Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Lu-Shun Zhang"'
Publikováno v:
Frontiers in Aging Neuroscience; 1/28/2024, p1-15, 15p
Publikováno v:
International Journal of Legal Medicine. 131:975-977
Application of X-STRs as complements of autosomal STR application in the forensic genetics has become a tendency for kinship testing, especially in deficiency paternity cases. Recently, a novel kit of 19 X-STR loci was developed, which permitted the
Publikováno v:
Andrologia. 48:193-197
Summary Growing evidences have suggested the association between interleukin-27 and cryptorchidism. We aimed to investigate the relationship between IL-27 polymorphisms and cryptorchidism susceptibility. A total of 519 males were enrolled in a case
Publikováno v:
Forensic Science International: Genetics Supplement Series. 5:e630-e632
MicroRNA is a promising marker for forensic body identification especially in compromised samples and mixtures because of its small size and tissue specific expression manner. Previously, five research groups have reported specific miRNAs screened fr
Autor:
Jingqiang Zhu, Weibo Liang, Li Wang, Hui Wang, Lu-Shun Zhang, Jiong Mao, Youjing Jiang, Qin Su, Zhilong Li, Duo Peng
Publikováno v:
Forensic Science International: Genetics Supplement Series. 5:e674-e676
MicroRNAs (miRNAs) have been proven to exist in forensically relevant body fluids. However, we need to know whether the result would be influenced by other species' saliva. This study aims to analyze the expression levels of 3 miRNA markers in differ
Autor:
M. Sirker, Weibo Liang, Markus A. Rothschild, Iva Gomes, Rolf Fimmers, Lu-Shun Zhang, Peter M. Schneider
Publikováno v:
Forensic Science International: Genetics Supplement Series. 5:e199-e201
For the analysis of cell type-specific miRNA expression patterns qPCR is currently the method of choice owing to its high accuracy. However, to obtain reliable results, a proper normalization strategy is an absolute prerequisite, which is often under
Publikováno v:
Forensic Science International: Genetics Supplement Series. 5:e598-e600
The short tandem repeat (STR) and single nucleotide polymorphisms (SNP) are widely distributed in human genomes. SNP-STR, a compound genetic marker combining a STR locus with tightly linked SNPs, is more informative than any single polymorphism. The
Association between genetic variants in pre-miRNA and colorectal cancer risk in a Chinese population
Publikováno v:
Journal of Cancer Research and Clinical Oncology. 139:1405-1410
Single-nucleotide polymorphisms (SNPs) in pre-miRNAs may alter microRNA expression levels or processing and then contribute to the susceptibility of cancer development. We hypothesized that SNPs in pre-miRNAs may be associated with the risk of colore
Publikováno v:
DNA and Cell Biology. 32:268-273
Growing evidence suggests that the angiotensin-converting enzyme (ACE) and endothelial nitric oxide synthase (eNOS) genes are associated with risk in a wide range of cancers. The objective of this study was to examine whether two DNA polymorphisms at
Publikováno v:
Molecular Medicine Reports. 7:1494-1500
Basigin may be involved in cardiovascular disease. In our previous study, suppression subtractive hybridization results indicated that basigin may be associated with the early phase of acute myocardial ischemia (AMI) within 1 h. However, little is kn