Regulation of focal adhesion turnover in SDF-1α-stimulated migration of mesenchymal stem cells in neural differentiation

por Hu, Ya’nan, Lu, Junhou, Xu, Xiaojing, Lyu, Jingya, Zhang, Huanxiang
Publicado 2017

Hypoglycemic Mechanism of the Berberine Organic Acid Salt under the Synergistic Effect of Intestinal Flora and Oxidative Stress

por Cui, Hong-Xin, Hu, Ya-Nan, Li, Jing-Wan, Yuan, Ke
Publicado 2018

Endothelial nitric oxide synthase (−786T>C) polymorphism and migraine susceptibility: A meta-analysis

por Dong, Han, Wang, Zhi Hao, Dong, Bin, Hu, Ya Nan, Zhao, Hui Ying
Publicado 2018

Preparation and Evaluation of Antidiabetic Agents of Berberine Organic Acid Salts for Enhancing the Bioavailability

por Cui, Hong-Xin, Hu, Ya-Nan, Li, Jing-Wan, Yuan, Ke, Guo, Ying
Publicado 2018

Population structure of Betula albosinensis and Betula platyphylla: evidence for hybridization and a cryptic lineage

por Hu, Ya-Nan, Zhao, Lei, Buggs, Richard J A, Zhang, Xue-Min, Li, Jun, Wang, Nian
Publicado 2019

A Series of Efficient Umbrella Modeling Strategies to Track Irradiation-Mutation Strains Improving Butyric Acid Production From the Pre-development Earlier Stage Point of View

por Cao, Li, Gao, Yue, Wang, Xue-Zhen, Shu, Guang-Yuan, Hu, Ya-Nan, Xie, Zong-Ping, Cui, Wei, Guo, Xiao-Peng, Zhou, Xiang
Publicado 2021

Independent manipulation of histone H3 modifications in individual nucleosomes reveals the contributions of sister histones to transcription

por Zhou, Zhen, Liu, Yu-Ting, Ma, Li, Gong, Ting, Hu, Ya-Nan, Li, Hong-Tao, Cai, Chen, Zhang, Ling-Li, Wei, Gang, Zhou, Jin-Qiu
Publicado 2017

Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations

por Zhang, Jian-hui, Ruan, Dan-dan, Hu, Ya-nan, Ruan, Xing-lin, Zhu, Yao-bin, Yang, Xiao, Wu, Jia-bin, Lin, Xin-fu, Luo, Jie-wei, Tang, Fa-qiang
Publicado 2021

Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A

por Zhu, Yao-Bin, Zhang, Jian-Hui, Ji, Yuan-Yuan, Hu, Ya-Nan, Wang, Han-Lu, Ruan, Dan-Dan, Meng, Xiao-Rong, Lin, Xin-Fu, Luo, Jie-Wei, Chen, Wei
Publicado 2022

Clinical and Genetic Analysis of a Family With Sitosterolemia Caused by a Novel ATP-Binding Cassette Subfamily G Member 5 Compound Heterozygous Mutation

por Shen, Ming-fang, Hu, Ya-nan, Chen, Wei-xiang, Liao, Li-sheng, Wu, Min, Wu, Qiu-yan, Zhang, Jian-hui, Zhang, Yan-ping, Luo, Jie-wei, Lin, Xin-fu
Publicado 2022

Retrospective Analysis of the Effect of Lidocaine Combined with Methylprednisolone on Pain Control After Uterine Artery Embolization

por Tang, Yi, Lin, Bin, Zhang, Yan-ping, Hu, Ya-nan, Zhang, Jian-hui, Wu, Shao-jie, Zhou, Yan-feng, Cai, Sen-lin, Luo, Jie-wei, Chi, Wu, Fang, Zhu-ting
Publicado 2022

Genetic Analysis and Functional Study of a Pedigree With Bruck Syndrome Caused by PLOD2 Variant

por Wang, Ruo-li, Ruan, Dan-dan, Hu, Ya-nan, Gan, Yu-mian, Lin, Xin-fu, Fang, Zhu-ting, Liao, Li-sheng, Tang, Fa-qiang, He, Wu-bing, Luo, Jie-wei
Publicado 2022

A thrombophilia family with protein S deficiency due to protein translation disorders caused by a Leu607Ser heterozygous mutation in PROS1

por Zhang, Yan-ping, Lin, Bin, Ji, Yuan-yuan, Hu, Ya-nan, Lin, Xin-fu, Tang, Yi, Zhang, Jian-hui, Wu, Shao-jie, Cai, Sen-lin, Zhou, Yan-feng, Chen, Ting, Fang, Zhu-ting, Luo, Jie-wei
Publicado 2021

Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency

por Wang, Han-lu, Ruan, Dan-dan, Wu, Min, Ji, Yuan-yuan, Hu, Xing-xing, Wu, Qiu-yan, Zhang, Yan-ping, Lin, Bin, Hu, Ya-nan, Wang, Hang, Tang, Yi, Fang, Zhu-ting, Luo, Jie-wei, Liao, Li-sheng, Gao, Mei-zhu
Publicado 2023