Luoying相关文献与解析，生知库 | 链接生命科学的每一步

Loss-of-function variations in solute carrier family 38 member 6 are associated with essential tremor.

溶质载体家族 38 成员 6 的功能丧失变异与特发性震颤有关

期刊:Signal Transduction and Targeted Therapy

Yuan Zhangqi, Sun Qiying, Luo Junyu, Zhang Lu, Zhang Yichi, Guo Jifeng, Wang Cheng, Yang Kangjuan, Yang Shumin, Cao Yanjie, Shen Yinhua, Cui Jiaming, Cui Hengxiang, Sun Hao, Ma Tingbin, Xu Xuan, Liu Chun-Jie, Wang Tao, Guo An-Yuan, Cheng Aifang, Zhang Luoying, Liu Jun, Jiang Man, Tang Beisha, Liu Jing Yu

发表日期：2025

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Gene Therapy vs Cochlear Implantation in Restoring Hearing Function and Speech Perception for Individuals With Congenital Deafness

基因疗法与人工耳蜗植入术在恢复先天性耳聋患者的听力功能和言语感知方面的比较

期刊:Jama Neurology

影响因子:21.3

doi:10.1001/jamaneurol.2025.2053

Cheng, Xiaoting; Zhong, Jiake; Zhang, Jiajia; Cui, Chong; Jiang, Luoying; Liu, Yang-Wenyi; Chen, Yuxin; Cao, Qi; Wang, Daqi; Cheng, Guiqing; Zong, Yuxin; Shen, Min; Xu, Chunxin; Lv, Jun; Wang, Hui; Zhang, Longlong; Zhu, Biyun; Tang, Honghai; Wang, Jinghan; Fan, Xintai; Fang, Yanqing; Guo, Luo; Guo, Jiawei; Chen, Liheng; Yin, Yanbo; Wang, Zijing; Han, Lei; Hu, Shaowei; Wang, Shengyi; Qin, Guoyou; Liu, Xuezhong; Sang, Jinqiu; Zeng, Fangang; Wang, Wuqing; Chen, Bing; Chen, Zheng-Yi; Li, Huawei; Shu, Yilai

发表日期：2025

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PAM-flexible adenine base editing rescues hearing loss in a humanized MPZL2 mouse model harboring an East Asian founder mutation

PAM 柔性腺嘌呤碱基编辑可挽救携带东亚创始突变的人源化 MPZL2 小鼠模型的听力损失

期刊:Nature Communications

影响因子:14.7

doi:10.1038/s41467-025-62562-8

Shao Wei Hu # ，Sohyang Jeong # ，Luoying Jiang # ，Hansol Koo # ，Zijing Wang ，Won Hoon Choi ，Biyun Zhu ，Heeyoung Seok ，Yi Zhou ，Min Gu Kim ，Dan Mu ，Huixia Guo ，Ziyi Zhou ，Sung Ho Jung ，Yingting Zhang ，Ho Byung Chae ，Liheng Chen ，Sung-Yeon Lee ，Luo Guo ，Myung-Whan Suh ，Yang Xiao ，Moo Kyun Park ，Honghai Tang ，Jae-Jin Song ，Xi Chen ，Ai Chen ，Jun Ho Lee ，Sangsu Bae ，Sang-Yeon Lee ，Yilai Shu

Decoding the mechanism of proanthocyanidins in central analgesia: redox regulation and KCNK3 blockade.

解码原花青素在中枢镇痛中的作用机制：氧化还原调节和 KCNK3 阻断

期刊:Experimental and Molecular Medicine

影响因子:12.9

doi:10.1038/s12276-025-01412-5

Gu Junxiang, Wang Jian, Fan Hongwei, Wei Yi, Li Yan, Ma Chengwen, Xing Keke, Wang Pan, Wu Zhenyu, Wu Teng, Li Xiaoyi, Zhang Luoying, Han Yunyun, Chen Tao, Qu Jianqiang, Yan Xianxia

其它

发表日期：2025

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Hearing restoration by gene replacement therapy for a multisite-expressed gene in a mouse model of human DFNB111 deafness

