Relevant bibliographies by topics / XENIX

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'XENIX'

Author: Grafiati
Published: 4 June 2021
Last updated: 11 February 2022

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Journal articles on the topic "XENIX"

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Gligor, V. D., C. S. Chandersekaran, R. S. Chapman, et al. "Design and Implementation of Secure Xenix." IEEE Transactions on Software Engineering SE-13, no. 2 (1987): 208–21. http://dx.doi.org/10.1109/tse.1987.232893.

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Gallagher, Kathleen M., Ahmed Kanna, Natalie Nesvaderani, Rana Dajani, Dima Hamadmad, and Ghufran Abudayyeh. "Reports." Anthropology of the Middle East 16, no. 1 (2021): 111–20. http://dx.doi.org/10.3167/ame.2021.160107.

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Melissa Fleming, A Hope More Powerful than the Sea: The Journey of Doaa Al Zamel (New York: Flatiron Books, 2017), 288 pp.Omar Dewachi, Ungovernable Life: Mandatory Medicine and Statecraft in Iraq (Stanford, CA: Stanford University Press, 2017), xviii + 239 pp.Rokhsareh Ghaemmaghami, Sonita (Zurich: Xenix Film, 2015), 90 min.Ron Bourke, Terror and Hope: The Science of Resilience (Portland: Collective Eye Films, 2019), 36 min.
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Wells, George C. "An evaluation of XENIX system V as a real-time operating system." Microprocessing and Microprogramming 33, no. 1 (1991): 57–66. http://dx.doi.org/10.1016/0165-6074(91)90015-l.

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Goel, L. R., Rakesh Gupta, and V. S. Rana. "Stochastic analysis of a xenix operating computer system with two down modes." Microelectronics Reliability 32, no. 6 (1992): 781–91. http://dx.doi.org/10.1016/0026-2714(92)90043-k.

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Gligor, V. D., C. S. Chandersekaran, Wen-Der Jiang, A. Johri, G. L. Luckenbaugh, and L. E. Reich. "A New Security Testing Method and Its Application to the Secure Xenix Kernel." IEEE Transactions on Software Engineering SE-13, no. 2 (1987): 169–83. http://dx.doi.org/10.1109/tse.1987.232890.

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Koppány, J. "A Dual-Computer Based Data Acquisition and Control System Using Xenix/Unix System V." IFAC Proceedings Volumes 19, no. 7 (1986): 123–26. http://dx.doi.org/10.1016/b978-0-08-034347-1.50019-x.

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Grochowski, Lechosław, Jan Kaczmarek, Władysław Kadłubiec, and Henryk Bujak. "Genetic variability of rye-xenic-hybrid traits." Acta Societatis Botanicorum Poloniae 65, no. 3-4 (2014): 329–33. http://dx.doi.org/10.5586/asbp.1996.050.

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In field experiments performed in two localities (Smolice, Wrocław) 18 xenic hybrids of winter rye, two testers and standard cultivar Dańkowskie Złote, were analysed. The objects of detailed evaluations were 11 traits. For six of them arithmetic means (x), standard deviations (S), coefficients of variation (cv), coefficients of genetic diversity (h<sup>2</sup>), correlation coefficients were calculated. Moreover, analyses of variance were carried out and the effects of general (GCA) and specific (SCA) combining ability were estimated. The existence of quantitative xenia in hybrids was confirmed. It was shown that xenic hybrids, in respect to most of the analysed traits, were insignificantly inferior to the testers and the standard cultivar. However, the decrease of plant height has shown to be significant and a tendency to higher yield was observed.
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Martin, Christine M. A., Vadivel Parthsarathy, Varun Pathak, Victor A. Gault, Peter R. Flatt, and Nigel Irwin. "Characterisation of the biological activity of xenin-25 degradation fragment peptides." Journal of Endocrinology 221, no. 2 (2014): 193–200. http://dx.doi.org/10.1530/joe-13-0617.

