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  • ¿µ¹®
    ÇѱÛ
  • D-xylose test
    D-ÀÚÀϷοÀ½º°Ë»ç
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  • D-xylose test
    Å©½Ç·Î¿À½º°Ë»ç
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  • ¿µ¹®
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  • D-dimer
    D-ÀÌÇÕü<ÀÌÁßü>
  • D-dimer
    µð ÀÌÁßü
  • D-JH rearrangement
    D-JH Àç¹è¿­
  • D-related antigen
    D-°ü·ÃÇ׿ø
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  • d-Glucose ceramide
    d-Æ÷µµ´ç ¼¼¶ó¹Ìµå
  • d-penicillamine
    D-Æä´Ï½Ç¶ó¹Î
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  • d-assay
    d-¾Æ½êÀÌ
  • D-configuration
    D-ÀÔüÇü»ó(Ø¡ô÷û¡ßÚ)
  • D-form
    "DÇü(û¡), (å²) dependent form"
  • D-loop
    D ·çÇÁ
  • D-loop synthesis
    D ·çÇÁ ÇÕ¼º(ùêà÷)
  • D-site
    D-ÀÚ¸® (ÔÒ) donor site
  • d-tubocurarine
    d-Åõº¸Äí¶ó¸°
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D-5-HS 5% dextrose in Harman's solution
D-5-S 5% dextrose in saline solution
D-A donor-acceptor
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d-A d-Amphetamine
D-AAO D-Amino acid oxidase
D-AMP D-amphetamine
D-AP5 D(-)-2-amino-5-phosphonovalerate
D-AP5 D-2-Amino-5-phosphonopentanoate
D-ARG D-Arginine
D-ASP D-Aspartic acid
D-ASP D-aspartate
d-cAMP Dibutyryl cyclic AMP
d-DNA denatured DNA
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  • D-amino acid polymer
    D-¾Æ¹Ì³ë»ê ÁßÇÕü
    D-amino »ê¿¡¼­ ÇÕ¼ºÇÏ¿© ¸¸µé¾îÁø Ç׿ø¼ºÀÌ °­ÇÑ ÆéŸÀ̵å, ¶Ç´Â Æú¸® ÆéŸÀ̵å.
  • D-myeloma protein
    D-°ñ¼öÁ¾ ´Ü¹é
    ¸é¿ª ±Û·ÎºÎ¸°ÀÇ ÇÑ ºÎ·ùÀÎ IgD¸¦ »ý»êÇÏ´Â °ñ¼öÁ¾¿¡¼­ ¸¸µé¾îÁø ´Ü¹éÁú.
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D-(-)-phenylglycyl-beta-lactamide amidohydrolase <enzyme> Highly specific for substrates containing an alpha-aminophenylacetic group in the acyl moiety; from xanthomonas sp.
Registry number: EC 3.5.1.-
Synonym: pg-lactamide amidohydrolase
(26 Jun 1999)
D-(-)-tartrate dehydratase <enzyme> From rhodopseudomonas spheroides; does not act on l-(+)-tartrate; forms oxaloacetate
Registry number: EC 4.2.1.-
Synonym: d-(-)-tartrate hydrolyase
(26 Jun 1999)
D-2-hydroxyacid dehydrogenase <enzyme> Substrate may be a specific hydroxy acid; enzyme from trypanosoma cruzi; has been sequenced; genbank u31175 (ddh gene product)
Registry number: EC 1.1.99.6
Synonym: alpha-hydroxyacid dehydrogenase, ddh gene product, staphylococcus aureus, d-lactate dehydrogenase (nad)
(26 Jun 1999)
D-3-hydroxyacyl CoA dehydratase <enzyme> From rat liver peroxisomes; catalyses the epimerization of d-3-hydroxyacyl CoA by the dehydration of 3-hydroxyacyl-CoA to 2-trans-enoyl-CoA followed by the hydration of the latter enzyme to l-3-hydroxyacyl-CoA by enoyl-CoA hydratase (EC 4.2.1.17); is not active on 2-cis-enoyl CoA; consider also EC 4.2.1.74
Registry number: EC 4.2.1.-
Synonym: d-3-hydroxyacyl coenzyme a dehydratase, beta-hydroxyacyl-CoA dehydratase
(26 Jun 1999)
D-alanyl-L-alanine endopeptidase <enzyme> Acts on peptidoglycan
Registry number: EC 3.4.99.-
Synonym: d-ala-l-ala endopeptidase
(26 Jun 1999)
d-altro-2-heptulose <biochemistry> Seven carbon sugar, whose phosphate derivatives are involved in the pentose phosphate pathway and the Calvin Benson cycle.
(18 Nov 1997)
D-amino acid malonyltransferase <enzyme> From mung beans
Registry number: EC 2.3.1.-
Synonym: 1-aminocyclopropanecarboxylate malonyltransferase, d-acc-malonyltransferase, acc n-malonyltransferase
(26 Jun 1999)
D-amino acid transaminase <enzyme> Catalyses the alpha,beta elimination of the (d)-isomer of beta-chloroalanine or other amino acids to yield pyruvate, chloride and ammonia
Registry number: EC 2.6.1.-
(26 Jun 1999)
D-amino acid transferase <enzyme> Mw 41 kD; catalyses d-amino acid transfer; d-configuration specific; recognises aromatic d-amino acid esters to form oligo d-amino acid esters
Registry number: EC 2.3.2.-
(26 Jun 1999)
d-amino-acid oxidase <enzyme> Chemical name: D-Amino-acid:oxygen oxidoreductase (deaminating)
Registry number: EC 1.4.3.3
(12 Dec 1998)
d-aminobutyric acid <enzyme> An enzyme catalyzing the reversible transfer of an amino group from d-aminobutyric acid to 2-oxoglutarate, thus forming a L-glutamic acid and succinate saemialdehyde. An important step in the catabolism of d-aminobutyric acid.
