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Journal articles on the topic 'Fox'

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Author: Grafiati

Published: 4 June 2021

Last updated: 28 July 2024

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1

Kurth, Florian, Sarah Strohmaier, and Eileen Luders. "Reduced Age-Related Gray Matter Loss in the Orbitofrontal Cortex in Long-Term Meditators." Brain Sciences 13, no. 12 (December 6, 2023): 1677. http://dx.doi.org/10.3390/brainsci13121677.

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The orbitofrontal cortex (OFC) is a functionally heterogeneous brain region contributing to mental processes relating to meditation practices. The OFC has been reported to decline in volume with increasing age and differs in volume between meditation practitioners and non-practitioners. We hypothesized that the age-related decline of the OFC is diminished in meditation practitioners. We tested this hypothesis in a sample of 50 long-term meditators and 50 matched controls by correlating chronological age with regional gray matter volumes of the left and right OFC, as well as in seven left and right cytoarchitectonically defined subregions of the OFC (Fo1–Fo7). In both meditators and controls, we observed a negative relationship between age and OFC (sub)volumes, indicating that older participants have smaller OFC volumes. However, in meditators, the age-related decline was less steep compared to controls. These age-related differences reached significance for left and right Fo2, Fo3, Fo4, and Fo7, as well as left Fo5 and right Fo6. Since different subregions of the OFC are associated with distinct brain functions, further investigations are required to explore the functional implications of these findings in the context of meditation and the aging brain.

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2

Honegger, Thomas. "'A Fox is a Fox is a Fox... ' The Fox and the Wolf Reconsidered." Reinardus / Yearbook of the International Reynard Society 9 (December 31, 1996): 59–74. http://dx.doi.org/10.1075/rein.9.06hon.

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Abstract The Middle English The Fox and the Wolf is the first piece of evidence that 'Renart' had crossed the 'linguistic channel' which separated the Anglo-Norman nobility from their English subjects. The article argues that the poet tries to take into account his audience's likely unfamiliarity with the scurrilous beast-epic hero by linking his poem with the already familiar traditions of the beast tale, the beast fable, as well as The Physiologus and the bestiary.

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3

Lyu, Tianshu, Lidong Bing, Zhao Zhang, and Yan Zhang. "FOX." ACM Transactions on Social Computing 3, no. 3 (August 5, 2020): 1–23. http://dx.doi.org/10.1145/3404970.

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4

Huang, Guocun, Qing Fan, Sigal Lechno-Yossef, Elizabeth Wojciuch, C. Peter Wolk, Takakazu Kaneko, and Satoshi Tabata. "Clustered Genes Required for the Synthesis of Heterocyst Envelope Polysaccharide in Anabaena sp. Strain PCC 7120." Journal of Bacteriology 187, no. 3 (February 1, 2005): 1114–23. http://dx.doi.org/10.1128/jb.187.3.1114-1123.2005.

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ABSTRACT As demonstrated with alr2835 (hepA) and alr2834 (hepC) mutants, heterocysts of Anabaena sp. strain PCC 7120, a filamentous cyanobacterium, must have an envelope polysaccharide layer (the Hep+ phenotype) to fix dinitrogen in an oxygen-containing milieu (the Fox+ phenotype). Transpositions presumptively responsible for a Fox− phenotype were localized in open reading frames (ORFs) near hepA and hepC. A mutation in each of nine of these ORFs was complemented by a clone bearing only that single, intact ORF. Heterocysts of the nine mutants were found to lack an envelope polysaccharide layer. Complementation of mutations in alr2832 and alr2840 may have resulted from recombination. However, alr2825, alr2827, alr2831, alr2833, alr2837, alr2839, and alr2841, like hepA and hepC, are required for a Hep+ Fox+ phenotype.

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5

Fox, Daniel M. "Fox Responds." American Journal of Public Health 106, no. 6 (June 2016): 976. http://dx.doi.org/10.2105/ajph.2016.303215.

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6

Smith, Dave. "February Fox." Literary Imagination 24, no. 1 (January 20, 2022): 40. http://dx.doi.org/10.1093/litimag/imab055.

