9,211 research outputs found
Deep Shape Matching
We cast shape matching as metric learning with convolutional networks. We
break the end-to-end process of image representation into two parts. Firstly,
well established efficient methods are chosen to turn the images into edge
maps. Secondly, the network is trained with edge maps of landmark images, which
are automatically obtained by a structure-from-motion pipeline. The learned
representation is evaluated on a range of different tasks, providing
improvements on challenging cases of domain generalization, generic
sketch-based image retrieval or its fine-grained counterpart. In contrast to
other methods that learn a different model per task, object category, or
domain, we use the same network throughout all our experiments, achieving
state-of-the-art results in multiple benchmarks.Comment: ECCV 201
SD-208, a novel protein kinase D inhibitor, blocks prostate cancer cell proliferation and tumor Growth in Vivo by inducing G2/M cell cycle arrest
Protein kinase D (PKD) has been implicated in many aspects of tumorigenesis and progression, and is an emerging molecular target for the development of anticancer therapy. Despite recent advancement in the development of potent and selective PKD small molecule inhibitors, the availability of in vivo active PKD inhibitors remains sparse. In this study, we describe the discovery of a novel PKD small molecule inhibitor, SD-208, from a targeted kinase inhibitor library screen, and the synthesis of a series of analogs to probe the structure-activity relationship (SAR) vs. PKD1. SD-208 displayed a narrow SAR profile, was an ATP-competitive pan-PKD inhibitor with low nanomolar potency and was cell active. Targeted inhibition of PKD by SD-208 resulted in potent inhibition of cell proliferation, an effect that could be reversed by overexpressed PKD1 or PKD3. SD-208 also blocked prostate cancer cell survival and invasion, and arrested cells in the G2/M phase of the cell cycle. Mechanistically, SD-208-induced G2/M arrest was accompanied by an increase in levels of p21 in DU145 and PC3 cells as well as elevated phosphorylation of Cdc2 and Cdc25C in DU145 cells. Most importantly, SD-208 given orally for 24 days significantly abrogated the growth of PC3 subcutaneous tumor xenografts in nude mice, which was accompanied by reduced proliferation and increased apoptosis and decreased expression of PKD biomarkers including survivin and Bcl-xL. Our study has identified SD-208 as a novel efficacious PKD small molecule inhibitor, demonstrating the therapeutic potential of targeted inhibition of PKD for prostate cancer treatment
Effect of helium ion irradiation on pure W, W-5Ta and W-5Re: a micro-tensile and nanoindentation investigation of mechanical properties
Micro-tensile testing has been used to study the response of pure tungsten and two tungsten alloys to helium ion irradiation. Commercially supplied plates of W, W-5Ta and W-5Re were irradiated using 6 MeV helium ions at room temperature. The ion energy was attenuated with an energy spreading device such that a uniform level of damage at 0.6 dpa (and 11,000 appm He) was deposited at the 3–9 µm depth. Focused ion beam milling was used to fabricate dog-bone shaped, micro-tensile samples 5 × 5 µm in cross-sectional area and 17 µm in length from the unirradiated and irradiated samples. All micro-tensile samples were tested at a quasi-static strain rate and the stress–strain curves were analysed to determine the mechanical properties. A close correlation was found between micro-tensile results and the bulk mechanical properties reported in the literature. Comparison between the unirradiated micro-tensile properties of W-5Re and W-5Ta with W showed that, as expected, W-5Re was softer than W whilst W-5Ta had only minor differences in micro-tensile properties compared with W. The micro-tensile results of the irradiated W, W-5Ta and W-5Re showed an increase in strength and an almost complete loss of ductility compared to the unirradiated samples. In comparing micro-tensile results to nanoindentation measurements, it was found that micro-tensile offers comparable level of precision in measurement of irradiation hardening amongst W, W-5Ta and W-5Re. The implications of the results with respect to the future performance of tungsten-based materials in the divertors in fusion reactors are discussed in detail. Graphical abstract: [Figure not available: see fulltext.
