| ¿µ¹® | sex identification | ÇÑ±Û | ¼º°¨º° |
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| ¿µ¹® | penicillin | ÇÑ±Û | Æä´Ï½Ç¸° |
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| ¼³¸í | Ç×»ýÁ¦ÀÇ ÀÏÁ¾. °¡Àå Ãʱ⿡ °³¹ßµÈ Ç×»ýÁ¦·Î ¸¹Àº Á¾·ùÀÇ º´±ÕÀ» Á×ÀÏ ¼ö ÀÖÀ¸¸ç, ºÎÀÛ¿ëÀº °ÅÀÇ ¾ø´Ù. ¾ÆÁ÷µµ °¡Àå ¸¹ÀÌ ¾²ÀÌ´Â Ç×»ýÁ¦ÀÇ ÇϳªÀÌÁö¸¸, ÀϺο¡¼ Æä´Ï½Ç¸°¼îÅ©(¾Ë·¹¸£±â¹ÝÀÀÀÇ ÀÏÁ¾À¸·Î »ý¸í¿¡ Å©°Ô À§ÇèÇÏ´Ù)°¡ ³ªÅ¸³ª±â ¶§¹®¿¡ ²¨¸®±âµµ ÇÑ´Ù. |
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| ChemID | Chemical Identification; Chemical Identification File |
|---|---|
| AUDIT | alcohol use disorders identification test |
| BAIT | bacterial automated identification technique |
| FPI | femoral pulsatility index; fluid percussion injury; formula protein intolerance; Freiburg Personalit... |
| HMIS | hazardous materials identification system; hospital medical information system |
| penicillin V | phenoxymethyl-penicillin |
|---|---|
| AUDIT | Alcohol Use Disorder Identification Test |
| MIS | Microbial Identification System |
| PIR | Protein Identification Resource |
| SSI | Synthetic Sentence Identification |
| animal identification systems | Procedures for recognizing individual animals and certain identifiable characteristics pertaining to them; includes computerised methods, ear tags, etc. (12 Dec 1998) |
|---|---|
| patient identification systems | Organised procedures for establishing patient identity, including use of bracelets, etc. (12 Dec 1998) |
| social identification | The process wherein the individual so strongly feels himself a member of a group that he adopts its ideas, beliefs, and habits. (12 Dec 1998) |
| denture identification marking | Any system of defining ownership of dentures or dental prostheses. (12 Dec 1998) |
| identification | <psychology> An unconscious defense mechanism by which an individual endeavors to pattern himself after another person. This process is also important in the development of the personality, particularly the superego or conscience, which is modeled largely on the behaviour of adult significant others. (18 Nov 1997) |
| field identification | <zoology> The determination of the taxonomic identity of an individual specimen, under field conditions, often with the aid of keys etc. See: Identification. (09 Jan 1998) |
| aluminum penicillin | The trivalent aluminum salt of an antibiotic substance or substances produced by the growth of the molds Penicillium notatum or P. Chrysogenum; used for oral or sublingual administration. (05 Mar 2000) |
| benzyl penicillin | <chemical> (2s-(2 alpha,5 alpha,6 beta))-3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid. A penicillin derivative commonly used in the form of its sodium or potassium salts in the treatment of a variety of infections. It is effective against most gram-positive bacteria and against gram-negative cocci. It has also been used as an experimental convulsant because of its actions on gaba mediated synaptic transmission. Pharmacological action: convulsants, gaba modulators, penicillins. Chemical name: 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)- (2S-(2alpha,5alpha,6beta))- (12 Dec 1998) |
| buffered crystalline penicillin G | Crystalline potassium penicillin G or crystalline sodium penicillin G buffered with not less than 4% and not more than 5% of sodium citrate. (05 Mar 2000) |
| penicillin | <drug> Probably the best known of the antibiotics, derived from the mould Penicillium notatum. It blocks the cross linking reaction in peptidoglycan synthesis and therefore destroys the bacterial cell wall making the bacterium very susceptible to damage. (18 Nov 1997) |
| penicillin amidase | <enzyme> An enzyme catalyzing the hydrolysis of penicillin to penicin and a carboxylic acid anion. Chemical name: Penicillin amidohydrolase Registry number: EC 3.5.1.11 (12 Dec 1998) |
| penicillin B | A penicillin preparation that is stable in gastric acid and is rapidly but only partially absorbed from the gastrointestinal tract. Synonym: alpha-phenoxyethylpenicillin potassium, penicillin B. (05 Mar 2000) |
| penicillin G | <chemical> (2s-(2 alpha,5 alpha,6 beta))-3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid. A penicillin derivative commonly used in the form of its sodium or potassium salts in the treatment of a variety of infections. It is effective against most gram-positive bacteria and against gram-negative cocci. It has also been used as an experimental convulsant because of its actions on gaba mediated synaptic transmission. Pharmacological action: convulsants, gaba modulators, penicillins. Chemical name: 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)- (2S-(2alpha,5alpha,6beta))- (12 Dec 1998) |
| penicillin G benzathine | <chemical> Semisynthetic antibiotic that is a relatively insoluble preparation that may remain in the body for 1 to 2 weeks, and prepared by combining the sodium salt of penicillin G with n,n'-dibenzylethylenediamine. Pharmacological action: penicillins. Chemical name: 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)- (2S-(2alpha,5alpha,6beta))-, compd. With N,N'-bis(phenylmethyl)-1,2-ethanediamine (2:1) (12 Dec 1998) |
| penicillin G hydrabamine | A dipenicillin compound, a mixture of penicillin G salts consisting chiefly of the salt of the diacidic base N,N '-bis-(dehydroabietyl) ethylenediamine. (05 Mar 2000) |
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