在人类 DFNB111 耳聋小鼠模型中，通过基因替代疗法恢复多位点表达基因的听力

期刊:American Journal of Human Genetics

影响因子:8.1

doi:10.1016/j.ajhg.2025.08.011

Jiang, Luoying; Hu, Shao Wei; Wang, Zijing; Zhou, Yi; Tang, Honghai; Chen, Yuxin; Wang, Daqi; Fan, Xintai; Han, Lei; Li, Huawei; Shi, Dazhi; He, Yingzi; Shu, Yilai

发表日期：2025

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Upstream open reading frames dynamically modulate CLOCK protein translation to regulate circadian rhythms and sleep

上游开放阅读框动态调节CLOCK蛋白的翻译，从而调控昼夜节律和睡眠。

期刊:PLoS Biology

影响因子:7.8

doi:10.1371/journal.pbio.3003173

Yuanqiang Sun,Ke Shui,Qinyu Li,Chenlu Liu,Wanting Jin,Jian-Quan Ni,Jian Lu,Luoying Zhang

Functional evidence supports the potential role of Tbx4-HLEA in the hindlimb degeneration of cetaceans.

功能性证据支持 Tbx4-HLEA 在鲸类后肢退化中的潜在作用

期刊:Evodevo

影响因子:3.6

doi:10.1186/s13227-025-00239-5

Zhang Zhenhua, Liu Yao, Liang Na, Yu Zhenpeng, Deme Luoying, Xu Duo, Liu Jia, Ren Wenhua, Xu Shixia, Yang Guang

其它

发表日期：2025

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Changes in human tear metabolome following topical 0.05% cyclosporine A on primary Sjögren's syndrome

局部应用0.05%环孢素A治疗原发性干燥综合征后，人泪液代谢组的变化

期刊:Frontiers in Medicine

影响因子:3

doi:10.3389/fmed.2025.1653585

Li, Yingsi; Huang, Meiting; Xie, Luoying; Yan, Xiaoming; Song, Wenjing

[The natural history of the relationship between OTOF mutation-related genotypes and audiological phenotypes]

[OTOF突变相关基因型与听力表型之间关系的自然史]

期刊:

影响因子:

doi:10.13201/j.issn.2096-7993.2025.04.016

Han, Lei; Chen, Liheng; Yu, Sha; Chen, Yuxin; Jiang, Luoying; Han, Shuang; Zhong, Jiake; Guo, Luo; Li, Huawei; Shu, Yilai

发表日期：2025

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Transcriptomic Profiling Reveals Divergent Immune Responses to AAV1 and AAV-ie in Mice Inner Ear

转录组分析揭示小鼠内耳对AAV1和AAV-ie的不同免疫反应

Loss-of-function variations in solute carrier family 38 member 6 are associated with essential tremor.

溶质载体家族 38 成员 6 的功能丧失变异与特发性震颤有关

Gene Therapy vs Cochlear Implantation in Restoring Hearing Function and Speech Perception for Individuals With Congenital Deafness

基因疗法与人工耳蜗植入术在恢复先天性耳聋患者的听力功能和言语感知方面的比较

PAM-flexible adenine base editing rescues hearing loss in a humanized MPZL2 mouse model harboring an East Asian founder mutation

PAM 柔性腺嘌呤碱基编辑可挽救携带东亚创始突变的人源化 MPZL2 小鼠模型的听力损失

Decoding the mechanism of proanthocyanidins in central analgesia: redox regulation and KCNK3 blockade.

解码原花青素在中枢镇痛中的作用机制：氧化还原调节和 KCNK3 阻断

Hearing restoration by gene replacement therapy for a multisite-expressed gene in a mouse model of human DFNB111 deafness

在人类 DFNB111 耳聋小鼠模型中，通过基因替代疗法恢复多位点表达基因的听力

Upstream open reading frames dynamically modulate CLOCK protein translation to regulate circadian rhythms and sleep

上游开放阅读框动态调节CLOCK蛋白的翻译，从而调控昼夜节律和睡眠。

Functional evidence supports the potential role of Tbx4-HLEA in the hindlimb degeneration of cetaceans.

功能性证据支持 Tbx4-HLEA 在鲸类后肢退化中的潜在作用

Changes in human tear metabolome following topical 0.05% cyclosporine A on primary Sjögren's syndrome

局部应用0.05%环孢素A治疗原发性干燥综合征后，人泪液代谢组的变化

[The natural history of the relationship between OTOF mutation-related genotypes and audiological phenotypes]

[OTOF突变相关基因型与听力表型之间关系的自然史]