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Cornelia Schönbauer

Researcher at Max Planck Society

Publications -  7
Citations -  701

Cornelia Schönbauer is an academic researcher from Max Planck Society. The author has contributed to research in topics: RNA interference & Drosophila Protein. The author has an hindex of 6, co-authored 7 publications receiving 618 citations.

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Systematic genetic analysis of muscle morphogenesis and function in Drosophila

TL;DR: A role in muscle is identified for 2,785 genes, many of which are phylogenetically conserved, including genes implicated in mammalian sarcomere organization and human muscle diseases.
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Three-Dimensional Reconstruction and Segmentation of Intact Drosophila by Ultramicroscopy

TL;DR: Ultramicroscopy reconstructions of the flight musculature, the nervous system, and the digestive tract of entire, chemically cleared, drosophila in autofluorescent light verify that the anatomy of a whole fly, including the filigree spatial organization of the direct flight muscles, can be analysed from a single ultramicroScopy reconstruction.
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Spalt mediates an evolutionarily conserved switch to fibrillar muscle fate in insects

TL;DR: It is proposed that Spalt proteins switch myofibres from tubular to fibrillar fate during development, a function potentially conserved in the vertebrate heart—a stretch-activated muscle sharing features with insect flight muscle.
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Ret rescues mitochondrial morphology and muscle degeneration of Drosophila Pink1 mutants

TL;DR: It is reported that a signaling active version of Ret (RetMEN2B) rescues muscle degeneration, disintegration of mitochondria and ATP content of Pink1 mutants, providing a novel mechanism underlying Ret‐mediated cell protection in a situation relevant for human PD.
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The RNA-binding protein Arrest (Bruno) regulates alternative splicing to enable myofibril maturation in Drosophila flight muscle

TL;DR: It is shown that spalt major (salm) determines fibrillar muscle physiology by regulating transcription and alternative splicing of a large set of sarcomeric proteins, and the RNA‐binding protein Arrest (Aret) is identified as downstream of salm.