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7

Brugaletta, John. "Fox Sparrow." Anglican Theological Review 99, no. 4 (September 2017): 765. http://dx.doi.org/10.1177/000332861709900411.

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8

Hascall, Nancy. "Fox Squirrel." English Journal 81, no. 8 (December 1992): 84. http://dx.doi.org/10.2307/820306.

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9

Desloovere, Martin. ""Dear Fox"." Documenta 8, no. 3 (May 3, 2019): 161–62. http://dx.doi.org/10.21825/doc.v8i3.11068.

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10

Lindholdt, P. "The Fox." Interdisciplinary Studies in Literature and Environment 8, no. 2 (July 1, 2001): 257. http://dx.doi.org/10.1093/isle/8.2.257.

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11

Milius, Susan. "Fox Selection." Science News 165, no. 9 (February 28, 2004): 132. http://dx.doi.org/10.2307/4014830.

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12

Case, Susan Howard. "Fox Fur." Red Cedar Review 44, no. 1 (2009): 55. http://dx.doi.org/10.1353/rcr.0.0041.

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13

Mayers, D. F., and J. E. Walsh. "Leslie Fox." Bulletin of the London Mathematical Society 31, no. 2 (March 1999): 241–47. http://dx.doi.org/10.1112/s0024609398004950.

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14

McCorkle, James. "Fox-Sparrow." Manoa 31, no. 2 (2019): 99–101. http://dx.doi.org/10.1353/man.2019.0127.

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15

Kirby, Tony. "Fiona Fox." Lancet 373, no. 9680 (June 2009): 2017. http://dx.doi.org/10.1016/s0140-6736(09)61099-0.

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16

Watts, Geoff. "Wallace Fox." Lancet 375, no. 9720 (March 2010): 1076. http://dx.doi.org/10.1016/s0140-6736(10)60467-9.

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17

Arguin, Paul. "Flying Fox." Emerging Infectious Diseases 8, no. 3 (March 2002): 340. http://dx.doi.org/10.3201/eid0803.030300.

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18

Waters, Michael. "The Fox." Missouri Review 11, no. 2 (1988): 34–35. http://dx.doi.org/10.1353/mis.1988.0100.

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19

Castro, Joy. "Fox Hollow." Ploughshares 45, no. 1 (2019): 17–21. http://dx.doi.org/10.1353/plo.2019.0004.

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20

Stevenson, Deborah. "Fox (review)." Bulletin of the Center for Children's Books 60, no. 9 (2007): 358–59. http://dx.doi.org/10.1353/bcc.2007.0320.

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21

Monserrate, Steven Gonzalez. "Silicon Fox." Anthropology and Humanism 45, no. 1 (June 2020): 130–38. http://dx.doi.org/10.1111/anhu.12276.

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22

Dyer, Christopher. "Harold Fox." Midland History 32, no. 1 (June 2007): 205. http://dx.doi.org/10.1179/mdh.2007.32.1.205.

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23

POISSANT, DAVID JAMES. "Fox King." Fairy Tale Review 8, no. 1 (March 2012): 111–20. http://dx.doi.org/10.1353/fair.2012.a812908.

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24

Mathis, Cleopatra. "Dead Fox." Ploughshares 37, no. 1 (March 2011): 133. http://dx.doi.org/10.1353/plo.2011.a435128.

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25

Smedley, Sue. "“Where’s the fox? You’ve got to read the fox.”." English in Education 25, no. 1 (March 1991): 12–20. http://dx.doi.org/10.1111/j.1754-8845.1991.tb00092.x.

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26

Rutherford-Johnson, Tim. "Christopher Fox - Christopher Fox, Trostlieder. EXAUDI, Weeks. Kairos, 0022005KAI." Tempo 77, no. 305 (July 2023): 80–81. http://dx.doi.org/10.1017/s0040298223000232.

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27

Skipper, Magdalena, Catherine A. Milne, and Jonathan Hodgkin. "Genetic and Molecular Analysis of fox-1, a Numerator Element Involved in Caenorhabditis elegans Primary Sex Determination." Genetics 151, no. 2 (February 1, 1999): 617–31. http://dx.doi.org/10.1093/genetics/151.2.617.

