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Drosophila embryo

Holes in the Plasma Membrane Mimic Torso-Like Perforin in Torso Tyrosine Kinase Receptor Activation in the Drosophila Embryo

Holes in the Plasma Membrane Mimic Torso-Like Perforin in Torso Tyrosine Kinase Receptor Activation in the Drosophila Embryo

... the Drosophila embryo at the blastoderm ...in Drosophila bearing a membrane attack complex/perforin (MACPF) domain — a motif present in proteins involved in pore formation at cell ...the ...

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Shaping BMP morphogen gradients in the Drosophila embryo and
pupal wing

Shaping BMP morphogen gradients in the Drosophila embryo and pupal wing

... Key to many developmental processes is the ability of cells to reproducibly interpret information regarding their spatial position within a developing field so that patterns and, ultimately, tissues form with the proper ...

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Quantitative Analysis of Gene Function in the Drosophila Embryo

Quantitative Analysis of Gene Function in the Drosophila Embryo

... HE Drosophila embryo provides a remarkable dem- Horowicz and Pinchin 1987; Morrissey et ...the embryo resulted in the interpretation of all of these experiments is the from studies on genes ...

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Origin and specification of type II neuroblasts in the Drosophila embryo

Origin and specification of type II neuroblasts in the Drosophila embryo

... of Drosophila embryo heads at early stage 11 (A,A ′ ), stage 12 (B-B ‴ ), stage 13 (C,C ′ ), stage 15 (D,D ′ ), stage 16 (E,E ′ ) and stage 17 (F,F ′ ...

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Non cell autonomous control of denticle diversity in the Drosophila embryo

Non cell autonomous control of denticle diversity in the Drosophila embryo

... en:spastin Drosophila embryo, showing phalloidin (magenta; to label actin) and b-tubulin (green) ...UAS-spastin embryo, showing phalloidin and b-tubulin ...

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Sec5, a member of the exocyst complex, mediates Drosophila embryo cellularization

Sec5, a member of the exocyst complex, mediates Drosophila embryo cellularization

... Cellularization of the Drosophila embryo is the process by which a syncytium of ~6000 nuclei is subdivided into discrete cells. In order to individualize the cells, massive membrane addition needs to occur ...

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A regulatory code for neurogenic gene expression in the
Drosophila embryo

A regulatory code for neurogenic gene expression in the Drosophila embryo

... Two of the previously identified enhancers are associated with the rhomboid (rho) and ventral nervous system defective (vnd) genes (White et al., 1983; Bier et al., 1990). Both enhancers are activated by intermediate ...

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Regulation of Gastrulation Through Dynamic Patterning in the Drosophila Embryo

Regulation of Gastrulation Through Dynamic Patterning in the Drosophila Embryo

... the Drosophila blastoderm, gives rise to precise gene expression ...the embryo thereby redistributing the overall concentration of Dorsal protein over ...

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Control of Denticle Diversity in the Drosophila Embryo

Control of Denticle Diversity in the Drosophila Embryo

... and Drosophila also requires a series of oriented cell divisions, also driven by PCP (da Silva and Vincent, 2007; Baena-Lopez, 2005; Ciruna, 2006; Fischer, 2006; Gong, ...

193

Myosin II is not required for Drosophila tracheal branch elongation and cell intercalation

Myosin II is not required for Drosophila tracheal branch elongation and cell intercalation

... The Drosophila tracheal system consists of an interconnected network of monolayered epithelial tubes that ensures oxygen transport in the larval and adult ...the Drosophila embryo that lead to ...

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The F actin microtubule crosslinker Shot is a platform for Krasavietz mediated translational regulation of midline axon repulsion

The F actin microtubule crosslinker Shot is a platform for Krasavietz mediated translational regulation of midline axon repulsion

... Axon extension and guidance require a coordinated assembly of F-actin and microtubules as well as regulated translation. The molecular basis of how the translation of mRNAs encoding guidance proteins could be closely ...

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Regulation of cytoskeletal organization and junctional remodeling by the atypical cadherin Fat

Regulation of cytoskeletal organization and junctional remodeling by the atypical cadherin Fat

... Fat and Ds are asymmetrically localized within cells (Ambegaonkar et al., 2012; Bosveld et al., 2012; Brittle et al., 2012) and could influence cell polarity directly or through the regulation of downstream effectors. ...

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Chromosomal Homology and Molecular Organization of Muller's Elements D and E in the Drosophila repleta Species Group

Chromosomal Homology and Molecular Organization of Muller's Elements D and E in the Drosophila repleta Species Group

... al., 1988 Abdominal segmentation of the Drosophila embryo requires a hormone receptor-like protein encoded by the gap gene knirps. FONTDEVILA, 1986 The evolutionary his[r] ...

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Dosage-Sensitive Maternal Modifiers of the Drosophila Segmentation Gene runt

Dosage-Sensitive Maternal Modifiers of the Drosophila Segmentation Gene runt

... The protein encoded by the pair-rule gene runt functions as a transcriptional regulator during anterior- posterior patterning of the Drosophila embryo.. Results of over-express[r] ...

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Differential Effects of Drosophila Mastermind on Asymmetric Cell Fate Specification and Neuroblast Formation

Differential Effects of Drosophila Mastermind on Asymmetric Cell Fate Specification and Neuroblast Formation

... the Drosophila stein and Posakony 1990; Bhat and Schedl 1994; Bhat embryo provides an important paradigm for investi- et ...the Drosophila embryo, ⵑ30 neuroblast et ...

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Myoblast fusion: lessons from flies and mice

Myoblast fusion: lessons from flies and mice

... the Drosophila embryo, the FCMs and founder cells/myotubes arise in close proximity to each other, and are often adjacent cells that are in direct contact ...the Drosophila system, it is often ...

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Cellular and molecular insights into Hox protein action

Cellular and molecular insights into Hox protein action

... early Drosophila embryo revealed that transcription factors with well-defined developmental functions show a surprisingly high number of genomic binding sites – up to 20,000 (Li et ...

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Wollknäuel is required for embryo patterning and encodes the
Drosophila ALG5 UDP glucose:dolichyl phosphate
glucosyltransferase

Wollknäuel is required for embryo patterning and encodes the Drosophila ALG5 UDP glucose:dolichyl phosphate glucosyltransferase

... A major activator of gt and kni expression is Caudal (Cad), which forms a posterior-anterior protein gradient, being translationally repressed by Bicoid in the anterior part of the embryo (Rivera-Pomar and Jackle, ...

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The Drosophila homologue of Rootletin is required for mechanosensory function and ciliary rootlet formation in chordotonal sensory neurons

The Drosophila homologue of Rootletin is required for mechanosensory function and ciliary rootlet formation in chordotonal sensory neurons

... A second feature of Drosophila is that it has very few ciliated cell types. The only somatic cells bearing cilia are the type I sensory neurons, in which olfactory, gus- tatory or mechanosensory reception are ...

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Wolbachia Transfer from Drosophila melanogaster into D. simulans: Host Effect and Cytoplasmic Incompatibility Relationships

Wolbachia Transfer from Drosophila melanogaster into D. simulans: Host Effect and Cytoplasmic Incompatibility Relationships

... Santamaria P., 1987 Injecting eggs, pp. 159–173 in Drosophila: A in insects, pp. 42–80 in Influential Passengers: Inherited Microorgan- Practical Approach, edited by D. B. Roberts. IRL Press, Oxford. isms and ...

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