Serpin-A3 is Associated with Persistent Albuminuria in Adolescents with Secondary Podocytopathy, in a Region with High Prevalence of Chronic Kidney Disease of Unknown Origin [0.03%]
塞拉尼蛋白A3与不明原因慢性肾脏病高发地区继发性肾小球足细胞病变青少年患者持续性尿蛋白相关
Leslie P Zúñiga-Macías,Ricardo E Ramírez-Orozco,Francisco J Avelar-González et al.
Leslie P Zúñiga-Macías et al.
Background: The state of Aguascalientes, Mexico, has been recognized as a chronic kidney disease hotspot. Screening studies have revealed a high prevalence of persistent albuminuria (pA), histologically characterized by g...
Importance of Confirmatory Tests for Sars-Cov-2 Infection in Hemodialysis Patients: A Multicenter Mexican Registry [0.03%]
墨西哥血液透析患者SARS-CoV-2感染确认检测的重要性：一项多中心 registry研究
Olynka Vega-Vega,Noemí Del Toro-Cisneros,Víctor M Sacoto-Romo et al.
Olynka Vega-Vega et al.
Background: Since the beginning of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic, patients with chronic kidney disease vulnerable to suffering more severe COVID-19 disease and worse outcomes ha...
Acute Kidney Injury in Critical Care COVID-19 Patients on Invasive Mechanical Ventilation: The Potential Preventive Role of Dexamethasone [0.03%]
危重症新冠肺炎患者有创机械通气患者的急性肾损伤：DEX预防潜在作用分析
Juan M Mejia-Vilet,Noemi Del Toro-Cisneros,Adrián E Caballero-Islas et al.
Juan M Mejia-Vilet et al.
Background: A high incidence of acute kidney injury (AKI) has been reported in coronavirus disease 2019 (COVID-19) patients in critical care units and those undergoing invasive mechanical ventilation (IMV). The introducti...
Activation of CTHRC1 by HOXB9 Promotes Angiogenesis through Fatty Acid Metabolism in Lung Adenocarcinoma [0.03%]
HOXB9激活CTHRC1通过脂肪酸代谢促进肺腺癌血管生成
Keqi Liu,Xiaomin Li,Zhouzhou Yang et al.
Keqi Liu et al.
Background: CTHRC1 is highly expressed in various cancers. Objectives: The aim of the study was to study the role of CTHRC1 played in l...
A simple painless solution to detach different materials from the skin of patients [0.03%]
一种简单无痛的从患者皮肤上去除不同材质的方法
Huberman-Wajsman Alberto
Huberman-Wajsman Alberto
Molecular and Genetic Mechanisms of Neurotoxicity During Anti-seizure Medications Use [0.03%]
抗癫痫药物使用过程中的分子和遗传神经毒性机制
Carmen Rubio,Fernando Gatica,Eric Uribe et al.
Carmen Rubio et al.
Epilepsy is a multifactorial pathology that has allowed the development of various drugs aiming to combat it. This effort was formally initiated in the 1940s when phenytoin began to be used. It eventually turned out to be a drug with great ...
Arterial Blood Gases in Normal Subjects at 2240 Meters Above Sea Level: Impact of Age, Gender, and Body Mass Index [0.03%]
海拔2240米正常人动脉血气的年龄、性别和体重指数的影响
Silvia Cid-Juárez,Norma A Téllez-Navarrete,Anaid Bautista-Bernal et al.
Silvia Cid-Juárez et al.
Background: The values of arterial blood gases (ABG) change with altitude above sea level; empirical verification is essential because ventilatory acclimatization varies with ethnicity and a population's adaptation. ...
At-risk Pregnant Woman with Sticky Platelet Syndrome, Previous Recurrent Preeclampsia, and Current Proteinuria - A Rare Experience [0.03%]
既往有反复妊娠高血压综合征及目前蛋白尿的粘附血小板综合征孕妇一例
Lucia Stančiaková,Miroslava Dobrotová,Jela Ivanková et al.
Lucia Stančiaková et al.
Editing the Human Genome with CRISPR/Cas: A Review of its Molecular Basis, Current Clinical Applications, and Bioethical Implications [0.03%]
CRISPR/Cas基因编辑技术：原理、临床应用及生物伦理学影响综述
Miguel Ahumada-Ayala,Regina Aguilar-López,Nicolai González-Stoylov et al.
Miguel Ahumada-Ayala et al.
CRISPR/Cas genes evolved in prokaryotic organisms as a mechanism of defense designed to identify and destroy genetic material from threatening viruses. A breakthrough discovery is that CRISPR/Cas system can be used in eukaryotic cells to ed...
Low expression of E-Cadherin and CDH1 variants associated with diffuse gastric cancer [0.03%]
E-钙粘蛋白低表达以及与弥漫性胃癌相关的CDH1变异类型
Azaria García-Ruvalcaba,Katia C Vázquez-Ibarra,María T Magaña-Torres et al.
Azaria García-Ruvalcaba et al.
Background: Reduced or null expression of E-cadherin protein is a frequent cause of diffuse gastric cancer (DGC). More than 50% of patients with DGC present somatic variants in CDH1 gene. ...