Search Results - "Lin, Keqin"
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FLT4 gene polymorphisms influence isolated ventricular septal defect predisposition in a Southwest China population
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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Exploring Genetic Diversity of SOD2 and POU5F1 for Congenital Heart Disease in the Southwest Chinese Population
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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Association study of FLT4 and HYDIN single nucleotide polymorphisms with atrial septal defect susceptibility in the Han Chinese population of Southwest China
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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Association between gene polymorphisms of voltage-dependent Ca2+ channels and hypertension in the Dai people of China: a case-control study
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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Mitochondrial haplogroup M9a1a1c1b is associated with hypoxic adaptation in the Tibetans
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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The Adaptive Change of HLA-DRB1 Allele Frequencies Caused by Natural Selection in a Mongolian Population That Migrated to the South of China
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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Molecular evolution of two asymptomatic echovirus 6 strains that constitute a novel branch of recently epidemic echovirus 6 in China
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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Autosomal STRs provide genetic evidence for the hypothesis that Tai people originate from southern China
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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Genetic relationships of ethnic minorities in Southwest China revealed by microsatellite markers
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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Correlation between the linguistic affinity and genetic diversity of Chinese ethnic groups
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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Distribution of HLA alleles and haplotypes in Jinuo and Wa populations in Southwest China
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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Difference in microbial community structure along a gradient of crater altitude: insights from the Nushan volcano
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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A novel mutation alters GNE bifunctional enzyme activity and leads to familial inherited GNE diseases
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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A novel splice site variant in the POPDC3 causes autosomal recessive limb‐girdle muscular dystrophy type 26
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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Comprehensive research on the distribution of HLA‐DRB1 in C hinese populations
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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Comprehensive research on the distribution of HLA‐DRB1 in Chinese populations
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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Three Novel Genetic Variants in the FAM110D, CACNA1A, and NLRP12 Genes Are Associated With Susceptibility to Hypertension Among Dai People
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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A novel mutation causes Hermansky-Pudlak syndrome type 4 with pulmonary fibrosis in 2 siblings from China
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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Molecular characterization of Coxsackievirus A16 strains isolated from children with severe hand, foot, and mouth disease in Yunnan, Southwest China, during 2009‐2015
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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Differences in mtDNA whole sequence between Tibetan and Han populations suggesting adaptive selection to high altitude
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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