Search Results - "Lin, Keqin"

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  1. 1

    FLT4 gene polymorphisms influence isolated ventricular septal defect predisposition in a Southwest China population by Zhang, Yunhan, Dong, Xiaoli, Zhang, Jun, Zhao, Miao, Wang, Jiang, Chu, Jiayou, Yang, Zhaoqing, Ma, Shaohui, Lin, Keqin, Sun, Hao, Luo, Zhiling

    Published in BMC medical genomics (06-08-2024)
    “…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…”
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  2. 2

    Exploring Genetic Diversity of SOD2 and POU5F1 for Congenital Heart Disease in the Southwest Chinese Population by Jin, Ye, Zhang, Jun, Guo, Qiuzhe, Dong, Xiaoli, Li, Jian, Wang, Jiang, Li, Shuang, Shen, Yan, Lin, Keqin, Yang, Zhaoqing, Chu, Jiayou, Sun, Hao, Luo, Zhiling

    Published in International Heart Journal (31-07-2024)
    “…Congenital heart disease (CHD) accounts for nearly one-third of all major congenital anomalies, with atrial septal defect (ASD) and ventricular septal defect…”
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  3. 3

    Association study of FLT4 and HYDIN single nucleotide polymorphisms with atrial septal defect susceptibility in the Han Chinese population of Southwest China by Jin, Ye, Zhao, Miao, Guo, Qiuzhe, Zhao, Wanyu, Lei, Min, Zhang, Yifei, Zhang, Yunhan, Shen, Yan, Lin, Keqin, Yang, Zhaoqing, Chu, Jiayou, Sun, Hao, Luo, Zhiling

    Published in Italian journal of pediatrics (05-04-2024)
    “…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…”
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  4. 4

    Association between gene polymorphisms of voltage-dependent Ca2+ channels and hypertension in the Dai people of China: a case-control study by Huang, Lifan, Chu, Yan, Huang, Xiaoqin, Ma, Shaohui, Lin, Keqin, Huang, Kai, Sun, Hao, Yang, Zhaoqing

    Published in BMC medical genetics (28-02-2020)
    “…Abstract Background Abnormal calcium homeostasis related to the development of hypertension. As the key regulator of intracellular calcium concentration,…”
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  5. 5

    Mitochondrial haplogroup M9a1a1c1b is associated with hypoxic adaptation in the Tibetans by Li, Qian, Lin, Keqin, Sun, Hao, Liu, Shuyuan, Huang, Kai, Huang, Xiaoqin, Chu, Jiayou, Yang, Zhaoqing

    Published in Journal of human genetics (01-12-2016)
    “…While hypoxic environment at high altitude remains a major challenge for travelers from low-altitude areas, Tibetans have adapted to the high-altitude…”
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  6. 6

    The Adaptive Change of HLA-DRB1 Allele Frequencies Caused by Natural Selection in a Mongolian Population That Migrated to the South of China by Sun, Hao, Yang, Zhaoqing, Lin, Keqin, Liu, Shuyuan, Huang, Kai, Wang, Xiuyun, Chu, Jiayou, Huang, Xiaoqin

    Published in PloS one (31-07-2015)
    “…Pathogen-driven balancing selection determines the richness of human leukocyte antigen (HLA) alleles. Changes in the pathogen spectrum may cause corresponding…”
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  7. 7

    Molecular evolution of two asymptomatic echovirus 6 strains that constitute a novel branch of recently epidemic echovirus 6 in China by Sun, Hao, Huang, Xiaoqin, Lin, Keqin, Huang, Kai, Chu, Jiayou, Yang, Zhaoqing, Ma, Shaohui

    Published in Virology journal (25-07-2017)
    “…Echovirus 6 (E6) infections are associated with aseptic meningitis and acute flaccid paralysis (AFP). But some infections, sometimes most of them, are…”
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  8. 8

    Autosomal STRs provide genetic evidence for the hypothesis that Tai people originate from southern China by Sun, Hao, Zhou, Chi, Huang, Xiaoqin, Lin, Keqin, Shi, Lei, Yu, Liang, Liu, Shuyuan, Chu, Jiayou, Yang, Zhaoqing

    Published in PloS one (08-04-2013)
    “…Tai people are widely distributed in Thailand, Laos and southwestern China and are a large population of Southeast Asia. Although most anthropologists and…”
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  9. 9

    Genetic relationships of ethnic minorities in Southwest China revealed by microsatellite markers by Lin, Hongbin, Fan, Hao, Zhang, Feng, Huang, Xiaoqin, Lin, Keqin, Shi, Lei, Hu, Songnian, Chu, Jiayou, Wang, Duen-Mei

    Published in PloS one (29-03-2010)
    “…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…”
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  10. 10

    Correlation between the linguistic affinity and genetic diversity of Chinese ethnic groups by Sun, Hao, Zhou, Chi, Huang, Xiaoqin, Liu, Shuyuan, Lin, Keqin, Yu, Liang, Huang, Kai, Chu, Jiayou, Yang, Zhaoqing

    Published in Journal of human genetics (01-10-2013)
    “…As the world's most populous nation, China exhibits a population with 56 nationalities. We already know the associations between genetic relationship of these…”
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  11. 11

