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Träfflista för sökning "WFRF:(Johansson Erik) srt2:(2020-2022)"

Sökning: WFRF:(Johansson Erik) > (2020-2022)

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1.
  • Andruszkiewicz, Aneta, et al. (författare)
  • Perovskite and quantum dot tandem solar cells with interlayer modification for improved optical semitransparency and stability
  • 2021
  • Ingår i: Nanoscale. - : Royal Society of Chemistry. - 2040-3364 .- 2040-3372. ; 13:12, s. 6234-6240
  • Tidskriftsartikel (refereegranskat)abstract
    • In this work, four-terminal (4T) tandem solar cells were fabricated by using a methylammonium lead iodide (MAPbI3) perovskite solar cell (PSC) as the front-cell and a lead sulfide (PbS) colloidal quantum dot solar cell (CQDSC) as the back-cell. Different modifications of the tandem interlayer, at the interface between the sub-cells, were tested in order to improve the infrared transparency of the perovskite sub-cell and consequently increase the utilization of infrared (IR) light by the tandem system. This included the incorporation of a semi-transparent thin gold electrode (Au) on the MAPbI3 solar cell, followed by adding a molybdenum(VI) oxide (MoO3) layer or a surlyn layer. These interlayer modifications resulted in an increase of the IR transmittance to the back cell and improved the optical stability, compared to that in the reference devices. This investigation shows the importance of the interlayer, connecting the PSC with a strong absorption in the visible region and the CQDSC with a strong infrared absorption to obtain efficient next-generation tandem photovoltaics (PVs).
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2.
  • Bohgard, Mats, et al. (författare)
  • Nu krävs satsning på forskning för ett hållbart arbetsliv
  • 2021
  • Ingår i: Dagens Medicin. - 1104-7488.
  • Tidskriftsartikel (populärvet., debatt m.m.)abstract
    • Debatt: Vi vill att forskningsråden skapar tvärvetenskapliga regionala forskningscentrum för arbetslivsforskning, som är internationellt konkurrenskraftiga och ger nationellt och regionalt kunskapsstöd. Dessa centrum ska ge kunskaper för både befintliga och framtida utmaningar. Stora vinster kan fås om forskning om folkhälsa och yttre miljö samordnas i centrumen. Arbetslivet är grunden för hälsa, välstånd och ett välfungerande samhälle. För att säkra att framtidens arbetsliv bidrar till hälsa och välstånd behövs både kunskap om hur det ska utformas och en uthållig infrastruktur för forskning. Tyvärr saknas detta. Gammal kunskap faller i glömska.
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3.
  • Dreyer, Joshua, et al. (författare)
  • Constraining the Positive Ion Composition in Saturn's Lower Ionosphere with the Effective Recombination Coefficient
  • 2021
  • Ingår i: The Planetary Science Journal. - : American Astronomical Society. - 2632-3338. ; 2:1
  • Tidskriftsartikel (refereegranskat)abstract
    • The present study combines Radio and Plasma Wave Science/Langmuir Probe and Ion and Neutral Mass Spectrometer data from Cassini's last four orbits into Saturn's lower ionosphere to constrain the effective recombination coefficient α300 from measured number densities and electron temperatures at a reference electron temperature of 300 K. Previous studies have shown an influx of ring material causes a state of electron depletion due to grain charging, which will subsequently affect the ionospheric chemistry. The requirement to take grain charging into account limits the derivation of α300 to upper limits. Assuming photochemical equilibrium and using an established method to calculate the electron production rate, we derive upper limits for α300 of ≲ 3 × 10−7 cm3 s−1 for altitudes below 2000 km. This suggests that Saturn's ionospheric positive ions are dominated by species with low recombination rate coefficients like HCO+. An ionosphere dominated by water group ions or complex hydrocarbons, as previously suggested, is incompatible with this result, as these species have recombination rate coefficients > 5 × 10−7 cm3 s−1 at an electron temperature of 300 K.
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4.
  • Dreyer, Joshua, et al. (författare)
  • Identifying Shadowing Signatures of C Ring Ringlets and Plateaus in Cassini Data from Saturn's Ionosphere
  • 2022
  • Ingår i: The Planetary Science Journal. - : Institute of Physics (IOP). - 2632-3338. ; 3:7
  • Tidskriftsartikel (refereegranskat)abstract
    • For orbits 288 and 292 of Cassini's Grand Finale, clear dips (sharp and narrow decreases) are visible in the H-2(+) densities measured by the Ion and Neutral Mass Spectrometer (INMS). In 2017, the southern hemisphere of Saturn was shadowed by its rings and the substructures within. Tracing a path of the solar photons through the ring plane to Cassini's position, we can identify regions in the ionosphere that were shadowed by the individual ringlets and plateaus (with increased optical depths) of Saturn's C ring. The calculated shadowed altitudes along Cassini's trajectory line up well with the dips in the H-2(+) data when adjusting the latter based on a detected evolving shift in the INMS timestamps since 2013, illustrating the potential for verification of instrument timings. We can further estimate the mean optical depths of the ringlets/plateaus by comparing the dips to inbound H-2(+) densities. Our results agree well with values derived from stellar occultation measurements. No clear dips are visible for orbits 283 and 287, whose periapsides were at higher altitudes. This can be attributed to the much longer chemical lifetime of H2+ at these higher altitudes, which in turn can be further used to estimate a lower limit for the flow speed along Cassini's trajectory. The resulting estimate of similar to 0.3 km s(-1) at an altitude of similar to 3400 km is in line with prior suggestions. Finally, the ringlet and plateau shadows are not associated with obvious dips in the electron density, which is expected due to their comparatively long chemical (recombination) lifetime.
