Evaluation of genetic parameters of 23 autosomal STR loci in a Southern Chinese Han population
Aim: To evaluate the 23 autosomal short tandem repeat (STR) loci included in GoldenEye™ 25 A kit using forensic human identification and paternity testing.
Hai-xia Li +6 more
doaj +1 more source
Association of polymorphisms in survivin gene with the risk of hepatocellular carcinoma in Chinese han population: a case control study [PDF]
Background Survivin, one of the strongest apoptosis inhibitors, plays a critical role in the development and progression of hepatocellular carcinoma (HCC).
Yuhua Li +4 more
core +2 more sources
Introduction Understanding the etiology and risk factors of lung cancer (LC) is the key to developing scientific and effective prevention and control strategies for LC. CYP4B1 genetic polymorphism has been reported to be associated with susceptibility to
Yongqin Yang +4 more
doaj +1 more source
Single nucleotide polymorphisms in thymic stromal lymphopoietin gene are not associated with allergic rhinitis susceptibility in Chinese subjects [PDF]
BACKGROUND: Thymic stromal lymphopoietin (TSLP) is an epithelial cell-derived cytokine, implicated in the development and progression of allergic diseases.
Claus Bachert +4 more
core +2 more sources
Background Short tandem repeats (STRs) are essential genetic markers for forensic applications and population estimations; thus the population genetics of STR loci have been extensively studied and discussed.
Zhihan Zhou +9 more
doaj +1 more source
Multiple genetic analyses for Chinese Hunan Han population via 46 A-STRs
Background Short tandem repeats (STRs) are important as common genetic markers in forensic identification and population genetics due to their highly polymorphic nature.
Yunying Zhang +7 more
doaj +1 more source
Regional surname affinity: a spatial network approach [PDF]
OBJECTIVE We investigate surname affinities among areas of modern‐day China, by constructing a spatial network, and making community detection.
Chen, Jiawei +5 more
core +1 more source
Identification of a novel neuregulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk haplotype. [PDF]
To access publisher full text version of this article. Please click on the hyperlink in Additional Links fieldTo determine if neuregulin 1 (NRG1) is associated with schizophrenia in Asian populations, we investigated a Han Chinese population using both a
Cai, G +13 more
core +1 more source
MUTYH Association with Esophageal Adenocarcinoma in a Han Chinese Population
Adenocarcinoma of esophagus (AE) is a complex disease, affected by a variety of genetic and environmental factors. Much evidence has shown that the MutY glycosylase homologue (MUTYH) plays a key role in the pathogenesis of many cancers. However, there have been no reports on influence on AE in the Han Chinese population. The objective of this study was
Feng, Kong +9 more
openaire +3 more sources
Spinocerebellar ataxia type 21 exists in the Chinese Han population [PDF]
AbstractRecently, mutations in transmembrane protein 240 (TMEM240) were identified as the cause of spinocerebellar ataxia type 21 (SCA21) in several French families. Clinically, SCA21 is characterized as an early-onset, slowly progressive cerebellar syndrome typically associated with cognitive impairment.
Sheng Zeng +12 more
openaire +2 more sources

