@article {958,
	title = {Comparative genomics of the eukaryotes.},
	journal = {Science},
	volume = {287},
	year = {2000},
	month = {2000 Mar 24},
	pages = {2204-15},
	abstract = {<p>A comparative analysis of the genomes of Drosophila melanogaster, Caenorhabditis elegans, and Saccharomyces cerevisiae-and the proteins they are predicted to encode-was undertaken in the context of cellular, developmental, and evolutionary processes. The nonredundant protein sets of flies and worms are similar in size and are only twice that of yeast, but different gene families are expanded in each genome, and the multidomain proteins and signaling pathways of the fly and worm are far more complex than those of yeast. The fly has orthologs to 177 of the 289 human disease genes examined and provides the foundation for rapid analysis of some of the basic processes involved in human disease.</p>
},
	keywords = {Animals, Apoptosis, Biological Evolution, Caenorhabditis elegans, Cell Adhesion, Cell Cycle, Drosophila melanogaster, Duplicate, Fungal Proteins, Genes, Genetic Diseases, Genetics, Genome, Helminth Proteins, Humans, Immunity, Inborn, Insect Proteins, Medical, Multigene Family, Neoplasms, Protein Structure, Proteome, Saccharomyces cerevisiae, Signal Transduction, Tertiary},
	issn = {0036-8075},
	doi = {10.1186/gb-2007-8-7-r145},
	author = {Rubin, G M and Yandell, M D and Wortman, J R and Gabor Miklos, G L and Nelson, C R and Hariharan, I K and Fortini, M E and Li, P W and Apweiler, R and Fleischmann, W and Cherry, J M and Henikoff, S and Skupski, M P and Misra, S and Ashburner, M and Birney, E and Boguski, M S and Brody, T and Brokstein, P and Celniker, S E and Chervitz, S A and Coates, D and Cravchik, A and Gabrielian, A and Galle, R F and Gelbart, W M and George, R A and Goldstein, L S and Gong, F and Guan, P and Harris, N L and Hay, B A and Hoskins, R A and Li, J and Li, Z and Hynes, R O and Jones, S J and Kuehl, P M and Lemaitre, B and Littleton, J T and Morrison, D K and Mungall, C and O{\textquoteright}Farrell, P H and Pickeral, O K and Shue, C and Vosshall, L B and Zhang, J and Zhao, Q and Zheng, X H and Lewis, S}
}
@article {961,
	title = {Drosophila homologs of baculovirus inhibitor of apoptosis proteins function to block cell death.},
	journal = {Cell},
	volume = {83},
	year = {1995},
	month = {1995 Dec 29},
	pages = {1253-62},
	abstract = {<p>Apoptotic cell death is a mechanism by which organisms eliminate superfluous or harmful cells. Expression of the cell death regulatory protein REAPER (RPR) in the developing Drosophila eye results in a small eye owing to excess cell death. We show that mutations in thread (th) are dominant enhancers of RPR-induced cell death and that th encodes a protein homologous to baculovirus inhibitors of apoptosis (IAPs), which we call Drosophila IAP1 (DIAP1). Overexpression of DIAP1 or a related protein, DIAP2, in the eye suppresses normally occurring cell death as well as death due to overexpression of rpr or head involution defective. IAP death-preventing activity localizes to the N-terminal baculovirus IAP repeats, a motif found in both viral and cellular proteins associated with death prevention.</p>
},
	keywords = {Amino Acid, Amino Acid Sequence, Animals, Apoptosis, Biological Evolution, Chromosome Deletion, Drosophila, Drosophila Proteins, Electron, Enhancer Elements, Eye, Genes, Genetic, Genetic Testing, Humans, Inhibitor of Apoptosis Proteins, Insect, Insect Proteins, Mammals, Microscopy, Molecular Sequence Data, Mutation, Neurons, Nucleic Acid, Peptides, Repetitive Sequences, Scanning, Sequence Homology, Viral Proteins},
	issn = {0092-8674},
	doi = {10.1186/gb-2007-8-7-r145},
	author = {Hay, B A and Wassarman, D A and Rubin, G M}
}
