74 research outputs found
Implementation of a Primary Tapped Transformer in a High Frequency Isolated Power Converter
Abstract: On load, transformer primary tap changing is not common in high frequency converters. This paper investigates a new converter topology to drive primary tapped transformers. The ideas that have been introduced previously are simply implemented into existing converter topologies which have been modified to accommodate a primary tapped transformer. The effects of efficiency with variation of source voltage and duty cycle are studied. It is shown that this topology can maintain a load voltage for a much wider source voltage variation without major sacrifices in efficiency
Some considerations for miniaturized measurement shunts in high frequency power electronic converters.
Abstract: Power semi-conductors are able to achieve switching transients within a few nanoseconds and possibly even faster. These fast switching transients will need to be measured and analyzed thoroughly. In this paper four different types of shunt constructions and installations are tested on the same power electronics circuit, giving widely diverse results. Interpreting and analyzing these measurement results will assist in developing accurate current measurement devices for fast switching transient power electronic converters of the future
An experimental study of switching GaN FETs in a coaxial transmission line
Abstract: The switching characteristics of GaN FETs have not yet been measured accurately because of their small electromagnetic size in relation to the circuit and the electromagnetic environment the measurements are exposed to. Switching GaN FETs in a transmission line will allow for measurements to be taken in an electromagnetically defined environment. The transmission line is adapted to take optimum measurements. This is proven by the waveforms presented
Albuminuria is associated with too few glomeruli and too much testosterone
Normally, the glomerular filtration barrier almost completely excludes circulating albumin from entering the urine. Genetic variation and both pre- and postnatal environmental factors may affect albuminuria in humans. Here we determine whether glomerular gene expression in mouse strains with naturally occurring variations in albuminuria would allow identification of proteins deregulated in relatively 'leaky' glomeruli. Albuminuria increased in female B6 to male B6 to female FVB/N to male FVB/N mice, whereas the number of glomeruli/kidney was the exact opposite. Testosterone administration led to increased albuminuria in female B6 but not female FVB/N mice. A common set of 39 genes, many expressed in podocytes, were significantly differentially expressed in each of the four comparisons: male versus female B6 mice, male versus female FVB/N mice, male FVB/N versus male B6 mice, and female FVB/N versus female B6 mice. The transcripts encoded proteins involved in oxidation/reduction reactions, ion transport, and enzymes involved in detoxification. These proteins may represent novel biomarkers and even therapeutic targets for early kidney and cardiovascular disease
Oxygenation and spontaneous deamination of 2-aminobenzenesulphonic acid in Alcaligenes sp. strain O-1 with subsequent meta ring cleavage and spontaneous desulphonation to 2-hydroxymuconic acid
Renal malformations associated with mutations of developmental genes: messages from the clinic
Renal tract malformations (RTMs) account for about 40% of children with end-stage renal failure. RTMs can be caused by mutations of genes normally active in the developing kidney and lower renal tract. Moreover, some RTMs occur in the context of multi-organ malformation syndromes. For these reasons, and because genetic testing is becoming more widely available, pediatric nephrologists should work closely with clinical geneticists to make genetic diagnoses in children with RTMs, followed by appropriate family counseling. Here we highlight families with renal cysts and diabetes, renal coloboma and Fraser syndromes, and a child with microdeletion of chromosome 19q who had a rare combination of malformations. Such diagnoses provide families with often long-sought answers to the question “why was our child born with kidney disease”. Precise genetic diagnoses will also help to define cohorts of children with RTMs for long-term clinical outcome studies
Expression of Fraser syndrome genes in normal and polycystic murine kidneys
