Zobrazeno 1 - 10
of 2 493
pro vyhledávání: '"YING BAI"'
Autor:
Ying Bai, Lynn M. Osikowicz, Jacoby Clark, Erik Foster, Christina Parise, Sarah Maes, Rebecca J. Eisen
Publikováno v:
Parasites & Vectors, Vol 17, Iss 1, Pp 1-9 (2024)
Abstract Background Ixodes scapularis and Ixodes pacificus are important vectors of multiple pathogens in the United States. However, their role in transmission of Bartonella spp., which are commonly reported in rodents and fleas, has been debated. O
Externí odkaz:
https://doaj.org/article/39585d9c55054ba3843e66319bac7f3b
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-13 (2024)
Abstract Background Molecular analysis of the CYP21A2 gene is highly important for understanding the aetiology of 21-hydroxylase deficiency (21-OHD). The aim of this study was to use a novel approach named CNVplex, together with the SNaPshot assay an
Externí odkaz:
https://doaj.org/article/643376abb7dc4856a79b7bcafc8cb11c
Autor:
Xinyi Liu, Cancan He, Ying Bai, Dandan Fan, Feifei Zang, Hongxing Zhang, Haisan Zhang, Honghong Yao, Zhijun Zhang, Chunming Xie, Peifang Wei
Publikováno v:
Chinese Medical Journal, Vol 137, Iss 17, Pp 2140-2142 (2024)
Externí odkaz:
https://doaj.org/article/9c51906317bb41cd803bbad9c49a80f8
Publikováno v:
Parasites & Vectors, Vol 17, Iss 1, Pp 1-7 (2024)
Abstract Background Bartonella spp. infect a variety of vertebrates throughout the world, with generally high prevalence. Several Bartonella spp. are known to cause diverse clinical manifestations in humans and have been recognized as emerging pathog
Externí odkaz:
https://doaj.org/article/5ef3c337542d4dee98ff50a2efee11a2
Autor:
Ying Bai, Rui Li, Jun-Feng Hao, Lian-Wan Chen, Si-Tong Liu, Xi-Lin Zhang, Gregory Y. H. Lip, Jin-Kui Yang, Yi-Xi Zou, Hao Wang
Publikováno v:
Journal of Translational Medicine, Vol 22, Iss 1, Pp 1-14 (2024)
Abstract Background Atrial fibrillation (AF) is associated with increased risk of stroke and mortality. It has been reported that the process of atrial fibrosis was regulated by β-catenin in rats with AF. However, pathophysiological mechanisms of th
Externí odkaz:
https://doaj.org/article/18f3d3c6c103462fbf8e8cbf3d60adc0
Publikováno v:
Journal of Animal Science and Technology, Vol 66, Iss 4, Pp 726-739 (2024)
This study was conducted to investigate whether lysophosphatidic acid (LPA) could improve the development of porcine somatic cell nuclear transfer (SCNT) embryos. Porcine SCNT-derived embryos were cultured in chemically defined polyvinyl alcohol (PVA
Externí odkaz:
https://doaj.org/article/26ae5b15bbd84491938b39b58248e438
Publikováno v:
BMC Geriatrics, Vol 24, Iss 1, Pp 1-13 (2024)
Abstract Objective Research the dose–response relationship between overall and certain types of exercise and cognitive function in older adults with Alzheimer's disease and dementia. Design Systemic and Bayesian Model-Based Network Meta-Analysis. M
Externí odkaz:
https://doaj.org/article/d0aabddb4da642d98de9edf5ed340264
Autor:
Yunyun Li, Xuelian Yang, Tao Han, Jiawei Zhou, Yafeng Liu, Jianqiang Guo, Ziqin Liu, Ying Bai, Yingru Xing, Xuansheng Ding, Jing Wu, Dong Hu
Publikováno v:
Translational Oncology, Vol 49, Iss , Pp 102095- (2024)
Background: The immune status is closely linked to cancer progression, metastasis, and prognosis. Lipid metabolism, crucial for reshaping immune status, plays a key role in regulating the advancement of lung adenocarcinoma (LUAD) and deserves further
Externí odkaz:
https://doaj.org/article/80317cf442284c7995e61e36305a3971
Publikováno v:
Journal of International Medical Research, Vol 52 (2024)
Pheochromocytoma crisis is rare but potentially fatal if not recognized early and properly managed. Here, a woman in her 20s with a paraganglioma-induced pheochromocytoma crisis, who was successfully treated by veno-arterial extracorporeal membrane o
Externí odkaz:
https://doaj.org/article/738749430309480b916da9fbde7523d8
Autor:
Ying Bai, Yue Sun, Chenguang Yu, Yanjie Xia, Jing Wu, Li Wang, Yong Gao, Xin Tu, Xiangdong Kong
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-12 (2024)
Abstract Background Marfan syndrome (MFS) is an autosomal dominant connective tissue disease with wide clinical heterogeneity, and mainly caused by pathogenic variants in fibrillin-1 (FBN1). Methods A Chinese 4-generation MFS pedigree with 16 family
Externí odkaz:
https://doaj.org/article/e2dfdbfc005a4eea8e99a59a626e9b05