All Articles

Translational insights into Duchenne muscular dystrophy: network biomarker identification and drug repositioning through multi-omics approaches

The role of long non-coding RNAs in breast cancer drug resistance: a comprehensive review

Artificial intelligence in forensic genetics: applications and ethical challenges

Autosomal dominant tibial muscular dystrophy in Estonia

Persistent IFN-γ signaling in acquired resistance to PD-(L)1 blockade in NSCLC

An appraisal of emerging dystrophin restoration therapies in Duchenne muscular dystrophy

Meeting abstracts of 3rd European Congress on Human Genetics

Association of PTPRC gene polymorphisms with TNF inhibitor efficacy in rheumatoid arthritis: a systematic review and meta-analysis

The crucial role of alveolar fibroblasts in pulmonary fibrosis

A review of the relationship between the SLC6A4 gene and mental disorders

SMN2 as a therapeutic target in spinal muscular atrophy: advances in gene expression modulation

Histone H3K18 lactylation and cisplatin resistance in bladder cancer: insights from single-cell transcriptomic analysis

IP3 receptors contribute to muscle atrophy and maintain ribosomal RNA content during 3-day hind limb suspension in rats

Bidirectional Mendelian randomization study of brain imaging-derived phenotypes unveils causal associations between thalamic nuclei volume and stroke risk

Genetic factors associated with dyslipidemia, T2DM and DKD: a cross-sectional study on FXR gene polymorphisms

Microhaplotype insights into the population structure of seven ethnic minorities in Guizhou, China

Cellular ATP levels alone do not reliably reflect overall mitochondrial bioenergetics or mitochondrial dysfunction in Barth syndrome

The relationship between serum alkaline phosphatase levels and sepsis: observational and Mendelian randomization studies