Song Ning-Ning相关文献与解析，生知库 | 链接生命科学的每一步

Liu, Wei-Tang; Hu, Zhi-Bin; Hu, Ling; Wang, Yu-Bing; Zhang, Qiong; Song, Ning-Ning; Liu, Xi-Yue; Chen, Jia-Yin; Zhu, Hong-Wen; Zhou, Bing-Yao; Tao, Yun-Chao; Zhao, Li; Li, Ze-Xuan; Li, Yi-Wei; Chen, Jia-Qi; Tu, Si-Xin; Qi, Cong-Cong; Ding, Sai-Dan; Peng, Gang; Xu, Lin; Ding, Yu-Qiang

信号转导

癫痫

神经科学

Nr4a2, A Key Factor Controlling the Development and Functional Maintenance of Forebrain Car3 Neurons.

Nr4a2，控制前脑Car3神经元发育和功能维持的关键因素。

期刊:Neuroscience Bulletin

影响因子:5.8

doi:10.1007/s12264-025-01496-z

Tao Yun-Chao, Zhao Li, Zhang Qiong, Liu Xi-Yue, Liu Wei-Tang, Li Ze-Xuan, Hu Ling, Zhang Lei, Chen Jia-Yin, Ding Yu-Qiang, Song Ning-Ning

Med13 is involved in the radial migration and contralateral projection of cortical neurons via PlxnA4.

Med13 通过 PlxnA4 参与皮层神经元的放射状迁移和对侧投射。

期刊:Communications Biology

影响因子:5.1

doi:10.1038/s42003-026-09704-w

Li Ze-Xuan, Tu Si-Xin, Li Yi-Wei, Hu Zhi-Bin, Liu Wei-Tang, Tao Yun-Chao, Zhao Li, Song Ning-Ning, Chen Jia-Yin, Zhang Qiong, Qi Cong-Cong, Zhu Hong-Wen, Ding Yu-Qiang, Hu Ling

The pathogenic factor of ZC4H2-associated rare disorder is a postsynaptic regulator for synaptic activity and cognitive function

ZC4H2相关罕见疾病的致病因子是突触后调节因子，该因子对突触活动和认知功能至关重要。

期刊:Proceedings of the National Academy of Sciences of the United States of America

影响因子:9.1

doi:10.1073/pnas.2426375122

Wan, Li Pear; Li, Yuwei; Zhao, Shuhua; Zhao, Shiping; Song, Ning-Ning; Yuan, Kai-Ming; Yang, Cuiping; Ding, Yu-Qiang; Mao, Bingyu; Sheng, Nengyin; Tao, Wucheng; Ma, Pengcheng

神经科学

发表日期：2025

文献求助收藏

A rat Satb1 truncation causes neurodevelopmental abnormalities recapitulating the symptoms of patients with SATB1 mutations

大鼠Satb1基因截断会导致神经发育异常，重现SATB1基因突变患者的症状。

期刊:Acta Pharmacologica Sinica

影响因子:8.4

doi:10.1038/s41401-025-01588-6

Hu, Zhi-Bin; Liu, Wei-Tang; Li, Yi-Wei; Hu, Ling; Huang, Ying; Liu, Xi-Yue; Zhang, Qiong; Wang, Yu-Bing; Chen, Jia-Yin; Li, Ze-Xuan; Tu, Si-Xin; Zhao, Li; Song, Ning-Ning; Klavir, Oded; Ding, Yu-Qiang

Central Med23 deficiency leads to malformation of dentate gyrus and ADHD-like behaviors in mice.

中枢 Med23 缺乏会导致小鼠齿状回畸形和类似 ADHD 的行为

期刊:Neuropsychopharmacology

影响因子:7.1

doi:10.1038/s41386-025-02088-1

Zhou Bing-Yao, Li Ze-Xuan, Li Yi-Wei, Li Jin-Nan, Liu Wei-Tang, Liu Xi-Yue, Hu Zhi-Bin, Zhao Li, Chen Jia-Yin, Hu Ling, Song Ning-Ning, Feng Xue, Wang Gang, Xu Lin, Ding Yu-Qiang

其它

发表日期：2025

文献求助收藏

Satb2 and Nr4a2 are required for the differentiation of cortical layer 6b.

