Crystal engineering using functionalized adamantane

We performed a first principles investigation on the structural, electronic, and optical properties of crystals made of chemically functionalized adamantane molecules. Several molecular building blocks, formed by boron and nitrogen substitutional functionalizations, were considered to build zincblende and wurtzite crystals, and the resulting structures presented large bulk moduli and cohesive energies, wide and direct bandgaps, and low dielectric constants (low-$\kappa$ materials). Those properties provide stability for such structures up to room temperature, superior to those of typical molecular crystals. This indicates a possible road map for crystal engineering using functionalized diamondoids, with potential applications ranging from space filling between conducting wires in nanodevices to nano-electro-mechanical systems

Functional interaction between BMPR-II and Tctex-1, a light chain of Dynein, is isoform-specific and disrupted by mutations underlying primary pulmonary hypertension

Diverse heterozygous mutations of bone morphogenetic receptor type II (BMPR-II) underlie the inherited form of the vascular disorder primary pulmonary hypertension (PPH). As yet, the molecular detail of how such defects contribute to the pathogenesis of PPH remains unclear. BMPR-II is a member of the transforming growth factor-beta cell signalling superfamily. Ligand binding induces cell surface receptor complex formation and activates a cascade of phosphorylation events of intracellular intermediaries termed Smads, which initiate transcriptional regulation. Some 30% of PPH-causing mutations localize to exon 12, which may be spliced out forming an isoform depleted of the unusually long BMPR-II cytoplasmic tail. To further elucidate the consequences of BMPR2 mutation, we sought to characterize aspects of the cytoplasmic domain function by seeking intracellular binding partners. We now report that Tctex-1, a light chain of the motor complex dynein, interacts with the cytoplasmic domain of BMPR-II and demonstrate that Tctex-1 is phosphorylated by BMPR-II, a function disrupted by PPH disease causing mutations within exon 12. Finally we show that BMPR-II and Tctex-1 co-localize to endothelium and smooth muscle within the media of pulmonary arterioles, key sites of vascular remodelling in PPH. Taken together, these data demonstrate a discrete function for the cytoplasmic domain of BMPR-II and justify further investigation of whether the interaction with and phosphorylation of Tctex-1 contributes to the pathogenesis of PPH

Primary pulmonary hypertension is associated with reduced pulmonary vascular expression of type II bone morphogenetic protein receptor

BACKGROUND: Mutations in the type II receptor for bone morphogenetic protein (BMPR-II), a receptor member of the transforming growth factor-beta (TGF-beta) superfamily, underlie many familial and sporadic cases of primary pulmonary hypertension (PPH). METHODS AND RESULTS: Because the sites of expression of BMPR-II in the normal and hypertensive lung are unknown, we studied the cellular localization of BMPR-II and the related type I and II receptors for TGF-beta by immunohistochemistry in lung sections from patients undergoing heart-lung transplantation for PPH (n=11, including 3 familial cases) or secondary pulmonary hypertension (n=6) and from unused donor lungs (n=4). In situ hybridization was performed for BMPR-II mRNA. Patients were screened for the presence of mutations in BMPR2. In normal lungs, BMPR-II expression was prominent on vascular endothelium, with minimal expression in airway and arterial smooth muscle. In pulmonary hypertension cases, the intensity of BMPR-II immunostaining varied between lesions but involved endothelial and myofibroblast components. Image analysis confirmed that expression of BMPR-II was markedly reduced in the peripheral lung of PPH patients, especially in those harboring heterozygous BMPR2 mutations. A less marked reduction was also observed in patients with secondary pulmonary hypertension. In contrast, there was no difference in level of staining for TGF-betaRII or the endothelial marker CD31. CONCLUSIONS: The cellular localization of BMPR-II is consistent with a role in the formation of pulmonary vascular lesions in PPH, and reduced BMPR-II expression may contribute to the process of vascular obliteration in severe pulmonary hypertension

Electronic properties and hyperfine fields of nickel-related complexes in diamond

We carried out a first principles investigation on the microscopic properties of nickel-related defect centers in diamond. Several configurations, involving substitutional and interstitial nickel impurities, have been considered either in isolated configurations or forming complexes with other defects, such as vacancies and boron and nitrogen dopants. The results, in terms of spin, symmetry, and hyperfine fields, were compared with the available experimental data on electrically active centers in synthetic diamond. Several microscopic models, previously proposed to explain those data, have been confirmed by this investigation, while some models could be discarded. We also provided new insights on the microscopic structure of several of those centers.Comment: 21 pages, 8 figure

Trial frequency effects in human temporal bisection : implications for theories of timing.

