1,588 research outputs found

    Menstrual disorders in rural Gambia.

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    As part of a community-based reproductive morbidity survey in rural Gambia, the prevalence and association of menstrual disorders with sociodemographic characteristics and other reproductive morbidities, and with knowledge, attitudes, and beliefs concerning menstrual problems were assessed. A questionnaire was administered by a field-worker and by a gynecologist, who also examined the women. Semistructured interviews were conducted to assess knowledge, attitudes, and beliefs in a subsample. Of 607 menstruating women not using hormonal contraceptives, 16 percent complained to the gynecologist of irregular cycles, 14 percent of dysmenorrhea, 8 percent of spotting, and 4 percent of heavy or prolonged bleeding. Each complaint was associated with other reproductive morbidities. A minority of women with menstrual problems had sought health care, and menstruation was revealed to be a highly personal and secretive topic in this population. Menstrual disorders constitute an important unaddressed area of reproductive health service needs in developing countries for which relatively simple and inexpensive therapies are often available. Information, education, and support combined with clinical management of menstrual problems should be core elements of reproductive health programs

    Hyperfine interaction and magnetoresistance in organic semiconductors

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    We explore the possibility that hyperfine interaction causes the recently discovered organic magnetoresistance (OMAR) effect. Our study employs both experiment and theoretical modelling. An excitonic pair mechanism model based on hyperfine interaction, previously suggested by others to explain magnetic field effects in organics, is examined. Whereas this model can explain a few key aspects of the experimental data, we, however, uncover several fundamental contradictions as well. By varying the injection efficiency for minority carriers in the devices, we show experimentally that OMAR is only weakly dependent on the ratio between excitons formed and carriers injected, likely excluding any excitonic effect as the origin of OMAR.Comment: 10 pages, 7 figures, 1 tabl

    Temperature dependent photoluminescence of organic semiconductors with varying backbone conformation

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    We present photoluminescence studies as a function of temperature from a series of conjugated polymers and a conjugated molecule with distinctly different backbone conformations. The organic materials investigated here are: planar methylated ladder type poly para-phenylene, semi-planar polyfluorene, and non-planar para hexaphenyl. In the longer-chain polymers the photoluminescence transition energies blue shift with increasing temperatures. The conjugated molecules, on the other hand, red shift their transition energies with increasing temperatures. Empirical models that explain the temperature dependence of the band gap energies in inorganic semiconductors can be extended to explain the temperature dependence of the transition energies in conjugated molecules.Comment: 8 pages, 9 figure

    Structure and dynamics of nondilute polyfluorene solutions

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    The rotational and translational diffusion dynamics of newly synthesized polyfluorenes were studied by dynamic light scattering over a broad concentration range up to the lyotropic state. On the basis of small-angle neutron scattering and translational diffusion measurements in dilute solutions. the single polymers were described as wormlike chains with a low persistent length l = 7 +/- 0.5 nm and cross-section diameter d = 1.8 +/- 0.5 nm. In the semidilute concentration regime, the rate of increase of the cooperative diffusion and the osmotic pressure with c/c* (c* being the overlap concentration) was lower than for linear flexible chains in good solvent. The intermediate scattering function displayed a second process assigned to chain relaxation, in reasonable agreement with the longest relaxation time obtained from shear rheometry. The bimodal shape of the orientation correlation function, which is a characteristic feature of shape persistent polymers and exhibits a peculiar dependence on the scattering angle, was also observed in this model system. The fuzzy cylinder model adequately represented the concentration dependence of the osmotic modulus and the chain orientation time, conforming to the wormlike nature of these polymers

    Involvement of Plasmodium falciparum protein kinase CK2 in the chromatin assembly pathway

