| 31. |
- Singh, B. S. Nara, et al.
(författare)
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Influence of the np interaction on the beta decay of Pd-94
- 2012
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Ingår i: Physical Review C. Nuclear Physics. - 0556-2813 .- 1089-490X. ; 86:4, s. 041301-
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Tidskriftsartikel (refereegranskat)abstract
- We present results from stopped beam rare isotope spectroscopic investigations at the GSI (RISING) experiment based on the detection of gamma-ray transitions following the beta decay of Pd-94. A comparison between the measured low-lying level scheme of Rh-94 and the prediction from shell-model calculations reveals the important roles of the g(7/2) and g(9/2) orbitals in explaining the structural features. The low values of the Gamow-Teller strengths B(GT) can be attributed to the influence of the neutron-proton interaction, which gives rise to an increased seniority mixing for the nuclear states, thereby leading to a fragmentation of the strength to several daughter levels. These results provide further strong indications that Pd-94 resides in the middle of a structural transition region in the Pd isotopes as the N = Z line is approached.
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| 32. |
- Wadsworth, R., et al.
(författare)
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Spin-gap Isomer in 96Cd
- 2012
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Ingår i: Journal of Physics: Conference Series. - : IOP Publishing. - 1742-6596 .- 1742-6588. ; 381:1
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Tidskriftsartikel (refereegranskat)abstract
- Evidence has been obtained for the existence of the long predicted 16+ spin-gap isomer in 96Cd. The decay of the isomer was identified and studied following the use of an 850 MeV/u beam of 124Xe impinging on a Be target and the fragment recoil separator at the GSI Laboratory. Gamma decays from the fragments were detected using the RISING gamma ray array, in its stopped beam configuration, plus a silicon active stopper. The data obtained have been compared with shell model predictions, which indicate that the isoscalar neutron-proton interaction plays a key role in the formation of the isomer.
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| 33. |
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| 34. |
- Berthold, R., et al.
(författare)
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Fusion protein-driven IGF-IR/PI3K/AKT signals deregulate Hippo pathway promoting oncogenic cooperation of YAP1 and FUS-DDIT3 in myxoid liposarcoma
- 2022
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Ingår i: Oncogenesis. - : Springer Science and Business Media LLC. - 2157-9024. ; 11:1
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Tidskriftsartikel (refereegranskat)abstract
- Myxoid liposarcoma (MLS) represents a common subtype of liposarcoma molecularly characterized by a recurrent chromosomal translocation that generates a chimeric FUS-DDIT3 fusion gene. The FUS-DDIT3 oncoprotein has been shown to be crucial in MLS pathogenesis. Acting as a transcriptional dysregulator, FUS-DDIT3 stimulates proliferation and interferes with adipogenic differentiation. As the fusion protein represents a therapeutically challenging target, a profound understanding of MLS biology is elementary to uncover FUS-DDIT3-dependent molecular vulnerabilities. Recently, a specific reliance on the Hippo pathway effector and transcriptional co-regulator YAP1 was detected in MLS; however, details on the molecular mechanism of FUS-DDIT3-dependent YAP1 activation, and YAP1 ' s precise mode of action remain unclear. In elaborate in vitro studies, employing RNA interference-based approaches, small-molecule inhibitors, and stimulation experiments with IGF-II, we show that FUS-DDIT3-driven IGF-IR/PI3K/AKT signaling promotes stability and nuclear accumulation of YAP1 via deregulation of the Hippo pathway. Co-immunoprecipitation and proximity ligation assays revealed nuclear co-localization of FUS-DDIT3 and YAP1/TEAD in FUS-DDIT3-expressing mesenchymal stem cells and MLS cell lines. Transcriptome sequencing of MLS cells demonstrated that FUS-DDIT3 and YAP1 co-regulate oncogenic gene signatures related to proliferation, cell cycle progression, apoptosis, and adipogenesis. In adipogenic differentiation assays, we show that YAP1 critically contributes to FUS-DDIT3-mediated adipogenic differentiation arrest. Taken together, our study provides mechanistic insights into a complex FUS-DDIT3-driven network involving IGF-IR/PI3K/AKT signals acting on Hippo/YAP1, and uncovers substantial cooperative effects of YAP1 and FUS-DDIT3 in the pathogenesis of MLS.
