Publications by authors named "Yeling Lu"

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Molecular genetic analysis of two novel ABO∗A alleles causing A phenotype in Chinese.
Hang Lei, Jiaming Li, Can Lou, Hui Zhang, Yuqing Shen, Yeling Lu

J Formos Med Assoc· September 2025

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Thrombomodulin Arg403Lys mutation impairs protein C activation and increases thrombosis risk.
Zhe Lai, Junwei Yuan, Fang Li, Shijie Zhou, Xi Wu, Yeling Lu

Thromb Res· August 2025

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The Prevalence and Associated Factors of Impaired Fasting Glucose among Children and Adolescents in Urban China: A Large-Scale Cross-Sectional Study.
Fenglian Huang, Zongyu Lin, Yeling Lu, Yueqin Zhou, Lewei Zhu

Pediatr Diabetes· April 2025

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Asn384Ser Mutation in Protein C is Associated with Multiple-Site Thrombosis in a Young Heterozygous Male.
Junwei Yuan, Shijie Zhou, Xi Wu, Fang Li, Zhe Lai, Yeling Lu

Thromb Haemost· April 2025

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Heterozygous Prothrombin Mutation-Associated Thrombophilia.
Xi Wu, Lei Li, Zhengjing Lu, Xiaobo Hu, Yeling Lu

Thromb Haemost· January 2025

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Neonatal Circulating Amino Acids and Lipid Metabolites Mediate the Association of Maternal Gestational Diabetes Mellitus with Offspring Neurodevelopment at 1 Year.
Yueqin Zhou, Xiaoyan Chen, Tianze Li, Pingming Gao, Saijun Huang, Yeling Lu

Nutrients· January 2025

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Association between vitamin D and cardiovascular health in Chinese children and adolescents: Basing on Life's Essential 8.
Fenglian Huang, Yueqin Zhou, Tianze Li, Zongyu Lin, Yeling Lu, Zhijun Lu

Nutr Metab Cardiovasc Dis· November 2024

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Molecular mechanisms and clinical manifestations of hereditary hemorrhagic telangiectasia.
Junwei Yuan, Xi Wu, Jialu Zhao, Qiulan Ding, Jing Dai, Yeling Lu

Thromb Res· September 2024

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Met343Val mutation disrupts the shuttling of Trp380 leading to a low-activity conformer of activated protein C and causes thrombosis.
Shijie Zhou, Fang Li, Zhe Lai, Xi Wu, Junwei Yuan, Yeling Lu

J Thromb Haemost· August 2024

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Mutation Ter462GlnextTer17 introduces a tail to C-terminus of protein C and causes venous thrombosis.
Zhe Lai, Jiaming Li, Shijie Zhou, Xi Wu, Junwei Yuan, Yeling Lu

Thromb Res· August 2024

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Clinical and Molecular Characteristics of Megakaryocytes in Myelodysplastic Syndrome.
Fangxiu Luo, Jialu Zhao, Yubao Chen, Zhenping Peng, Ran An, Yeling Lu

Glob Med Genet· June 2024

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Ser252Asn Mutation Introduces a New N-Linked Glycosylation Site and Causes Type IIb Protein C Deficiency.
Shijie Zhou, Xi Wu, Ying Song, Lei Li, Chunli Shi, Yeling Lu

Thromb Haemost· May 2024

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Antithrombin Resistance Rescues Clotting Defect of Homozygous Prothrombin-Y510N Dysprothrombinemia.
Yeling Lu, Bruno O Villoutreix, Indranil Biswas, Qiulan Ding, Xuefeng Wang

Thromb Haemost· May 2022

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Unraveling the molecular basis underlying nine putative splice site variants of von Willebrand factor.
Qian Liang, Xiaoyi Lin, Xi Wu, Yanyan Shao, Changming Chen, Yeling Lu

Hum Mutat· February 2022

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Role of Gly197 in the structure and function of protein C.
Yeling Lu, Indranil Biswas, Bruno O Villoutreix, Alireza R Rezaie

Biochim Biophys Acta Gen Subj· June 2021

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Thr90Ser Mutation in Antithrombin is Associated with Recurrent Thrombosis in a Heterozygous Carrier.
Yeling Lu, Bruno O Villoutreix, Indranil Biswas, Qiulan Ding, Xuefeng Wang

Thromb Haemost· July 2020

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Ile73Asn mutation in protein C introduces a new N-linked glycosylation site on the first EGF-domain of protein C and causes thrombosis.
Yeling Lu, Padmaja Mehta-D'souza, Indranil Biswas, Bruno O Villoutreix, Xuefeng Wang

Haematologica· June 2020

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Gly197Arg mutation in protein C causes recurrent thrombosis in a heterozygous carrier.
Yeling Lu, Hemant Giri, Bruno O Villoutreix, Qiulan Ding, Xuefeng Wang

J Thromb Haemost· May 2020

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Maternal microchimerism protects hemophilia A patients from inhibitor development.
Yeling Lu, Zhenping Chen, Jing Dai, Xi Wu, Hao Gu

Blood Adv· May 2020

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Prothrombin Arg541Trp Mutation Leads to Defective PC (Protein C) Pathway Activation and Constitutes a Novel Genetic Risk Factor for Venous Thrombosis.
Xi Wu, Jing Dai, Xiaoqian Xu, Fang Li, Lei Li, Yeling Lu

Arterioscler Thromb Vasc Biol· February 2020

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The characteristics and spectrum of F9 mutations in Chinese sporadic haemophilia B pedigrees.
Yeling Lu, Xi Wu, Jing Dai, Qiulan Ding, Wenman Wu

Haemophilia· March 2019

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Complex recombination with deletion in the F8 and duplication in the TMLHE mediated by int22h copies during early embryogenesis.
Changming Chen, Xiaoling Xie, Xi Wu, Yeling Lu, Xuefeng Wang

Thromb Haemost· July 2017

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Dysfibrinogenemia-associated novel heterozygous mutation, Shanghai (FGA c.169_180+2 del), leads to N-terminal truncation of fibrinogen Aα chain and impairs fibrin polymerization.
Jingyi Zhou, Qiulan Ding, Wenman Wu, Qi Ouyang, Yinyin Xie, Yeling Lu

J Clin Pathol· February 2017

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Vps33b regulates Vwf-positive vesicular trafficking in megakaryocytes.
Jing Dai, Yeling Lu, Conghui Wang, Xue Chen, Xuemei Fan

J Pathol· September 2016

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AccuCopy quantification combined with pre-amplification of long-distance PCR for fast analysis of intron 22 inversion in haemophilia A.
Qianlan Ding, Xi Wu, Yeling Lu, Changming Chen, Rui Shen

Clin Chim Acta· July 2016

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