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Journal articles on the topic 'N411'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Hopkins, Robert L., David J. Eisenhour, Lisa J. Hopman, and David K. Peyton. "Morphological Analysis of a Hybrid Minnow Swarm." Northeastern Naturalist 16, no. 4 (2009): 621–28. http://dx.doi.org/10.1656/045.016.n411.

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2

Cole, Aidan J., Conor K. McGarry, Karl T. Butterworth, Kevin M. Prise, Joe M. O'Sullivan, and Alan R. Hounsell. "Development of a novel experimental model to investigate radiobiological implications of respiratory motion in advanced radiotherapy." Physics in Medicine and Biology 57, no. 22 (2012): N411—N420. http://dx.doi.org/10.1088/0031-9155/57/22/n411.

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3

Ubani, Chikwendu, and Ubong Ikpaisong. "Use of CNG as Autofuel in Nigeria." European Journal of Engineering Research and Science 3, no. 10 (2018): 66–69. http://dx.doi.org/10.24018/ejers.2018.3.10.668.

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Natural gas is a clean-burning, safe fuel that can save you money at the pump while benefitting the environment and reducing Nigeria’s dependence on petroleum. It is a naturally occurring mixture of gaseous hydrocarbon, non-gaseous non-hydrocarbons and gaseous non-hydrocarbons found in underground reservoir rocks either on its own (non-associated gas) or in association with crude oil (associated gas). Natural gas is today accepted as one of the best sources of energy for the world and for the future because of its environmentally-friendly nature compared to other kinds of fossil fuels. Nigeria is ranked as the seventh most natural gas endowed nation in the world and relaxes on number one spot in Africa as she seats on about one hundred and eighty-eight trillion cubic feet of natural gas deposits.Current opportunities to utilize gas in Nigeria include: Gas to reinjection schemes, Gas to power schemes, Gas to petrochemicals (as feedstock), LNG-Liquefied Natural Gas, LPG- Liquefied Petroleum Gas, and CNG- Compressed Natural Gas. The use of CNG as auto fuel in Nigeria presents so much benefits as have been highlighted in this paper with emphasis on the economic advantage. Compressed Natural Gas (CNG) is a product of compressing natural gas to one hundredth the volume it occupies at standard atmospheric pressure.A comprehensive economic analysis to determine the cost savings from driving a car on CNG against PMS considered the case of a motorist who covers an average of 100 km every day in the approximately thirty days that make a month was employed. Results established that running a car on CNG amounts to saving N1 143 daily and N34 284 monthly, the cost of converting the car from PMS - driven to CNG - driven is recovered before the end of the sixth month. From the sixth month to the end of the first year, savings of N211 402 is made. Savings of N411 408 is enjoyed each year after the first year.Running vehicles on CNG will greatly reduce the friction and troubles encountered in importing fuel into the country. This will also cut down largely the hardly available foreign exchange expended in bringing in PMS for fuelling vehicles. To this end, the Nigerian Government should as a matter of national development ensure legal and regulatory framework encompassing both technical and commercial aspects for natural gas utilization in Nigeria. Worthy of note is the aspect of gas gathering, gas transmission and distribution which will further encourage the planting of CNG refuelling stations that will serve the expected large fleet of natural gas vehicles. Currently, Green Gas Limited, a joint venture between Nigeria Gas Company (NGC) a Nigerian National Petroleum Corporation (NNPC) and NIPCO Plc. that has nine operational CNG refuelling stations and others under construction is the only company driving the CNG revolution in the country.

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4

Resende, Marilene Ribeiro. "Editorial v19 n41." Revista Profissão Docente 19, no. 41 (2019): 1–2. http://dx.doi.org/10.31496/rpd.v19i41.1328.

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5

Aluri, Srinivas, Rongbao Zhao, Charlotte Lubout, Susanna M. I. Goorden, Andras Fiser, and I. David Goldman. "Hereditary folate malabsorption due to a mutation in the external gate of the proton-coupled folate transporter SLC46A1." Blood Advances 2, no. 1 (2018): 61–68. http://dx.doi.org/10.1182/bloodadvances.2017012690.

