IGC Research in a Nutshell. Dr Aneta Mikulasova.Institute of Genetics and Cancer, The University of Edinburgh.(Epi)genomic Instability in Multiple Myeloma.

Isoforms are seldom considered in genetic variant interpretation. Here the authors map common and rare variants to alternative isoforms, which can be highly expressed and tissue-specific. A common DPP...

The reduced risk of heart disease seen in people who are overweight or have obesity taking the weight loss drug semaglutide may not be due to a drop in weight alone, a study shows.

Professor Riccardo Marioni Institute of Genetics and Cancer.

YouTube video by STV News

An exciting postdoctoral position is available to research the role of epigenetic marks in gene regulation.

IGC Research in a Nutshell Professor Sara Brown, Institute of Genetics and Cancer and NHS Lothian. investigating genetic mechanisms in atopic eczema to design better treatments.

A collaborative research programme led by the Institute of Genetics and Cancer has been awarded £1.92 million from the Advanced Research + Invention Agency (ARIA).

How oncogenes increase protein levels may shape PROTAC response and help identify tumors most likely to benefit from targeted protein degradation.

The way cancer-causing proteins accumulate in tumours may influence how effectively a promising new generation of medicines can remove them, a study has found.

Explore how Dr. Andrew Jackson's research on rare genetic disorders reveals connections between growth, aging, and cancer biology.

YouTube video by Sano Genetics

Atopic dermatitis (AD), asthma, food allergy, and respiratory allergy are common childhood conditions with significant disease burden. Current understanding implicates the skin-barrier and the dual-a....

An experimental mRNA vaccine developed by pharmaceutical companies Moderna and Merck helped prevent the return and spread of cancer in high-risk melanoma patients.

Jimenez-Moreno et al. reveal that ER-phagy receptors directly control cytosolic signaling events. Upon stimulation, cytoplasmic PRKAR1A condensates interact with FAM134B/C, forming inter-organellar co...

Long-read sequencing technology has been used to make notable strides in identifying elusive genetic causes of diseases that previously remained undiagnosed.

European Journal of Human Genetics - Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project