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Claudia Quedenau

Researcher at Max Delbrück Center for Molecular Medicine

Publications -  25
Citations -  1928

Claudia Quedenau is an academic researcher from Max Delbrück Center for Molecular Medicine. The author has contributed to research in topics: Medicine & Human leukocyte antigen. The author has an hindex of 14, co-authored 21 publications receiving 1497 citations. Previous affiliations of Claudia Quedenau include Max Planck Society.

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Neural circular RNAs are derived from synaptic genes and regulated by development and plasticity

TL;DR: The data indicate that brain circRNAs are positioned to respond to and regulate synaptic function and exhibited substantial up- or downregulation following a homeostatic downscaling of neuronal activity.
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Polylox barcoding reveals haematopoietic stem cell fates realized in vivo

TL;DR: The development of an artificial DNA recombination locus (termed Polylox) is reported that enables broadly applicable endogenous barcoding based on the Cre–loxP recombination system and reaches a practical diversity of several hundred thousand barcodes, allowing tagging of single cells.
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Amorfrutins are potent antidiabetic dietary natural products

TL;DR: In diet-induced obese and db/db mice, amorfrutin treatment strongly improves insulin resistance and other metabolic and inflammatory parameters without concomitant increase of fat storage or other unwanted side effects such as hepatoxicity.
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Integrative analysis revealed the molecular mechanism underlying RBM10‐mediated splicing regulation

TL;DR: RBM10 is established as an important regulator of alternative splicing, presented a mechanistic model for RBM10‐mediated splicing regulation and provided a molecular link to understanding a human congenital disorder.
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Pervasive isoform‐specific translational regulation via alternative transcription start sites in mammals

TL;DR: This study demonstrated the extensive translational regulation by usage of alternative transcription start sites and offered comprehensive understanding of translationalregulation by diverse sequence features embedded in 5ʹUTRs.