Genetic variants influencing SR B-ALL relapse risk identified
Genome and transcriptome sequencing revealed that subtypes such as TCF3/4::HLF were associated with an increased risk of relapse.
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Genome and transcriptome sequencing revealed that subtypes such as TCF3/4::HLF were associated with an increased risk of relapse.
Increased gene activity in the SYK pathway could be the basis of a blood test to identify melanoma patients most susceptible to severe side effects.
The novel strategy demonstrates a strong immune response, both body-wide and specifically in the upper respiratory tract, in porcine models.
Scientists discovered the number of Tr1 cells increased as tumours grew larger, making mice insensitive to immunotherapy.
Researchers have developed a new form of immunotherapy that could provide a longer life expectancy to men with prostate cancer.
A biomaterial that improved hyaline cartilage repair could be used to avoid knee replacements and treat injuries and degenerative diseases.
The new technique could be adapted to produce a wide range of antibodies to combat chronic conditions like HIV.
Researchers utilised AI to identify genes that reprogramme GBM cancer cells into dendritic cells within the tumour.
Organoids with SMA-pathology uncovered key findings about the disease, which could be utilised to develop new therapeutic options.
The new study demonstrated that a small molecule inhibitor, BLZ945, could be used as a potential therapeutic to achieve viral clearance.
The study’s results indicate that spatial sequencing of mixed-type breast cancers could inform personalised treatment.
Researchers discovered two potential new drug applications with the possible clinical use of surfactant early in COVID-19 cases.
The agreement between Cartherics, The University of Sydney and The University of Queensland will further stem cell-derived heart muscle therapy for heart failure.
The new agent, DIF-1(+3), proved to be as effective against drug-resistant malaria as it was against susceptible strains.
Mice with rod-specific VPS35 deletion demonstrate a pathology more similar to human Parkinson’s disease, compared to other mouse models.