444 research outputs found
Magnetization reversal in Kagome artificial spin ice studied by first-order reversal curves
Magnetization reversal of interconnected Kagome artificial spin ice was
studied by the first-order reversal curve (FORC) technique based on the
magneto-optical Kerr effect and magnetoresistance measurements. The
magnetization reversal exhibits a distinct six-fold symmetry with the external
field orientation. When the field is parallel to one of the nano-bar branches,
the domain nucleation/propagation and annihilation processes sensitively depend
on the field cycling history and the maximum field applied. When the field is
nearly perpendicular to one of the branches, the FORC measurement reveals the
magnetic interaction between the Dirac strings and orthogonal branches during
the magnetization reversal process. Our results demonstrate that the FORC
approach provides a comprehensive framework for understanding the magnetic
interaction in the magnetization reversal processes of spin-frustrated systems
Recommended from our members
Plasma Apolipoprotein B-48, Hepatic Apolipoprotein B mRNA Editing and Apolipoprotein B mRNA Editing Catalytic Subunit-1 mRNA Levels Are Altered in Zinc-Deficient Rats
Apolipoprotein B (apoB) exists as two major isoforms and serves as an obligatory component of lipid-rich plasma lipoprotein particles. Apolipoprotein B mRNA editing is a zinc-dependent, site-specific cytidine deamination that determines whether the apoB-100 or apoB-48 isoform is synthesized. The objective of this work was to examine whether dietary zinc levels affect apoB mRNA editing in vivo. Adult male Sprague-Dawley rats were randomly assigned to zinc-deficient (ZD, Ͻ0.5 mg Zn/kg diet), zinc-adequate (ZA, 30 mg Zn/kg diet) or zincreplenished (ZDA, ZD rats fed the ZA diet for last 2 d) dietary groups for 18 d. The ratio of plasma apolipoprotein B-48 (apoB-48) to total apoB was significantly lower in zinc-deficient compared with zinc-adequate rats. Primer extension analysis indicated a modest but significant reduction in hepatic apoB mRNA editing in ZD rats compared with that of the ZA group. In ZDA rats, hepatic apoB mRNA editing and the percentage of plasma apoB-48 to total apoB were not different from ZA rats. The mRNA abundance of hepatic apobec-1 (apoB mRNA editing catalytic subunit 1) was significantly lower in ZD and ZDA rats than in ZA rats. In summary, the plasma ratio of apoB-48 to total apoB protein as well as hepatic apoB mRNA editing and hepatic apobec-1 mRNA levels were reduced in rats consuming a zinc-deficient diet. These data suggest that one or more components of apoB metabolism may be influenced by dietary zinc status. J. Nutr. 129: 1855–1861, 1999
Recommended from our members
Regulation of Intestinal Apolipoprotein B mRNA Editing Levels by a Zinc-Deficient Diet and cDNA Cloning of Editing Protein in Hamsters
This study was conducted to investigate the influence of dietary zinc on intestinal apoB mRNA editing in hamsters. Apolipoprotein B-48 (apoB-48) is synthesized from the same gene as apoB-100 by a post-transcriptional, site-specific cytidine deamination, a process known as apoB mRNA editing. A cDNA encoding the hamster apoB mRNA editing enzyme was obtained by reverse transcriptase-polymerase chain reaction (RT-PCR) and the deduced amino acid sequence was found to possess high amino acid sequence identity to apoB mRNA editing enzymes from several other species. Editing activity was detected in the small intestine and colon but, like humans, none was detected in the liver. Analysis by RT-PCR indicated that the small intestine possessed the highest expression of editing enzyme mRNA abundance, whereas both liver and small intestine expressed relatively high levels of apoB mRNA. The influence of dietary zinc on intestinal apoB mRNA editing levels was examined in Golden Syrian hamsters (7 wk old) assigned to one of the following three dietary treatments: Zn-adequate (ZA, 30 mg Zn/kg diet), Zn-deficient (ZD, Ͻ0.5 mg Zn/kg diet), or Zn-replenished (ZDA, ZD hamsters receiving ZA diet for last 2 d) for 7 wk. Hamsters consuming the ZD diet had modestly but significantly lower intestinal editing activity than ZA hamsters. Intestinal editing activity in the ZDA group was not different from that of ZA hamsters. Data derived from these studies contribute to the understanding of lipoprotein metabolism in hamsters, a suitable model for the study of atherosclerosis. J. Nutr. 130: 2166 –2173, 2000
Identification and characterization of a novel nasopharyngeal carcinoma-associated peptide: NAP-1
