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Institution

University of Oklahoma

EducationNorman, Oklahoma, United States
About: University of Oklahoma is a education organization based out in Norman, Oklahoma, United States. It is known for research contribution in the topics: Population & Radar. The organization has 25269 authors who have published 52609 publications receiving 1821706 citations. The organization is also known as: OU & Oklahoma University.


Papers
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Journal ArticleDOI
Georges Aad1, Brad Abbott2, Jalal Abdallah3, S. Abdel Khalek4  +2815 moreInstitutions (169)
TL;DR: In this article, a search for new phenomena in final states with an energetic jet and large missing transverse momentum was performed using 20.3 fb(-1) of root s = 8 TeV data collected in 2012.
Abstract: Results of a search for new phenomena in final states with an energetic jet and large missing transverse momentum are reported. The search uses 20.3 fb(-1) of root s = 8 TeV data collected in 2012 ...

414 citations

Journal ArticleDOI
TL;DR: In addition to taxonomic and metabolic differences between urban and traditional lifestyles, hunter-gatherers form a distinct sub-group among traditional peoples and Treponema are discovered, which are symbionts lost in urban-industrialized societies.
Abstract: Recent studies suggest that gut microbiomes of urban-industrialized societies are different from those of traditional peoples. Here we examine the relationship between lifeways and gut microbiota through taxonomic and functional potential characterization of faecal samples from hunter-gatherer and traditional agriculturalist communities in Peru and an urban-industrialized community from the US. We find that in addition to taxonomic and metabolic differences between urban and traditional lifestyles, hunter-gatherers form a distinct sub-group among traditional peoples. As observed in previous studies, we find that Treponema are characteristic of traditional gut microbiomes. Moreover, through genome reconstruction (2.2-2.5 MB, coverage depth × 26-513) and functional potential characterization, we discover these Treponema are diverse, fall outside of pathogenic clades and are similar to Treponema succinifaciens, a known carbohydrate metabolizer in swine. Gut Treponema are found in non-human primates and all traditional peoples studied to date, suggesting they are symbionts lost in urban-industrialized societies.

413 citations

Journal ArticleDOI
01 Jun 2011-Diabetes
TL;DR: Investigating whether chronic activation of the AMP-activated protein kinase (AMPK) by metformin restores cardiac function and cardiomyocyte autophagy in OVE26 diabetic mice found that stimulation of AMPK may represent a novel approach to treat diabeticCardiomyopathy.
Abstract: OBJECTIVE—Autophagy is a critical cellular system for removal of aggregated proteins and damaged organelles. Although dysregulated autophagy is implicated in the development of heart failure, the role of autophagy in the development of diabetic cardiomyopathy has not been studied. We investigated whether chronic activation of the AMP-activated protein kinase (AMPK) by metformin restores cardiac function and cardiomyocyte autophagy in OVE26 diabetic mice. RESEARCH DESIGN AND METHODS—OVE26 mice and cardiac-specific AMPK dominant negative transgenic (DN)-AMPK diabetic mice were treated with metformin or vehicle for 4 months, and cardiac autophagy, cardiac functions, and cardiomyocyte apoptosis were monitored. RESULTS—Compared with control mice, diabetic OVE26 mice exhibited a significant reduction of AMPK activity in parallel with reduced cardiomyocyte autophagy and cardiac dysfunction in vivo and in isolated hearts. Furthermore, diabetic OVE26 mouse hearts exhibited aggregation of chaotically distributed mitochondria between poorly organized myofibrils and increased polyubiquitinated protein and apoptosis. Inhibition of AMPK by overexpression of a cardiac-specific DN-AMPK gene reduced cardiomyocyte autophagy, exacerbated cardiac dysfunctions, and increased mortality in diabetic mice. Finally, chronic metformin therapy significantly enhanced autophagic activity and preserved cardiac functions in diabetic OVE26 mice but not in DN-AMPK diabetic mice. CONCLUSIONS—Decreased AMPK activity and subsequent reduction in cardiac autophagy are important events in the development of diabetic cardiomyopathy. Chronic AMPK activation by metformin prevents cardiomyopathy by upregulating autophagy activity in diabetic OVE26 mice. Thus, stimulation of AMPK may represent a novel approach to treat diabetic cardiomyopathy. Diabetes 60:1770–1778, 2011