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Key Points An N411K mutation in the external gate of the proton-coupled folate transporter within the aqueous channel results in impaired function. The N411K mutation produces a substrate-specific defect in transport, resulting in hereditary folate malabsorption.

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6

Metlay, J. P., M. D. Witmer-Pack, R. Agger, M. T. Crowley, D. Lawless, and R. M. Steinman. "The distinct leukocyte integrins of mouse spleen dendritic cells as identified with new hamster monoclonal antibodies." Journal of Experimental Medicine 171, no. 5 (1990): 1753–71. http://dx.doi.org/10.1084/jem.171.5.1753.

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Hybridoma fusions with hamster hosts were undertaken to generate mAbs to mouse spleen dendritic cells. Two mAb were obtained and used to uncover the distinct integrins of these APC. One, 2E6, bound a determinant common to all members of the CD11/CD18 family, most likely the shared 90 kD CD18 beta chain. 2E6 immunoprecipitated the characteristic beta 2 integrin heterodimers from lymphocytes (p180, 90; CD11a) and macrophages (p170,90; CD11b), but from dendritic cells, a p150,90 (presumably CD11c) integrin was the predominant species. 2E6 inhibited the binding function of the CD11a and CD11b integrins on B cells and macrophages in appropriate assays, but 2E6 exerted little or no inhibition on the clustering of dendritic cells to T cells early in primary MLR, suggesting a CD11/CD18-independent mechanism for this binding. The second mAb, N418, precipitated a 150, 90 kD heterodimer that shared the 2E6 CD18 epitope. This N418 epitope may be the murine homologue of the previously characterized human CD11c molecule, but the epitope was only detected on dendritic cells. N418 did not react with peritoneal macrophages, anti-Ig-induced spleen B blasts, or bulk lymph node cells. When used to stain sections of spleen, N418 stained dendritic cells in the T-dependent areas, much like anti-class II mAbs that were also generated in these fusions. In addition, N418 revealed nests of dendritic cells that punctuated the rim of marginal zone macrophages between red and white pulp. This localization positioned most dendritic cells at regions where arterial vessels and T cells enter the white pulp. We conclude that the p150, 90 heterodimer is the major beta 2 integrin of spleen dendritic cells, and we speculate that it may function to localize these APC at sites that permit access to the recirculating pool of resting T cells.

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7

Witmer-Pack, M. D., M. T. Crowley, K. Inaba, and R. M. Steinman. "Macrophages, but not dendritic cells, accumulate colloidal carbon following administration in situ." Journal of Cell Science 105, no. 4 (1993): 965–73. http://dx.doi.org/10.1242/jcs.105.4.965.

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The dendritic cell system operates in situ to capture and present antigens in a form that is immunogenic to T cells. It is likely that dendritic cells require endocytic activity in order to process antigens. On the other hand, macrophages are considered to be the principal cells that internalize substrates in situ. We therefore investigated the phenotype of cells that scavenge the indigestible endocytic tracer, colloidal carbon, by phenotyping the endocytic cells with monoclonal antibodies that help distinguish macrophages from dendritic cells. Of some importance was the monoclonal N418, an antibody to the p150/90 leukocyte beta 2 integrin. FACS analyses on isolates from blood, spleen and peritoneal cavity showed that N418 reacts primarily with dendritic cells. N418 also stained dendritic profiles strongly in tissue sections of liver and spleen, but most of the cells that actively endocytosed carbon in both organs showed little or no N418 staining. Likewise, carbon could not be identified in cells that react with M342, which stains intracellular granules of dendritic cells. In contrast, the carbon-labeled cells in both liver and spleen were labeled with antibodies (SER-4, F4/80, FA11) that bind primarily to isolated macrophages. Therefore the clearance of colloidal carbon in situ reflects the scavenging activity of macrophages and not the endocytic activity that underlies the antigen presenting function of dendritic cells.