To contrast the classic version of the Scalar Expectancy Theory (SET) with the Behavioral Economic Model (BEM), we examined the effects of trial frequency on human temporal judgments. Mathematical analysis showed that, in a temporal bisection task, SET predicts that participants should show almost exclusive preference for the response associated with the most frequent duration, whereas BEM predicts that, even though participants will be biased, they will still display temporal control. Participants learned to emit one response (R[S]) after a 1.0-s stimulus and another (R[L]) after a 1.5-s stimulus. Then the effects of varying the frequencies of the 1.0-s and 1.5-s stimuli were assessed. Results were more consistent with BEM than with SET. Overall, this research illustrates how the impact of non-temporal factors on temporal discrimination may help us to contrast associative models such as BEM with cognitive models such as SET. Deciding between these two classes of models has important implications regarding the relations between associative learning and timing. This article is part of a Special Issue entitled: Associative and Temporal Learning.This research was supported by NIH grant MH033881. Jeremie Jozefowiez and Armando Machado acknowledge support from the Fundacao para a Ciencia e a Tecnologia as well as from the European project COST ISCH Action TD0904 "Time in Mental activity" (www.timely-cost.eu). We would like to thank Sean Gannon and Sarah Sterling for help running parts of the experiments, Mario Laborda, Bridget McConnell, Gonzalo Miguez, and James Witnauer for comments on an earlier version of this manuscript. Correspondence concerning this article should be addressed to Jeremie Jozefowiez, laboratoire URECA, Universite Lille Nord de France, Campus de Lille3, Domaine Universitaire du Pont de Bois, BP 60149, 58653 Villeneuve d'Ascq Cedex, France. jeremie.jozefowiez@univ-lille3fr

Avaliação da composição química das espigas de três híbridos de milho (Zea mays L.) em quatro estádios de maturação.

O objetivo deste experimento foi avaliar a composição química das espigas dos três híbridos de milho BRS 1035, BRS 1031 e BRS 1001 em quatro idades de corte, a partir da determinação dos parâmetros: matéria seca (MS), proteína bruta (PB), fibra detergente neutro (FDN) e fibra detergente ácido (FDA). O delineamento utilizado foi inteiramente casualizado com fatorial3 (híbridos) x 4 (idades de corte), sendo as médias comparadas pelo teste SNK (P<0,05). Todos os híbridos demonstraram um aumento do teor de MS de 87 para 171 dias, com diferença (P<0,05) entre todos os cortes. Não houve diferença (P<0,05) nos valores de PB entre os cortes em todos os híbridos. Aos 94 dias o híbrido BRS 1001 (5,67%) demonstrou um valor de PB superior (P<0,05) ao BRS 1031 (4,66%) e ambos foram semelhantes (P<0,05) ao BRS 1035 (5,11%). Todos os híbridos apresentaram uma queda dos valores de FDN com o avanço da maturidade até 101 dias. A variação dos valores de FDA da espiga foi muito semelhante à variação do FDN já que a correlação dessas características foi 0,97 (P<0,001). Não houve diferença (P<0,05) nos valores de FDA entre os híbridos dentro dos cortes. Os híbridos avaliados neste experimento apresentaram as mesmas tendências de aumento da MS da' espiga com o avançar da maturidade fisiológica com provável acúmulo de amido na espiga, reduzindo os teores de carboidratos estruturais como FDN e FDA nessa fração da planta

Effectiveness of Surgery for Lumbar Spinal Stenosis : A Systematic Review and Meta-Analysis

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