O-GlcNAcylated YTHDF2 promotes bladder cancer progression by regulating the tumor suppressor gene PER1 via m6A modification [0.03%]
O-GlcNAc修饰的YTHDF2通过m6A修饰调控肿瘤抑制基因PER1促进膀胱癌进展
Li Wang,Da Ren,Zeqiang Cai et al.
Li Wang et al.
Objectives: Bladder cancer is a common malignancy with high incidence and poor prognosis. N6-methyladenosine (m6A) modification is widely involved in diverse physiological processes, among which the m6A recognition protei...
FTO - regulated m6A modification of pri - miR - 139 represses papillary thyroid carcinoma metastasis [0.03%]
FTO通过调节pri-miR-139的m6A修饰抑制乳头状甲状腺癌转移
Jiale Li,Ping Zhou,Juan DU et al.
Jiale Li et al.
Objectives: Increasing detection of low-risk papillary thyroid carcinoma (PTC) is associated with overdiagnosis and overtreatment. N6-methyladenosine (m6A)-mediated microRNA (miRNA) dysregulation plays a critical role in ...
Radiogenomics-based prediction of KRAS and EGFR gene mutation in non-small cell lung cancer patients [0.03%]
基于影像组学预测非小细胞肺癌患者KRAS和EGFR基因突变
Jianing Lin,Zhihang Yan,Longyu He et al.
Jianing Lin et al.
Objectives: Non-small cell lung cancer (NSCLC) is associated with poor prognosis, with 30% of patients diagnosed at an advanced stage. Mutations in the EGFR and KRAS genes are important prognostic factors for NSCLC, and t...
Value and validation of a nomogram model based on the Charlson comorbidity index for predicting in-hospital mortality in patients with acute myocardial infarction complicated by ventricular arrhythmias [0.03%]
基于Charlson合并症指数的预测急性心肌梗死并发室性心律失常住院死亡率预测列线图价值及效度研究
Nan Xie,Weiwei Liu,Pengzhu Yang et al.
Nan Xie et al.
Objectives: The Charlson comorbidity index reflects overall comorbidity burden and has been applied in cardiovascular medicine. However, its role in predicting in-hospital mortality in patients with acute myocardial infar...
Correlation between cardiovascular magnetic resonance features and clinical characteristics of cardiac involvement in connective tissue diseases [0.03%]
结缔组织病心脏受累的心血管磁共振影像特征与临床特点的相关性研究
Jing Luo,Hui Zhou,Yisha Li et al.
Jing Luo et al.
Objectives: Patients with connective tissue diseases (CTD) have a high incidence of cardiac involvement, which often presents insidiously and can progress rapidly, making it one of the leading causes of death. Multiparame...
Association between remnant cholesterol and atherosclerosis plaques in single and multiple vascular territories [0.03%]
残余胆固醇与单个和多个血管区域动脉粥样硬化斑块的关系
Xuelian Liu,Kui Chen,Yaqin Wang et al.
Xuelian Liu et al.
Objectives: In recent years, the role of remnant cholesterol (RC) in the development and progression of cardiovascular diseases has gained increasing attention. However, evidence on the association between RC and subclini...
Mendelian randomization studies on cardiometabolic factors and intracranial aneurysms: A systematic literature analysis [0.03%]
颅内动脉瘤遗传学研究系统回顾及孟德尔随机化分析
Yuge Wang,Junyu Liu,Fang Cao et al.
Yuge Wang et al.
Objectives: Intracranial aneurysm (IA) has an insidious onset, and once ruptured, it carries high rates of mortality and disability. Cardiometabolic factors may be associated with the formation and rupture of IA. This stu...
Application of stereotactic radiotherapy in the treatment of cardiovascular diseases through sympathectomy [0.03%]
立体定向放射治疗交感神经治疗心血管疾病的应用
Zhangli Xie,Liyi Liao,Shuang Zhang et al.
Zhangli Xie et al.
Sympathectomy, as an emerging treatment method for cardiovascular diseases, has received extensive attention in recent years. Stereotactic radiotherapy (SRT), a precise and noninvasive therapeutic technique, has gradually been introduced in...
Mechanism of post cardiac arrest syndrome based on animal models of cardiac arrest [0.03%]
基于心脏停搏动物模型的心肺复苏后综合征机制研究
Halidan Abudu,Yiping Wang,Kang He et al.
Halidan Abudu et al.
Cardiac arrest (CA) is a critical condition in the field of cardiovascular medicine. Despite successful resuscitation, patients continue to have a high mortality rate, largely due to post CA syndrome (PCAS). However, the injury and pathophy...
Genetic analysis of UMOD gene mutation in autosomal dominant tubulointerstitial kidney disease [0.03%]
UMOD基因突变在常染色体显性遗传型髓质间质性肾炎中的遗传学分析
Yingying Zhang,Nannan Li,Min Lu et al.
Yingying Zhang et al.
Autosomal dominant tubulointerstitial kidney disease (ADTKD) is a rare autosomal dominant hereditary disorder characterized by hyperuricemia, gout, impaired urinary concentration, and progressive renal failure. It is primarily caused by mut...