Direct Profiling of Extracellular Vesicle Surface Markers in Plasma: A Proof-of-Concept Study. [PDF]
Clegg LA +7 more
europepmc +1 more source
Global Delivery of Foetal Sequencing: Do We Need Some Standardisation?
ABSTRACT Objective The development of sequencing technologies has resulted in rapid expansion in the testing available for foetuses with structural anomalies to diagnose monogenic disorders. To understand the variability in how foetal sequencing services are delivered, we developed a survey that focussed on the scope of testing, any parallel testing ...
Natalie J. Chandler, Zandra C. Deans
wiley +1 more source
Proteome-Wide Mapping of Artesunate Targets Reveals Enrichment of the Ubiquitin-Proteasome System. [PDF]
Wang G, Tang X, Zhang F.
europepmc +1 more source
The Prediction of Pre‐Eclampsia Using Low Fetal Fraction in a Machine Learning Model
ABSTRACT Objective To investigate the association between low fetal fraction (FF) in non‐invasive prenatal testing (NIPT) and pregnancy complications or adverse pregnancy outcomes. Methods Sixty‐four pregnant women undergoing NIPT at the Second Affiliated Hospital of Wenzhou Medical University between 13 June 2019 and 6 January 2023 had an initial NIPT
Jinyuan Wang +9 more
wiley +1 more source
New Generation of Clinical Epigenetics Analysis and Diagnosis for Precision Medicine. [PDF]
Song P, Li B.
europepmc +1 more source
Prenatal Diagnosis of Paternal Uniparental Isodisomy 14 Arising From the Transfer of a Mosaic Monosomy 14 Embryo. [PDF]
Minick J, Lende M.
europepmc +1 more source
<i>Staphylococcus aureus</i> transcriptomics and single-cell sequencing approaches. [PDF]
Malachowa N, DeLeo FR.
europepmc +1 more source
Unveiling complex patterns: An information-theoretic approach to high-order behaviors in microarray data. [PDF]
Lacalamita A +14 more
europepmc +1 more source
AttBiomarker: unveiling preeclampsia biomarkers and molecular pathways through two-stage gene selection techniques and attention-based CNN with gene regulatory network analysis. [PDF]
Sarker S +4 more
europepmc +1 more source
Turner Syndrome With 45,X/46,XX Mosaicism and a Derivative X Chromosome (Xqter → Xq13?::Xp11.4 → Xqter): A Case Report. [PDF]
Jiang W, Ji T, Wu Q, Xu Z, Xia X.
europepmc +1 more source

