Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Jiayou Chu"'
Autor:
Yunhan Zhang, Xiaoli Dong, Jun Zhang, Miao Zhao, Jiang Wang, Jiayou Chu, Zhaoqing Yang, Shaohui Ma, Keqin Lin, Hao Sun, Zhiling Luo
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-9 (2024)
Abstract Background Ventricular septal defect (VSD) is the most common congenital heart disease. Although a small number of genes associated with VSD have been found, the genetic factors of VSD remain unclear. In this study, we evaluated the associat
Externí odkaz:
https://doaj.org/article/ff512aae6b6c42bfaf5f7b813cff6f10
Autor:
Ye Jin, Miao Zhao, Qiuzhe Guo, Wanyu Zhao, Min Lei, Yifei Zhang, Yunhan zhang, Yan Shen, Keqin Lin, Zhaoqing Yang, Jiayou Chu, Hao Sun, Zhiling Luo
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-7 (2024)
Abstract Background Atrial septal defect (ASD) is a common form of congenital heart disease. Although several genes related to ASD have been found, the genetic factors of ASD remain unclear. This study aimed to evaluate the correlation between 10 can
Externí odkaz:
https://doaj.org/article/90687a0c3b5f438e9a49a84b71660ddf
Autor:
Zhaoqing Yang, Hao Chen, Yan Lu, Yang Gao, Hao Sun, Jiucun Wang, Li Jin, Jiayou Chu, Shuhua Xu
Publikováno v:
BMC Biology, Vol 21, Iss 1, Pp 1-2 (2023)
Externí odkaz:
https://doaj.org/article/81abe6340fba4dea9a9e1a19e658a825
Autor:
Zhaoqing Yang, Hao Chen, Yan Lu, Yang Gao, Hao Sun, Jiucun Wang, Li Jin, Jiayou Chu, Shuhua Xu
Publikováno v:
BMC Biology, Vol 20, Iss 1, Pp 1-20 (2022)
Abstract Background Yunnan is located in Southwest China and consists of great cultural, linguistic, and genetic diversity. However, the genomic diversity of ethnic minorities in Yunnan is largely under-investigated. To gain insights into population
Externí odkaz:
https://doaj.org/article/bf96d34c8d514cb7bb08f44d1ecdc222
Publikováno v:
Virology Journal, Vol 14, Iss 1, Pp 1-10 (2017)
Abstract Background Echovirus 6 (E6) infections are associated with aseptic meningitis and acute flaccid paralysis (AFP). But some infections, sometimes most of them, are asymptomatic. The mechanism of E6 virulence is unknown. Analyses of the molecul
Externí odkaz:
https://doaj.org/article/59d84826936e4b48a2ba79feb84605d2
Autor:
Hao Sun, Zhaoqing Yang, Keqin Lin, Shuyuan Liu, Kai Huang, Xiuyun Wang, Jiayou Chu, Xiaoqin Huang
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0134334 (2015)
Pathogen-driven balancing selection determines the richness of human leukocyte antigen (HLA) alleles. Changes in the pathogen spectrum may cause corresponding changes in HLA loci. Approximately 700 years ago, a Mongolian population moved from the nor
Externí odkaz:
https://doaj.org/article/0dd72992db58410f8839a589ab27bca5
Autor:
Hao Sun, Chi Zhou, Xiaoqin Huang, Keqin Lin, Lei Shi, Liang Yu, Shuyuan Liu, Jiayou Chu, Zhaoqing Yang
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e60822 (2013)
Tai people are widely distributed in Thailand, Laos and southwestern China and are a large population of Southeast Asia. Although most anthropologists and historians agree that modern Tai people are from southwestern China and northern Thailand, the
Externí odkaz:
https://doaj.org/article/03ca97e38e5a495283f979d5fa0a285c
Autor:
Hongbin Lin, Hao Fan, Feng Zhang, Xiaoqin Huang, Keqin Lin, Lei Shi, Songnian Hu, Jiayou Chu, Duen-Mei Wang
Publikováno v:
PLoS ONE, Vol 5, Iss 3, p e9895 (2010)
Population migrations in Southwest and South China have played an important role in the formation of East Asian populations and led to a high degree of cultural diversity among ethnic minorities living in these areas. To explore the genetic relations
Externí odkaz:
https://doaj.org/article/ed17c8834ee14cbcb5fd323f875d8007
Autor:
Baitong, Fan, Xiaoqin, Huang, Xiaochao, Zhang, Lifan, Huang, Zhaoqing, Yang, Shaohui, Ma, Jiayou, Chu, Kai, Huang, Yuting, Weng, Lin, Zhang, Keqin, Lin, Hao, Sun
Publikováno v:
HLA. 101:239-248
By presenting antigen peptides, HLA-DRB1 plays an important role in the immune system. However, the allele frequency of HLA-DRB1 exon 2 across China has not been comprehensively studied, especially in minority populations. We sampled 3757 individuals
Autor:
Lin, Zhang, Wenwu, Li, Yuting, Weng, Keqin, Lin, Kai, Huang, Shaohui, Ma, Jiayou, Chu, Zhaoqing, Yang, Xiaochao, Zhang, Hao, Sun
Publikováno v:
Clinical Genetics. 102:345-349
Limb-Girdle muscular dystrophy (LGMD) is a group of muscle disorders with highly heterogeneous genetic patterns and clinical phenotypes, and this group includes multiple subtypes. Different LGMD subtypes have similar phenotypes and clinical overlaps,