Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Feiyue Zhao"'
Publikováno v:
Remote Sensing, Vol 16, Iss 11, p 2003 (2024)
Small object detection poses significant challenges in the realm of general object detection, primarily due to complex backgrounds and other instances interfering with the expression of features. This research introduces an uncomplicated and efficien
Externí odkaz:
https://doaj.org/article/677cbf02842a4abda3648c2b0fac6d87
Publikováno v:
Stem Cells International, Vol 2024 (2024)
Chronic gastric ulcer (CGU), a prevalent digestive disease, has a high incidence and is seriously harmful to human health. Mesenchymal stem cells (MSCs) have been proven to have beneficial therapeutic effects in many human diseases. Here, a CGU model
Externí odkaz:
https://doaj.org/article/f883dde13ecb4cd58c27fc3e2caed289
Autor:
Hai Huang, Xing Wang, Yuan Chen, Qing Zhang, FeiYue Zhao, Xin Ren, XingGuo Zeng, Wei Yan, WangLi Chen, Bin Liu, DaWei Liu, LianBo Fu, JianJun Liu
Publikováno v:
Earth and Planetary Physics, Vol 7, Iss 3, Pp 331-346 (2023)
China’s first Mars exploration mission, Tianwen-1, successfully landed in southern Utopia Planitia on Mars on May 15, 2021. This work presents a detailed investigation of the geologic context of the landing area surface for this mission based on or
Externí odkaz:
https://doaj.org/article/9f35b68f67864afea13492d84959d114
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Synpolydactyly (SPD) is caused by mutations in the transcription factor gene HOXD13. Such mutations include polyalanine expansion (PAE), but further study is required for the phenotypic spectrum characteristics of HOXD13 PAE. We investigated four unr
Externí odkaz:
https://doaj.org/article/57d1c2ca592d495da1572a637e0304db
Autor:
Na Song, Jia Liu, Ke Zhang, Jie Yang, Kai Cui, Zhuang Miao, Feiyue Zhao, Hongjing Meng, Lu Chen, Chong Chen, Yushan Li, Minglong Shao, Wei Su, Haijun Wang
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
Purpose: The LIM (Lin-11, Isl1, MEC-3) domain protein AJUBA is involved in multiple biological functions, and its aberrant expression is related to the occurrence and progression of various cancers. However, there are no analytical studies on AJUBA i
Externí odkaz:
https://doaj.org/article/b5967c98385d416f87c876785180f139
Autor:
Na Song, Kai Cui, Ke Zhang, Jie Yang, Jia Liu, Zhuang Miao, Feiyue Zhao, Hongjing Meng, Lu Chen, Chong Chen, Yushan Li, Minglong Shao, Jinghang Zhang, Haijun Wang
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
N6-methyladenosine (m6A) RNA methylation is identified as the most common, abundant and reversible RNA epigenetic modification in messenger RNA (mRNA) and non-coding RNA, especially within eukaryotic messenger RNAs (mRNAs), which post-transcriptional
Externí odkaz:
https://doaj.org/article/4787355bfb6e49cc85ec77e6d3c399a6
Publikováno v:
Remote Sensing, Vol 15, Iss 9, p 2463 (2023)
Taking the Chang’e-5 (CE-5) sampling area as an example, this study carried out an investigation on improving the crater size-frequency distribution (CSFD) dating accuracy of lunar surface geologic units based on the crater degradation model. We co
Externí odkaz:
https://doaj.org/article/986b65113acd4b068b86ffd994603390
Genotypic and Phenotypic Analysis in Chinese Cohort With Autosomal Recessive Osteogenesis Imperfecta
Autor:
Shan Li, Yixuan Cao, Han Wang, Lulu Li, Xiuzhi Ren, Huan Mi, Yanzhou Wang, Yun Guan, Feiyue Zhao, Bin Mao, Tao Yang, Yi You, Xin Guan, Yujiao Yang, Xue Zhang, Xiuli Zhao
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Osteogenesis imperfecta (OI) is a rare heritable skeletal disorder which is mainly caused by defected type I collagen. Autosomal recessive OI (AR-OI) is caused by mutations of genes that are responsible for type I collagen modification and folding, a
Externí odkaz:
https://doaj.org/article/d3682e35ac7446f7aaa3bc4f382dd13e
Autor:
Lulu Li, Yixuan Cao, Feiyue Zhao, Bin Mao, Xiuzhi Ren, Yanzhou Wang, Yun Guan, Yi You, Shan Li, Tao Yang, Xiuli Zhao
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Osteogenesis Imperfecta (OI) is a rare inherited bone dysplasia, which is mainly caused by mutations in genes encoding type I collagen including COL1A1 and COL1A2. It has been well established to identify the classical variants as well as consensus s
Externí odkaz:
https://doaj.org/article/1c150d65762a4cf283e82c2cf413d861
Autor:
Shuang Li, Xiuzhi Ren, Yun Guan, Feiyue Zhao, Yixuan Cao, Xingzhu Geng, Yanzhou Wang, Nan Wu, Lingqian Wu, Xiuli Zhao
Publikováno v:
PAIN; Sep2024, Vol. 165 Issue 9, p1926-1943, 18p