Analysis of 33 tumour types identifies new immunotherapy targets
The researchers identified 1,068 transposable element-derived transcripts with the potential to produce tumour antigens that could serve as targets for new immunotherapies.
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Genomics is the branch of molecular biology concerned with the structure, function, evolution, and mapping of genomes.
The researchers identified 1,068 transposable element-derived transcripts with the potential to produce tumour antigens that could serve as targets for new immunotherapies.
A mechanism linked to a genetic mutation could help identify patients who are at higher risk of developing leukaemia.
Scientists from Spain have identified genes that regulate Alzheimer’s disease, including Surf4, which alters the regulation of calcium within Alzheimer’s cells.
The scientists from Texas A&M have developed GTX-102, a novel therapeutic candidate to target Angelman syndrome by reactivating expression of deficient protein.
The scientists revealed in mice models that endogenous retrovirus activation increases a foetus’s susceptibility to autism.
Lipid nanoparticles have been used to encapsulate CRISPR-Cas9 and deliver it to cells in mice, where it was highly effective at knocking down expression of a target protein.
The team used these models to show drug responses and established a CRISPR-screening platform to identify potential therapeutic targets for non-alcoholic fatty liver disease.
Japanese researchers combine cutting edge mass spectrometry with software analysis to elucidate mRNA structure.
US researchers uncover the amino acid: arginine, that prompts genetic mutations in cancer cells.
US researchers found that serotonin impacts the mitral valve in the heart which can lead to heart valve disease.
30 January 2023 | By Thermo Fisher Scientific
Watch this webinar to learn how an integrated structural biology workflow can be used to get crucial structural insights on key protein targets that are of therapeutic interest.
The scientists say that the engineered CRISPR enzymes could overcome key limitations for eventual use to treat genetic diseases irrespective of a patient’s particular mutation.
Using lung basal cell organoids, researchers identify a gene that directs the development of lung cancer and offers a better understanding of its disease treatment.
Researchers found that proteins made by stem cells that regenerate the cornea could be new targets for treating dry eye disease.
US researchers have developed a mouse model that holds promise in identifying the best organ donor and showing early signs of transplant rejection.