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| 35. |
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| 36. |
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| 37. |
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| 38. |
- Kluza, Ewelina, et al.
(författare)
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Diverse ultrastructural landscape of atherosclerotic endothelium
- 2021
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Ingår i: Atherosclerosis. - : Elsevier BV. - 0021-9150. ; 339, s. 35-45
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Tidskriftsartikel (refereegranskat)abstract
- Background and aims: The endothelium plays a major role in atherosclerosis, yet the endothelial plaque surface is a largely uncharted territory. Here we hypothesize that atherosclerosis-driven remodeling of the endothelium is a dynamic process, involving both damaging and regenerative mechanisms. Methods: Using scanning electron microscopy (SEM) and immuno-SEM, we studied endothelial junction ultrastructure, endothelial openings and immune cell-endothelium interactions in eight apoe−/− mice and two human carotid plaques. Results: The surface of early mouse plaques (n = 11) displayed a broad range of morphological alterations, including junctional disruptions and large transcellular endothelial pores with the average diameter between 0.6 and 3 μm. The shoulder region of advanced atherosclerotic lesions (n = 7) had a more aggravated morphology with 8 μm-size paracellular openings at two-fold higher density. In contrast, the central apical surface of advanced plaques, i.e., the plaque body (n = 7), displayed endothelial normalization, as shown by a significantly higher frequency of intact endothelial junctions and a lower incidence of paracellular pores. This normalized endothelial phenotype correlated with low immune cell density (only 5 cells/mm2). The human carotid plaque surface (n = 2) displayed both well-organized and disrupted endothelium with similar features as described above. In addition, they were accompanied by extensive thrombotic areas. Conclusions: Our study unveils the spectrum of endothelial abnormalities associated with the development of atherosclerosis. These were highly abundant in early lesions and in the shoulder region of advanced plaques, while normalized at the advanced plaque's body. Similar endothelial features were observed in human atherosclerotic plaques, underlining the versatility of endothelial transformations in atherosclerosis.
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| 39. |
- Litnovsky, Andrey, et al.
(författare)
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Carbon transport, deposition and fuel accumulation in castellated structures exposed in TEXTOR
- 2007
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Ingår i: Journal of Nuclear Materials. - : Elsevier BV. - 0022-3115 .- 1873-4820. ; 367, s. 1481-1486
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Tidskriftsartikel (refereegranskat)abstract
- In order to maintain the thermo-mechanical durability of ITER it is proposed to castellate the interior surface of the first wall and divertor by splitting them into small-size cells [W. Daener et a]., Fusion Eng. Des. 61&62 (2002) 61]. A concern is the accumulation of fuel in the gaps of the castellation. In TEXTOR, molybdenum limiters were exposed in the scrape-off layer (SOL) plasma to assess fuel accumulation. The first limiter was exposed under deposition-dominated conditions. Carbon deposits were formed both on top surfaces and in the gaps. About 0.12% of the impinging D-fluence was found in the gaps. Another castellated limiter was exposed under erosion-dominated conditions. Deposited layers were found only on the plasma shadowed areas of the gaps. A significant amount of molybdenum from the limiter was found intermixed in the deposit. The gaps contained similar to 0.03% of the impinging D-fluence. Modeling was performed to simulate carbon transport into the gaps.
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| 40. |
- Meurisch, Christian, et al.
(författare)
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SmartGuidance'17 : 2nd Workshop on Intelligent Personal Support of Human Behavior
- 2017
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Konferensbidrag (refereegranskat)abstract
- In today's fast-paced environment, humans are faced with various problems such as information overload, stress, health and social issues. So-called anticipatory systems promise to approach these issues through personal guidance or support within a user's daily and professional life. The Second Workshop on Intelligent Personal Support of Human Behavior (SmartGuidance'17) aims to build on the success of the previous workshop (namely Smarticipation) organized in conjunction with UbiComp 2016, to continue discussing the latest research outcomes of anticipatory mobile systems. We invite the submission of papers within this emerging, interdisciplinary research field of anticipatory mobile computing that focuses on understanding, design, and development of such ubiquitous systems. We also welcome contributions that investigate human behaviors, underlying recognition and prediction models; conduct field studies; as well as propose novel HCI techniques to provide personal support. All workshop contributions will be published in supplemental proceedings of the UbiComp 2017 conference and included in the ACM Digital Library.
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