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Xenin-25, a peptide co-secreted with the incretin hormone glucose-dependent insulinotropic polypeptide (GIP), possesses promising therapeutic actions for obesity-diabetes. However, native xenin-25 is rapidly degraded by serum enzymes to yield the truncated metabolites: xenin 9–25, xenin 11–25, xenin 14–25 and xenin 18–25. This study has examined the biological activities of these fragment peptides. In vitro studies using BRIN-BD11 cells demonstrated that native xenin-25 and xenin 18–25 possessed significant (P<0.05 to P<0.001) insulin-releasing actions at 5.6 and 16.7 mM glucose, respectively, but not at 1.1 mM glucose. In addition, xenin 18–25 significantly (P<0.05) potentiated the insulin-releasing action of the stable GIP mimetic (d-Ala2)GIP. In contrast, xenin 9–25, xenin 11–25 and xenin 14–25 displayed neither insulinotropic nor GIP-potentiating actions. Moreover, xenin 9–25, xenin 11–25 and xenin 14–25 significantly (P<0.05 to P<0.001) inhibited xenin-25 (10−6 M)-induced insulin release in vitro. I.p. administration of xenin-based peptides in combination with glucose to high fat-fed mice did not significantly affect the glycaemic excursion or glucose-induced insulin release compared with controls. However, when combined with (d-Ala2)GIP, all xenin peptides significantly (P<0.01 to P<0.001) reduced the overall glycaemic excursion, albeit to a similar extent as (d-Ala2)GIP alone. Xenin-25 and xenin 18–25 also imparted a potential synergistic effect on (d-Ala2)GIP-induced insulin release in high fat-fed mice. All xenin-based peptides lacked significant satiety effects in normal mice. These data demonstrate that the C-terminally derived fragment peptide of xenin-25, xenin 18–25, exhibits significant biological actions that could have therapeutic utility for obesity-diabetes.
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Khan, Dawood, Srividya Vasu, R. Charlotte Moffett, Victor A. Gault, Peter R. Flatt та Nigel Irwin. "Locally produced xenin and the neurotensinergic system in pancreatic islet function and β-cell survival". Biological Chemistry 399, № 1 (2017): 79–92. http://dx.doi.org/10.1515/hsz-2017-0136.

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AbstractModulation of neuropeptide receptors is important for pancreatic β-cell function. Here, islet distribution and effects of the neurotensin (NT) receptor modulators, xenin and NT, was examined. Xenin, but not NT, significantly improved glucose disposal and insulin secretion, in mice. However, both peptides stimulated insulin secretion from rodent β-cells at 5.6 mmglucose, with xenin having similar insulinotropic actions at 16.7 mmglucose. In contrast, NT inhibited glucose-induced insulin secretion. Similar observations were made in human 1.1B4 β-cells and isolated mouse islets. Interestingly, similar xenin levels were recorded in pancreatic and small intestinal tissue. Arginine and glucose stimulated xenin release from islets. Streptozotocin treatment decreased and hydrocortisone treatment increased β-cell mass in mice. Xenin co-localisation with glucagon was increased by streptozotocin, but unaltered in hydrocortisone mice. This corresponded to elevated plasma xenin levels in streptozotocin mice. In addition, co-localisation of xenin with insulin was increased by hydrocortisone, and decreased by streptozotocin. Furtherin vitroinvestigations revealed that xenin and NT protected β-cells against streptozotocin-induced cytotoxicity. Xenin augmented rodent and human β-cell proliferation, whereas NT displayed proliferative actions only in human β-cells. These data highlight the involvement of NT signalling pathways for the possible modulation of β-cell function.
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Yang, Qin, Yan Fu, Yalan Liu, Tingting Zhang, Shu Peng, and Jie Deng. "Novel Classification Forms for Xenia." HortScience 55, no. 7 (2020): 980–87. http://dx.doi.org/10.21273/hortsci14939-20.

