá°í·¹µå, Æí±¤»ó(³ì»ö) µîÀ¸·Î È®ÀÎÇÑ´Ù. ±¸Á¶ÀûÀ¸·Î´Â ¾Æ¹Ð·ÎÀ̵堼¶À¯ÀÇ ÁýÇÕÀ¸·Î ÀÌ·ç¾îÁö´Â ¿©·¯ °¡Áö ¾Æ¹Ð·ÎÀ̵å Ä§ÂøÀÌ ÀÖÀ¸¸ç ±×°Íµé¿¡ ´ëÇÑ º´ÇüÀÌ ºÐ·ùµÇ¾î ÀÖ´Ù. °¡Á·Çü, ´Ù¹ß¼º °ñ¼öÁ¾°ú ¼ö¹ÝÇϴ Çü ±×¸®°í °¡Á·¼º ÁöÁßÇØ¿­À» ¼ö¹ÝÇϴ Çü µîÀÌ ÀÖ´Ù.
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  • ¿µ¹®
    ÇѱÛ
  • amyloid angiopathy
    ¾Æ¹Ð·ÎÀ̵åÇ÷°üº´(Áõ)
  • amyloid kidney
    ¾Æ¹Ð·ÎÀ̵åÄáÆÏ, ¾Æ¹Ð·ÎÀ̵å½ÅÀå
  • amyloid nephrosis
    ¾Æ¹Ð·ÎÀ̵åÄáÆÏÁõ, ¾Æ¹Ð·ÎÀ̵å½ÅÀåÁõ
  • amyloid plaque
    ¾Æ¹Ð·ÎÀ̵åÆÇ
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ
  • amylopectinosis
    ¾Æ¹Ð·ÎÆåƾÁõ
  • amylorrhea
    ³ì¸»´ëº¯(Áõ)
  • amylose
    ¾Æ¹Ð·Î¿À½º
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 6 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • amyloid angiopathy
    ¾Æ¹Ð·ÎÀ̵åÇ÷°üº´Áõ
  • amyloid kidney
    ¾Æ¹Ð·ÎÀ̵åÄáÆÏ, ¾Æ¹Ð·ÎÀ̵å½ÅÀå
  • amyloid nephrosis
    ¾Æ¹Ð·ÎÀ̵åÄáÆÏÁõ
  • amyloid plaque
    ¾Æ¹Ð·ÎÀ̵åÆÇ
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ
  • amylose
    ¾Æ¹Ð·Î¿À½º
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • amylo-1
    6-glucosidase
  • amyloid
    ¾Æ¹Ð·ÎÀ̵å.
  • amyloid
    ¾Æ¹Ð·ÎÀ̵å
  • amyloid angiopathy
    À¯ÀüºÐÇ÷°üº´Áõ(ëºîþÝÏ úìηܻñø)
  • amyloid bodies<³ª> corpora amylacea
    ¾Æ¹Ð·ÎÀ̵å¼Òü(¡­á³ô÷).
  • amyloid degeneration
    ¾Æ¹Ð·ÎÀ̵庯¼º(¡­Ü¨àõ).
  • amyloid disease
    ¾Æ¹Ð·ÎÀ̵庴(¡­Ü»).
  • amyloid kidney
    ¾Æ¹Ð·ÎÀÌµå ½Å
  • amyloid nephrosis
    ¾Æ¹Ð·ÎÀ̵å½ÅÁõ(¡­ãìñø).
  • amyloid precurssor protein
    ¾Æ¹Ð·ÎÀ̵å Àü±¸ ´Ü¹éÁú
  • amyloid tumor
    ¾Æ¹Ð·ÎÀ̵åÁ¾¾ç.
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ, À¯ÀüºÐÁõ
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ, À¯ÀüºÐÁõ.
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ(¡­ñø), À¯ÀüºÐÁõ(ëºîþÝÏñø)
  • amyloidosis
    À¯ÀüºÐÁõ
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • amylo-1
    6-glucosidase
  • amyloid
    ¾Æ¹Ð·ÎÀ̵å.
