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The additional content of clinical features of specimens are showed in Supplementary Table 1

Interfaces 2019, 11 , 3715 3721, DOI: 10.1021/acsami.8b1849762An Enzyme-Free "ON-OFF" Electrochemiluminescence Biosensor for Ultrasensitive Detection of PML/RAR based on Target-Switched DNA NanotweezerBian, Xintong

121 Mutations in the progranulin gene, GRN , which cause a genetic familial FTD, downregulate expression of EAAT2 astrocyte glutamate transporter, which mediates synaptic degeneration

Results depend on baseline health status, treatment adherence, lifestyle factors, genetics, and other variables

Control Release 353 , 490506 (2023)