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The xenia effect refers to the phenomenon whereby the pollen genotype directly affects seed and fruit development during the period from fertilization to seed germination, which leads to different characteristics in phenotypic traits. The xenia effect can create differences in the endosperm and embryo formed after double fertilization and can also alter various fruit parameters, such as the fruit-ripening period; the fruit shape, size, and color; the flavor quality, such as sugars and acids; as well as the nutrient quality, such as anthocyanins. The xenia effect manifests in various ways, playing an important role in increasing the yield of fruit trees, improving fruit appearance and internal quality, as well as in directional breeding. Compared with other pomology research areas, our understanding of the xenia effect is still in its infancy. Currently, xenia is classified into two types: xenia and metaxenia. In the former, the direct effects of the pollen genotype are exhibited in the syngamous parts of the ovules; that is, the embryo and endosperm only. In the latter, the effects of the pollen genotype are demonstrated in structures other than the embryo and endosperm; that is, in tissues derived wholly from the mother plant material, in seed parts such as the nucellus and testa, as well as in the carpels and accessory tissues. However, the current classification has various shortcomings. In the present study, we propose a novel classification based on whether the appearance of xenia results from the tissue formed by double fertilization. Three xenia types are proposed: double-fertilization xenia, non–double-fertilization xenia, and combined xenia. The new classification has great theoretical and practical significance for future studies on the xenia effect and its mechanisms and also provides a more effective, broader application of xenia in improving the yield and quality of fruit trees.
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Dissertations / Theses on the topic "XENIX"

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Kim, Eun Ran. "Roles of xenin in the regulation of energy balance: central nervous system control of food intake and body weight by xenin." Elsevier, 2010. http://hdl.handle.net/1993/5006.

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Xenin, a gastrointestinal peptide, is structurally similar to neurotensin which functions as a satiety factor via neurotensin receptor 1 (Ntsr1). Metabolic effect of the adipocyte hormone leptin is partially mediated through the Ntsr1 and interleukin 1 type I receptor (IL-1RI) in the central nervous system (CNS). Xenin reduces food intake when administered centrally and peripherally. Apart from its acute feeding-suppressing effect, the distinct metabolic action of xenin and the mechanism of xenin-induced anorexia remain to be elucidated. We hypothesized that prolonged xenin treatment reduces food intake and body weight and increases energy expenditure. We also hypothesized that xenin reduces food intake by activating CNS signalling pathways including Ntsr1 and IL-1RI and by interacting with leptin. To address these hypotheses, we examined (1) the effect of xenin treatment on food intake, energy expenditure and body weight in wild-type, Ntsr1-deficient and IL-1RI-deficient mice, (2) the effect of xenin on hypothalamic Fos and interleukin 1β (IL-1β) expression in wild-type mice, and (3) the effect of co-injection of xenin and leptin on food intake and body weight in wild-type mice. Daily intraperitoneal (i.p.) or intracerebroventricular (i.c.v.) xenin treatment (6-10 days) significantly reduced body weight gain and adiposity with a transient reduction in food intake in wild-type mice. Xenin treatment (i.p.) caused a significant reduction in respiratory quotient without changes in energy expenditure. Xenin treatment increased hormone sensitive lipase (HSL) mRNA levels and reduced acyl-coenzyme A: diacylglycerol acyltransferase 2 (DGAT2) mRNA levels in white adipose tissue. Xenin (i.p.) increased the number of Fos-immunoreactive cells in the hypothalamus and the brainstem and increased hypothalamic IL-1β mRNA levels. The anorectic effects of xenin and leptin were abolished or attenuated in mice lacking Ntsr1 or IL-1RI. I.p. co-administration of xenin and leptin caused greater reductions in food intake and body weight compared to leptin alone and xenin alone. These data suggest that long-term xenin treatment reduces body weight by reducing food intake and increasing fat oxidization. Xenin reduces food intake by activating CNS signalling pathways involving Ntsr1 and IL-1 possibly through the interaction with leptin. These findings implicate xenin and its downstream mediators as potential targets for anti-obesity drugs.
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Ebert, Antonia Xenia [Verfasser]. "Chromogranin A im Rahmen von gastrointestinalen und endokrinen Autoimmunerkrankungen / Antonia Xenia Ebert." Mainz : Universitätsbibliothek der Johannes Gutenberg-Universität Mainz, 2020. http://d-nb.info/122489569X/34.

