Dokument 1.pdf - OPUS - Friedrich-Alexander-Universität Erlangen ...

Literatur
Deshpande, G., Calhoun, G., Yanowitz, J. L. und Schedl, P. D., 1999. Novel functions of
nanos in downregulating mitosis and transcription during the development of the Drosophila
germline. Cell. 99, 271-81.
Dettner, K., 2003. Lehrbuch der Entomologie. Spektrum Akademischer Verlag, Heidelberg.
Dietzl, G., Chen, D., Schnorrer, F., Su, K. C., Barinova, Y., Fellner, M., Gasser, B., Kinsey,
K., Oppel, S., Scheiblauer, S., Couto, A., Marra, V., Keleman, K. und Dickson, B. J.,
2007. A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila.
Nature. 448, 151-6.
Dill, K. K. und Seaver, E. C., 2008. Vasa and nanos are coexpressed in somatic and germ
line tissue from early embryonic cleavage stages through adulthood in the polychaete
Capitella sp. I. Dev Genes Evol. 218, 453-63.
DiNardo, S., Kuner, J. M., Theis, J. und O'Farrell, P. H., 1985. Development of embryonic
pattern in D. melanogaster as revealed by accumulation of the nuclear engrailed protein.
Cell. 43, 59-69.
DiNardo, S. und O'Farrell, P. H., 1987. Establishment and refinement of segmental pattern in
the Drosophila embryo: spatial control of engrailed expression by pair-rule genes. Genes
Dev. 1, 1212-25.
Draper, B. W., McCallum, C. M. und Moens, C. B., 2007. nanos1 is required to maintain
oocyte production in adult zebrafish. Dev Biol. 305, 589-98.
Driever, W. und Nüsslein-Volhard, C., 1988a. A gradient of bicoid protein in Drosophila
embryos. Cell. 54, 83-93.
Driever, W. und Nüsslein-Volhard, C., 1988b. The bicoid protein determines position in the
Drosophila embryo in a concentration-dependent manner. Cell. 54, 95-104.
Driever, W. und Nüsslein-Volhard, C., 1989. The bicoid protein is a positive regulator of
hunchback transcription in the early Drosophila embryo. Nature. 337, 138-43.
Droll, D., Archer, S., Fenn, K., Delhi, P., Matthews, K. und Clayton, C., 2010. The trypanosome
Pumilio-domain protein PUF7 associates with a nuclear cyclophilin and is involved
in ribosomal RNA maturation. FEBS Lett.
Dubnau, J., Chiang, A. S., Grady, L., Barditch, J., Gossweiler, S., McNeil, J., Smith, P.,
Buldoc, F., Scott, R., Certa, U., Broger, C. und Tully, T., 2003. The staufen/pumilio
pathway is involved in Drosophila long-term memory. Curr Biol. 13, 286-96.
Dubnau, J. und Struhl, G., 1996. RNA recognition and translational regulation by a homeodomain
protein. Nature. 379, 694-9.
Duffy, J. B., Kania, M. A. und Gergen, J. P., 1991. Expression and function of the Drosophila
gene runt in early stages of neural development. Development. 113, 1223-30.
Eckert, C., Aranda, M., Wolff, C. und Tautz, D., 2004. Separable stripe enhancer elements
for the pair-rule gene hairy in the beetle Tribolium. EMBO Rep. 5, 638-42.
Edwards, T. A., Pyle, S. E., Wharton, R. P. und Aggarwal, A. K., 2001. Structure of Pumilio
reveals similarity between RNA and peptide binding motifs. Cell. 105, 281-9.
Eldon, E. D. und Pirrotta, V., 1991. Interactions of the Drosophila gap gene giant with maternal
and zygotic pattern-forming genes. Development. 111, 367-78.
Engsontia, P., Sanderson, A. P., Cobb, M., Walden, K. K., Robertson, H. M. und Brown, S.,
2008. The red flour beetle's large nose: an expanded odorant receptor gene family in
Tribolium castaneum. Insect Biochem Mol Biol. 38, 387-97.
Enslee, E. C. und Riddiford, L. M., 1981. Blastokinesis in embryos of the bug, Pyrrhocoris
apterus. A light and electron microscopic study 1. Normal blastokinesis. J Embryol Exp
Morphol. 61, 35-49.
Ephrussi, A., Dickinson, L. K. und Lehmann, R., 1991. Oskar organizes the germ plasm and
directs localization of the posterior determinant nanos. Cell. 66, 37-50.
Extavour, C. G., Pang, K., Matus, D. Q. und Martindale, M. Q., 2005. vasa and nanos expression
patterns in a sea anemone and the evolution of bilaterian germ cell specification
mechanisms. Evol Dev. 7, 201-15.
Farzana, L. und Brown, S. J., 2008. Hedgehog signaling pathway function conserved in
Tribolium segmentation. Dev Genes Evol. 218, 181-92.
247