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Abstract fox-1 was previously identified as a candidate numerator element based on its overexpression phenotype. FOX-1 is an RRM-type RNA-binding protein, which can bind RNAs in vitro. Western analysis detects FOX-1 throughout development. fox-1::lacZ comes on ubiquitously early during embryogenesis. Postembryonically, fox-1::lacZ is expressed sex specifically in a subset of cells in the head and tail. We describe a Tc1derived deletion allele [fox-1(Δ)] that removes the RRM domain. fox-1(Δ) confers no phenotype in XXs, but can rescue XO-specific lethality and feminization caused by duplications of the left end of the X. fox-1(Δ) synergizes with putative numerators, resulting in abnormal XX development. Genetic analysis indicated that fox-1(Δ) leads to a slight increase in xol-1 activity, while fox-1(gf) leads to partial loss of xol-1 activity, and xol-1 is epistatic to fox-1. RNase protection experiments revealed increased levels of the 2.2-kb xol-1 message in fox-1(Δ) animals, and reduced levels in fox-1(gf) animals. Additionally, fox-1(Δ) impairs male mating efficiency, which, we propose, represents another function of fox-1, independent of xol-1 and its role in sex determination.

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28

Pérez-Llarena, Francisco José, Frédéric Kerff, Laura Zamorano, María Carmen Fernández, Maria Luz Nuñez, Elisenda Miró, Antonio Oliver, Ferran Navarro, and Germán Bou. "Characterization of the New AmpC β-Lactamase FOX-8 Reveals a Single Mutation, Phe313Leu, Located in the R2 Loop That Affects Ceftazidime Hydrolysis." Antimicrobial Agents and Chemotherapy 57, no. 10 (July 22, 2013): 5158–61. http://dx.doi.org/10.1128/aac.00818-13.

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ABSTRACTA novel class C β-lactamase (FOX-8) was isolated from a clinical strain ofEscherichia coli. The FOX-8 enzyme possessed a unique substitution (Phe313Leu) compared to FOX-3. IsogenicE. colistrains carrying FOX-8 showed an 8-fold reduction in resistance to ceftazidime relative to FOX-3. In a kinetic analysis, FOX-8 displayed a 33-fold reduction inkcat/Kmfor ceftazidime compared to FOX-3. In the FOX family of β-lactamases, the Phe313 residue located in the R2 loop affects ceftazidime hydrolysis and alters the phenotype ofE. colistrains carrying this variant.

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29

Shirley, Mark D. F., Bodil Elmhagen, Peter W. W. Lurz, Steve P. Rushton, and Anders Angerbjörn. "Modelling the spatial population dynamics of arctic foxes: the effects of red foxes and microtine cycles." Canadian Journal of Zoology 87, no. 12 (December 2009): 1170–83. http://dx.doi.org/10.1139/z09-104.

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The Fennoscandian arctic fox ( Vulpes lagopus (L., 1758)) population is critically endangered, possibly because of increased interference competition from red foxes ( Vulpes vulpes (L., 1758)) and fading cycles in microtine rodents, which cause food shortage. It is not known how these factors drive arctic fox population trends. To test their role in arctic fox decline, we developed a spatially explicit and individual-based model that allowed us to simulate fox interactions and food availability in a real landscape. A sensitivity analysis revealed that simulated arctic fox population size and den occupancy were strongly correlated with fecundity and mortality during the microtine crash phase, but also with red fox status. Model simulations suggested that arctic fox population trends depended on microtine cycles and that arctic fox distributions were restricted by red fox presence. We compared the model predictions with field data collected at Vindelfjällen, Sweden. The model recreated the observed arctic fox trend only with the inclusion of arctic fox avoidance of red fox home ranges. The results indicate that avoidance behaviours can affect population trends and hence that relatively small numbers of red foxes can have a strong negative impact on arctic fox population size and distribution.

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30

Yang, Xiong, Bo Wang, Kai Zhao, Dongkui Zhao, Yafeng Huang, and Xiaofeng Wang. "Calculation of binding energy and mechanical properties of FOX-7 with three kinds of binders." Journal of Physics: Conference Series 2478, no. 3 (June 1, 2023): 032022. http://dx.doi.org/10.1088/1742-6596/2478/3/032022.

