Electronic Spectrum of Dihydrogenated Buckminsterfullerene in a 6 K Neon Matrix

Vibrationally resolved electronic absorption spectrum of 1,2-dihydrogenated[60]fullerene has been recorded in a 6 K neon matrix after mass-selected deposition of m/z = 722 cations produced from reaction of protonated methane and C60 in an ion source. One system has the origin band at 688.5 ± 0.1 nm and another commencing at 404.8 ± 0.1 nm. Theoretical computations were used to calculate the relative energies of three isomers of dihydrogenated[60]fullerene and time-dependent density functional theory predicted the vertical excitations to 50 electronic states

Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies

BACKGROUND: Genetic determinants of stroke, the leading neurological cause of death and disability, are poorly understood and have seldom been explored in the general population. Our aim was to identify additional loci for stroke by doing a meta-analysis of genome-wide association studies. METHODS: For the discovery sample, we did a genome-wide analysis of common genetic variants associated with incident stroke risk in 18 population-based cohorts comprising 84 961 participants, of whom 4348 had stroke. Stroke diagnosis was ascertained and validated by the study investigators. Mean age at stroke ranged from 45·8 years to 76·4 years, and data collection in the studies took place between 1948 and 2013. We did validation analyses for variants yielding a significant association (at p<5 × 10(-6)) with all-stroke, ischaemic stroke, cardioembolic ischaemic stroke, or non-cardioembolic ischaemic stroke in the largest available cross-sectional studies (70 804 participants, of whom 19 816 had stroke). Summary-level results of discovery and follow-up stages were combined using inverse-variance weighted fixed-effects meta-analysis, and in-silico lookups were done in stroke subtypes. For genome-wide significant findings (at p<5 × 10(-8)), we explored associations with additional cerebrovascular phenotypes and did functional experiments using conditional (inducible) deletion of the probable causal gene in mice. We also studied the expression of orthologs of this probable causal gene and its effects on cerebral vasculature in zebrafish mutants. FINDINGS: We replicated seven of eight known loci associated with risk for ischaemic stroke, and identified a novel locus at chromosome 6p25 (rs12204590, near FOXF2) associated with risk of all-stroke (odds ratio [OR] 1·08, 95% CI 1·05-1·12, p=1·48 × 10(-8); minor allele frequency 21%). The rs12204590 stroke risk allele was also associated with increased MRI-defined burden of white matter hyperintensity-a marker of cerebral small vessel disease-in stroke-free adults (n=21 079; p=0·0025). Consistently, young patients (aged 2-32 years) with segmental deletions of FOXF2 showed an extensive burden of white matter hyperintensity. Deletion of Foxf2 in adult mice resulted in cerebral infarction, reactive gliosis, and microhaemorrhage. The orthologs of FOXF2 in zebrafish (foxf2b and foxf2a) are expressed in brain pericytes and mutant foxf2b(-/-) cerebral vessels show decreased smooth muscle cell and pericyte coverage. INTERPRETATION: We identified common variants near FOXF2 that are associated with increased stroke susceptibility. Epidemiological and experimental data suggest that FOXF2 mediates this association, potentially via differentiation defects of cerebral vascular mural cells. Further expression studies in appropriate human tissues, and further functional experiments with long follow-up periods are needed to fully understand the underlying mechanisms

Finishing the euchromatic sequence of the human genome

The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead

Electronic Spectra of Protonated Fluoranthene in a Neon Matrix and Gas Phase at 10 K

Four electronic systems with origin bands at 759.5, 559.3, 476.3, and 385.5 nm are detected in a 6 K neon matrix following deposition of mass-selected protonated fluoranthene C16H11+ produced from a reaction of neutral vapor and ethanol in a hot-cathode ion source. Two cationic isomers are identified as the carriers of these band systems. The 559.3, 476.3, and 385.5 nm absorptions are assigned to 4,3,2 1A′ ← X 1A′ transitions of isomer E+ (γ−) and the 2 1A′ ← X 1A′ system at 759.5 nm is of isomer C+ (α−) of protonated fluoranthene on the basis of theoretical predictions. The electronic spectrum of E+ was also recorded in the gas phase using a resonant 1 + 1 two-photon excitation–dissociation technique in an ion trap at vibrational and rotational temperatures of 10 K. The 3,2 1A′ ← X 1A′ transitions have origin band maxima at 558.28 ± 0.01 and 474.92 ± 0.01 nm. Both the 2 1A′ and 3 1A′ excited states have a distinct vibrational pattern with lifetimes on the order of 1 ps

Plastic Zone Size for Nanoindentation of Irradiated Fe–9%Cr ODS

The objective of this study is to determine irradiation effects on the nanoindentation plastic zone morphology in a model Fe–9%Cr ODS alloy. Specimens are irradiated to 50 displacements per atom at 400°C with Fe++ self-ions or to 3 dpa at 500°C with neutrons. The as-received specimen is also studied as a control. The nanoindentation plastic zone size is calculated using two approaches: (1) an analytical model based on the expanding spherical cavity analogy, and (2) finite element modeling (FEM). Plastic zones in all specimen conditions extend radially outward from the indenter, ∼4–5 times the tip radius, indicative of fully plastic contact. Non-negligible plastic flow in the radial direction requires the experimentalist to consider the plastic zone morphology when nanoindenting ion-irradiated specimens; a single nanoindent may sample non-uniform irradiation damage, regardless of whether the indent is made top-down or in cross-section. Finally, true stress-strain curves are generated