934 research outputs found
Narratives of Expert Speech-Language Pathologists: Defining Clinical Expertise and Supporting Knowledge Transfer
Clinical expertise is a component of evidence-based practice; however, relatively little attention has been paid to this phenomenon in the professional literature of speech-language pathology. This may have negative impacts on the training of pre-professional and novice speech-language pathologists. The purpose of this study was to examine professional narratives of expert Speech-Language Pathologists (SLPs) to consider applications for knowledge transfer between expert clinicians and novice clinicians. Collection of the professional narratives of 10 expert SLPs were obtained through in-depth interviews. Interviews were transcribed and coded for themes. Themes that impacted expertise in SLP included: training; work sites; individual and clinician traits; a holistic versus disorder-specific view; technical excellence; acknowledgment of and reflection upon mistakes; professional networking; peer and patient recognition; and, embracing the creative. Within the narratives, implications toward knowledge transfer for novice clinicians were evident. Narratives of expert SLPs may facilitate knowledge transfer of clinical expertise. Of the nine themes identified, seven were consistent with previous literature, and two were not. The themes provide an opportunity for further research and development, largely concerning knowledge transfer in clinical education
Regulation of trophoblast beta1-integrin expression by contact with endothelial cells
BACKGROUND: In human and non-human primates, migratory trophoblasts penetrate the uterine epithelium, invade uterine matrix, and enter the uterine vasculature. Invasive trophoblasts show increased expression of β1 integrin. Since trophoblast migration within the uterine vasculature involves trophoblast attachment to endothelial cells lining the vessel walls, this raises the possibility that cell-cell contact and/or factors released by endothelial cells could regulate trophoblast integrin expression. To test this, we used an in vitro system consisting of early gestation macaque trophoblasts co-cultured on top of uterine microvascular endothelial cells. RESULTS: When cultured alone, trophoblasts expressed low levels of β1 integrin as determined by quantitative immunofluorescence microscopy. When trophoblasts were cultured on top of endothelial cells for 24 h, the expression of trophoblast β1 integrin was significantly increased as determined by image analysis. β1 Integrin expression was not increased when trophoblasts were cultured with endothelial cell-conditioned medium, suggesting that upregulation requires direct contact between trophoblasts and endothelial cells. To identify endothelial cell surface molecules responsible for induction of trophoblast integrin expression, trophoblasts were cultured in dishes coated with recombinant platelet endothelial cell adhesion molecule-1 (PECAM-1), intercellular adhesion molecule-1 (ICAM-1), or αVβ3 integrin. Trophoblast β1 integrin expression (assessed by immunofluorescence microscopy and Western blotting) was increased when PECAM-1 or αVβ3 integrin, but not ICAM-1, was used as substrate. CONCLUSIONS: Direct contact between trophoblasts and endothelial cells increases the expression of trophoblast β1 integrin
Distribution of plasma folate forms in hemodialysis patients receiving high daily doses of l-folinic or folic acid
Distribution of plasma folate forms in hemodialysis patients receiving high daily doses of l-folinic or folic acid.BackgroundWe have previously reported that a daily oral high dose of l-folinic acid for the treatment of hyperhomocysteinemia in hemodialysis patients does not provide significantly greater reduction in fasting total homocysteine (tHcy) levels than an equimolar dose of folic acid. The present study uses the affinity/HPLC method to analyze the distribution of plasma folate forms in patients who received l-folinic acid versus those who received folic acid. This was done to investigate claims that renal insufficiency is associated with impaired folate interconversion, a stance that is supportive of the premise that tHcy lowering in these patients is more efficacious with folinic acid and other reduced folates, than folic acid.MethodsForty-eight chronic and stable hemodialysis patients were block-randomized, based on their screening predialysis tHcy levels, sex, and dialysis center, into two groups treated for 12 weeks with oral folic acid at 15 mg/day or an equimolar amount (20 mg/day) of oral l-folinic acid. All 48 subjects also received 50 mg/day of oral vitamin B6 and 1 mg/day of oral vitamin B12. Folate distribution was determined in plasma of 46 participants (Folinic acid group, N = 22; Folic acid group, N = 24) by using the affinity/HPLC method, with electrochemical (coulometric) detection.ResultsBoth groups had similar baseline geometric means of plasma total folate and similar folate forms distribution. Following treatment, both groups demonstrated similar marked elevation in plasma total folate (geometric mean of the increase: Folinic acid group, +337 ng/mL; Folic acid group, +312 ng/mL; P = 0.796). In the folinic acid-treated group, practically all of the increase in total folate was due to 5-methyltetrahydrofolate. In the folic acid-treated group 5-methyltetrahydrofolate accounted for 35% of the increase in total folate and the remainder was unmethylated folic acid.ConclusionsData from the present findings suggest that defects in folate absorption or impairment in folate interconversion are not the cause of the persistent hyperhomocysteinemia in hemodialysis patients
Nicotinamide mononucleotide supplementation reverses vascular dysfunction and oxidative stress with aging in mice