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8

ZHAO, Dan, Ping MIN, Longquan YANG, Shili LU та Cangwen JIAO. "N451 γ Spectrometry Logging Probe and Logging Techniques". Acta Geologica Sinica - English Edition 88, s2 (2014): 1434–35. http://dx.doi.org/10.1111/1755-6724.12381_46.

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9

Carter, James Richard, Cara Theresia Pager, Stephen Derrick Fowler, and Rebecca Ellis Dutch. "Role of N-Linked Glycosylation of the Hendra Virus Fusion Protein." Journal of Virology 79, no. 12 (2005): 7922–25. http://dx.doi.org/10.1128/jvi.79.12.7922-7925.2005.

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ABSTRACT The Hendra virus fusion (F) protein contains five potential sites for N-linked glycosylation in the ectodomain. Examination of F protein mutants with single asparagine-to-alanine mutations indicated that two sites in the F2 subunit (N67 and N99) and two sites in the F1 subunit (N414 and N464) normally undergo N-linked glycosylation. While N-linked modification at N414 is critical for protein folding and transport, F proteins lacking carbohydrates at N67, N99, or N464 remained fusogenically active. As N464 lies within heptad repeat B, these results contrast with those seen for several paramyxovirus F proteins.

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10

Liang, Zu-Pei, Jian Li, and Hua Yang. "N2,N4,1-Tribenzyl-2,5-dimethyl-3-oxopyrrolidine-2,4-dicarboxamide." Acta Crystallographica Section E Structure Reports Online 63, no. 6 (2007): o2817—o2818. http://dx.doi.org/10.1107/s1600536807021290.

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11

Beresten, Sergey F., Rodica Stan, Anja J. van Brabant, Tian Ye, Saule Naureckiene, and Nathan A. Ellis. "Purification of Overexpressed Hexahistidine-Tagged BLM N431 as Oligomeric Complexes." Protein Expression and Purification 17, no. 2 (1999): 239–48. http://dx.doi.org/10.1006/prep.1999.1135.

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12

Kelsall, B. L., and W. Strober. "Distinct populations of dendritic cells are present in the subepithelial dome and T cell regions of the murine Peyer's patch." Journal of Experimental Medicine 183, no. 1 (1996): 237–47. http://dx.doi.org/10.1084/jem.183.1.237.

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Despite the fact that the Peyer's patch (PP) is the primary site for antigen uptake in the intestine, the cellular basis of antigen handling after transport into the PP is poorly understood. We performed immunohistology of murine PPs using the dendritic cell (DC)-reactive monoclonal antibodies N418, NLDC-145, M342, and 2A1, as well as antibodies to other T cell, B cell, and macrophage markers. N418+, 2A1+, NLDC-145-, M342- cells form a dense layer of cells in the subepithelial dome (SED), just beneath the follicle epithelium, and are scattered throughout the follicle, sparing the germinal center. In contrast, N418+, 2A1+, NLDC-145+, and M342+ DCs are present in the interfollicular T cell regions (IFR). CD3+ and CD4+, but no CD8+ T cells were present in the SED and the follicle, including the germinal center, while CD3+, CD4+, and CD8+ T cells were present in the IFR. B cells and macrophages were poorly represented in the SED as no B220+ cells, only few Mac-1lo cells, and no F4/80+ cells were present at this site. In contrast, Mac-1hi cells were found in the IFR and lamina propria of intestinal villi, while F4/80+ cells were found only in the latter. In further phenotypic studies, we analyzed surface molecules of PP and spleen DCs by flow cytometry and found that these cells had similar fluorescence profiles when stained with N418, NLDC-145, and 33D1 DC-reactive antibodies, and antibodies to the costimulatory molecules B7-1 (1G10) and B7-2 (GL1). In contrast, PP DCs expressed 5-10-fold higher levels of major histocompatibility complex class II antigens (IEk) than spleen DCs. Finally, in functional studies, we demonstrated that both PP and spleen DCs process soluble protein antigens during overnight culture and induce similar levels of proliferation in CD3+ T cells, and CD4+/Mel 14hi T cells from T cell receptor transgenic mice. The in vivo relevance of such presentation was shown by the fact that PP DCs isolated from Balb/c mice after being fed ovalbumin stimulated proliferation in ovalbumin T cell receptor T cells. Taken together, our data suggest that DCs in the SED of the PP are uniquely positioned for the processing of antigens passed into the PP from the overlying M cell, and that PP DCs are effective at processing and presenting oral antigens to naive T cells.

