Publications by authors named "Lin Faquan"

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Split biosensor based on nano-enzymatic ferrocene-tyramine deposition reaction for detection of SMP30 antibody.
Yanping Xing, Xixiang Xie, Jiangtao Liu, Tao Zhao, Xiyu Liu, Faquan Lin

Anal Chim Acta· January 2026

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The Prevalence of Abnormal Glucose Metabolism and Its Correlates in the Zhuang Nationality, Nanning, Guangxi Province.
Qin Yuanyuan, Liao Lin, Chen Qingyun, Huang Yunhua, Lin Faquan

J Clin Lab Anal· November 2025

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Bubble Multimer-Enhanced Fluorescence Enables Self-Contained Profiling of Colorectal Cancer Extracellular Vesicles.
Yinghong Wei, Binqi Wei, Xifeng Mo, Xiaohuan Xu, Jiahao Huang, Faquan Lin

Nano Lett· November 2025

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Congenital hypofibrinogenemia with bleeding risk: mutations in the FGA, FGB, and FGG genes.
Yangyang Wu, Kaili Qin, Liqun Xiang, Meiling Luo, Min Chen, Faquan Lin

Lab Med· November 2025

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Pulmonary Vascular Endothelial Cells in Lung Diseases: Mechanisms, Therapeutic Strategies, and Future Directions.
Qianyue Liu, Hongshuai Zheng, Jing Liu, Ming Gao, Faquan Lin

Cell Prolif· October 2025

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Ultrasensitive Single-Molecule Immunoassays Built on Digital Techniques for Low Amounts of Biomarker Detection.
Ningneng Zhai, Xiaoting Ling, Yunhua Huang, Yuling Qiu, Chenghan Wang, Faquan Lin

ACS Sens· August 2025

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Barcodes based on nucleic acid sequences: Applications and challenges (Review).
Ying Hong Wei, Faquan Lin

Mol Med Rep· July 2025

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The clinical application value of the KU-F40 fully automatic fecal analyzer for the detection of fecal parasites: A large-sample retrospective study.
Chu Huang, Yunhua Huang, Faquan Lin, Lin Liao

Sci Rep· July 2025

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Case report: Novel multi-exon homozygous deletion of causes immunodeficiency, centromeric instability, and facial anomalies syndrome 2.
Yan Long, Chenghan Wang, Jie Xiao, Yunhua Huang, Xiaoting Ling, Faquan Lin

Front Immunol· May 2025

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4-phenylbutyric acid attenuates diabetes mellitus secondary to thiamine-responsive megaloblastic anaemia syndrome by modulating endoplasmic reticulum stress.
Yumei Qin, Xuan Zhang, Yuping Ye, Min Chen, Yuanyuan Qin, Faquan Lin

Endokrynol Pol· May 2025

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Rosa roxburghii juice alleviates DEHP-induced reproductive system damage in male mice via the PI3K/AKT signaling pathway.
Chaoyu Huang, Chen Qian, Zongxian Li, Yuanyuan Qin, Wuning Mo, Faquan Lin

J Ethnopharmacol· May 2025

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The diagnostic value of a breast cancer diagnosis model based on serum MiRNAs and serum tumor markers.
Xiaohui Li, Feng Wang, Faquan Lin, Binbin Xie, Yi Liu

World J Surg Oncol· March 2025

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A nomogram model for predicting advanced liver fibrosis in patients with hepatitis B: A multicenter study.
Bo Hu, Li Yang, Rui-Bing Li, Jiao Gong, Er-Hei Dai

Clin Chim Acta· February 2025

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Heterogeneity of tumor-associated neutrophils in hepatocellular carcinoma.
Guixiang Fan, Jintong Na, Zhen Shen, Faquan Lin, Liping Zhong

Mol Immunol· January 2025

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Corrigendum to "A novel duplication mutation of SLC2A1 gene causing glucose transporter 1 deficiency syndrome" [Gene 928 (2024) 148762].
Chaoyu Huang, Yunhua Huang, Liqiu Pan, Linlin Li, Xiaoting Ling, Faquan Lin

Gene· December 2024

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A novel duplication mutation of SLC2A1 gene causing glucose transporter 1 deficiency syndrome.
Chaoyu Huang, Yunhua Huang, Liqiu Pan, Linlin Li, Xiaoting Ling, Faquan Lin

Gene· November 2024

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Ultrasensitive Biosensors Detecting mA in Blood: Achieving Early Screening and Typing of Tumors.
Haiping Li, Xixiang Xie, Xiyu Liu, Pan Wu, Jian He, Faquan Lin

ACS Sens· November 2024

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A clinical update of compound heterozygosity for hemoglobin Hekinan II [a27(B8)Glu-Asp; HBA1: c.84G>T] variant in China.
Liqiu Pan, Yuling Qiu, Lihua Ye, Linlin Li, Yuanyuan Huang, Faquan Lin

Lab Med· September 2024

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Association of rs2241766 and rs1501299 polymorphisms in the adiponectin gene with metabolic syndrome.
Yinghua Tang, Lianli Yin, Faquan Lin

Immun Inflamm Dis· September 2024

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Evaluation of alarm notification of artificial intelligence in automated analyzer detection of parasites.
Zila Wang, Lin Liao, Ximei Huang, Jinguang Tang, Faquan Lin

Medicine (Baltimore)· September 2024

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Novel splice site and nonsense variants in PKHD1 cause autosomal recessive polycystic kidney disease in a Chinese Zhuang ethnic family.
Chen Qian, Jie Yan, Ximei Huang, Zila Wang, Faquan Lin

Medicine (Baltimore)· August 2024

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Guideline for diagnosis and management of congenital dysfibrinogenemia.
Jie Yan, Lin Liao, Donghong Deng, Weijie Zhou, Peng Cheng, Faquan Lin

Clin Chim Acta· July 2024

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A novel discriminant algorithm for differential diagnosis of mild to moderate thalassemia and iron deficiency anemia.
Liqiu Pan, Linlin Li, Yuling Qiu, Xiaoting Ling, Chenghan Wang, Faquan Lin

Medicine (Baltimore)· May 2024

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The combined detection of hematological indicators is used for the differential diagnosis of colorectal cancer and benign-colorectal lesions.
Xuan Zhang, Yang-Yang Wu, Yuan-Yuan Qin, Fa-Quan Lin

Cancer Biomark· April 2024

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Patient with congenital factor VII deficiency undergoing brain tumor neurosurgery successfully treated with recombinant factor VIIa and fresh frozen plasma: A case report and literature review.
Chaoyu Huang, Yongjia Yu, Ningneng Zhai, Wuning Mo, Faquan Lin

Medicine (Baltimore)· December 2023

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