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The effects of laser-plasma interactions (LPI) on the dynamics of inertial confinement fusion hohlraums are investigated via a new approach that self-consistently couples reduced LPI models into radiation-hydrodynamics numerical codes. The interplay between hydrodynamics and LPI-specifically stimulated Raman scatter and crossed-beam energy transfer (CBET)-mostly occurs via momentum and energy deposition into Langmuir and ion acoustic waves. This spatially redistributes energy coupling to the target, which affects the background plasma conditions and thus, modifies laser propagation. This model shows reduced CBET and significant laser energy depletion by Langmuir waves, which reduce the discrepancy between modeling and data from hohlraum experiments on wall x-ray emission and capsule implosion shape.
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INTRODUCTION: An awareness of Professional Identity (PI), an individual's identity in relation to their professional group, and Role Perception (RP), an individual's view of their specific role, may enable safe and effective practice by providing an understanding of professional boundaries, behaviours and activities. This research aimed to explore and gain an understanding of the PI and RP of Radiographers and Clinical Technologists working as Nuclear Medicine Technologists (NMT's). METHODS: 10 NMT's were recruited from a large National Health Service (NHS) Trust. Utilising the established methodology of Qualitative Description, data was obtained using semi-structured interviews and analysed using inductive thematic analysis. RESULTS: Four themes were identified: "Becoming the Unexpected" which detailed various training pathways; "Caring with Science" which described the NMT's role and defined their PI; "Same View, Different Lens" which portrayed how Radiographers and Clinical Technologists practise as team of NMT's; and "Confirmation of Professional Self" which presented how individuals view their professional status. CONCLUSION: The study showed that the NMT role is highly specialised, multi-faceted and patient-centred. Their professional status is based on the nature of their role and their university level education and training. They work together under the umbrella title of NMT with a dual professional identity of "provider of care" and "user of science and technology". However, they may have an individual identity of Radiographer or Clinical Technologist that is determined by their training pathway. IMPLICATIONS FOR PRACTICE: This research has provided valuable understanding of the PI and RP of NMT's. By highlighting the differences in the regulatory status of this workforce, an insight into the future implications in the context of national healthcare planning has been provided, highlighting potentially significant issues that may impact on the manner in which NMT's can practice.
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Medicina Nuclear , Humanos , Medicina Estatal , Técnicos Medios en Salud , Cintigrafía , PercepciónRESUMEN
First observations of the Cabibbo-suppressed decays B(0) â D(+)K(-)π(+)π(-) and B(-) â D(0)K(-)π(+)π(-) are reported using 35 pb(-1) of data collected with the LHCb detector. Their branching fractions are measured with respect to the corresponding Cabibbo-favored decays, from which we obtain B(B(0) â D(+)K(-)π(+)π(-))/B(B(0) â D(+)π(-)π(+)π(-))=(5.9±1.1±0.5)×10(-2) and B(B(-) â D(0)K(-)π(+)π(-))/B(B(-) â D(0)π(-)π(+)π(-))=(9.4±1.3±0.9)×10(-2), where the uncertainties are statistical and systematic, respectively. The B(-) â D(0)K(-)π(+)π(-) decay is particularly interesting, as it can be used in a similar way to B(-) â D(0)K(-) to measure the Cabibbo-Kobayashi-Maskawa phase γ.
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The angular distributions and the partial branching fraction of the decay B0 â K*0 µ+ µ- are studied by using an integrated luminosity of 0.37 fb(-1) of data collected with the LHCb detector. The forward-backward asymmetry of the muons, A(FB), the fraction of longitudinal polarization, F(L), and the partial branching fraction dB/dq2 are determined as a function of the dimuon invariant mass. The measurements are in good agreement with the standard model predictions and are the most precise to date. In the dimuon invariant mass squared range 1.00-6.00 GeV2/c4, the results are A(FB)=-0.06(-0.14)(+0.13)±0.04, F(L)=0.55±0.10±0.03, and dB/dq2=(0.42±0.06±0.03)×10(-7) c4/GeV2. In each case, the first error is statistical and the second systematic.
