mRNA expression of NLRP3 and IL1B in inflammatory bowel diseases: a systematic review and meta-analysis. [PDF]
Metselaar PI +4 more
europepmc +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
Erratum: IGFBP3 induced by the TGF-β/EGFRvIII transactivation contributes to the malignant phenotype of glioblastoma. [PDF]
Zhang X +12 more
europepmc +1 more source
Differential Gene Expression Across Species Following Spinal Cord Injury: A Systematic Review and Meta-Analysis. [PDF]
AbouZekry SS +4 more
europepmc +1 more source
Chromosomal microarray analysis for the prenatal diagnosis in fetuses with fetal echogenic bowel: a retrospective cohort study. [PDF]
Wu W, Tian M, Liu M, Man D, Wang F.
europepmc +1 more source
Optimizing feature selection in cancer microarray data using a heap-driven evolutionary framework for high-dimensional spaces. [PDF]
Alweshah M +5 more
europepmc +1 more source
Multi‐omic profiling reveals immune cell priming signature linked to lupus prognosis
Objective Systemic lupus erythematosus (SLE) is a multi‐organ disease with widespread immune dysregulation and significant unmet clinical need. Blood‐based gene expression studies have advanced our understanding of SLE pathogenesis but may overlook critical tissue‐specific mechanisms that drive disease heterogeneity and progression.
Michael A. Smith +23 more
wiley +1 more source
SEMA3B is associated with disease activity and infliximab response in IBD patients but does not contribute to the development of intestinal inflammation <i>in vivo</i>. [PDF]
Arosa L +4 more
europepmc +1 more source
5‐Methylcytosine Analysis of miRNAs in Minimal Change Disease
ABSTRACT Minimal change disease (MCD) is a glomerular disorder, which is the most common cause of nephrotic syndrome in children. Additionally, the prevalence of MCD in adults has been increasing in recent years. During protein synthesis, noncoding RNAs can be regulated through a variety of modifications, which helps preserve biological diversity and ...
Huiyi Zeng +14 more
wiley +1 more source