Generic 3D Representation via Pose Estimation and Matching
Though a large body of computer vision research has investigated developing
generic semantic representations, efforts towards developing a similar
representation for 3D has been limited. In this paper, we learn a generic 3D
representation through solving a set of foundational proxy 3D tasks:
object-centric camera pose estimation and wide baseline feature matching. Our
method is based upon the premise that by providing supervision over a set of
carefully selected foundational tasks, generalization to novel tasks and
abstraction capabilities can be achieved. We empirically show that the internal
representation of a multi-task ConvNet trained to solve the above core problems
generalizes to novel 3D tasks (e.g., scene layout estimation, object pose
estimation, surface normal estimation) without the need for fine-tuning and
shows traits of abstraction abilities (e.g., cross-modality pose estimation).
In the context of the core supervised tasks, we demonstrate our representation
achieves state-of-the-art wide baseline feature matching results without
requiring apriori rectification (unlike SIFT and the majority of learned
features). We also show 6DOF camera pose estimation given a pair local image
patches. The accuracy of both supervised tasks come comparable to humans.
Finally, we contribute a large-scale dataset composed of object-centric street
view scenes along with point correspondences and camera pose information, and
conclude with a discussion on the learned representation and open research
questions.Comment: Published in ECCV16. See the project website
http://3drepresentation.stanford.edu/ and dataset website
https://github.com/amir32002/3D_Street_Vie
Structural analysis and corrosion studies on an ISO 5832-9 biomedical alloy with TiO2 sol–gel layers
The aim of this study was to demonstrate the
relationship between the structural and corrosion properties
of an ISO 5832-9 biomedical alloy modified with titanium
dioxide (TiO2) layers. These layers were obtained via the
sol–gel method by acid-catalyzed hydrolysis of titanium
isopropoxide in isopropanol solution. To obtain TiO2 layers
with different structural properties, the coated samples
were annealed at temperatures of 200, 300, 400, 450, 500,
600 and 800 C for 2 h. For all the prepared samples,
accelerated corrosion measurements were performed in
Tyrode’s physiological solution using electrochemical
methods. The most important corrosion parameters were
determined: corrosion potential, polarization resistance,
corrosion rate, breakdown and repassivation potentials.
Corrosion damage was analyzed using scanning electron
microscopy. Structural analysis was carried out for selected
TiO2 coatings annealed at 200, 400, 600 and 800 C. In
addition, the morphology, chemical composition, crystallinity,
thickness and density of the deposited TiO2 layers
were determined using suitable electron and X-ray measurement
methods. It was shown that the structure and
character of interactions between substrate and deposited
TiO2 layers depended on annealing temperature. All the
obtained TiO2 coatings exhibit anticorrosion properties, but
these properties are related to the crystalline structure and
character of substrate–layer interaction. From the point of
view of corrosion, the best TiO2 sol–gel coatings for stainless steel intended for biomedical applications seem to
be those obtained at 400 C.This study was supported by Grant No. N N507
501339 of the National Science Centre. The authors wish to express
their thanks to J. Borowski (MEDGAL, Poland) for the Rex 734 alloy
Structure and function of a spectrin-like regulator of bacterial cytokinesis
© 2014 Macmillan Publishers Limited. All rights reserved. Bacterial cell division is facilitated by a molecular machine - the divisome - that assembles at mid-cell in dividing cells. The formation of the cytokinetic Z-ring by the tubulin homologue FtsZ is regulated by several factors, including the divisome component EzrA. Here we describe the structure of the 60-kDa cytoplasmic domain of EzrA, which comprises five linear repeats of an unusual triple helical bundle. The EzrA structure is bent into a semicircle, providing the protein with the potential to interact at both N- and C-termini with adjacent membrane-bound divisome components. We also identify at least two binding sites for FtsZ on EzrA and map regions of EzrA that are responsible for regulating FtsZ assembly. The individual repeats, and their linear organization, are homologous to the spectrin proteins that connect actin filaments to the membrane in eukaryotes, and we thus propose that EzrA is the founding member of the bacterial spectrin family
