Identification of senescence-related biomarkers for osteoporosis based on microarray analysis, Mendelian randomization, and experimental validation. [PDF]
Zhu Y, Zhao J, Li Z, Chen Y.
europepmc +1 more source
Facilitating Genetic Testing for Perinatal Demise: Development of a Multidisciplinary Workflow
ABSTRACT Genetic contributors to perinatal demise are common but frequently undiagnosed due to clinical and logistical barriers. We aimed to improve access to genetic for intrauterine fetal demise (IUFD), stillbirth, and early neonatal death by developing a multidisciplinary workflow.
Mackenzie Mosera +15 more
wiley +1 more source
Prenatal Evaluation of RNU4‐2 Variants in Fetuses With Central Nervous System Anomalies
ABSTRACT Fetal central nervous system (CNS) anomalies are among the most common congenital malformations, yet the overall prenatal diagnostic yield of current genetic testing remains below 40%. Variants in RNU4‐2, a non‐coding gene encoding the U4 small nuclear RNA (snRNA), have recently been linked to a novel highly recurrent dominant ...
Yiyao Chen +13 more
wiley +1 more source
Microarray Analysis Reveals Sepsis Is a Syndrome with Hyperactivity of TH17 Immunity, with Over-Presentation of the Treg Cell Cytokine TGF-β. [PDF]
Chen YJ, Lu JJ, Lin CP, Hu WC.
europepmc +1 more source
Unveiling biomarker detection in Alzheimer's disease: a computational approach to microarray analysis. [PDF]
Khan NS +5 more
europepmc +1 more source
Glycomic profiling of parathyroid neoplasms via lectin microarray analysis. [PDF]
Zheng Q +7 more
europepmc +1 more source
Chromosomal Microarray Analysis in Fetuses with Ultrasound Abnormalities. [PDF]
Chen X +7 more
europepmc +1 more source
Chromosomal Microarray Analysis and Karyotype Analysis for Prenatal Diagnosis of Fetuses With Abnormal Ultrasound Soft Markers. [PDF]
Liu L, She L, Zheng Z, Huang S, Wu H.
europepmc +1 more source

