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Ferritin Is Required in Multiple Tissues during Drosophila melanogaster Development.

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Academic year: 2017

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Fig 1. Ferritin mutants result in a variety of cuticle phenotypes quantified by different colors
Fig 2. Fer1HCH 451 lacZ enhancer trap is expressed in the embryonic CNS. Using an antibody against Anti- Beta-Galactosidase (green) and an antibody against the neuronal marker Elav (red), colocalization is observed in (A) heterozygous Fer1HCH 451/+ and (B)
Fig 3. Ferritin mutants result in CNS phenotypes, as revealed by ɑ -Elav staining. (A) Mutant CNS (B-H) appear twisted and irregular (E, G); often, holes are seen within the ventral nerve cord (white arrows)
Fig 4. Neuroblast and ganglion mother cells populations and neuronal axons derived from embryonic neurons are affected in ferritin mutants.
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