We tested the hypothesis that supplementation of nicotinamide mononucleotide (NMN), a key NAD (+) intermediate, increases arterial SIRT1 activity and reverses age‐associated arterial dysfunction and oxidative stress. Old control mice (OC) had impaired carotid artery endothelium‐dependent dilation (EDD) (60 ± 5% vs. 84 ± 2%), a measure of endothelial function, and nitric oxide (NO)‐mediated EDD (37 ± 4% vs. 66 ± 6%), compared with young mice (YC). This age‐associated impairment in EDD was restored in OC by the superoxide ([Formula: see text]) scavenger TEMPOL (82 ± 7%). OC also had increased aortic pulse wave velocity (aPWV, 464 ± 31 cm s(−1) vs. 337 ± 3 cm s(−1)) and elastic modulus (EM, 6407 ± 876 kPa vs. 3119 ± 471 kPa), measures of large elastic artery stiffness, compared with YC. OC had greater aortic [Formula: see text] production (2.0 ± 0.1 vs. 1.0 ± 0.1 AU), nitrotyrosine abundance (a marker of oxidative stress), and collagen‐I, and reduced elastin and vascular SIRT1 activity, measured by the acetylation status of the p65 subunit of NFκB, compared with YC. Supplementation with NMN in old mice restored EDD (86 ± 2%) and NO‐mediated EDD (61 ± 5%), reduced aPWV (359 ± 14 cm s(−1)) and EM (3694 ± 315 kPa), normalized [Formula: see text] production (0.9 ± 0.1 AU), decreased nitrotyrosine, reversed collagen‐I, increased elastin, and restored vascular SIRT1 activity. Acute NMN incubation in isolated aortas increased NAD (+) threefold and manganese superoxide dismutase (MnSOD) by 50%. NMN supplementation may represent a novel therapy to restore SIRT1 activity and reverse age‐related arterial dysfunction by decreasing oxidative stress
Kepler Observations of Transiting Hot Compact Objects
Kepler photometry has revealed two unusual transiting companions orbiting an
early A-star and a late B-star. In both cases the occultation of the companion
is deeper than the transit. The occultation and transit with follow-up optical
spectroscopy reveal a 9400 K early A-star, KOI-74 (KIC 6889235), with a
companion in a 5.2 day orbit with a radius of 0.08 Rsun and a 10000 K late
B-star KOI-81 (KIC 8823868) that has a companion in a 24 day orbit with a
radius of 0.2 Rsun. We infer a temperature of 12250 K for KOI-74b and 13500 K
for KOI-81b.
We present 43 days of high duty cycle, 30 minute cadence photometry, with
models demonstrating the intriguing properties of these object, and speculate
on their nature.Comment: 12 pages, 3 figures, submitted to ApJL (updated to correct KOI74
lightcurve
Transit Timing Observations from Kepler: VI. Potentially interesting candidate systems from Fourier-based statistical tests
We analyze the deviations of transit times from a linear ephemeris for the
Kepler Objects of Interest (KOI) through Quarter six (Q6) of science data. We
conduct two statistical tests for all KOIs and a related statistical test for
all pairs of KOIs in multi-transiting systems. These tests identify several
systems which show potentially interesting transit timing variations (TTVs).
Strong TTV systems have been valuable for the confirmation of planets and their
mass measurements. Many of the systems identified in this study should prove
fruitful for detailed TTV studies.Comment: 32 pages, 6 of text and one long table, Accepted to Ap
Recommended from our members
Kepler-4B: A Hot Neptune-Like Planet of A G0 Star Near Main-Sequence Turnoff
Early time-series photometry from NASA's Kepler spacecraft has revealed a planet transiting the star we term Kepler-4, at R.A. = 19(h)02(m)27.(s)68, delta = +50 degrees 08'08 '' 7. The planet has an orbital period of 3.213 days and shows transits with a relative depth of 0.87 x 10(-3) and a duration of about 3.95 hr. Radial velocity (RV) measurements from the Keck High Resolution Echelle Spectrometer show a reflex Doppler signal of 9.3(-1.9)(+1.1) m s(-1), consistent with a low-eccentricity orbit with the phase expected from the transits. Various tests show no evidence for any companion star near enough to affect the light curve or the RVs for this system. From a transit-based estimate of the host star's mean density, combined with analysis of high-resolution spectra, we infer that the host star is near turnoff from the main sequence, with estimated mass and radius of 1.223(-0.091)(+0.053) M(circle dot) and 1.487(-0.084)(+0.071) R(circle dot).We estimate the planet mass and radius to be {M(P), R(P)} = {24.5 +/- 3.8 M(circle plus), 3.99 +/- 0.21 R(circle plus)}. The planet's density is near 1.9 g cm(-3); it is thus slightly denser and more massive than Neptune, but about the same size.W. M. Keck FoundationNASA's Science Mission DirectorateAstronom
Terrestrial Planet Occurrence Rates for the Kepler GK Dwarf Sample
We measure planet occurrence rates using the planet candidates discovered by
the Q1-Q16 Kepler pipeline search. This study examines planet occurrence rates
for the Kepler GK dwarf target sample for planet radii, 0.75<Rp<2.5 Rearth, and
orbital periods, 50<Porb<300 days, with an emphasis on a thorough exploration
and identification of the most important sources of systematic uncertainties.
Integrating over this parameter space, we measure an occurrence rate of F=0.77
planets per star, with an allowed range of 0.3<F<1.9. The allowed range takes
into account both statistical and systematic uncertainties, and values of F
beyond the allowed range are significantly in disagreement with our analysis.
We generally find higher planet occurrence rates and a steeper increase in
planet occurrence rates towards small planets than previous studies of the
Kepler GK dwarf sample. Through extrapolation, we find that the one year
orbital period terrestrial planet occurrence rate, zeta_1=0.1, with an allowed
range of 0.01<zeta_1<2, where zeta_1 is defined as the number of planets per
star within 20% of the Rp and Porb of Earth. For G dwarf hosts, the zeta_1
parameter space is a subset of the larger eta_earth parameter space, thus
zeta_1 places a lower limit on eta_earth for G dwarf hosts. From our analysis,
we identify the leading sources of systematics impacting Kepler occurrence rate
determinations as: reliability of the planet candidate sample, planet radii,
pipeline completeness, and stellar parameters.Comment: 19 Pages, 17 Figures, Submitted ApJ. Python source to support Kepler
pipeline completeness estimates available at
http://github.com/christopherburke/KeplerPORTs
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