422 research outputs found
Floral morphology and structure of Emblingia calceoliflora (Emblingiaceae, Brassicales): questions and answers
Temporal diffeomorphic Free Form Deformation to quantify changes induced by left and right bundle branch block and pacing
International audienceThis paper presents motion and deformation quantification results obtained from synthetic and in vitro phantom data provided by the second cardiac Motion Analysis Challenge at STACOM-MICCAI. We applied the Temporal Diffeomorphic Free Form Deformation (TDFFD) algorithm to the datasets. This algorithm builds upon a diffeomorphic version of the FFD, to provide a 3D + t continuous and differentiable transform. The similarity metric includes a comparison between consecutive images, and between a reference and each of the following images. Motion and strain accuracy were evaluated on synthetic 3D ultrasound sequences with known ground truth motion. Experiments were also conducted on in vitro acquisitions
Temporal diffeomorphic Free Form Deformation (TDFFD) applied to motion and deformation quantification of tagged MRI sequences
International audienceThis paper presents strain quantification results obtained from the Tagged Magnetic Resonance Imaging (TMRI) sequences acquired for the 1 st cardiac Motion Analysis Challenge (cMAC). We applied the Temporal Diffeomorphic Free Form Deformation (TDFFD) algorithm to the phantom and the 15 healthy volunteers of the cMAC database. The TDFFD was modified in two ways. First, we modified the similarity metric to incorporate frame to frame intensity differences. Second, on volunteer sequences, we performed the tracking backward in time since the first frames did not show the contrast between blood and myocardium, making these frames poor choices of reference. On the phantom, we propagated a grid adjusted to tag lines to all frames for visually assessing the influence of the different algorithmic parameters. The weight between the two metric terms appeared to be a critical parameter for making a compromise between good tag tracking while preventing drifts and avoiding tag jumps. For each volunteer, a volumet-ric mesh was defined in the Steady-State Free Precession (SSFP) image, at the closest cardiac time from the last frame of the tagging sequence. Uniform strain patterns were observed over all myocardial segments, as physiologically expected
Laser capture microdissection of intestinal tissue from sea bass larvae using an optimized RNA integrity assay and validated reference genes
The increasing demand for a sustainable larviculture has promoted research regarding environmental parameters, diseases and nutrition, intersecting at the mucosal surface of the gastrointestinal tract of fish larvae. The combination of laser capture microdissection (LCM) and gene expression experiments allows cell specific expression profiling. This study aimed at optimizing an LCM protocol for intestinal tissue of sea bass larvae. Furthermore, a 3'/5' integrity assay was developed for LCM samples of fish tissue, comprising low RNA concentrations. Furthermore, reliable reference genes for performing qPCR in larval sea bass gene expression studies were identified, as data normalization is critical in gene expression experiments using RT-qPCR. We demonstrate that a careful optimization of the LCM procedure allows recovery of high quality mRNA from defined cell populations in complex intestinal tissues. According to the geNorm and Normfinder algorithms, ef1a, rpl13a, rps18 and faua were the most stable genes to be implemented as reference genes for an appropriate normalization of intestinal tissue from sea bass across a range of experimental settings. The methodology developed here, offers a rapid and valuable approach to characterize cells/tissues in the intestinal tissue of fish larvae and their changes following pathogen exposure, nutritional/environmental changes, probiotic supplementation or a combination thereof
Incompressible image registration using divergence-conforming B-splines
Anatomically plausible image registration often requires volumetric
preservation. Previous approaches to incompressible image registration have
exploited relaxed constraints, ad hoc optimisation methods or practically
intractable computational schemes. Divergence-free velocity fields have been
used to achieve incompressibility in the continuous domain, although, after
discretisation, no guarantees have been provided. In this paper, we introduce
stationary velocity fields (SVFs) parameterised by divergence-conforming
B-splines in the context of image registration. We demonstrate that sparse
linear constraints on the parameters of such divergence-conforming B-Splines
SVFs lead to being exactly divergence-free at any point of the continuous
spatial domain. In contrast to previous approaches, our framework can easily
take advantage of modern solvers for constrained optimisation, symmetric
registration approaches, arbitrary image similarity and additional
regularisation terms. We study the numerical incompressibility error for the
transformation in the case of an Euler integration, which gives theoretical
insights on the improved accuracy error over previous methods. We evaluate the
proposed framework using synthetically deformed multimodal brain images, and
the STACOM11 myocardial tracking challenge. Accuracy measurements demonstrate
that our method compares favourably with state-of-the-art methods whilst
achieving volume preservation.Comment: Accepted at MICCAI 201
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COVID-19 Roundtable
The past year was an unprecedentedly challenging period to humanity. The very concept of a pandemic indicates a profound impact across different regions and societal strata, rendering the idea of unscathed human lives almost unimaginable. Still, this image of COVID-19 as a global threat menacing us all must not be allowed to efface the specificity of individual or communal struggles. This caveat is particularly relevant in the context of gender and diversity studies – the pertinence of which has been underscored countlessly over the past months, especially in policy recommendations to the COVID-19 pandemic. From the disproportionately severe measures aggravating isolation and destitution among the elderly to the coalescence of sanitary regulations and the BLM protests or the fire in the Moria refugee camp and the resulting urgency to address the wellbeing of displaced people: issues that relate intimately to notions of marginalization continually surface adjacent to the health crisis proper. Whether explicitly or implicitly, these circumstances call for gender and diversity scholars to commit their expertise to the benefit of those inordinately affected by COVID-19 and the array of responses it has evoked worldwide. At the same time, the conditions affecting these groups and individuals also affect research activities and advocacy work on gender and diversity, inhibiting the active commitment and scholarly involvement the situation demands. In this Spring 2021 General Issue, the Journal of Diversity and Gender Studies (DiGeSt) sought to explore the paradoxes, contradictions and tensions scholars in our field have faced and continue to face during the current COVID-19 crisis. Transcending a formally academic register, the roundtable includes personal, situated accounts that engage tensions between the pandemic and scholarly work in diversity and gender studies
Fumarate is an epigenetic modifier that elicits epithelial-to-mesenchymal transition.
