@article {2720,
	title = {Limiting amounts of centrosome material set centrosome size in C.elegans embryos.},
	journal = {Current Biology},
	volume = {21},
	year = {2011},
	month = {2011 Aug 9},
	pages = {1259-67},
	abstract = {<p>The ways in which cells set the size of intracellular structures is an important but largely unsolved problem [1]. Early embryonic divisions pose special problems in this regard. Many checkpoints common in somatic cells are missing from these divisions, which are characterized by rapid reductions in cell size and short cell cycles [2]. Embryonic cells must therefore possess simple and robust mechanisms that allow the size of many of their intracellular structures to rapidly scale with cell size.</p>
},
	issn = {1879-0445},
	doi = {10.1016/j.cub.2011.06.002},
	author = {Decker, Markus and Jaensch, Steffen and Pozniakovsky, A and Zinke, A and O{\textquoteright}Connell, K F and Zachariae, W and Myers, Eugene and Hyman, Anthony A}
}
@article {2327,
	title = {Automated tracking and analysis of centrosomes in early Caenorhabditis elegans embryos.},
	journal = {Bioinformatics},
	volume = {26},
	year = {2010},
	month = {2010 Jun 15},
	pages = {i13-20},
	abstract = {<p>The centrosome is a dynamic structure in animal cells that serves as a microtubule organizing center during mitosis and also regulates cell-cycle progression and sets polarity cues. Automated and reliable tracking of centrosomes is essential for genetic screens that study the process of centrosome assembly and maturation in the nematode Caenorhabditis elegans.</p>
},
	keywords = {Animals, Caenorhabditis elegans, Caenorhabditis elegans Proteins, Cell Division, Cell Lineage, Centrosome, Embryo, Fluorescence, Microscopy, Mitotic Spindle Apparatus, Nonmammalian},
	issn = {1367-4811},
	doi = {10.1093/bioinformatics/btq190},
	author = {Jaensch, Steffen and Decker, Markus and Hyman, Anthony A and Myers, Eugene W}
}
