David Haberthür

Dr. David Haberthür

orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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24 May 2011 in Annals of Biomedical Engineering
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Journal Article
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SRS. M. K. Rausch
S. M. K. Rausch
DHDavid Haberthür
David Haberthür
MSM. Stampanoni
M. Stampanoni
JSJohannes C. Schittny
Johannes C. Schittny
WWW. A. Wall
W. A. Wall

1 September 2008 in Journal of Applied Physiology
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Journal Article
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ATA. Tsuda
A. Tsuda
NFN. Filipovic
N. Filipovic
DHDavid Haberthür
David Haberthür
RDR. Dickie
R. Dickie
YMY. Matsui
Y. Matsui
JSJohannes C. Schittny
Johannes C. Schittny
The alveolated structure of the pulmonary acinus plays a vital role in gas exchange function. Three-dimensional (3D) analysis of the parenchymal region is fundamental to understanding this structure-function relationship, but only a limited number of attempts have been conducted in the past because of technical limitations. In this study, we developed a new image processing methodology based on finite element (FE) analysis for accurate 3D structural reconstruction of the gas exchange regions of the lung. Stereologically well characterized rat lung samples ( Pediatr Res 53: 72–80, 2003) were imaged using high-resolution synchrotron radiation-based X-ray tomographic microscopy. A stack of 1,024 images (each slice: 1024 × 1024 pixels) with resolution of 1.4 μm3 per voxel were generated. For the development of FE algorithm, regions of interest (ROI), containing ∼7.5 million voxels, were further extracted as a working subunit. 3D FEs were created overlaying the voxel map using a grid-based hexahedral algorithm. A proper threshold value for appropriate segmentation was iteratively determined to match the calculated volume density of tissue to the stereologically determined value ( Pediatr Res 53: 72–80, 2003). The resulting 3D FEs are ready to be used for 3D structural analysis as well as for subsequent FE computational analyses like fluid dynamics and skeletonization.

22 August 2016 in Solid Earth
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KSKathleen Sell
Kathleen Sell
ESErik H. Saenger
Erik H. Saenger
AFAndrzej Falenty
Andrzej Falenty
MCMarwen Chaouachi
Marwen Chaouachi
DHDavid Haberthür
David Haberthür
MKMichael Kersten
Michael Kersten
To date, very little is known about the distribution of natural gas hydrates in sedimentary matrices and its influence on the seismic properties of the host rock, in particular at low hydrate concentration. Digital rock physics offers a unique approach to this issue yet requires good quality, high-resolution 3-D representations for the accurate modeling of petrophysical and transport properties. Although such models are readily available via in situ synchrotron radiation X-ray tomography, the analysis of such data asks for complex workflows and high computational power to maintain valuable results. Here, we present a best-practice procedure complementing data from Chaouachi et al. (2015) with data post-processing, including image enhancement and segmentation as well as exemplary numerical simulations of an acoustic wave propagation in 3-D using the derived results. A combination of the tomography and 3-D modeling opens a path to a more reliable deduction of properties of gas hydrate-bearing sediments without a reliance on idealized and frequently imprecise models.

12 October 2020 in Nature Communications
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ENElis Newham
Elis Newham
PGPamela G. Gill
Pamela G. Gill
PBPhilippa Brewer
Philippa Brewer
MBMichael J. Benton
Michael J. Benton
VFVincent Fernandez
Vincent Fernandez
ICIan Corfe
Ian Corfe
Despite considerable advances in knowledge of the anatomy, ecology and evolution of early mammals, far less is known about their physiology. Evidence is contradictory concerning the timing and fossil groups in which mammalian endothermy arose. To determine the state of metabolic evolution in two of the earliest stem-mammals, the Early JurassicMorganucodonandKuehneotherium, we use separate proxies for basal and maximum metabolic rate. Here we report, using synchrotron X-ray tomographic imaging of incremental tooth cementum, that they had maximum lifespans considerably longer than comparably sized living mammals, but similar to those of reptiles, and so they likely had reptilian-level basal metabolic rates. Measurements of femoral nutrient foramina showMorganucodonhad blood flow rates intermediate between living mammals and reptiles, suggesting maximum metabolic rates increased evolutionarily before basal metabolic rates. Stem mammals lacked the elevated endothermic metabolism of living mammals, highlighting the mosaic nature of mammalian physiological evolution.

7 June 2021 in Nature Communications
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HNHenry Nording
Henry Nording
LBLasse Baron
Lasse Baron
DHDavid Haberthür
David Haberthür
FEFrederic Emschermann
Frederic Emschermann
MMMatthias Mezger
Matthias Mezger
HLHarald Langer
Harald Langer
Platelets contribute to the regulation of tissue neovascularization, although the specific factors underlying this function are unknown. Here, we identified the complement anaphylatoxin C5a-mediated activation of C5a receptor 1 (C5aR1) on platelets as a negative regulatory mechanism of vessel formation. We showed that platelets expressing C5aR1 exert an inhibitory effect on endothelial cell functions such as migration and 2D and 3D tube formation. Growth factor- and hypoxia-driven vascularization was markedly increased in C5ar1−/− mice. Platelet-specific deletion of C5aR1 resulted in a proangiogenic phenotype with increased collateralization, capillarization and improved pericyte coverage. Mechanistically, we found that C5a induced preferential release of CXC chemokine ligand 4 (CXCL4, PF4) from platelets as an important antiangiogenic paracrine effector molecule. Interfering with the C5aR1-CXCL4 axis reversed the antiangiogenic effect of platelets both in vitro and in vivo.In conclusion, we identified a mechanism for the control of tissue neovascularization through C5a/C5aR1 axis activation in platelets and subsequent induction of the antiangiogenic factor CXCL4.

9 July 2010 in Journal of Synchrotron Radiation
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DHDavid Haberthür
David Haberthür
CHChristoph Hintermüller
Christoph Hintermüller
FMFederica Marone
Federica Marone
JSJohannes C. Schittny
Johannes C. Schittny
MSMarco Stampanoni
Marco Stampanoni
Volumetric data at micrometer level resolution can be acquired within a few minutes using synchrotron-radiation-based tomographic microscopy. The field of view along the rotation axis of the sample can easily be increased by stacking several tomograms, allowing the investigation of long and thin objects at high resolution. On the contrary, an extension of the field of view in the perpendicular direction is non-trivial. This paper presents an acquisition protocol which increases the field of view of the tomographic dataset perpendicular to its rotation axis. The acquisition protocol can be tuned as a function of the reconstruction quality and scanning time. Since the scanning time is proportional to the radiation dose imparted to the sample, this method can be used to increase the field of view of tomographic microscopy instruments while optimizing the radiation dose for radiation-sensitive samples and keeping the quality of the tomographic dataset on the required level. This approach, dubbed wide-field synchrotron radiation tomographic microscopy, can increase the lateral field of view up to five times. The method has been successfully applied for the three-dimensional imaging of entire rat lung acini with a diameter of 4.1 mm at a voxel size of 1.48 microm.