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13

Almansa-Villatoro, M. Victoria. "The Cultural Indexicality of the N41 Sign for bjȝ: The Metal of the Sky and the Sky of Metal." Journal of Egyptian Archaeology 105, no. 1 (2019): 73–81. http://dx.doi.org/10.1177/0307513319899948.

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This article explores the cultural implications of the sign N41 [Formula: see text] used in an apparently random constellation of words related to women, water and metals. The symbolic meaning of iron and its consistent relation with the sky in religious texts is explored to determine that the Egyptian cosmovision contemplated the sky as an iron container of water, pieces of which fell to the earth in the shape of meteors and were used to produce ritual objects. The indexicality of the N41 sign suggests that the relation between birth, afterlife, and iron existed even before the first attested long religious texts in Egypt. Finally, the lexical parallels between Egypt and Mesopotamia can be explained as a common reaction to the phenomena of falling iron meteorites.

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14

Oluški, Nikola. "ISTRAŽIVANJE STRUJANJA JONSKE TEČNOSTI PRIMENOM RAČUNARSKE DINAMIKE FLUIDA." Zbornik radova Fakulteta tehničkih nauka u Novom Sadu 35, no. 01 (2019): 9–12. http://dx.doi.org/10.24867/06am01oluski.

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Predmet rada jeste strujanje jonske tečnosti N-butil N,N,N trimetilamonijum bis(trihlormetilsulfonil)imid, skraćeno [N4111][NTf2], kroz pravu cev. Cilj rada jeste istraživanje prinudne konvekcije i hidrauličkih karakteristika pri strujanju jonske tečnosti kroz pravu cevnu deonicu. Istraživanje je urađeno primenom računarske dinamike fluida pomoću programskog paketa StarCCM+. Pri analizi termičkih i hidrauličkih karakteristika zaključeno je da predmetna jonska tečnost ne predstavlja najbolje rešenje kao medijum za prenos toplote za date uslove.

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15

Turner, Brie E., Melinda Christensen, Janusz Lange, et al. "Conditioning Intensity and Dendritic Cell (DC) Activation: Implications for GVHD Control Using DC Depleting Antibodies." Blood 106, no. 11 (2005): 3112. http://dx.doi.org/10.1182/blood.v106.11.3112.3112.

