Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mengzhen Fu"'
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
De novo inflammatory bowel disease (IBD) in response to rituximab (RTX) has been documented on multiple occasions as a severe adverse effect. However, none of these reports mentioned any genetic variation associated with this complication. We describ
Externí odkaz:
https://doaj.org/article/8289f7a5b1044fc9a63501aa401e4922
Autor:
Tingting Han, Mei Xue, Yafei Guan, Tao Ju, Kaili Shi, Mengzhen Fu, Lili Jia, Chunlin Gao, Zhengkun Xia
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundMinimal change disease (MCD) is one of the most common primary glomerular disorders with high serum IgE levels. This study was aimed to investigate the clinical features of different serum IgE levels in pediatric MCD and evaluate the progno
Externí odkaz:
https://doaj.org/article/dd0b01f715a2498dbecd6674ebe5aba2
Publikováno v:
Immunology
Genome-wide association studies (GWAS) have identified many loci for systemic lupus erythematosus (SLE). However, identification of functionally relevant genes remains a challenge. The aim of this study was to highlight potential causal genes for SLE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b9b7efcf7714510de49ad6c5bd5f42b
https://doi.org/10.1111/imm.13144
https://doi.org/10.1111/imm.13144
Publikováno v:
Rheumatology. 59:889-898
Objectives Phosphorylation-related single-nucleotide polymorphisms (phosSNPs) are missense SNPs that may influence protein phosphorylation. The aim of this study was to evaluate the effect of phosSNPs on lipid levels and RA. Methods We examined the a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6573a39d56a27954920f42b7eeba0295
https://doi.org/10.1093/rheumatology/kez466
https://doi.org/10.1093/rheumatology/kez466