日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Human C1-Inhibitor Suppresses Malaria Parasite Invasion and Cytoadhesion via Binding to Parasite Glycosylphosphatidylinositol and Host Cell Receptors.

人类 C1 抑制剂通过与寄生虫糖基磷脂酰肌醇和宿主细胞受体结合来抑制疟原虫入侵和细胞粘附

Mejia Pedro, Diez-Silva Monica, Kamena Faustin, Lu Fengxin, Fernandes Stacey M, Seeberger Peter H, Davis Alvin E 3rd, Mitchell James R

C1 inhibitor: biologic activities that are independent of protease inhibition

C1抑制剂:不依赖于蛋白酶抑制的生物活性

Davis, Alvin E 3rd; Cai, Shenghe; Liu, Dongxu

N-linked glycosylation at Asn3 and the positively charged residues within the amino-terminal domain of the c1 inhibitor are required for interaction of the C1 Inhibitor with Salmonella enterica serovar typhimurium lipopolysaccharide and lipid A

C1抑制剂与鼠伤寒沙门氏菌脂多糖和脂质A的相互作用需要Asn3位点的N-连接糖基化以及氨基末端结构域内的带正电荷残基。

Liu, Dongxu; Cramer, Cort C; Scafidi, Jennifer; Davis, Alvin E 3rd

N-linked glycosylation is required for c1 inhibitor-mediated protection from endotoxin shock in mice

N-连接糖基化是c1抑制剂介导的小鼠内毒素休克保护作用所必需的。

Liu, Dongxu; Gu, Xiaogang; Scafidi, Jennifer; Davis, Alvin E 3rd