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1.
Appl Radiat Isot ; 208: 111280, 2024 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-38508066

RESUMO

Natural antimony targets were irradiated in a 60 MeV bremsstrahlung beam and gamma spectrometric measurements were performed. The goal was to establish the yield of 117mSn, a radionuclide with great potential for application in medicine. Considering that 117mSn is predominantly produced through a photonuclear reaction in which an charged particle is emitted (121Sb(γ,p3n)), the yield of this tin isotope is much lower than the yields of several antimony isotopes produced in (γ,xn) reactions. It has been estimated that photonuclear reactions on natural antimony could produce 117mSn activities needed for therapeutic applications, with accelerators having electron currents of the order of mA. For the used bremsstrahlung energy of 60 MeV, it was estimated how much 119mSn activity can be expected when exposing the antimony target.

2.
Nature ; 611(7935): 265-270, 2022 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-36261531

RESUMO

The visible world is founded on the proton, the only composite building block of matter that is stable in nature. Consequently, understanding the formation of matter relies on explaining the dynamics and the properties of the proton's bound state. A fundamental property of the proton involves the response of the system to an external electromagnetic field. It is characterized by the electromagnetic polarizabilities1 that describe how easily the charge and magnetization distributions inside the system are distorted by the electromagnetic field. Moreover, the generalized polarizabilities2 map out the resulting deformation of the densities in a proton subject to an electromagnetic field. They disclose essential information about the underlying system dynamics and provide a key for decoding the proton structure in terms of the theory of the strong interaction that binds its elementary quark and gluon constituents. Of particular interest is a puzzle in the electric generalized polarizability of the proton that remains unresolved for two decades2. Here we report measurements of the proton's electromagnetic generalized polarizabilities at low four-momentum transfer squared. We show evidence of an anomaly to the behaviour of the proton's electric generalized polarizability that contradicts the predictions of nuclear theory and derive its signature in the spatial distribution of the induced polarization in the proton. The reported measurements suggest the presence of a new, not-yet-understood dynamical mechanism in the proton and present notable challenges to the nuclear theory.

3.
Phys Rev Lett ; 123(18): 182501, 2019 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-31763910

RESUMO

Backward-angle meson electroproduction above the resonance region, which was previously ignored, is anticipated to offer unique access to the three quark plus sea component of the nucleon wave function. In this Letter, we present the first complete separation of the four electromagnetic structure functions above the resonance region in exclusive ω electroproduction off the proton, ep→e^{'}pω, at central Q^{2} values of 1.60, 2.45 GeV^{2}, at W=2.21 GeV. The results of our pioneering -u≈-u_{min} study demonstrate the existence of a unanticipated backward-angle cross section peak and the feasibility of full L/T/LT/TT separations in this never explored kinematic territory. At Q^{2}=2.45 GeV^{2}, the observed dominance of σ_{T} over σ_{L}, is qualitatively consistent with the collinear QCD description in the near-backward regime, in which the scattering amplitude factorizes into a hard subprocess amplitude and baryon to meson transition distribution amplitudes: universal nonperturbative objects only accessible through backward-angle kinematics.

4.
Phys Rev Lett ; 123(2): 022501, 2019 Jul 12.
Artigo em Inglês | MEDLINE | ID: mdl-31386522

RESUMO

We present extractions of the nucleon nonsinglet moments utilizing new precision data on the deuteron F_{2} structure function at large Bjorken-x determined via the Rosenbluth separation technique at Jefferson Lab Experimental Hall C. These new data are combined with a complementary set of data on the proton previously measured in Hall C at similar kinematics and world datasets on the proton and deuteron at lower x measured at SLAC and CERN. The new Jefferson Lab data provide coverage of the upper third of the x range, crucial for precision determination of the higher moments. In contrast to previous extractions, these moments have been corrected for nuclear effects in the deuteron using a new global fit to the deuteron and proton data. The obtained experimental moments represent an order of magnitude improvement in precision over previous extractions using high x data. Moreover, recent exciting developments in lattice QCD calculations provide a first ever comparison of these new experimental results with calculations of moments carried out at the physical pion mass, as well as a new approach that first calculates the quark distributions directly before determining moments.