  • amyloid
    ¾Æ¹Ð·ÎÀ̵å
  • amyloid angiopathy
    À¯ÀüºÐÇ÷°üº´Áõ(ëºîþÝÏ úìηܻñø)
  • amyloid bodies<³ª> corpora amylacea
    ¾Æ¹Ð·ÎÀ̵å¼Òü(¡­á³ô÷).
  • amyloid degeneration
    ¾Æ¹Ð·ÎÀ̵庯¼º(¡­Ü¨àõ).
  • amyloid disease
    ¾Æ¹Ð·ÎÀ̵庴(¡­Ü»).
  • amyloid kidney
    ¾Æ¹Ð·ÎÀÌµå ½Å
  • amyloid nephrosis
    ¾Æ¹Ð·ÎÀ̵å½ÅÁõ(¡­ãìñø).
  • amyloid precurssor protein
    ¾Æ¹Ð·ÎÀ̵å Àü±¸ ´Ü¹éÁú
  • amyloid tumor
    ¾Æ¹Ð·ÎÀ̵åÁ¾¾ç.
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ, À¯ÀüºÐÁõ.
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ(¡­ñø), À¯ÀüºÐÁõ(ëºîþÝÏñø)
  • amyloidosis
    À¯ÀüºÐÁõ
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ, À¯ÀüºÐÁõ
´ëÇѽŰæ¿Ü°úÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 3 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ÇÑÀÚ
  • amyloid a.
    ¾Æ¹Ð·ÎÀ̵åÇ÷°üº´Áõ
    ¾Æ¹Ð·ÎÀ̵åúìηܻñø
  • amyloid angiopathy
    ¾Æ¹Ð·ÎÀ̵åÇ÷°üº´Áõ
    ¾Æ¹Ð·ÎÀ̵åúìηܻñø
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ
    ¾Æ¹Ð·ÎÀ̵åñø
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 14 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • amylo-
    ¾Æ¹Ð·Î-
  • amyloclastic
    ¾Æ¹Ð·ÎºÐÇØ (ÝÂú°)
  • amyloclastic method
    ¾Æ¹Ð·ÎºÐÇØ¹ý(ÝÂú°Ûö)
  • amylodextrin
    ¾Æ¹Ð·Îµ¦½ºÆ®¸°
  • amyloid
    ¾Æ¹Ð·ÎÀ̵å
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ(ñø)
  • amylolysis
    "³ì¸»ºÐÇØ(ÝÂú°), ¾Æ¹Ð·ÎÀ̵åºÐÇØ(ÝÂú°)"
  • amylometric method
    "¾Æ¹Ð·ÎÀ̵åÃøÁ¤¹ý(ö´ïÒÛö), ¾Æ¹Ð·ÎÀ̵å¹ý(Ûö)"
  • amylopectin
    ¾Æ¹Ð·ÎÆåƾ
  • amylopectinosis
    ¾Æ¹Ð·ÎÆåƾÁõ(ñø)
  • amyloplast
    ¾Æ¹Ð·ÎÇÃ¶ó½ºÆ®
  • amylopsin
    ¾Æ¹Ð·Ó½Å
  • amylose
    ¾Æ¹Ð·ÎÁî
  • amylose synthetase(synthase)
    "¾Æ¹Ð·Î½º½ÅÅ×Å×À̽º, ¾Æ¹Ð·Î½º½ÅÅ×À̽º"
KI ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 2 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • amyloid infiltration
    ¾Æ¹Ð·ÎÀ̵åħÀ±
  • amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ, À¯ÀüºÐÁõ
ÀÇÇÐ³í¹® ¾àÀÚ(Pubmed/Entrez) °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • JrId: 20942
    JournalTitle: the official journal of the International Society of Amyloidosis.
