Zobrazeno 1 - 10
of 215
pro vyhledávání: '"Lidong Zhao"'
Publikováno v:
Journal of Materials Research and Technology, Vol 32, Iss , Pp 915-925 (2024)
In the present study, X-ray diffraction, electron probe microanalysis, and transmission electron microscopy, among other advanced characterization methods, were used to analyze the microstructure and mechanical properties of the 9Ni steel treated at
Externí odkaz:
https://doaj.org/article/33a169461faa4dceb092e9d6bd907821
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 19, Iss 1, Pp 1-7 (2024)
Abstract Background Molecular biology has been applied to the diagnosis, prognosis and treatment of various diseases, and long noncoding RNA LINC00943 (lncRNA LINC00943; LINC00943) plays an important role in a variety of cancers. Therefore, this stud
Externí odkaz:
https://doaj.org/article/b57d6a65ddd9419297af7223273626c9
Autor:
Wenke Wu, Lei Miao, Lidong Zhao, Yuanxin Zhu, Jianping Mao, Zhimei Cai, Yajun Ji, Lei Wang, Ying Wang, Tao Jia
Publikováno v:
Hematology, Vol 29, Iss 1 (2024)
ABSTRACTObjective To investigate the prognostic value of lactate dehydrogenase (LDH), serum albumin (ALB) and the lactate dehydrogenase/albumin ratio (LAR) in diffuse large B-cell lymphoma (DLBCL) before primary treatment.Methods The clinical data of
Externí odkaz:
https://doaj.org/article/c4412c04fb9f4f55aaf31e5389499b97
Publikováno v:
Buildings, Vol 14, Iss 10, p 3196 (2024)
The tailings microcrystalline foamed plate (TMF plate), produced from industrial waste tailings, has limited research regarding its use in high-performance building walls. Its brittleness under stress poses challenges. To improve its mechanical prope
Externí odkaz:
https://doaj.org/article/adb7a1334e644882b4b30ca2d13f32ca
Publikováno v:
Frontiers in Environmental Science, Vol 12 (2024)
Green innovation possesses dual externalities of “innovation” and “environmental protection”, and enhancing energy efficiency serves as a crucial means to promote high-quality economic development. Building upon the energy rebound effect, we
Externí odkaz:
https://doaj.org/article/0884a991687146d7beb184d233f13e8b
Autor:
Lingyu Wang, Jie Zhang, Linna Lu, Juan Ren, Yaofang Zhang, Lidong Zhao, Wukang Shen, Xucheng Hu, Shuai Fang, Xiaomei Lu, Gang Wang, Linhua Yang
Publikováno v:
International Journal of Genomics, Vol 2024 (2024)
Wiskott-Aldrich syndrome (WAS) is a rare X-linked recessive genetic disease characterized by clinical symptoms such as eczema, thrombocytopenia with small platelets, immune deficiency, prone to autoimmune diseases, and malignant tumors. This disease
Externí odkaz:
https://doaj.org/article/ec4f4c2a81e4410688ba379459d443df
Publikováno v:
Frontiers in Neurology, Vol 14 (2024)
Externí odkaz:
https://doaj.org/article/d29ec1c3bc804f9ba4c4f6c4687596ce
Autor:
Jun Li, Qi Han, Yanqing Huang, Yanhui Wei, Jie Zi, Lidong Zhao, Zhimei Cai, Xuzhang Lu, Rong Xiao, Yanming Zhang, Xiaotian Yang, Hao Xu, Naitong Sun, Wanchuan Zhuang, Zhengdong Wu, Yuan Xia, Yanli Xu, Bin He, Wei Zhu, Fengling Min, Yongchun Chen, Banghe Ding, Peimin Shi, Jing Xie, Hua Tang, Zefa Liu, Bingzong Li, Yu Sun, Hongxia Qiu, Limin Duan, Elanora Dovat, Chunhua Song, Laszlo SzeKely, Sinisa Dovat, Zheng Ge
Publikováno v:
Blood Cancer Journal, Vol 12, Iss 10, Pp 1-5 (2022)
Externí odkaz:
https://doaj.org/article/6ea1178c6595485da129eb16f7140eef
Autor:
Yanchun Ma, Wenwen Sun, Lidong Zhao, Mingze Yao, Changxin Wu, Pengfei Su, Linhua Yang, Gang Wang
Publikováno v:
Stem Cell Research & Therapy, Vol 13, Iss 1, Pp 1-11 (2022)
Abstract Background Hemophilia B is a rare inherited genetic bleeding disorder caused by a deficiency or lack of coagulation factor IX, the gene for which (F9) is located on the X chromosome. Hemophilia B is currently incurable and the standard treat
Externí odkaz:
https://doaj.org/article/98f5b9af77da4bc98f5aa9e975b97949
Autor:
Linna Lu, Lingyu Wang, Wukang Shen, Shuai Fang, Lidong Zhao, Xuchen Hu, Linhua Yang, Gang Wang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 5, Pp n/a-n/a (2023)
Abstract Background Hemophilia B (HB), a rare bleeding disorder, shows X‐linked recessive inheritance and is caused by heterogeneous variants in the FIX gene (F9) encoding coagulation factor IX (FIX). This study aimed to investigate the molecular p
Externí odkaz:
https://doaj.org/article/03ef4656e4e4417eb81fc58e6c95abbb