Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Wenzhou LIU"'
Publikováno v:
Journal of Orthopaedic Surgery and Research, Vol 18, Iss 1, Pp 1-13 (2023)
Abstract Purpose Tenosynovial giant cell tumour (TGCT) is a benign hyperplastic and inflammatory disease of the joint synovium or tendon sheaths, which may be misdiagnosed due to its atypical symptoms and imaging features. We aimed to identify biomar
Externí odkaz:
https://doaj.org/article/bda92bcabce94b73b102f106978cda48
Autor:
Qing He, Peng Hao, Gang He, Hantao Mai, Wenzhou Liu, Weiqiong Zhang, Kelin Zhang, Guifang Zhong, Ruilian Guo, Changzhi Yu, Yang Li, Chipiu Wong, Qian Chen, Yantao Chen
Publikováno v:
Journal of Translational Medicine, Vol 20, Iss 1, Pp 1-14 (2022)
Abstract Doxorubicin (Dox) is the standard treatment approach for osteosarcoma (OS), while acquired drug resistance seriously attenuates its treatment efficiency. The present study aimed to investigate the potential roles of metabolic reprogramming a
Externí odkaz:
https://doaj.org/article/dd785fd8469b467992a1fb0c652956d4
Autor:
Hongyu Li, Xin Shen, Mengjun Ma, Wenzhou Liu, Wen Yang, Peng Wang, Zhaopeng Cai, Rujia Mi, Yixuan Lu, Jiahao Zhuang, Yuhang Jiang, Yihui Song, Yanfeng Wu, Huiyong Shen
Publikováno v:
Journal of Experimental & Clinical Cancer Research, Vol 40, Iss 1, Pp 1-16 (2021)
Abstract Background The zinc transporters Zrt- and Irt-related protein (ZIP/SLC39) are overexpressed in human tumors and correlate with poor prognosis; however, their contributions to carcinogenesis and chemoresistance in osteosarcoma (OS) remain unc
Externí odkaz:
https://doaj.org/article/584d29c39cfa4f6cb48eb6e906ddad12
Publikováno v:
BMC Pulmonary Medicine, Vol 21, Iss 1, Pp 1-6 (2021)
Abstract Background LINC01116 is a recently identified oncogenic lncRNA in glioma. Differential expression analysis using the public gene expression analysis tool GEPIA revealed the upregulation of LINC01116 in lung cancer. We studied the functions o
Externí odkaz:
https://doaj.org/article/b59e5839ed644aacbbef22ac11058a65
Publikováno v:
Frontiers in Surgery, Vol 9 (2022)
BackgroundThis study reported the individual surgical treatment of 12 cases with stage IV Müller-Weiss disease (MWD) according to CT/MRI examination.MethodsIn total, 12 cases diagnosed with stage IV MWD in our hospital from 2015 to 2019 were include
Externí odkaz:
https://doaj.org/article/a049ea6f26db42698b76ee5615cc6330
Publikováno v:
Frontiers in Molecular Biosciences, Vol 8 (2022)
Objective: Osteoarthritis (OA) is the most common chronic degenerative joint disease, which represents the leading cause of age-related disability. Here, this study aimed to depict the intercellular heterogeneity of OA synovial tissues.Methods: Singl
Externí odkaz:
https://doaj.org/article/6f3651a1cf444d389f70bf483632d096
Publikováno v:
STEMedicine, Vol 1, Iss 3 (2020)
Chimeric antigen receptor T (CAR-T) technology is the pinnacle of modern immunology, system biology, synthetic biology and cellular engineering. It is the powerful new player of cancer therapy since the concept of adoptive cell therapy. Clinical succ
Externí odkaz:
https://doaj.org/article/60f6ce257ae04f0798884f15692b7ae3
Publikováno v:
BMC Surgery, Vol 18, Iss 1, Pp 1-4 (2018)
Abstract Background Spleen leaves its normal anatomical position and appears in other locations, which is called ectopic spleen. It is most commonly found in the abdomen or pelvis with seeding of the peritoneum, omentum or mesentery. A few of cases o
Externí odkaz:
https://doaj.org/article/e5dade026df246e28407d6d045e5cb0c
Publikováno v:
Chinese Journal of Lung Cancer, Vol 15, Iss 11, Pp 642-645 (2012)
Background and objective Lung cancer is the most common cancer in the world. The gene expression profiling of lung cancer has been extensively investigated. However, only a few studies have identified the possible pathways and significant genes relat
Externí odkaz:
https://doaj.org/article/a0f7fa64356d447b955cf5c13e341c90
Autor:
Weining Rong, Xue Chen, Kanxing Zhao, Yani Liu, Xiaoxing Liu, Shaoping Ha, Wenzhou Liu, Xiaoli Kang, Xunlun Sheng, Chen Zhao
Publikováno v:
PLoS ONE, Vol 9, Iss 5, p e97808 (2014)
Usher syndrome (USH) is a group of disorders manifested as retinitis pigmentosa and bilateral sensorineural hearing loss, with or without vestibular dysfunction. Here, we recruited three Chinese families affected with autosomal recessive USH for deta
Externí odkaz:
https://doaj.org/article/77cf01d4717d4c5786519671daac2ee8