1000 resultados para Bray-1


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Em Latossolo Vermelho-Amarelo textura arenosa, do submedio Sao Francisco, avaliou-se a dispnibilidade de fosforo no solo extraido pelos extratores de Mehlich e Bray 1 e estimaram-se niveis adequados de adubacao fosfatada para o tomateiro rasteiro (Lycopersicum esculentum Mill) no periodo de 1982 a 1983. Diferentes niveis de fosforo no solo foram criados atraves da adicao previa de quantidades crescentes de fosfato sob a forma de superfosfato triplo. Obtiveram-se correlacoes significativas dos teores de fosforo no solo com os niveis de fosfato aplicado e a produtividade da cultura. Os teores de P no solo obtidos pelos extratores de Mehlich e Bray 1 foram classificados, respectivamente, nos seguintes niveis: muito baixo, inferiores a 5 ppm e 7 ppm; baixo, de 5 ppm a 10 ppm e 7 ppm a 12 ppm; medio, de 11 ppm a 16 ppm e 13 ppm a 18 ppm; alto, de 17 ppm a 29 ppm e 19 ppm a 31 ppm; e muito alto, superiores a 19 ppm e 31ppm. As doses estimadas de fosforo a serem aplicadas ao solo em sulco para obter a produtividade otima esperada seriam: 120, 100, 70, 30 e 0 kg/ha de P2O5 para os niveis muito baixo, baixo, medio, alto e muito alto, respectivamente.

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Neste trabalho é apresentada uma modificação ao método de BRAY (1948) para se construir uma curva de calibração de nutrientes disponíveis no solo. Basicamente, trata-se de se estimar o valor da constante da equação de Mitscherlich, na forma linear, por meio de regressão linear e com esse valor construir uma curva de calibração.

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Macvicaria crassigula (Linton, 1910) (Opecoelidae) is referred from the intestine of Micropogonias furnieri and from Stellifer rastrifer; and from Stellifer rastrifer, and Saturnius maurepasi Overstreet, 1977 (Bunocotylidae) from the stomach of Mugil liza. This is the first report of these species in Brazil, and a new host records are presented.

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Original eingebunden in: Senckenberg, Johann Christian: [Undatiertes und Varia zu den ärztlichen und nicht ärztlichen Tagebüchern]

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This study aimed at evaluating the functional activation and activating receptors expression on resting, short- and long-term NK and NK-like T cells from blood of ovarian neoplasia patients. Blood from patients with adnexal benign alterations (n = 10) and ovarian cancer (grade I-IV n = 14) were collected after signed consent. Effector cells activation was evaluated by the expression of the CD107a molecule. Short-term culture was conducted overnight with IL-2 and long-term culture for 21 days, by a method designed to expand CD56(+) lymphocytes. Short-term culture significantly increased NK cells activation compared to resting NK cells (p<0.05), however, the long-term procedure supported an even higher increase (p<0.001). Resting NK-like T cells showed poor activation, which was not altered by the culture procedures. The long-term culture effectively increased the expression of the activating receptors on NK and NK-like T cells, either by increasing the number of cells expressing a given receptor and/or by up-regulating their expression intensity. As a conclusion, the long-term culture system employed, resulted in a high number of functional NK cells. The culture system was particularly efficient on the up-regulation of NKp30 and DNAM-1 receptors on NK cells.

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Human bocavirus 1 (HBoV1) is associated with respiratory infections worldwide, mainly in children. Similar to other parvoviruses, it is believed that HBoV1 can persist for long periods of time in humans, probably through maintaining concatemers of the virus single-stranded DNA genome in the nuclei of infected cells. Recently, HBoV-1 was detected in high rates in adenoid and palatine tonsils samples from patients with chronic adenotonsillar diseases, but nothing is known about the virus replication levels in those tissues. A 3-year prospective hospital-based study was conducted to detect and quantify HBoV1 DNA and mRNAs in samples of the adenoids (AD), palatine tonsils (PT), nasopharyngeal secretions (NPS), and peripheral blood (PB) from patients undergoing tonsillectomy for tonsillar hypertrophy or recurrent tonsillitis. HBoV1 was detected in 25.3% of the AD samples, while the rates of detection in the PT, NPS, and PB samples were 7.2%, 10.5%, and 1.7%, respectively. The viral loads were higher in AD samples, and 27.3% of the patients with HBoV had mRNA detectable in this tissue. High viral loads and detectable mRNA in the AD were associated with HBoV1 detection in the other sample sites. The adenoids are an important site of HBoV1 replication and persistence in children with tonsillar hypertrophy. The adenoids contain high HBoV1 loads and are frequently positive for HBoV mRNA, and this is associated with the detection of HBoV1 in secretions.

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This study aimed to identify novel biomarkers for thyroid carcinoma diagnosis and prognosis. We have constructed a human single-chain variable fragment (scFv) antibody library that was selected against tumour thyroid cells using the BRASIL method (biopanning and rapid analysis of selective interactive ligands) and phage display technology. One highly reactive clone, scFv-C1, with specific binding to papillary thyroid tumour proteins was confirmed by ELISA, which was further tested against a tissue microarray that comprised of 229 thyroid tissues, including: 110 carcinomas (38 papillary thyroid carcinomas (PTCs), 42 follicular carcinomas, 30 follicular variants of PTC), 18 normal thyroid tissues, 49 nodular goitres (NG) and 52 follicular adenomas. The scFv-C1 was able to distinguish carcinomas from benign lesions (P=0.0001) and reacted preferentially against T1 and T2 tumour stages (P=0.0108). We have further identified an OTU domain-containing protein 1, DUBA-7 deubiquitinating enzyme as the scFv-binding antigen using two-dimensional polyacrylamide gel electrophoresis and mass spectrometry. The strategy of screening and identifying a cell-surface-binding antibody against thyroid tissues was highly effective and resulted in a useful biomarker that recognises malignancy among thyroid nodules and may help identify lower-risk cases that can benefit from less-aggressive management.

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The present study investigated the effects of running at 0.8 or 1.2 km/h on inflammatory proteins (i.e., protein levels of TNF- α , IL-1 β , and NF- κ B) and metabolic proteins (i.e., protein levels of SIRT-1 and PGC-1 α , and AMPK phosphorylation) in quadriceps of rats. Male Wistar rats at 3 (young) and 18 months (middle-aged rats) of age were divided into nonexercised (NE) and exercised at 0.8 or 1.2 km/h. The rats were trained on treadmill, 50 min per day, 5 days per week, during 8 weeks. Forty-eight hours after the last training session, muscles were removed, homogenized, and analyzed using biochemical and western blot techniques. Our results showed that: (a) running at 0.8 km/h decreased the inflammatory proteins and increased the metabolic proteins compared with NE rats; (b) these responses were lower for the inflammatory proteins and higher for the metabolic proteins in young rats compared with middle-aged rats; (c) running at 1.2 km/h decreased the inflammatory proteins and increased the metabolic proteins compared with 0.8 km/h; (d) these responses were similar between young and middle-aged rats when trained at 1.2 km. In summary, the age-related increases in inflammatory proteins, and the age-related declines in metabolic proteins can be reversed and largely improved by treadmill training.