    MedAbbr: Amyloid
    ISSN: 1350-6129
    ESSN:
    IsoAbbr: Amyloid
    NlmId: 9433802
Çѱ¹Ç¥ÁØÁúº´»çÀκзù ¾àÀÚ ¸ÂÃã °Ë»ö °á°ú : 3 ÆäÀÌÁö: 1
  • ÄÚµå
    ¿µ¹®
    ÇѱÛ
  • E85
    Amyloidosis
    ¾Æ¹Ð·ÎÀ̵åÁõ
  • L99.0*
    Amyloidosis of skin)(E85.-
    ÇǺÎÀÇ ¾Æ¹Ð·ÎÀ̵åÁõ
  • E85.9
    Amyloidosis, unspecified
    »ó¼¼ºÒ¸íÀÇ ¾Æ¹Ð·ÎÀ̵åÁõ
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü ¸ÂÃã °Ë»ö °á°ú : 7 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • amylocoagulase
    ¾Æ¹Ð·ÎÄھƱ¼·¹À̽º
    °¡¿ë¼º ÀüºÐÀ» ÀÀ°í½ÃŰ´Â È¿¼Ò.
  • amylodyspepsia
    ÀüºÐ ¼ÒÈ­ ºÒ·®Áõ
    ÀüºÐÀ» ÇÔÀ¯ÇÑ ½Ä¹°À» ¼ÒÈ­ÇÏÁö ¸øÇÏ´Â °Í.
  • amyloid degeneration
    ¾Æ¹Ð·ÎÀÌµå º¯¼º
  • amyloid infiltration
    ¾Æ¹Ð·ÎÀ̵å ħÀ±
  • Amylomyces
    ¾ÆÀϷαÕ
    ´çÈ­¿Í ¾ËÄÚ¿Ã ¹ßÈ¿¸¦ ¿µÀ§ÇÏ´Â ÅаõÆÎÀÌ¼Ó ¹× °Å¹ÌÁÙ°õÆÎÀÌ¼Ó ±ÕÀÇ ÃÑĪ. Á¶±Õ·ù¿¡ ¼ÓÇÑ´Ù. ÇöÀç ¾Æ¹Ð·Î ¹ßÈ¿¹ý¿¡ »ç¿ëµÇ´Â °õÆÎÀÌ´Â ´çÈ­·ÂÀÌ ¶Ù¾î³­ ¶óÀÌÁ¶Çª½º
  • amylopectin
    ¾Æ¹Ð·ÎÆäƾ
    ÀüºÐÀÇ ºÒ¿ë¼º ¼ººÐ. ¿ä¿Àµå·Î ÀÚÀû»öÀÇ ¹ÝÀÀÀ» ³ªÅ¸³»¸ç, ¿­ÅÁÀ» °¡Çϸé Ç®À» Çü¼ºÇÑ´Ù. ÀüºÐÀÇ °¡¿ë ¼ººÐÀº amyloseÀÌ´Ù.
  • amylophagia
    ÀüºÐ ޽Ä
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
amylo- Starch, or polysaccharide nature or origin.
Origin: G. Amylon, unmilled; starch, fr. A-+ myle, a mill
(05 Mar 2000)
amylo-1,4:1,6-glucantransferase 1,4-alpha-d-glucan branching enzyme
amylo-1,6-glucosidase <enzyme> Catalyses endohydrolysis of 1,6-alpha-d-glucoside linkages at points of branching in chains of 1,4-linked alpha-d-glucose residues
Registry number: EC 3.2.1.33
(26 Jun 1999)
amylobacter <biology> A microorganism (Bacillus amylobacter) which develops in vegetable tissue during putrefaction.
Origin: L. Amylum starch + NL. Bacterium. See Bacterium.
Source: Websters Dictionary
(01 Mar 1998)
amylocaine hydrochloride 1-(Dimethylaminomethyl)-1-methylpropyl benzoate hydrochloride; benzoylethyldimethylaminopropanol hydrochloride;an early local anaesthetic once widely used but eventually abandoned because of side effects.
