SwePub
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "WFRF:(Judson G) "

Sökning: WFRF:(Judson G)

  • Resultat 31-40 av 52
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
31.
  • Såmark-Roth, A., et al. (författare)
  • Spectroscopy along flerovium decay chains. III. Details on experiment, analysis, 282Cn, and spontaneous fission branches
  • 2023
  • Ingår i: Physical Review C. - 2469-9985. ; 107:2
  • Tidskriftsartikel (refereegranskat)abstract
    • Flerovium isotopes (element Z = 114) were produced in the fusion-evaporation reactions 48Ca+242,244Pu and studied with an upgraded TASISpec decay station placed in the focal plane of the gas-filled separator TASCA at the GSI Helmholtzzentrum für Schwerionenforschung in Darmstadt, Germany. Twenty-nine flerovium decay chains were identified by means of correlated implantation, α decay, and spontaneous fission events. Data analysis aspects and statistical assessments, primarily based on measured rates of various events, which laid the foundation for the comprehensive spectroscopic information on the flerovium decay chains, are presented in detail. Various decay scenarios of an excited state observed in 282Cn are examined in depth with the help of GEANT4 simulations and assessed by predictions of beyond mean-field calculations including triaxial shape degrees of freedom. Previous, revised, and newly derived fission probabilities of even-even superheavy nuclei are compared with various theoretical predictions.
  •  
32.
  •  
33.
  •  
34.
  • Darby, I. G., et al. (författare)
  • Decay of the high-spin isomer in Re-160 : Changing single-particle structure beyond the proton drip line
  • 2011
  • Ingår i: Physics Letters B. - : Elsevier BV. - 0370-2693 .- 1873-2445. ; 695:1-4, s. 78-81
  • Tidskriftsartikel (refereegranskat)abstract
    • A new high-spin isomeric state (t(1/2) = 2.8 +/- 0.1 mu s) in Re-160 has been identified. This high-spin isomer is unique in that it only decays by gamma-decay and not by proton or alpha-particle emission as is the case in every other proton emitter between Z = 64 and 80. Shell model calculations indicate how the convergence of the h(9/2) and f(7/2) neutron levels in this region could open up a gamma-decay path from the high-spin isomer to the low-spin ground state of 160Re. providing a natural explanation for this anomalous absence of charged-particle emission. The consequences of these observations for future searches for proton emission from even more exotic nuclei and in-beam spectroscopic studies are considered.
  •  
35.
  • Darby, I. G., et al. (författare)
  • Precision measurements of proton emission from the ground states of Ta-156 and Re-160
  • 2011
  • Ingår i: Physical Review C. Nuclear Physics. - 0556-2813 .- 1089-490X. ; 83:6, s. 064320-
  • Tidskriftsartikel (refereegranskat)abstract
    • The decays of the pi d(3/2) ground states of Ta-156 and Re-160 have been studied in detail using the GREAT spectrometer. More than 7000 Re-160 nuclei were produced in reactions of 290- and 300-MeV Ni-58 ions with an isotopically enriched Cd-106 target and separated in flight using the RITU separator. The proton and alpha decays of the pi d(3/2) level were confirmed and the half-life and branching ratios of this state were determined with improved precision to be t(1/2) = 611 +/- 7 mu s and b(p) = 89 +/- 1% and b(alpha) = 11 +/- 1%, respectively. The alpha-decay branch populated the ground state of Ta-156, allowing improved values for the proton-decay energy and half-life to be obtained (E-p = 1011 +/- 5 keV; t(1/2) = 106 +/- 4 ms). The beta decay of this level was identified for the first time and a branching ratio of b(beta) = 29 +/- 3% was deduced. The spectroscopic factors deduced from these measurements are compared with predictions.
  •  
36.
