Recent Articles

Open access

ISSN: 2352-3042
CN: 50-1221/R
p-ISSN: 2352-4820

Comprehensive analysis and experimental verification of the role of mitochondrial dynamics-related genes in liver hepatocellular carcinoma

MSC-EVs alleviate osteoarthritic joint pain and degeneration by suppressing IL-1β/NGF signaling

Systematic druggable genome-wide analysis to identify potential therapeutic targets for urologic diseases

Epigenetic insights into minimal residual disease detection in cancer

Molecular characterization of a new R1925X point mutation mouse model for dysferlinopathy

Deubiquitinase USP17 negatively regulates 3T3-L1 adipocyte differentiation via HDAC1

Data-driven identification of core tumor-secreted factors associated with cachexia prevalence

TNFAIP8/TIPE2 inactivation modulates extracellular matrix organization gene expression and preserves the intervertebral disc structure in mice

Spatial transcriptomic characterization of the pathologic niche in a patient with pulmonary crystal-storing histiocytosis

A novel truncating variant in PRDM16 causes severe familial cardiomyopathy with variable clinical presentations

CBS promotes tumor immune evasion by reducing MHC-I stability

Serum tRF-4575 may regulate osteoclast differentiation and serve as a promising biomarker for enthesitis-related arthritis diagnosis

Rare variants in NRSN2 cause non-syndromic orofacial cleft through dysregulation of TGF-β signaling

Identification and functional characterization of a novel nonsense mutation of CASR gene in a familial hypocalciuric hypercalcemia pedigree

Genetic variability in the PLIN4 gene: A new sequence duplication causing autophagic vacuolar myopathy

Lactylation-driven METTL3 regulates wound healing by enhancing m6A/HNRNPA2B1/DNMT1 signaling in keratinocytes

Identification and analysis of extrachromosomal circular DNAs in pancreatic islets during the early and late stages of T2DM mice

Pathogenic variation in human DNA damage repair genes was originated from the evolutionary process of modern humans

DNA damage repair (DDR) genes play critical roles in maintaining genome stability. However, they are prone to genetic variation, of which pathogenic variation (PV) is a predisposing factor for high...

Sox11 deficiency induces paravertebral muscle injury and scoliosis via Mlxipl upregulation

Roles of efferocytosis in wound repair: Process, cells, and signals

Efficient clearance of apoptotic cells, termed efferocytosis, is essential for resolving excessive inflammation, promoting wound repair, and maintaining homeostasis. Defective clearance results in the...

DNA methylation heterogeneity in complex tumor microenvironment: Quantitative methods, influencing factors, and clinical implications

5-Methylcytosine (5-mC) is the most prevalent DNA methylation modification in the human genome, and its abnormal patterns are strongly associated with tumor progression. Intratumoral and intertumoral...

eQTL analysis: A bridge from genome to mechanism

Expression quantitative trait locus (eQTL) refers to a genetic variation associated with the expression of specific genes. It has been widely applied to explain the regulatory mechanisms linking genetic...

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