2,962 research outputs found
Non-invasive Diabetes Detection using Gabor Filter: A Comparative Analysis of Different Cameras
This paper compares and explores the performance of both mobile device camera
and laptop camera as convenient tool for capturing images for non-invasive
detection of Diabetes Mellitus (DM) using facial block texture features.
Participants within age bracket 20 to 79 years old were chosen for the dataset.
12mp and 7mp mobile cameras, and a laptop camera were used to take the photo
under normal lighting condition. Extracted facial blocks were classified using
k-Nearest Neighbors (k-NN) and Support Vector Machine (SVM). 100 images were
captured, preprocessed, filtered using Gabor, and iterated. Performance of the
system was measured in terms of accuracy, specificity, and sensitivity. Best
performance of 96.7% accuracy, 100% sensitivity, and 93% specificity were
achieved from 12mp back camera using SVM with 100 images.Comment: 11 pages, 5 figures, 3 tables, conferenc
Lamellar Structures of MUC2-Rich Mucin: A Potential Role in Governing the Barrier and Lubricating Functions of Intestinal Mucus
Mucus is a ubiquitous feature of mammalian wet epithelial surfaces, where it lubricates and forms a selective barrier that excludes a range of particulates, including pathogens, while hosting a diverse commensal microflora. The major polymeric component of mucus is mucin, a large glycoprotein formed by several MUC gene products, with MUC2 expression dominating intestinal mucus. A satisfactory answer to the question of how these molecules build a dynamic structure capable of playing such a complex role has yet to be found, as recent reports of distinct layers of chemically identical mucin in the colon and anomalously rapid transport of nanoparticles through mucus have emphasized. Here we use atomic force microscopy (AFM) to image a MUC2-rich mucus fraction isolated from pig jejunum. In the freshly isolated mucin fraction, we find direct evidence for trigonally linked structures, and their assembly into lamellar networks with a distribution of pore sizes from 20 to 200 nm. The networks are two-dimensional, with little interaction between lamellae. The existence of persistent cross-links between individual mucin polypeptides is consistent with a non-self-interacting lamellar model for intestinal mucus structure, rather than a physically entangled polymer network. We only observe collapsed entangled structures in purified mucin that has been stored in nonphysiological conditions
Evidence for Height and Immune Function Trade-offs Among Preadolescents in a High Pathogen Population
Background
In an energy-limited environment, caloric investments in one characteristic should trade-off with investments in other characteristics. In high pathogen ecologies, biasing energy allocation towards immune function over growth would be predicted, given strong selective pressures against early-life mortality.
Methodology
In the present study, we use flow cytometry to examine trade-offs between adaptive immune function (T cell subsets, B cells), innate immune function (natural killer cells), adaptive to innate ratio and height-for-age z scores (HAZ) among young children (N = 344; aged 2 months–8 years) in the Bolivian Amazon, using maternal BMI and child weight-for-height z scores (WHZ) as proxies for energetic status.
Results
Markers of adaptive immune function negatively associate with child HAZ, a pattern most significant in preadolescents (3+ years). In children under three, maternal BMI appears to buffer immune and HAZ associations, while child energetic status (WHZ) moderates relationships in an unexpected direction: HAZ and immune associations are greater in preadolescents with higher WHZ. Children with low WHZ maintain similar levels of adaptive immune function, but are shorter compared to high WHZ peers.
Conclusions
Reduced investment in growth in favor of immunity may be necessary for survival in high pathogen contexts, even under energetic constraints. Further, genetic and environmental factors are important considerations for understanding variation in height within this population. These findings prompt consideration of whether there may be a threshold of investment into adaptive immunity required for survival in high pathogen environments, and thus question the universal relevance of height as a marker of health.
Lay Summary
Adaptive immune function is negatively associated with child height in this high pathogen environment. Further, low weight-for-height children are shorter but maintain similar immune levels. Findings question the relevance of height as a universal health marker, given that costs and benefits of height versus immunity may be calibrated to local ecology
The Relation Between Activity and Environment in Compact Groups of Galaxies
We present the results of the classification of spectral activity types for
193 galaxies from a new sample of 49 compact groups of galaxies in the southern
hemisphere (SCGs). This sample was selected in automated fashion from a
digitized galaxy catalogue, covering an area of ~5200 sq deg, around the South
Galactic Pole. It is complete up to m ~14.5 in b_j for the brightest galaxy of
the group.
The spectral analysis of the SCG galaxies confirms the results previously
obtained for a smaller sample of Hickson's compact groups (HCG). We confirm the
luminosity-activity and morphology-activity relations, as well as the
predominance of AGNs (41% of SCGs galaxies). We verified also that the number
of early-type non-emission-line galaxies increases with the number of members
in the group.
