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Träfflista för sökning "WFRF:(Torres V.) srt2:(2000-2004)"

Sökning: WFRF:(Torres V.) > (2000-2004)

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1.
  • Markevich, V.P., et al. (författare)
  • Electronic properties of vacancy-oxygen complexes in SiGe alloys
  • 2003
  • Ingår i: Physica. B, Condensed matter. - : Elsevier BV. - 0921-4526 .- 1873-2135. ; 340, s. 790-4
  • Tidskriftsartikel (refereegranskat)abstract
    • Capacitance transient techniques, combined with ab initio modeling, were employed to study the electronic properties and structure of vacancy-oxygen (VO) complexes in unstrained Czochralski-grown Si1-xGex crystals (0
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  • Von Clarmann, T., et al. (författare)
  • A blind test retrieval experiment for infrared limb emission spectrometry
  • 2003
  • Ingår i: Journal of Geophysical Research - Atmospheres. - 2169-897X .- 2169-8996. ; 108:D23
  • Tidskriftsartikel (refereegranskat)abstract
    • The functionality and characteristics of six different data processors (i.e., retrieval codes in their actual software and hardware environment) for analysis of high-resolution limb emission infrared spectra recorded by the space-borne Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) have been validated by means of a blind test retrieval experiment based on synthetic spectra. For this purpose a self-consistent set of atmospheric state parameters, including pressure, temperature, vibrational temperatures, and abundances of trace gases and aerosols, has been generated and used as input for radiative transfer calculations for MIPAS measurement geometry and configuration. These spectra were convolved with the MIPAS field of view, spectrally degraded by the MIPAS instrument line shape, and, finally, superimposed with synthetic measurement noise. These synthetic MIPAS measurements were distributed among the participants of the project “Advanced MIPAS level-2 data analysis” (AMIL2DA), who performed temperature and species abundance profile retrievals by inverse radiative transfer calculations. While the retrieved profiles of atmospheric state parameters reflect some characteristics of the individual data processors, it was shown that all the data processors under investigation are capable of producing reliable results in the sense that deviations of retrieved results from the reference profiles are within the margin that is consistent with analytical error estimation.
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  • Coutinho, J., et al. (författare)
  • Electronic structure of divacancy-hydrogen complexes in silicon
  • 2003
  • Ingår i: Journal of Physics. - : IOP Publishing. - 0953-8984 .- 1361-648X. ; 15:39, s. S2809-S2814
  • Tidskriftsartikel (refereegranskat)abstract
    • Divacancy-hydrogen complexes (V2H and V2H2) in Si are studied by ab initio modelling using large supercells. Here we pay special attention to their electronic structure, showing that these defects produce deep carrier traps. Calculated electrical gap levels indicate that V2H2 is an acceptor, whereas V2H is amphoteric, with levels close to those of the well known divacancy. Finally our results are compared with the available data from deep level transient spectroscopy and electron paramagnetic resonance experiments.
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  • Leigh, R. S., et al. (författare)
  • Vibrational modes of sulfur defects in GaP
  • 2003
  • Ingår i: Physical Review B. Condensed Matter and Materials Physics. - 1098-0121 .- 1550-235X. ; 68:3
  • Tidskriftsartikel (refereegranskat)abstract
    • First principles calculations carried out on GaP containing sulfur donors 32SP (95%) and34SP (5%) show that both the neutral and ionized donors are located on substitutional sites and have weak S-Ga bonds. For the sulfur impurity in its positive charge state the calculations give gap modes for 32S and34S at frequencies close to those found experimentally. Modes within the gap are also predicted for neutral sulfur at frequencies within a few cm-1 of their charged-state counterparts. However, the SP0 donor has a very low apparent charge (i.e. oscillator strength), its calculated integrated absorption cross section being only ∼3% of that for the SP+ defect. These results support an earlier explanation of the failure to detect gap modes from SP0 in infrared measurements. Calculated and observed apparent charges for the SP+ donor are compared, and the importance of taking due account of the different geometries that apply to the theoretical calculations and infrared experiments is emphasized.
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  • Millar, D S, et al. (författare)
  • Molecular genetic analysis of severe protein C deficiency
  • 2000
  • Ingår i: Human Genetics. - : Springer Science and Business Media LLC. - 1432-1203 .- 0340-6717. ; 106:6, s. 646-653
  • Tidskriftsartikel (refereegranskat)abstract
    • Severe protein C deficiency is a rare, early onset, venous thrombotic condition that is inherited as an autosomal recessive trait. The protein C (PROC) genes of nine unrelated individuals with severe protein C deficiency were sequenced yielding a total of 13 different lesions. Eight of these were novel, including a gross gene deletion, three missense mutations, two micro-deletions, a splicing mutation and a single base-pair substitution in the HNF-3 binding site in the PROC gene promoter. Evidence for the pathogenicity of the mutations detected was obtained by molecular modelling, in vitro splicing assay and reporter gene assay. Neither the plasma protein C activity level nor the nature of the PROC gene lesions detected were found to be a good prognostic indicator of the age of onset or clinical severity of thrombotic symptoms. Other factors may thus complicate the relationship between genotype and clinical phenotype. Indeed, in two patients, the inheritance of either one or two Factor V Leiden alleles in addition to two PROC gene lesions could have served to precipitate the thrombotic events. No association was however apparent between clinical severity and the possession of a particular promoter polymorphism genotype. Despite the absence of a clear genotype-phenotype relationship, the molecular genetic analysis of the severe recessive form of protein C deficiency potentiates both the counselling of affected families and the provision of antenatal exclusion diagnosis.
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