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- Aoyama, T., et al.
(författare)
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The anomalous magnetic moment of the muon in the Standard Model
- 2020
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Ingår i: Physics reports. - : Elsevier BV. - 0370-1573 .- 1873-6270. ; 887, s. 1-166
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Forskningsöversikt (refereegranskat)abstract
- We review the present status of the Standard Model calculation of the anomalous magnetic moment of the muon. This is performed in a perturbative expansion in the fine-structure constant α and is broken down into pure QED, electroweak, and hadronic contributions. The pure QED contribution is by far the largest and has been evaluated up to and including O(α5) with negligible numerical uncertainty. The electroweak contribution is suppressed by (mμ/MW)2 and only shows up at the level of the seventh significant digit. It has been evaluated up to two loops and is known to better than one percent. Hadronic contributions are the most difficult to calculate and are responsible for almost all of the theoretical uncertainty. The leading hadronic contribution appears at O(α2) and is due to hadronic vacuum polarization, whereas at O(α3) the hadronic light-by-light scattering contribution appears. Given the low characteristic scale of this observable, these contributions have to be calculated with nonperturbative methods, in particular, dispersion relations and the lattice approach to QCD. The largest part of this review is dedicated to a detailed account of recent efforts to improve the calculation of these two contributions with either a data-driven, dispersive approach, or a first-principle, lattice-QCD approach. The final result reads aμSM = 116 591 810(43) x 10-11 and is smaller than the Brookhaven measurement by 3.7 σ. The experimental uncertainty will soon be reduced by up to a factor four by the new experiment currently running at Fermilab, and also by the future J-PARC experiment. This and the prospects to further reduce the theoretical uncertainty in the near future - which are also discussed here - make this quantity one of the most promising places to look for evidence of new physics.
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| 2. |
- Busayavalasa, Kiran, et al.
(författare)
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Leveraging a gain-of-function allele of Caenorhabditis elegans paqr-1 to elucidate membrane homeostasis by PAQR proteins
- 2020
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Ingår i: Plos Genetics. - : Public Library of Science (PLoS). - 1553-7404. ; 16:8
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Tidskriftsartikel (refereegranskat)abstract
- TheC.elegansproteins PAQR-2 (a homolog of the human seven-transmembrane domain AdipoR1 and AdipoR2 proteins) and IGLR-2 (a homolog of the mammalian LRIG proteins characterized by a single transmembrane domain and the presence of immunoglobulin domains and leucine-rich repeats in their extracellular portion) form a complex that protects against plasma membrane rigidification by promoting the expression of fatty acid desaturases and the incorporation of polyunsaturated fatty acids into phospholipids, hence increasing membrane fluidity. In the present study, we leveraged a novel gain-of-function allele of PAQR-1, a PAQR-2 paralog, to carry out structure-function studies. We found that the transmembrane domains of PAQR-2 are responsible for its functional requirement for IGLR-2, that PAQR-1 does not require IGLR-2 but acts via the same pathway as PAQR-2, and that the divergent N-terminal cytoplasmic domains of the PAQR-1 and PAQR-2 proteins serve a regulatory function and may regulate access to the catalytic site of these proteins. We also show that overexpression of human AdipoR1 or AdipoR2 alone is sufficient to confer increased palmitic acid resistance in HEK293 cells, and thus act in a manner analogous to the PAQR-1 gain-of-function allele. Author summary Cells are enclosed within membranes primarily composed of fat. When membranes contain much saturated fats, they tend to become more rigid, as with butter. Conversely, when membranes are rich in unsaturated fats, they become more fluid, as with vegetable oils. Our goal is to better understand how cells monitor and adjust the composition and properties of their membranes. We focus on a small group of proteins found in all animals, and called AdipoR1 and AdipoR2 in humans, and PAQR-1 and PAQR-2 in the wormCaenorhabditis elegans. We now found a version of PAQR-1 that is more "active", and promotes increased levels of unsaturated fats in membranes. By swapping different parts of the PAQR-1 protein with those of PAQR-2, we were able to determine which protein parts played which roles. We found that it is the transmembrane domains of PAQR-2 that dictate its requirements for another protein called IGLR-2 and that the intracellular domains of PAQR-1 and PAQR-2 play a regulatory role. These studies help understand how AdipoR1 and AdipoR2 regulate membrane composition in human cells, which is a vital function for us to thrive on diets that vary greatly in the types of fats that they contain.
