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Träfflista för sökning "WFRF:(Wan P) "

Sökning: WFRF:(Wan P)

  • Resultat 221-230 av 257
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221.
  • McBrien, Owen R., et al. (författare)
  • SN2018kzr : A Rapidly Declining Transient from the Destruction of a White Dwarf
  • 2019
  • Ingår i: Astrophysical Journal Letters. - : American Astronomical Society. - 2041-8205 .- 2041-8213. ; 885:1
  • Tidskriftsartikel (refereegranskat)abstract
    • We present SN2018kzr, the fastest declining supernova-like transient, second only to the kilonova, AT2017gfo. SN2018kzr is characterized by a peak magnitude of M-r & xfffd;=& xfffd;?17.98, a peak bolometric luminosity of ?1.4 & xfffd;& x5e0;10(43) erg s(?1), and a rapid decline rate of 0.48 & xfffd;& xfffd;0.03 mag day(?1) in the r band. The bolometric luminosity evolves too quickly to be explained by pure Ni-56 heating, necessitating the inclusion of an alternative powering source. Incorporating the spin-down of a magnetized neutron star adequately describes the lightcurve and we estimate a small ejecta mass of M-ej & xfffd;=& xfffd;0.10 & xfffd;& xfffd;0.05 M. Our spectral modeling suggests the ejecta is composed of intermediate mass elements including O, Si, and Mg and trace amounts of Fe-peak elements, which disfavors a binary neutron star merger. We discuss three explosion scenarios for SN2018kzr, given the low ejecta mass, intermediate mass element composition, and high likelihood of additional powering?the core collapse of an ultra-stripped progenitor, the accretion induced collapse (AIC) of a white dwarf, and the merger of a white dwarf and neutron star. The requirement for an alternative input energy source favors either the AIC with magnetar powering or a white dwarf?neutron star merger with energy from disk wind shocks.
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222.
  • Meister, Mikael, 1969, et al. (författare)
  • High-energy breakup of 8B
  • 2003
  • Ingår i: Nucl. Phys. A. ; 718, s. 431-433
  • Konferensbidrag (refereegranskat)
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223.
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224.
  • Osborn, D. P. S., et al. (författare)
  • Autosomal recessive cardiomyopathy and sudden cardiac death associated with variants in MYL3
  • 2021
  • Ingår i: Genetics in Medicine. - : Elsevier BV. - 1098-3600 .- 1530-0366. ; 23:4, s. 787-792
  • Tidskriftsartikel (refereegranskat)abstract
    • Purpose Variants in genes encoding sarcomeric proteins are the most common cause of inherited cardiomyopathies. However, the underlying genetic cause remains unknown in many cases. We used exome sequencing to reveal the genetic etiology in patients with recessive familial cardiomyopathy. Methods Exome sequencing was carried out in three consanguineous families. Functional assessment of the variants was performed. Results Affected individuals presented with hypertrophic or dilated cardiomyopathy of variable severity from infantile- to early adulthood-onset and sudden cardiac death. We identified a homozygous missense substitution (c.170C>A, p.[Ala57Asp]), a homozygous translation stop codon variant (c.106G>T, p.[Glu36Ter]), and a presumable homozygous essential splice acceptor variant (c.482-1G>A, predicted to result in skipping of exon 5). Morpholino knockdown of the MYL3 orthologue in zebrafish, cmlc1, resulted in compromised cardiac function, which could not be rescued by reintroduction of MYL3 carrying either the nonsense c.106G>T or the missense c.170C>A variants. Minigene assay of the c.482-1G>A variant indicated a splicing defect likely resulting in disruption of the EF-hand Ca2+ binding domains. Conclusions Our data demonstrate that homozygous MYL3 loss-of-function variants can cause of recessive cardiomyopathy and occurrence of sudden cardiac death, most likely due to impaired or loss of myosin essential light chain function.
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225.