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A search is performed for the lepton number violating decay B+ â h- µ+ µ+, where h- represents a K- or a π-, using an integrated luminosity of 36 pb(-1) of data collected with the LHCb detector. The decay is forbidden in the standard model but allowed in models with a Majorana neutrino. No signal is observed in either channel and limits of B(B+ â K- µ+ µ+) < 5.4×10(-8) and B(B+ â π- µ+ µ+) < 5.8×10(-8) are set at the 95% confidence level. These improve the previous best limits by factors of 40 and 30, respectively.
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We present a measurement of the time-dependent CP-violating asymmetry in B(s)(0) â J/ψÏ decays, using data collected with the LHCb detector at the LHC. The decay time distribution of B(s)(0) â J/ψÏ is characterized by the decay widths Γ(H) and Γ(L) of the heavy and light mass eigenstates, respectively, of the B(s)(0) - B(s)(0) system and by a CP-violating phase Ï(s). In a sample of about 8500 B(s)(0) â J/ψÏ events isolated from 0.37 fb(-1) of pp collisions at sqrt[s] = 7 TeV, we measure Ï(s) = 0.15 ± 0.18(stat) ± 0.06(syst) rad. We also find an average B(s)(0) decay width Γ(s) ≡ (Γ(L) + Γ(H))/2 = 0.657 ± 0.009(stat) ± 0.008(syst) ps(-1) and a decay width difference ΔΓ(s) ≡ Γ(L) - Γ(H) = 0.123 ± 0.029(stat) ± 0.011(syst) ps(-1). Our measurement is insensitive to the transformation (Ï(s),ΔΓ(s)) ⦠(π - Ï(s), -ΔΓ(s)).
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A search for time-integrated CP violation in D(0)âh(-)h(+) (h=K, π) decays is presented using 0.62 fb(-1) of data collected by LHCb in 2011. The flavor of the charm meson is determined by the charge of the slow pion in the D(*+)âD(0)π(+) and D(*-)âD[over ¯](0)π(-) decay chains. The difference in CP asymmetry between D(0)âK(-)K(+) and D(0)âπ(-)π(+), ΔA(CP)≡A(CP)(K(-)K(+))-A(CP)(π(-)π(+)), is measured to be [-0.82±0.21(stat)±0.11(syst)]%. This differs from the hypothesis of CP conservation by 3.5 standard deviations.
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The decay B(s)(0) â J/ψK+ K- is investigated using 0.16 fb(-1) of data collected with the LHCb detector using 7 TeV pp collisions. Although the J/ψÏ channel is well known, final states at higher K+ K- masses have not previously been studied. In the K+ K- mass spectrum we observe a significant signal in the f(2)'(1525) region as well as a nonresonant component. After subtracting the nonresonant component, we find B(B(s)(0) â J/ψf(2)'(1525))/B(B(s)(0) â J/ψÏ) = (26.4 ± 2.7 ± 2.4)%.
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The interference between the K+ K- S-wave and P-wave amplitudes in B(s)(0) â J/ψK+ K- decays with the K+ K- pairs in the region around the Ï(1020) resonance is used to determine the variation of the difference of the strong phase between these amplitudes as a function of K+ K- invariant mass. Combined with the results from our CP asymmetry measurement in B(s)(0) â J/ψÏ decays, we conclude that the B(s)(0) mass eigenstate that is almost CP = +1 is lighter and decays faster than the mass eigenstate that is almost CP = -1. This determines the sign of the decay width difference ΔΓ(s) ≡ Γ(L) - Γ(H) to be positive. Our result also resolves the ambiguity in the past measurements of the CP violating phase Ï(s) to be close to zero rather than π. These conclusions are in agreement with the standard model expectations.
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The relative abundance of the three decay modes B(0)âD(-)K(+), B(0)âD(-)π(+), and B(s)(0)âD(s)(-)π(+) produced in 7 TeV pp collisions at the LHC is determined from data corresponding to an integrated luminosity of 35 pb(-1). The branching fraction of B(0)âD(-)K(+) is found to be B(B(0)âD(-)K(+)) = (2.01 ± 0.18(stat) ± 0.14(syst)) × 10(-4). The ratio of fragmentation fractions f(s)/f(d) is determined through the relative abundance of B(s)(0)âD(s)(-)π(+) to B(0)âD(-)K(+) and B(0)âD(-)π(+), leading to f(s)/f(d) = 0.253 ± 0.017 ± 0.017 ± 0.020, where the uncertainties are statistical, systematic, and theoretical, respectively.
