| 1. |
- Forsberg, Ulrika, et al.
(författare)
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Spectroscopic Tools Applied to Element Z = 115 Decay Chains
- 2014
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Ingår i: EPJ Web of Conferences. - : EDP Sciences. - 2100-014X .- 2101-6275. - 9782759811755 - 9782759811762 ; 66, s. 02036-02036
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Konferensbidrag (refereegranskat)abstract
- Nuclides that are considered to be isotopes of element Z = 115 were produced in the reaction 48Ca + 243Am at the GSI Helmholtzzentrum für Schwerionenforschung Darmstadt. The detector setup TASISpec was used. It was mounted behind the gas-filled separator TASCA. Thirty correlated α-decay chains were found, and the energies of the particles were determined with high precision. Two important spectroscopic aspects of the offline data analysis are discussed in detail: the handling of digitized preamplified signals from the silicon strip detectors, and the energy reconstruction of particles escaping to upstream detectors relying on pixel-by-pixel dead-layer thicknesses.
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| 2. |
- Rudolph, Dirk, et al.
(författare)
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Alpha-Photon Coincidence Spectroscopy Along Element 115 Decay Chains
- 2014
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Ingår i: Acta Physica Polonica. Series B: Elementary Particle Physics, Nuclear Physics, Statistical Physics, Theory of Relativity, Field Theory. - 0587-4254. ; 45, s. 263-272
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Tidskriftsartikel (refereegranskat)abstract
- Produced in the reaction 48Ca+243Am, thirty correlated α-decay chains were observed in an experiment conducted at the GSI Helmholzzentrum für Schwerionenforschung, Darmstadt, Germany. The decay chains are basically consistent with previous findings and are considered to originate from isotopes of element 115 with mass numbers 287, 288, and 289. A set-up aiming specifically for high-resolution charged particle and photon coincidence spectroscopy was placed behind the gas-filled separator TASCA. For the first time, γ rays as well as X-ray candidates were observed in prompt coincidence with the α-decay chains of element 115.
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| 3. |
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| 4. |
- Rudolph, Dirk, et al.
(författare)
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Spectroscopy of Element 115 Decay Chains
- 2013
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Ingår i: Physical Review Letters. - 1079-7114. ; 111:11
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Tidskriftsartikel (refereegranskat)abstract
- A high-resolution , X-ray and gamma-ray coincidence spectroscopy experiment was conducted at the GSI Helmholtzzentrum für Schwerionenforschung. Thirty correlated alpha-decay chains were detected following the fusion-evaporation reaction 48Ca + 243Am. The observations are consistent with previous assignments of similar decay chains to originate from element Z = 115. For the first time, precise spectroscopy allows the derivation of excitation schemes of isotopes along the decay chains starting with elements Z > 112. Comprehensive Monte-Carlo simulations accompany the data analysis. Nuclear structure models provide a first level interpretation.
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| 6. |
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| 7. |
- Ragnarsson, Ingemar, et al.
(författare)
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Terminating States In Z=71 Lu Nuclei With N Approximate To 90
- 2010
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Ingår i: International Journal of Modern Physics E. - 0218-3013. ; 19:4, s. 590-600
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Tidskriftsartikel (refereegranskat)abstract
- The high-spin yrast states in Lu-161 are calculated in a Cranked Nilsson-Strutinsky approach keeping track of configurations and their evolution with spin. The outcome from calculations neglecting pairing and including pairing are compared. It is predicted that several yrast region configurations terminate at a very favored energy around I = 50 and that one of the observed bands is two transitions short of termination.
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| 8. |
- Sukalo, Maja, et al.
(författare)
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Mutations in the Human UBR1 Gene and the Associated Phenotypic Spectrum
- 2014
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Ingår i: Human Mutation. - : Hindawi Limited. - 1059-7794 .- 1098-1004. ; 35:5, s. 521-531
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Tidskriftsartikel (refereegranskat)abstract
- Johanson-Blizzard syndrome (JBS) is a rare, autosomal recessive disorder characterized by exocrine pancreatic insufficiency, typical facial features, dental anomalies, hypothyroidism, sensorineural hearing loss, scalp defects, urogenital and anorectal anomalies, short stature, and cognitive impairment of variable degree. This syndrome is caused by a defect of the E3 ubiquitin ligase UBR1, which is part of the proteolytic N-end rule pathway. Herein, we review previously reported (n=29) and a total of 31 novel UBR1 mutations in relation to the associated phenotype in patients from 50 unrelated families. Mutation types include nonsense, frameshift, splice site, missense, and small in-frame deletions consistent with the hypothesis that loss of UBR1 protein function is the molecular basis of JBS. There is an association of missense mutations and small in-frame deletions with milder physical abnormalities and a normal intellectual capacity, thus suggesting that at least some of these may represent hypomorphic UBR1 alleles. The review of clinical data of a large number of molecularly confirmed JBS cases allows us to define minimal clinical criteria for the diagnosis of JBS. For all previously reported and novel UBR1 mutations together with their clinical data, a mutation database has been established at LOVD.
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