日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Essential role of NONO-HOXA1-Wnt axis in cardiomyocyte differentiation.

NONO-HOXA1-Wnt轴在心肌细胞分化中起着至关重要的作用。

Feng Zhiyu, Gao Yuan, Gao Han, Sun Siyu, Na Weilan, Huang Xianghui, Li Shuolin, Tan Chaozhong, Min Shaojie, Lu Yuquan, Zhuang Quannan, Lin Siyi, Ma Xiaojing, Liu Ying, Shou Weinian, Wang Mei, Wang Jing, Gu Zhongkai, Sheng Wei, Wu Feizhen, Huang Guoying

Identification of candidate genes harboring pathogenic variants in congenital heart disease and laterality defects in Chinese population.

鉴定中国人群先天性心脏病和侧向性缺陷中致病变异的候选基因

Wang Jinxin, Chen Weicheng, Huang Xianghui, Gao Han, Feng Zhiyu, Tan Chaozhong, Zhuang Quannan, Gao Yuan, Min Shaojie, Lu Yuquan, Wu Feizhen, Qian Maoxiang, Yan Weili, Sheng Wei, Huang Guoying

Association of copy number variation in X chromosome-linked PNPLA4 with heterotaxy and congenital heart disease.

X染色体连锁PNPLA4拷贝数变异与异位症和先天性心脏病的关联

Gao Han, Huang Xianghui, Chen Weicheng, Feng Zhiyu, Zhao Zhengshan, Li Ping, Tan Chaozhong, Wang Jinxin, Zhuang Quannan, Gao Yuan, Min Shaojie, Yao Qinyu, Qian Maoxiang, Ma Xiaojing, Wu Feizhen, Yan Weili, Sheng Wei, Huang Guoying

Circadian Regulator-Mediated Molecular Subtypes Depict the Features of Tumor Microenvironment and Indicate Prognosis in Head and Neck Squamous Cell Carcinoma

昼夜节律调节因子介导的分子亚型描绘了头颈部鳞状细胞癌的肿瘤微环境特征并指示其预后

Aye, Ling; Wang, Zhanying; Chen, Fanghua; Xiong, Yujun; Zhou, Jiaying; Wu, Feizhen; Hu, Li; Wang, Dehui

Analysis of the CHD7 gene mutations in patients of congenital heart disease with extracardiac malformations

对伴有心脏外畸形的先天性心脏病患者进行CHD7基因突变分析

Huang, Xianghui; Gao, Han; Chen, Weicheng; Feng, Zhiyu; Tan, Chaozhong; Zhuang, Quannan; Wang, Jinxin; Gao, Yuan; Min, Shaojie; Yao, Qinyu; Sun, Jingwei; Yan, Weili; Ma, Xiaojing; Wu, Feizhen; Sheng, Wei; Huang, Guoying

Intrahepatic transcriptomics reveals gene signatures in chronic hepatitis B patients responded to interferon therapy

肝内转录组学揭示了对干扰素治疗有反应的慢性乙型肝炎患者的基因特征

Li, Ning; Yu, Kangkang; Dong, Minhui; Wang, Jinyu; Yang, Feifei; Zhu, Haoxiang; Yu, Jie; Yang, Jingshu; Xie, Wentao; Mitra, Bidisha; Mao, Richeng; Wu, Feizhen; Guo, Haitao; Zhang, Jiming

Copy number variant analysis for syndromic congenital heart disease in the Chinese population

中国人群中综合征性先天性心脏病的拷贝数变异分析

Li, Ping; Chen, Weicheng; Li, Mengru; Zhao, Zhengshan; Feng, Zhiyu; Gao, Han; Suo, Meijiao; Xu, Ziqing; Tian, Guixiang; Wu, Feizhen; Wei, Sheng; Huang, Guoying

Zfp57 Exerts Maternal and Sexually Dimorphic Effects on Genomic Imprinting.

Zfp57 对基因组印记发挥母系和性别二态性效应

Xu Zhen, Shi Jiajia, Zhang Yu, Liu Yuhan, Zhao Junzheng, Chen Qian, Song Chenglin, Geng Shuhui, Xie Wei, Wu Feizhen, Bai Yun, Yang Yang, Li Xiajun

DNMT3A reads and connects histone H3K36me2 to DNA methylation

DNMT3A 读取组蛋白 H3K36me2 并将其与 DNA 甲基化连接起来。

Xu, Wenqi; Li, Jiahui; Rong, Bowen; Zhao, Bin; Wang, Mei; Dai, Ruofei; Chen, Qilong; Liu, Hang; Gu, Zhongkai; Liu, Shuxian; Guo, Rui; Shen, Hongjie; Wu, Feizhen; Lan, Fei

Correction to: DNMT3A reads and connects histone H3K36me2 to DNA methylation

更正:DNMT3A 读取组蛋白 H3K36me2 并将其与 DNA 甲基化连接起来

Xu, Wenqi; Li, Jiahui; Rong, Bowen; Zhao, Bin; Wang, Mei; Dai, Ruofei; Chen, Qilong; Liu, Hang; Gu, Zhongkai; Liu, Shuxian; Guo, Rui; Shen, Hongjie; Wu, Feizhen; Lan, Fei