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forensic
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  法医学
    A Study of Quadriplex PCR with Chimeric Primers for STR Loci and Validation in Forensic Science
    STR基因座嵌合引物复合扩增及其法医学应用研究
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    The Study of HLA-B Gene Polymorphism to Forensic Medicine Applications
    HLA-B基因多态性在法医学中的应用研究
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    A Systemic Study of Whole Genome Amplification Technology and Its Applications in Forensic Science
    全基因组扩增技术应用于法医学实践的系统研究
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    Analysis of Mitochondrial DNA Polymorphisms Based on Denaturing High-Performance Liquid Chromatography and Its Study in Forensic Application
    线粒体DNA多态的变性高效液相色谱分析及其法医学应用研究
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    Forensic medical autopsy findings on 600 cases with fatal traffic accidents
    600起重、特大交通事故死亡的法医学分析
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  法医
    A Study of Species Identification Based on Molecular Biology in Forensic Entomology
    法医昆虫种属鉴定的分子生物学方法研究
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    Exploring Novel STR Loci on Human Chromosome 21 for Forensic and Medical Genetics
    人类21号染色体新STR遗传标记的法医及医学遗传学研究
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    A Study of Species Identification for Forensic Ichthyology
    法医鱼类学种属鉴别初步研究
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    The Forensic Pathological Studies of Brain Death Ⅰ.—35 Cases of Morphological Studies of Brain Trauma.
    脑死亡法医病理学研究—Ⅰ.钝力所致35例脑损伤形态学研究
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    Forensic Pathological Study of Brain Death in 120 Cases and Application of Posterior Arch-Ectomy (P.A.E) of Atlas
    120例脑死亡法医病理学研究及《环椎后弓切除术式》应用
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  “forensic”译为未确定词的双语例句
    The study of forensic application of DNA amplification for sex determination(Ⅰ)
    DNA体外扩增技术在法庭科学性别鉴定中的应用研究(Ⅰ)
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    A New Statistical Model and Method for Testing Check Samples and Control Samples in Forensic Science
    检验检材和比对的一种新的统计模型和方法
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    ANALYSIS OF FORENSIC PSYCHIATERIC EVALUATION OF 64 HOMCIDE CASES
    64例凶杀案司法精神鉴定
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    SUBSCRIPTION FOR 1996 JOURNAL OF FORENSIC MEDICE
    SUBSCRIPTION FOR 1996 JOURNAL OF FORENSIC MEDICE
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    Application of MS/MS to Forensic Science
    MS/MS在刑事科学技术中的一些应用
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  forensic
A method for identifying the writing age of blue ballpoint pen ink has been established due to the imperative demand in forensic laboratories.
      
A procedure is developed for the quantitative determination of diacetylmorphine and its concomitants, including acetylated opioid derivatives, in forensic samples.
      
Chromatographic Techniques in Forensic Chemical Examinations
      
Some aspects of the use of chromatographic analytical techniques in the forensic chemical examination of materials, substances, and products were considered.
      
The procedure is intended for forensic chemical analysis in cases of opiate poisoning.
      
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Since the HLA system is one of the most complex human genetic polym- orphisms,its application in forensic medicine included disputed paternity and criminal identification,have been fairly recognized. The present paper reported the results of our study about the HLA typing in human blood stain,serum and saliva,it was concluded that:(1).The existed strong anti-complementary activity in human blood stain when the amount of complement used in microlym-phocytotoxicity inhibition test(MLIT) was incresed to 10μl,it...

Since the HLA system is one of the most complex human genetic polym- orphisms,its application in forensic medicine included disputed paternity and criminal identification,have been fairly recognized. The present paper reported the results of our study about the HLA typing in human blood stain,serum and saliva,it was concluded that:(1).The existed strong anti-complementary activity in human blood stain when the amount of complement used in microlym-phocytotoxicity inhibition test(MLIT) was incresed to 10μl,it was found that the results of HLA-All,-B 5 typing in bloodstains were all correct,and the detectable period was at least 90 days; (2).The soluble HLA-A antigens in human serum could reliable detected with MLIT;(3).The soluble HLA-A antigens were also present in the human siliva.

HLA 是迄今人类最复杂的遗传多态性系统,其在法医学上的应用,包括亲子鉴定和个人识别的重要性日益被认识。作者等对血痕、血清和唾液的 HLA 测定的研究结果证明:(1)血痕中存在较强的抗补体作用。应用淋巴细胞毒抑制试验测定血痕的 HLA 时,增加补体用量可使测定的正确率达100%,经90天的血痕仍能完全正确检出 HLA 型。(2)血清的 HLA 测定是可行的,这对远道送检血清及尸体血清测定 HLA 有一定价值。(3)唾液中有可溶性 HLA 抗原存在。

A high performance liquid chromatographic method has been improved for determination of aconitine in rabbit blood using a reversed phase chromatographic column (YWG-C_(18)H_(37),10μm) and a precolumn(Micro-pak, 5μm, 40×4mm I.D.), with tetracaine as internal standard and methanal-0.05mol/L ammonium carb onate-dichlormethane(90:10:2) as mobile phase. It is more simple, more precise, more specific, more rapid and ecnomical than other assays using in forensic toxicological poison analysis at present. The procedure...

