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| 3. |
- Kipling, D, et al.
(författare)
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Telomere-dependent senescence
- 1999
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Ingår i: NATURE BIOTECHNOLOGY. - : NATURE AMERICA INC. ; 17:4
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Annan publikation (övrigt vetenskapligt/konstnärligt)
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| 5. |
- Buyanova, Irina, 1960-, et al.
(författare)
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Electronic structure of the 0.88-eV luminescence center in electron-irradiated gallium nitride
- 1999
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Ingår i: Physical review. B, Condensed matter and materials physics. ; 60:3, s. 1746-1751
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Tidskriftsartikel (refereegranskat)abstract
- Photoluminescence (PL) spectroscopy is employed to determine the nature of a near-infrared PL emission with a no-phonon line at ∼0.88 eV, commonly present in electron-irradiated GaN. This PL emission is suggested to originate from an internal transition between a moderately shallow excited state (with an ionization energy ∼21 meV) and the deep ground state (with an ionization energy ∼900 meV) of a deep defect. The existence of a higher-lying second excited state related to the 0.88-eV PL center is also shown from temperature-dependent studies. A different electronic character of the wave functions related to the first and second excited states has been revealed by PL polarization measurements. Since the PL emission has been observed with comparable intensity in all electron-irradiated GaN samples independent of doping on the starting material, it is proposed that either native defects, or common residual contaminants or their complexes are involved. The substitutional ON donor (or related complex) is considered as the most probable candidate, based on the observed striking similarity in the local vibrational properties between the 0.88-eV PL centers and the substitutional OP donor in GaP.
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| 6. |
- López-Puertas, M., et al.
(författare)
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Non-local thermodynamic equilibrium limb radiances for the mipas instrument on Envisat-1
- 1998
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Ingår i: Journal of Quantitative Spectroscopy and Radiative Transfer. - 0022-4073 .- 1879-1352. ; 59:3-5, s. 377-403
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Tidskriftsartikel (refereegranskat)abstract
- An evaluation of the effects that the assumption of local thermodynamic equilibrium (LTE) has on the retrieval of pressure, temperature and the five primary target gases (O3, H2O, CH4, N2O, and HNO3) from spectra to be taken by Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) on the Envisat-1 platform has been conducted. For doing so, non-LTE and LTE limb radiances in the spectral range of 680–2275 cm−1 (4.15–14.6 μm) with a resolution of 0.05 cm−1 at tangent heights from 10 to 70 km have been computed. These calculations included the most updated non-LTE populations of a large number of vibrational levels of the CO2, O3, H2O, CH4, N2O and HNO3 molecules which cause the most prominent atmospheric infrared emissions. A discussion of the most important non-LTE effects on the limb radiances as well as on the retrievals of pressure-temperature and volume mixing ratios of O3, H2O, CH4, N2O, and HNO3 is presented, together with the most important non-LTE issues that could be studied with the future coming of MIPAS data.
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| 7. |
- Newman, D J, et al.
(författare)
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Serum cystatin C measured by automated immunoassay : a more sensitive marker of changes in GFR than serum creatinine
- 1995
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Ingår i: Kidney International. - : Elsevier BV. - 0085-2538. ; 47, s. 312-318
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Tidskriftsartikel (refereegranskat)abstract
- Serum cystatin C has been suggested as a new marker of GFR. For the introduction of this marker into clinical use a rapid and automated method is required. We have developed and validated an assay for serum cystatin C using latex particle-enhanced immunoturbidimetry. Intra- and inter-assay precision were < 3% and < 5% across the assay range. Analytical recovery was 93 +/- 3.8% and no lack of parallelism was demonstrated. Regression analysis of a method comparison with an enzyme-enhanced radial-immunodiffusion method, gave PETIA = 0.074 + 0.93 x SRID, r = 0.98, N = 100. Inter-assay precision profiles showed cystatin C was measured with two-fold better precision than creatinine on the same analyzer. Cystatin C measurement was neither interfered with by icterus nor by hemolysis. 1/cystatin C versus 1/creatinine concentrations gave r = 0.67, N = 469. Comparison of Cr EDTA GFR with 1/cystatin C and 1/creatinine gave r = 0.81 and 0.50, respectively, N = 206. Calculating diagnostic sensitivity for abnormal GFR showed cystatin C to be significantly (P < 0.05) more sensitive than creatinine (71.4 vs. 52.4%). Cystatin C measurement using PETIA technology can be automated on the same instruments used routinely for the measurement of creatinine and offers better analytical performance and probably improved clinical sensitivity as a screening test for early renal damage.
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