    Distribution of HLA alleles and haplotypes in Jinuo and Wa populations in Southwest China by Shi, Li, Ogata, Saeko, Yu, Jian Kun, Ohashi, Jun, Yu, Liang, Shi, Lei, Sun, Hao, Lin, Keqin, Huang, Xiao Qin, Matsushita, Masaki, Horai, Satoshi, Muramatsu, Masaaki, Chu, Jia You, Tokunaga, Katsushi

    Published in Human immunology (2008)
    “…Summary The frequencies of human leukocyte antigen (HLA) alleles HLA-A, -B, and -DRB1 alleles and A-B-DRB1, A-B, and B-DRB1 haplotypes were studied in Jinuo…”
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  12. 12

    Difference in microbial community structure along a gradient of crater altitude: insights from the Nushan volcano by Chen, Jin, Cui, Ye, Xiao, Qingchen, Lin, Keqin, Wang, Boyan, Zhou, Jing, Li, Xiaoyu

    Published in Applied and environmental microbiology (21-08-2024)
    “…The variation in the soil microbial community along the altitude gradient has been widely documented. However, the structure and function of the microbial…”
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  13. 13

    A novel mutation alters GNE bifunctional enzyme activity and leads to familial inherited GNE diseases by Li, Yufei, Li, Wenwu, Fan, Baitong, Zhang, Yao, Li, Zhaoqing, Lin, Keqin, Huang, Kai, Yang, Zhaoqing, Ma, Shaohui, Sun, Hao

    Published in Gene (15-11-2024)
    “…•Identified a novel pathogenic GNE gene mutation: NP_005467.1:p.S663L.•p.S663L reduces GNE enzyme activity without changing protein expression.•Mutation…”
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  14. 14

    A novel splice site variant in the POPDC3 causes autosomal recessive limb‐girdle muscular dystrophy type 26 by Zhang, Lin, Li, Wenwu, Weng, Yuting, Lin, Keqin, Huang, Kai, Ma, Shaohui, Chu, Jiayou, Yang, Zhaoqing, Zhang, Xiaochao, Sun, Hao

    Published in Clinical genetics (01-10-2022)
    “…Limb‐Girdle muscular dystrophy (LGMD) is a group of muscle disorders with highly heterogeneous genetic patterns and clinical phenotypes, and this group…”
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  15. 15

    Comprehensive research on the distribution of HLA‐DRB1 in C hinese populations by Fan, Baitong, Huang, Xiaoqin, Zhang, Xiaochao, Huang, Lifan, Yang, Zhaoqing, Ma, Shaohui, Chu, Jiayou, Huang, Kai, Weng, Yuting, Zhang, Lin, Lin, Keqin, Sun, Hao

    Published in HLA : immune response genetics (01-03-2023)
    “…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…”
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  16. 16

    Comprehensive research on the distribution of HLA‐DRB1 in Chinese populations by Fan, Baitong, Huang, Xiaoqin, Zhang, Xiaochao, Huang, Lifan, Yang, Zhaoqing, Ma, Shaohui, Chu, Jiayou, Huang, Kai, Weng, Yuting, Zhang, Lin, Lin, Keqin, Sun, Hao

    Published in HLA (01-03-2023)
    “…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…”
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  17. 17

    Three Novel Genetic Variants in the FAM110D, CACNA1A, and NLRP12 Genes Are Associated With Susceptibility to Hypertension Among Dai People by Zhang, Lin, Sun, Yun, Zhang, Xiaochao, Shan, Xiyun, Li, Jianmei, Yao, Yao, Shu, Yun, Lin, Keqin, Huang, Xiaoqin, Yang, Zhaoqing, Chu, Jiayou, Huang, Lifan, Sun, Hao

    Published in American journal of hypertension (09-08-2021)
    “…Abstract BACKGROUND Although the genetic factors associated with hypertension remain unknown, genetic variations in genes related to ion channels,…”
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  18. 18

    A novel mutation causes Hermansky-Pudlak syndrome type 4 with pulmonary fibrosis in 2 siblings from China by Wu, Wenjuan, Lin, Keqin, Yang, Yanni, Dong, ZhaoXing, Zhang, Tao, Lei, Wen, Yang, Weimin, Yang, Zhaoqing

    Published in Medicine (Baltimore) (01-08-2019)
    “…Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive multisystem disorder characterized by oculocutaneous albinism (OCA) and bleeding diathesis,…”
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  19. 19

    Molecular characterization of Coxsackievirus A16 strains isolated from children with severe hand, foot, and mouth disease in Yunnan, Southwest China, during 2009‐2015 by Zhang, Ming, Zhao, Yilin, Zhang, Haihao, Lin, Keqin, Liu, Hongbo, Zhang, Jie, Ding, Lisha, Huang, Xiaoqin, Yang, Zhaoqing, Ma, Shaohui

    Published in Journal of medical virology (01-01-2019)
    “…Coxsackievirus A16 (CV‐A16) commonly causes mild symptoms, but severe diseases, such as aseptic meningitis, encephalitis, and even fatal cases, have been…”
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  20. 20

    Differences in mtDNA whole sequence between Tibetan and Han populations suggesting adaptive selection to high altitude by Gu, Mingliang, Dong, Xiaoqun, Shi, Li, Shi, Lei, Lin, Keqin, Huang, Xiaoqin, Chu, Jiayou

    Published in Gene (15-03-2012)
    “…We performed a mitochondrial whole-genome comparison study in 40 Tibetan and 50 Han Chinese. All subjects could be classified into 13 haplogroups pertained to…”
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