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

A comprehensive cancer analysis investigating the oncogenic role of zinc finger protein 36 (ZFP36) in human tumors

一项全面的癌症分析研究了锌指蛋白36(ZFP36)在人类肿瘤中的致癌作用

Xie, Shuyuan; Wu, Huidan; Li, Xuanwen; Wang, Bingye; Liu, Yuxuan; Li, Congying; Huang, Qing; Yang, Yang; Gu, Shinong

P4HA2 Participates in Pathogenesis of Refractive Error by Regulating Collagen Posttranslational Modification and Extracellular Matrix Balance.

P4HA2 通过调节胶原蛋白翻译后修饰和细胞外基质平衡参与屈光不正的发病机制。

Liu Yanling, Dong Shanshan, Huang Furong, Li Ruotong, He Xi, Jiang Yizheng, Tian Qi, Xiong Haofeng, Jin Liangyun, Wang Qiongsi, Xia Lu, Chen Jingjing, Wu Huidan, Guo Hui, Zhou Xiangtian, Xia Kun, Hu Zhengmao

Ultrafast synthesis of L-His-Fe(3)O(4) nanozymes with enhanced peroxidase-like activity for effective antibacterial applications.

超快速合成具有增强的类过氧化物酶活性的 L-His-Fe(3)O(4) 纳米酶,用于有效的抗菌应用

Yuan Ye, Liu Yuan, Shen Zhipeng, Wu Huidan, Meng Lantian, Guo Xiaoxiao, Jiang Bing, Fang Ling

A pan-cancer analysis targeting the oncogenic role of ATP-binding cassette transporter A1 in human tumors

针对ATP结合盒转运蛋白A1在人类肿瘤中致癌作用的泛癌分析

Wu, Huidan; Gu, Shinong; Xie, Shuyuan; Li, Xuanwen; Wang, Bingye; Liu, Yuxuan; Huang, Qing

LncRNA34977 promotes the proliferation, migration, and invasion and inhibits the apoptosis of canine mammary tumors by regulating the expression of miR-8881/ELAVL4

LncRNA34977通过调控miR-8881/ELAVL4表达促进犬乳腺肿瘤增殖、迁移、侵袭并抑制其凋亡

Baochun Lu, Yufan Zhu, Juye Wu, Huidan Qiu, Jinyu Wang, Zihang Ma, Kun Jia

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

大规模靶向测序可识别神经发育障碍的风险基因

Wang, Tianyun; Hoekzema, Kendra; Vecchio, Davide; Wu, Huidan; Sulovari, Arvis; Coe, Bradley P; Gillentine, Madelyn A; Wilfert, Amy B; Perez-Jurado, Luis A; Kvarnung, Malin; Sleyp, Yoeri; Earl, Rachel K; Rosenfeld, Jill A; Geisheker, Madeleine R; Han, Lin; Du, Bing; Barnett, Chris; Thompson, Elizabeth; Shaw, Marie; Carroll, Renee; Friend, Kathryn; Catford, Rachael; Palmer, Elizabeth E; Zou, Xiaobing; Ou, Jianjun; Li, Honghui; Guo, Hui; Gerdts, Jennifer; Avola, Emanuela; Calabrese, Giuseppe; Elia, Maurizio; Greco, Donatella; Lindstrand, Anna; Nordgren, Ann; Anderlid, Britt-Marie; Vandeweyer, Geert; Van Dijck, Anke; Van der Aa, Nathalie; McKenna, Brooke; Hancarova, Miroslava; Bendova, Sarka; Havlovicova, Marketa; Malerba, Giovanni; Bernardina, Bernardo Dalla; Muglia, Pierandrea; van Haeringen, Arie; Hoffer, Mariette J V; Franke, Barbara; Cappuccio, Gerarda; Delatycki, Martin; Lockhart, Paul J; Manning, Melanie A; Liu, Pengfei; Scheffer, Ingrid E; Brunetti-Pierri, Nicola; Rommelse, Nanda; Amaral, David G; Santen, Gijs W E; Trabetti, Elisabetta; Sedláček, Zdeněk; Michaelson, Jacob J; Pierce, Karen; Courchesne, Eric; Kooy, R Frank; Nordenskjöld, Magnus; Romano, Corrado; Peeters, Hilde; Bernier, Raphael A; Gecz, Jozef; Xia, Kun; Eichler, Evan E

