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Although considerable progress has been achieved in detecting common driver mutations (such as EGFR, ALK and ROS1), there is an urgent need for more sensitive and comprehensive biomarker platforms capable of detecting rare mutations, gene fusions and intricate molecular profiles (306308)

Molecular mapping of the tubulin PTMs in human photoreceptor cell outer segment Next, we wanted to assess whether the observed distribution of tubulin PTMs is conserved in human retina, as mutations of AGBL5 , coding for CCP5, lead to retinitis pigmentosa in human (Fig

PdZn/CoSA-NC nanozymes with highly efficient SOD/CAT activities for treatment of osteoarthritis via regulating immune microenvironment

10.1093/ageing/afl108 248 TikhonovaL