Nasopharyngeal carcinoma (NPC) is one of the most commons cancers in Southeast Asia and Southern China. Several NPC-associated genes have been so far described and here we describe the identification and the characterization of a novel nasopharyngeal carcinoma-associated peptide: NAP-1. NAP-1 was identified with the human genome draft searching method combined with nested PCR mapping of the chromosome 4q13 region. NAP-1 encodes an 85 amino acid alkaline peptide with a calculated isoelectric point of 9.3, three phosphorilation sites and a proline-rich region. Northern blot analysis revealed that NAP-1 is expressed as a 0.6 kb transcript in normal lymph nodes and trachea. In addition, reverse transcription (RT)-PCR showed that NAP-1 is expressed not only in NPC but in normal nasopharynx (NP) and various other tumors and tissues of the head and neck including: tonsils, lymph nodes, carcinoma of the tonsil, T cell lymphomas, squamous cell carcinoma of the hard palate, papilloma of the nasopharynx, nasopharyngitis, lymphoma of the tongue root and follicular dendritic cells (FDC). In addition, NAP-1 is not expressed in normal tissues or tumors from other anatomical regions and was not expressed by NPC cell lines. Surprisingly, differential RT-PCR demonstrated decreased expression of NAP-1 in NPC compared with paired NP biopsies in 42.5 % of cases (17 out of 40). In addition, in situ hybridization and immunohistochemistry demonstrated that NAP-1 is expressed by S100(+) CD35(+) FDCs of the germinal center and not in other normal immune cells infiltrating NP or NPC. Therefore, it is likely that NAP-1 is secreted by FDC in the NP and may play an immune modulatory role in NPC
Study of and
The decays and have been
investigated with a sample of 225.2 million events collected with the
BESIII detector at the BEPCII collider. The branching fractions are
determined to be and . Distributions of the angle
between the proton or anti-neutron and the beam direction are well
described by the form , and we find
for and
for . Our branching-fraction
results suggest a large phase angle between the strong and electromagnetic
amplitudes describing the decay.Comment: 16 pages, 13 figures, the 2nd version, submitted to PR
First observation of the M1 transition
Using a sample of 106 million \psi(3686) events collected with the BESIII
detector at the BEPCII storage ring, we have made the first measurement of the
M1 transition between the radially excited charmonium S-wave spin-triplet and
the radially excited S-wave spin-singlet states: \psi(3686)\to\gamma\eta_c(2S).
Analyses of the processes \psi(2S)\to \gamma\eta_c(2S) with \eta_c(2S)\to
\K_S^0 K\pi and K^+K^-\pi^0 gave an \eta_c(2S) signal with a statistical
significance of greater than 10 standard deviations under a wide range of
assumptions about the signal and background properties. The data are used to
obtain measurements of the \eta_c(2S) mass (M(\eta_c(2S))=3637.6\pm
2.9_\mathrm{stat}\pm 1.6_\mathrm{sys} MeV/c^2), width
(\Gamma(\eta_c(2S))=16.9\pm 6.4_\mathrm{stat}\pm 4.8_\mathrm{sys} MeV), and the
product branching fraction (\BR(\psi(3686)\to \gamma\eta_c(2S))\times
\BR(\eta_c(2S)\to K\bar K\pi) = (1.30\pm 0.20_\mathrm{stat}\pm
0.30_\mathrm{sys})\times 10^{-5}). Combining our result with a BaBar
measurement of \BR(\eta_c(2S)\to K\bar K \pi), we find the branching fraction
of the M1 transition to be \BR(\psi(3686)\to\gamma\eta_c(2S)) = (6.8\pm
1.1_\mathrm{stat}\pm 4.5_\mathrm{sys})\times 10^{-4}.Comment: 7 pages, 1 figure, 1 tabl
Search for the Lepton Flavor Violation Process at BESIII
We search for the lepton-flavor-violating decay of the into an
electron and a muon using events
collected with the BESIII detector at the BEPCII collider. Four candidate
events are found in the signal region, consistent with background expectations.
An upper limit on the branching fraction of (90% C.L.) is obtained
Search for Baryonic Decays of \psi(3770) and \psi(4040)
By analyzing data samples of 2.9 fb^{-1} collected at \sqrt s=3.773 GeV, 482
pb^{-1} collected at \sqrt s=4.009 GeV and 67 pb^{-1} collected at \sqrt
s=3.542, 3.554, 3.561, 3.600 and 3.650 GeV with the BESIII detector at the
BEPCII storage ring, we search for \psi(3770) and \psi(4040) decay to baryonic
final states, including \Lambda\bar\Lambda\pi^+\pi^-, \Lambda \bar\Lambda\pi^0,
\Lambda\bar\Lambda\eta, \Sigma^+ \bar\Sigma^-, \Sigma^0 \bar\Sigma^0,
\Xi^-\bar\Xi^+ and \Xi^0\bar\Xi^0 decays. None are observed, and upper limits
are set at the 90% confidence level.Comment: 9 pages, 3 figure
Two-photon widths of the states and helicity analysis for \chi_{c2}\ar\gamma\gamma}
Based on a data sample of 106 M events collected with the
BESIII detector, the decays \psi^{\prime}\ar\gamma\chi_{c0, 2},\chi_{c0,
2}\ar\gamma\gamma are studied to determine the two-photon widths of the
states. The two-photon decay branching fractions are determined
to be {\cal B}(\chi_{c0}\ar\gamma\gamma) = (2.24\pm 0.19\pm 0.12\pm
0.08)\times 10^{-4} and {\cal B}(\chi_{c2}\ar\gamma\gamma) = (3.21\pm 0.18\pm
0.17\pm 0.13)\times 10^{-4}. From these, the two-photon widths are determined
to be keV,
keV, and
, where the uncertainties
are statistical, systematic, and those from the PDG {\cal
B}(\psi^{\prime}\ar\gamma\chi_{c0,2}) and errors,
respectively. The ratio of the two-photon widths for helicity and
helicity components in the decay \chi_{c2}\ar\gamma\gamma is
measured for the first time to be .Comment: 10 pages, 4 figure
- …