From gene to heart: the impact of a novel SGCD variant in familial dilated cardiomyopathy [0.03%]
从基因到心脏：新型SGCD变异在家族性扩张型心肌病中的影响
Samira Kalayinia,Amirhossein Poopak,Mahdieh Soveizi et al.
Samira Kalayinia et al.
Unraveling the temporal dynamics of radiation-induced lung injury: a multi-omics integration of transcriptomic, proteomic, and metabolic reprogramming [0.03%]
解开辐射诱导的肺损伤的时间动态变化：转录组学、蛋白质组学和代谢重组多组学整合分析
Dabin Wu,Fei Tang,Yixin Zhang et al.
Dabin Wu et al.
Cellular senescence in gastric cancer: a novel prognostic stratification and immune predictor [0.03%]
细胞衰老在胃癌中的作用：一种新型的预后分层和免疫标志
Cheng-Zhi Wei,Yu-Ting Li,Zhi-Hao Lin et al.
Cheng-Zhi Wei et al.
Shared molecular signatures between atrial fibrillation and chronic obstructive pulmonary disease: an integrated bioinformatic analysis with experimental validation [0.03%]
房颤与慢性阻塞性肺疾病之间共享的分子特征：综合生物信息学分析及实验验证
Wei Zhou,Qian Tang,Dandan Chen et al.
Wei Zhou et al.
Apolipoprotein D downregulation in OSCC: multi-database validation and clinical significance [0.03%]
口腔鳞癌中载脂蛋白D的下调：多数据库验证及临床意义
Shuting Wang,Jun Zhao,Rui Bai et al.
Shuting Wang et al.
Background: Apolipoprotein D (APOD), a member of the lipocalin superfamily, plays a pivotal role in apoptosis, cancer, immune responses, and neural injury repair. Its association with various cancer types has been well-do...
Evaluation and management of DMD gene copy number variations detected by prenatal SNP-array testing [0.03%]
产前SNP芯片检测到的DMD基因拷贝数变异的评估与管理
Jiancheng Hu,Jialun Pang,Rong Hu et al.
Jiancheng Hu et al.
Prenatal diagnosis and clinical evaluation of fetuses with structural X chromosome abnormalities: a ten-year single-center retrospective study [0.03%]
胎儿结构异常的产前诊断及临床评估:X染色体异常单中心十年回顾性研究
Lixian Zhang,Jianlong Zhuang,Wenli Chen et al.
Lixian Zhang et al.
Identification of novel compound heterozygote variants in the PCCB gene in a fetus with undetectable fetal phenotype [0.03%]
在胎儿表型无法检测的情况下识别PCCB基因新型复合杂合变异
Xingyu Feng,Yao Hu,Huiming Yan et al.
Xingyu Feng et al.
Propionic acidemia (PA) is a rare autosomal recessive metabolic disorder caused by functional deficiency of propionyl-CoA carboxylase, clinically characterized by life-threatening ketoacidosis, hyperammonemia, and multiorgan dysfunction. Du...
Genetic modulators of metabolic dysfunction-associated steatotic liver disease (MASLD) and their epistatic interactions: from in vitro and animal models to clinical outcomes [0.03%]
与代谢功能障碍相关肝脂肪变性疾病的遗传调节因子及其显性相互作用：从体外和动物模型到临床结局
Fernanda G Arriaga-González,Felipe de Jesús Castañeda-Córdova,Mauricio Díaz-Muñoz et al.
Fernanda G Arriaga-González et al.
Association of VDR BsmI polymorphism and vitamin D status with osteoarthritis susceptibility [0.03%]
维生素D受体基因多态性及维生素D水平与骨关节炎易感性的关联研究
Shawnim M Maaruf,Dara K Mohammad,Treska S Hassan et al.
Shawnim M Maaruf et al.
Background: Osteoarthritis (OA) is a chronic degenerative joint disease influenced by genetic, environmental, and immunological factors. Vitamin D exerts immunomodulatory and anti-inflammatory effects through the vitamin ...