Results 41 to 50 of about 6,558 (158)
Abstract Background Over the past decade, the ascent of personalized medicine (PM) has catalyzed pivotal transformations in healthcare systems on a global scale. Recognizing its crucial importance, the European Commission has prioritized PM within its research directives, allocating funding for international collaborative projects, such as the ...
Marzia Di Marcantonio +6 more
wiley +1 more source
Evaluating the Efficiency of REPLI-g?? Single Cell Kit for Trace DNA Amplification [PDF]
Objective To evaluate the efficiency of REPLI-g?? Single Cell Kit for sample DNA amplification, and explore its application value in forensic trace DNA amplification. Methods Three DNA extraction kits were selected to extract DNA from peripheral blood of
XU Qian-nan, SHEN Qiong, ZHANG Jia-yi,et al.
core +1 more source
Cardiac Disease Associated Genetic Variants in Yi Nationality in Regions with High Incidence of Yunnan Sudden Unexplained Death [PDF]
Objective To explore the association of cardiac disease associated genetic variants and the high incidence of Yunnan sudden unexplained death (YNSUD) in Yi nationality.
LIU Kai, WANG Yue-bing, DU Jin-liang,et al
core +1 more source
Geolocation Inference of Forensic Individual Origin by Soil Metagenomic Analysis [PDF]
Objective To preliminarily discuss the feasibility of geolocation inference of forensic individual origin by soil metagenomic analysis. Methods The 33 soil samples from Heilongjiang, Qinghai and Tibet were collected, total bacterial DNA in the samples ...
LIU Wen-li, CHENG Feng, QIAN Jia-lin, et al.
core +1 more source
ABSTRACT Objectives An increased nuchal translucency (NT) thickness of ≥ 3.5 mm is a well‐established marker for congenital anomalies and adverse pregnancy outcome between 11 and 14 weeks' gestation, but little is known about its performance as a screening tool before 11 weeks.
B. B. Bet +5 more
wiley +1 more source
目的探讨光学基因组图谱技术(OGM)在复杂染色体重排中的应用。方法收集2022年1月到2023年6月期间,在中山大学附属第六医院生殖医学中心进行辅助生殖助孕的染色体复杂重排患者5例,对患者进行OGM检测,纳米孔三代测序和胚胎植入前遗传学检测(PGT),并与核型分析、染色体微阵列分析技术(CMA)/基因组拷贝数变异测序(CNV-Seq)的结果分析对比。结果相互易位合并插入,相互易位合并倒位,三联易位均能被OGM成功检测,且与纳米孔测序和CMA/CNV-Seq结果相符。OGM成功定位断裂点位置 ...
何姝婧 +6 more
doaj
自从1975年Kompf等发现乙二醛酶Ⅰ(Glyoxalase Ⅰ GLOI)具有多态性以来,作为一种遗传标记,受到广大人类遗传学及法医学工作者的注意。在法医学上应用于亲权鉴定及个体识别。GLOI的表现型有1—1,2—1,2—2三种,由第6号染色体短臂2区1带2亚带(6P212)上的一对共显性等位基因GLOI~1,GLOI~2控制。虽然后来Rittner等,发现GLOI~0“隐性”基因,但非常罕见 ...
李建金
doaj
Analysis of 28S rRNA and COⅠ Gene Sequence of Nine Necrophagous Calliphorid Flies from Luoyang#br# [PDF]
Objective To assess the feasibility of using 28S ribosomal RNA (28S rRNA) and mitochondrial cytochrome c oxidase subunit Ⅰ (COⅠ) gene sequences of nine necrophagous Calliphorid flies for the identification of common necrophagous Calliphorid flies, and to
ZHAO Lin-lin, ZHAI Xian-dun, ZHENG Zhe,et al.
core +1 more source
CiteSpace-based Document Information Visualization of Literature Published by Journal of Forensic Medicine from 1985 to 2018 [PDF]
Objective To analyze a knowledge web of the literature published by Journal of Forensic Medicine from its founding in 1985 to 2018, describe the evolving process of forensic science research and explore the research hotspots and frontiers at present ...
XIE Xiao-ping, PAN Zhen-jie, WANG Kang,et al
core +1 more source
Research Progresses of Tri-Allelic Patterns in Autosomal STR in Forensic DNA Analysis [PDF]
Tri-allelic pattern in autosomal STR is a common abnormal typing phenomenon in forensic DNA analysis, which brings difficulties and uncertainties to the evaluation of the evidence weight in actual cases. This paper reviews the types, formation mechanism,
Xiao-yan MA, Hong-yu SUN, Qing LI
core +1 more source

