Morphology and Photoluminescence of HfO2Obtained by Microwave-Hydrothermal

In this letter, we report on the obtention of hafnium oxide (HfO2) nanostructures by the microwave-hydrothermal method. These nanostructures were analyzed by X-ray diffraction (XRD), field-emission gum scanning electron microscopy (FEG-SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectrometry (EDXS), ultraviolet–visible (UV–vis) spectroscopy, and photoluminescence (PL) measurements. XRD patterns confirmed that this material crystallizes in a monoclinic structure. FEG-SEM and TEM micrographs indicated that the rice-like morphologies were formed due to an increase in the effective collisions between the nanoparticles during the MH processing. The EDXS spectrum was used to verify the chemical compositional of this oxide. UV–vis spectrum revealed that this material have an indirect optical band gap. When excited with 488 nm wavelength at room temperature, the HfO2nanostructures exhibited only one broad PL band with a maximum at around 548 nm (green emission)

Natural Course of Cysts in Birt-Hogg-Dube Syndrome

Pathogenesis and treatment of chronic pulmonary disease

Differential Requirement for the Nonhelical Tailpiece and the C Terminus of the Myosin Rod in Caenorhabditis elegans Muscle

Myosin heavy chain (MHC) is a large, multidomain protein important for both cellular structure and contraction. To examine the functional role of two C-terminal domains, the end of the coiled-coil rod and the nonhelical tailpiece, we have generated constructs in which residues within these domains are removed or mutated, and examined their behavior in Caenorhabditis elegans striated muscle. Genetic tests demonstrate that MHC lacking only tailpiece residues is competent to support the timely onset of embryonic contractions, and therefore viability, in animals lacking full-length MHC. Antibody staining experiments show that this truncated molecule localizes as wild type in early stages of development, but may be defective in processes important for thick filament organization later in embryogenesis. Ultrastructural analysis reveals thick filaments of normal morphology in disorganized arrangement, as well as occasional abnormal assemblages. In contrast, molecules in which the four terminal residues of the coiled coil are absent or mutated fail to rescue animals lacking endogenous MHC. Loss of these four residues is associated with delayed protein localization and delayed contractile function during early embryogenesis. Our results suggest that these two MHC domains, the rod and the tailpiece, are required for distinct steps during muscle development

Modelling of 3D Objects Using Unconstrained and Uncalibrated Images Taken with a Handheld Camera

Abstract. 3D models are an essential part of computer graphics applications such as games, movie special effects, urban and landscape design, architecture, virtual heritage, visual impact studies, and virtual environments such as Second Life. We have developed a novel technique which allows the construction of 3D models using image sequences acquired by a handheld low-cost digital camera. In contrast to alternative technologies, such as laser scanners, structured lighting, and sets of calibrated cameras, our approach can be used by everyone having access to a consumer-level camera. The user only has to create a set of images from different view directions, input them into our algorithm, and a 3D model is returned. We use a novel combination of advanced computer vision algorithms for feature detection, feature matching, and projection matrix estimation in order to reconstruct a 3D point cloud representing the location of geometric features estimated from input images. In a second step a full 3D model is reconstructed using the projection matrix and a triangulation process. We tested our algorithm using a variety of data sets of objects of different scales acquired under different weather and lighting conditions. The results show that our algorithm is stable and enables inexperienced users to easily create complex 3D content using a simple consumer level camera.

Optimizing Mutation and Fusion Detection in NSCLC by Sequential DNA and RNA Sequencing

Introduction: Frequently, patients with locally advanced or metastatic NSCLC are screened for mutations and fusions. In most laboratories, molecular workup includes a multitude of tests: immunohistochemistry (ALK, ROS1, and programmed death-ligand 1 testing), DNA sequencing, in situ hybridization for fusion, and amplification detection. With the fast-emerging new drugs targeting specific fusions and exon-skipping events, this procedure harbors a growing risk of tissue exhaustion.Methods: In this study, we evaluated the benefit of anchored, multiplexed, polymerase chain reaction-based targeted RNA sequencing (RNA next-generation sequencing [NGS]) in the identification of gene fusions and exon-skipping events in patients, in which no pathogenic driver mutation was found by DNA-based targeted cancer hotspot NGS (DNA NGS). We analyzed a cohort of stage IV NSCLC cases from both in-house and referral hospitals, consisting 38.5% cytology samples and 61.5% microdissected histology samples, mostly core needle biopsies. We compared molecular findings in a parallel workup (DNA NGS and RNA NGS, cohort 1, n = 198) with a sequential workup (DNA NGS followed by RNA NGS in selected cases, cohort 2, n = 192). We hypothesized the sequential workup to be the more efficient procedure.Results: In both cohorts, a maximum of one oncogenic driver mutation was found per case. This is in concordance with large, whole-genome databases and suggests that it is safe to omit RNA NGS when a clear oncogenic driver is identified in DNA NGS. In addition, this reduced the number of necessary RNA NGS to only 53% of all cases. The tumors of never smokers, however, were enriched for fusions and exon-skipping events (32% versus 4% in former and current smokers, p = 0.00), and therefore benefited more often from the shorter median turnaround time of the parallel approach (15 d versus only 9 d in the parallel workup).Conclusions: We conclude that sequentially combining DNA NGS and RNA NGS is the most efficient strategy for mutation and fusion detection in smoking-associated NSCLC, whereas for never smokers we recommend a parallel approach. This approach was shown to be feasible on small tissue samples including for cytology tests, can drastically reduce the complexity and cost of molecular workup, and also provides flexibility in the constantly evolving landscape of actionable targets in NSCLC. (C) 2020 International Association for the Study of Lung Cancer. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).MTG

Métodos alternativos do teste de frio para avaliação do vigor de sementes de milho Alternative methods of the cold test for evaluation of corn seed vigor

O presente trabalho teve como objetivo básico estudar comparativamente quatro métodos para a condução do teste de frio, visando a avaliação do potencial fisiológico das sementes de milho. Para tanto, foram utilizados dois cultivares de milho (AG 3010 e AG 5011), cada um representado por 5 lotes com potenciais fisiológicos distintos. Amostras de sementes de todos os lotes foram submetidas a quatro procedimentos do teste de frio, a saber: "terra" (mistura de terra e areia) em caixas empilhadas (método tradicional); "terra" em caixas dispostas lado a lado; bandeja com "terra"; bandeja com "terra" + papel toalha. Estes procedimentos foram comparados com os testes de germinação padrão, envelhecimento acelerado e emergência das plântulas em campo. O teste de frio em bandeja oferece maior facilidade para padronização e permite a obtenção de resultados mais consistentes do que o teste de frio utilizando-se "terra" em caixas, inclusive quanto à relação com a emergência das plântulas em campo.<br>This research was conducted with the objective of comparing different procedures of the cold test to evaluate corn seed vigor. Two cultivars (AG 3010 and AG 5011) represented by 5 lots each were used. Seed samples of all lots were submitted to four procedures of the cold test: stacked deep-box (Brazilian traditional method), deep-box disposed side by side, tray with soil and tray with soil + paper towel, in cold chamber at 10°C for seven days followed by germination at 25°C. Those procedures were also compared with germination, accelerated aging and seedling field emergence tests. The cold test in tray exhibited a great level of standardization than the procedure known as deep-box, allowing for more consistent results and a closer relationship to seedling field emergence