BACKGROUND: Fraser syndrome (FS) features renal agenesis and cystic kidneys. Mutations of FRAS1 (Fraser syndrome 1)and FREM2 (FRAS1-related extracellular matrix protein 2)cause FS. They code for basement membrane proteins expressed in metanephric epithelia where they mediate epithelial/mesenchymal signalling. Little is known about whether and where these molecules are expressed in more mature kidneys. METHODS: In healthy and congenital polycystic kidney (cpk)mouse kidneys we sought Frem2 expression using a LacZ reporter gene and quantified Fras family transcripts. Fras1 immunohistochemistry was undertaken in cystic kidneys from cpk mice and PCK (Pkhd1 mutant) rats (models of autosomal recessive polycystic kidney disease) and in wildtype metanephroi rendered cystic by dexamethasone. RESULTS: Nascent nephrons transiently expressed Frem2 in both tubule and podocyte epithelia. Maturing and adult collecting ducts also expressed Frem2. Frem2 was expressed in cpk cystic epithelia although Frem2 haploinsufficiency did not significantly modify cystogenesis in vivo. Fras1 transcripts were significantly upregulated, and Frem3 downregulated, in polycystic kidneys versus the non-cystic kidneys of littermates. Fras1 was immunodetected in cpk, PCK and dexamethasone-induced cystepithelia. CONCLUSIONS: These descriptive results are consistent with the hypothesis that Fras family molecules play diverse roles in kidney epithelia. In future, this should be tested by conditional deletion of FS genes in nephron segments and collecting ducts
Isoflavone metabolism in domestic cats (Felis catus): comparison of plasma metabolites detected after ingestion of two different dietary forms of genistein and daidzein
Some felid diets contain isoflavones but the metabolic capacity of cats toward isoflavones is relatively unknown, despite the understanding that isoflavones have divergent biological potential according to their metabolite end products. The objective of this study was to determine the plasma metabolites detectable in domestic cats after exposure to 2 different dietary forms of isoflavones, either as a soy extract tablet ( n = 6) or as part of a dietary matrix ( n = 4). Serial blood samples were collected after isoflavone exposure to identify the plasma metabolites of each cat. Genistein was detected in its unconjugated form or as a monosulfate. Daidzein was detected as both a mono- and disulfate as well as in its unconjugated form. Other daidzein metabolites detected included equol mono- and disulfate, dihydrodaidzein, and O -desmethylangolensin. No β -glucuronide metabolites of either isoflavone were detected. Equol was produced in markedly fewer cats after ingestion of a soy extract tablet as a single oral bolus compared with cats consuming an isoflavone-containing diet. The detectable metabolites of the isoflavones, genistein and daidzein, in domestic cat plasma after dietary ingestion has been described in the present study for the first time. The metabolic capacity for isoflavones by domestic cats appears to be efficient, with only minimal proportions of the ingested amount detected in their unconjugated forms. This has implications for the potential of isoflavones to exert physiological activity in the domestic cat when consumed at concentrations representative of typical dietary intake
Writing Class In and Out: Constructions of Class in Elite Businesswomen's Autobiographies
The final version of this paper has been published in Sociology, November 2020 by SAGE Publications Ltd, All rights reserved. © The Authors, 2020. It is available at: https://journals.sagepub.com/home/socThis article explores how meanings of class are constructed in elite businesswomen’s autobiographies. It extends existing sociological studies of elites in two ways. First, by theorising the cultural mechanisms that contribute to the reproduction of business elites, and second, by examining the hitherto under-researched gendered aspects of the reproduction of business elites, and the legitimisation of wealth. We show how these autobiographical texts acknowledge class yet render it irrelevant through discursive repertoires of ordinariness, a universal gender struggle and the unimportance of wealth. We argue that in doing so the genre of elite businesswomen autobiographies contributes to the cultural erasure of class, perpetuating messages that contribute to the creation of a cultural milieu in which class and wealth inequalities remain unquestioned. In an economic context where social disparities continue to grow, the article importantly furthers our understanding of the cultural means by which a plutocratic elite holds on to power
Enhancement of the activity of phenoxodiol by cisplatin in prostate cancer cells
Phenoxodiol is a novel isoflav-3-ene, currently undergoing clinical trials, that has a broad in vitro activity against a number of human cancer cell lines. Phenoxodiol alone inhibited DU145 and PC3 in a dose- and time-dependent manner with IC50 values of 8±1 and 38±9 μM, respectively. The combination of phenoxodiol and cisplatin was synergistic in DU145, and additive in PC3, as assessed by the Chou–Talalay method. Carboplatin was also synergistic in combination with phenoxodiol in DU145 cells. The activity of the phenoxodiol and cisplatin combination was confirmed in vivo using a DU145 xenograft model in nude mice. Pharmacokinetic data from these mice suggest that the mechanism of synergy may occur through a pharmacodynamic mechanism. An intracellular cisplatin accumulation assay showed a 35% (P<0.05) increase in the uptake of cisplatin when it was combined in a ratio of 1 μM: 5 μM phenoxodiol, resulting in a 300% (P<0.05) increase in DNA adducts. Taken together, our results suggest that phenoxodiol has interesting properties that make combination therapy with cisplatin or carboplatin appealing
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