Institution
University of Nebraska–Lincoln
Education•Lincoln, Nebraska, United States•
About: University of Nebraska–Lincoln is a education organization based out in Lincoln, Nebraska, United States. It is known for research contribution in the topics: Population & Poison control. The organization has 28059 authors who have published 61544 publications receiving 2139104 citations. The organization is also known as: Nebraska & UNL.
Topics: Population, Poison control, Large Hadron Collider, Gene, Laser
Papers published on a yearly basis
Papers
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TL;DR: The current techniques, challenges of the currentBioactive peptide production techniques, the oral use and gastrointestinal bioavailability of these food-derived bioactive peptides, and the overall regulatory environment are discussed.
Abstract: Recent scientific evidence suggests that food proteins not only serve as nutrients, but can also modulate the body’s physiological functions. These physiological functions are primarily regulated by some peptides that are encrypted in the native protein sequences. These bioactive peptides can exert health beneficial properties and thus are considered as a lead compound for the development of nutraceuticals or functional foods. In the past few decades, a wide range of food-derived bioactive peptide sequences have been identified, with multiple health beneficial activities. However, the commercial application of these bioactive peptides has been delayed because of the absence of appropriate and scalable production methods, proper exploration of the mechanisms of action, high gastro-intestinal digestibility, variable absorption rate, and the lack of well-designed clinical trials to provide the substantial evidence for potential health claims. This review article discusses the current techniques, challenges of the current bioactive peptide production techniques, the oral use and gastrointestinal bioavailability of these food-derived bioactive peptides, and the overall regulatory environment.
376 citations
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TL;DR: The genome of the pathogenic North American PRRSV isolate 16244B has been sequenced and compared with LV, and genomic differences confirm the presence of distinct North American and EuropeanPRRSV genotypes.
Abstract: Although North American and European serotypes of porcine reproductive and respiratory syndrome virus (PRRSV) are recognized, only the genome of the European Lelystad strain (LV) has been sequenced completely. Here, the genome of the pathogenic North American PRRSV isolate 16244B has been sequenced and compared with LV. The genomic organization of 16244B was the same as LV but with only 63.4% nucleotide identity. The 189 nucleotide 5' non-coding region (NCR) of 16244B was distinct from the LV NCR, with good conservation (83%) only over a 43 base region immediately upstream of open reading frame (ORF) 1a. Major differences were found in the region encoding the non-structural part of the ORF1a polyprotein, which shared only 47% amino acid identity over 2503 residues of the six non-structural proteins (Nsps) encoded. Nsp2, thought to have a species-specific function, showed the greatest divergence, sharing only 32% amino acid identity with LV and containing 120 additional amino acids in the central region. Nsps encoded by the 5'-proximal and central regions of ORF1b had from 66 to 75% amino acid identity; however, the carboxy-terminal protein CP4 was distinct (42% identity). The ORF 1a-1b frameshift region of 16244B had 98% nucleotide identity with LV. Consistent with previous reports for North American isolates, the six structural proteins encoded were 58 to 79% identical to LV proteins. The 3' NCR (150 nucleotides) was 76% identical between isolates. These genomic differences confirm the presence of distinct North American and European PRRSV genotypes.
376 citations
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TL;DR: A newly designed 2D COF with incorporated Re complex, which exhibits intrinsic light absorption and charge separation properties and can efficiently reduce CO2 to form CO under visible light illumination with high electivity and better activity than its homogeneous Re counterpart.
Abstract: Covalent organic framework (COF) represents an emerging class of porous materials that have exhibited great potential in various applications, particularly in catalysis. In this work, we report a newly designed 2D COF with incorporated Re complex, which exhibits intrinsic light absorption and charge separation (CS) properties. We show that this hybrid catalyst can efficiently reduce CO2 to form CO under visible light illumination with high electivity (98%) and better activity than its homogeneous Re counterpart. More importantly, using advanced transient optical and X-ray absorption spectroscopy and in situ diffuse reflectance spectroscopy, we unraveled three key intermediates that are responsible for CS, the induction period, and rate limiting step in catalysis. This work not only demonstrates the potential of COFs as next generation photocatalysts for solar fuel conversion but also provide unprecedented insight into the mechanistic origins for light-driven CO2 reduction.
375 citations
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TL;DR: In this article, the fifth-order corrected expressions for the electromagnetic field components of a monochromatic fundamental Gaussian beam (i.e., a focused TEM00 mode laser beam) propagating within a homogeneous dielectric media are derived.
Abstract: Fifth‐order corrected expressions for the electromagnetic field components of a monochromatic fundamental Gaussian beam (i.e., a focused TEM00 mode laser beam) propagating within a homogeneous dielectric media are derived and presented. Calculations of relative error indicate that the fifth‐order Gaussian beam description provides a significantly improved solution to Maxwell’s equations in comparison with commonly used paraxial (zeroth‐order) and first‐order Gaussian beam descriptions.
375 citations
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TL;DR: The data indicate that in compatible plant–pathogen interactions apoptosis-like programmed cell death occurs, and these animal antiapoptotic genes function in plants and should be useful to delineate resistance pathways.
Abstract: An emerging topic in plant biology is whether plants display analogous elements of mammalian programmed cell death during development and defense against pathogen attack. In many plant–pathogen interactions, plant cell death occurs in both susceptible and resistant host responses. For example, specific recognition responses in plants trigger formation of the hypersensitive response and activation of host defense mechanisms, resulting in restriction of pathogen growth and disease development. Several studies indicate that cell death during hypersensitive response involves activation of a plant-encoded pathway for cell death. Many susceptible interactions also result in host cell death, although it is not clear how or if the host participates in this response. We have generated transgenic tobacco plants to express animal genes that negatively regulate apoptosis. Plants expressing human Bcl-2 and Bcl-xl, nematode CED-9, or baculovirus Op-IAP transgenes conferred heritable resistance to several necrotrophic fungal pathogens, suggesting that disease development required host–cell death pathways. In addition, the transgenic tobacco plants displayed resistance to a necrogenic virus. Transgenic tobacco harboring Bcl-xl with a loss-of-function mutation did not protect against pathogen challenge. We also show that discrete DNA fragmentation (laddering) occurred in susceptible tobacco during fungal infection, but does not occur in transgenic-resistant plants. Our data indicate that in compatible plant–pathogen interactions apoptosis-like programmed cell death occurs. Further, these animal antiapoptotic genes function in plants and should be useful to delineate resistance pathways. These genes also have the potential to generate effective disease resistance in economically important crops.
375 citations
Authors
Showing all 28272 results
Name | H-index | Papers | Citations |
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Donald P. Schneider | 242 | 1622 | 263641 |
Suvadeep Bose | 154 | 960 | 129071 |
David D'Enterria | 150 | 1592 | 116210 |
Aaron Dominguez | 147 | 1968 | 113224 |
Gregory R Snow | 147 | 1704 | 115677 |
J. S. Keller | 144 | 981 | 98249 |
Andrew Askew | 140 | 1496 | 99635 |
Mitchell Wayne | 139 | 1810 | 108776 |
Kenneth Bloom | 138 | 1958 | 110129 |
P. de Barbaro | 137 | 1657 | 102360 |
Randy Ruchti | 137 | 1832 | 107846 |
Ia Iashvili | 135 | 1676 | 99461 |
Yuichi Kubota | 133 | 1695 | 98570 |
Ilya Kravchenko | 132 | 1366 | 93639 |
Andrea Perrotta | 131 | 1380 | 85669 |