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In an attempt to generate antibodies which recognize novel tumor-associated antigens we have immunized Rhesus monkeys (Macaca mulatta) with human colon carcinoma cells prepared from freshly excised tumors. Immunohistochemical characterization of polyclonal antisera from one monkey (DF6) revealed preferential reactivity with primary and metastatic colon carcinoma tissue, and a general lack of recognition of nonneoplastic mucosa. Immunoreactivity was localized to the luminal contents of glandular structures and to the apical surfaces of cells lining these glands. Immunoreactivity was not observed with any normal tissue examined. Examination of neoplastic tissues revealed reactivity with two gastric carcinoma specimens (n = 2) and one breast carcinoma (n = 7). In reactive colon carcinoma tissues, the pattern of staining with DF6 was similar to that of several other antibodies including anti-carcinoembryonic antigen, B72.3, anti-Le(x) and anti-Le(y). However, the panel of tissues recognized by these antibodies and DF6 differed significantly, suggesting that the DF6-reactive epitopes are unique. Human colon carcinoma cell lines maintained in vitro also expressed antigens recognized by DF6 in a pattern similar to that of surgically excised tissue. This preliminary characterization of DF6 antiserum suggests that immunization of Rhesus monkeys is a potentially useful protocol for identifying antigens preferentially expressed by human colon carcinoma.
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Anticuerpos Antineoplásicos/inmunología , Antígenos de Neoplasias/inmunología , Carcinoma/inmunología , Neoplasias del Colon/inmunología , Animales , Antígeno Carcinoembrionario/inmunología , Reacciones Cruzadas , Técnica del Anticuerpo Fluorescente , Humanos , Macaca mulatta , Células Tumorales Cultivadas/inmunologíaRESUMEN
The adult guinea-pig small intestinal microvillus membrane was purified approximately 25-fold by both cation-precipitation and differential centrifugation methods. Comparison by sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) revealed no substantial differences in polypeptide composition between the two preparations. One-dimensional SDS-PAGE and two-dimensional isoelectric focussing (IEF)/SDS-PAGE, together with Coomassie-blue, silver and lectin-staining, showed three major high molecular weight polypeptides, Mr 108 000, 116 000 and 127 000, as well as a 47 kDa protein (actin), as major constituents of the membrane. The proteins of Mr 108 000 and 116 000 were strongly concanavalin A reactive. A detailed two-dimensional IEF/SDS-PAGE map of the membrane was constructed. Sodium carbonate treatment showed the two concanavalin A-reactive glycoproteins, Mr 108 000 and 116 000, comprising the sucrase-isomaltase complex, to be loosely-associated 'extrinsic' microvillus membrane proteins. Two proteins, Mr 127 000 and 135 000, were tightly-associated 'intrinsic' microvillus proteins. Despite regional differences in specific activity of some small intestinal microvillar enzymes, most noticeably enterokinase (EC 3.4.21.9) and dipeptidyl peptidase IV (EC 3.4.14.x), no substantial regional differences were seen in microvillus membrane polypeptide composition. In contrast, a substantial increase in the major high molecular weight proteins of Mr 108 000 and 116 000 accompanied a 10-fold rise in sucrase-isomaltase activity, and loss of a major protein of Mr 131 000 accompanied the complete loss of lactase activity from the membrane during postnatal development.
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Mucosa Intestinal/análisis , Proteínas de la Membrana/análisis , Microvellosidades/análisis , Factores de Edad , Animales , Fraccionamiento Celular/métodos , Membrana Celular/análisis , Membrana Celular/enzimología , Cobayas , Mucosa Intestinal/enzimología , Mucosa Intestinal/crecimiento & desarrollo , Punto Isoeléctrico , Microvellosidades/enzimología , Peso MolecularRESUMEN
An intrinsic membrane glycoprotein, Mr 131 000, is a major developmentally specific component of the neonatal guinea-pig small intestinal microvillar membrane. Such high-molecular-weight proteins are often difficult to translate in vitro. In this study we report a successful strategy for the identification of the primary translation product of this glycoprotein, a high-molecular-weight precursor polypeptide of approximate Mr 225 000.
