Biohydrogen production from traditional Chinese medicine wastewater in anaerobic packed bed reactor system

por Sun, Caiyu, Sheng, Tao, Li, Lixin, Yang, Lisha
Publicado 2021

Paradoxical effects on voltage-gated Na(+) conductance in adrenal chromaffin cells by twin vs single high intensity nanosecond electric pulses

por Yang, Lisha, Pierce, Sophia, Chatterjee, Indira, Craviso, Gale L., Leblanc, Normand
Publicado 2020

Genetic Polymorphism and Population Genetic Structure Analysis of 21 Autosomal STR Loci for a Han-Chinese Population from Luzhou of Southwest China

por Song, Binghui, Fu, Jiewen, Qian, Jie, Yang, Lisha, Cheng, Jingliang, Fu, Junjiang
Publicado 2023

Nanosecond electric pulses differentially affect inward and outward currents in patch clamped adrenal chromaffin cells

por Yang, Lisha, Craviso, Gale L., Vernier, P. Thomas, Chatterjee, Indira, Leblanc, Normand
Publicado 2017

Novel, heterozygous, de novo pathogenic variant (c.4963delA: p.Thr1656Glnfs*42) of the NF1 gene in a Chinese family with neurofibromatosis type 1

por Yang, Lisha, Fu, Jiewen, Cheng, Jingliang, Zhou, Baixu, Chen, Maomei, Anuchapreeda, Songyot, Fu, Junjiang
Publicado 2023

Comprehensive analysis, immune, and cordycepin regulation for SOX9 expression in pan-cancers and the matched healthy tissues

por Liu, Shuguang, Yang, Lisha, Fu, Jiewen, Li, Ting, Zhou, Baixu, Wang, Kai, Wei, Chunli, Fu, Junjiang
Publicado 2023

Study on core competencies of midwives in China

por Sun, Kejuan, Qi, Jinghan, Luo, Bin, Yang, Lisha, Shu, Chang, Tang, Huijun, Qin, Yanyue, Zang, Yu
Publicado 2023

Novel compound heterozygous EYS variants may be associated with arRP in a large Chinese pedigree

por Wei, Chunli, Xiao, Ting, Cheng, Jingliang, Fu, Jiewen, Zhou, Qi, Yang, Lisha, Lv, Hongbin, Fu, Junjiang
Publicado 2020

Evaluation of amplification refractory mutation system (ARMS) technique for quick and accurate prenatal gene diagnosis of CHM variant in choroideremia

por Yang, Lisha, Ijaz, Iqra, Cheng, Jingliang, Wei, Chunli, Tan, Xiaojun, Khan, Md Asaduzzaman, Fu, Xiaodong, Fu, Junjiang
Publicado 2017

Thymoquinone Inhibits the Migration and Invasive Characteristics of Cervical Cancer Cells SiHa and CaSki In Vitro by Targeting Epithelial to Mesenchymal Transition Associated Trans...

por Li, Jun, Khan, Md. Asaduzzaman, Wei, Chunli, Cheng, Jingliang, Chen, Hanchun, Yang, Lisha, Ijaz, Iqra, Fu, Junjiang
Publicado 2017

A novel, homozygous nonsense variant of the CDHR1 gene in a Chinese family causes autosomal recessive retinal dystrophy by NGS‐based genetic diagnosis

por Fu, Jiewen, Ma, Lu, Cheng, Jingliang, Yang, Lisha, Wei, Chunli, Fu, Shangyi, Lv, Hongbin, Chen, Rui, Fu, Junjiang
Publicado 2018

A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree

por Cheng, Jingliang, Fu, Jiewen, Zhou, Qi, Xiang, Xiaohong, Wei, Chunli, Yang, Lisha, Fu, Shangyi, Khan, Md. Asaduzzaman, Lv, Hongbin, Fu, Junjiang
Publicado 2019

A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing

por Wei, Chunli, Yang, Lisha, Cheng, Jingliang, Imani, Saber, Fu, Shangyi, Lv, Hongbin, Li, Yumei, Chen, Rui, Leung, Elaine Lai-Han, Fu, Junjiang
Publicado 2018

Descriptive statistics of dataset from the meta-analysis and meta-regression analysis on prognostic significance of pre-treatment systemic hemato-immunological indices of cervical...

por Han, Xingping, Liu, Shuya, Hosseinifard, Hossein, Imani, Saber, Yang, Gang, Yang, Lisha, Maghsoudloo, Mazaher, Fu, ShaoZhi, Wen, QingLian, Liu, Qiang
Publicado 2021

Novel splicing variant c. 208+2T>C in BBS5 segregates with Bardet–Biedl syndrome in an Iranian family by targeted exome sequencing

por Imani, Saber, Cheng, Jingliang, Fu, Jiewen, Mobasher-Jannat, Abdolkarim, Wei, Chunli, Mohazzab-Torabi, Saman, Jadidi, Khosrow, Khosravi, Mohammad Hossein, Shasaltaneh, Marzieh Dehghan, Yang, Lisha, Khan, Md. Asaduzzaman, Fu, Junjiang
Publicado 2019

Identification of a novel RPGRIP1 mutation in an Iranian family with leber congenital amaurosis by exome sequencing

por Imani, Saber, Cheng, Jingliang, Mobasher‐Jannat, Abdolkarim, Wei, Chunli, Fu, Shangyi, Yang, Lisha, Jadidi, Khosrow, Khosravi, Mohammad Hossein, Mohazzab‐Torabi, Saman, Shasaltaneh, Marzieh Dehghan, Li, Yumei, Chen, Rui, Fu, Junjiang
Publicado 2017

High body mass index is a significant risk factor for the progression and prognosis of imported COVID-19: a multicenter, retrospective cohort study

por Cai, Huan, Yang, Lisha, Lu, Yingfeng, Zhang, Shanyan, Ye, Chanyuan, Zhang, Xiaoli, Yu, Guodong, Gu, Jueqing, Lian, Jiangshan, Hao, Shaorui, Hu, Jianhua, Zhang, Yimin, Jin, Ciliang, Sheng, Jifang, Yang, Yida, Jia, Hongyu
Publicado 2021

Genetic identification and molecular modeling characterization reveal a novel PROM1 mutation in Stargardt4-like macular dystrophy

por Imani, Saber, Cheng, Jingliang, Shasaltaneh, Marzieh Dehghan, Wei, Chunli, Yang, Lisha, Fu, Shangyi, Zou, Hui, Khan, Md. Asaduzzaman, Zhang, Xianqin, Chen, Hanchun, Zhang, Dianzheng, Duan, Chengxia, Lv, Hongbin, Li, Yumei, Chen, Rui, Fu, Junjiang
Publicado 2017

Immunomodulatory and Antiviral Therapy Improved Functional Cure Rate in CHB Patients with High HBsAg Level Experienced NA

por Jia, Hongyu, Yu, Guodong, Yu, Jiong, Zhang, Xiaoli, Yang, Lisha, Wang, Bin, Zhang, Jiming, Bai, Lang, Zhang, Xinxin, Wang, Kai, Zhao, Ping, Yang, Dongliang, Zhao, Yingren, Yu, Yanyan, Zhang, Yimin, Gu, Jueqing, Ye, Chanyuan, Cai, Huan, Lu, Yingfeng, Xiang, Dairong, Yu, Liang, Lian, Jiangshan, Hu, Jianhua, Zhang, Shanyan, Jin, Ciliang, Yang, Yida
Publicado 2023