A. Shah

This study identifies KMT2D as a tumor suppressor in melanoma, showing its loss leads to metabolic reprogramming toward glycolysis and dependence on IGF signaling, suggesting therapeutic targeting of these pathways.

This study shows that obesity-induced metabolically activated macrophages in mammary adipose tissue promote triple-negative breast cancer stemness and tumorigenesis through GP130 signaling.

This study evaluates baseline variability in haemoglobin and blood oxygenation in tumours using photoacoustic imaging, showing trends and correlations with tumour growth.

The paper introduces LACIS, a microfluidic method for identifying and sorting edited clones using Opto-Electronic Positioning, enabling rapid and efficient clonal selection after CRISPR-Cas9 editing.