101 research outputs found
Spectroscopy of P using the one-proton knockout reaction
The structure of P was studied with a one-proton knockout reaction
at88~MeV/u from a S projectile beam at NSCL. The rays from
thedepopulation of excited states in P were detected with GRETINA,
whilethe P nuclei were identified event-by-event in the focal plane of
theS800 spectrograph. The level scheme of P was deduced up to 7.5 MeV
using coincidences. The observed levels were attributed to
protonremovals from the -shell and also from the deeply-bound
orbital.The orbital angular momentum of each state was derived from the
comparisonbetween experimental and calculated shapes of individual
(-gated)parallel momentum distributions. Despite the use of different
reactions andtheir associate models, spectroscopic factors, , derived
from theS knockout reaction agree with those obtained earlier
fromS(,\nuc{3}{He}) transfer, if a reduction factor , as
deducedfrom inclusive one-nucleon removal cross sections, is applied to the
knockout transitions.In addition to the expected proton-hole configurations,
other states were observedwith individual cross sections of the order of
0.5~mb. Based on their shiftedparallel momentum distributions, their decay
modes to negative parity states,their high excitation energy (around 4.7~MeV)
and the fact that they were notobserved in the (,\nuc{3}{He}) reaction, we
propose that they may resultfrom a two-step mechanism or a nucleon-exchange
reaction with subsequent neutronevaporation. Regardless of the mechanism, that
could not yet be clarified, thesestates likely correspond to neutron core
excitations in \nuc{35}{P}. Thisnewly-identified pathway, although weak, offers
the possibility to selectivelypopulate certain intruder configurations that are
otherwise hard to produceand identify.Comment: 5 figures, 1 table, accepted for publication in Physical Review
Spectroscopy of Na: shell evolution toward the drip line
Excited states in Na have been studied using the -decay of
implanted Ne ions at GANIL/LISE as well as the in-beam -ray
spectroscopy at the NSCL/S800 facility. New states of positive
(J=3,4) and negative (J=1-5) parity are proposed. The
former arise from the coupling between 0d protons and a 0d
neutron, while the latter are due to couplings with 1p or 0f
neutrons. While the relative energies between the J=1-4 states are
well reproduced with the USDA interaction in the N=17 isotones, a progressive
shift in the ground state binding energy (by about 500 keV) is observed between
F and Al. This points to a possible change in the proton-neutron
0d-0d effective interaction when moving from stability to the
drip line. The presence of J=1-4 negative parity states around 1.5
MeV as well as of a candidate for a J=5 state around 2.5 MeV give
further support to the collapse of the N=20 gap and to the inversion between
the 0f and 1p levels below Z=12. These features are discussed
in the framework of Shell Model and EDF calculations, leading to predicted
negative parity states in the low energy spectra of the F and O
nuclei.Comment: Exp\'erience GANIL/LISE et NSCL/S80
Control of human adenovirus type 5 gene expression by cellular Daxx/ATRX chromatin-associated complexes
Death domain–associated protein (Daxx) cooperates with X-linked α-thalassaemia retardation syndrome protein (ATRX), a putative member of the sucrose non-fermentable 2 family of ATP-dependent chromatin-remodelling proteins, acting as the core ATPase subunit in this complex, whereas Daxx is the targeting factor, leading to histone deacetylase recruitment, H3.3 deposition and transcriptional repression of cellular promoters. Despite recent findings on the fundamental importance of chromatin modification in host-cell gene regulation, it remains unclear whether adenovirus type 5 (Ad5) transcription is regulated by cellular chromatin remodelling to allow efficient virus gene expression. Here, we focus on the repressive role of the Daxx/ATRX complex during Ad5 replication, which depends on intact protein–protein interaction, as negative regulation could be relieved with a Daxx mutant that is unable to interact with ATRX. To ensure efficient viral replication, Ad5 E1B-55K protein inhibits Daxx and targets ATRX for proteasomal degradation in cooperation with early region 4 open reading frame protein 6 and cellular components of a cullin-dependent E3-ubiquitin ligase. Our studies illustrate the importance and diversity of viral factors antagonizing Daxx/ATRX-mediated repression of viral gene expression and shed new light on the modulation of cellular chromatin remodelling factors by Ad5. We show for the first time that cellular Daxx/ATRX chromatin remodelling complexes play essential roles in Ad gene expression and illustrate the importance of early viral proteins to counteract cellular chromatin remodelling
Single-neutron orbits near Ni-78: Spectroscopy of the N=49 isotope Zn-79
5 pags., 6 figs.Single-neutron states in the , isotope 79Zn have been populated using the 78Zn(d, p)79Zn transfer reaction at REX-ISOLDE, CERN. The experimental setup allowed the combined detection of protons ejected in the reaction, and of γ rays emitted by 79Zn. The analysis reveals that the lowest excited states populated in the reaction lie at approximately 1 MeV of excitation, and involve neutron orbits above the shell gap. From the analysis of γ-ray data and of proton angular distributions, characteristic of the amount of angular momentum transferred, a configuration was assigned to a state at 983 keV. Comparison with large-scale-shell-model calculations supports a robust neutron shell-closure for 78Ni. These data constitute an important step towards the understanding of the magicity of 78Ni and of the structure of nuclei in the region.This work was supported by the European Commission through the Marie Curie Actions Contracts Nos. PIEFGA-2011-30096 (R.O.) and PIEFGA-2008-219175 (J.P.), by the Spanish Ministerio de Ciencia e Innovación under contracts FPA2009-13377-C02 and FPA2011-29854-C04, by the Spanish MEC Consolider – Ingenio 2010, Project No. CDS2007-00042 (CPAN), by FWO-Vlaanderen (Belgium), by GOA/2010/010 (BOF KU Leuven), by the Interuniversity Attraction Poles Programme initiated by the Belgian Science Policy Office (BriX network P7/12), by the European Union Seventh Framework Programme through ENSAR, contract no. RII3-CT-2010-262010, and by the German BMBF under contracts 05P09PKCI5, 05P12PKFNE, 05P12RDCIA and 06DA9036I. R.O., R.C., J.F.W.L., V.L. and J.F.S. also acknowledge support from STFC, Grant Nos. PP/F000944/1, ST/F007590/1, and ST/J000183/2
Study of the deformation-driving vd5/2 orbital in 6728Ni39 using one-neutron transfer reactions
Abstract The ν g 9 / 2 , d 5 / 2 , s 1 / 2 orbitals are assumed to be responsible for the swift onset of collectivity observed in the region below 68Ni. Especially the single-particle energies and strengths of these orbitals are of importance. We studied such properties in the nearby 67Ni nucleus, by performing a ( d , p ) -experiment in inverse kinematics employing a post-accelerated radioactive ion beam (RIB) at the REX-ISOLDE facility. The experiment was performed at an energy of 2.95 MeV/u using a combination of the T-REX particle detectors, the Miniball γ-detection array and a newly-developed delayed-correlation technique as to investigate μs-isomers. Angular distributions of the ground state and multiple excited states in 67Ni were obtained and compared with DWBA cross-section calculations, leading to the identification of positive-parity states with substantial ν g 9 / 2 (1007 keV) and ν d 5 / 2 (2207 keV and 3277 keV) single-particle strengths up to an excitation energy of 5.8 MeV. 50% of the ν d 5 / 2 single-particle strength relative to the ν g 9 / 2 -orbital is concentrated in and shared between the first two observed 5 / 2 + levels. A comparison with extended Shell Model calculations and equivalent (3He, d) studies in the region around 9040Zr50 highlights similarities for the strength of the negative-parity pf and positive-parity g 9 / 2 state, but differences are observed for the d 5 / 2 single-particle strength
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation
Purpose
By incorporating major developments in genetics, ophthalmology, dermatology, and neuroimaging, to revise the diagnostic criteria for neurofibromatosis type 1 (NF1) and to establish diagnostic criteria for Legius syndrome (LGSS).
Methods
We used a multistep process, beginning with a Delphi method involving global experts and subsequently involving non-NF experts, patients, and foundations/patient advocacy groups.
Results
We reached consensus on the minimal clinical and genetic criteria for diagnosing and differentiating NF1 and LGSS, which have phenotypic overlap in young patients with pigmentary findings. Criteria for the mosaic forms of these conditions are also recommended.
Conclusion
The revised criteria for NF1 incorporate new clinical features and genetic testing, whereas the criteria for LGSS were created to differentiate the two conditions. It is likely that continued refinement of these new criteria will be necessary as investigators (1) study the diagnostic properties of the revised criteria, (2) reconsider criteria not included in this process, and (3) identify new clinical and other features of these conditions. For this reason, we propose an initiative to update periodically the diagnostic criteria for NF1 and LGSS
Nurses' perceptions of aids and obstacles to the provision of optimal end of life care in ICU
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