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5.
  • Folkersen, Lasse, et al. (författare)
  • Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
  • 2020
  • Ingår i: Nature metabolism. - : Springer Science and Business Media LLC. - 2522-5812. ; 2:10, s. 1135-1148
  • Tidskriftsartikel (refereegranskat)abstract
    • Circulating proteins are vital in human health and disease and are frequently used as biomarkers for clinical decision-making or as targets for pharmacological intervention. Here, we map and replicate protein quantitative trait loci (pQTL) for 90 cardiovascular proteins in over 30,000 individuals, resulting in 451 pQTLs for 85 proteins. For each protein, we further perform pathway mapping to obtain trans-pQTL gene and regulatory designations. We substantiate these regulatory findings with orthogonal evidence for trans-pQTLs using mouse knockdown experiments (ABCA1 and TRIB1) and clinical trial results (chemokine receptors CCR2 and CCR5), with consistent regulation. Finally, we evaluate known drug targets, and suggest new target candidates or repositioning opportunities using Mendelian randomization. This identifies 11 proteins with causal evidence of involvement in human disease that have not previously been targeted, including EGF, IL-16, PAPPA, SPON1, F3, ADM, CASP-8, CHI3L1, CXCL16, GDF15 and MMP-12. Taken together, these findings demonstrate the utility of large-scale mapping of the genetics of the proteome and provide a resource for future precision studies of circulating proteins in human health.
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6.
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7.
  • Furukawa, Toshi A., et al. (författare)
  • Dismantling, optimising, and personalising internet cognitive behavioural therapy for depression : a systematic review and component network meta-analysis using individual data
  • 2021
  • Ingår i: Lancet psychiatry. - London, United Kingdom : Elsevier. - 2215-0374 .- 2215-0366. ; 8:6, s. 500-511
  • Forskningsöversikt (refereegranskat)abstract
    • Findings We identified 76 RCTs, including 48 trials contributing individual participant data (11 704 participants) and 28 trials with aggregate data (6474 participants). The participants' weighted mean age was 42.0 years and 12 406 (71%) of 17 521 reported were women. There was suggestive evidence that behavioural activation might be beneficial (iMD -1.83 [95% credible interval (CrI) -2.90 to -0.80]) and that relaxation might be harmful (1.20 [95% CrI 0.17 to 2.27]). Baseline severity emerged as the strongest prognostic factor for endpoint depression. Combining human and automated encouragement reduced dropouts from treatment (incremental odds ratio, 0.32 [95% CrI 0.13 to 0.93]). The risk of bias was low for the randomisation process, missing outcome data, or selection of reported results in most of the included studies, uncertain for deviation from intended interventions, and high for measurement of outcomes. There was moderate to high heterogeneity among the studies and their components. 511
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8.
  • Ghoreishi, Farzaneh S., et al. (författare)
  • Enhanced performance of CH3NH3PbI3 perovskite solar cells via interface modification using phenyl ammonium iodide derivatives
  • 2020
  • Ingår i: Journal of Power Sources. - : Elsevier. - 0378-7753 .- 1873-2755. ; 473
  • Tidskriftsartikel (refereegranskat)abstract
    • Interface modification in perovskite solar cells is a key factor for achieving high power conversion efficiency by suppressing electron-hole recombination and accelerating charge carrier extraction. Here, we use a series of phenyl ammonium derivatives, phenyl ammonium iodide (PAI), benzyl ammonium iodide (BAI), and phenyl ethyl ammonium iodide (PEAI), to modify the interface between methylammonium lead triiodide (MAPbI3) perovskite and Spiro-OMeTAD as a hole transport layer in solar cell devices. The structural and optical properties of the perovskite films are studied and the results reveal the formation of two-dimensional perovskite interfacial layers on the surface of the MAPbI3 film modified with PEAI and BAI whereas the MAPbI3 layer modified with PAI gives an interface layer with slightly different properties compared to the two-dimensional perovskite. Impedance spectroscopy shows that the charge transport resistance of the interface engineered solar cells decreases when compared to pristine MAPbI3. In addition, slower open-circuit voltage decay and longer carrier lifetime are also observed for the modified cells which in total lead to the improvement of the photovoltaic performance. The investigation therefore gives insight in the effect of interface modifications, and especially how different sizes of the molecular interface modifier results in different interface formation and characteristics.
