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- Moberg, Christina, et al.
(författare)
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De unga gör helt rätt när de stämmer staten
- 2022
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Ingår i: Aftonbladet. - 1103-9000.
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Tidskriftsartikel (populärvet., debatt m.m.)abstract
- 1 620 forskare och lärare i forskarvärlden: Vi ställer oss bakom Auroras klimatkrav
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| 3. |
- Ahlberg, Erik, et al.
(författare)
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"Vi klimatforskare stödjer Greta och skolungdomarna"
- 2019
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Ingår i: Dagens nyheter (DN debatt). - 1101-2447.
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Tidskriftsartikel (populärvet., debatt m.m.)abstract
- DN DEBATT 15/3. Sedan industrialiseringens början har vi använt omkring fyra femtedelar av den mängd fossilt kol som får förbrännas för att vi ska klara Parisavtalet. Vi har bara en femtedel kvar och det är bråttom att kraftigt reducera utsläppen. Det har Greta Thunberg och de strejkande ungdomarna förstått. Därför stödjer vi deras krav, skriver 270 klimatforskare.
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| 5. |
- Andersson, Mattias, et al.
(författare)
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A 7.5 mW 9 MHz CT Delta-Sigma Modulator in 65 nm CMOS with 69 dB SNDR and Reduced Sensitivity to Loop Delay Variations
- 2012
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Ingår i: IEEE Asian Solid State Circuits Conference (A-SSCC), 2012. ; , s. 245-248
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Konferensbidrag (refereegranskat)abstract
- This paper presents a 3rd-order, 3-bit continuous time (CT) Delta-Sigma modulator for an LTE radio receiver. By adopting a return-to-zero (RZ) pulse in the innermost DAC, the modulator shows a reduced sensitivity to loop-delay variations, and the additional loop delay compensation usually needed in CT modulators can be omitted. The modulator has been implemented in a 65nm CMOS process, where it occupies an area of 0.2mmx0.4mm. It achieves an SNR of 71dB and an SNDR of 69dB over a 9MHz bandwidth with an oversampling ratio of 16. Power consumption is 7.5mW from a 1.2V supply, for a figure-of-merit of 181fJ/conversion.
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| 7. |
- Andersson, Mattias, et al.
(författare)
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A Filtering Delta Sigma ADC for LTE and Beyond
- 2014
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Ingår i: IEEE Journal of Solid-State Circuits. - 0018-9200. ; 49:7, s. 1535-1547
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Tidskriftsartikel (refereegranskat)abstract
- Abstract in UndeterminedThis paper presents a filtering ADC for the LTE communication standard, where a second-order Delta-Sigma modulator (DSM) is incorporated into the third-order Chebychev channel-select filter (CSF) of the radio receiver. The CSF introduces an additional third-order suppression of both thermal and quantization DSM noise, while the CSF transfer function is maintained. A design method for the filtering ADC accounting for unavoidable DSM-DAC delays is developed and experimentally demonstrated. The 65 nm CMOS prototype is clocked at 576/288 MHz with an 18.5/9.0 MHz LTE bandwidth, has an in-band gain of 26 dB, an SNDR of 56.4/58.1 dB, an input-referred noise of 5 nV/root Hz, and an out-of-band (half-duplex) IIP3 of 20/12 dBV(rms), with a power consumption of 7.9/5.4 mW and an overall state-of-the art performance.
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| 9. |
- Andersson, Mattias, et al.
(författare)
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Intrinsic and extrinsic influences on the temperature dependence of mobility in conjugated polymers
- 2008
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Ingår i: Organic electronics. - : Elsevier. - 1566-1199 .- 1878-5530. ; 9:5, s. 569-574
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Tidskriftsartikel (refereegranskat)abstract
- The temperature dependence of charge carrier mobility in conjugated polymers and their blends with fullerenes is investigated with different electrical methods, through field effect transistor (FET), space charge limited current (SCLC) and charge extraction (CELIV) measurements. Simple models, such as the Gaussian disorder model (GDM), are shown to accurately predict the temperature behavior, and a good correlation between the different measurement methods is obtained. Inconsistent charge carrier concentrations in the modeling are explained through intrinsic non-equilibrium effects, and are responsible for the limited applicability of existing numerical models. A severe extrinsic influence from water in FETs with a hydrophilic insulator interface is also demonstrated. The presence of water leads to a significant overestimate of the disorder in the materials from measurements close to room temperature and erratic behavior in the 150-350 K range. To circumvent this problem it is shown to be necessary to measure under ultra high vacuum (UHV) conditions. © 2008 Elsevier B.V. All rights reserved.
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| 10. |
- Andersson, Mattias K., et al.
(författare)
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The extended substrate cleavage specificity of the human mast cell chymase reveals a serine protease with well-defined substrate recognition profile
- 2009
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Ingår i: International Immunology. - : Oxford University Press (OUP). - 0953-8178 .- 1460-2377. ; 21:1, s. 95-104
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Tidskriftsartikel (refereegranskat)abstract
- The human chymase (HC) is a major granule constituent of mast cells (MCs) residing in the connective tissue and the sub-mucosa. Although many potential substrates have been described for this important MC enzyme, its full range of in vivo substrates has most likely not yet been identified. A major step toward a better understanding of the function of the HC is therefore to determine its extended cleavage specificity. Using a phage-displayed random nonapeptide library, we show that the HC has a rather stringent substrate recognition profile. Only aromatic amino acids (aa) are accepted in position P1, with a strong preference for Tyr and Phe over Trp. Aliphatic aa are preferred in positions P2 to P4 N-terminal of the cleaved bond. In the P1' position C-terminal of the cleaved bond, Ser is clearly over-represented and acidic aa Asp and Glu are strongly preferred in the P2' position. In P3', the small aliphatic aa Ala, Val and Gly were frequently observed. The consensus sequence, from P4 to P3': Gly/Leu/Val-Val/Ala/Leu-Ala/Val/Leu-Tyr/Phe-Ser-Asp/Glu-Ala/Val/Gly, provides an instrument for the identification of novel in vivo substrates for the HC. Interestingly, a very similar cleavage specificity was recently reported for the major chymase in mouse connective tissue mast cells (CTMCs), the beta-chymase mouse mast cell protease-4, suggesting functional homology between these two enzymes. This indicates that a rather stringent chymotryptic substrate recognition profile has been evolutionary conserved for the dominant CTMC chymase in mammals.
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