268 research outputs found
First observation of excited states in 173Hg
The neutron-deficient nucleus 173Hg has been studied following
fusion-evaporation reactions. The observation of gamma rays decaying from
excited states are reported for the first time and a tentative level scheme is
proposed. The proposed level scheme is discussed within the context of the
systematics of neighbouring neutron-deficient Hg nuclei. In addition to the
gamma-ray spectroscopy, the alpha decay of this nucleus has been measured
yielding superior precision to earlier measurements.Comment: 5 pages, 4 figure
Practitioner accounts and knowledge production: an analysis of three marketing discourses
Responding to repeated calls for marketing academicians to connect with marketing actors, we offer an empirically-sourced discourse analysis of the ways in which managers portray their practices. Focusing on the micro-discourses and narratives that marketing actors draw upon to represent their work we argue that dominant representations of marketing knowledge production present a number of critical concerns for marketing theory and marketing education. We also evidence that the often promoted idea of a need to close the gap between theory - as a dominant discourse - and practice, as a way of doing marketing, is problematic to pursue. We suggest that a more fruitful agenda resides in the development of a range of polyphonic and creative micro-discourses of management, promoting context, difference and individual meaning in marketing knowledge production
Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development
De novo loss of function mutations in the ubiquitin ligase-encoding gene Cullin3 (CUL3) lead to autism spectrum disorder (ASD). Here, we used Cul3 mouse models to evaluate the consequences of Cul3 mutations in vivo. Our results show that Cul3 haploinsufficient mice exhibit deficits in motor coordination as well as ASD-relevant social and cognitive impairments. Cul3 mutant brain displays cortical lamination abnormalities due to defective neuronal migration and reduced numbers of excitatory and inhibitory neurons. In line with the observed abnormal columnar organization, Cul3 haploinsufficiency is associated with decreased spontaneous excitatory and inhibitory activity in the cortex. At the molecular level, employing a quantitative proteomic approach, we show that Cul3 regulates cytoskeletal and adhesion protein abundance in mouse embryos. Abnormal regulation of cytoskeletal proteins in Cul3 mutant neuronal cells results in atypical organization of the actin mesh at the cell leading edge, likely causing the observed migration deficits. In contrast to these important functions early in development, Cul3 deficiency appears less relevant at adult stages. In fact, induction of Cul3 haploinsufficiency in adult mice does not result in the behavioral defects observed in constitutive Cul3 haploinsufficient animals. Taken together, our data indicate that Cul3 has a critical role in the regulation of cytoskeletal proteins and neuronal migration and that ASD-associated defects and behavioral abnormalities are primarily due to Cul3 functions at early developmental stages
Shape coexistence at the proton drip-line: First identification of excited states in 180Pb
Excited states in the extremely neutron-deficient nucleus, 180Pb, have been
identified for the first time using the JUROGAM II array in conjunction with
the RITU recoil separator at the Accelerator Laboratory of the University of
Jyvaskyla. This study lies at the limit of what is presently achievable with
in-beam spectroscopy, with an estimated cross-section of only 10 nb for the
92Mo(90Zr,2n)180Pb reaction. A continuation of the trend observed in 182Pb and
184Pb is seen, where the prolate minimum continues to rise beyond the N=104
mid-shell with respect to the spherical ground state. Beyond mean-field
calculations are in reasonable correspondence with the trends deduced from
experiment.Comment: 5 pages, 4 figures, submitted to Phys.Rev.
Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development
De novo loss of function mutations in the ubiquitin ligase-encoding gene Cullin3 lead to autism spectrum disorder (ASD). In mouse, constitutive haploinsufficiency leads to motor coordination deficits as well as ASD-relevant social and cognitive impairments. However, induction of Cul3 haploinsufficiency later in life does not lead to ASD-relevant behaviors, pointing to an important role of Cul3 during a critical developmental window. Here we show that Cul3 is essential to regulate neuronal migration and, therefore, constitutive Cul3 heterozygous mutant mice display cortical lamination abnormalities. At the molecular level, we found that Cul3 controls neuronal migration by tightly regulating the amount of Plastin3 (Pls3), a previously unrecognized player of neural migration. Furthermore, we found that Pls3 cell-autonomously regulates cell migration by regulating actin cytoskeleton organization, and its levels are inversely proportional to neural migration speed. Finally, we provide evidence that cellular phenotypes associated with autism-linked gene haploinsufficiency can be rescued by transcriptional activation of the intact allele in vitro, offering a proof of concept for a potential therapeutic approach for ASDs
From Social Democracy back to No Ideology? - The Scottish National Party and Ideological Change in a Multi-level Electoral Setting
This article examines the development of ideology in the Scottish National Party since its formation in 1934, focusing on the recent period of the party’s history. It examines ideological development within the context of the party’s adaptation to multi-level elections and party system, especially in the decade since devolution began in 1999. It also provides a brief consideration of the party’s office success and governmental performance since 2007 to examine the effect of office on the SNP and its autonomy goal of Scottish independence
A coding polymorphism in matrix metalloproteinase 9 reduces risk of scarring sequelae of ocular Chlamydia trachomatis infection.
BACKGROUND: Trachoma, an infectious disease of the conjunctiva caused by Chlamydia trachomatis, is an important global cause of blindness. A dysregulated extracellular matrix (ECM) proteolysis during the processes of tissue repair following infection and inflammation are thought to play a key role in the development of fibrotic sequelae of infection, which ultimately leads to blindness. Expression and activity of matrix metalloproteinase 9 (MMP-9), a major effector of ECM turnover, is up-regulated in the inflamed conjunctiva of trachoma subjects. Genetic variation within the MMP9 gene affects in vitro MMP9 expression levels, enzymatic activity and susceptibility to various inflammatory and fibrotic conditions. METHODS: We genotyped 651 case-control pairs from trachoma endemic villages in The Gambia for coding single nucleotide polymorphisms (SNPs) in the MMP9 gene using the high-throughput Sequenom system. Single marker and haplotype conditional logistic regression (CLR) analysis for disease association was performed. RESULTS: The Q279R mutation located in exon 6 of MMP9 was found to be associated with lower risk for severe disease sequelae of ocular Chlamydia trachomatis infection. This mutation, which leads to a nonsynonymous amino-acid change within the active site of the enzyme may reduce MMP-9-induced degradation of the structural components of the ECM during inflammatory episodes in trachoma and its associated fibrosis. CONCLUSION: This work supports the hypothesis that MMP-9 has a role in the pathogenesis of blinding trachoma
The JUROGAM 3 spectrometer
The jurogam 3 spectrometer has been constructed for in-beam gamma-ray spectroscopy experiments in the Accelerator Laboratory of the University of Jyvaskyla, Finland. jurogam 3 consists of germanium-detector modules in a compact geometry surrounding a target to measure. rays emitted from radioactive nuclei. jurogam 3 can be employed in conjunction with one of two recoil separators, the mara vacuum-mode separator or the ritu gas-filled separator, and other ancillary devices.Peer reviewe
Study of Intermediate-spin States of Y-98
The nuclear structure of the oddâodd nucleus 98Y has been re-investigated
by observing prompt Îł rays emitted following the proton-induced fission
of a 238U target, using the JUROGAM-II multidetector array. New highspin
decays have been observed and placed in the level schemes using triple
coincidences. The experimental level energies and Îł-decay patterns are
compared to GICM and QPRM calculations, assuming that this neutronrich
N = 59 isotone is spherical at low energies and prolate deformed at
intermediate spins.Web of Science47391691
In-beam spectroscopic study of 244Cf
The ground-state rotational band of the neutron-deficient californium (Z = 98) isotope 244Cf was identified for the first time and measured up to a tentative spin and parity of I = 20+. The observation of the rotational band indicates that the nucleus is deformed. The kinematic and dynamic moments of inertia were deduced from the measured gamma-ray transition energies. The behavior of the dynamic moment of inertia revealed an up-bend due to a possible alignment of coupled nucleons in high-j orbitals starting at a rotational frequency of about hw = 0.20 MeV. The results were compared with the systematic behavior of the even-even N = 146 isotones as well as with available theoretical calculations that have been performed for nuclei in the region
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