5.
Sci Rep ; 9(1): 6253, 2019 Apr 18.
Artigo em Inglês | MEDLINE | ID: mdl-31000757

RESUMO

The natural electron accelerator in the clouds above Aragats high-altitude research station in Armenia operates continuously in 2017 providing more than 100 Thunderstorm Ground enhancements (TGEs). Most important discovery based on analysis of 2017 data is observation and detailed description of the long-lasting TGEs. We present TGE catalog for 2 broad classes according to presence or absence of the high-energy particles. In the catalog was summarized several key parameters of the TGEs and related meteorological and atmospheric discharge observations. The statistical analysis of the data collected in tables reveals the months when TGEs are more frequent, the daytime when TGEs mostly occurred, the mean distance to lightning flash that terminates TGE and many other interesting relations. Separately was discussed the sharp count rate decline and following removal of high-energy particles from the TGE flux after a lightning flash. ADEI multivariate visualization and statistical analysis platform make analytical work on sophisticated problems rather easy; one can try and test many hypotheses very fast and come to a definite conclusion allowing crosscheck and validation.

6.
Phys Rev Lett ; 115(15): 152001, 2015 Oct 09.
Artigo em Inglês | MEDLINE | ID: mdl-26550716

RESUMO

Wide-angle exclusive Compton scattering and single-pion photoproduction from the proton have been investigated via measurement of the polarization transfer from a circularly polarized photon beam to the recoil proton. The wide-angle Compton scattering polarization transfer was analyzed at an incident photon energy of 3.7 GeV at a proton scattering angle of θ_{cm}^{p}=70°. The longitudinal transfer K_{LL}, measured to be 0.645±0.059±0.048, where the first error is statistical and the second is systematic, has the same sign as predicted for the reaction mechanism in which the photon interacts with a single quark carrying the spin of the proton. However, the observed value is ~3 times larger than predicted by the generalized-parton-distribution-based calculations, which indicates a significant unknown contribution to the scattering amplitude.

7.
Tsitologiia ; 55(4): 259-60, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23875460

RESUMO

Multicolor banding approach, first introduced for human chromosomes only, was established as an optimal approach for karyotyping of murine chromosomes. Here we present the established mcb probe sets for all murine autosomes and the X-chromosome and review their potential application.


Assuntos
Bandeamento Cromossômico/métodos , Coloração Cromossômica/métodos , Cromossomos de Mamíferos , Animais , Bandeamento Cromossômico/normas , Coloração Cromossômica/normas , Hibridização in Situ Fluorescente , Cariotipagem , Camundongos
8.
Acta Haematol ; 130(1): 23-6, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23363773

RESUMO

Acute promyelocytic leukemia (APL) is usually associated with a favorable outcome, but about 10% of patients tend to relapse. The genetic hallmark of APL is a balanced translocation involving chromosomes 15 and 17, and the PML-RARa gene fusion is found in more than 90% of these cases. Other chromosomal abnormalities are commonly found in APL, but their clinical significance has yet to be determined. Here we report a case of childhood APL that was studied by conventional cytogenetics along with molecular cytogenetic techniques. The patient showed a complex karyotype with an unusual cytogenetic rearrangement originating from two different abnormalities in a single chromosome 6. Our case is an exceptional example of a cryptic cytogenetic anomaly in APL and underscores the importance of detailed genetic characterization.


Assuntos
Cromossomos Humanos Par 6 , Rearranjo Gênico , Leucemia Promielocítica Aguda/genética , Translocação Genética/genética , Criança , Bandeamento Cromossômico , Cromossomos Humanos Par 15 , Cromossomos Humanos Par 17 , Humanos , Hibridização in Situ Fluorescente , Masculino
9.
Phys Rev Lett ; 108(12): 122002, 2012 Mar 23.
Artigo em Inglês | MEDLINE | ID: mdl-22540573

RESUMO

The parity-violating (PV) asymmetry of inclusive π- production in electron scattering from a liquid deuterium target was measured at backward angles. The measurement was conducted as a part of the G0 experiment, at a beam energy of 360 MeV. The physics process dominating pion production for these kinematics is quasifree photoproduction off the neutron via the Δ0 resonance. In the context of heavy-baryon chiral perturbation theory, this asymmetry is related to a low-energy constant d(Δ)- that characterizes the parity-violating γNΔ coupling. Zhu et al. calculated d(Δ)- in a model benchmarked by the large asymmetries seen in hyperon weak radiative decays, and predicted potentially large asymmetries for this process, ranging from A(γ)-=-5.2 to +5.2 ppm. The measurement performed in this work leads to A(γ)-=-0.36±1.06±0.37±0.03 ppm (where sources of statistical, systematic and theoretical uncertainties are included), which would disfavor enchancements considered by Zhu et al. proportional to V(ud)/V(us). The measurement is part of a program of inelastic scattering measurements that were conducted by the G0 experiment, seeking to determine the N-Δ axial transition form factors using PV electron scattering.

