ALP : KMLE 의학 검색 엔진 - 의학사전, 의학용어, 의학약어, 의학논문, 약품/의약품 검색

MeSH(Medical Subject Headings) 맞춤 검색 (http://www.nlm.nih.gov) 결과 : 5 페이지: 5

alpha-L-Fucosidase - 새창 An enzyme that catalyzes the hydrolysis of an alpha L-fucoside to yield an alcohol and L-fucose. Deficiency of this enzyme can cause FUCOSIDOSIS. EC 3.2.1.51.
Synonyms : alpha-Fucosidase, alpha Fucosidase, alpha L Fucosidase
alpha-Linolenic Acid - 새창 A fatty acid that is found in plants and involved in the formation of prostaglandins.
Synonyms : Linolenate, alpha-Linolenic Acid, (E, E, E)-Isomer, alpha-Linolenic Acid, (E, E, Z)-Isomer, alpha-Linolenic Acid, (E, Z, E)-Isomer, alpha-Linolenic Acid, (E, Z, Z)-Isomer, alpha-Linolenic Acid, (Z, E, E)-Isomer, alpha-Linolenic Acid, (Z, E, Z)-Isomer
alpha-Macroglobulins - 새창 Glycoproteins with a molecular weight of approximately 620,000 to 680,000. Precipitation by electrophoresis is in the alpha region. They include alpha 1-macroglobulins and alpha 2-macroglobulins. These proteins exhibit trypsin-, chymotrypsin-, thrombin-, and plasmin-binding activity and function as hormonal transporters.
Synonyms : 45S RNP, Acute-Phase alpha 1-Protein, Slow alpha 2-Globulin, alpha 1-Acute Phase Globulin, alpha 1-Acute Phase Protein, alpha 1-Macroglobulin, alpha 2-Acute Phase Globulin, alpha 2-Glucoprotein, alpha 2-Macroglobulin, alpha-Macrofetoprotein, alpha2-Macroglobulin
alpha-Mannosidase - 새창 An enzyme that catalyzes the HYDROLYSIS of terminal, non-reducing alpha-D-mannose residues in alpha-D-mannosides. The enzyme plays a role in the processing of newly formed N-glycans and in degradation of mature GLYCOPROTEINS. There are multiple isoforms of alpha-mannosidase, each having its own specific cellular location and pH optimum. Defects in the lysosomal form of the enzyme results in a buildup of mannoside intermediate metabolites and the disease ALPHA-MANNOSIDOSIS.
Synonyms : LAMAN, Neutral alpha-Mannosidase, alpha Mannosidase B, alpha-D-Mannosidase, alpha-D-Mannoside Mannohydrolase, Lysosomal alpha Mannosidase, Mannohydrolase, alpha-D-Mannoside, Mannosidase B, alpha, Neutral alpha Mannosidase, alpha D Mannosidase, alpha Mannosidase
alpha-Mannosidosis - 새창 An inborn error of metabolism marked by a defect in the lysosomal isoform of ALPHA-MANNOSIDASE activity that results in lysosomal accumulation of mannose-rich intermediate metabolites. Virtually all patients have psychomotor retardation, facial coarsening, and some degree of dysostosis multiplex. It is thought to be an autosomal recessive disorder.
Synonyms : alpha-Mannosidase Deficiency, Deficiencies, alpha-Mannosidase, Deficiency, alpha-Mannosidase, alpha Mannosidase Deficiency, alpha Mannosidosis, alpha-Mannosidase Deficiencies, alpha-Mannosidoses