413 citations

Journal ArticleDOI
TL;DR: The DLVO model has been found unable to fully describe the behavior of abiotic and abiotic colloidal behavior inaqueous media as mentioned in this paper, and it is reasonable to believe that the structure of water may participate in a more significant fashion.
Abstract: The interaction and behavior of surfaces orcolloids is of quantitative significance inunderstanding the transport and fate ofcompounds and microorganisms in environmentalsystems. Historically, the DLVO model ofcolloid stability has described theseinteractions. This model finds its basis in aforce (energy) balance that comprisesattractive van der Waals and repulsiveelectrostatic interactions. Recently, the DLVOmodel has been found unable to fully describebiotic and abiotic colloidal behavior inaqueous media. The suspending phase (commonlywater) is often treated as a force (energy)transmitting or propagating medium. It isreasonable to believe that the structure ofwater may participate in a more significantfashion. Moreover, other moieties (sorbed anddissolved) may also have non-DLVO effects. Significant work has been focused on extendingthe precepts of the traditional DLVO model toaccommodate these non-DLVO forces (energies). This paper reviews many of the interactionsthat play a role in environmental systems andare not commonly subsumed by the traditionalDLVO model: e.g., hydrogen bonding and thehydrophobic effect, hydration pressure,non-charge transfer Lewis acid baseinteractions, and steric interactions.

413 citations

Journal ArticleDOI
TL;DR: It is proved here for the first time that, despite the narrow diameter of the carbon nanotubes considered which may suggest the existence of single-file diffusion, when the trajectories of confined water are studied at time scales in excess of 500 ps, a Fickian-type diffusion mechanism prevails.
Abstract: Carbon nanotubes show exceptional physical properties that render them promising candidates as building blocks for nanostructured materials. Many ambitious applications, ranging from gene therapy to membrane separations, require the delivery of fluids, in particular aqueous solutions, through the interior of carbon nanotubes. To foster these and other applications, it is necessary to understand the thermodynamic and transport properties of water confined within long narrow carbon nanotubes. Previous theoretical work considered either short carbon nanotubes or short periods of time. By conducting molecular dynamics simulations in the microcanonical ensemble for water confined in infinitely long carbon nanotubes of diameter 1.08 nm, we show here that confined water molecules diffuse through a fast ballistic motion mechanism for up to 500 ps at room temperature. By comparing the results obtained for the diffusion of water to those obtained for the diffusion of a reference Lennard-Jones fluid, we prove here that long-lasting hydrogen bonds are responsible for the ballistic diffusion of water clusters in narrow carbon nanotubes, as opposed to spatial mismatches between pore-fluid and fluid-fluid attractive interactions which, as shown previously by others, are responsible for the concerted motion of simple fluids in molecular sieves. Additionally we prove here for the first time that, despite the narrow diameter of the carbon nanotubes considered which may suggest the existence of single-file diffusion, when the trajectories of confined water are studied at time scales in excess of 500 ps, a Fickian-type diffusion mechanism prevails. Our results are important for designing nano fluidic apparatuses to develop, for example, novel drug-delivery devices.

412 citations


Authors

Showing all 25490 results

NameH-indexPapersCitations
Ronald C. Kessler2741332328983
Michael A. Strauss1851688208506
Derek R. Lovley16858295315
Ashok Kumar1515654164086
Peter J. Schwartz147647107695
Peter Buchholz143118192101
Robert Hirosky1391697106626
Elizabeth Barrett-Connor13879373241
Brad Abbott137156698604
Lihong V. Wang136111872482
Itsuo Nakano135153997905
Phillip Gutierrez133139196205
P. Skubic133157397343
Elizaveta Shabalina133142192273
Richard Brenner133110887426
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202392
2022348
20212,425
20202,481
20192,433
20182,396