Effect of Emi1 gene silencing on the proliferation and invasion of human breast cancer cells

por Kuang, Ying, Huang, Shengwen, Tang, Shifan, Zhuo, Zhaozhen, Linghu, Keyan
Publicado 2023

The oral microbiome of patients with ischemic stroke predicts their severity and prognosis

por Sun, Wenbo, Huang, Shengwen, Yang, Xiaoli, Luo, Yufan, Liu, Luqiong, Wu, Danhong
Publicado 2023

LncRNA VPS9D1-AS1 promotes cell proliferation in acute lymphoblastic leukemia through modulating GPX1 expression by miR-491-5p and miR-214-3p evasion

por Xiao, Shishan, Xu, Na, Ding, Qian, Huang, Shengwen, Zha, Yan, Zhu, Hongqian
Publicado 2020

Carotid Siphon Calcification Predicts the Symptomatic Progression in Branch Artery Disease With Intracranial Artery Stenosis—Brief Report

por Hou, Duanlu, Yang, Xiaoli, Wang, Yuanyuan, Huang, Shengwen, Tang, Yuping, Wu, Danhong
Publicado 2022

Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review

por Chen, Weijie, Wang, Yuanyuan, Huang, Shengwen, Yang, Xiaoli, Shen, Liwei, Wu, Danhong
Publicado 2022

A novel heterozygous mutation of the NPHS1 gene in a Chinese child with congenital nephrotic syndrome: A case report

por Xie, Dan, Wu, Jiangfen, Zhang, Wenyi, Jin, Tingting, Wu, Peng, An, Banquan, Huang, Shengwen
Publicado 2023

Two novel mutations in PADI6 and TLE6 genes cause female infertility due to arrest in embryonic development

por Liu, Juan, Tan, Zongjian, He, Jun, Jin, Tingting, Han, Yuanyuan, Hu, Li, Huang, Shengwen
Publicado 2021

A Three-Year Prospective Study Assessing the Application of Chromosomal Microarray Analysis in 576 High-Risk Pregnant Women

por Jiang, Minmin, Huang, Shengwen, Ma, Xingwei, Xie, Ping, Ren, Lingyan, Jin, Qian, Linghu, Keyan
Publicado 2022

Identification of three molecular subtypes based on immune infiltration in ovarian cancer and its prognostic value

por Liu, Juan, Tan, Zongjian, He, Jun, Jin, Tingting, Han, Yuanyuan, Hu, Li, Song, Jukun, Huang, Shengwen
Publicado 2020

Whole‐exome sequencing identified five novel de novo variants in patients with unexplained intellectual disability

por Zhang, Wenqiu, Hu, Li, Huang, Xinyi, Xie, Dan, Wu, Jiangfen, Fu, Xiaoling, Liang, Daiyi, Huang, Shengwen
Publicado 2022

Identification of Two Novel Variants of the DMD Gene in Chinese Families with Duchenne Muscular Dystrophy

por Wu, Jiangfen, Ren, Lingyan, Huang, Xinyi, Hu, Li, Zhang, Liangliang, Xie, Dan, Li, Zhimin, Han, Naijian, Huang, Shengwen
Publicado 2023

Identification of two CUL7 variants in two Chinese families with 3‐M syndrome by whole‐exome sequencing

por Hu, Li, Wang, Xike, Jin, Tingting, Han, Yuanyuan, Liu, Juan, Jiang, Minmin, Yan, Shujuan, Fu, Xiaoling, An, Bangquan, Huang, Shengwen
Publicado 2020

Long noncoding RNA PCED1B-AS1 promotes erythroid differentiation coordinating with GATA1 and chromatin remodeling

por Zhu, Junwei, Ren, Yunxiao, Han, Yuanyuan, Jin, Tingting, Li, Yanming, Ruan, Xiuyan, Qu, Hongzhu, Huang, Shengwen, Zhang, Zhaojun, Fang, Xiangdong
Publicado 2019

Association of polymorphisms in the HBG1‐HBD intergenic region with HbF levels

por Hu, Li, Huang, Ling, Han, Yuanyuan, Jin, Tingting, Liu, Juan, Jiang, Minmin, Liu, Xingmei, Li, Yuanyuan, Han, Wenping, An, Bangquan, Huang, Shengwen
Publicado 2020

ANTXR1 Regulates Erythroid Cell Proliferation and Differentiation through wnt/β-Catenin Signaling Pathway In Vitro and in Hematopoietic Stem Cell

por Jin, Tingting, Zhang, Zhaojun, Han, Yuanyuan, Li, Di, Liu, Juan, Jiang, Minmin, Kurita, Ryo, Nakamura, Yukio, Hu, Fangfang, Fang, Xiangdong, Huang, Shengwen, Sun, Zhaolin
Publicado 2022

Transmembrane Protein ANTXR1 Regulates γ-Globin Expression by Targeting the Wnt/β-Catenin Signaling Pathway

por Jin, Tingting, Zhang, Zhaojun, Han, Yuanyuan, Li, Di, Liu, Juan, Jiang, Minmin, Zhu, Junwei, Kurita, Ryo, Nakamura, Yukio, Hu, Fangfang, Xu, Yongjie, Fang, Xiangdong, Huang, Shengwen, Sun, Zhaolin
Publicado 2022