Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Weidi, Wang"'
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-13 (2024)
Abstract Background Elucidating the dynamics of gene expression across developmental stages, including the genomic characteristics of brain expression during infancy, is pivotal in deciphering human psychiatric and neurological disorders and providin
Externí odkaz:
https://doaj.org/article/59909c54b2dd4a7db8fda85819518850
Autor:
Jiayuan Zhao, Dan Wang, Ruojiao Wang, Yonglan He, Congwei Jia, Lingya Pan, Shuiqing Ma, Ming Wu, Weidi Wang, Xinghan Cheng, Junjun Yang, Yang Xiang
Publikováno v:
Journal of Ovarian Research, Vol 17, Iss 1, Pp 1-9 (2024)
Abstract Objective To describe the characteristics of children and adolescents with borderline ovarian tumors (BOTs) and evaluate the efficacy and safety of fertility-sparing surgery (FSS) in these patients. Methods Patients with BOTs younger than 20
Externí odkaz:
https://doaj.org/article/f2386d03fa7f4773914734acc112bf27
Publikováno v:
Materials & Design, Vol 237, Iss , Pp 112550- (2024)
Mechanical metamaterials (MMs) are micro-structured systems that have long attracted research as well as application interests due to their exotic dynamic functionalities and properties not seen in ordinary materials. Graded MM arrays further enrich
Externí odkaz:
https://doaj.org/article/e1f0052ecfd14f1495171207f04102f4
Autor:
Zheqin Li, Jian Gao, Liangjun Lin, Zifeng Zheng, Susu Yan, Weidi Wang, Dongdong Shi, Zhen Wang
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
IntroductionObsessive–compulsive disorder (OCD), characterized by the presence of obsessions and/or compulsions, is often difficult to diagnose and treat in routine clinical practice. The candidate circulating biomarkers and primary metabolic pathw
Externí odkaz:
https://doaj.org/article/657893a3b1a740948b6a3d6777ace827
Autor:
Zhe Liu, Wei Qian, Wenxiang Cai, Weichen Song, Weidi Wang, Dhruba Tara Maharjan, Wenhong Cheng, Jue Chen, Han Wang, Dong Xu, Guan Ning Lin
Publikováno v:
Research, Vol 6 (2023)
Identifying pathogenetic variants and inferring their impact on protein–protein interactions sheds light on their functional consequences on diseases. Limited by the availability of experimental data on the consequences of protein interaction, most
Externí odkaz:
https://doaj.org/article/c895377255434f57b709ced30e8eff90
Publikováno v:
BMC Medical Genomics, Vol 14, Iss S1, Pp 1-11 (2021)
Abstract Background Huntington’s disease is a kind of chronic progressive neurodegenerative disease with complex pathogenic mechanisms. To data, the pathogenesis of Huntington’s disease is still not fully understood, and there has been no effecti
Externí odkaz:
https://doaj.org/article/34c3f356a3ea48648d1f2f47447d660e
Autor:
Ying Sun, Le Ma, Jianhua Chen, Weidi Wang, Shiyu Peng, Ying Cheng, Yu Zhang, Jinghong Chen, Peijun Ju
Publikováno v:
Molecular Brain, Vol 14, Iss 1, Pp 1-12 (2021)
Abstract Anxiety disorders are the most common psychiatric disorders, and the change in the activity of the prefrontal cortex (PFC) is considered as the underlying pathological mechanism. Parvalbumin-expressing (PV+) inhibition contributes to the ove
Externí odkaz:
https://doaj.org/article/29280de6bbf94de0bbb5a73c0705f5f3
Publikováno v:
BMC Genomics, Vol 22, Iss S3, Pp 1-11 (2021)
Abstract Background Observational studies have identified various associations between neuroimaging alterations and neuropsychiatric disorders. However, whether such associations could truly reflect causal relations remains still unknown. Results Her
Externí odkaz:
https://doaj.org/article/07f356b7a4c34ed6b1d77e6fad502066
Publikováno v:
Endocrine Connections, Vol 10, Iss 6, Pp 656-666 (2021)
Background: The presence of clinically negative nodules on the contralater al lobe is common in patients with unilateral papillary thyroid microcarci noma (PTMC). The appropriate operational strategies of contralateral thyroid nodules remain controve
Externí odkaz:
https://doaj.org/article/524b58826f4a48fa9752ea659f44b96d
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Recurrent deletions and duplications of chromosome 7q11.23 copy number variants (CNVs) are associated with several psychiatric disorders. Although phenotypic abnormalities have been observed in patients, causal genes responsible for CNV-asso
Externí odkaz:
https://doaj.org/article/880c847ab3384d7fa5f731deebc2754e