  • Das, P., et al. (författare)
  • Study of exotic decay of Cs isotope close to the proton drip line
  • 2020
  • Ingår i: 27th International Nuclear Physics Conference (INPC2019) 29 July - 2 August 2019, Glasgow, UK. - : IOP Publishing. - 1742-6588. ; 1643
  • Konferensbidrag (refereegranskat)abstract
    • The neutron-deficient 115Cs was produced at ISOLDE, CERN by spallation reaction using 1.4 GeV proton on LaC2 target. The exotic decay modes were studied by using a charged particle array (DSSD and pad detectors) and a γ-detector array (four Clovers) at the ISOLDE decay station (IDS). In this report, results on observed β-delayed particle emission from 115Cs, a nucleus close to proton drip line, is presented. By measuring the time distribution in the delayed proton spectrum, the half-life of the ground state of 115Cs was extracted. The obtained half-life is in agreement with previous reported value. For the first time, the p-unbound states of 115Xe, obtained by measuring beta-delayed protons from 115Cs is reported.
  •  
37.
  • Ekhtiari, Hamed, et al. (författare)
  • A methodological checklist for fMRI drug cue reactivity studies : development and expert consensus
  • 2022
  • Ingår i: Nature Protocols. - : Nature Portfolio. - 1754-2189 .- 1750-2799. ; 17:3, s. 567-595
  • Tidskriftsartikel (refereegranskat)abstract
    • Cue reactivity measured by functional magnetic resonance imaging is used in studies of substance-use disorders. This Consensus Statement is the result of a Delphi process to arrive at parameters that should be reported in describing these studies. Cue reactivity is one of the most frequently used paradigms in functional magnetic resonance imaging (fMRI) studies of substance use disorders (SUDs). Although there have been promising results elucidating the neurocognitive mechanisms of SUDs and SUD treatments, the interpretability and reproducibility of these studies is limited by incomplete reporting of participants characteristics, task design, craving assessment, scanning preparation and analysis decisions in fMRI drug cue reactivity (FDCR) experiments. This hampers clinical translation, not least because systematic review and meta-analysis of published work are difficult. This consensus paper and Delphi study aims to outline the important methodological aspects of FDCR research, present structured recommendations for more comprehensive methods reporting and review the FDCR literature to assess the reporting of items that are deemed important. Forty-five FDCR scientists from around the world participated in this study. First, an initial checklist of items deemed important in FDCR studies was developed by several members of the Enhanced NeuroImaging Genetics through Meta-Analyses (ENIGMA) Addiction working group on the basis of a systematic review. Using a modified Delphi consensus method, all experts were asked to comment on, revise or add items to the initial checklist, and then to rate the importance of each item in subsequent rounds. The reporting status of the items in the final checklist was investigated in 108 recently published FDCR studies identified through a systematic review. By the final round, 38 items reached the consensus threshold and were classified under seven major categories: Participants Characteristics, General fMRI Information, General Task Information, Cue Information, Craving Assessment Inside Scanner, Craving Assessment Outside Scanner and Pre- and Post-Scanning Considerations. The review of the 108 FDCR papers revealed significant gaps in the reporting of the items considered important by the experts. For instance, whereas items in the General fMRI Information category were reported in 90.5% of the reviewed papers, items in the Pre- and Post-Scanning Considerations category were reported by only 44.7% of reviewed FDCR studies. Considering the notable and sometimes unexpected gaps in the reporting of items deemed to be important by experts in any FDCR study, the protocols could benefit from the adoption of reporting standards. This checklist, a living document to be updated as the field and its methods advance, can help improve experimental design, reporting and the widespread understanding of the FDCR protocols. This checklist can also provide a sample for developing consensus statements for protocols in other areas of task-based fMRI.
  •  
38.
  •  
39.