The SCGs contain more star-forming galaxies (SFGs) and less non-emission-line
galaxies than HCGs, which suggests that they probe a wider range of physical
properties. The SFGs are composed in majority of HII Nucleus Galaxies, which
have less intense star formation than starburst galaxies. The star formation
activity in SCGs is, consequently, remarkably low. The SFGs show also evidence
for nuclear activity. If these results are further confirmed, 70% of the
galaxies in SCGs would then have an active nucleus, making these systems
remarkably rich in AGNs. Curiously, however, this characteristic of CGs
generally excludes Seyfert 1 galaxies.(Abridged)Comment: 53 pages, Latex, 9 encapsulated postscript figures, Accepted for
publication in The Astronomical Journa
How Prosecutors and Defense Attorneys Differ in Their Use of Neuroscience Evidence
Much of the public debate surrounding the intersection of neuroscience and criminal law is based on assumptions about how prosecutors and defense attorneys differ in their use of neuroscience evidence. For example, according to some commentators, the defense’s use of neuroscience evidence will abdicate criminals of all responsibility for their offenses. In contrast, the prosecution’s use of that same evidence will unfairly punish the most vulnerable defendants as unfixable future dangers to society. This “double- edged sword” view of neuroscience evidence is important for flagging concerns about the law’s construction of criminal responsibility and punishment: it demonstrates that the same information about the defendant can either be mitigating or aggravating depending on who is raising it. Yet empirical assessments of legal decisions reveal a far more nuanced reality, showing that public beliefs about the impact of neuroscience on the criminal law can often be wrong. This Article takes an evidence-based and multidisciplinary approach to examining how courts respond to neuroscience evidence in capital cases when the defense presents it to argue that the defendant’s mental state at the time of the crime was below the given legal requisite due to some neurologic or cognitive deficiency
Sex Hormones Regulate Tenofovir-Diphosphate in Female Reproductive Tract Cells in Culture
The conflicting results of recent pre-exposure prophylaxis (PrEP) trials utilizing tenofovir (TFV) to prevent HIV infection in women led us to evaluate the accumulation of intracellular TFV-diphosphate (TFV-DP) in cells from the female reproductive tract (FRT) and whether sex hormones influence the presence of TFV-DP in these cells. Following incubation with TFV, isolated epithelial cells, fibroblasts, CD4+ T cells and CD14+ cells from the FRT as well as blood CD4+ T cells and monocyte-derived macrophages convert TFV to TFV-DP. Unexpectedly, we found that TFV-DP concentrations (fmol/million cells) vary significantly with the cell type analyzed and the site within the FRT. Epithelial cells had 5-fold higher TFV-DP concentrations than fibroblasts; endometrial epithelial cells had higher TFV-DP concentrations than cells from the ectocervix. Epithelial cells had 125-fold higher TFV-DP concentrations than FRT CD4+ T cells, which were comparable to that measured in peripheral blood CD4+ T cells. These findings suggest the existence of a TFV-DP gradient in the FRT where epithelial cells \u3e fibroblasts \u3e CD4+ T cells and macrophages. In other studies, estradiol increased TFV-DP concentrations in endometrial and endocervical/ectocervical epithelial cells, but had no effect on fibroblasts or CD4+ T cells from FRT tissues. In contrast, progesterone alone and in combination with estradiol decreased TFV-DP concentrations in FRT CD4+ T cells. Our results suggest that epithelial cells and fibroblasts are a repository of TFV-DP that is under hormonal control. These cells might act either as a sink to decrease TFV availability to CD4+ T cells and macrophages in the FRT, or upon conversion of TFV-DP to TFV increase TFV availability to HIV-target cells. In summary, these results indicate that intracellular TFV-DP varies with cell type and location in the FRT and demonstrate that estradiol and/or progesterone regulate the intracellular concentrations of TFV-DP in FRT epithelial cells and CD4+ T cells
A 4 Gyr M-dwarf Gyrochrone from CFHT/MegaPrime Monitoring of the Open Cluster M67
We present stellar rotation periods for late K- and early M-dwarf members of
the 4 Gyr old open cluster M67 as calibrators for gyrochronology and tests of
stellar spin-down models. Using Gaia EDR3 astrometry for cluster membership and
Pan-STARRS (PS1) photometry for binary identification, we build this set of
rotation periods from a campaign of monitoring M67 with the
Canada-France-Hawaii Telescope's MegaPrime wide field imager. We identify 1807
members of M67, of which 294 are candidate single members with significant
rotation period detections. Moreover, we fit a polynomial to the period versus