On the Effectiveness of Image Rotation for Open Set Domain Adaptation
Open Set Domain Adaptation (OSDA) bridges the domain gap between a labeled
source domain and an unlabeled target domain, while also rejecting target
classes that are not present in the source. To avoid negative transfer, OSDA
can be tackled by first separating the known/unknown target samples and then
aligning known target samples with the source data. We propose a novel method
to addresses both these problems using the self-supervised task of rotation
recognition. Moreover, we assess the performance with a new open set metric
that properly balances the contribution of recognizing the known classes and
rejecting the unknown samples. Comparative experiments with existing OSDA
methods on the standard Office-31 and Office-Home benchmarks show that: (i) our
method outperforms its competitors, (ii) reproducibility for this field is a
crucial issue to tackle, (iii) our metric provides a reliable tool to allow
fair open set evaluation.Comment: accepted at ECCV 202
Tracking Target Signal Strengths on a Grid using Sparsity
Multi-target tracking is mainly challenged by the nonlinearity present in the
measurement equation, and the difficulty in fast and accurate data association.
To overcome these challenges, the present paper introduces a grid-based model
in which the state captures target signal strengths on a known spatial grid
(TSSG). This model leads to \emph{linear} state and measurement equations,
which bypass data association and can afford state estimation via
sparsity-aware Kalman filtering (KF). Leveraging the grid-induced sparsity of
the novel model, two types of sparsity-cognizant TSSG-KF trackers are
developed: one effects sparsity through -norm regularization, and the
other invokes sparsity as an extra measurement. Iterative extended KF and
Gauss-Newton algorithms are developed for reduced-complexity tracking, along
with accurate error covariance updates for assessing performance of the
resultant sparsity-aware state estimators. Based on TSSG state estimates, more
informative target position and track estimates can be obtained in a follow-up
step, ensuring that track association and position estimation errors do not
propagate back into TSSG state estimates. The novel TSSG trackers do not
require knowing the number of targets or their signal strengths, and exhibit
considerably lower complexity than the benchmark hidden Markov model filter,
especially for a large number of targets. Numerical simulations demonstrate
that sparsity-cognizant trackers enjoy improved root mean-square error
performance at reduced complexity when compared to their sparsity-agnostic
counterparts.Comment: Submitted to IEEE Trans. on Signal Processin
Benefits and risks of the hormetic effects of dietary isothiocyanates on cancer prevention
The isothiocyanate (ITC) sulforaphane (SFN) was shown at low levels (1-5 µM) to promote cell proliferation to 120-143% of the controls in a number of human cell lines, whilst at high levels (10-40 µM) it inhibited such cell proliferation. Similar dose responses were observed for cell migration, i.e. SFN at 2.5 µM increased cell migration in bladder cancer T24 cells to 128% whilst high levels inhibited cell migration. This hormetic action was also found in an angiogenesis assay where SFN at 2.5 µM promoted endothelial tube formation (118% of the control), whereas at 10-20 µM it caused significant inhibition. The precise mechanism by which SFN influences promotion of cell growth and migration is not known, but probably involves activation of autophagy since an autophagy inhibitor, 3-methyladenine, abolished the effect of SFN on cell migration. Moreover, low doses of SFN offered a protective effect against free-radical mediated cell death, an effect that was enhanced by co-treatment with selenium. These results suggest that SFN may either prevent or promote tumour cell growth depending on the dose and the nature of the target cells. In normal cells, the promotion of cell growth may be of benefit, but in transformed or cancer cells it may be an undesirable risk factor. In summary, ITCs have a biphasic effect on cell growth and migration. The benefits and risks of ITCs are not only determined by the doses, but are affected by interactions with Se and the measured endpoint
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