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Abstract Graft versus Host Disease (GVHD) and treatment related mortality (TRM) are the major limitations to the widespread application of allogeneic haematopoietic stem cell transplantation (HSCT) for haematological and non-haematological malignancies. Dendritic cells (DC) as the key initiators and directors of the immune response are central to allogeneic transplant interactions. Preparative conventional conditioning (CC) regimens aim to control disease and ablate the host immune response to facilitate normal haematopoietic reconstitution. The conditioning also unleashes a cytokine storm that activates the residual host immune system, driving host DC and donor T cell interactions that result in GVHD. Reducing the intensity of conditioning (RIC) regimens maintains immune anti-leukaemic activity of T replete HSCT, reduces TRM and delays the onset of GVHD, but the overall incidence of GVHD is unchanged. We hypothesise that this is due to increased persistence of host DC. We propose that strategic administration of DC depleting antibodies could be an effective means to control GVHD. Whilst there is some information on the effects of CC on DC; we have shown that mature plasmacytoid (p) DC are increased in mouse spleen after conditioning by radiation, there is no information on the effects of RIC on DC. We have established murine models of conditioning (CC = Cyclophosphamide [CY] + 800cGy and RIC = Fludarabine [FLU] + CY + 200cGy). The effects on DC numbers, activation and subset composition (myeloid (m) DC and DC), cytokine and systemic endotoxin levels were studied on each day of the conditioning regimens in the absence of HSCT. Mice receiving CC have a significantly higher percentage of DC which are pDC compared to RIC (p&lt;0.001) which results in a decrease in the overall percentage of mDC. However, mice that received RIC have significantly higher absolute numbers of host pDC than CC mice. Preliminary data shows no difference in endotoxin levels in mice receiving RIC or CC without HSCT. However, there may be a transient increase in endotoxin levels in mice after 2 FLU injections (p=0.12). No such increase was seen after CC. There were significantly higher levels of TNF-α (p=0.02) and IL1-β (p=0.03) in mice receiving RIC rather than CC without HSCT. The higher absolute numbers of DC, altered subset ratio and cytokine production appears to account for the delayed onset of GVHD in RIC transplant recipients. Intra-peritoneal (ip) injection of N418, a monoclonal antibody to mouse leukocyte integrin CD11c depleted murine DC in vivo. Preliminary experiments show elimination of 50% of DC after injection of N418 (500mg). Subsequent experiments show that 1mg of N418 is sufficient to significantly delay, but not prevent, GVHD in a full MHC mismatched model of HSCT (p=0.025). The action of N418 is specific, as DC depletion was not seen in mice treated with 1 mg hamster Ig. Together, these observations suggest that increasing antibody concentration and prolonged administration may be required to prevent GVHD. The successful application of DC depletion to control GVHD will improve the safety of HSCT for patients with leukaemia.

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16

WEN Lei, 温. 磊., 陈. 林. CHEN Lin, 陈. 伟. CHEN Wei, 胡丽丽 HU Li-li, and 吴谊群 WU Yi-qun. "Small signal gain of glass N41 in large aperture Nd:laser." Optics and Precision Engineering 24, no. 12 (2016): 2925–30. http://dx.doi.org/10.3788/ope.20162412.2925.

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17

Yuhong Du, Kamalika Moulick, Anna Rodina, et al. "High-Throughput Screening Fluorescence Polarization Assay for Tumor-Specific Hsp90." Journal of Biomolecular Screening 12, no. 7 (2007): 915–24. http://dx.doi.org/10.1177/1087057107306067.

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Heat shock protein 90 (Hsp90) is a molecular chaperone that has emerged as an important target in cancer and several other diseases, such as neurodegenerative diseases, nerve injuries, inflammation, and infection. Discovery of novel agents that inhibit Hsp90 and have druglike properties is therefore a major focus in several academic and industrial laboratories. In this study, the authors describe the development and optimization in a 384-well format of a novel assay for the identification of Hsp90 inhibitors using fluorescence polarization, which measures competitive binding of red-shifted fluorescently labeled geldanamycin (GM-cy3B) to Hsp90 found in the NCI-N417 small-cell lung carcinoma cells. The authors demonstrate that GMcy3B binds with high affinity and specificity to cellular Hsp90. The assay results in excellent signal-to-noise ratios (>10) and Z′ values (>0.75) at tracer concentrations greater than 4 nM and 1 µg/well of total NCI-N417 protein, indicating a robust assay. It also equilibrates after 5 h of incubation at room temperature and remains stable for up to 24 h. Furthermore, it is a simple mix-and-read format that is cost-effective and uses only low amounts of fluorophore and cell lysates. A study using more than 15,000 compounds from the National Institutes of Health Molecular Libraries Screening Center Network was performed to validate its performance in a high-throughput screening format. ( Journal of Biomolecular Screening 2007:915-924)

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18

Crowley, M., K. Inaba, and R. M. Steinman. "Dendritic cells are the principal cells in mouse spleen bearing immunogenic fragments of foreign proteins." Journal of Experimental Medicine 172, no. 1 (1990): 383–86. http://dx.doi.org/10.1084/jem.172.1.383.

