105 research outputs found
Late growth stages and post-growth diffusion in organic epitaxy: PTCDA on Ag(111)
The late growth stages and the post-growth diffusion of crystalline organic
thin films have been investigated for 3,4,9,10-perylenetetracarboxylic
dianhydride (PTCDA) on Ag(111), a model system in organic epitaxy. In situ
x-ray measurements at the anti-Bragg point during the growth show intensity
oscillations followed by a time-independent intensity which is independent of
the growth temperature. At T > 350 K, the intensity increases after growth up
to a temperature-dependent saturation value due to a post-growth diffusion
process. The time-independent intensity and the subsequent intensity recovery
have been reproduced by models based on the morphology change as a function of
the growth temperature. The morphology found after the post-growth diffusion
processes has been studied by specular rod measurements.Comment: 9 pages, 8 figures, accepted for publication in Surface Scienc
Axonal Preservation in Deep Subcortical White Matter Lesions in the Ageing Brain
Cerebral white matters lesions (WML) are seen in 94% of the population aged 64 and over and are associated
with cognitive decline and depression. We used immunohistochemistry and stereological methods on post mortem
brain samples derived from the Medical Research Council Cognitive Function and Ageing Study (MRC-CFAS) cohort
to investigate the axonal density within deep subcortical lesions. There was no significant difference between the
lesional and control white matter, therefore, we conclude that there is axonal preservation within these lesions that
are characterized by demyelination
Diffusion of gold nanoclusters on graphite
We present a detailed molecular-dynamics study of the diffusion and
coalescence of large (249-atom) gold clusters on graphite surfaces. The
diffusivity of monoclusters is found to be comparable to that for single
adatoms. Likewise, and even more important, cluster dimers are also found to
diffuse at a rate which is comparable to that for adatoms and monoclusters. As
a consequence, large islands formed by cluster aggregation are also expected to
be mobile. Using kinetic Monte Carlo simulations, and assuming a proper scaling
law for the dependence on size of the diffusivity of large clusters, we find
that islands consisting of as many as 100 monoclusters should exhibit
significant mobility. This result has profound implications for the morphology
of cluster-assembled materials
A abordagem do DNA nos livros de biologia e química do ensino médio: Uma análise crítica
Biological Control of Charcoal Rot of Mungbean by Trichoderma harzianum and Shoot Dry Biomass of Sisymbrium irio
Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium
Background
Genome-wide association studies have identified multiple genomic loci associated with coronary artery disease, but most are common variants in non-coding regions that provide limited information on causal genes and etiology of the disease. To overcome the limited scope
that common variants provide, we focused our investigation on low-frequency and rare
sequence variations primarily residing in coding regions of the genome.
Methods and results
Using samples of individuals of European ancestry from ten cohorts within the Cohorts for
Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium, both crosssectional and prospective analyses were conducted to examine associations between
genetic variants and myocardial infarction (MI), coronary heart disease (CHD), and allcause mortality following these events. For prevalent events, a total of 27,349 participants of
European ancestry, including 1831 prevalent MI cases and 2518 prevalent CHD cases were
used. For incident cases, a total of 55,736 participants of European ancestry were included
(3,031 incident MI cases and 5,425 incident CHD cases). There were 1,860 all-cause
deaths among the 3,751 MI and CHD cases from six cohorts that contributed to the analysis
of all-cause mortality. Single variant and gene-based analyses were performed separately
in each cohort and then meta-analyzed for each outcome. A low-frequency intronic variant
(rs988583) in PLCL1 was significantly associated with prevalent MI (OR = 1.80, 95% confidence interval: 1.43, 2.27; P = 7.12
A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure
Elevated blood pressure (BP), a leading cause of global morbidity and mortality, is influenced by both genetic and lifestyle factors. Cigarette smoking is one such lifestyle factor. Across five ancestries, we performed a genome-wide gene–smoking interaction study of mean arterial pressure (MAP) and pulse pressure (PP) in 129 913 individuals in stage 1 and follow-up analysis in 480 178 additional individuals in stage 2. We report here 136 loci significantly associated with MAP and/or PP. Of these, 61 were previously published through main-effect analysis of BP traits, 37 were recently reported by us for systolic BP and/or diastolic BP through gene–smoking interaction analysis and 38 were newly identified (P < 5 × 10−8, false discovery rate < 0.05). We also identified nine new signals near known loci. Of the 136 loci, 8 showed significant interaction with smoking status. They include CSMD1 previously reported for insulin resistance and BP in the spontaneously hypertensive rats. Many of the 38 new loci show biologic plausibility for a role in BP regulation. SLC26A7 encodes a chloride/bicarbonate exchanger expressed in the renal outer medullary collecting duct. AVPR1A is widely expressed, including in vascular smooth muscle cells, kidney, myocardium and brain. FHAD1 is a long non-coding RNA overexpressed in heart failure. TMEM51 was associated with contractile function in cardiomyocytes. CASP9 plays a central role in cardiomyocyte apoptosis. Identified only in African ancestry were 30 novel loci. Our findings highlight the value of multi-ancestry investigations, particularly in studies of interaction with lifestyle factors, where genomic and lifestyle differences may contribute to novel findings
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
Genome-wide association analysis advanced understanding of blood pressure (BP), a major risk factor for vascular conditions such as coronary heart disease and stroke. Accounting for smoking behavior may help identify BP loci and extend our knowledge of its genetic architecture. We performed genome-wide association meta-analyses of systolic and diastolic BP incorporating gene-smoking interactions in 610,091 individuals. Stage 1 analysis examined ~18.8 million SNPs and small insertion/deletion variants in 129,913 individuals from four ancestries (European, African, Asian, and Hispanic) with follow-up analysis of promising variants in 480,178 additional individuals from five ancestries. We identified 15 loci that were genome-wide significant (p < 5 X 10 -8) in stage 1 and formally replicated in stage 2. A combined stage 1 and 2 meta-analysis identified 66 additional genome-wide significant loci (13, 35, and 18 loci in European, African, and trans-ancestry, respectively). A total of 56 known BP loci were also identified by our results (p < 5 X 10 -8). Of the newly identified loci, ten showed significant interaction with smoking status, but none of them were replicated in stage 2. Several loci were identified in African ancestry, highlighting the importance of genetic studies in diverse populations. The identified loci show strong evidence for regulatory features and support shared pathophysiology with cardiometabolic and addiction traits. They also highlight a role in BP regulation for biological candidates such as modulators of vascular structure and function (CDKN1B, BCAR1-CFDP1, PXDN, EEA1), ciliopathies (SDCCAG8, RPGRIP1L), telomere maintenance (TNKS, PINX1, AKTIP), and central dopaminergic signaling (MSRA, EBF2)
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