(05 Mar 2000)
d-aminolevulinate dehydratase <enzyme> An enzyme that catalyses the formation of porphobilinogen from two molecules of 5-aminolevulinic acid.
Chemical name: 5-Aminolevulinate hydro-lyase (adding 5-aminolevulinate and cyclizing)
Registry number: EC 4.2.1.24
(12 Dec 1998)
d-aminolevulinate dehydratase porphyria An inherited disorder in which there is a deficiency of porphobilinogen synthase; d-aminolevulinate levels are elevated, leading to neurological disturbances.
Synonym: porphobilinogen synthase porphyria.
(05 Mar 2000)
d-aminolevulinic acid NH2CH2COCH2CH2COOH;an acid formed by d-aminolevulinate synthase from glycine and succinyl-coenzyme A; a precursor of porphobilinogen, hence an important intermediate in the biosynthesis of haematin. ALA levels are elevated in cases of lead poisoning.
(05 Mar 2000)
d-aminolevulinic acid synthase <enzyme> An enzyme that catalyses the reaction of succinyl-CoA with glycine to form d-aminolevulinic acid, coenzyme A, and CO2. The committed step in porphyrin biosynthesis.
Acronym: ALA
(05 Mar 2000)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 1
  • D-Ala(2),MePhe(4),Met(0)-ol-enkephalin - »õâ A stable synthetic analog of methionine enkephalin (ENKEPHALIN, METHIONINE). Actions are similar to those of methionine enkephalin. Its effects can be reversed by narcotic antagonists such as naloxone.
    Synonyms : FK 33-824, FK-33-824, FK-33824, Tyr-Ala-Gly-MePhe-Met-OH, FK 33 824, FK 33824, FK33824, Tyr Ala Gly MePhe Met OH
  • D-Alanine Transaminase - »õâ A PYRIDOXAL PHOSPHATE containing enzyme that catalyzes the reversible transfer of an amino group between D-Alanine and ALPHA-KETOGLUTARATE to form PYRUVATE and D-GLUTAMATE, respectively. It plays a role in the synthesis of the bacterial CELL WALL. This enzyme was formerly classified as EC 2.6.1.10.
    Synonyms : D-Alanine Aminotransferase, D-Glutamate-D-Alanine Transaminase, Aminotransferase, D-Alanine, D Alanine Aminotransferase, D Alanine Transaminase, D Glutamate D Alanine Transaminase, Transaminase, D-Alanine, Transaminase, D-Glutamate-D-Alanine
  • D-Amino-Acid Oxidase - »õâ
    Synonyms : D-Amino Acid Dehydrogenase, Acid Dehydrogenase, D-Amino, Acid Oxidase, dextro-Amino, D Amino Acid Dehydrogenase, D Amino Acid Oxidase, Dehydrogenase, D-Amino Acid, Oxidase, D-Amino-Acid, Oxidase, dextro-Amino Acid, dextro Amino Acid Oxidase
  • D-Aspartate Oxidase - »õâ An FAD-dependent peroxisomal flavoenzyme, this catalyzes the oxidative deamination of D-ASPARTATE to OXALOACETATE and AMMONIA using oxygen as electron acceptor.
    Synonyms : Aspartic Oxidase, D-aspartic Oxidase, D Aspartate Oxidase, D aspartic Oxidase, Oxidase, Aspartic, Oxidase, D-Aspartate, Oxidase, D-aspartic
  • D-Aspartic Acid - »õâ The D-isomer of ASPARTIC ACID.
    Synonyms : 3-hydroxy-N-(2-methyl-1-oxo-2-propenyl)-, D Aspartate, D Aspartic Acid
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A12950241 Alfacalcidol
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A15103742 D-sorbitol, L-arginine, L-histidine, L-leucine, L-lsoleucine, L-lysine HCl, L-methionine, L-phenylalanine, L-proline, L-threonine, L-tryptophan, L-valine
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A07102101 D-sorbitol, L-arginine, L-histidine, L-leucine, L-lsoleucine, L-lysine HCl, L-methionine, L-phenylalanine, L-proline, L-threonine, L-tryptophan, L-valine
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D-amino-acid oxidase (D-ami
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D-dimer D-dimer is an end product derived from plasmin-mediated degradation of crosslinked fibrin clots. D-dimer measurement has proved to be a sensitive marker for the evaluation of disseminated intravascular coagulation (DIC). In addition, D-dimer can effectively rule out those patients with a low or a moderate probability of venous thromboembolism (VTE) such as deep vein thrombosis (DVT) or pulmonary embolism (PE).
Ãâó: www.dpcweb.com/medical/heartdisease/glossary.html
D-dimer a. an immunoassay for the fibrin degradation product D dimer. Levels are elevated in deep venous thrombosis, acute myocardial infarction, pulmonary embolism, unstable angina, and disseminated intravascular coagulation (DIC). Called also D-dimer test.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
D-dimer t. see under assay.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
d-xylose absorption t. (for differential diagnosis in malabsorption syndromes): after the oral administration to a fasting adult of 25 g (or sometimes 5 g) of D-xylose dissolved in 250 mL of water, followed immediately by an additional 250 mL of water, the amount excreted in the urine during a 5-hour period is determined. Since poor renal function may also result in low xylose absorption, blood levels are also determined at two hours. Normally, more than 4.0 g of xylose should be excreted over the 5-hour period; less than this amount suggests intestinal malabsorption. Blood values are normally more than 25 mg xylose per 100 mL of blood.
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d- day of the allied landing in France, World War II
d- the lowest region of the ionosphere (35 to 50 miles up) that reflects low-frequency radio waves
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