1. Volume 22, Issue 16, Pages R620-R622 (August 2012)
Candida albicans 
Judith Berman 
Current Biology 
Volume 22, Issue 16, Pages R620-R622 (August 2012)
DOI: /j.cub
Copyright © 2012 Elsevier Ltd Terms and Conditions

2. Figure 1 Fluorescent protein fusions in Candida albicans.
Useful fluorescent markers for tracking subcellular structures in C. albicans include: DAPI (DNA); Nop1-GFP (green fluorescent protein, localizing to the nucleolus); Hhf1-GFP (chromatin); Tub2-GFP (microtubules, green); and Tub4-mCherry fluorescent protein (spindle pole bodies, red). Micrographs courtesy of Shelly Applen and Benjamin Harrison.
Current Biology  , R620-R622DOI: ( /j.cub )
Copyright © 2012 Elsevier Ltd Terms and Conditions

3. Figure 2 Phenotypic switching in Candida albicans.
Growth of C. albicans cells on phloxine plates detects colonies of cells that are either white (white colonies) or opaque (pink colonies) (left panel). A subset of cells in a mostly white colony switched to the opaque state, forming a sector in the colony (right panel). Photos courtesy of Meleah Hickman.
Current Biology  , R620-R622DOI: ( /j.cub )
Copyright © 2012 Elsevier Ltd Terms and Conditions