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Abstract In order to select the binder suitable for FOX-7 polymer bonded explosives system, the binding energy and mechanical properties of FOX-7 with three binders were calculated by molecular dynamics method. The results show that the binding energies of the three systems are in the order of FOX-7+BA> FOX-7+F2603> FOX-7+EVA, and that the binding energies of F2603, BA with FOX-7 are basically the same. FOX-7+F2603 and FOX-7+ BA systems exhibit better comprehensive mechanical properties, and thus are more suitable for polymer bonded explosive systems.

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31

Li, Xiaodong, Yue Yang, Changgui Song, Yantao Sun, Yuanqi Han, Yue Zhao, and Jingyu Wang. "Fabrication and Characterization of Viton@FOX-7@Al Spherical Composite with Improved Thermal Decomposition Property and Safety Performance." Materials 14, no. 5 (February 26, 2021): 1093. http://dx.doi.org/10.3390/ma14051093.

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To achieve a uniform distribution of the components and a better performance of aluminized composite explosives, Viton (dipolymers of hexafluoropropylene and vinylidene fluoride) @ FOX-7 (1,1-diamino-2,2-dinitroethylene) @Al microspheres and FOX-7/Viton@Al were synthesized by spray-drying strategy contrastively. Viton@FOX-7@Al owned porous and loose morphology and good sphericity with a retained crystal phase of FOX-7 and aluminum. The 23.56% fluorine content on Viton@FOX-7@Al surface indicated that Viton was completely coated on the surface of the particles. Nanosized aluminum (nAl) in Viton@FOX-7@Al had a certain catalytic activity on the thermal decomposition process of FOX-7 resulting in a depressed exothermic peak temperature and reduced apparent activation energy relative to nAl in FOX-7/Viton@Al. Because of the specific structure and the synergies between each individual component, Viton@FOX-7@Al showed reduced impact sensitivity and friction sensitivity than those of FOX-7/Viton@Al. In brief, Viton@FOX-7@Al with multilevel coating structure possessed comparatively low thermal decomposition energy requirement and improved safety performance.

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32

VIVALLO, FELIPE. "Lectotype designations, taxonomic notes and new synonymy in some species of the bee genus Centris Fabricius, 1804 described by William Henry Fox (Hymenoptera: Apidae)." Zootaxa 4624, no. 4 (July 2, 2019): 478–90. http://dx.doi.org/10.11646/zootaxa.4624.4.2.

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In this paper, the primary types of Centris described by the American doctor and naturalist William Henry Fox deposited at the Academy of Natural Sciences, Drexel University, Philadelphia and in the United States National Museum, Washington, United States were studied. To stabilize the application of some names, lectotypes were designated for C. atriventris Fox (= C. foxi Friese), C. cockerellii Fox, C. eisenii Fox, C. errans Fox, C. pallida Fox, C. subhyalina Fox (= C. lanosa Cresson), and C. xylocopoides Fox. This latter species is withdrawn from the synonymy of C. braccata Packard and subsequently revalidated. Centris foxi is removed from synonymy of C. atripes Mocsáry and revalidated, proposing this latter species as its new junior synonym. A taxonomic note on the primary type of C. marginata Fox (= C. caesalpiniae Cockerell) is also provided.

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33

Baraniak, Andrew P., Jing R. Chen, and Mariano A. Garcia-Blanco. "Fox-2 Mediates Epithelial Cell-Specific Fibroblast Growth Factor Receptor 2 Exon Choice." Molecular and Cellular Biology 26, no. 4 (February 15, 2006): 1209–22. http://dx.doi.org/10.1128/mcb.26.4.1209-1222.2006.

