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Katharina Höhn

Researcher at University of Ulm

Publications -  10
Citations -  316

Katharina Höhn is an academic researcher from University of Ulm. The author has contributed to research in topics: Transmission electron microscopy & Freeze substitution. The author has an hindex of 7, co-authored 10 publications receiving 285 citations. Previous affiliations of Katharina Höhn include Heidelberg University.

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Journal ArticleDOI

FoxO3 induces reversible cardiac atrophy and autophagy in a transgenic mouse model.

TL;DR: Heart-specific expression of constitutively active FoxO3 leads to reversible heart atrophy, which suggests a remarkable ability of the adult myocardium to respond to different regulatory cues.
Journal ArticleDOI

FIB/SEM tomography with TEM-like resolution for 3D imaging of high-pressure frozen cells

TL;DR: Small features, so far only visible in transmission electron microscope (TEM) (e.g., the two leaflets of the membrane bi-layer, clathrin coats and cytoskeletal elements), can be resolved directly in the FIB/SEM in the 3D context of whole cells.
Book ChapterDOI

Three-dimensional imaging of adherent cells using FIB/SEM and STEM.

TL;DR: Three different approaches for three-dimensional imaging of electron microscopic samples are described, in which a sample is repeatedly milled with a focused ion beam (FIB) and each newly produced block face is imaged with the scanning electron microscope (SEM), and resolution is considerably improved when the secondary electron signal is used.
Journal ArticleDOI

Preparation of cryofixed cells for improved 3D ultrastructure with scanning transmission electron tomography

TL;DR: This combination of novel light transparent sapphire specimen carrier for high-pressure freezing and a freeze substitution protocol for better contrast of membranes allows for imaging membranes and other subcellular structures with unsurpassed quality.
Book ChapterDOI

High-Pressure Freezing for Scanning Transmission Electron Tomography Analysis of Cellular Organelles

TL;DR: This chapter describes optimized high-pressure freezing and freeze substitution protocols for STEM tomography in order to obtain high membrane contrast and adapted protocols for high- pressure freezing of cultivated cells from a physiological state.