(Q52676250)

5 May 2018

title

Proteomic analysis of steroid-triggered autophagic programmed cell death during Drosophila development. (English)

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5 May 2018

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2

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Don L DeVoe

8

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author name string

Martin DN

1

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5 May 2018

Dutta S

3

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Chen J

4

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Rudnick P

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Cranford J

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Kantartzis S

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Lee C

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Baehrecke EH

10

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publication date

26 January 2007

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5 May 2018

Cell Death & Differentiation

published in

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volume

14

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issue

5

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page(s)

916-923

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https://scigraph.springernature.com/pub.10.1038/sj.cdd.4402098

exact match

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cites work

Developmental cell death: morphological diversity and multiple mechanisms

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The morphology of various types of cell death in prenatal tissues

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Apoptosis: A Basic Biological Phenomenon with Wideranging Implications in Tissue Kinetics

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Mechanisms of caspase activation and inhibition during apoptosis

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Caspases function in autophagic programmed cell death in Drosophila

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The role of apoptosis in creating and maintaining luminal space within normal and oncogene-expressing mammary acini.

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Autophagic programmed cell death in Drosophila

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Autophagy: dual roles in life and death?

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Regulation of an ATG7-beclin 1 program of autophagic cell death by caspase-8

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Role of Bcl-2 family proteins in a non-apoptotic programmed cell death dependent on autophagy genes

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Drosophila ultraspiracle modulates ecdysone receptor function via heterodimer formation

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The Drosophila beta FTZ-F1 orphan nuclear receptor provides competence for stage-specific responses to the steroid hormone ecdysone.

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A molecular mechanism for the stage specificity of the Drosophila prepupal genetic response to ecdysone

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E93 directs steroid-triggered programmed cell death in Drosophila

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Genome-wide analyses of steroid- and radiation-triggered programmed cell death in Drosophila.

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The Drosophila melanogaster Apaf-1 homologue ARK is required for most, but not all, programmed cell death

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The Drosophila caspase Ice is important for many apoptotic cell deaths and for spermatid individualization, a nonapoptotic process

21 January 2018

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Steroid regulation of programmed cell death during Drosophila development

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Functional ecdysone receptor is the product of EcR and Ultraspiracle genes.

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Drosophila caspase DRONC is required for specific developmental cell death pathways and stress-induced apoptosis

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Dissociation of the dorsal-cactus complex and phosphorylation of the dorsal protein correlate with the nuclear localization of dorsal

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kelch encodes a component of intercellular bridges in Drosophila egg chambers

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crumbs encodes an EGF-like protein expressed on apical membranes of Drosophila epithelial cells and required for organization of epithelia

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The villin-like protein encoded by the Drosophila quail gene is required for actin bundle assembly during oogenesis

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Highwire regulates synaptic growth in Drosophila

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Osa associates with the Brahma chromatin remodeling complex and promotes the activation of some target genes

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Highwire regulates presynaptic BMP signaling essential for synaptic growth.

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Capillary isoelectric focusing-based multidimensional concentration/separation platform for proteome analysis.

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Hrs regulates endosome membrane invagination and tyrosine kinase receptor signaling in Drosophila

21 January 2018

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Role and regulation of starvation-induced autophagy in the Drosophila fat body

21 January 2018

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The Salvador partner Hippo promotes apoptosis and cell-cycle exit in Drosophila.

21 January 2018

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Autophagy occurs upstream or parallel to the apoptosome during histolytic cell death.

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A SAGE Approach to Discovery of Genes Involved in Autophagic Cell Death

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The reaction with polytene chromosomes of antibodies raised against Drosophila E75A protein.

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

The Drosophila insulin receptor homolog: a gene essential for embryonic development encodes two receptor isoforms with different signaling potential

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https://api.crossref.org/works/10.1038%2FSJ.CDD.4402098

inferred from DOI database lookup

7 January 2021

based on heuristic

The Drosophila tumor suppressor gene warts encodes a homolog of human myotonic dystrophy kinase and is required for the control of cell shape and proliferation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402098

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.CDD.4402098

1 reference

5 May 2018

1 reference

5 May 2018