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Hengesch, Xenia [Verfasser]. "Impact of adverse early life events on physiological stress responses / Xenia Hengesch." Trier : Universität Trier, 2018. http://d-nb.info/1197808043/34.

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Große, Xenia [Verfasser], and Norbert [Akademischer Betreuer] Hampp. "Bioinspirierte Partikeladsorption: Polyelektrolyt-Multilayer auf strukturierten Substraten / Xenia Große. Betreuer: Norbert Hampp." Marburg : Philipps-Universität Marburg, 2014. http://d-nb.info/1057000019/34.

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Junior, José de Ribamar Braga Pinheiro. "Xenia: um sistema de segurança para grades computacionais baseado em cadeias de confiança." Universidade de São Paulo, 2008. http://www.teses.usp.br/teses/disponiveis/45/45134/tde-05082008-152432/.

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Os Sistemas de Grades Computacionais são intrinsecamente mais vulneráveis às ameaças de segurança que os Sistemas tradicionais, uma vez que abrangem um grande número de usuários e os recursos e as aplicações são geridas por diferentes domínios administrativos. A autenticação e a autorização são fatores imperativos para os Sistemas de Grade Computacional. Da mesma forma, a escalabilidade e a distribuição de dados vêm também sendo objeto de estudo de vários pesquisadores da área. Os serviços providos pelas Grades Computacionais devem evitar implementações centralizadas pela dificuldade do gerenciamento global. Outro importante requisito das Grades Computacionais é prover mecanismos para a delegação de direitos de acesso aos recursos. O proprietário do recurso deve ser capaz de delegar permissões para outro usuário, talvez por um tempo limitado, com base na confiança que possui neste. No entanto, a delegação deve ser usada com cuidado, pois uma longa cadeia de delegações poderia conduzir a uma utilização abusiva dos recursos pelos usuários maliciosos. Para tratar os principais requisitos de segurança das Grades Computacionais, desenvolvemos uma Arquitetura de Segurança denominada Xenia. Esta arquitetura é baseada em SPKI/SDSI, um modelo de segurança flexível, extensível e descentralizado que fornece autenticação, confidencialidade e controle de acesso. Propusemos uma extensão ao modelo SPKI/SDSI baseada em lógica subjetiva para representar relações de confiança entre indivíduos.<br>Grid Computing Systems are inherently more vulnerable to security threats than traditional systems, since they potentially encompass a large number of users, resources, and applications managed by different administrative domains. Authentication and authorization are imperative for grid systems. Since scalability and distribution are major concerns on grid environments, those services implementations should avoid centralized solutions. Another relevant requirement to consider is the provision of mechanisms for delegating access rights, since they minimize the overhead of grid administrators on providing access rights to grid resources. The owner of an access right should be able to delegate permissions to another user, maybe for a limited time, based on his trust on that user. However, delegation must be used with care. A long chain of delegations could lead to improper use of resources by malicious users. Confidentiality and integrity are also important security requirements for many grid applications. To address these problems, we designed a Security Architecture for Grid Systems named Xenia. This architecture is based on SPKI/SDSI, a flexible and extensible decentralized security model that provides authentication, confidentiality, and access control. We proposed an extension to the SPKI/SDSI model to represent trust relations between subjects based on subjective logic.
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Daase, Deborah Xenia [Verfasser]. "Das kartellrechtliche Konzept der wirtschaftlichen Einheit unter besonderer Berücksichtigung von Gemeinschaftsunternehmen / Deborah Xenia Daase." Frankfurt a.M. : Peter Lang GmbH, Internationaler Verlag der Wissenschaften, 2019. http://d-nb.info/1212760050/34.

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Gorny, Xenia [Verfasser]. "Das Adapterprotein AKAP79/150 : Charakterisierung eines genetischen Polymorphismus und eines neuen Bindungspartners / Xenia Gorny." Magdeburg : Universitätsbibliothek, 2012. http://d-nb.info/105413555X/34.

