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

Runx2 controls the osteogenic fate of growth plate chondrocytes

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The abnormal splicing regulation network caused by synonymous mutations in FBN1 exon 39 leads to Marfan syndrome

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Phosphorylation-related genes in lupus nephritis: Single-cell and machine learning insights

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Prognostic significance and multidimensional roles of interferon regulatory factors in cancer biology: A comprehensive analysis

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HOXB6 down-regulation induced by retinoic acid pathway repression leads to chondrocyte proliferation inhibition and apoptosis in microtia

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Construction of a prognostic model based on the cuproptosis-related genes in pancreatic cancer

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AUTS2 expression within mammalian lineage: A predictor of neural networks involved in autism spectrum disorders

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Predicting anti-cancer drug sensitivity through WRE-XGBoost algorithm with weighted feature selection

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Reduction of Atp5b protects mice from diet-induced obesity

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Transcriptional programs associated with luminal play a vital role in invasive mucinous lung adenocarcinoma

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Expanding the spectrum of novel candidate genes using trio exome sequencing and identification of monogenic cause in 27.5% of 320 families with steroid-resistant nephrotic syndrome

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Unique presentation of a novel gain-of-function mutation in MTOR

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The important role and core marker gene of tumor-infiltrating plasma cells in the microenvironment of lung adenocarcinoma

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Glucose metabolism perturbations influence tumor microenvironments via LINC01139 pathway and facilitate immunotherapy in hepatocellular carcinoma

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The AKT1-mTOR signaling cascade is crucial for SOX3 to promote hepatocarcinogenesis

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PinX1 suppresses cancer progression by inhibiting telomerase activity in cervical squamous cell carcinoma and endocervical adenocarcinoma

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Construction and validation of a novel SUMOylation-related lncRNAs signature for predicting the prognosis, tumor immune microenvironment, and therapeutic sensitivity of lung adenocarcinoma

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SNORD3B-2 promotes endometrial carcinoma progression by 2′-O-methylation modification of PLK1 and regulating RAB17 alternative splice

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De novo missense variants of UNC13A are implicated in epileptic encephalopathies and neurodevelopmental disorders

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