33 resultados para 22-218
Resumo:
Neste estudo, objetivou-se contrastar os efeitos de sombreamento sobre o crescimento de S. orientalis, utilizando a análise de crescimento. Os experimentos foram conduzidos em vasos, a pleno sol (A) e sob sombrite 50% (B). As plantas tiveram seus índices de crescimento determinados aos 14, 28, 42, 56, 80, 94 e 108 dias após o transplante (DAT), para A; e aos 14, 28, 42, 56, 70, 84, 108, 122 e 136 DAT, para B. O delineamento experimental foi o inteiramente casualizado, com quatro repetições. Os dados foram analisados por meio de análise de regressão. Os modelos foram escolhidos com base na significância dos coeficientes de regressão, utilizando-se o teste t até 10%, no coeficiente de determinação e no fenômeno em estudo. As plantas apresentaram comportamento semelhante em A e B para a maioria das variáveis analisadas, embora as plantas sombreadas (radiação média de 218 µmol m-² s-¹) tivessem maior duração do ciclo cultural, cerca de 140 DAT, retardando os valores máximos e/ou mínimos, em relação às plantas a luz plena (média de 658 µmol m-² s-¹), com aproximadamente 110 DAT. Em B, foram obtidas também as maiores médias para a maioria dos índices avaliados - área foliar, altura, números de folhas e capítulos florais, biomassa seca total, taxa de crescimento absoluto, taxa de crescimento relativo, razão de peso foliar, razão de área foliar e área foliar específica -, sugerindo que a espécie é favorecida pelo sombreamento.
Resumo:
The Thr(118)Met substitution in the peripheral myelin protein 22 (PMP22) gene has been detected in a number of families with demyelinating Charcot-Marie-Tooth (CMT1) neuropathy or with the hereditary neuropathy with liability to pressure palsy, but in none of them has it consistently segregated with the peripheral neuropathy. We describe here a CMT1 family (a 63-year-old man, his brother and his niece) in which two mutations on different chromosomes were found in the PMP22 gene, the 17p duplication, detected by fluorescent semiquantitative polymerase chain reaction (PCR) of microsatellite markers localized within the duplicated region on chromosome 17p11.2-p12, and the Thr(118)Met substitution, detected by direct sequencing the four coding exons of the PMP22 gene. A genotype/phenotype correlation study showed that the neuropathy segregates with the duplication and that the amino acid substitution does not seem to modify the clinical characteristics or the severity of the peripheral neuropathy. We did not find any evidence to characterize this substitution as a polymorphism in the population studied and we propose that the high frequency reported for this point mutation in the literature suggests that the Thr(118)Met substitution may be a hotspot for mutations in the PMP22 gene.
Resumo:
Preterm delivery is the main cause of neonatal death and ultrasonographic cervical assessment has been shown to be more accurate than digital examination in recognizing a short cervix. This is a cross-sectional study, involving 1131 women at 22-24 weeks of pregnancy, designed to determine the distribution of cervical length and to examine which variables of demographic characteristics and obstetric history increase the risk of a short cervix (15 mm or less). The distribution of maternal demographic and obstetric history characteristics among patients with cervical length £15 mm was analyzed and compared to the findings for the general population. Risk ratios (RR) between subgroups were generated from this comparison. Median cervical length was 37 mm and in 1.5% of cases it was 15 mm or less. The proportion of women with a short cervix (<=15 mm) was significantly higher among patients with a low body mass index (RR = 3.5) and in those with previous fetal losses between 16-23 weeks (RR = 33.1) or spontaneous preterm deliveries between 24-32 weeks (RR = 14.1). We suggest that transvaginal sonographic measurement of cervical length be performed as part of a routine midtrimester ultrasound evaluation. There are specific variables of demographic characteristics and obstetric history which increase the risk of detecting a short cervix at 22-24 weeks.