Satb2 和 Nr4a2 是皮质层 6b 分化所必需的

期刊:Cell Death Discovery

影响因子:7

doi:10.1038/s41420-025-02402-2

Zhao Li, Tao Yun-Chao, Hu Ling, Liu Xi-Yue, Zhang Qiong, Zhang Lei, Ding Yu-Qiang, Song Ning-Ning

其它

发表日期：2025

文献求助收藏

Neural plasticity and depression treatment

神经可塑性和抑郁症治疗

期刊:IBRO Neuroscience Reports

影响因子:2.9

doi:10.1016/j.ibneur.2022.09.001

Wang, Yu-Bing; Song, Ning-Ning; Ding, Yu-Qiang; Zhang, Lei

Deletion of Schizophrenia Susceptibility Gene Ulk4 Leads to Abnormal Cognitive Behaviors via Akt-GSK-3 Signaling Pathway in Mice.

精神分裂症易感基因Ulk4的缺失通过Akt-GSK-3信号通路导致小鼠认知行为异常

期刊:Schizophrenia Bulletin

影响因子:4.8

doi:10.1093/schbul/sbac040

Hu Ling, Zhou Bing-Yao, Yang Cui-Ping, Lu Da-Yun, Tao Yun-Chao, Chen Lin, Zhang Lei, Su Jun-Hui, Huang Ying, Song Ning-Ning, Chen Jia-Yin, Zhao Li, Chen Yi, He Chun-Hui, Wang Yu-Bing, Lang Bing, Ding Yu-Qiang

Enhanced Photocatalytic Degradation of Perfluorooctanoic Acid by Mesoporous Sb(2)O(3)/TiO(2) Heterojunctions

介孔Sb(2)O(3)/TiO(2)异质结增强全氟辛酸的光催化降解

期刊:Frontiers in Chemistry

影响因子:4.2

doi:10.3389/fchem.2021.690520

Yao, Xinyun; Zuo, Jiaqi; Wang, Yu-Jue; Song, Ning-Ning; Li, Huang-Hao; Qiu, Kaipei

发表日期：2021

文献求助收藏

Cortical Somatostatin Neurons Regulate Seizure Susceptibility via MINAR1/Gαs-cAMP Signaling

皮质生长抑素神经元通过MINAR1/Gαs-cAMP信号通路调节癫痫易感性

Nr4a2, A Key Factor Controlling the Development and Functional Maintenance of Forebrain Car3 Neurons.

Nr4a2，控制前脑Car3神经元发育和功能维持的关键因素。

Med13 is involved in the radial migration and contralateral projection of cortical neurons via PlxnA4.

Med13 通过 PlxnA4 参与皮层神经元的放射状迁移和对侧投射。

The pathogenic factor of ZC4H2-associated rare disorder is a postsynaptic regulator for synaptic activity and cognitive function

ZC4H2相关罕见疾病的致病因子是突触后调节因子，该因子对突触活动和认知功能至关重要。

A rat Satb1 truncation causes neurodevelopmental abnormalities recapitulating the symptoms of patients with SATB1 mutations

大鼠Satb1基因截断会导致神经发育异常，重现SATB1基因突变患者的症状。

Central Med23 deficiency leads to malformation of dentate gyrus and ADHD-like behaviors in mice.

中枢 Med23 缺乏会导致小鼠齿状回畸形和类似 ADHD 的行为

Satb2 and Nr4a2 are required for the differentiation of cortical layer 6b.

Satb2 和 Nr4a2 是皮质层 6b 分化所必需的

Neural plasticity and depression treatment

神经可塑性和抑郁症治疗

Deletion of Schizophrenia Susceptibility Gene Ulk4 Leads to Abnormal Cognitive Behaviors via Akt-GSK-3 Signaling Pathway in Mice.

精神分裂症易感基因Ulk4的缺失通过Akt-GSK-3信号通路导致小鼠认知行为异常

Enhanced Photocatalytic Degradation of Perfluorooctanoic Acid by Mesoporous Sb(2)O(3)/TiO(2) Heterojunctions

介孔Sb(2)O(3)/TiO(2)异质结增强全氟辛酸的光催化降解