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We monitored the APC function of cells taken from the spleen and peritoneal cavity of mice that had been given protein antigens via the intravenous or intraperitoneal routes. Using the mAb 33D1 and N418 to negatively and positively select dendritic cells, we obtained evidence that dendritic cells are the main cell type in spleen that carries the protein in a form that is immunogenic for antigen-specific T cells. In vivo pulsed macrophages were not immunogenic and did not appear capable of transferring peptide fragments to dendritic cells.

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19

He Shaobo, 贺少勃, 陈林 Chen Lin, 陈远斌 Chen Yuanbin, 刘建国 Liu Jianguo, 刘勇 Liu Yong, and 祖小涛 Zu Xiaotao. "Thermal Effect of N41 Nd∶Glass Slab with 400 mm Aperture." Chinese Journal of Lasers 44, no. 5 (2017): 0501007. http://dx.doi.org/10.3788/cjl201744.0501007.

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20

Kobal, Michael. "Nonlinear Mean Reversion in Stock Prices." CFA Digest 38, no. 4 (2008): 37–38. http://dx.doi.org/10.2469/dig.v38.n4.1.

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21

Hubbard, Jonathan Wheeler. "First Come First Disserved." CFA Digest 38, no. 4 (2008): 28–29. http://dx.doi.org/10.2469/dig.v38.n4.11.

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22

Hubbard, Jonathan Wheeler. "Utility-Adjusted Performance." CFA Digest 39, no. 4 (2009): 88–89. http://dx.doi.org/10.2469/dig.v39.n4.1.

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23

Magiera, Frank T. "Homeownership and Mixed–Asset Portfolio Allocations." CFA Digest 39, no. 4 (2009): 98–100. http://dx.doi.org/10.2469/dig.v39.n4.11.

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Sule, Ahmed. "The Moving Average Ratio and Momentum." CFA Digest 40, no. 4 (2010): 60–62. http://dx.doi.org/10.2469/dig.v40.n4.1.

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Gunasingham, Brindha. "Are Member Firms of Corporate Groups Less Risky?" CFA Digest 40, no. 4 (2010): 26–27. http://dx.doi.org/10.2469/dig.v40.n4.11.

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MacIsaac, Keith Joseph. "Hedge Funds: Pricing Controls and the Smoothing of Self-Reported Returns." CFA Digest 41, no. 4 (2011): 5–7. http://dx.doi.org/10.2469/dig.v41.n4.1.

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Ishmael, Tokunboh. "The Forgotten History of Domestic Debt." CFA Digest 41, no. 4 (2011): 64–66. http://dx.doi.org/10.2469/dig.v41.n4.11.

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Balakrishna, Sridhar. "What’s Wrong with Today’s Economics? The Current Crisis Calls for an Approach to Economics Rooted More on Data than on Rationality." CFA Digest 42, no. 4 (2012): 179–82. http://dx.doi.org/10.2469/dig.v42.n4.1.

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Ennis, Richard M. "The New Organizational Paradigm: A Single Portfolio Manager and a Band of Scouts." Financial Analysts Journal 64, no. 4 (2008): 8–10. http://dx.doi.org/10.2469/faj.v64.n4.1.

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Sullivan, Rodney N. "Governance: Travel and Destinations." Financial Analysts Journal 65, no. 4 (2009): 6–10. http://dx.doi.org/10.2469/faj.v65.n4.1.

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Do, Binh, and Robert Faff. "Does Simple Pairs Trading Still Work?" Financial Analysts Journal 66, no. 4 (2010): 83–95. http://dx.doi.org/10.2469/faj.v66.n4.1.

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Sullivan, Rodney N. "“Speculative Leverage: A False Cure for Pension Woes”: Author Response." Financial Analysts Journal 66, no. 4 (2010): 14–16. http://dx.doi.org/10.2469/faj.v66.n4.11.

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Willenbrock, Scott. "Diversification Return, Portfolio Rebalancing, and the Commodity Return Puzzle." Financial Analysts Journal 67, no. 4 (2011): 42–49. http://dx.doi.org/10.2469/faj.v67.n4.1.