(05 Mar 2000)
amyloclast An obsolete term for amylase.
Origin: amylo-+ G. Klastos, broken in pieces
(05 Mar 2000)
amylodextrin End product of hydrolysis of amylopectin by beta-amylase; further hydrolysis requires amylo-1,6-glucosidase, which attacks the branch points. Identified by its colour reaction with iodine (amylodextrin turns blue).
Compare: achroodextrin, erythrodextrin.
(05 Mar 2000)
amylogenesis Biosynthesis of starch.
Origin: amylo-+ G. Genesis, production
(05 Mar 2000)
amylogenic Relating to amylogenesis.
(05 Mar 2000)
amylogenic body A plant plastid involved in the synthesis and storage of starch. Found in many cell types, but particularly storage tissues. Characteristically has starch grains in the plastid stroma.
(18 Nov 1997)
amyloglucosidase A hydrolase removing terminal alpha-1,4-linked d-glucose residues from nonreducing ends of chains, with release of beta-d-glucose.
Synonym: acid maltase, amyloglucosidase, gamma-amylase, glucoamylase.
(05 Mar 2000)
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)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 1
  • Amyloid - »õâ A type of extracellularly deposited substance composed of an amyloid protein and additional components including HEPARAN SULFATE PROTEOGLYCAN; LAMININ; COLLAGEN TYPE IV; SERUM AMYLOID P-COMPONENT; and APOLIPOPROTEINS E which together form characteristic amyloid fibrils. The core of amyloid fibrils is formed by the stacking of overlapping beta-pleated sheet domains of the amyloid protein. There are many different amyloid proteins that have been found forming the core of the fibrils in vivo. However, amyloid can be formed from any protein that exposes beta-pleated strand conformations during unfolding or refolding. A common characteristic of amyloid is the ability to bind such dyes as CONGO RED and thioflavine.
    Synonyms : Amyloid Fibrils, Amyloid Proteins, Amyloid Substance, Fibrils, Amyloid, Proteins, Amyloid, Substance, Amyloid
  • Amyloid beta-Protein - »õâ A 4-kDa 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.
    Synonyms : ABP (Alzheimer's), Amyloid AD-AP, AD-AP, Amyloid, Alzheimer beta Protein, Amyloid AD AP, Amyloid beta Protein, Protein A4, Amyloid, Protein, beta-Amyloid, beta Amyloid Protein, beta-Protein, Alzheimer, beta-Protein, Amyloid
  • Amyloid beta-Protein Precursor - »õâ 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.
    Synonyms : Amyloid beta Precursor Protein, Amyloid beta Protein Precursor, beta Amyloid Protein Precursor, beta-Protein Precursor, Amyloid
  • Amyloid Neuropathies - »õâ Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary forms have been described. Some familial subtypes demonstrate an autosomal dominant pattern of inheritance. Clinical manifestations include sensory loss, mild weakness, autonomic dysfunction, and CARPAL TUNNEL SYNDROME. (Adams et al., Principles of Neurology, 6th ed, p1349)
    Synonyms : Amyloid Neuropathy, Secondary, Amyloid Polyneuropathies, Amyloid Neuropathies, Secondary, Amyloid Neuropathy, Amyloid Polyneuropathy, Neuropathies, Secondary Amyloid, Neuropathy, Amyloid, Neuropathy, Secondary Amyloid, Polyneuropathies, Amyloid
  • Amyloid Neuropathies, Familial - »õâ Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN.