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ABSTRACT Alternative splicing of fibroblast growth factor receptor 2 (FGFR2) transcripts occurs in a cell-type-specific manner leading to the mutually exclusive use of exon IIIb in epithelia or exon IIIc in mesenchyme. Epithelial cell-specific exon choice is dependent on (U)GCAUG elements, which have been shown to bind Fox protein family members. In this paper we show that FGFR2 exon choice is regulated by (U)GCAUG elements and Fox protein family members. Fox-2 isoforms are differentially expressed in IIIb+ cells in comparison to IIIc+ cells, and expression of Fox-1 or Fox-2 in the latter led to a striking alteration in FGFR2 splice choice from IIIc to IIIb. This switch was absolutely dependent on the (U)GCAUG elements present in the FGFR2 pre-mRNA and required critical residues in the C-terminal region of Fox-2. Interestingly, Fox-2 expression led to skipping of exon 6 among endogenous Fox-2 transcripts and formation of an inactive Fox-2 isoform, which suggests that Fox-2 can regulate its own activity. Moreover, the repression of exon IIIc in IIIb+ cells was abrogated by interfering RNA-mediated knockdown of Fox-2. We also show that Fox-2 is critical for the FGFR2(IIIb)-to-FGFR2(IIIc) switch observed in T Rex-293 cells grown to overconfluency. Overconfluent T Rex-293 cells show molecular and morphological changes consistent with a mesenchymal-to-epithelial transition. If overconfluent cells are depleted of Fox-2, the switch from IIIc to IIIb is abrogated. The data in this paper place Fox-2 among critical regulators of gene expression during mesenchymal-epithelial transitions and demonstrate that this action of Fox-2 is mediated by mechanisms distinct from those described for other cases of Fox activity.

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34

Roepstorff, Carsten, Bodil Vistisen, Kirstine Roepstorff, and Bente Kiens. "Regulation of plasma long-chain fatty acid oxidation in relation to uptake in human skeletal muscle during exercise." American Journal of Physiology-Endocrinology and Metabolism 287, no. 4 (October 2004): E696—E705. http://dx.doi.org/10.1152/ajpendo.00001.2004.

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In the present study, we investigated possible sites of regulation of long-chain fatty acid (LCFA) oxidation in contracting human skeletal muscle. Leg plasma LCFA kinetics were determined in eight healthy men during bicycling (60 min, 65% peak oxygen uptake) with either high (H-FOX) or low (L-FOX) leg fat oxidation (H-FOX: 1,098 ± 140; L-FOX: 494 ± 84 μmol FA/min, P < 0.001), which was achieved by manipulating preexercise muscle glycogen (H-FOX: 197 ± 21; L-FOX: 504 ± 25 mmol/kg dry wt, P < 0.001). Several blood metabolites and hormones were kept nearly similar between trials by allocating a preexercise meal and infusing glucose intravenously during exercise. During exercise, leg plasma LCFA fractional extraction was identical between trials (H-FOX: 17.8 ± 1.6; L-FOX: 18.2 ± 1.8%, not significant), suggesting similar LCFA transport capacity in muscle. On the contrary, leg plasma LCFA oxidation was 99% higher in H-FOX than in L-FOX (421 ± 47 vs. 212 ± 37 μmol/min, P < 0.001). Probably due to the slightly higher ( P < 0.01) plasma LCFA concentration in H-FOX than in L-FOX, leg plasma LCFA uptake was nonsignificantly ( P = 0.17) higher (25%) in H-FOX than in L-FOX, yet the fraction of plasma LCFA uptake oxidized was 61% higher ( P < 0.05) in H-FOX than in L-FOX. Accordingly, the muscle content of several lipid-binding proteins did not differ significantly between trials, although fatty acid translocase/CD36 and caveolin-1 were elevated ( P < 0.05) by the high-intensity exercise and dietary manipulation allocated on the day before the experimental trial. The present data suggest that, in contracting human skeletal muscle with different fat oxidation rates achieved by manipulating preexercise glycogen content, transsarcolemmal transport is not limiting plasma LCFA oxidation. Rather, the latter seems to be limited by intracellular regulatory mechanisms.

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35

Blamires, David, and Thomas W. Best. "Reynard the Fox." Modern Language Review 80, no. 1 (January 1985): 113. http://dx.doi.org/10.2307/3729378.

