Women in Architecture: Learning from the Past to Change the Future

Until recently the inclusion of women in the history of architecture in America was non-existent. The current pedagogy of architectural programs, internship training, and practice is gender biased, focusing on the male stars of architecture thus creating a male biased narrow definition of success in the profession. This one-sided view of the profession’s history and vision of success is not only inaccurate, but is detrimental to women in the field. Many women, after entering practice and obtaining their licenses, leave the profession as a result. This study reflects on the progression of the profession and summarizes the lives and careers of five historically significant women pioneers in the profession beginning in 1880 through 1980 who were outstanding, not only because they were exceptional women but because they were competent architects. Louise Blanchard Bethune, Marion Mahony, Julia Morgan, Denise Scott Brown, and Beverly Willis were talented, multifaceted architects who created notable architectural projects, established successful selfdefined practices, and have interesting personal stories of their road to success. Women currently in practice have benefitted from the achievements of these historical role models. Architects like Jeanne Gang, Anna Franz, Maya Lin, Monica Ponce de Leon are some of the women in practice today who, like their predecessors, have created their own career paths and do not let obstacles stop them from pursuing their attainment of success. If women in school, training, and practice were exposed to the history of these pioneers, they would realize that they, these pioneers have faced numerous obstacles in their careers and lives and did not let anyone or anything deter them from pursuing their dreams and defining their careers and lives in their own way. The entire architectural profession including education, training, and practice, along with architectural organizations, needs to change and work collaboratively to embrace and promote the true history of the profession that includes both men and women. The profession must progress to best service the twenty-first century society

Insufficient weight at birth and preschool-age growth in children attending charitably funded crèches in the municipality of Santo André , in the State of São Paulo , Brazil

OBJETIVOS: comparar o crescimento alcançado e a prevalência de baixa estatura na idade pré-escolar entre recém-nascidos de peso insuficiente (PNI) e de peso adequado (PNA). MÉTODOS: foram estudadas 323 crianças com PNI e 886 com PNA de famílias de baixa renda de quinze creches filantrópicas de Santo André, São Paulo, Brasil, em 2001 e 2002. As variáveis foram o escore Z de peso e de estatura para a idade, pelo referencial Center for Disease Control (CDC) and National Center for Health Statistics (NCHS) 2000, comparando-se as médias dos dois grupos. Calculou-se a razão de prevalência (RP) de baixa estatura na idade pré-escolar em decorrência do peso insuficiente ao nascer. RESULTADOS: o escore z médio de peso foi -0,09 e 0,39 e o escore z médio de estatura foi de -0,06 e de 0,24 para as crianças de PNI e de PNA, respectivamente. A prevalência de baixa estatura foi de 2,78% para as crianças com PNI e de 0,79% para aquelas com PNA. A RP de baixa estatura na idade pré-escolar para as crianças de PNI foi de 3,5 (IC95% 1,3-9,4). CONCLUSÕES: as crianças com PNI apresentaram crescimento inferior e maior risco de falhas de crescimento até a idade pré-escolar, sugerindo um efeito negativo do peso insuficiente ao nascer sobre o crescimento infantil.OBJECTIVES: to compare rate of growth and prevalence of low stature at preschool age in children who were underweight at birth and in children born with a normal weight. METHODS: the study covered 323 children born underweight and 886 born with a normal weight from low-income families in fifteen charitably funded crèches in the municipality of Santo André, in the State of São Paulo, Brazil, in 2001 and 2002. The variables used were the z score for weight and height for age, using the Center for Disease Control (CDC) and National Center for Health Statistics (NCHS) 2000 benchmark, comparing the means for the two groups. The prevalence ratio was calculated for low stature in preschool age children resulting from insufficient weight at birth. RESULTS: the z score for weight was -0.09 and 0.39 and the average z score for height was -0.06 and 0.24 for underweight and normal weight at birth, respectively. The prevalence of low stature was 2.78% for children born underweight and 0.79% for normal weight. The PR for low stature at preschool age for children born underweight was 3.5 (CI95% 1.3-9.4). CONCLUSIONS: children born underweight had a lower rate of growth and greater risk of developing a growth disorder up to preschool age, suggesting a negative effect of insufficient birth weight on child growth

