Embryonic development seemingly proceeds with almost perfect precision. However, it is largely unknown how much microscopic variability is hidden beneath this macroscopic accuracy. Here, we quantified
Raw dataset of transmitted images from a transgenic Tg(spon1b:GFP) zebrafish brain at 24 hpf. Planes were acquired from a frontal view and are used as anatomical reference for the fluorescence
Purpose: study of function of ATG5 protein on zebrafish larvae development Methods: Using morpholino oligos for atg5 gene knock down and overexpression, injected into one- to four-cell-stage embryos,e