  • Parrag, Eleonora, et al. (författare)
  • SN 2019hcc : a Type II supernova displaying early Oɪɪ lines
  • 2021
  • Ingår i: Monthly notices of the Royal Astronomical Society. - : Oxford University Press (OUP). - 0035-8711 .- 1365-2966. ; 506:4, s. 4819-4840
  • Tidskriftsartikel (refereegranskat)abstract
    • We present optical spectroscopy together with ultraviolet, optical, and near-infrared photometry of SN 2019hcc, which resides in a host galaxy at redshift 0.044, displaying a sub-solar metallicity. The supernova spectrum near peak epoch shows a ‘w’ shape at around 4000 Å which is usually associated with O II lines and is typical of Type I superluminous supernovae. SN 2019hcc post-peak spectra show a well-developed H α P-Cygni profile from 19 d past maximum and its light curve, in terms of its absolute peak luminosity and evolution, resembles that of a fast-declining Hydrogen-rich supernova (SN IIL). The object does not show any unambiguous sign of interaction as there is no evidence of narrow lines in the spectra or undulations in the light curve. Our TARDIS spectral modelling of the first spectrum shows that carbon, nitrogen, and oxygen (CNO) at 19 000 K reproduce the ‘w’ shape and suggests that a combination of non-thermally excited CNO and metal lines at 8000 K could reproduce the feature seen at 4000 Å. The Bolometric light-curve modelling reveals that SN 2019hcc could be fit with a magnetar model, showing a relatively strong magnetic field (B > 3 × 1014 G), which matches the peak luminosity and rise time without powering up the light curve to superluminous luminosities. The high-energy photons produced by the magnetar would then be responsible for the detected Oɪɪ lines. As a consequence, SN 2019hcc shows that a ‘w’ shape profile at around 4000 Å, usually attributed to O II, is not only shown in superluminous supernovae and hence it should not be treated as the sole evidence of the belonging to such a supernova type. 
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226.
  • Pu, X., et al. (författare)
  • A wireless 8-channel ECG biopotential acquisition system for dry electrodes
  • 2012
  • Ingår i: Proceedings of the 2012 IEEE International Symposium on Radio-Frequency Integration Technology. - Singapore : IEEE Press. - 9781467323048 ; , s. 140-142
  • Konferensbidrag (refereegranskat)abstract
    • A wireless 8-channel biopotential acquisition system for capturing electrocardiogram (ECG) using dry electrodes is presented. The ECG system consists of copper electrodes, a micropowered 8-channel custom ASIC, and an off-the-shelf microprocessor and bluetooth radio. Each analog channel of the custom ECG front-end is composed of a chopper-modulated instrumentation amplifier (CMIA) with chopping spike filter (CSF), a programmable gain amplifier (PGA), and a output buffer. Implemented in standard a 0.35 μm CMOS technology, the ECG front-end consumes 101 μA from a 2.7 V supply, occupying 5 mm2 of chip area. Measurement results show an input impedance of 1 G Ω, an input-referred noise of 0.97 μVrms (0.5 ∼ 100 Hz), and a CMRR of 114 dB. Finally, a complete wireless 8-channel ECG monitoring system incorporating this analog front-end is demonstrated, showing successful recordings of a capture ECG waveform using a smart phone.
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229.
  • Rogers, Simon N., et al. (författare)
  • Variations in concerns reported on the patient concerns inventory in patients with head and neck cancer from different health settings across the world
  • 2020
  • Ingår i: Head and Neck. - : Wiley. - 1043-3074 .- 1097-0347. ; 42:3, s. 498-512
  • Tidskriftsartikel (refereegranskat)abstract
    • Background The aim was to collate and contrast patient concerns from a range of different head and neck cancer follow-up clinics around the world. Also, we sought to explore the relationship, if any, between responses to the patient concerns inventory (PCI) and overall quality of life (QOL). Methods Nineteen units participated with intention of including 100 patients per site as close to a consecutive series as possible in order to minimize selection bias. Results There were 2136 patients with a median total number of PCI items selected of 5 (2-10). "Fear of the cancer returning" (39%) and "dry mouth" (37%) were most common. Twenty-five percent (524) reported less than good QOL. Conclusion There was considerable variation between units in the number of items selected and in overall QOL, even after allowing for case-mix variables. There was a strong progressive association between the number of PCI items and QOL.
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230.
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