Mutations of the tricarboxylic acid cycle enzyme fumarate hydratase cause hereditary leiomyomatosis and renal cell cancer. Fumarate hydratase-deficient renal cancers are highly aggressive and metastasize even when small, leading to a very poor clinical outcome. Fumarate, a small molecule metabolite that accumulates in fumarate hydratase-deficient cells, plays a key role in cell transformation, making it a bona fide oncometabolite. Fumarate has been shown to inhibit α-ketoglutarate-dependent dioxygenases that are involved in DNA and histone demethylation. However, the link between fumarate accumulation, epigenetic changes, and tumorigenesis is unclear. Here we show that loss of fumarate hydratase and the subsequent accumulation of fumarate in mouse and human cells elicits an epithelial-to-mesenchymal-transition (EMT), a phenotypic switch associated with cancer initiation, invasion, and metastasis. We demonstrate that fumarate inhibits Tet-mediated demethylation of a regulatory region of the antimetastatic miRNA cluster mir-200ba429, leading to the expression of EMT-related transcription factors and enhanced migratory properties. These epigenetic and phenotypic changes are recapitulated by the incubation of fumarate hydratase-proficient cells with cell-permeable fumarate. Loss of fumarate hydratase is associated with suppression of miR-200 and the EMT signature in renal cancer and is associated with poor clinical outcome. These results imply that loss of fumarate hydratase and fumarate accumulation contribute to the aggressive features of fumarate hydratase-deficient tumours.This work was supported by the Medical Research Council (UK). S.F. was supported by a Herchel Smith Research Studentship and K.F. by an MRC Career Development Award. E.R.M is supported by the ERC Advanced Researcher award 323004–ONCOTREAT. P.H.M. is supported by Senior Investigator Awards from the Wellcome Trust and NIHR. The Cambridge Human Research Tissue Bank and A.W. are supported by the NIHR Cambridge Biomedical Research Centre.This is the author accepted manuscript. The final version is available from Nature Publishing at http://dx.doi.org/10.1038/nature19353
Atlas construction and image analysis using statistical cardiac models
International audienceThis paper presents a brief overview of current trends in the construction of population and multi-modal heart atlases in our group and their application to atlas-based cardiac image analysis. The technical challenges around the construction of these atlases are organized around two main axes: groupwise image registration of anatomical, motion and fiber images and construction of statistical shape models. Application-wise, this paper focuses on the extraction of atlas-based biomarkers for the detection of local shape or motion abnormalities, addressing several cardiac applications where the extracted information is used to study and grade different pathologies. The paper is concluded with a discussion about the role of statistical atlases in the integration of multiple information sources and the potential this can bring to in-silico simulations
Pits and fissures: etch resistance in prismless enamel walls
The document attached has been archived with permission from the Australian Dental Association. An external link to the publisher’s copy is included.Background: In a previous study to examine the nature of etching on the walls of fissures, there was a consistent result of resistance to deep etching on parts of the walls and a zone of lesser etching on part of the walls as evidenced by the uptake of stain. The staining had been used to examine the nature of the etch pattern. The aims of this study were to define the nature of this etch resistant area. Methods: A sample of 55 teeth, both molars and premolars, were divided into three groups. In the first group the wetting of fissures by the etchant was examined; the second group tested for the effects of pellicle-cuticle-debris or air entrapment on the etching process. The final group looked at alternative mechanical treatments of the fissure prior to etching. Results: The specimens split along the fissures showed clearly that the etch resistant zone was not due to lack of contact with the etchant or the presence of a pellicle-cuticle-debris covering, but to the presence of a prismless enamel structure. This study showed that this zone inhibited tag development on the fissure walls. Conclusions: The mechanical removal of this prismless layer of enamel within the fissure system should result in an improved bonding of a fissure sealant through better tag development, in turn leading to a reduction in the failure rate of a sealant used to prevent caries.MF Burrow, JF Burrow and OF Makinso
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