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  • 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
  • amyloidosis cutis
    ÇǺξƹзÎÀ̵åÁõ
  • amyloidosis primary
    ¿ø¹ß¼º(ê«Û¡àõ) ¾Æ¹Ð·ÎÀ̵åÁõ.
  • amyloidosis ulcer
    À¯ÀüºÐÁõ(ëºîþÝÏñø) ±Ë¾ç(Ï÷åË)
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  • 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
  • amyloidosis cutis
    ÇǺξƹзÎÀ̵åÁõ
  • amyloidosis primary
    ¿ø¹ß¼º(ê«Û¡àõ) ¾Æ¹Ð·ÎÀ̵åÁõ.
  • amyloidosis ulcer
    À¯ÀüºÐÁõ(ëºîþÝÏñø) ±Ë¾ç(Ï÷åË)
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amylin Natural hormone produced by pancreatic beta cells that moderates the glucose lowering effects of insulin.
(18 Nov 1997)
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)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 2
  • 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
  • Amyloid Precursor Protein Secretases - »õâ Endopeptidases that are specific for AMYLOID PROTEIN PRECURSOR. Three secretase subtypes referred to as alpha, beta, and gamma have been identified based upon the region of amyloid protein precursor they cleave.
    Synonyms : APP Secretase, Amyloid Precursor Protein Secretase, Secretase, Secretases, alpha-Secretase, beta-Secretase, gamma-Secretase, Secretase, APP, alpha Secretase, beta Secretase, gamma Secretase
  • Amyloidosis - »õâ A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits.
    Synonyms : Amyloidoses
  • Amyloidosis, Familial - »õâ Diseases in which there is a familial pattern of AMYLOIDOSIS.
    Synonyms : Amyloidoses, Familial, Amyloidoses, Hereditary, Familial Amyloidoses, Familial Amyloidosis, Hereditary Amyloidoses, Hereditary Amyloidosis
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amylase any of a group of proteins found in saliva and pancreatic juice and parts of plants; help convert starch to sugar
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...
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amyl of or related to the process of amylolysis
amyl a complex carbohydrate found chiefly in seeds, fruits, tubers, roots and stem pith of plants, notably in corn, potatoes, wheat, and rice
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