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

作者更正:大规模靶向测序可识别神经发育障碍的风险基因

Wang, Tianyun; Hoekzema, Kendra; Vecchio, Davide; Wu, Huidan; Sulovari, Arvis; Coe, Bradley P; Gillentine, Madelyn A; Wilfert, Amy B; Perez-Jurado, Luis A; Kvarnung, Malin; Sleyp, Yoeri; Earl, Rachel K; Rosenfeld, Jill A; Geisheker, Madeleine R; Han, Lin; Du, Bing; Barnett, Chris; Thompson, Elizabeth; Shaw, Marie; Carroll, Renee; Friend, Kathryn; Catford, Rachael; Palmer, Elizabeth E; Zou, Xiaobing; Ou, Jianjun; Li, Honghui; Guo, Hui; Gerdts, Jennifer; Avola, Emanuela; Calabrese, Giuseppe; Elia, Maurizio; Greco, Donatella; Lindstrand, Anna; Nordgren, Ann; Anderlid, Britt-Marie; Vandeweyer, Geert; Van Dijck, Anke; Van der Aa, Nathalie; McKenna, Brooke; Hancarova, Miroslava; Bendova, Sarka; Havlovicova, Marketa; Malerba, Giovanni; Bernardina, Bernardo Dalla; Muglia, Pierandrea; van Haeringen, Arie; Hoffer, Mariette J V; Franke, Barbara; Cappuccio, Gerarda; Delatycki, Martin; Lockhart, Paul J; Manning, Melanie A; Liu, Pengfei; Scheffer, Ingrid E; Brunetti-Pierri, Nicola; Rommelse, Nanda; Amaral, David G; Santen, Gijs W E; Trabetti, Elisabetta; Sedláček, Zdeněk; Michaelson, Jacob J; Pierce, Karen; Courchesne, Eric; Kooy, R Frank; Nordenskjöld, Magnus; Romano, Corrado; Peeters, Hilde; Bernier, Raphael A; Gecz, Jozef; Xia, Kun; Eichler, Evan E

Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model

自闭症/发育迟缓风险基因的遗传突变和多个新发突变提示存在多因素模型

Guo, Hui; Wang, Tianyun; Wu, Huidan; Long, Min; Coe, Bradley P; Li, Honghui; Xun, Guanglei; Ou, Jianjun; Chen, Biyuan; Duan, Guiqin; Bai, Ting; Zhao, Ningxia; Shen, Yidong; Li, Yun; Wang, Yazhe; Zhang, Yu; Baker, Carl; Liu, Yanling; Pang, Nan; Huang, Lian; Han, Lin; Jia, Xiangbin; Liu, Cenying; Ni, Hailun; Yang, Xinyi; Xia, Lu; Chen, Jingjing; Shen, Lu; Li, Ying; Zhao, Rongjuan; Zhao, Wenjing; Peng, Jing; Pan, Qian; Long, Zhigao; Su, Wei; Tan, Jieqiong; Du, Xiaogang; Ke, Xiaoyan; Yao, Meiling; Hu, Zhengmao; Zou, Xiaobing; Zhao, Jingping; Bernier, Raphael A; Eichler, Evan E; Xia, Kun

De novo genic mutations among a Chinese autism spectrum disorder cohort

中国自闭症谱系障碍患者群体中的新生基因突变

Wang, Tianyun; Guo, Hui; Xiong, Bo; Stessman, Holly A F; Wu, Huidan; Coe, Bradley P; Turner, Tychele N; Liu, Yanling; Zhao, Wenjing; Hoekzema, Kendra; Vives, Laura; Xia, Lu; Tang, Meina; Ou, Jianjun; Chen, Biyuan; Shen, Yidong; Xun, Guanglei; Long, Min; Lin, Janice; Kronenberg, Zev N; Peng, Yu; Bai, Ting; Li, Honghui; Ke, Xiaoyan; Hu, Zhengmao; Zhao, Jingping; Zou, Xiaobing; Xia, Kun; Eichler, Evan E