1,448 research outputs found
Experimental observation of plasmons in a graphene monolayer resting on a two-dimensional subwavelength silicon grating
We experimentally demonstrate graphene-plasmon polariton excitation in a
continuous graphene monolayer resting on a two-dimensional subwavelength
silicon grating. The subwavelength silicon grating is fabricated by a
nanosphere lithography technique with a self-assembled nanosphere array as a
template. Measured transmission spectra illustrate the excitation of
graphene-plasmon polaritons, which is further supported by numerical
simulations and theoretical prediction of plasmonband diagrams. Our
grating-assisted coupling to graphene-plasmon polaritons forms an important
platform for graphene-based opto-electronics applications.Comment: 13 pages, 4 figures, revised version accepted by AP
Genetic ancestry of participants in the National Children's Study.
BackgroundThe National Children's Study (NCS) is a prospective epidemiological study in the USA tasked with identifying a nationally representative sample of 100,000 children, and following them from their gestation until they are 21 years of age. The objective of the study is to measure environmental and genetic influences on growth, development, and health. Determination of the ancestry of these NCS participants is important for assessing the diversity of study participants and for examining the effect of ancestry on various health outcomes.ResultsWe estimated the genetic ancestry of a convenience sample of 641 parents enrolled at the 7 original NCS Vanguard sites, by analyzing 30,000 markers on exome arrays, using the 1000 Genomes Project superpopulations as reference populations, and compared this with the measures of self-reported ethnicity and race. For 99% of the individuals, self-reported ethnicity and race agreed with the predicted superpopulation. NCS individuals self-reporting as Asian had genetic ancestry of either South Asian or East Asian groups, while those reporting as either Hispanic White or Hispanic Other had similar genetic ancestry. Of the 33 individuals who self-reported as Multiracial or Non-Hispanic Other, 33% matched the South Asian or East Asian groups, while these groups represented only 4.4% of the other reported categories.ConclusionsOur data suggest that self-reported ethnicity and race have some limitations in accurately capturing Hispanic and South Asian populations. Overall, however, our data indicate that despite the complexity of the US population, individuals know their ancestral origins, and that self-reported ethnicity and race is a reliable indicator of genetic ancestry
Lattice vibrations and structural instability in Cesium near the cubic to tetragonal transition
Under pressure cesium undergoes a transition from a high-pressure fcc phase
(Cs-II) to a collapsed fcc phase (Cs-III) near 4.2GPa. At 4.4GPa there follows
a transition to the tetragonal Cs-IV phase. In order to investigate the lattice
vibrations in the fcc phase and seek a possible dynamical instability of the
lattice, the phonon spectra of fcc-Cs at volumes near the III-IV transition are
calculated using Savrasov's density functional linear-response LMTO method.
Compared with quasiharmonic model calculations including non-central
interatomic forces up to second neighbours, at the volume (
is the experimental volume of bcc-Cs with =6.048{\AA}), the
linear-response calculations show soft intermediate wavelength
phonons. Similar softening is also observed for
short wavelength and phonons and intermediate
wavelength phonons. The Born-von K\'{a}rm\'{a}n analysis of
dispersion curves indicates that the interplanar force constants exhibit
oscillating behaviours against plane spacing and the large softening of
intermediate wavelength phonons results from a
negative (110)-interplanar force-constant . The frequencies of the
phonons with around 1/3 become imaginary
and the fcc structure becomes dynamically unstable for volumes below .
It is suggested that superstructures corresponding to the
soft mode should be present as a precursor of tetragonal Cs-IV structure.Comment: 12 pages, 5 figure
Consanguinity and rare mutations outside of MCCC genes underlie nonspecific phenotypes of MCCD.
Purpose3-Methylcrotonyl-CoA carboxylase deficiency (MCCD) is an autosomal recessive disorder of leucine catabolism that has a highly variable clinical phenotype, ranging from acute metabolic acidosis to nonspecific symptoms such as developmental delay, failure to thrive, hemiparesis, muscular hypotonia, and multiple sclerosis. Implementation of newborn screening for MCCD has resulted in broadening the range of phenotypic expression to include asymptomatic adults. The purpose of this study was to identify factors underlying the varying phenotypes of MCCD.MethodsWe performed exome sequencing on DNA from 33 cases and 108 healthy controls. We examined these data for associations between either MCC mutational status, genetic ancestry, or consanguinity and the absence or presence/specificity of clinical symptoms in MCCD cases.ResultsWe determined that individuals with nonspecific clinical phenotypes are highly inbred compared with cases that are asymptomatic and healthy controls. For 5 of these 10 individuals, we discovered a homozygous damaging mutation in a disease gene that is likely to underlie their nonspecific clinical phenotypes previously attributed to MCCD.ConclusionOur study shows that nonspecific phenotypes attributed to MCCD are associated with consanguinity and are likely not due to mutations in the MCC enzyme but result from rare homozygous mutations in other disease genes.Genet Med 17 8, 660-667
Exploring 'The autisms' at a cognitive level
The autism spectrum is characterized by genetic and behavioral heterogeneity. However, it is still unknown whether there is a universal pattern of cognitive impairment in autism spectrum disorder (ASD) and whether multiple cognitive impairments are needed to explain the full range of behavioral symptoms. This study aimed to determine whether three widely acknowledged cognitive abnormalities (Theory of Mind (ToM) impairment, Executive Function (EF) impairment, and the presence of a Local Processing Bias (LB)) are universal and fractionable in autism, and whether the relationship between cognition and behavior is dependent on the method of behavioral assessment. Thirty-one high-functioning children with ASD and thirty-seven children with neurotypical development (NTD), comparable in age, gender and Intelligence Quotient (IQ), completed several tasks tapping into ToM, EF, and LB, and autistic symptomatology was assessed through parental and teacher questionnaires, parental interview and direct observation. We found that ToM and EF deficits differentiated the groups and some ToM and EF tasks were related to each other. ToM and EF were together able to correctly classify more than three-quarters of the children into cases and controls, despite relating to none of the specific behavioral measures. Only a small subgroup of individuals displayed a LB, which was unrelated to ToM and EF, and did not aid diagnostic classification, most likely contributing to non-diagnostic symptoms in a subgroup. Despite the characteristic heterogeneity of the autism spectrum, it remains a possibility therefore that a single cognitive cause may underlie the range of diagnostic symptoms in all individuals with autism
Research Activities Report for the Project:living Aquatic Resources - management and knowledge base
Technical report with results from the fish sampling and analyses from the Joint Danube Survey 2007
Coulomb-Enhanced Spin-Orbit Splitting: The Missing Piece in the Sr2RhO4 Puzzle
The outstanding discrepancy between the measured and calculated
(local-density approximation) Fermi surfaces in the well-characterized,
paramagnetic Fermi liquid Sr2RhO4 is resolved by including the spin-orbit
coupling and Coulomb repulsion. This results in an effective spin-orbit
coupling constant enhanced 2.15 times over the bare value. A simple formalism
allows discussion of other systems. For Sr2RhO4, the experimental specific-heat
and mass enhancements are found to be 2.2.Comment: 4 pages, 2 figure
Potential of interferon-Îł-inducible protein 10 in improving tuberculosis diagnosis in HIV-infected patients
The use of combined heart rate response and accelerometry to assess the level and predictors of physical activity in tuberculosis patients in Tanzania
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