Esophageal squamous cell carcinoma (ESCC) is one of the main types of esophageal cancer (EC), accounting for more than 90% of patients with EC in China. Although the treatment has been improved in recent years, […]
Hepatocellular carcinoma (HCC) is a highly malignant tumor. Previous studies have shown that lots of genes are involved in the development of HCC and may be used as prognostic biomarkers of HCC. However, there are […]
Parkinson’s disease is a neurodegenerative disorder characterized by motor and non-motor symptoms. Furthermore, the Parkinson’s disease is a second most common neurodegenerative disorder, after Alzheimer’s disease. In the study published in BJBMS, the authors from […]
COVID-19 is a current pandemic, caused by the SARS-CoV-2 virus. Diverse abnormalities in immune cells, such as neutrophils, macrophages and T-cells have been found in SARS-CoV-2 infection, and such abnormalities cause a massive inflammatory status […]
We are living in a world of great technological advances, which is inevitably also linked to production of huge amounts of data. By using machine learning, the idea that a computer can form algorithms from […]
Neonatal sepsis (NS) occurs in neonates within 28 days of birth, and the current diagnostic biomarkers are unsatisfactory as a result of their poor specificity. During the past decades, a series of differentially expressed microRNAs […]
Kaposi sarcoma (KS) is a rare disease, and there is no specific treatment protocol agreed upon, especially for the classical type. Chemotherapeutics such as paclitaxel, pegylated liposomal doxorubicin (PLD), etoposide, gemcitabine are used in the […]
Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection has become a global threat since its emergence in 2019 from Wuhan, China. As of 1 March 2021, SARS-CoV-2 has affected over 113 million people and has been […]
Cervical cancer is the fourth most common female malignant tumor in the world. In the study published in BJBMS, the authors sought to establish a mathematical model to predict the 3-, 5-, and 10- year […]
Background Sarcotubular myopathy (STM) is a rare autosomal recessive disease characterized predominantly by weakness of the proximal limb. Mutations in the TRIM32 gene are often associated with STM and the limb-girdle muscular dystrophy R8 (LGMDR8). […]
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