Single-cell RNA sequencing of adenoid cystic carcinoma of the breast reveals cellular heterogeneity and tumor microenvironment features [0.03%]
乳腺腺样囊性癌单细胞RNA测序揭示了细胞异质性和肿瘤微环境特征
Zhenning Tang,Jufen Zhao,Xiaoying Huang et al.
Zhenning Tang et al.
The functional minisatellite at the 3'-UTR of SLC6A3/DAT1 and dementia spectrum disorders: an association study in a population of Central Italy [0.03%]
SLC6A3/DAT1 3′-UTR功能性微卫星与痴呆连续性疾病：意大利中部地区人群中的关联研究
Benedetta Torbidoni-Baldassari,Anna Giulia Guazzarini,Gabriele Rezza et al.
Benedetta Torbidoni-Baldassari et al.
Background: Dementia comprises a spectrum of neurodegenerative disorders marked by progressive cognitive and behavioural decline, with Alzheimer's disease (AD) being the most prevalent form. While several genetic factors ...
Short-term exposure of sleep deprivation male model rats to dutasteride promotes the discovery of gene profiles related to fertility impairments [0.03%]
短期睡眠剥夺雄性大鼠暴露于度他雄胺促进与生育能力损伤相关的基因谱型的发现
Shengxiao Zhang,Wei Li,Guirong Zhang
Shengxiao Zhang
Identification of a novel signature in progression of non-small cell lung cancer based on HdWGCNA and in vitro validation [0.03%]
基于HdWGCNA和体外验证的非小细胞肺癌进展新标志物的鉴定
Kunpeng Zhang,Wenqiang Xia,Yi Li et al.
Kunpeng Zhang et al.
Whole-exome sequencing for the genetic diagnosis of early-onset high myopia and associated hereditary eye disorders [0.03%]
外全基因组测序在早发性高度近视及遗传性眼病的基因诊断中的应用
Chunxiao Han,Shanshan Wu,Yang Yang et al.
Chunxiao Han et al.
The implementation of next-generation sequencing (NGS) in a Brazilian public hospital: a systematic review of challenges and perspectives in oncology [0.03%]
下一代测序（NGS）在巴西公立医院的实施：肿瘤学中的挑战和前景系统评价
Stêphanie Rocha Vieira Elexias,Bruno A Lopes,Rodolfo Acatauassú et al.
Stêphanie Rocha Vieira Elexias et al.
Differentially expressed exosome miRNA profiles as putative prognostic biomarkers for profound sudden sensorineural hearing loss [0.03%]
差异表达的外泌体miRNA谱作为重度突发性感音神经性聋预后生物标志物的假说研究
Hongru Zhang,Haoliang Xie,Qiran Cao et al.
Hongru Zhang et al.
Background: Sudden sensorineural hearing loss (SSNHL) is an abrupt, often idiopathic hearing decline with uncertain prognosis and multifactorial pathophysiology. Among its subtypes, total deafness-also referred to as prof...
Diagnostic value of karyotyping, CMA/CNV-seq, and WES in fetuses with thickened nuchal translucency: perinatal and two-year follow-up outcomes [0.03%]
核型分析、CMA/CNV-seq和WES在厚颈项透明层胎儿中的诊断价值：围产儿及2年随访结局
Mohan Wang,Yizhen Ji,Yasong Xu et al.
Mohan Wang et al.
Hub genes and molecular mechanisms related to hypospadias based on transcriptome sequencing data and bioinformatics analysis [0.03%]
基于转录组测序数据和生物信息学分析的尿道下裂相关的重要基因及分子机制研究
Haoyu Yao,Yingzhong Fan,Luping Li et al.
Haoyu Yao et al.
A novel inversion at 17q12 disrupting HNF1B gene in a patient with renal cysts and diabetes syndrome [0.03%]
染色体17q12区段倒位破坏HNF1B基因导致肾囊肿和糖尿病综合征
Yue Wang,Qiu Wang,Lijie Guan et al.
Yue Wang et al.
Background and objective: This study aims to elucidate the genetic cause of polycystic kidney disease detected in the proband during the fetal period and progressively worsening, thereby providing a reference for research...