Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mali Lin"'
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
ObjectiveThe purpose of this study is to evaluate the efficacy of Vitamin A (VitA) as an adjuvant therapy for pediatric Mycoplasma Pneumoniae Pneumonia (MPP) through meta-analysis, and to investigate its impact on inflammation levels (IL-6, IL-10), i
Externí odkaz:
https://doaj.org/article/2efd7fb8aedb435ebaeeedb57089e749
Publikováno v:
Frontiers in Bioengineering and Biotechnology, Vol 11 (2023)
The incidence and mortality of cancer are gradually increasing. The highly invasive and metastasis of tumor cells increase the difficulty of diagnosis and treatment, so people pay more and more attention to the diagnosis and treatment of cancer. Conv
Externí odkaz:
https://doaj.org/article/57215dea338e44bc8a0fc366f41dfae0
Autor:
Lingzhang, Meng, Shan, Cao, Na, Lin, Jingjie, Zhao, Xulong, Cai, Yonghua, Liang, Ken, Huang, Mali, Lin, Xiajing, Chen, Dongming, Li, Junli, Wang, Lijuan, Yang, Aibo, Wei, Genliang, Li, Qingmei, Lu, Yuxiu, Guo, Qiuju, Wei, Junhua, Tan, Meiying, Huang, Yuming, Huang, Jie, Wang, Yunguang, Liu
Publikováno v:
BioMed Research International
ACTN4, a gene which codes for the protein α-actinin-4, is critical for the maintenance of the renal filtration barrier. It is well known that ACTN4 mutations can lead to kidney dysfunction, such as familial focal segmental glomerulosclerosis (FSGS),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5a31049b89661b99d66c8f63d389ad02
https://pubmed.ncbi.nlm.nih.gov/31930129
https://pubmed.ncbi.nlm.nih.gov/31930129
Autor:
Jingjie Zhao, Mali Lin, Aibo Wei, Xiajing Chen, Dongming Li, Junhua Tan, Qiuju Wei, Junli Wang, Xulong Cai, Na Lin, Lingzhang Meng, Yuming Huang, Yuxiu Guo, Jie Wang, Shan Cao, Ken Huang, Yonghua Liang, Lijuan Yang, Genliang Li, Meiying Huang, Yunguang Liu, Qingmei Lu
Publikováno v:
BioMed Research International, Vol 2019 (2019)
ACTN4, a gene which codes for the protein α-actinin-4, is critical for the maintenance of the renal filtration barrier. It is well known that ACTN4 mutations can lead to kidney dysfunction, such as familial focal segmental glomerulosclerosis (FSGS),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fad0b98c72973b30cfa0fcc5a1879ac7
https://doaj.org/article/da62753665274fc29f14d11aa196bf88
https://doaj.org/article/da62753665274fc29f14d11aa196bf88
Publikováno v:
Annals of human genetics. 82(3)
Asthma is a common, heterogeneous chronic respiratory disease characterized by chronic inflammation of the airway, airway hyperreactivity, and airway remodeling. The RAR-related orphan receptor A (RORA) gene has been identified for the pathogenesis o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fe897b1e0fa0fcebdf8e72129664ba3
https://pubmed.ncbi.nlm.nih.gov/29282706
https://pubmed.ncbi.nlm.nih.gov/29282706