Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Shiqiu Xiong"'
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background Persistent airflow limitation (PAL) in childhood asthma is associated with a poor prognosis. The aim of this study was to categorize asthmatic children with PAL into distinct phenotypes and investigate the risk factors associated
Externí odkaz:
https://doaj.org/article/291a167651c943d0ae72e613fc143e5e
Publikováno v:
Heliyon, Vol 10, Iss 18, Pp e37866- (2024)
Background: Previous studies have demonstrated that immune cells release exosomes, which act as antigen-presenting vesicles to activate T cells. In our previous study, we discovered that podocytes, a type of kidney cell, can also exhibit antigen-pres
Externí odkaz:
https://doaj.org/article/ba87ce7f4981460fa51b78a453c0ff28
Autor:
Chunyu Tian, Shiqiu Xiong, Shuo Li, Xin Song, Yantao Zhang, Xinmei Jiang, Xinyue Hou, Yifan Zhang, Chuanhe Liu
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background Cough variant asthma (CVA) is one of the most common causes of chronic cough in children worldwide. The diagnosis of CVA in children remains challenging. This study aimed to assess the diagnostic utility of impulse oscillometry (I
Externí odkaz:
https://doaj.org/article/666763e46b5b4fbe852efa84bea06ce6
Publikováno v:
BMC Pulmonary Medicine, Vol 23, Iss 1, Pp 1-15 (2023)
Abstract Background Asthma exacerbations reduce the patient’s quality of life and are also responsible for significant disease burdens and economic costs. Machine learning (ML)-based prediction models have been increasingly developed to predict ast
Externí odkaz:
https://doaj.org/article/781f799ef34841efb31cc12d5c7b0df1
Autor:
Yan Yin, Shengrong Ouyang, Qin Li, Yuyang Du, Shiqiu Xiong, Min Zhang, Wei Wang, Ting Zhang, Chuanhe Liu, Ying Gao
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionFood allergies have a substantial impact on patient health, but their mechanisms are poorly understood, and strategies for diagnosing, preventing, and treating food allergies are not optimal. This study explored the levels of and relation
Externí odkaz:
https://doaj.org/article/deb7f8e15cc4448380d1112a13970dd9
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Persistent allergies affect the quality of life of patients and increase economic burdens. Many clinical observations indicate the presence of IgE+ long-lived plasma cells (LLPCs), which account for the persistent secretion of specific IgE; however,
Externí odkaz:
https://doaj.org/article/40bc703c0804438da4d3499dd67ef9e2
Autor:
Xueqiong Meng, Xiaoxi Cui, Xiaoya Shao, Yanqi Liu, Yihao Xing, Victoria Smith, Shiqiu Xiong, Salvador Macip, Yixiang Chen
Publikováno v:
Translational Oncology, Vol 18, Iss , Pp 101362- (2022)
Cervical cancer is one of the most common malignancies in women, with a poor survival rate. Thus, there is a need to define effective combination strategies to improve therapy. In this study, we report that dsRNA poly(I:C) up-regulated the expression
Externí odkaz:
https://doaj.org/article/aebb55d5c84d48e683c0fca68c13add5
Podocytic infolding in Schimke immuno-osseous dysplasia with novel SMARCAL1 mutations: a case report
Publikováno v:
BMC Nephrology, Vol 21, Iss 1, Pp 1-5 (2020)
Abstract Background Schimke immuno-osseous dysplasia (SIOD) is a rare autosomal recessive disorder characterized by spondyloepiphyseal dysplasia, progressive renal insufficiency and defective cellular immunity. Podocytic infolding glomerulopathy (PIG
Externí odkaz:
https://doaj.org/article/efaad6d5494e4ba8b33800da22814804
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
X-linked sideroblastic anemia with ataxia (XLSA/A) is a rare X-liked inherited disease, which was linked to the ABCB7 gene mutations. So far, five families have been reported worldwide. We present the first Chinese family of XLSA/A with novel ABCB7 g
Externí odkaz:
https://doaj.org/article/660e050a90084eeaa2434f53caf226e3
Autor:
Caiqiong Liu, Xiaoyan Li, Lanjun Shuai, Xiqiang Dang, Fangrong Peng, Mingyi Zhao, Shiqiu Xiong, Ying Liu, Qingnan He
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
Purpose: The factor associated with IgA nephropathy (IgAN) is an abnormality of IgA known as galactose-deficient IgA1 (Gd-IgA1). The purpose of this study was to determine the molecular role played by miRNAs in the formation of Gd-IgA1 in IgAN and in
Externí odkaz:
https://doaj.org/article/12e13f9cdc2f4ea2a7a3033d9be883bd