Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kunna, Lu"'
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
BackgroundSystemic inflammation and immune response are involved in the pathogenesis of diabetic nephropathy (DN). However, the specific immune-associated signature during DN development is unclear. Our study aimed to reveal the roles of immune-relat
Externí odkaz:
https://doaj.org/article/e992d7ff3c7c490bbe5461147ed92919
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
We investigated the effects of high- vs. standard-dose vitamin D supplementation on kidney function and bone metabolism in children with chronic kidney disease (CKD). Children were randomized to receive one of two formulations: 75 participants receiv
Externí odkaz:
https://doaj.org/article/fb980b14e56848a1ac8e162f50100cef
We investigated the effects of high VS. standard dose of vitamin D supplementation on kidney function and bone metabolism in children with chronic kidney disease (CKD). In all, 75 participants receive 2000 IU/D of vitamin D oral supplementation vs 75
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::610e523b2468d23ec5388f9171c5e899
https://doi.org/10.21203/rs.3.rs-1843828/v1
https://doi.org/10.21203/rs.3.rs-1843828/v1
Publikováno v:
Human Cell. 34:825-835
Subclinical hypothyroidism (SCH) is associated with increased risks of endothelial dysfunction and atherosclerosis, but the mechanisms remain unclear. In our previous study, microRNA-126-3p was downregulated in SCH, but the role and regulatory mechan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab097f6b2ffdc1200e56c3a7f4d54dd3
https://doi.org/10.1007/s13577-021-00508-0
https://doi.org/10.1007/s13577-021-00508-0
Autor:
Shiguo, Liu, Wenhui, Zhang, Liqin, Zhang, Hui, Zou, Kunna, Lu, Qiang, Li, Hongfei, Xia, Shengli, Yan, Xu, Ma
Publikováno v:
Oncotarget
Mutations in the dual oxidase 2 gene (DUOX2) impair hydrogen peroxide (H2O2) production and cause dyshormonogenesis. In addition, these mutations have been implicated in autosomal recessive congenital hypothyroidism (CH) with goiter. In this study, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e1a9d25770f9083a1c551d46e8b66a24
https://pubmed.ncbi.nlm.nih.gov/29435108
https://pubmed.ncbi.nlm.nih.gov/29435108