Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Xiu-Qi Chen"'
Publikováno v:
Frontiers in Surgery, Vol 11 (2024)
ObjectiveTo study the effectiveness of liver transplantation (LT) in treating mitochondrial DNA depletion syndrome (MDS) caused by the MPV17 gene variant.Case presentationA boy aged 2.8 years presented with edema of the lower limbs and abdomen, which
Externí odkaz:
https://doaj.org/article/b7b09c359eb54948adfb5003686da897
Autor:
Jun-Yu Wei, Miao-Yue Hu, Xiu-Qi Chen, Feng-Ying Lei, Jin-Shuang Wei, Jie Chen, Xuan-Kai Qin, Yuan-Han Qin
Publikováno v:
Renal Failure, Vol 44, Iss 1, Pp 2056-2065 (2022)
Background In recent years, peroxisome proliferator-activated receptor γ (PPARγ) has been found to be closely associated with hypoxia renal disease. The aim of this study was to investigate the relationship between rosiglitazone and mitochondrial a
Externí odkaz:
https://doaj.org/article/f4c5616171c14922b98fdc155cfb658f
Publikováno v:
PLoS ONE, Vol 18, Iss 10, p e0291592 (2023)
BackgroundIn the past two years, studies have found a significant increase in neutrophil extracellular traps (NETs) in patients with IgA vasculitis (IgAV), which is correlated with the severity of the disease. NETs have been reported as an interventi
Externí odkaz:
https://doaj.org/article/291cefe9cb294a3a83f1d9ad72ae1332
Publikováno v:
PLoS ONE, Vol 18, Iss 7, p e0288538 (2023)
BackgroundNeutrophil extracellular traps (NETs) have been found to play a role in the development of autoimmune diseases. In the past two years, studies have demonstrated a significantly increase of NETs in skin tissues during the early stages of IgA
Externí odkaz:
https://doaj.org/article/a2e0785c92b24dc5890b8ebd20c3531e
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundWilson’s disease (WD) is a rare cause of acute liver failure (ALF) and has a high fatality rate. Rapid and accurate diagnosis is important for ALF because of WD (ALF-WD). Our objective was to establish a simple, rapid, and accurate diagno
Externí odkaz:
https://doaj.org/article/2503bf80b150405abbb2b8f1bbbad694
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Immunoglobulin A vasculitis (IgAV) is the most common systemic small vessel vasculitis in childhood. Its clinical manifestations are non-thrombocytopenic purpura, accompanied by gastrointestinal tract, joint, kidney and other organ system involvement
Externí odkaz:
https://doaj.org/article/bf6feb49f02a435e9be615de82521824
The Involvement of Neutrophil Extracellular Traps in Disease Activity Associated With IgA Vasculitis
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
ObjectivesThis aim of this study was to determine whether neutrophil extracellular traps (NETs) are involved in the pathogenesis of IgA vasculitis (IgAV) and investigate whether the circulating NETs levels are associated with disease activity in chil
Externí odkaz:
https://doaj.org/article/0db5f7837204482eae36b3a78df95d43
Autor:
Mei-Xiong Yang, Zi-Li Lv, Li Huang, Lian-Cheng Lan, Xiu-Qi Chen, Qing Tang, Xia Yang, Qing-Wen Shan
Publikováno v:
World Journal of Clinical Cases
BACKGROUND The ATP6AP1 gene coding for the accessory protein Ac45 of the vacuolar-type adenosine triphosphatases (V-ATPase) is located on chromosome Xq28. Defects in certain subunits or accessory subunits of the V-ATPase can lead to congenital disord
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59be7223ac84519eeb7a54e9ff82223e
http://europepmc.org/articles/PMC8462236
http://europepmc.org/articles/PMC8462236
Publikováno v:
Indian journal of pediatrics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3f4a2da0dc78878b1471182b181764d
https://pubmed.ncbi.nlm.nih.gov/36598634
https://pubmed.ncbi.nlm.nih.gov/36598634
Background To explore t function of peroxisome proliferator-activated receptor γ(PPARγ) in renal tissue in acute hypoxic renal rat model injury. Methods 24 male SD rats were randomly divided into normal control group, PPARγ agonist group (rosiglit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86d20777c4f6ec4a310d076a607e6035
https://doi.org/10.21203/rs.3.rs-1299965/v1
https://doi.org/10.21203/rs.3.rs-1299965/v1