Leptin and high glucose stimulate cell proliferation in MCF-7 human breast cancer cells: reciprocal involvement of PKC-α and PPAR expression

AbstractGlucose concentration may be an important factor in breast cancer cell proliferation, and the prevalence of breast cancer is high in diabetic patients. Leptin may also be an important factor since plasma levels of leptin correlated with TNM staging for breast cancer patients. The effects of glucose and leptin on breast cancer cell proliferation were evaluated by examining cell doubling time, DNA synthesis, levels of cell cycle related proteins, protein kinase C (PKC) isozyme expression, and peroxisome proliferator-activated receptor (PPAR) subtypes were determined following glucose exposure at normal (5.5 mM) and high (25 mM) concentrations with/without leptin in MCF-7 human breast cancer cells. In MCF-7 cells, leptin and high glucose stimulated cell proliferation as demonstrated by the increases in DNA synthesis and expression of cdk2 and cyclin D1. PKC-α, PPARγ, and PPARα protein levels were up-regulated following leptin and high glucose treatment in drug-sensitive MCF-7 cells. However, there was no significant effect of leptin and high glucose on cell proliferation, DNA synthesis, levels of cell cycle proteins, PKC isozymes, or PPAR subtypes in multidrug-resistant human breast cancer NCI/ADR-RES cells. These results suggested that hyperglycemia and hyperleptinemia increase breast cancer cell proliferation through accelerated cell cycle progression with up-regulation of cdk2 and cyclin D1 levels. This suggests the involvement of PKC-α, PPARα, and PPARγ

Year 2030: the dawn of the millennium profession: nursing - a prospective vision of under-graduate students

Estudo sobre cartas-testamento escritas por estudantes do 1º ano de graduação em enfermagem, que deveriam imaginar-se estar no ano 2030. Tudo o que esses alunos imaginaram que poderia ter acontecido nas três décadas anteriores a 2030 foi objeto dessa atividade, tais como conquistas profissionais e da profissão, cura de doenças, exercício de cargos e prestígio social.Study based on testament-letters written by freshmen students of the undergraduate course in Nursing, who should imagine to be in the year 2030. Everything imagined by these students and that might have happened in the three earlier decades was the subject of this study, such as professional and nurses achievements, outbtreak of cure for illnesses, social prestige and positions

DNA Methylation of the ABO Promoter Underlies Loss of ABO Allelic Expression in a Significant Proportion of Leukemic Patients

Background: Loss of A, B and H antigens from the red blood cells of patients with myeloid malignancies is a frequent occurrence. Previously, we have reported alterations in ABH antigens on the red blood cells of 55% of patients with myeloid malignancies. Methodology/Principal Findings: To determine the underlying molecular mechanisms of this loss, we assessed ABO allelic expression in 21 patients with ABH antigen loss previously identified by flow cytometric analysis as well as an additional 7 patients detected with ABH antigen changes by serology. When assessing ABO mRNA allelic expression, 6/12 (50%) patients with ABH antigen loss detected by flow cytometry and 5/7 (71%) of the patients with ABH antigen loss detected by serology had a corresponding ABO mRNA allelic loss of expression. We examined the ABO locus for copy number and DNA methylation alterations in 21 patients, 11 with loss of expression of one or both ABO alleles, and 10 patients with no detectable allelic loss of ABO mRNA expression. No loss of heterozygosity (LOH) at the ABO locus was observed in these patients. However in 8/11 (73%) patients with loss of ABO allelic expression, the ABO promoter was methylated compared with 2/10 (20%) of patients with no ABO allelic expression loss (P = 0.03). Conclusions/Significance: We have found that loss of ABH antigens in patients with hematological malignancies is associated with a corresponding loss of ABO allelic expression in a significant proportion of patients. Loss of ABO allelic expression was strongly associated with DNA methylation of the ABO promoter.Tina Bianco-Miotto, Damian J. Hussey, Tanya K. Day, Denise S. O'Keefe and Alexander Dobrovi

