Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Jiadi Li"'
Autor:
Ronglin Tu, Xiaoming Liu, Lin Xu, Xuemin Yao, Ran Zhang, Jiadi Li, Wenjun Zhang, Jinrong Liu, Xiuping Wu, Bing Li
Publikováno v:
Frontiers in Materials, Vol 11 (2024)
Objectives: Due to the complexity and importance of oral bone structure, oral bone regeneration materials differ from those used in other parts of the body. To study the research trends and hotspots of oral bone regeneration materials, this paper con
Externí odkaz:
https://doaj.org/article/7605a5c9b852400da532ae1ecb7583b1
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
IntroductionTriple-negative breast cancer (TNBC) is linked to a poorer outlook, heightened aggressiveness relative to other breast cancer variants, and limited treatment choices. The absence of conventional treatment methods makes TNBC patients susce
Externí odkaz:
https://doaj.org/article/6e84ec196ca146e1bcbe548e0b3e4ae6
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract This study used a Mendelian randomization (MR) approach to investigate the causal relationship between genetically predicted endometriosis (EMS) and breast cancer risk. A total of 122,977 cases and 105,974 controls were included in the analy
Externí odkaz:
https://doaj.org/article/55c6584ca604498fa73d3df4e8e8b04d
Publikováno v:
Arabian Journal of Chemistry, Vol 16, Iss 11, Pp 105229- (2023)
Potential cancer therapy can be accomplished by utilizing nano-based platforms that supply facilitated drug penetration inside cancer cells. In this paper, an intelligent therapeutic nano-based system derived from metal–organic framework (MOF) core
Externí odkaz:
https://doaj.org/article/cb08b72bce764431a9990f70a4f874e8
Autor:
Huilong Yin, Zhuan Ju, Minhua Zheng, Xiang Zhang, Wenjie Zuo, Yidi Wang, Xiaochen Ding, Xiaofang Zhang, Yingran Peng, Jiadi Li, Angang Yang, Rui Zhang
Publikováno v:
PLoS Biology, Vol 21, Iss 3, p e3002017 (2023)
Alzheimer's disease (AD) is a heterogeneous disease with complex clinicopathological characteristics. To date, the role of m6A RNA methylation in monocyte-derived macrophages involved in the progression of AD is unknown. In our study, we found that m
Externí odkaz:
https://doaj.org/article/4526e8330c154eafbd02f5408613b99f
Autor:
Jiafeng Chen, Xinrong Li, Shuixin Yan, Jiadi Li, Yuxin Zhou, Minhua Wu, Jinhua Ding, Jiahui Yang, Yijie Yuan, Ye Zhu, Weizhu Wu
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
IntroductionBreast cancer (BRCA) is the most common malignancy among women worldwide. It was widely accepted that autophagy and the tumor immune microenvironment play an important role in the biological process of BRCA. Long non-coding RNAs (lncRNAs)
Externí odkaz:
https://doaj.org/article/3c134895f8f244c1b6f2c5b8163e2a82
Autor:
Jingjing Shi, Jie Tian, Yu Fan, Xiaoyan Hao, Mengjie Li, Jiadi Li, Dongrui Ma, Mengnan Guo, Shuangjie Li, Yuming Xu, Changhe Shi
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: A high level of education or intelligence (IQ) is reported to be a risk factor for Parkinson’s disease (PD). The purpose of this study was to systematically examine the causal relationships between IQ, educational attainment (EA), cogni
Externí odkaz:
https://doaj.org/article/7e69d8f57d954cd5948c2537b2c7e686
Autor:
Jiadi Li, Yu Fan, Liyuan Fan, Fen Liu, Xiaoyan Hao, Mengjie Li, Chengyuan Mao, Yuming Xu, Changhe Shi
Publikováno v:
Stem Cell Research, Vol 63, Iss , Pp 102844- (2022)
Neuronal intranuclear inclusion disease (NIID) is a neurodegenerative disease characterized by cognitive impairment, extrapyramidal symptoms, white matter lesions and muscle weakness. The cause of NIID is a repeat amplification of a GGC mutation in t
Externí odkaz:
https://doaj.org/article/d96367e95ee544efb66391d141e727eb
Autor:
Mengjie Li, Fen Liu, Xiaoyan Hao, Yu Fan, Jiadi Li, Zhengwei Hu, Jingjing Shi, Liyuan Fan, Shuo Zhang, Dongrui Ma, Mengnan Guo, Yuming Xu, Changhe Shi
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
Spinocerebellar ataxia 19/22 (SCA19/22) is a rare neurodegenerative disorder caused by mutations of the KCND3 gene, which encodes the Kv4. 3 protein. Currently, only 22 KCND3 single-nucleotide mutation sites of SCA19/22 have been reported worldwide,
Externí odkaz:
https://doaj.org/article/f185e50cbd9f4d29aff921d16b8e2b27
Autor:
Shuixin Yan1, Jiadi Li1, Jiafeng Chen1, Yuxin Zhou1, Yu Qiu1, Yan Chen1, Weizhu Wu1 wuweizhu1128@163.com
Publikováno v:
Alternative Therapies in Health & Medicine. Jan2024, Vol. 30 Issue 1, p260-264. 5p.