Results 211 to 220 of about 708,274 (274)
Long Noncoding RNA TRIBAL Links the 8q24.13 Locus to Hepatic Lipid Metabolism and Coronary Artery Disease. [PDF]
Soubeyrand S+5 more
europepmc +1 more source
ABSTRACT The primary degradation pathway for antisense oligonucleotides (ASOs) involves endonuclease and exonuclease‐mediated breakdown. The effect of various chemical modifications on the stability of oligonucleotides has not been systematically investigated.
Jelena Lovrić+7 more
wiley +1 more source
Discovery of RNA Biomarkers for Prostate Cancer Using Cross-Platform Transcriptomics. [PDF]
Visser WCH+8 more
europepmc +1 more source
Abstract Cell state‐specific synthetic promoters are essential tools for studying and manipulating cellular function, yet their design remains challenging, particularly for complex states such as T cell exhaustion. Here we present SPECIFIC (Synthetic Promoter Engineering for Cellular State Identification and Functional Analysis), an integrated ...
Zhaoyu Zhang+6 more
wiley +1 more source
Novel SMARCA4 Variant in an Infant With Atypical Teratoid Rhabdoid Tumor. [PDF]
Haldipurkar SK+5 more
europepmc +1 more source
Droplet Microfluidics for Advanced Single‐Cell Analysis
This paper reviews the transformative impact of droplet microfluidics on single‐cell research. It highlights current advancements in encapsulation techniques, applications in high‐throughput screening, and the study of intercellular and cell‐microorganism interactions.
Chang Liu, Xiaoyu Xu
wiley +1 more source
Investigating Single-Molecule Molecular Inversion Probes for Medium-Scale Targeted DNA Methylation Analysis. [PDF]
Simons RB+3 more
europepmc +1 more source
Prenatal Diagnosis of Proteus Syndrome: About a Case
ABSTRACT Proteus syndrome (PS) is a rare disorder (< 1/1000000), marked by progressive overgrowth commonly impacting the skeleton, skin, adipose tissue, and central nervous system. Clinical criteria were established in 2019. PS arises from a somatic activating variation in the AKT1 gene.
Luana Giovannangeli+10 more
wiley +1 more source
Whole genome sequencing for copy number variant detection to improve diagnosis and management of rare diseases. [PDF]
Bowman P+6 more
europepmc +1 more source