10.
Phys Rev Lett ; 108(9): 092502, 2012 Mar 02.
Artigo em Inglês | MEDLINE | ID: mdl-22463628

RESUMO

We present new measurements of electron scattering from high-momentum nucleons in nuclei. These data allow an improved determination of the strength of two-nucleon correlations for several nuclei, including light nuclei where clustering effects can, for the first time, be examined. The data also include the kinematic region where three-nucleon correlations are expected to dominate.

11.
Phys Rev Lett ; 107(2): 022501, 2011 Jul 08.
Artigo em Inglês | MEDLINE | ID: mdl-21797598

RESUMO

We have measured the beam-normal single-spin asymmetries in elastic scattering of transversely polarized electrons from the proton, and performed the first measurement in quasielastic scattering on the deuteron, at backward angles (lab scattering angle of 108°) for Q² = 0.22 GeV²/c² and 0.63 GeV²/c² at beam energies of 362 and 687 MeV, respectively. The asymmetry arises due to the imaginary part of the interference of the two-photon exchange amplitude with that of single-photon exchange. Results for the proton are consistent with a model calculation which includes inelastic intermediate hadronic (πN) states. An estimate of the beam-normal single-spin asymmetry for the scattering from the neutron is made using a quasistatic deuterium approximation, and is also in agreement with theory.

12.
Phys Rev Lett ; 105(10): 101601, 2010 Sep 03.
Artigo em Inglês | MEDLINE | ID: mdl-20867509

RESUMO

We have extracted QCD matrix elements from our data on doubly polarized inelastic scattering of electrons on nuclei. We find the higher twist matrix element d˜2, which arises strictly from quark-gluon interactions, to be unambiguously nonzero. The data also reveal an isospin dependence of higher twist effects if we assume that the Burkhardt-Cottingham sum rule is valid. The fundamental Bjorken sum rule obtained from the a0 matrix element is satisfied at our low momentum transfer.

13.
Phys Rev Lett ; 104(1): 012001, 2010 Jan 08.
Artigo em Inglês | MEDLINE | ID: mdl-20366359

RESUMO

We have measured parity-violating asymmetries in elastic electron-proton and quasielastic electron-deuteron scattering at Q2=0.22 and 0.63 GeV2. They are sensitive to strange quark contributions to currents in the nucleon and the nucleon axial-vector current. The results indicate strange quark contributions of approximately < 10% of the charge and magnetic nucleon form factors at these four-momentum transfers. We also present the first measurement of anapole moment effects in the axial-vector current at these four-momentum transfers.

14.
Phys Rev Lett ; 105(21): 212502, 2010 Nov 19.
Artigo em Inglês | MEDLINE | ID: mdl-21231294

RESUMO

We present new data on electron scattering from a range of nuclei taken in Hall C at Jefferson Lab. For heavy nuclei, we observe a rapid falloff in the cross section for x>1, which is sensitive to short-range contributions to the nuclear wave function, and in deep inelastic scattering corresponds to probing extremely high momentum quarks. This result agrees with higher energy muon scattering measurements, but is in sharp contrast to neutrino scattering measurements which suggested a dramatic enhancement in the distribution of the "superfast" quarks probed at x>1. The falloff at x>1 is noticeably stronger in 2H and 3He, but nearly identical for all heavier nuclei.

15.
Genet Couns ; 21(4): 397-404, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-21290969

RESUMO

Infertility is defined as the inability to conceive after one year of regular unprotected intercourse. Constitutional numerical and/or structural chromosomal aberrations like sex-chromosome aberrations are one of the possible factors involved in fertility problems. Reciprocal translocations between an X-chromosome and an autosome are rarely seen in men. Male carriers of an X-autosome translocation are invariably sterile, regardless of the position of the breakpoint in the X-chromosome. Breakpoints in autosomal chromosomes could also be involved in male infertility. In this paper, we describe a 31-year-old male with azoospermia. GTG banding with high resolution multicolor-banding (MCB) techniques revealed a karyotype 46,Y,t(X;1)(p22.3;q25), and we discuss how the breakpoint of this translocation could affect male infertility. As a conclusion, cytogenetic evaluation of infertile subjects with azoospermia should be considered in the first place before in vitro fertilisation procedures are planned.