A high performance liquid chromatographic method has been improved for determination of aconitine in rabbit blood using a reversed phase chromatographic column (YWG-C_(18)H_(37),10μm) and a precolumn(Micro-pak, 5μm, 40×4mm I.D.), with tetracaine as internal standard and methanal-0.05mol/L ammonium carb onate-dichlormethane(90:10:2) as mobile phase. It is more simple, more precise, more specific, more rapid and ecnomical than other assays using in forensic toxicological poison analysis at present. The procedure is as follows: Take 2 mL of rabbit blood, add 20 μL of the internal standard (50μg/mL), 5 mL of ether and TmL of ammonia(2.5%). Shake for 10 minutes and centrifuge for 10 minutes at 5000r/min. The residue is extracted with the same ammount fresh ether for two times as above. The combination of ether which is taken out three times is mixed with 1 mL of 0.1 N hydrochloric acid. Evaporate the ether to 5 mL at 40℃ and under nitrogen gas flow, then draw the remaining ether out. Mix the acid phase with 1 mL of dichlormethane and 1 mL of ammonia (2.5%), centrifuge for 5 minutes. Take the upper layer out and evaporate the lower in the changed KD enrichment installation to dryness at 40℃ under nitrogen gas flow and lower preesure. Reconstitute the residue with 100μL of methanol and inject 40μL into the chromatograph. The mean recovery of aconitine was 96.75% and coefficient variation was 5.49%. The method was liner from 0.1 to 5.0μg/2mL with correlation coefficient of 0.9992. Toxicokinetics of aconitine was studied with HPLC as above in 10 rabbits after intravenous injection at a dose of 0.06mg/kg. The results showed that the curve of the logarithm of the concentration of aconitine in blood versus time fitted well to a two compartment model. The following toxicokinetic parameters were obtained: T1/2α 1.4682min, T1/2β 34.1379min, K_(12) 0.2418min~(-1), K_(21) 0.2035 min~(-1), V_1 31.6012 mL/kg, V_2 41.7181 mL/kg, Cl 1.4885 mL/min. Elimination of aconitine from rabbit was mainly in urine and within 6 hours after injection.

本文应用甲醇-0.05mol/L碳酸铵水溶液-二氯甲烷(90:10:2)作流动相,在YWGC_(18)H_(37)反相键合相色谱柱上分离乌头碱和内标,用紫外分光检测器在235nm外定量,改进了动物组织内痕量乌头碱的HPLC检测法。运用该法检测家兔静脉注射乌头碱后的血毒物浓度,初步研究了乌头碱在家兔体内的代谢动力学过程,表明其体内过程符合开放二室模型,T_(1/2α)=1.4682min,T_(1/2β)=34.1379min。体内乌头碱可以原形由尿和胆汁中排出,但以前6h尿排泄为主。

Methaqualone and 2-methyl-3 [2- (hydroxymethyl) phenyl]- 4 (3H) quinazolinone (metabolite I) concentrations in human serum wereanalyzed quantitatively by reverse high performance liquid chromatography (RP-HPLC). The concentrations of methaqualone ranging from 1-35μg/ml were in good linear relationship(Correlation coefficient r = 0. 9980, regression line y = 0. 06324x-0. 1029), The average recovery of methaqualone reached as high as 102.08±9. 987(SD)% (n= 5). The detective limit was 1 ng. The relative quantity...

Methaqualone and 2-methyl-3 [2- (hydroxymethyl) phenyl]- 4 (3H) quinazolinone (metabolite I) concentrations in human serum wereanalyzed quantitatively by reverse high performance liquid chromatography (RP-HPLC). The concentrations of methaqualone ranging from 1-35μg/ml were in good linear relationship(Correlation coefficient r = 0. 9980, regression line y = 0. 06324x-0. 1029), The average recovery of methaqualone reached as high as 102.08±9. 987(SD)% (n= 5). The detective limit was 1 ng. The relative quantity of metabolite I was determined according to the linear concentration of methaqulone. RP-HPLC assay is proved to be useful in determening blood methaqualone and metabolite I concentrations in forensic toxicology.

本文建立了用反相高效液相色谱法(RP-HPLC)测定人血清中安眠酮及其苯甲基羟化代谢物-2-甲基-3[2-(羟甲基)-苯基]-4(3H)喹唑酮(Ⅰ)的浓度。安眠酮浓度在1-35μg/ml范围内呈直线相关(相关系数r=0.9980;回归方程y=0.06324x—0.1029),方法回收率平均为102.08±9.987(SD)%(n=5),检出限为1ng。其代谢物Ⅰ按原型安眠酮的线性浓度测定其相对量。本法为测定中毒者体内安眠酮及其代谢物Ⅰ的血浓度提供可行的手段。

 
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