Effect of major CYP2C19 genetic polymorphisms on Helicobacter pylori eradication based on different treatment regimens [0.03%]
不同治疗方案中主要的CYP2C19基因多态性对幽门螺旋杆菌根除的影响
Malek Zihlif,Banan Bashaireh,Mohammed Rashid et al.
Malek Zihlif et al.
Helicobacter pylori (H. pylori) infection is a global issue. Its eradication in affected individuals is important to prevent several further complications that may occur if left untreated. Proton pump inhibitors (PPIs) serve an important ro...
Association between promoter methylation and gene expression of CGB3 and NOP56 in HPV-infected cervical cancer cells [0.03%]
CGB3和NOP56基因启动子甲基化与HPV感染的宫颈癌细胞中的基因表达的关系研究
Palak Singh,Kanwalat Chalertpet,Juthamard Sukbhattee et al.
Palak Singh et al.
Overexpression of the E7 gene of human papillomavirus (HPV) type 16 is one of the primary causes of cervical cancer. The E7 protein can bind with DNA methyltransferase I and induce methylation of tumor suppressor genes, such as cyclin-A1 (C...
Asymptomatic SARS-CoV-2 infection in an unvaccinated 97-year-old woman: A case report [0.03%]
未接种疫苗的97岁女性SARS-CoV-2无症状感染的病例报告
Vasiliki Epameinondas Georgakopoulou,Petros Papalexis,Christos Sanos et al.
Vasiliki Epameinondas Georgakopoulou et al.
Coronavirus disease (COVID-19) is an infection caused by the newly detected coronavirus, SARS-CoV-2. The majority of individuals will exhibit mild to moderate illness. Older individuals, and those suffering from co-existing diseases have a ...
Case Reports
Biomedical reports. 2021 Dec;15(6):107. DOI:10.3892/br.2021.1483 2021
Mitochondria-related TFAM gene variants and their effects on patients with cervical cancer [0.03%]
与线粒体相关的TFAM基因变异及其对宫颈癌患者的影响
Ieva Golubickaite,Rasa Ugenskiene,Juste Cepaite et al.
Ieva Golubickaite et al.
Cervical cancer is the fourth most common type of cancer in women worldwide, with high incidence and mortality rates, particularly in developing countries. There are human papillomavirus vaccines and cytological screening programs available...
Preliminary investigation of two promoter region polymorphisms of the TNFA gene in patients with recurrent depressive disorder [0.03%]
TNFA基因启动子区两个多态性在复发抑郁障碍患者中的初步研究
Agnieszka Jeleń,Marta Żebrowska-Nawrocka,Dagmara Szmajda-Krygier et al.
Agnieszka Jeleń et al.
Immune system dysregulation plays a role in the pathogenesis of complex human diseases, including psychiatric disorders. In addition, elevated levels of pro-inflammatory cytokines, including tumor necrosis factor α (TNF-α) may be conditio...
Staphylococcus aureus mediastinitis following a skin infection in a non-immunocompromised patient: A case report [0.03%]
皮肤感染后的金黄色葡萄球菌非免疫抑制患者的纵隔炎病例报告
Konstantinos Mantzouranis,Vasiliki Epameinondas Georgakopoulou,Dimitrios Mermigkis et al.
Konstantinos Mantzouranis et al.
Mediastinitis is a severe inflammation of the structures located in the mid-chest cavity. Three main causes of infective mediastinitis are traditionally recognized: Deep infection of a sternal wound following cardiothoracic surgery, perfora...
A case of Bardet-Biedl syndrome caused by a recurrent variant in BBS12: A case report [0.03%]
BBS12基因突变引起的Bardet-Biedl综合征一例报告
Ina Ofelia Focșa,Magdalena Budișteanu,Carmen Burloiu et al.
Ina Ofelia Focșa et al.
Bardet-Biedl syndrome (BBS) is a clinically and genetically heterogenous disorder that manifests as a result of primary cilia impairment. Cilia are present on most cell types, thus BBS is a multisystemic condition involving the majority of ...
Jalil Daher
Jalil Daher
It is hypothesized that several comorbidities increase the severity of COVID-19 symptoms. Cardiovascular disease including hypertension was shown to play a critical role in the severity of COVID-19 infection by affecting the survival of pat...
Influence of the SOD2 A16V gene polymorphism on alterations of redox markers and erythrocyte membrane fatty acid profiles in patients with multiple chemical sensitivity [0.03%]
SOD2 A16V基因多态性对多重化学敏感患者氧化还原标志物及红细胞膜脂肪酸谱变化的影响
Attilio Cannata,Chiara De Luca,Giulia Andolina et al.
Attilio Cannata et al.
Chronically increased oxidative stress has been reported in patients with multiple chemical sensitivity (MCS). Recently, a single nucleotide polymorphism of the gene coding for mitochondrial superoxide dismutase (SOD2), namely the missense ...
Potential protective role of a NOD2 polymorphism in the susceptibility to multiple sclerosis is not associated with interferon therapy [0.03%]
NOD2基因多态性在多发性硬化易感性的潜在保护作用与干扰素治疗无关
Aida Zečkanović,Aleš Maver,Smiljana Ristić et al.
Aida Zečkanović et al.
Pattern recognition receptors, such as specific nucleotide-binding oligomerization domain protein 2, and their polymorphisms may be involved in the pathogenesis of multiple sclerosis (MS). They may also play a role in the formation of neutr...