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The data warehousing, CWM and MOF resource page. http://www. omg.org/cwm
, 2002
"... Arg-16 and Arg-21 in the N-terminal region of the triple-gene-block protein 1 of Bamboo mosaic virus are essential for virus movement ..."
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Arg-16 and Arg-21 in the N-terminal region of the triple-gene-block protein 1 of Bamboo mosaic virus are essential for virus movement
in Real Estate Development
, 1990
"... in Real Estate Development This thesis analyzes the factors affecting distressed property and identifies the principal reasons for default. The thesis further analyzes the impact of financial structure, principal factors of default, and the probability of an individual property successfully emerging ..."
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in Real Estate Development This thesis analyzes the factors affecting distressed property and identifies the principal reasons for default. The thesis further analyzes the impact of financial structure, principal factors of default, and the probability of an individual property successfully emerging from foreclosure. The central question being explored is: From the vast pool of distressed properties, can opportunities for long term appreciation be identified by analyzing the primary reasons for default and the associated financial structure? The real estate market is
Against a Better Prison: Gender Responsiveness and the Changing Terrain of Abolition by
, 2010
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WRITING WITHOUT THE ‘PROTECTION OF ANGELS’: NOTES FROM THE MIDDLE VOICE
"... As a plainly-dressed six-year-old, I was fascinated with our neighbor woman’s jewelry and her make-up, particularly her red nail polish. I often wondered how my nails would look if they were transformed by the color red. One day in the first grade at our local Mennonite elementary school, I wondered ..."
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As a plainly-dressed six-year-old, I was fascinated with our neighbor woman’s jewelry and her make-up, particularly her red nail polish. I often wondered how my nails would look if they were transformed by the color red. One day in the first grade at our local Mennonite elementary school, I wondered no more. I colored my fingernails with my new bright red crayon. When we stood to pray before eating our lunches packed by our mothers, a few of the students called the teacher’s attention to the forbidden color on my nails. She seemed dismissive at first, but then she said, «If she’s not satisfied with how God made her nails... » My memory trails off at that point, but I do remember that I felt guilty, condemned, and different from my classmates. I hadn’t realized I was dissatisfied with my nail color. I only knew red was beautiful. Later in the year, over-attentive female students scrutinized my coloring and printing. My coloring was out of the lines, and my printing was «turkey scratches». However, on the night of the annual fall open house, I couldn’t wait to show my parents my very own writing. We walked around the block walls looking at the lined paper torn from orange Golden Rod tablets holding our printing. That night, for the first time, I saw my writing in comparison to my peers. And it did, indeed, look like scratches in the dirt. Even the teacher told Mom and Dad that the printing efforts were scratches. One feeble attempt at making me right-handed made her abandon the attempt to «correct » my left-handedness. The frustration experienced because of my less than acceptable attempts to form letters and the realization that I did not measure up to my peers in this activity were rendered insignificant, however, when it came to opening books and learning to read. When I sat at the small table in school with the other children in my reading group, I was a Bluebird. I took pride in the fact that the Bluebirds were the best, smarter than the Redbirds, smarter for sure than the Yellowbirds. Everyone knew that. What everyone knows now is how deficient and how damaging to some young children those specialized groups were.
Historical/Analytical Study of the Contributions of Alma E. McKibbin to the Seventh-Day Adventist
"... Please honor the copyright of this document by not duplicating or distributing additional copies in any form without the author’s express written permission. Thanks for your cooperation. INFORMATION TO USERS This manuscript has been reproduced from the microfilm master. U M I films the text directly ..."
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Please honor the copyright of this document by not duplicating or distributing additional copies in any form without the author’s express written permission. Thanks for your cooperation. INFORMATION TO USERS This manuscript has been reproduced from the microfilm master. U M I films the text directly from the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter face, while others may be from any type of computer printer. The quality of this reproduction is dependent upon the quality o f the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send U M I a complete manuscript and there are missing pages, these will be noted. Also, if
GOOD FOOD, GOOD FUN, AND GOOD GIRLS: USO HOSTESSES AND WORLD WAR TWO
"... Rights Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the aut ..."
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Rights Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.
In Bacillus subtilis LutR is part of the global complex regulatory network governing the adaptation to the transition from exponential growth to stationary phase
"... The lutR gene, encoding a product resembling a GntR-family transcriptional regulator, has previously been identified as a gene required for the production of the dipeptide antibiotic bacilysin in Bacillus subtilis. To understand the broader regulatory roles of LutR in B. subtilis, we studied the ge ..."
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The lutR gene, encoding a product resembling a GntR-family transcriptional regulator, has previously been identified as a gene required for the production of the dipeptide antibiotic bacilysin in Bacillus subtilis. To understand the broader regulatory roles of LutR in B. subtilis, we studied the genome-wide effects of a lutR null mutation by combining transcriptional profiling studies using DNA microarrays, reverse transcription quantitative PCR, lacZ fusion analyses and gel mobility shift assays. We report that 65 transcriptional units corresponding to 23 monocistronic units and 42 operons show altered expression levels in lutR mutant cells, as compared with lutR + wild-type cells in early stationary phase. Among these, 11 single genes and 25 operons are likely to be under direct control of LutR. The products of these genes are involved in a variety of physiological processes associated with the onset of stationary phase in B. subtilis, including degradative enzyme production, antibiotic production and resistance, carbohydrate utilization and transport, nitrogen metabolism, phosphate uptake, fatty acid and phospholipid biosynthesis, protein synthesis and translocation, cell-wall metabolism, energy production, transfer of mobile genetic elements, induction of phage-related genes, sporulation, delay of sporulation and cannibalism, and biofilm formation. Furthermore, an electrophoretic mobility shift assay performed in the presence of both SinR and LutR revealed a close overlap between the LutR and SinR targets. Our data also revealed a significant overlap with the AbrB regulon. Together, these findings reveal that LutR is part of the global complex, interconnected regulatory systems governing adaptation of bacteria to the transition from exponential growth to stationary phase.
Correspondence
, 2010
"... Calcium-transporting ATPases (Ca 2+ pumps) are major players in maintaining calcium homeostasis in the cell and have been detected in all cellular organisms. Here, we report the identification of two putative Ca 2+ pumps, M535L and C785L, encoded by chlorella viruses MT325 and AR158, respectively, a ..."
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Calcium-transporting ATPases (Ca 2+ pumps) are major players in maintaining calcium homeostasis in the cell and have been detected in all cellular organisms. Here, we report the identification of two putative Ca 2+ pumps, M535L and C785L, encoded by chlorella viruses MT325 and AR158, respectively, and the functional characterization of M535L. Phylogenetic and sequence analyses place the viral proteins in group IIB of P-type ATPases even though they lack a typical feature of this class, a calmodulin-binding domain. A Ca 2+ pump gene is present in 45 of 47 viruses tested and is transcribed during virus infection. Complementation analysis of the triple yeast mutant K616 confirmed that M535L transports calcium ions and, unusually for group IIB pumps, also manganese ions. In vitro assays show basal ATPase activity. This activity is inhibited by vanadate, but, unlike that of other Ca 2+ pumps, is not significantly stimulated by either calcium or manganese. The enzyme forms a 32 P-phosphorylated intermediate, which is inhibited by vanadate and not stimulated by the transported substrate Ca 2+, thus confirming the peculiar properties of this viral pump. To our knowledge this is the first report of a functional P-type Ca 2+-transporting ATPase encoded by a virus.
