511 research outputs found

    Three-dimensional effects in polarization signatures as observed from precipitating clouds by low frequency ground-based microwave radiometers

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    International audienceConsistent negative polarization differences (i.e. differences between the vertical and the horizontal brightness temperature) are observed when looking at precipitating systems by ground-based radiometers at slant angles. These signatures can be partially explained by one-dimensional radiative transfer computations that include oriented non-spherical raindrops. However some cases are characterized by polarization values that exceed differences expected from one-dimensional radiative transfer. A three-dimensional fully polarized Monte Carlo model has been used to evaluate the impact of the horizontal finiteness of rain shafts with different rain rates at 10, 19, and 30 GHz. The results show that because of the reduced slant optical thickness in finite clouds, the polarization signal can strongly differ from its one-dimensional counterpart. At the higher frequencies and when the radiometer is positioned underneath the cloud, significantly higher negative values for the polarization are found which are also consistent with some observations. When the observation point is located outside of the precipitating cloud, typical polarization patterns (with troughs and peaks) as a function of the observation angle are predicted. An approximate 1-D slant path radiative transfer model is considered as well and results are compared with the full 3-D simulations to investigate whether or not three-dimensional effects can be explained by geometry effects alone. The study has strong relevance for low-frequency passive microwave polarimetric studies

    Purification and analytical characterization of an anti- CD4 monoclonal antibody for human therapy

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    A purification process for the monclonal anti-CD4 antibody MAX.16H5 was developed on an analytical scale using (NH&SO, precipitation, anion-exchange chromatography on MonoQ or Q-Sepharose, hydrophobic interaction chromatography on phenyl- Sepharose and gel filtration chromatography on Superdex 200. The purification schedule was scaled up and gram amounts of MAX.16H5 were produced on corresponding BioPilot columns. Studies of the identity, purity and possible contamination by a broad range of methods showed that the product was highly purified and free from contaminants such as mouse DNA, viruses, pyrogens and irritants. Overall, the analytical data confirm that the monoclonal antibody MAX.16H5 prepared by this protocol is suitable for human therapy

    Statistical characteristics of surrogate data based on geophysical measurements

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    In this study, the statistical properties of a range of measurements are compared with those of their surrogate time series. Seven different records are studied, amongst others, historical time series of mean daily temperature, daily rain sums and runoff from two rivers, and cloud measurements. Seven different algorithms are used to generate the surrogate time series. The best-known method is the iterative amplitude adjusted Fourier transform (IAAFT) algorithm, which is able to reproduce the measured distribution as well as the power spectrum. Using this setup, the measurements and their surrogates are compared with respect to their power spectrum, increment distribution, structure functions, annual percentiles and return values. It is found that the surrogates that reproduce the power spectrum and the distribution of the measurements are able to closely match the increment distributions and the structure functions of the measurements, but this often does not hold for surrogates that only mimic the power spectrum of the measurement. However, even the best performing surrogates do not have asymmetric increment distributions, i.e., they cannot reproduce nonlinear dynamical processes that are asymmetric in time. Furthermore, we have found deviations of the structure functions on small scales

    Human Periodontal Fibroblast Response to Enamel Matrix Derivative, Amelogenin, and Platelet‐Derived Growth Factor‐BB

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    Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/142271/1/jper1242.pd

    RDE-2 interacts with MUT-7 to mediate RNA interference in Caenorhabditis elegans

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    In Caenorhabditis elegans, the activity of transposable elements is repressed in the germline. One of the mechanisms involved in this repression is RNA interference (RNAi), a process in which dsRNA targets cleavage of mRNAs in a sequence-specific manner. The first gene found to be involved in RNAi and transposon silencing in C.elegans is mut-7, a gene encoding a putative exoribonuclease. Here, we show that the MUT-7 protein resides in complexes of ∼250 kDa in the nucleus and in the cytosol. In addition, we find that upon triggering of RNAi the cytosolic MUT-7 complex increases in size. This increase is independent of the presence of target RNA, but does depend on the presence of RDE-1 and RDE-4, two proteins involved in small interfering RNA (siRNA) production. Finally, using a yeast two-hybrid screen, we identified RDE-2/MUT-8 as one of the other components of this complex. This protein is encoded by the rde-2/mut-8 locus, previously implicated in RNAi and transposon silencing. Using genetic complementation analysis, we show that the interaction between these two proteins is required for efficient RNAi in vivo. Together these data support a role for the MUT-7/RDE-2 complex downstream of siRNA formation, but upstream of siRNA mediated target RNA recognition, possibly indicating a role in the siRNA amplification step

    A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II

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    The dentin sialophosphoprotein (DSPP) gene (4q21.3) encodes two major noncollagenous dentin matrix proteins: dentin sialoprotein (DSP) and dentin phosphoprotein (DPP). Defects in the human gene encoding DSPP cause inherited dentin defects, and these defects can be associated with bilateral progressive high-frequency sensorineural hearing loss. Clinically, five different patterns of inherited dentin defects are distinguished and are classified as dentinogenesis imperfecta (DGI) types I, II, and III, and dentin dysplasia types I and II. The genetic basis for this clinical heterogeneity is unknown. Among the 11 members recruited from the studied kindred, five were affected with autosomal dominant DGI type II. The mutation (g.1188C→G, IVS2-3C→G) lay in the third from the last nucleotide of intron 2 and changed its sequence from CAG to GAG. The mutation was correlated with the affection status and was absent in 104 unaffected individuals (208 alleles) with the same ethnic and geological background. The proband was in the primary dentition stage and presented with multiple pulp exposures. The occlusal surface of his dental enamel was generally abraded, and the dentin was heavily worn and uniformly shaded brown. The dental pulp chambers appeared originally to be within normal limits without any sign of obliteration, but over time (by age 4), the pulp chambers became partially or completely obliterated. The oldest affected member (age 59) showed mild hearing loss at high-frequency (8 kHz). Permanent dentition was severely affected in the adults, who had advanced dental attrition, premature loss of teeth, and extensive dental reconstruction.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/47593/1/439_2004_Article_1143.pd
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