军用子弹的鉴定

军用子弹的鉴定结论关系到犯罪嫌疑罪轻罪重的判断。检验军用子弹,首先要从外观、外形、底火等部分进行特征检验,测量子弹各部分是否符合军用子弹的规定的尺寸,对其称量是否达到一定数值,最后检验子弹的标识。     

新时期统一战线制度建设的理论思考

统一战线制度是对统一战线内部关系的社会规范。加强新时期统一战线建设是党的执政方式发展的需要,是对我国统一战线历史经验教训的深刻总结;在统一战线制度建设上,应从统一战线范围、对象入手,依据统一战线的性质,从政策制度、政治制度、政治体系和机制等方面加以发展和完善。     

高血压大鼠挤压伤后心功能指标与伤病关系分析

目的观察高血压病大鼠肢体挤压后的早期心肌损伤情况,并分析其在伤病关系分析中的意义。方法原发性高血压大鼠按打击程度随机分为4组,用自由落体装置打击大鼠右侧大腿,然后观察血压、心率变化,测量血清生化指标(肌酸激酶、肌酸激酶同功酶、乳酸脱氢酶、肌酐、尿素氮、α-羟丁酸脱氢酶、天门冬氨酸转移酶),并观察大鼠心、脑、肾的形态学改变。结果打击后大鼠血压、心率均有不同程度的上升,并且随着打击力度的增加而增加,但打击组间没有显著性差异。各组血清生化物表现为随打击力度的增加而上升,轻中重打击作为整体损伤组与对照组比较有显著性差异,天门冬氨酸转移酶、肌酸激酶、肌酸激酶同功酶在打击组间比较具有显著性差异。结论挤压性打击损伤造成了SHR早期心肌损伤,并且此指标可以运用于高血压病与损伤共存下的伤病关系分析。     

刑法上之“类推禁止”如何可能? 一个方法论上的悬疑

<正>一、问题的提出在当下中国的刑法理论中,"类推禁止"无疑构成了一种常识。尽管在一般法学方法论上,类推之漏洞补充功能仍然得到普遍承认,但在刑事法领域,基于"法律保留原则"的顽强坚守,此项漏洞补充技术遭到了极为严酷的拒绝。这不仅是因为,类推在形式推理上十分可疑,无法获致完全可靠的逻辑结论;也不仅仅是因为,一旦承认类推,它就极有可能随时突破制定法的文字边界,从而使刑法的客观性、明确性及可预测性等诸多重要价值被彻底虚置;更为重要的是因为,类推从始至终都是罪刑法定原则的"死     

利他合同的基本理论问题

基于“不得为他人缔约”的规则,罗马法上不承认利他合同。欧洲共同法时期受自然法学思想的影响,承认了利他合同,但以第三人的接受作为前提。因为其在实践上的缺陷,这一理论逐渐为新理论所取代,直接承认合同可以对第三人产生效力。建立中国法上的利他合同制度,不宜通过对合同法第64条的解释来实现,而应在完整借鉴大陆法系利他合同理论的基础上,在未来民法典中通过立法的方式来实现。     

9个Y-STR基因座荧光复合扩增系统的法医学应用

目的建立9个Y-STR基因座的复合扩增系统,提高Y-STR的法医学检测效能。方法6-FAM标记DYS434、Y-GATA-A10、DYS438、DYS439,HEX标记DYS531、DYS557、DYS448,TAMRA标记DYS456、DYS444引物,PCR复合扩增,毛细管电泳得到结果,考察扩增系统的个体识别能力、灵敏度、特异性、组织同一性。结果所建立的9个Y-STR复合扩增系统分型清晰,单倍型多样性达0.9968,特异性好,灵敏度高(0.5ngDNA),并且在男女混合斑检验上较常染色体STR分型更有优势。结论9个Y-STR复合扩增系统具有较高的识别能力,对建立Y染色体STR数据库,研究群体遗传学和进行法医学混合斑物证鉴定有重要意义。     

