Results 51 to 60 of about 771,775 (343)

Regional surname affinity: a spatial network approach [PDF]

open access: yes, 2019
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

RETRACTED: Genetic polymorphism and phylogenetic analyses of 21 non‐CODIS STR loci in a Chinese Han population from Shanghai

open access: yesMolecular Genetics & Genomic Medicine, 2020
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

Missense variants in CYP4B1 associated with increased risk of lung cancer among Chinese Han population

open access: yesWorld Journal of Surgical Oncology, 2023
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

Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population [PDF]

open access: yes, 2015
Background: Ventricular septal defects (VSDs) constitute the most prevalent congenital heart disease (CHD), occurs either in isolation (isolated VSD) or in combination with other cardiac defects (complex VSD).
Bailin Wu   +12 more
core   +1 more source

Platelet to lymphocyte ratio is associated with the severity of coronary artery disease and clinical outcomes of percutaneous coronary intervention in the Chinese Han population.

open access: yesExperimental and Therapeutic Medicine, 2017
The aim of the present study was to evaluate whether the ratio of the absolute number of platelets to the number of lymphocytes (PLR) correlates with the severity of coronary artery disease (CAD) and major adverse cardiovascular disease (CVD) events in ...
Dong Zhou   +4 more
semanticscholar   +1 more source

MMP8 and MMP9 gene polymorphisms were associated with breast cancer risk in a Chinese Han population

open access: yesScientific Reports, 2018
Matrix metalloproteinases (MMPs) are a group of zinc-dependent endopeptidases that can breakdown almost all extracellular matrix components. MMP8 and MMP9 have been shown to be associated with breast cancer (BC) risk in European and American populations.
Kai Wang   +10 more
semanticscholar   +1 more source

Single nucleotide polymorphisms in thymic stromal lymphopoietin gene are not associated with allergic rhinitis susceptibility in Chinese subjects [PDF]

open access: yes, 2012
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

Association between SNPs in microRNA machinery genes and gastric cancer susceptibility, invasion, and metastasis in Chinese Han population

open access: yesOncoTarget, 2017
Objective The present study investigates the influence of genetic variants in miRNA machinery genes (DROSHA, DICER, AGO1, and GEMIN4) on gastric cancer in Chinese Han population, further revealing the genetic mechanisms of gastric cancer occurrence and ...
Xing-bo Song   +7 more
semanticscholar   +1 more source

MUTYH Association with Esophageal Adenocarcinoma in a Han Chinese Population

open access: yesAsian Pacific Journal of Cancer Prevention, 2013
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]

open access: yesScientific Reports, 2016
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

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