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The segment polarity gene dishevelled (dsh) of Drosophila is required for pattern formation of the embryonic segments and the adult imaginal discs.
Using the Arabidopsis kpl mutant, in which single-fertilization events are frequent, we showed that endosperm development is not required for pattern formation during early embryogenesis.
We extended the use of Drosophila beyond being a model for signaling pathways required for pattern recognition immune signaling and show that the fly can be used to identify genes required for pathogenesis and host-pathogen interactions.
In fault diagnosis system designers or engineers should analyse systems in order to define their input patterns, features, classes required for pattern recognition, and corresponding residuals, fault symptoms, faults needed for fault diagnosis, respectively.
Thus, our genetic analyses suggest that the NMDA receptor is not required for pattern completion during associative memory recall.
Nested feedback loops were required for pattern formation at early embryogenesis, and for neurogenesis at middle embryogenesis.
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Since the resulting air-particle jet is divergent, erosion resistant masks are required for patterning.
Furthermore, we show that coordinated activation of UNC-104/Kinesin3 UNC-104/Kinesin3quired for panderning newly formeDyneinpses.
Furthermore, overexpression of sprouty in wing veins and ovarian follicle cells, two other tissues where EGF signaling is required for patterning, results in phenotypes that resemble the loss-of-function phenotypes of Egf receptor.
The pair-rule gene, hairy, encodes a basic helix-loop-helix transcription factor and is required for patterning of the early Drosophila embryo and for morphogenesis of the embryonic salivary gland.
These findings support the idea that the gastrulation arrest phenotype is a true result of XMeis3 loss-of-function and that XMeis3 is required for patterning (a part of) the primary axis in Xenopus embryos.
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