Height, VKORC1 1173, and CYP2C9 Genotypes Determine Warfarin Dose for Pediatric Patients with Kawasaki Disease in Southwest China

por Yang, Dan, Kuang, Hongyu, Zhou, Yuanlin, Cai, Chunqiong, Lu, Tiewei
Publicado 2018

An EGLN1 mutation may regulate hypoxic response in cyanotic congenital heart disease through the PHD2/HIF-1A pathway

por Zhou, Yuanlin, Ouyang, Na, Liu, Lingjuan, Tian, Jie, Huang, Xupei, Lu, Tiewei
Publicado 2018

Synthesis and Preparation of (Acrylic Copolymer) Ternary System Peelable Sealing Decontamination Material

por He, Zhiyu, Li, Yintao, Xiao, Zhiqiang, Jiang, Huan, Zhou, Yuanlin, Luo, Deli
Publicado 2020

Comprehensive Diagnostic Criteria for MELAS Syndrome; a Case Study Involving an Elderly Patient With MT-TWm.5541C>T Mutation

por Wu, Gang, Shen, Yuguang, Zhu, Feng, Tao, Weiwei, Zhou, Yuanlin, Ke, Shaofa, Jiang, Huihua
Publicado 2022

A de novo Mutation in the MTUS1 Gene Decreases the Risk of Non-compaction of Ventricular Myocardium via the Rac1/Cdc42 Pathway

por Bai, Xuehan, Zhou, Yuanlin, Ouyang, Na, Liu, Lingjuan, Huang, Xupei, Tian, Jie, Lv, Tiewei
Publicado 2019

[Corrigendum] The tetraspanin CD151‑ARSA mutant inhibits angiogenesis via the YRSL sequence

por Peng, Dan, Zuo, Houjuan, Liu, Zhengxiang, Qin, Jin, Zhou, Yuanlin, Li, Pengcheng, Wang, Daowen, Zeng, Hesong, Zhang, Xin A.
Publicado 2023

The tetraspanin CD151-ARSA mutant inhibits angiogenesis via the YRSL sequence

por PENG, DAN, ZUO, HOUJUAN, LIU, ZHENGXIANG, QIN, JIN, ZHOU, YUANLIN, LI, PENGCHENG, WANG, DAOWEN, ZENG, HESONG, ZHANG, XIN A.
Publicado 2013

Ataxia with oculomotor apraxia type 2 caused by a novel homozygous mutation in SETX gene, and literature review

por Chen, Shuaishuai, Du, Juping, Jiang, Huihua, Zhao, Weibo, Wang, Na, Ying, Anna, Li, Jun, Chen, Shiyong, Shen, Bo, Zhou, Yuanlin
Publicado 2022