Shared genetic architecture between Alzheimer's disease and psychiatric disorders revealed by multi-trait genome-wide analyses [0.03%]
多性状全基因组分析揭示了阿尔茨海默病与精神障碍之间的共享遗传结构
Huajun Zhang,Liangzhuo Xie,Facai Meng et al.
Huajun Zhang et al.
Multi-omics single-cell dissection of malignant epithelial heterogeneity identifies GJB2 as an EMT-driving biomarker in triple-negative breast cancer [0.03%]
多组学单细胞解剖恶性上皮异质性鉴定出连接蛋白GJB2是三阴性乳腺癌上皮间质转化驱动生物标志物
Hongjie Xu,Chengzhi Zhang,Xinyi Zhang et al.
Hongjie Xu et al.
A novel androgen receptor gene splice site mutation induces aberrant mRNA splicing and internal in-frame deletion in androgen insensitivity syndrome [0.03%]
新型雄激素受体基因剪接位点突变导致雄激素不敏感综合征异常的mRNA剪接及内部插入型缺失
Baoqiong Liao,Mei Shuai,Lin Xiao et al.
Baoqiong Liao et al.
Bioinformatics analyses of a potential miRNA‒mRNA regulatory axis in lumbar degenerative disc disease [0.03%]
腰椎退行性 discs疾病的潜在miRNA-mRNA调控轴的生物信息学分析
Jiagang Wang,Lifan Zhu,Fengbiao Weng et al.
Jiagang Wang et al.
Whole-exome sequencing identifies PRSS56 variants in Chinese patients with microphthalmia [0.03%]
全外显子组测序识别出中国小眼症患者的PRSS56基因变异
Jingyi Luo,Kaijing Li,Runcai Yang et al.
Jingyi Luo et al.
Genetic polymorphisms and expression of SARS-CoV-2 host entry genes associate with COVID-19 severity in an unvaccinated Moroccan cohort [0.03%]
摩洛哥未接种疫苗人群的冠状病毒病严重程度与SARS-CoV-2宿主进入基因多态性和表达的关系
Safaa Aqillouch,Oumaima Laazaazia,Ahd Ouladlahsen et al.
Safaa Aqillouch et al.
Association of TP53 polymorphic variants rs1042522 and rs1642785 with susceptibility and prognosis of acute lymphoblastic leukemia in a Brazilian Amazon population [0.03%]
TP53基因多态性变异体rs1042522和rs1642785与巴西亚马逊地区急性淋巴细胞白血病易感性和预后的关系研究
Glenda Menezes Nogueira,Luca Gabriel Marques Gonçalves,Thaís Lohana Pereira-Ribeiro et al.
Glenda Menezes Nogueira et al.
Lingjuan Jia,Meng Zhu,Xiaqiu Wu et al.
Lingjuan Jia et al.
CRABP2 upregulation in perichondral stem cells is associated with microtia [0.03%]
软骨外干细胞CRABP2上调与小耳畸形相关
Jingheng Zhang,Feiyang Chu,Xuzhong Hu et al.
Jingheng Zhang et al.
Downward bias in the association between APOE and Alzheimer's disease using prevalent and by-proxy disease sampling in the All of Us research program [0.03%]
APOE与阿尔茨海默病关联的向下偏倚：来自“全民参与”研究项目的患病率和代理表型抽样结果
Clayton O Mansel,Valentina Ghisays,Jonathan D Mahnken et al.
Clayton O Mansel et al.