Assuntos
Azoospermia/genética , Cromossomos Humanos Par 1 , Cromossomos Humanos X , Aberrações dos Cromossomos Sexuais , Transtornos dos Cromossomos Sexuais/genética , Translocação Genética , Adulto , Bandeamento Cromossômico , Humanos , Masculino , Turquia
16.
Cytogenet Genome Res ; 126(4): 313-7, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19864871

RESUMO

The immortalized human cerebral microvessel endothelial cell line hCMEC/D3 has been repeatedly used as a model of human blood-brain barrier (BBB). hCMEC/D3 cells between passage 25 and 35 are most often applied in research, remained phenotypically nontransformed, and cells maintained many characteristics of human brain endothelial cells. Also hCMEC/D3 was thought to have conserved a normal diploid karyotype over all these passages. Here we characterized the cell line using high-resolution multicolor fluorescence in situ hybridization (FISH) approaches and revealed a complex karyotype in the 30th passage. Clonal cryptic unbalanced structural rearrangements and numerical aberrations were discovered and described as follows: 45 approximately 48,XX, -X,del(5)(q11)[2],del(9)(q11)[3],+9[3],del(11)(q13 approximately 14)[2], der(14)t(14;21)(q32.33;q22.3)[28],der(15)t(9;15)(p11;p11)[13], dup(15)(p11q11)[5],der(21)t(17;21)(p12;q22)[9],-22[6][cp28]. In summary, a complex karyotype with clonal unbalanced chromosomal rearrangements is present in hCMEC/D3. Thus, we solicit to include molecular cytogenetics in the testing of all cell lines prior to application of their use in complex studies.


Assuntos
Encéfalo/irrigação sanguínea , Encéfalo/citologia , Células Endoteliais/citologia , Microvasos/citologia , Linhagem Celular , Aberrações Cromossômicas , Humanos , Cariotipagem
17.
Phys Rev Lett ; 103(20): 202301, 2009 Nov 13.
Artigo em Inglês | MEDLINE | ID: mdl-20365978

RESUMO

New Jefferson Lab data are presented on the nuclear dependence of the inclusive cross section from (2)H, (3)He, (4)He, (9)Be and (12)C for 0.3 < x < 0.9, Q(2) approximately 3-6 GeV(2). These data represent the first measurement of the EMC effect for (3)He at large x and a significant improvement for (4)He. The data do not support previous A-dependent or density-dependent fits to the EMC effect and suggest that the nuclear dependence of the quark distributions may depend on the local nuclear environment.

18.
Int J Mol Med ; 21(2): 189-200, 2008 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-18204785

RESUMO

The differentiation of homologous chromosomes as well as their parental origin can presently be conducted and determined exclusively by molecular genetic methods using microsatellite or SNP analysis. Only in exceptional cases is a distinction on a single-cell level possible, e.g. due to variations within the heterochromatic regions of chromosomes 1, 9, 16 and Y or the p-arms of the acrocentric chromosomes. In the absence of such polymorphisms, an individual distinction of the homologous chromosomes is not currently possible. Consequently, various questions of scientific and diagnostic relevance are unable to be answered. Based on the recently detected large-scale copy-number variations (LCV) or copy-number polymorphisms (CNP) spanning up to several megabase pairs of DNA, in this study, a molecular cytogenetic technique for the inter-individual differentiation of homologous chromosomes called parental-origin-determination fluorescence in situ hybridization (pod-FISH) is presented. All human chromosomes were covered with 225 LCV- and/or CNP-specific BAC probes, and one- to five-color chromosome-specific pod-FISH sets were created, evaluated and optimized. We demonstrated that pod-FISH is suitable for single-cell analysis of uniparental disomy (UDP) in clinical cases such as Prader-Willi syndrome caused by maternal UPD. A rare clinical case with a mosaic form of a genome-wide isodisomy was used to determine the detection limits of pod-FISH. Additionally we analyzed the informativeness of conventional microsatellite analysis for the first time and compared the results to pod-FISH. With this new possibility to study the parental origin of individual human chromosomes on a single-cell level, new doors for diagnostic and basic research are opened.


Assuntos
Cromossomos Humanos/metabolismo , Hibridização in Situ Fluorescente/métodos , Alelos , Cromossomos Artificiais Bacterianos , Células Clonais , Humanos , Repetições de Microssatélites/genética , Dissomia Uniparental
20.
Phys Rev Lett ; 98(14): 142301, 2007 Apr 06.
Artigo em Inglês | MEDLINE | ID: mdl-17501267

RESUMO

We report on a study of the longitudinal to transverse cross section ratio, R=sigmaL/sigmaT, at low values of x and Q2, as determined from inclusive inelastic electron-hydrogen and electron-deuterium scattering data from Jefferson Laboratory Hall C spanning the four-momentum transfer range 0.06

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