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9.
  • Grönlund, Eric, 1987-, et al. (författare)
  • Robust treatment planning of dose painting for prostate cancer based on ADC-to-Gleason score mappings : what is the potential to increase the tumor control probability?
  • 2021
  • Ingår i: Acta Oncologica. - : Taylor & Francis. - 0284-186X .- 1651-226X. ; 60:2, s. 199-206
  • Tidskriftsartikel (refereegranskat)abstract
    • Background and Purpose The aim of this study was to evaluate the potential to increase the tumor control probability (TCP) with ‘dose painting by numbers’ (DPBN) plans optimized in a treatment planning system (TPS) compared to uniform dose plans. The DPBN optimization was based on our earlier published formalism for prostate cancer that is driven by dose-responses of Gleason scores mapped from apparent diffusion coefficients (ADC).Material and MethodsFor 17 included patients, a set of DPBN plans were optimized in a TPS by maximizing the TCP for an equal average dose to the prostate volume (CTVT) as for a conventional uniform dose treatment. For the plan optimizations we applied different photon energies, different precisions for the ADC-to-Gleason mappings, and different CTVT positioning uncertainties. The TCP increasing potential was evaluated by the DPBN efficiency, defined as the ratio of TCP increases for DPBN plans by TCP increases for ideal DPBN prescriptions (optimized without considering radiation transport phenomena, uncertainties of the CTVT positioning, and uncertainties of the ADC-to-Gleason mapping).ResultsThe median DPBN efficiency for the most conservative planning scenario optimized with a low precision ADC-to-Gleason mapping, and a positioning uncertainty of 0.6 cm was 10%, meaning that more than half of the patients had a TCP gain of at least 10% of the TCP for an ideal DPBN prescription. By increasing the precision of the ADC-to-Gleason mapping, and decreasing the positioning uncertainty the median DPBN efficiency increased by up to 40%.ConclusionsTCP increases with DPBN plans optimized in a TPS were found more likely with a high precision mapping of image data into dose-responses and a high certainty of the tumor positioning. These findings motivate further development to ensure precise mappings of image data into dose-responses and to ensure a high spatial certainty of the tumor positioning when implementing DPBN clinically.
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10.
  • Hofving, Tobias, 1989, et al. (författare)
  • SMAD4 haploinsufficiency in small intestinal neuroendocrine tumors
  • 2021
  • Ingår i: BMC Cancer. - : Springer Science and Business Media LLC. - 1471-2407. ; 21:1
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: Patients with small intestinal neuroendocrine tumors (SINETs) frequently present with lymph node and liver metastases at the time of diagnosis, but the molecular changes that lead to the progression of these tumors are largely unknown. Sequencing studies have only identified recurrent point mutations at low frequencies with CDKN1B being the most common harboring heterozygous mutations in less than 10% of all tumors. Although SINETs are genetically stable tumors with a low frequency of point mutations and indels, they often harbor recurrent hemizygous copy number alterations (CNAs) yet the functional implications of these CNA are unclear. Methods: Utilizing comparative genomic hybridization (CGH) arrays we analyzed the CNA profile of 131 SINETs from 117 patients. Two tumor suppressor genes and corresponding proteins i.e. SMAD4, and CDKN1B, were further characterized using a tissue microarray (TMA) with 846 SINETs. Immunohistochemistry (IHC) was used to quantify protein expression in TMA samples and this was correlated with chromosome number evaluated with fluorescent in-situ hybridization (FISH). Intestinal tissue from a Smad4+/− mouse model was used to detect entero-endocrine cell hyperplasia with IHC. Results: Analyzing the CGH arrays we found loss of chromosome 18q and SMAD4 in 71% of SINETs and that focal loss of chromosome 12 affecting the CDKN1B was present in 9.4% of SINETs. No homozygous loss of chromosome 18 was detected. Hemizygous loss of SMAD4, but not CDKN1B, significantly correlated with reduced protein levels but hemizygous loss of SMAD4 did not induce entero-endocrine cell hyperplasia in the Smad4+/− mouse model. In addition, patients with low SMAD4 protein expression in primary tumors more often presented with metastatic disease. Conclusions: Hemizygous loss of chromosome 18q and the SMAD4 gene is the most common genetic event in SINETs and our results suggests that this could influence SMAD4 protein expression and spread of metastases. Although SMAD4 haploinsufficiency alone did not induce tumor initiation, loss of chromosome 18 could represent an evolutionary advantage in SINETs explaining the high prevalence of this aberration. Functional consequences of reduced SMAD4 protein levels could hypothetically be a potential mechanism as to why loss of chromosome 18 appears to be clonally selected in SINETs.
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