All Articles

Extraembryonic mesoderm in primate and rodent embryos and models

EQTL Mendelian randomization to identify genetic insights and regulatory mechanisms in benign prostatic hyperplasia

Osimertinib in EGFR-mutated non-small cell lung cancer: a comprehensive narrative review of clinical evidence

Rewriting hepatic fate: emerging gene therapy strategies for liver disease

RNA-binding proteins in skeletal disorders: insights into molecular mechanisms and possible therapeutic targets

Context-dependent roles of alpha-ketoglutarate in brain disorders: molecular mechanisms and translational opportunities

Integrating innovation and insight in reproductive genetics and genomics: the essential role of advanced counseling

Inclusion of human centromeres in genomic browsers – will it finally come?

ADAM9 in cancer: a comprehensive analysis of mutation, prognostic value, expression and TQFL12-induced inhibition

Kinship classification from a machine learning perspective: a pilot study based on genotyping data

Decoding the DHX36-m6A-G4 axis: exploring its role in health and disease through epigenetic and molecular insights

Membrane-bound or soluble, mesenchymal or myeloid: which RANKL drives osteoclastogenesis?

Oral microbiota for diagnosis of etomidate abuse via machine learning

Novel gene-editing technologies: applications of CRISPR-Cas9, base editing, and prime editing in SCID gene therapy

Genetic and ultrasound assessment in recurrent fetal malformations: a case report on TUBA1A gene variation

The association of PGC-1α and its single-nucleotide polymorphism with the lipid metabolic disorders of diabetic kidney disease in patients with type 2 diabetes

Machine learning and maximum entropy for rational AAV library-design: technical commentary and analysis

The value of ctDNA tumor fraction in interpreting negative liquid biopsy results