| 1. |
- Abt, I, et al.
(author)
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Inclusive V-0 production cross sections from 920 GeV fixed target proton-nucleus collisions
- 2003
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In: European Physical Journal C. Particles and Fields. - : Springer Science and Business Media LLC. - 1434-6044. ; 29:2, s. 181-190
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Journal article (peer-reviewed)abstract
- Inclusive differential cross sections dsigma(pA)/dx(F) and dsigma(pA)/dp(t)(2) for the production of K-S(0), Lambda, and (&ULambda;) over bar particles are measured at HERA in proton-induced reactions on C, Al, Ti, and W targets. The incident beam energy is 920 GeV, corresponding to roots = 41.6 GeV in the proton-nucleon system. The ratios of differential cross sections dsigma(pA)(K-S(0))/dsigma(pA)(Lambda) and dsigma(pA)((&ULambda;) over bar)/dsigma(pA) (Lambda) are measured to be 6.2 +/- 0.5 and 0.66 +/- 0.07, respectively, for x(F) approximate to -0.06. No significant dependence upon the target material is observed. Within errors, the slopes of the transverse momentum distributions da,Ald t also show no significant dependence upon the target material. The dependence of the extrapolated total cross sections sigma(pA) on the atomic mass A of the target material is discussed, and the deduced cross sections per nucleon sigma(pN) are compared with results obtained at other energies.
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| 2. |
- Abt, I, et al.
(author)
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Measurement of the b(b)over-bar production cross section in 920 GeV fixed-target proton-nucleus collisions
- 2003
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In: European Physical Journal C. Particles and Fields. - : Springer Science and Business Media LLC. - 1434-6044. ; 26:3, s. 345-355
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Journal article (peer-reviewed)abstract
- Using the HERA-B detector, the b (b) over bar production cross section has been measured in 920 GeV proton collisions on carbon and titanium targets. The b (b) over bar production was tagged via inclusive bottom quark decays into J/psi by exploiting the longitudinal separation of J/psi --> l(+)l(-) decay vertices from the primary proton-nucleus interaction. Both e(+)e(-) and mu(+)mu(-) channels have been reconstructed and the combined analysis yields the cross section sigma(b (b) over bar) = 32(-12)(+14)(stat) (+6)(-7)(sys) nb/nucleon.
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| 3. |
- Ivarsson, Stefan, et al.
(author)
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Improved oscillator strengths and wavelengths for Os I and Ir I, and new results on early r-process nucleosynthesis
- 2003
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In: Astronomy & Astrophysics. - : EDP Sciences. - 0004-6361 .- 1432-0746. ; 409:3, s. 1141-1149
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Journal article (peer-reviewed)abstract
- The radioactive decay of 238U and 232Th has recently been used to determine ages for some of the oldest stars in the Universe. This has highlighted the need for accurate observational constraints on production models for the heaviest r-process elements which might serve as stable references, notably osmium and iridium. In order to provide a firmer basis for the observed abundances, we have performed laser-induced fluorescence measurements and Fourier Transform Spectroscopy to determine new radiative lifetimes and branching fractions for selected levels in Os I and Ir I. From these data, we determine new absolute oscillator strengths and improved wavelengths for18 Os I and 4 Ir I lines. A reanalysis of VLT spectra of CS 31082-001and new results for other stars with Os and Ir detections show that (i):the lines in the UV and lambda 4260 yield reliable Os abundances, while those at lambda lambda 4135, 4420 are heavily affected by blending; (ii): the Os and Ir abundances are identical in all the stars; (iii): the heavy-element abundances in very metal-poor stars conform closely to the scaled solar r-process pattern throughout the range 56 <= Z <= 77; and (iv): neither Os or Ir nor any lighter species are suitable as reference elements for the radioactive decay of Th and U.Based in part on observations obtained with the Very Large Telescope of the European Southern Observatory at Paranal, Chile.
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| 7. |
- Nilsson, H., et al.
(author)
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Measurements of Transition Probabilities for Complex Ions
- 2003
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In: Physica Scripta. - : Institute of Physics Publishing (IOPP). - 0031-8949 .- 1402-4896. ; T105:1, s. 61-61
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Journal article (peer-reviewed)abstract
- Fourier transform spectroscopy has proven to be a useful tool when measuring wavelengths and branching fractions. The high spectral resolution makes it possible to extend and improve term analyses of complex spectra. We present an overview of our measurements with the Fourier transform spectrometer at Lund Observatory. Much of our work is motivated by astrophysical problems, and we show an application of some of our measurements related to the age determination of the Galaxy.
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| 8. |
- Spentchian, M, et al.
(author)
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Severe hypophosphatasia: Characterization of fifteen novel mutations in the ALPL gene
- 2003
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In: Human Mutation. - : Hindawi Limited. - 1059-7794. ; 22:1, s. 105-106
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Journal article (peer-reviewed)abstract
- Hypophosphatasia is an inherited disorder characterized by defective bone mineralization and deficiency of serum and tissue liver/bone/kidney alkaline phosphatase (L/B/K ALP) activity. We report the characterization of ALPL gene mutations in a series of 11 families from various origins affected by perinatal and infantile hypophosphatasia. Sixteen distinct mutations were found, fifteen of them not previously reported: M45V, G46R, 388-391delGTAA, 389delT, T131I, G145S, D172E, 662delG, G203A, R255L, 876-881delAGGGGA, 962delG, E294K, E435K, and A451T. This confirms that severe hypophosphatasia is due to a large spectrum of mutations in Caucasian populations.
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| 9. |
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| 10. |
- Weng, J., et al.
(author)
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Functional consequences of mutations in the MODY4 gene (IPF1) and coexistence with MODY3 mutations
- 2001
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In: Diabetologia. - : Springer Science and Business Media LLC. - 1432-0428 .- 0012-186X. ; 44:2, s. 249-258
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Journal article (peer-reviewed)abstract
- Aims/hypothesis. The aim of this study was to examine the putative role of mutations in the insulin promoter 1 (IPF1) gene in early-onset diabetes. Methods. We carried out mutation screening of the IPF1 gene in 115 Scandinavian families with at least two members with onset of diabetes younger than 40 years. The allele frequencies were also tested in 183 unrelated patients with late-onset Type II (noninsulin-dependent) diabetes mellitus and in 92 nondiabetic control subjects. Results. Two novel IPF1 variants (G212R and P239Q) and one previously reported (D76N) IPF1 variant were identified in the 115 families (3.5%). The D76N variant was found in one MODY3 family (S315fsinsA of HNF1 alpha) and also in two families with late-onset Type II diabetes. The P239Q variant was identified in two families with early-onset diabetes including one with MODY3 (R272C of HNF1 alpha) and in three families with late-onset Type II diabetes. Despite the fact that the variants did not segregate completely with diabetes, the non-diabetic carriers of the IPF1 variants had increased blood glucose concentrations (p < 0.05) and reduced insulin:glucose ratios (p < 0.05) during an oral glucose tolerance test compared with non-diabetic family members without these variants. In addition, when the G212R and P239Q variants were expressed in cells without IPF1 i.e.. Nes2y cells, both variants showed about a 50% reduction in their ability to activate insulin gene transcription compared to wild-type IPF1, as measured by reporter gene assay. Conclusion/interpretation. Although mutations in the IPF-1 gene are rare in early- (3.5%) and late-onset (2.7%) Type II diabetes, they are functionally important and occur also in families with other MODY mutations.
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