  • Fiorentino, M., et al. (författare)
  • Immunohistochemical Expression of BRCA1 in Prostate Cancer
  • 2009
  • Ingår i: Laboratory Investigation. - : Nature Publishing Group. - 0023-6837 .- 1530-0307. ; 22, s. 169A-169A
  • Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
    • Background: BRCA1 is a multifunctional protein involved in DNA repair, gene transcription and the regulation of cell-cycle check-points. While germline mutations of BRCA1 are rare in prostate cancer and seem to play a limited role in tumor susceptibility, BRCA1 expression has not been investigated to date.Design: We analyzed the immunohistochemical expression of BRCA1 in paraffin embedded samples from 524 men with prostate cancer belonging to the Physicians’ Health Study and the Swedish Watchful Waiting cohorts of prostate cancer patients. High density tissue micro-arrays (TMA) including at least three tumor cores for each case were utilized for the immunohistochemical staining with the monoclonal MS110 antibody specific for the N-terminus of the 220 kDa BRCA1 protein. Cases were scored as negative or positive for BRCA1 immunostaining. The Ki67 proliferation index was also assessed on the same TMAs and evaluated by quantitative image analysis.Results: A positive nuclear immunostaining for BRCA1 was revealed in 62 of 524 (11.9%) patients while normal prostate control cores were all negative. BRCA1 positive tumors were associated with 4 times greater proliferation rate compared to BRCA1 negative tumors (p ∼ 0.0003). In addition, we found a linear trend such that tumors with greater number of TMA cores expressing BRCA1 had stronger extent of proliferation. Men with BRCA1 positive tumors had a slightly higher Gleason’s score (mean 7.5) compared to those negative for BRCA1 (mean 7) No significant correlation was found between BRCA1 staining and cancer-specific death.Conclusions: BRCA1 protein is expressed in a small subset of prostate cancers characterized by high proliferation index but not in normal prostate tissue. Expression of BRCA1 might be acquired in selected tumors to prevent DNA damage in actively replicating cells. A different role independent of germline mutations might be disclosed for BRCA1 as cell cycle regulator in prostate cancer.
  •  
40.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 31-40 av 52
Typ av publikation
tidskriftsartikel (47)
konferensbidrag (4)
forskningsöversikt (1)
Typ av innehåll
refereegranskat (50)
övrigt vetenskapligt/konstnärligt (2)
Författare/redaktör
Judson, D. S. (27)
Mengoni, D. (25)
Eberth, J. (25)
Pullia, A. (24)
Reiter, P. (24)
Recchia, F. (23)
visa fler...
Hess, H. (23)
Menegazzo, R. (22)
Michelagnoli, C. (22)
Stezowski, O. (21)
Birkenbach, B. (20)
Gadea, A. (20)
Leoni, S. (20)
Salsac, M. D. (20)
Benzoni, G. (19)
Jungclaus, A. (19)
Korten, W. (19)
Million, B. (19)
Theisen, Ch. (19)
Napoli, D. R. (19)
Valiente-Dobón, J. J ... (18)
Crespi, F.C.L. (18)
Gottardo, A. (18)
Bracco, A. (16)
Maj, A. (16)
Quintana, B. (16)
Simpson, J (15)
de Angelis, G. (15)
Désesquelles, P. (15)
Zielinska, M (14)
Bazzacco, D. (14)
Clement, E. (14)
Harkness-Brennan, L. ... (13)
Boston, H.C. (13)
Gonzalez, V. (12)
Sanchis, E. (12)
Nyberg, Johan, 1955- (12)
Cullen, D. M. (12)
de France, G. (12)
Labiche, M. (12)
Ljungvall, J. (12)
Şahin, E. (12)
Boston, A. J. (12)
Bednarczyk, P. (11)
Camera, F. (11)
Farnea, E. (11)
Lunardi, S. (11)
Podolyak, Zs. (11)
Grebosz, J. (11)
Ciemala, M. (11)
visa färre...
Lärosäte
Uppsala universitet (22)
Lunds universitet (20)
Kungliga Tekniska Högskolan (17)
Karolinska Institutet (5)
Stockholms universitet (3)
Chalmers tekniska högskola (3)
visa fler...
Umeå universitet (2)
Linköpings universitet (2)
Göteborgs universitet (1)
Högskolan Väst (1)
Örebro universitet (1)
visa färre...
Språk
Engelska (52)
Forskningsämne (UKÄ/SCB)
Naturvetenskap (40)
Medicin och hälsovetenskap (6)
Teknik (1)
Samhällsvetenskap (1)

År

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy