scispace - formally typeset
D

Daniela Penzkofer

Researcher at Goethe University Frankfurt

Publications -  7
Citations -  483

Daniela Penzkofer is an academic researcher from Goethe University Frankfurt. The author has contributed to research in topics: Reperfusion injury & Ischemia. The author has an hindex of 5, co-authored 7 publications receiving 424 citations.

Papers
More filters
Journal ArticleDOI

Inhibition of MicroRNA-92a Protects Against Ischemia/Reperfusion Injury in a Large-Animal Model

TL;DR: Regional LNA-92a delivery reduces miR- 92a levels and infarct size and postischemic loss of function and might be a novel therapeutic tool to preserve cardiac function after ischemia.
Journal ArticleDOI

Inhibition of miR-92a improves re-endothelialization and prevents neointima formation following vascular injury.

TL;DR: It is indicated that inhibition of endothelial miR-92a attenuates neointimal lesion formation by accelerating re-endothelialization and thus represents a putative novel mechanism to enhance the functional recovery following vascular injury.
Journal ArticleDOI

The Early Activation of Toll-Like Receptor (TLR)-3 Initiates Kidney Injury after Ischemia and Reperfusion

TL;DR: Overall, the absence of TLR-3 is associated with lower cumulative kidney damage and maintained renal blood perfusion within the first 24 hours of reperfusion and it is concluded that TLr-3 seems to participate in the pathogenesis of early acute kidney injury.
Journal ArticleDOI

Phenotypic Characterization of miR-92a−/− Mice Reveals an Important Function of miR-92a in Skeletal Development

TL;DR: It is demonstrated that deletion of miR-92a is sufficient to induce a developmental skeletal defect in mice and not reduce circulating or bone marrow-derived hematopoietic cells, but induces skeletal defects.
Journal ArticleDOI

The small fibrinopeptide Bβ15-42 as renoprotective agent preserving the endothelial and vascular integrity in early ischemia reperfusion injury in the mouse kidney.

TL;DR: It is shown that Bβ15–42 alleviates early functional and morphological kidney damage as soon as 1 h and 3 h after ischemia and reperfusion, and may act as a potent renoprotective agent by preserving the endothelial and vascular integrity.