ADF/cofilin-mediated actin dynamics regulate AMPA receptor trafficking during synaptic plasticity von Zheng, James Q, Gu, Jiaping, Lee, Chi Wai, Fan, Yanjie, Komlos, Daniel, Tang, Xin, Sun, Chicheng, Yu, Kuai, Hartzell, H Criss, Chen, Gong, Bamburg, James R

Volltext

Neuronal-Specific TUBB3 Is Not Required for Normal Neuronal Function but Is Essential for Timely Axon Regeneration von Latremoliere, Alban, Cheng, Long, DeLisle, Michelle, Wu, Chen, Chew, Sheena, Hutchinson, Elizabeth B., Sheridan, Andrew, Alexandre, Chloe, Latremoliere, Frederic, Sheu, Shu-Hsien, Golidy, Sara, Omura, Takao, Huebner, Eric A., Fan, Yanjie, Whitman, Mary C., Nguyen, Elaine, Hermawan, Crystal, Pierpaoli, Carlo, Tischfield, Max A., Woolf, Clifford J., Engle, Elizabeth C.

Volltext

Combining optical genome mapping and RNA-seq for structural variants detection and interpretation in unsolved neurodevelopmental disorders von Xiao, Bing, Luo, Xiaomei, Liu, Yi, Ye, Hui, Liu, Huili, Fan, Yanjie, Yu, Yongguo

Volltext

Incentive measures to avoid the illegal parking of dockless shared bikes: the relationships among incentive forms, intensity and policy compliance von Gao, Liangpeng, Ji, Yanjie, Yan, Xingchen, Fan, Yao, Guo, Weihong

Volltext

A comparison of the clinical characteristics of pediatric urolithiasis patients with positive and negative molecular diagnoses von Zhao, Yining, Fang, Xiaoliang, He, Lei, Fan, Yanjie, Li, Yueyan, Xu, Guofeng, Yu, Yongguo, Geng, Hongquan

Volltext

Lipid Droplet-Mitochondria Contacts in Health and Disease von Fan, Hongjun, Tan, Yanjie

Volltext

A 29 Mainland Chinese cohort of patients with Phelan-McDermid syndrome: genotype-phenotype correlations and the role of SHANK3 haploinsufficiency in the important phenotypes von Xu, Na, Lv, Hui, Yang, Tingting, Du, Xiujuan, Sun, Yu, Xiao, Bing, Fan, Yanjie, Luo, Xiaomei, Zhan, Yongkun, Wang, Lili, Li, Fei, Yu, Yongguo

Volltext

PQ-RRT: An improved path planning algorithm for mobile robots von Li, Yanjie, Wei, Wu, Gao, Yong, Wang, Dongliang, Fan, Zhun

Volltext

Novel PYGL mutations in Chinese children leading to glycogen storage disease type VI: two case reports von Luo, Xiaomei, Hu, Jiacheng, Gao, Xueren, Fan, Yanjie, Sun, Yu, Gu, Xuefan, Qiu, Wenjuan

Volltext

Diagnostic yield of additional exome sequencing after the detection of long continuous stretches of homozygosity (LCSH) in SNP arrays von Fan, Yanjie, Wang, Lili, Sun, Yu, Xu, Ting, Gong, Zhuwen, Zhao, Qianfeng, Qiu, Wenjuan, Liang, Lili, Xiao, Bing, Zhang, Huiwen, Han, Lianshu, Lin, Fujun, Xu, Rang, Gu, Xuefan, Yu, Yongguo

Volltext

Changes in Homogalacturonan Metabolism in Banana Peel during Fruit Development and Ripening von Ning, Tong, Chen, Chengjie, Yi, Ganjun, Chen, Houbin, Liu, Yudi, Fan, Yanjie, Liu, Jing, Chen, Shule, Wei, Sixuan, Li, Zexuan, Tan, Yehuan, He, Zhenting, Xu, Chunxiang

Volltext

Chronic Neuroinflammation Induced by Lipopolysaccharide Injection into the Third Ventricle Induces Behavioral Changes von Na, Shufang, Duan, Xuejiao, Wang, Rongyan, Fan, Yanjie, Xue, Ke, Tian, Shuwei, Yang, Zheqiong, Li, Ke, Yue, Jiang

Volltext

Integration of exome sequencing and metabolic evaluation for the diagnosis of children with urolithiasis von Zhao, Yining, Fang, Xiaoliang, Fan, Yanjie, Sun, Yu, He, Lei, Xu, Maosheng, Xu, Guofeng, Li, Yufeng, Huang, Yunteng, Yu, Yongguo, Geng, Hongquan

Volltext

Effect of contact stress and slip amplitude on fretting fatigue behaviour of ultrasonic surface nanocrystallized TC11 titanium alloy von Fan, Kaifa, Liu, Daoxin, Wang, Can, Yang, Jing, Liu, Yanjie, Zhang, Xiaohua, Xiang, Junfeng, Abdel Wahab, Magd

Volltext

Actin capping protein regulates postsynaptic spine development through CPI-motif interactions von Myers, Kenneth R., Fan, Yanjie, McConnell, Patrick, Cooper, John A., Zheng, James Q.

Volltext

A Novel Nonsense Mutation of PHF6 in a Female with Extended Phenotypes of Borjeson-Forssman-Lehmann Syndrome von Zhang, Xia, Fan, Yanjie, Liu, Xiaomin, Zhu, Ming-Ang, Sun, Yu, Yan, Hui, He, Yunjuan, Ye, Xiantao, Gu, Xuefan, Yu, Yongguo

Volltext

Genetic Evaluation of 114 Chinese Short Stature Children in the Next Generation Era: a Single Center Study von Huang, Zhuo, Sun, Yu, Fan, Yanjie, Wang, Lili, Liu, Huili, Gong, Zhuwen, Wang, Jianguo, Yan, Hui, Wang, Yu, Hu, Guorui, Wang, Ruifang, Ye, Jun, Han, Lianshu, Qiu, Wenjuan, Zhang, Huiwen, Liang, Lili, Yang, Yu, Dauber, Andrew, Yu, Yongguo, Gu, Xue-Fan

Volltext

Genetic Diagnostic Evaluation of Trio-Based Whole Exome Sequencing Among Children With Diagnosed or Suspected Autism Spectrum Disorder von Du, Xiujuan, Gao, Xueren, Liu, Xin, Shen, Lixiao, Wang, Kai, Fan, Yanjie, Sun, Yu, Luo, Xiaomei, Liu, Huili, Wang, Lili, Wang, Yu, Gong, Zhuwen, Wang, Jianguo, Yu, Yongguo, Li, Fei

Volltext

Rare Copy Number Variations in a Chinese Cohort of Autism Spectrum Disorder von Fan, Yanjie, Du, Xiujuan, Liu, Xin, Wang, Lili, Li, Fei, Yu, Yongguo

Volltext

A novel compound heterozygous mutation of the CLCN7 gene is associated with autosomal recessive osteopetrosis von Wang, Xia, Wang, Yingcan, Xu, Ting, Fan, Yanjie, Ding, Yifeng, Qian, Jihong

Volltext