9 research outputs found
Surface-enhanced pair transfer in quadrupole states of neutron-rich Sn isotopes
We investigate the neutron pair transfer modes associated with the low-lying
quadrupole states in neutron-rich Sn isotopes by means of the quasiparticle
random phase approximation based on the Skyrme-Hartree-Fock-Bogoliubov mean
field model. The transition strength of the quadrupole pair-addition mode
feeding the state is enhanced in the Sn isotopes with . The
transition density of the pair-addition mode has a large spatial extension in
the exterior of nucleus, reaching far to fm. The quadrupole
pair-addition mode reflects sensitively a possible increase of the effective
pairing interaction strength in the surface and exterior regions of
neutron-rich nuclei.Comment: 14 page
Di-neutron correlation and soft dipole excitation in medium mass neutron-rich nuclei near drip-line
The neutron pairing correlation and the soft dipole excitation in medium-mass
nuclei near drip-line are investigated from a viewpoint of the di-neutron
correlation. Numerical analyses by means of the coordinate-space HFB and the
continuum QRPA methods are performed for even-even O, Ca
and Ni. A clear signature of the di-neutron correlation is found in
the HFB ground state; two neutrons are correlated at short relative distances
\lesim 2 fm with large probability . The soft dipole excitation is
influenced strongly by the neutron pairing correlation, and it accompanies a
large transition density for pair motion of neutrons. This behavior originates
from a coherent superposition of two-quasiparticle configurations consisting of continuum states with high orbital angular momenta
reaching an order of . It raises a picture that the soft dipole
excitation under the influence of neutron pairing is characterized by motion of
di-neutron in the nuclear exterior against the remaining subsystem.
Sensitivity to the density dependence of effective pair force is discussed.Comment: 35 pages, 22 figure
Di-neutron correlation in soft octupole excitations of neutron-rich Ni isotopes beyond N=50
We investigate low-lying octupole response of neutron-rich Ni isotopes beyond
the N=50 shell closure using the Skyrme-Hartree-Fock-Bogoliubov mean-fields and
the continuum quasi-particle random phase approximation. Performing detailed
numerical analyses employing the Skyrme parameter set SLy4 and a
density-dependent delta interaction of the mixed type, we show that a neutron
mode emerges above the neutron separation energy as a consequence of the weak
binding of neutrons and it exhibits strong influences of the di-neutron
correlation
Immunemodulatory Effects of 5-Azacitidin Through Expansion of Functional Regulatory T Cells on Paraneoplastic Inflammation Associated With Myelodysplastic Syndromes: A Case Report
Myelodysplastic syndrome (MDS) is a heterogeneous group of clonal disorders of hematopoietic stem cells, characterized by dysplastic hematopoiesis and dysregulated immune system resulting in various clinical conditions. Paraneoplastic inflammatory syndromes, which are well known to be associated with MDS, show response to immune-modulated therapy and often disappear during the course of hematologic management. Azacitidine (5-Aza) was shown to prolong survival of high-risk MDS patients, however, the effects of 5-Aza on paraneoplastic inflammation in MDS have yet to be elucidated. 5-Aza was administered to a 60-year-old man with MDS accompanying Sweet’s syndrome at a dose of 75 mg/m2/daily subcutaneously for 7 days every 28 days. 5-Aza was not only effective in controlling systemic symptoms caused by paraneoplastic inflammation, but hematologic improvements were also observed after four cycles of the 5-Aza treatment. Immune profiling in peripheral blood before and after 5-Aza treatment revealed that the effector and naive regulatory T cells in lymphocytes drastically increased after the 5-Aza treatment, i.e., 5-Aza might induce a shift in lymphocytic populations toward immunosuppression in this patient. Our results raised the immune-mediated effect of 5-Aza on both dysplastic hematopoiesis and paraneoplastic inflammation in myelodyplastic syndromes