Espectroscopia mecânica em ruteno-cupratos: mobilidade de vacâncias de oxigênio intersticial

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

O Brasil rural nas obras de Monteiro Lobato nas décadas de 1910 a 1930

Pós-graduação em Ciências Sociais - FFC

Enxertos venosos ao avesso e normal, preenchidos com plasma rico em plaquetas em nervo misto de rato

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Determinação do percentual de malte de cevada em cervejas tipo Pilsen utilizando os isótopos estáveis do carbono ('delta' 'inpot.13C') e do nitrogênio ('delta' 'inpot15N')

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Efeito do lodo de esgoto sobre a atividade microbiana e fitopatógenos habitantes do solo

Pós-graduação em Agronomia (Proteção de Plantas) - FCA

Influência da adição de reforço e ciclagem mecânica na resistência ao impacto de resinas para base e para reembasamento imediato

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Influência da altura da coroa em implantes osseointegrados: estudo pelo método dos elementos finitos tridimensionais

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Comportamento de lek, frugivora e dispersão de sementes por Manacus Manacus (Linnaeus 1766, Pipridae) em áres de restinga no sudeste do Brasil

Pós-graduação em Ciências Biológicas (Zoologia) - IBRC

Expressão de fatores relacionados à morte celular programada em embriões bovinos infectados com BHV-5

Pós-graduação em Microbiologia - IBILCE

Culture of equine bone marrow mononuclear fraction and adipose tissue-derived stromal vascular fraction cells in different media

The objective of this study was to evaluate the culture of equine bone marrow mononuclear fraction and adipose tissue - derived stromal vascular fraction cells in two different cell culture media. Five adult horses were submitted to bone marrow aspiration from the sternum, and then from the adipose tissue of the gluteal region near the base of the tail. Mononuclear fraction and stromal vascular fraction were isolated from the samples and cultivated in DMEM medium supplemented with 10% fetal bovine serum or in AIM-V medium. The cultures were observed once a week with an inverted microscope, to perform a qualitative analysis of the morphology of the cells as well as the general appearance of the cell culture. Colony-forming units (CFU) were counted on days 5, 15 and 25 of cell culture. During the first week of culture, differences were observed between the samples from the same source maintained in different culture media. The number of colonies was significantly higher in samples of bone marrow in relation to samples of adipose tissue.

Artificial activation of bovine and equine oocytes with cycloheximide, roscovitine, strontium, or 6-dimethylaminopurine in low or high calcium concentrations

Knowledge on parthenogenetic activation of oocytes is important to improve the efficiency of nuclear transfer (NT) and intracytoplasmic sperm injection (ICSI) because artificial activation of oocyte (AOA) is an essential step to achieve embryo production. Although different procedures for AOA have been established, the efficiency of in vitro production of embryos remains low, especially in equines and Bos taurus bovines. In an attempt to improve the techniques of NT and ICSI in bovine and equine species, we tested different combinations of drugs that had different mechanisms of action for the parthenogenetic activation of oocytes in these animals. The oocytes were collected, in vitro matured for 24 to 30 h and activated artificially, in the presence of low or high concentrations of calcium, with combinations of calcium ionophore (ionomycin) with cycloheximide, roscovitine, strontium, or 6-dimethylaminopurine (6-DMAP). For assessment of activation rates, oocytes were stained with Hoechst 33342 and observed under an inverted microscope. We showed that all combinations of drugs were equally efficient in activating bovine oocytes, with the best results obtained when high concentrations of calcium were adopted. For equine oocytes, high concentrations of calcium were not beneficial for the parthenogenetic activation and the combination of ionomycin with either 6-DMAP or roscovitine was effective in inducing artificial activation of oocytes. We believe that our preliminary findings provide some clues for the development of a better AOA protocol to be used with these species.

Chromatic changes to artificial irises produced using different techniques

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

O agostinismo político: contribuições e limites para as discussões políticas medievais

Pós-graduação em História - FCLAS

Heterochromatin and molecular characterization of DsmarMITE transposable element in the beetle Dichotomius schiffleri (Coleoptera: Scarabaeidae)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Lumped element modeling of operational structures by inverting the mobility models

This paper is concerned with what a source precisely sees when it drives a receiver such as a continuous structural object. An equivalent lumped element system consisting of masses, springs and dampers is developed to visually represent the operational structural dynamics of a single-input structure at the driving point. The development is solely based on the mobility model of the driving point response. The mobility model is mathematically inverted to give the impedance model that is suitable for lumped element modeling. The two types of structures studied are unconstrained inertial objects and constrained resilient objects. The lumped element systems presented suggest a new view to dynamics that a single-input flexible structure in operation can be decomposed into the two subsystems: a base system of single degree of freedom (or of a mass for an inertial object) whose mass is in contact with the source and an appendage system consisting of a series of oscillators each of which is attached to the base mass. The driving point response is a result of the coupling between the two subsystems. (C) 2014 Elsevier Ltd. All rights reserved.