人体器官肺的体积、密度检测及其医学和法医学意义

目的积累不同种族人体器官组织体积和密度的基本数据。为病理学和法医学尸检提供简便、可靠的诊断方法。方法应用电子智能化体积-密度仪,同步检测正常人及各种疾病死者肺的质量、体积、密度。结果获得正常肺和不同程度弥漫性肺水肿病变器官体积和组织密度;在2例医源性循环超负荷和水中毒案件的法医病理学鉴定中,用肺密度值证实了常规病理组织学形态不典型的严重低渗性肺水肿。结论大体检测器官密度对尸体解剖的综合病理诊断具有一定的辅助意义。     

基层派出所的新增效点:警务基础BT模型——以曹杨派出所"社区综合联动机制"为实践样本的思考

上海市公安局普陀分局受网络下载方式的启发,围绕夯实公安基层基础的目标,提出了构建警务基础BT模型的新设想,以"统筹运作、自觉承受、互助共享、实时交互、多点齐动"为要点进行制度设计,并在曹杨派出所进行试点,创建了以"多元化管控、分流化接报、专业化服务"为特点的"社区综合联动机制",在整合社会力量夯实派出所工作基础方面进行了有益探索.可预见,警务基础BT模型在经历"拓展互动范畴、统筹呼应渠道、创新发动手段、发展信息优势、强化市场运作"等方面的升级完善后,必能为基层派出所开辟新的增效空间.     

Forensic genetic analysis of mitochondrial DNA hypervariable region I/II sequences: an expanded Korean population database

We have analyzed variation of the mitochondrial DNA (mtDNA) hypervariable segments I and II (HVS-I and HVS-II) in 185 randomly chosen individuals from Korea to provide an expanded and reliable Korean database. Combined sequence comparison of HVS-I and HVS-II led to the identification of 167 different haplotypes characterized by 154 variable sites. One hundred and fifty-one of the haplotypes were individual-specific, 14 were found in two individuals and 2 were found in three individuals. A pairwise comparison of the 185 HVS-I/II sequences found an average of 10.11 +/- 4.63 differences between individuals. The random match probability and gene diversity for the combined hypervariable regions were estimated at 0.66% and 0.9988, respectively. Analyzing the expanded database including three previously reported data sets and the present data using haplogroup-based comparisons and comparison with closely related sequences allowed errors to be detected and eliminated, thus considerably improving data quality. Sample division comparisons based on PhiST genetic distance measures revealed no significant population differentiation in the distribution of mtDNA sequence variations between the present data set and a database in The Scientific Working Group on DNA Analysis Methods (SWGDAM), but did indicate differences from other sets of data. Based on the results of mtDNA profiles, almost all of the mtDNA types studied here could be classified into subsets of haplogroups common in east Asia, and show that the Koreans possess lineages from both the southern and the northern haplogroup complexes of east Asian populations. The new data, combined with other mtDNA sequences, demonstrate how useful comparison with closely related mtDNA sequences can be for improving database quality, as well as providing haplotype information for forensic and population genetic analyses in the Korean population.     

Genetic polymorphisms for 11 Y-STRs haplotypes of Chinese Yi ethnic minority group

Eleven Y-STRs loci including minimal haplotypes (DYS19, DYS389I, DYS389II, DYS390, DYS391, DYS392, DYS393, and DYS385a,b) and two additional loci, namely DYS438 and DYS439 have been co-amplified in 100 healthy unrelated males of Chinese Yi minority ethnic group using the Y-PLEX 5 and Y-PLEX 6 kit, in order to investigate allele and haplotype frequencies of Yi population, evaluate their usefulness in forensic paternity testing and human identification, and enrich Chinese population genetic informational resources. Out of a total of 100 individuals 85 showed different haplotypes, while 8 haplotypes occurred more than once. The overall haplotype diversity for 11 Y-STRs loci was 0.9945.