Invasiveness as a putative additional virulence mechanism of some atypical Enteropathogenic Escherichia coli strains with different uncommon intimin types

<p>Abstract</p> <p>Background</p> <p>Enteropathogenic <it>Escherichia coli </it>(EPEC) produce attaching/effacing (A/E) lesions on eukaryotic cells mediated by the outer membrane adhesin intimin. EPEC are sub-grouped into typical (tEPEC) and atypical (aEPEC). We have recently demonstrated that aEPEC strain 1551-2 (serotype O non-typable, non-motile) invades HeLa cells by a process dependent on the expression of intimin sub-type omicron. In this study, we evaluated whether aEPEC strains expressing other intimin sub-types are also invasive using the quantitative gentamicin protection assay. We also evaluated whether aEPEC invade differentiated intestinal T84 cells.</p> <p>Results</p> <p>Five of six strains invaded HeLa and T84 cells in a range of 13.3%–20.9% and 5.8%–17.8%, respectively, of the total cell-associated bacteria. The strains studied were significantly more invasive than prototype tEPEC strain E2348/69 (1.4% and 0.5% in HeLa and T84 cells, respectively). Invasiveness was confirmed by transmission electron microscopy. We also showed that invasion of HeLa cells by aEPEC 1551-2 depended on actin filaments, but not on microtubules. In addition, disruption of tight junctions enhanced its invasion efficiency in T84 cells, suggesting preferential invasion via a non-differentiated surface.</p> <p>Conclusion</p> <p>Some aEPEC strains may invade intestinal cells <it>in vitro </it>with varying efficiencies and independently of the intimin sub-type.</p

HeLa-cell adherence patterns and actin aggregation of enteropathogenic Escherichia coli (EPEC) and Shiga-toxin-producing E. coli (STEC) strains carrying different eae and tir alleles

A collection of 69 eae-positive strains expressing 29 different intimin types and eight tir alleles was characterized with respect to their adherence patterns to HeLa cells, ability to promote actin accumulation in vitro, the presence of bfpA alleles in positive strains, and bundle-forming pilus (BFP) expression. All of the nine typical enteropathogenic Escherichia coli (tEPEC) studied harbored the enteropathogenic E. coli adherence factor (EAF) plasmid, as shown by PCR and/or EAF probe results. In addition, they were positive for bfpA, as shown by PCR, and BFP expression, as confirmed by immunofluorescence (IFL) and/or immunoblotting (IBL) assays. Localized adherence (LA) was exclusively displayed by those nine tEPEC, while localized-adherence-like (LAL) was the most frequent pattern among atypical EPEC (aEPEC) and Shiga-toxinproducing E. coli (STEC). All LA and LAL strains were able to cause attaching and effacing (AE) lesions, as established by means of the FAS test. There was a significant association between the presence of tir allele α1 and bfpA-positive strains, and consequently, with the LA pattern. However, intimin type or bfpA was not associated with the adherence pattern displayed in HeLa cells. Among the eight bfpA alleles detected, a new type (β10; accession number FN391178) was identified in a strain of serotype O157:H45, and a truncated variant (β3.2-t; accession number FN 391181) in four strains belonging to different pathotypes. [Int Microbiol 2009; 12(4):243-251

Draft whole-genome sequences of 10 atypical enteropathogenic Escherichia coli strains isolated in Brazil

The number of diarrhea cases caused by atypical enteropathogenic Escherichia coli (aEPEC) has been increasing worldwide. Here, we report the draft whole-genome sequences of 10 aEPEC strains isolated in Brazil. These sequences will provide an important source for future studies concerning aEPEC pathogenicity and genetic markers of potentially virulent strains