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36

Miao, Chaoyang, He Zhang, Miao Zhang, and Xiaoyan Zhang. "Fox-Fordyce disease." Anais Brasileiros de Dermatologia 93, no. 1 (February 2018): 161–62. http://dx.doi.org/10.1590/abd1806-4841.20187348.

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37

Ginter, Donald E., and L. G. Mitchell. "Charles James Fox." American Historical Review 98, no. 5 (December 1993): 1607. http://dx.doi.org/10.2307/2167127.

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38

Downing, Jane. "The Fox Hunter." Antipodes 32, no. 1-2 (2018): 85–93. http://dx.doi.org/10.1353/apo.2018.0010.

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39

Diaz-Brown, William, Luis Rubio, and Susan Kaufman Purcell. "Mexico Under Fox." History Teacher 39, no. 1 (November 1, 2005): 134. http://dx.doi.org/10.2307/30036762.

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40

Diaz-Brown, William, Luis Rubio, and Susan Kaufman Purcell. "Mexico Under Fox." History Teacher 38, no. 3 (May 1, 2005): 420. http://dx.doi.org/10.2307/30037033.

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41

Schvey. "After the Fox." Tennessee Williams Annual Review, no. 17 (2018): 115. http://dx.doi.org/10.2307/48615446.

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42

Opyr, Linda. "Seeing a Fox." Hudson Review 56, no. 3 (2003): 494. http://dx.doi.org/10.2307/3852696.

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43

Femia, Natalie. "My Friend Fox." Psychosis 13, no. 4 (October 2, 2021): 379–80. http://dx.doi.org/10.1080/17522439.2021.1991991.

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44

Blasco-Morente, Gonzalo, María J. Naranjo-Díaz, Israel Pérez-López, Antonio Martínez-López, Ricardo Ruiz-Villaverde, and José Aneiros-Fernández. "Fox-Fordyce Disease." Sultan Qaboos University Medical Journal 16, no. 1 (February 2, 2016): e119-120. http://dx.doi.org/10.18295/squmj.2016.16.01.025.

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45

Feinberg, Richard, Luis Rubio, and Susan Kaufman Purcell. "Mexico under Fox." Foreign Affairs 84, no. 2 (2005): 161. http://dx.doi.org/10.2307/20034312.

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46

Allan, James. "Fantastic Mr Fox." King's Law Journal 23, no. 3 (December 11, 2012): 329–41. http://dx.doi.org/10.5235/klj.23.3.329.

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47

Osmond-Smith, David. "Beyond Fox-Hunting." Musical Times 138, no. 1853 (July 1997): 5. http://dx.doi.org/10.2307/1004027.

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48

Harnden, D. G. "Professor Brian Fox." British Journal of Cancer 81, no. 2 (August 27, 1999): 189. http://dx.doi.org/10.1038/sj.bjc.6690675.

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49

Ingle, H. Larry. "George Fox, Millenarian." Albion 24, no. 2 (1992): 261–78. http://dx.doi.org/10.2307/4050813.

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“Friends, take heed of setting up that which God will throw down, lest you be found fighters against God.”The nearly two decades comprising the period of the English Revolution were marked by a widespread interest in the timely appearance of the millennium, the thousand year period of Christ's promised earthly reign. From scholarly biblical studies of Daniel and Revelation to omens such as total eclipses of the sun and rumors of a Nottingham girl returning from the dead to warn a sinful world of approaching destruction, people in revolutionary England were bombarded with “evidence” of divine intervention and the expected arrival of the new kingdom. Parliament's victory in the English civil wars and its execution of Charles I in 1649 dramatically blew away the aura of divinity surrounding the monarchy and promised a new and glorious age. As they read prophecies in Revelation about a New Jerusalem where God would dry all tears and banish death, sorrow, and pain, enthusiasts of the seventeenth century anxiously looked for the Christ who promised, “Behold, I come quickly.” So prevalent were such notions that, as one authority has stressed, popular millenarianism seemed only a small step beyond received orthodoxy.

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50

Wells, Michael. "Professor Harold Fox." International Journal of Gynecological Pathology 31, no. 4 (July 2012): 395–96. http://dx.doi.org/10.1097/pgp.0b013e31825ebac2.

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