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In this manuscript, we propose that an integrative neurogenomics workflowcombining multi-omic phenotypeoriented whole-exome sequencing, biologically-oriented common variant burden profiling, biochemical markers, functional metagenomic data, and multidisciplinary clinical interpretationcan generate testable, personalized diagnostic and therapeutic hypotheses in neurodegenerative disorders

A., Alwutayd, K

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Antibiotic susceptibility was determined through measurement of the diameter of the inhibition zones in accordance with the disk manufacturers guidelines ( 2.8 In vivo safety assessment of the M22 in mice 2.8.1 Animal experiments Forty ICR mice (provided by Nanjing Huimiaoxin, China) randomly divided into four groups following a 7-days acclimation period under controlled conditions (25 C, unlimited access to food and water)