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Progeria is a disease that leads to rapid ageing and is caused by a mutation leading to a dysfunctional Lamin A protein. Based on your knowledge of lamina-associated domains (LADs), what would be a potential phenotype of progeria patients?
UTX is a lysine demethylase that removes methylation marks specifically from lysine 27 on Histone H3. If a cell has a mutation that decreases the function of UTX, what would be the effect on gene expression in general?
Why might gene editing be preferred over gene therapy in some personalised medicine strategies?
What does the use of biomarkers to guide treatment decisions illustrate about the philosophy of personalised medicine?
What makes the clinical standards framework a robust tool for assessing the pathogenicity of mutations?
In the context of personalised medicine, what problem does detecting genomic variants aim to address?
Why is under-expressing a gene of interest useful to help understand the function of the gene product of interest?
How does genomics assist in making gene editing possible, where a disease-causing mutation is implicated in a genetic disease?