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Baltussen, Guido, Bart van der Grient, Wilma de Groot, Erik Hennink, and Weili Zhou. "Exploiting Option Information in the Equity Market." Financial Analysts Journal 68, no. 4 (2012): 56–72. http://dx.doi.org/10.2469/faj.v68.n4.1.

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Erb, Claude B., and Campbell R. Harvey. "The Golden Dilemma." Financial Analysts Journal 69, no. 4 (2013): 10–42. http://dx.doi.org/10.2469/faj.v69.n4.1.

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Asness, Clifford S., Andrea Frazzini, and Lasse H. Pedersen. "Low-Risk Investing without Industry Bets." Financial Analysts Journal 70, no. 4 (2014): 24–41. http://dx.doi.org/10.2469/faj.v70.n4.1.

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Doeswijk, Ronald, Trevin Lam, and Laurens Swinkels. "“The Global Multi-Asset Market Portfolio, 1959–2012”: Author Response." Financial Analysts Journal 70, no. 4 (2014): 9–12. http://dx.doi.org/10.2469/faj.v70.n4.11.

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Brockman, Paul, Xu Li, and S. McKay Price. "Differences in Conference Call Tones: Managers vs. Analysts." Financial Analysts Journal 71, no. 4 (2015): 24–42. http://dx.doi.org/10.2469/faj.v71.n4.1.

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L’Her, Jean-François, Rossitsa Stoyanova, Kathryn Shaw, William Scott, and Charissa Lai. "A Bottom-Up Approach to the Risk-Adjusted Performance of the Buyout Fund Market." Financial Analysts Journal 72, no. 4 (2016): 36–48. http://dx.doi.org/10.2469/faj.v72.n4.1.

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Baker, Malcolm, Ryan Taliaferro, and Terence Burnham. "Optimal Tilts: Combining Persistent Characteristic Portfolios." Financial Analysts Journal 73, no. 4 (2017): 75–89. http://dx.doi.org/10.2469/faj.v73.n4.1.

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Wang, Peng, Laura Chapman, Steven Peterson, and Jon Spinney. "Evaluating Spending Policies in a Low-Return Environment." Financial Analysts Journal 74, no. 4 (2018): 11–23. http://dx.doi.org/10.2469/faj.v74.n4.1.

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Barukcic, Marinko, Srete Nikolovski, and Zeljko Hederic. "Estimation of Power Losses on Radial Feeder Using Minimum Electrical Measurements and Differential Evolution Method." International Journal of Soft Computing and Software Engineering 2, no. 4 (2012): 1–13. http://dx.doi.org/10.7321/jscse.v2.n4.1.

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Diermeier, Jeff. "The View from Vancouver." CFA Institute Magazine 19, no. 4 (2008): 5. http://dx.doi.org/10.2469/cfm.v19.n4.1.

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McCarthy, Ed. "When Values Clash." CFA Institute Magazine 19, no. 4 (2008): 18–19. http://dx.doi.org/10.2469/cfm.v19.n4.11.

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Stith, Jeffrey. "Questions about Self-Reporting." CFA Institute Magazine 20, no. 4 (2009): 28–29. http://dx.doi.org/10.2469/cfm.v20.n4.11.

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Rogers, John. "Reaching Out." CFA Institute Magazine 21, no. 4 (2010): 6. http://dx.doi.org/10.2469/cfm.v21.n4.1.

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Trammell, Susan. "Middle March." CFA Institute Magazine 21, no. 4 (2010): 40–45. http://dx.doi.org/10.2469/cfm.v21.n4.11.

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Rogers, John. "The CFA Network." CFA Institute Magazine 22, no. 4 (2011): 7. http://dx.doi.org/10.2469/cfm.v22.n4.1.

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Barnes, Jonathan. "“A Very Exciting Time”." CFA Institute Magazine 22, no. 4 (2011): 38–41. http://dx.doi.org/10.2469/cfm.v22.n4.11.

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Barnes, Jonathan. "The Value of Financial Innovation." CFA Institute Magazine 23, no. 4 (2012): 36–39. http://dx.doi.org/10.2469/cfm.v23.n4.11.

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