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Institution

University of Kentucky

EducationLexington, Kentucky, United States
About: University of Kentucky is a education organization based out in Lexington, Kentucky, United States. It is known for research contribution in the topics: Population & Poison control. The organization has 43933 authors who have published 92195 publications receiving 3256087 citations. The organization is also known as: UK.


Papers
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Journal ArticleDOI
TL;DR: Significant findings related to nomenclature and protein methodology are elucidation of several new genetic variants of the major milk proteins, establishment by sequencing techniques and sequence alignment of the bovine caseins and whey proteins as the reference point for the nomenClature of all homologous milk proteins.

1,185 citations

Journal ArticleDOI
TL;DR: Inoculation of the first true leaf of cucumber with Colletotrichum lagenarium enhanced peroxidase activity in leaf 2, and the increased activity was associated, at least in part, with the fastest moving anodic isozymes during polyacrylamide gel electrophoresis.
Abstract: Inoculation of the first true leaf of cucumber with Colletotrichum lagenarium enhanced peroxidase activity in leaf 2. The increased activity was associated, at least in part, with the fastest moving anodic isozymes during polyacrylamide gel electrophoresis. All plant parts and cellular fractions exhibited enhanced peroxidase activity in protected as compared to control plants. Injury of leaf 1 with dry ice neither induced systemic resistance to C. lagenarium nor enhanced peroxidase activity of leaf 2. Inoculation of leaf 1 with C. lagenarium followed by inoculation of leaf 2, 1 week later, elicited a higher degree of protection and higher peroxidase activity in leaf 3 than did single inoculations. Increasing numbers of C. lagenarium lesions on leaf 1 progressively increased peroxidase activity and resistance in leaf 2. Induced resistance was detected 3 to 4 days after inoculation of leaf 1, whereas peroxidase activity increased after the 4th day.

1,184 citations

Journal ArticleDOI
TL;DR: A theoretical overview of some critical issues relevant to conditioned place preference is provided and it seems clear that CPP measures a learning process that is fundamentally distinct from drug self-administration.
Abstract: Rationale: Among the various experimental protocols that have been used to measure drug reward in laboratory animals, conditioned place preference (CPP) has been one of the most popular. However, a number of controversial issues have surrounded the use of this experimental protocol. Objective: The present review provides a theoretical overview of some critical issues relevant to CPP. The advantages and limitations of CPP are also covered. Results: Based on modern and traditional theoretical formulations of Pavlovian conditioning, CPP appears to reflect a preference for a context due to the contiguous association between the context and a drug stimulus. Within this theoretical framework, it seems clear that CPP measures a learning process that is fundamentally distinct from drug self-administration. The main advantages of CPP are that it: (1) tests animals in a drug-free state; (2) is sensitive to both reward and aversion; (3) allows for simultaneous determination of CPP and locomotor activity; (4) is adaptable to a variety of species; (5) typically yields dose-effect curves that are monophasic rather than biphasic; and (6) has utility in probing the neural circuits involved in drug reward. The main limitations of CPP are that it: (1) is subject to interpretation based on the notion of novelty seeking; (2) is cumbersome for providing the graded dose-effect curves needed for answering some pharmacological questions; (3) is difficult to interpret when animals prefer one context prior to drug conditioning; and (4) lacks face validity as an experimental protocol of drug reward in humans. Conclusion: Despite some limitations, CPP provides unique information about the rewarding effect of contextual cues associated with a drug stimulus.

1,184 citations

Journal ArticleDOI
TL;DR: A novel implementation of perfectly matched layer (PML) media is presented for the termination of FDTD lattices based on the stretched coordinate form of the PML, a recursive convolution, and the use of complex frequency, shifted (CFS) PML parameters.
Abstract: A novel implementation of perfectly matched layer (PML) media is presented for the termination of FDTD lattices. The implementation is based on the stretched coordinate form of the PML, a recursive convolution, and the use of complex frequency, shifted (CFS) PML parameters. The method, referred to here as the convolutional PML (CPML), offers a number of advantages over the traditional implementations of the PML. Specifically, the application of the CPML is completely independent of the host medium. Thus, no modifications are necessary when applying it to inhomogeneous, lossy, anisotropic, dispersive, or nonlinear media. Secondly, it is shown that the CFS–PML is highly absorptive of evanescent modes and can provide significant memory savings when computing the wave interaction of elongated structures, sharp corners, or low-frequency excitations. © 2000 John Wiley & Sons, Inc. Microwave Opt Technol Lett 27: 334–339, 2000.

1,176 citations

Journal ArticleDOI
TL;DR: A second generation splice detection algorithm, MapSplice, whose focus is high sensitivity and specificity in the detection of splices as well as CPU and memory efficiency is introduced, which indicates that Map Splice is a highly accurate algorithm for the alignment of RNA-seq reads to splice junctions.
Abstract: The accurate mapping of reads that span splice junctions is a critical component of all analytic techniques that work with RNA-seq data. We introduce a second generation splice detection algorithm, MapSplice, whose focus is high sensitivity and specificity in the detection of splices as well as CPU and memory efficiency. MapSplice can be applied to both short (<75 bp) and long reads (≥ 75 bp). MapSplice is not dependent on splice site features or intron length, consequently it can detect novel canonical as well as non-canonical splices. MapSplice leverages the quality and diversity of read alignments of a given splice to increase accuracy. We demonstrate that MapSplice achieves higher sensitivity and specificity than TopHat and SpliceMap on a set of simulated RNA-seq data. Experimental studies also support the accuracy of the algorithm. Splice junctions derived from eight breast cancer RNA-seq datasets recapitulated the extensiveness of alternative splicing on a global level as well as the differences between molecular subtypes of breast cancer. These combined results indicate that MapSplice is a highly accurate algorithm for the alignment of RNA-seq reads to splice junctions. Software download URL: http://www.netlab.uky.edu/p/bioinfo/MapSplice.

1,173 citations


Authors

Showing all 44305 results

NameH-indexPapersCitations
Mark P. Mattson200980138033
Carlo M. Croce1981135189007
Charles A. Dinarello1901058139668
Richard A. Gibbs172889249708
Gang Chen1673372149819
David A. Bennett1671142109844
Carl W. Cotman165809105323
Rodney S. Ruoff164666194902
David Tilman158340149473
David Cella1561258106402
Richard E. Smalley153494111117
Deepak L. Bhatt1491973114652
Kevin Murphy146728120475
Jian Yang1421818111166
Thomas J. Smith1401775113919
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023108
2022532
20214,329
20204,216
20193,965
20183,605