    Synonyms : Amyloid Polyneuropathy, British Type, Amyloid Polyneuropathy, Iowa Type, Amyloid Polyneuropathy, Swiss Type, Appalachian Type Familial Amyloid Polyneuropathy, British Type Amyloid Polyneuropathy, Familial Amyloid Neuropathy, Andrade Type
¿ÜºÎ ¸µÅ© - Merriam-Webster's ÀÇÇлçÀü ¸ÂÃã °Ë»ö (https://www.merriam-webster.com) °á°ú: 5 ÆäÀÌÁö: 1
¿ÜºÎ ¸µÅ© - A.D.A.M. Medical Encyclopedia ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú: 5 ÆäÀÌÁö: 1
¿ÜºÎ ¸µÅ© - µå·¯±×ÀÎÆ÷ ¾àÇÐ Á¤º¸ ¸ÂÃã °Ë»ö (http://www.druginfo.co.kr) °á°ú: 3 ÆäÀÌÁö: 1
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ÆÇ¸Å»ç
º¸ÇèÄÚµå ¼ººÐ/ÇÔ·®
±¸ºÐ/º¸Çè±Þ¿©
ºñ¹ÙŸÁ¦Ä°¼¿ - »õâ
»ïõ´çÁ¦¾à
A08400801 Amyloliquifase-x conc., Cellulosin AP conc., Pancreatin, Samprose-f conc.
ÀϹÝÀǾàǰ | ºñ±Þ¿©
Äܱ×Áüݼ¿ - »õâ
µ¿±¸Á¦¾à
A11102231 Amylolisin, Bionattomin, Cellulase AP3, Samprose-f conc.
ÀϹÝÀǾàǰ | ºñ±Þ¿©
À寮·Ñݼ¿ - »õâ
»ïõ´çÁ¦¾à
A08402361 Amylolisin, Bionattomin, Cellulase AP3, Samprose-f conc.
ÀϹÝÀǾàǰ | »èÁ¦
KMLE À¥ ¿ë¾î ¸ÂÃã °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
amylolytic of or related to the process of amylolysis
Ãâó: wordnet.princeton.edu/perl/webwn
amyloid a non-nitrogenous food substance consisting chiefly of starch; any substance resembling starch (pathology) a waxy translucent complex protein resembling starch that results from degeneration of tissue starchlike: resembling starch
Ãâó: wordnet.princeton.edu/perl/webwn
amyloidosis a disorder characterized by deposit of amyloid in organs or tissues; often secondary to chronic rheumatoid arthritis or tuberculosis or multiple myeloma
Ãâó: wordnet.princeton.edu/perl/webwn
amylolysis conversion of starch to sugar
Ãâó: wordnet.princeton.edu/perl/webwn
amyloid A protein a pathological fibrillar low-molecular-weight protein occurring in reactive systemic amyloidosis and familial Mediterranean fever; it is antigenically related to the high-molecular-weight serum amyloid A (SAA) protein. Called also AA p. See also amyloid (def. 3).
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
ÇÑ¿µ/¿µÇÑ »çÀü ¸ÂÃã °Ë»ö °á°ú : 4 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • amyloid
    ¾Æ¹Ð·ÎÀ̵å;À¯ÀüºÐü
  • amylopectin
    ¾Æ¹Ð·ÎÆåƾ(ÀüºÐ ÁÖ¼ººÐÀÇ Çϳª)
  • amylopsin
    ¾Æ¹Ð·Ó½Å(³ì¸» ´çÈ­¼Ò)
  • amylose
    ¾Æ¹Ð·Î¿À½º
WordNet ÀÏ¹Ý ¿µ¿µ »çÀü °Ë»ö °á°ú : 9 ÆäÀÌÁö: 1
amylo (pathology) a waxy translucent complex protein resembling starch that results from degeneration of tissue
amylo a nonnitrogenous food substance consisting chiefly of starch
amylo resembling starch
amylo a plaque consisting of tangles of amyloid protein in nervous tissue (a pathological mark of Alzheimer's disease)
amylo a plaque consisting of tangles of amyloid protein in nervous tissue (a pathological mark of Alzheimer's disease)
amylo resembling starch
amylo a disorder characterized by deposit of amyloid in organs or tissues
amylo conversion of starch to sugar
amylo of or related to the process of amylolysis
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