Identification of RNA-binding protein genes associated with renal rejection and graft survival [0.03%]
与肾排斥和移植物存活相关的RNA结合蛋白基因的鉴定
Zhaozhong Zhong,Yongrong Ye,Liubing Xia et al.
Zhaozhong Zhong et al.
Rejection is one of the major factors affecting the long-term prognosis of kidney transplantation, and timely recognition and aggressive treatment of rejection is essential to prevent disease progression. RBPs are proteins that bind to RNA ...
Risk factors and clinical prediction models for osteoporosis in pre-dialysis chronic kidney disease patients [0.03%]
透前慢性肾脏病患者骨质疏松的风险因素及临床预测模型
Chaoying Kuang,Jingjie Shang,Mingming Ma et al.
Chaoying Kuang et al.
Background: Osteoporosis in pre-dialysis chronic kidney disease (CKD) patients has been overlooked, and the risk factors of osteoporosis in these patients have not been adequately studied. ...
Decrease in platelet count in patients with AKI and its association with major adverse kidney events [0.03%]
急性肾损伤患者的血小板计数下降及其与主要不良肾脏事件的相关性
Ramón Medina-González,Jose J Zaragoza,Eduardo M Hernández-Barajas et al.
Ramón Medina-González et al.
Introduction: A reduction in platelet count in critically ill patients is a marker of severity of the clinical condition. However, whether this association holds true in acute kidney injury (AKI) is unknown. We analyzed t...
The role of sacubitril/valsartan in abnormal renal function patients combined with heart failure: a meta-analysis and systematic analysis [0.03%]
萨库布韦/缬沙坦在肾功能异常的心衰患者中的作用：一项Meta分析和系统分析
Xinyue Yang,Jingjing Jin,Meijuan Cheng et al.
Xinyue Yang et al.
Aims: This study aimed to investigate the efficacy and safety of sacubitril/valsartan in abnormal renal function (eGFR < 60 ml/min/1.73m2) patients combined with heart failure based on randomized controlled trials (RCTs) ...
Contralateral renal change in a unilateral ureteral obstruction rat model using intravoxel incoherent motion diffusion-weighted imaging [0.03%]
单侧尿路梗阻大鼠模型的对侧肾脏改变的体素内不相干运动扩散加权成像研究
Lingtao Zhang,Xukai Mo,Zijie Jiang et al.
Lingtao Zhang et al.
Objectives: Most functional magnetic resonance research has primarily examined alterations in the affected kidney, often neglecting the contralateral kidney. Our study aims to investigate whether imaging parameters accura...
H-151 attenuates lipopolysaccharide-induced acute kidney injury by inhibiting the STING-TBK1 pathway [0.03%]
H-151通过抑制STING-TBK1信号通路缓解脂多糖诱导的急性肾损伤
Lei Xia,Jia-Hui Jiang,Jie-Yu Liu et al.
Lei Xia et al.
Sepsis is a severe systemic infectious disease that often leads to multi-organ dysfunction. One of the common and serious complications of sepsis is renal injury. In this study, we aimed to investigate the potential mechanistic role of a no...
Pattern and outcome of renal diseases in hospitalized patients at a tertiary hospital in Mogadishu, Somalia [0.03%]
索马里摩加迪沙三级医院住院患者的肾脏疾病模式和结局
Abdirahman Abdikadir Osman,Nasteho Mohamed Sheikh Omar,Marian Muse Osman et al.
Abdirahman Abdikadir Osman et al.
Remnant cholesterol, preinflammatory state and chronic kidney disease: association and mediation analyses [0.03%]
残余胆固醇、前期炎症状态与慢性肾脏病的关联及中介效应分析
Yougen Yuan,Xiangming Hu,Shanghong Zhang et al.
Yougen Yuan et al.
Blood lipid management is a key approach in the prevention of chronic kidney disease (CKD). Remnant cholesterol (RC) plays an important role in the development of multiple diseases via chronic inflammation. The aim of our study was to deter...
Serum antineutrophil cytoplasmic antibody positivity at the time of renal biopsy is associated with disease activity of lupus nephritis [0.03%]
肾活检时血清抗中性粒细胞胞浆抗体阳性与狼疮性肾炎的疾病活动相关
Jing Zhang,Ruoshan Lian,Yi Chen et al.
Jing Zhang et al.
Objective: To investigate the correlations between serum antineutrophil cytoplasmic antibody (ANCA) and clinicopathological features, induction treatment response, and prognosis of lupus nephritis (LN) patients. ...
Identification of a novel nonsense mutation in α-galactosidase A that causes Fabry disease in a Chinese family [0.03%]
在中国一个家庭中鉴定出一种全新的终止密码子突变的α-半乳糖苷酶A导致法布瑞病
Yushi Peng,Meize Pan,Yuchen Wang et al.
Yushi Peng et al.
Fabry disease, a lysosomal storage disease, is an uncommon X-linked recessive genetic disorder stemming from abnormalities in the alpha-galactosidase gene (GLA) that codes human alpha-Galactosidase A (α-Gal A). To date, over 800 GLA mutati...
Case Reports
Renal failure. 2024 Dec;46(2):2362391. DOI:10.1080/0886022X.2024.2362391 2024