N-glycosylation in the SERPIN domain of C1-Esterase Inhibitor in hereditary angioedema
Z Ren, J Bao, S Zhao, N Pozzi, H Wedner, JP Atkinson - JCI insight, 2025 - insight.jci.org
185548-INS-RG-V3_Clean full_1230 Page 1 1 Title: 1 N-glycosylation in the SERPIN Domain
of the C1-Esterase Inhibitor in Hereditary 2 Angioedema 3 4 Zhen Ren,1 John Bao,1 Shuangxia …
of the C1-Esterase Inhibitor in Hereditary 2 Angioedema 3 4 Zhen Ren,1 John Bao,1 Shuangxia …
A mechanism for hereditary angioedema caused by a methionine-379–to–lysine substitution in kininogens
Hereditary angioedema (HAE) is associated with episodic kinin-induced swelling of the skin
and mucosal membranes. Most patients with HAE have low plasma C1-inhibitor activity …
and mucosal membranes. Most patients with HAE have low plasma C1-inhibitor activity …
Integrated Analysis of Bulk RNA Sequencing, eQTL, GWAS, and Single‐Cell RNA Sequencing Reveals Key Genes in Hepatocellular Carcinoma
M Gong, X Zhao, Q Li, Q Hao, L Cha… - Journal of Cellular …, 2025 - Wiley Online Library
Hepatocellular carcinoma (HCC) poses a continual therapeutic challenge owing to its
elevated incidence and unfavourable prognosis, underscoring the critical need for the …
elevated incidence and unfavourable prognosis, underscoring the critical need for the …
Phenotypic and molecular characterization of the largest worldwide cluster of hereditary angioedema type 1
JS Arias-Flórez, SX Ramirez, B Bayona-Gomez… - PloS one, 2024 - journals.plos.org
Hereditary angioedema type 1 (HAE1) is a rare, genetically heterogeneous, and autosomal
dominant disease. It is a highly variable, insidious, and potentially life-threatening condition …
dominant disease. It is a highly variable, insidious, and potentially life-threatening condition …