Roles of MicroRNA-34a in Epithelial to Mesenchymal Transition, Competing Endogenous RNA Sponging and Its Therapeutic Potential

por Nie, Dongsong, Fu, Jiewen, Chen, Hanchun, Cheng, Jingliang, Fu, Junjiang
Publicado 2019

A case of Usher syndrome type IIA caused by a rare USH2A homozygous frameshift variant with maternal uniparental disomy (UPD) in a Chinese family

por Fu, Jiewen, Shen, Shiyi, Cheng, Jingliang, Lv, Hongbin, Fu, Junjiang
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

Genetic polymorphism of 19 autosomal STR loci in the Yi ethnic minority of Liangshan Yi autonomous prefecture from Sichuan province in China

por Cheng, Jingliang, Song, Binghui, Fu, Jiewen, Zheng, Xiaoli, He, Tao, Fu, Junjiang
Publicado 2021

New progresses on cell surface protein HSPA5/BiP/GRP78 in cancers and COVID-19

por Li, Ting, Fu, Jiewen, Cheng, Jingliang, Elfiky, Abdo A., Wei, Chunli, Fu, Junjiang
Publicado 2023

Thymoquinone upregulates IL17RD in controlling the growth and metastasis of triple negative breast cancer cells in vitro

por Khan, Md. Asaduzzaman, Zheng, Meiling, Fu, Jiewen, Tania, Mousumi, Li, Jun, Fu, Junjiang
Publicado 2022

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

Genetic Polymorphism Analysis of 24 Y-STRs in a Han Chinese Population in Luzhou, Southwest China

por Fu, Jiewen, Song, Binghui, Qian, Jie, He, Ting, Chen, Hanchun, Cheng, Jingliang, Fu, Junjiang
Publicado 2023

A novel missense variant c.G644A (p.G215E) of the RPGR gene in a Chinese family causes X-linked retinitis pigmentosa

por Fu, Jiewen, Cheng, Jingliang, Zhou, Qi, Wei, Chunli, Chen, Hanchun, Lv, Hongbin, Fu, Junjiang
Publicado 2019

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

Impacts of transmembrane serine protease 4 expression on susceptibility to severe acute respiratory syndrome coronavirus 2

por Tan, Qi, Fu, Jiewen, Liu, Zhiying, Deng, Haoyue, Zhang, Lianmei, He, Jiayue, Li, Xiaotao, Fu, Junjiang
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

Prostate adenocarcinoma and COVID‐19: The possible impacts of TMPRSS2 expressions in susceptibility to SARS‐CoV‐2

por Cheng, Jingliang, Zhou, Ju, Fu, Shangyi, Fu, Jiewen, Zhou, Baixu, Chen, Hanchun, Fu, Junjiang, Wei, Chunli
Publicado 2021

Effect of DPP4/CD26 expression on SARS-CoV-2 susceptibility, immune response, adenosine (derivatives m(6)(2)A and CD) regulations on patients with cancer and healthy individuals

por Du, Jiaman, Fu, Jiewen, Zhang, Wenqian, Zhang, Lianmei, Chen, Hanchun, Cheng, Jingliang, He, Tao, Fu, Junjiang
Publicado 2023

Novel compound heterozygous nonsense variants, p.L150* and p.Y3565*, of the USH2A gene in a Chinese pedigree are associated with Usher syndrome type IIA

por Fu, Jiewen, Cheng, Jingliang, Zhou, Qi, Khan, Md. Asaduzzaman, Duan, Chengxia, Peng, Jiangzhou, Lv, Hongbin, Fu, Junjiang
Publicado 2020

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

Identification of a novel germline BRCA2 variant in a Chinese breast cancer family

por Cheng, Jingliang, Peng, Jiangzhou, Fu, Jiewen, Khan, Md. Asaduzzaman, Tan, Pingping, Wei, Chunli, Deng, Xiyun, Chen, Hanchun, Fu, Junjiang
Publicado 2019

Targeted Next-Generation Sequencing Identified Novel Compound Heterozygous Variants in the CDH23 Gene Causing Usher Syndrome Type ID in a Chinese Patient

por Zhang, Lianmei, Cheng, Jingliang, Zhou, Qi, Khan, Md. Asaduzzaman, Fu, Jiewen, Duan, Chengxia, Sun, Suan, Lv, Hongbin, Fu, Junjiang
Publicado 2020

Expressions and significances of the angiotensin-converting enzyme 2 gene, the receptor of SARS-CoV-2 for COVID-19

por Fu, Jiewen, Zhou, Baixu, Zhang, Lianmei, Balaji, Kyathegowdanadoddi Srinivasa, Wei, Chunli, Liu, Xiaoyan, Chen, Hanchun, Peng, Jiangzhou, Fu, Junjiang
Publicado 2020

The speckle-type POZ protein (SPOP) inhibits breast cancer malignancy by destabilizing TWIST1

por Wei, Chunli, Liu, Yun, Liu, Xiaoyan, Cheng, Jingliang, Fu, Jiewen, Xiao, Xiuli, Moses, Robb E., Li, Xiaotao, Fu, Junjiang
Publicado 2022