color-derived effective temperature sequence observed in our data. We find that
the rotation of very cool dwarfs can be explained by a simple solid-body
spin-down between 2.7 and 4 Gyr. We compare this rotational sequence to the
predictions of gyrochronological models and find that the best match is
Skumanich-like spin-down, P_rot \propto t^0.62, applied to the sequence of
Ruprecht 147. This suggests that, for spectral types K7-M0 with near-solar
metallicity, once a star resumes spinning down, a simple Skumanich-like is
sufficient to describe their rotation evolution, at least through the age of
M67. Additionally, for stars in the range M1-M3, our data show that spin-down
must have resumed prior to the age of M67, in conflict with predictions of the
latest spin-down models.Comment: 21 pages, 16 figures, Accepted for publication by Ap
Identifying alemtuzumab as an anti-myeloid cell antiangiogenic therapy for the treatment of ovarian cancer
<p>Abstract</p> <p>Background</p> <p>Murine studies suggest that myeloid cells such as vascular leukocytes (VLC) and Tie2<sup>+ </sup>monocytes play a critical role in tumor angiogenesis and vasculogenesis. Myeloid cells are a primary cause of resistance to anti-VEGF therapy. The elimination of these cells from the tumor microenvironment significantly restricts tumor growth in both spontaneous and xenograft murine tumor models. Thus animal studies indicate that myeloid cells are potential therapeutic targets for solid tumor therapy. Abundant VLC and Tie2<sup>+ </sup>monocytes have been reported in human cancer. Unfortunately, the importance of VLC in human cancer growth remains untested as there are no confirmed therapeutics to target human VLC.</p> <p>Methods</p> <p>We used FACS to analyze VLC in ovarian and non-ovarian tumors, and characterize the relationship of VLC and Tie2-monocytes. We performed qRT-PCR and FACS on human VLC to assess the expression of the CD52 antigen, the target of the immunotherapeutic Alemtuzumab. We assessed Alemtuzumab's ability to induce complement-mediated VLC killing in vitro and in human tumor ascites. Finally we assessed the impact of anti-CD52 immuno-toxin therapy on murine ovarian tumor growth.</p> <p>Results</p> <p>Human VLC are present in ovarian and non-ovarian tumors. The majority of VLC appear to be Tie2+ monocytes. VLC and Tie2+ monocytes express high levels of CD52, the target of the immunotherapeutic Alemtuzumab. Alemtuzumab potently induces complement-mediated lysis of VLC in vitro and ex-vivo in ovarian tumor ascites. Anti-CD52 immunotherapy targeting VLC restricts tumor angiogenesis and growth in murine ovarian cancer.</p> <p>Conclusion</p> <p>These studies confirm VLC/myeloid cells as therapeutic targets in ovarian cancer. Our data provide critical pre-clinical evidence supporting the use of Alemtuzumab in clinical trials to test its efficacy as an anti-myeloid cell antiangiogenic therapeutic in ovarian cancer. The identification of an FDA approved anti-VLC agent with a history of clinical use will allow immediate proof-of-principle clinical trials in patients with ovarian cancer.</p
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Quantifying particle size and turbulent scale dependence of dust uplift in the Sahara using aircraft measurements
The first size-resolved airborne measurements of dust fluxes and the first dust flux measurements from the central Sahara are presented and compared with a parameterization by Kok (2011a). High-frequency measurements of dust size distribution were obtained from 0.16 to 300 µm diameter, and eddy covariance fluxes were derived. This is more than an order of magnitude larger size range than previous flux estimates. Links to surface emission are provided by analysis of particle drift velocities. Number flux is described by a −2 power law between 1 and 144 µm diameter, significantly larger than the 12 µm upper limit suggested by Kok (2011a). For small particles, the deviation from a power law varies with terrain type and the large size cutoff is correlated with atmospheric vertical turbulent kinetic energy, suggesting control by vertical transport rather than emission processes. The measured mass flux mode is in the range 30–100 µm. The turbulent scales important for dust flux are from 0.1 km to 1–10 km. The upper scale increases during the morning as boundary layer depth and eddy size increase. All locations where large dust fluxes were measured had large topographical variations. These features are often linked with highly erodible surface features, such as wadis or dunes. We also hypothesize that upslope flow and flow separation over such features enhance the dust flux by transporting large particles out of the saltation layer. The tendency to locate surface flux measurements in open, flat terrain means these favored dust sources have been neglected in previous studies
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