(Strutt and White, 1994)

(Schulz et al., 1993, Schulz et al., 1993, Tearle and Nusslein-Volhard, 1987)

(Strutt and White, 1994)

(Strutt and White, 1994)

(Strutt and White, 1994, Schulz et al., 1993, Tearle and Nusslein-Volhard, 1987)

(Strutt and White, 1994)

(Strutt and White, 1994)

Identification: in a germline clone screen for mutants that are defective in localisation of an Avic\GFP-stau marker in living oocytes. 1 allele of Ets97D has been identified in the screen.

(Martin et al., 2003)

Ets97D function is required for the correct localisation of the posterior determinants in the oocyte. It is also required for dorsoventral polarity in the follicle cells.

(Gajewski and Schulz, 1995)

Complementation analysis and sequence analysis of the female sterile mutant tiny eggs demonstrates that tiny eggs is an allele of Ets97D. Mutations of Ets97D demonstrate that the Ets97D gene product is required for proper follicle cell migration, chorion formation and nurse cell chromosome decondensation during oogenesis.

(Schulz et al., 1993)

Ets97D has been cloned, sequenced and its RNA expression pattern characterised.

(Chen et al., 1992)

Pattern and mode of coding gene divergence in the ets gene family examined. Results suggest that gene evolution recapitulates species divergence, though at different rates imposed by apparent selective constraints on 3 domains, and that there have been a minimum of 5 ets-primordial gene duplication events: one during X.laevis speciation, one near the time of vertebrate emergence and three prior to the divergence of vertebrates from the Echinodermata and Arthropoda.

(Lautenberger et al., 1992)

Isolated from a pupal cDNA library using pnt and viral ets gene fragments as probes, under low stringency conditions.

(Pribyl et al., 1991)

An Ets97D cDNA has been cloned and sequenced, and Ets97D mRNA expression has been analysed.

(Pribyl et al., 1991)