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    <p>Abstract</p> <p>Background</p> <p>Protein kinase CK2 is a pleiotropic serine/threonine protein kinase with hundreds of reported substrates, and plays an important role in a number of cellular processes. The cellular functions of <it>Plasmodium falciparum </it>CK2 (PfCK2) are unknown. The parasite's genome encodes one catalytic subunit, PfCK2α, which we have previously shown to be essential for completion of the asexual erythrocytic cycle, and two putative regulatory subunits, PfCK2β1 and PfCK2β2.</p> <p>Results</p> <p>We now show that the genes encoding both regulatory PfCK2 subunits (PfCK2β1 and PfCK2β2) cannot be disrupted. Using immunofluorescence and electron microscopy, we examined the intra-erythrocytic stages of transgenic parasite lines expressing hemagglutinin (HA)-tagged catalytic and regulatory subunits (HA-CK2α, HA-PfCK2β1 or HA-PfCK2β2), and localized all three subunits to both cytoplasmic and nuclear compartments of the parasite. The same transgenic parasite lines were used to purify PfCK2β1- and PfCK2β2-containing complexes, which were analyzed by mass spectrometry. The recovered proteins were unevenly distributed between various pathways, with a large proportion of components of the chromatin assembly pathway being present in both PfCK2β1 and PfCK2β2 precipitates, implicating PfCK2 in chromatin dynamics. We also found that chromatin-related substrates such as nucleosome assembly proteins (Naps), histones, and two members of the Alba family are phosphorylated by PfCK2α <it>in vitro</it>.</p> <p>Conclusions</p> <p>Our reverse-genetics data show that each of the two regulatory PfCK2 subunits is required for completion of the asexual erythrocytic cycle. Our interactome study points to an implication of PfCK2 in many cellular pathways, with chromatin dynamics being identified as a major process regulated by PfCK2. This study paves the way for a kinome-wide interactomics-based approach to elucidate protein kinase function in malaria parasites.</p

    Effect of side-chain asymmetry on the intermolecular structure and order-disorder transition in alkyl-substituted polyfluorenes

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    We study relations among the side-chain asymmetry, structure, and order-disorder transition (ODT) in hairy-rod-type poly(9,9-dihexylfluorene) (PF6) with two identical side chains and atactic poly(9-octyl-9-methylfluorene) (PF1-8) with two different side chains per repeat. PF6 and PF1-8 organize into alternating side-chain and backbone layers that transform into an isotropic phase at T-ODT(PF6) and T-bi(ODT)(PF1-8). We interpret polymers in terms of monodisperse and bidisperse brushes and predict scenarios T-ODT <T-bi(ODT) and T-ODT similar to T-bi(ODT) for high and low grafting densities (the side-chain length above or below the average grafting distance). Calorimetry and x-ray scattering indicate the condition T-ODT(PF6) similar to T-bi(ODT)(PF1-8) following the low grafting prediction. PF6 side chains coming from the alternating backbone layers appear as two separate layers with thickness H(PF6), whereas PF1-8 side chains appear as an indistinguishable bilayer with a half thickness H-bilayer(PF1-8)/2 approximate to H(PF6). The low grafting density region is structurally possible but not certain for PF6 and confirmed for PF1-8.Peer reviewe

    Spectral and Photophysical Studies of Poly[2,6-(1,5-dioctylnaphthalene)]thiophenes

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    A complete spectroscopic and photophysical study of three alternating naphthalene-α-thiophene copolymers was undertaken in solution (room and low temperature) and in the solid state (thin films in a Zeonex matrix). The study comprises absorption, emission, and triplet−triplet spectra together with quantitative measurements of quantum yield (fluorescence, intersystem-crossing, internal conversion, and singlet oxygen formation) lifetimes and singlet and triplet energies. The overall data allow the determination of the rate constants for all the decay processes. Comparison between the behavior of analogous 1-naphthyl(oligo)thiophenes and the 2,6-naphthalene(oligo)thiophene copolymers allows several important observations. First, the polymers display higher fluorescence quantum yields and lower S1→T1 intersystem-crossing yields than the oligomers. This can be attributed to the presence of the 1,5-dioctyloxynaphthalene groups in the copolymers leading to a more rigid polymer backbone, which decreases radiationless deactivation and increases the radiative efficiency. Second, the singlet and triplet energies are significantly lower in the polymers than with the corresponding oligomers. This implies a lower HOMO−LUMO energy difference in the polymers due to an extended π-delocalization. Third, the singlet-to-triplet (S1−T1) energy splitting is higher in the oligomers than with the polymers, even though the former display higher intersystem-crossing yields. It is suggested that this may result from intersystem-crossing in the oligomers involving significant charge-transfer (CT) character (spin-orbit coupling is mediated by CT mixing involving the singlet and triplet states in matrix elements of the type 1ΨCT |H‘|3Ψ1) of the relevant excited states but that is less important with the polymers. We believe that this may be relevant to understanding the nature of CT states in conjugated copolymers

    Excited States of Ladder-type Poly-p-phenylene Oligomers

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    Ground state properties and excited states of ladder-type paraphenylene oligomers are calculated applying semiempirical methods for up to eleven phenylene rings. The results are in qualitative agreement with experimental data. A new scheme to interpret the excited states is developed which reveals the excitonic nature of the excited states. The electron-hole pair of the S1-state has a mean distance of approximately 4 Angstroem.Comment: 24 pages, 21 figure
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