Integrin αV and β5 partner to drive cancer cell growth
A novel cellular mechanism has been uncovered with the use of CRISPR gene-tiling technology, which could advance oncologic therapies.
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A novel cellular mechanism has been uncovered with the use of CRISPR gene-tiling technology, which could advance oncologic therapies.
Researchers found that resolvinT4 restores protective macrophage biological activities in rheumatoid arthritis patients.
Researchers conducted a proteogenomic characterisation and found that drug exposure changes drug sensitivity.
A new study proves that organoid drug testing is highly accurate at predicting effective treatments and finds a novel therapeutic option.
The computer model enables a better understanding of how drugs affect fibroblasts and finds a promising candidate to prevent heart scarring.
Researchers suggest that DA histology slowly emerges by accumulating burdens of DNA damage and copy number aberrations.
A deep learning model developed using circulating cell-free DNA outperformed traditional screening methods for gestational diabetes mellitus.
Regenerating bladder tissue with bone marrow stem and progenitor cells gives hope to patients with end-stage bladder dysfunction.
A new study has identified targets to refine diagnostic tests, track disease progression, and discover more effective therapies.
The interactions linking intestinal microbiota with the functionality of basally resident alveolar macrophages and severity of infection are revealed.
The new study suggests that this gene therapy method may combat ARVC in both early and more advanced stages of the condition.
A novel technology can reduce tumour sizes significantly and improve treatment efficacy when used with existing immunotherapy.
A new project plans to elucidate the relationship between the glucosylceramidase beta gene and Parkinson’s disease.
For the first time, mitochondrial DNA mutations could be used with immunotherapy to increase the chances of successful treatments.
A new learning-based framework enables patients and caregivers to predict the timing of any of the five clinical groups of AD development.