Resultados de procura - Fujun Lin

Identification and functional characterization of the first deep intronic GLA mutation (IVS4+1326C>T) causing renal variant of Fabry disease por Xuantong Dai, Xue Zong, Xiaoxia Pan, Wei Lu, Geng-Ru Jiang, Fujun Lin

Ligazón do recurso

Deciphering the complexity: a case of kidney failure with co-inheritance of COL4A5 and APOE variants por Xiaoyan Zhang, Shi Jin, Xuantong Dai, Chenlin Yao, Ziyi Zhao, Fujun Lin, Yiqin Shi

Ligazón do recurso

Coenzyme Q10 supplementation in adult-onset focal segmental glomerulosclerosis caused by the Chinese common pathogenic variant c.737G > A (p.Ser246Asn) in the COQ8B gene por Shi Jin, Yiqin Shi, Pan Lin, Hong Liu, Xialian Xu, Xuantong Dai, Gengru Jiang, Xiaoqiang Ding, Fujun Lin

Ligazón do recurso

Homozygous FAT1 frameshift mutation linked to glomerulotubular nephropathy with impaired cell adhesion and Rap1 signaling por Yang Fei, Zhouhui Jin, Li He, Meng Zhang, Qiong Jiao, Qiye Liu, Fujun Lin, Wei Wang, Niansong Wang, Aili Cao, Dongsheng Cheng

Ligazón do recurso

A comprehensive immune repertoire signature distinguishes pulmonary infiltration in SARS-CoV-2 Omicron variant infection por Xuechuan Li, Hongyi Zhu, Peipei Xu, Jie Zhang, Zhe Wang, Hui He, Fang Shen, Yi Jiang, Lijuan Shen, Jing Xiang, Linhua Yang, Chao Yang, Hao Jiang, Ganglong Gao, Junshuo Jin, Huojian Shen, Yinping Wang, Linshi Wu, Changlin Qian, Dejun Liu, Weiqing Qiu, Qiwei Li, Yuanwen Chen, Fujun Lin, Yun Liu

Ligazón do recurso