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Intestino Delgado/ultraestructura , Biosíntesis de Péptidos , Animales , Sistema Libre de Células , Electroforesis en Gel de Poliacrilamida , Cobayas , Microvellosidades/metabolismo , Peso Molecular , Biosíntesis de ProteínasRESUMEN
New technologies in both combinatorial chemistry and combinatorial biology promise to unlock new opportunities for drug discovery and lead optimisation. Using such genome-based technologies to measure the dynamic properties of pharmacological systems, pharmacogenomics can now provide an objective measure of a drug's biological efficacy, including its potential adverse effects.
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ADN/genética , Quimioterapia , Genoma , Farmacogenética , Animales , Biotecnología , ADN/química , Bases de Datos como Asunto , Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos , Variación Genética , Humanos , Polimorfismo GenéticoRESUMEN
The demands on drug discovery organizations have increased dramatically in recent years, partly because of the need to identify novel targets that are both relevant to disease and chemically tractable. This is leading to an industrial approach to traditional biology and chemistry, inspired in part by the revolution in genomics. The purpose of this article is to highlight the flow of investigation from gene sequence of potential therapeutic targets, through mRNA and protein expression, to protein structure and drug design. To deal with this scale of activity, many commercial and public organizations have been established and some of the key players will be listed in this article.
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Diseño de Fármacos , Genoma , Expresión Génica , Análisis de Secuencia por Matrices de Oligonucleótidos , Farmacogenética , Proteínas/genética , Proteoma , ARN Mensajero/genéticaRESUMEN
The results of phase noise measurement for high-overtone bulk-acoustic resonators (HBARs) for use in high-performance oscillators, operating at 640 MHz with insertion losses of 10-15 dB and unmatched Qs greater than 110 K are reported. Noise measurements made on these resonators with input drive levels of 16 dBm have shown self-noise levels of S(y)(f=100 Hz)=8.0x10(-26) for 1/f noise which represents state-of-the-art for a UHF resonator.
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The calibration and performance of the opposite-side flavour tagging algorithms used for the measurements of time-dependent asymmetries at the LHCb experiment are described. The algorithms have been developed using simulated events and optimized and calibrated with B+âJ/ψK+, B0âJ/ψK∗0 and B0âD∗-µ+νµ decay modes with 0.37 fb-1 of data collected in pp collisions at [Formula: see text] during the 2011 physics run. The opposite-side tagging power is determined in the B+âJ/ψK+ channel to be (2.10±0.08±0.24) %, where the first uncertainty is statistical and the second is systematic.
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The production of Ï(1S), Ï(2S) and Ï(3S) mesons in proton-proton collisions at the centre-of-mass energy of [Formula: see text] is studied with the LHCb detector. The analysis is based on a data sample of 25 pb-1 collected at the Large Hadron Collider. The Ï mesons are reconstructed in the decay mode Ïâµ+µ- and the signal yields are extracted from a fit to the µ+µ- invariant mass distributions. The differential production cross-sections times dimuon branching fractions are measured as a function of the Ï transverse momentum pT and rapidity y, over the range pT <15 GeV/c and 2.0
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The differential cross-section for the inclusive production of ψ(2S) mesons in pp collisions at [Formula: see text] has been measured with the LHCb detector. The data sample corresponds to an integrated luminosity of 36 pb-1. The ψ(2S) mesons are reconstructed in the decay channels ψ(2S)âµ+µ- and ψ(2S)âJ/ψπ+π-, with the J/ψ meson decaying into two muons. Results are presented both for promptly produced ψ(2S) mesons and for those originating from b-hadron decays. In the kinematic range pT(ψ(2S))≤16 GeV/c and 2
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A plasma-membrane fraction was isolated from the alga Hydrodictyon africanum by micro-dissection and its phospholipid components were analysed. Phosphatidylcholine was the major phospholipid of the preparation. Both phosphatidylserine and diphosphatidylglycerol were enriched in the fraction compared with the whole cell, but the relative amount of phosphatidylglycerol present was less than that in the whole cell. Phosphatidylinositol was absent from the plasma-membrane preparation.