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| 4. |
- Engqvist, Håkan, et al.
(författare)
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Flexural strength measurement of ceramic dental restorative materials
- 2007
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Ingår i: Journal of Advanced Materials. - 1070-9789. ; 39:1, s. 41-45
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Tidskriftsartikel (refereegranskat)abstract
- Flexural strength of a dental material reflects its ability to withstand tensile stresses and as such has an impact of the fracture risk of a filling. There are several methods to measure flexural strength of a material. The flexural strength of a bioceramic calciumaluminate-based dental restorative material (DoxaDent) has been measured in three different methods with a composite (Tetric Ceram), a glass ionomer cement (Fuji 11) and a phosphate cement (Harward) as references. The three test methods were: a) ISO 4049 for dental composites, three-point bend test of 2*2*25 mm rods, non-polished surface, b) EN 843-1 for ceramic materials, three-point bend test of 3*4*40 mm, polished surface, and c) biaxial ball-on-disc for ceramic materials (ASTM F-394), polished surface. The results obtained clearly show the difficulty in performing flexural strength testing of a bioceramic material. By using the ball-on-disc method the defect size was reduced and thus the resulting flexural strength higher. The strength of DoxaDent tested in the ball-on-disc method is close to the theoretical strength based on the microstructure of the material (maximum grain size of 15 mu m). The composite material and the phosphate cement were rather insensitive to the test method whereas the glass ionomer cement also showed sensitivity towards the test method. Based on fracture mechanics the flexural strength of bioceramic materials is discussed. A modified biaxial test method for evaluation of strength of dental materials in a close to real-life component is proposed.
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| 8. |
- Hermansson, Leif, et al.
(författare)
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Flexural Strength Measurement of Ceramic Dental Restorative Materials
- 2008
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Ingår i: BIOCERAMICS, VOL 20, PTS 1 AND 2. ; , s. 873-876
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Konferensbidrag (refereegranskat)abstract
- Flexural strength of a dental material reflects its ability to withstand tensile stresses and thus the fracture risk of a filling. The flexural strength of an experimental bioceramic Calcium aluminate-based (CA) dental restorative material was measured using three different methods with a composite (Tetric Ceram), a glass ionomer cement (Fuji II) and a phosphate cement (Harward) as references. The three test methods were: a) ISO 4049 for dental composites, 3-point bend test b) EN 843-1 for ceramic materials, 3-point bend test and c) ASTM F-394, biaxial ball-on-disc for ceramic materials. The strength of the CA-material, tested in the ball-on-disc method, is close to the theoretical strength based on the microstructure of the material (max. grain size of 15 mu m). The composite material and the phosphate cement were rather insensitive to the test method, while the glass ionomer cement as the CA-material showed sensitivity towards the test method. A modified biaxial test method for evaluation of strength of dental materials in a close to real-life component is proposed.
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| 10. |
- Peng, B, et al.
(författare)
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LipidCreator workbench to probe the lipidomic landscape
- 2020
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Ingår i: Nature communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 11:1, s. 2057-
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Tidskriftsartikel (refereegranskat)abstract
- Mass spectrometry (MS)-based targeted lipidomics enables the robust quantification of selected lipids under various biological conditions but comprehensive software tools to support such analyses are lacking. Here we present LipidCreator, a software that fully supports targeted lipidomics assay development. LipidCreator offers a comprehensive framework to compute MS/MS fragment masses for over 60 lipid classes. LipidCreator provides all functionalities needed to define fragments, manage stable isotope labeling, optimize collision energy and generate in silico spectral libraries. We validate LipidCreator assays computationally and analytically and prove that it is capable to generate large targeted experiments to analyze blood and to dissect lipid-signaling pathways such as in human platelets.
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