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Martin, Christine Margaret Anne. "Characterisation, biological activity and therapeutic potential of xenin and modified forms in obesity-diabetes." Thesis, Ulster University, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.667745.

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Novel therapeutic approaches are required to restore normoglycaemia in type 2 diabetes mellitus (T2DM). This thesis characterised and elucidated biological activity and therapeutic applicability of xenin and modified forms in obesity-diabetes. The plasma enzymatic degradation products of xenin-25 have now been characterised, namely xenin 9-25, xenin 11-25, xenin 14-25 and xenin 18-25. Xenin- 25 and enzyme resistant synthetic xenin-25[Lys13PAL] enhanced insulin secretion and potentiated GIP-induced insulin release in vitro, improved anti-hyperglycaemic and insulin-releasing activity and reduced food intake in vivo. Moreover, xenin- 25 [Lys 13p AL] demonstrated enhanced biological activity compared to native xenin- 25. Twice daily administration of xenin-25[Lys13PAL] for 14 days significantly improved metabolic control in dietary-induced diabetes. Once daily administration of xenin-25[Lys13PAL], in combination with a novel acylated GIP agonist, (DAla2) GIP[Lys37PAL], for 21 days did not have any additive effects. Nonetheless, (DAla2) GIP[Lys37PAL] treated mice exhibited significant improvements in glycaemic control and insulin sensitivity. The biological role of xenin-25 degradation fragments was also assessed. As such, xenin 9-25, xenin 11-25 and xenin 14-25 had no insulinotropic, glucose-lowering or satiety effects. Nonetheless, xenin 18-25 demonstrated in vitro insulinotropic effects, and mild glucose-lowering effects in vivo. The novel xenin 18-25 analogue, xenin 18-25[Lys20PAL], demonstrated similar biological effects, but these were not enhanced compared to xenin 18-25. In addition, the amino acid substituted xenin analogues, namely xenin-25 GIn and xenin 18-25 GIn, induced in vitro insulin secretion, reduced glycaemic excursion and enhanced insulin secretion in vivo. Furthermore, xenin-25 GIn potentiated the insulinotropic action of GIP and acutely inhibited food intake. Sub-chronic administration of xenin-25 GIn or xenin 18-25 Gin improved glucose tolerance and metabolic response to GIP in high fat mice. Collectively, this thesis has demonstrated that xenin, and modified forms, possess beneficial independent biological actions in addition to GIP additive actions, and appear to have dual therapeutic properties that merit further investigation for T2DM therapy.
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Erler, Xenia [Verfasser], and Peter [Akademischer Betreuer] Strasser. "In-situ investigation of metal nanoparticle stability during electrocatalysis / Xenia Erler. Betreuer: Peter Strasser." Berlin : Universitätsbibliothek der Technischen Universität Berlin, 2012. http://d-nb.info/1028912935/34.

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Kuhlman, Leslie Charles. "Investigation of a xenia effect for yield caused by the waxy gene in grain sorghum." Texas A&M University, 2005. http://hdl.handle.net/1969.1/2624.

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Sorghum grain with a waxy endosperm is more digestible and has a higher feeding efficiency compared to sorghum grain with a non-waxy (or normal) endosperm. However, waxy sorghums (Sorghum bicolor (L.) Moench) yield 10-15% less than normal sorghum and the cause of the yield reduction is unclear. The objective of this research is to determine if the yield decrease could be due to the waxy phenotype itself. The waxy phenotype is an example of a xenia effect, where the pollen not only contributes to the genotype of the resulting hybrid, but also immediately influences the phenotype of the resulting seed. Sterile hybrids under different pollination types, and different genotypes of fertile hybrids, both resulted in hybrids that produced different ratios of waxy phenotype seed. The effects on yield and 500 kernel weight were investigated in Weslaco, College Station, and Halfway, Texas over two years. Yields of sterile heterozygous waxy hybrids under waxy pollination, which produced an average 27% waxy seed over all environments, were nearly identical to homozygous nonwaxy hybrids that produced 0% waxy seed. Average 500 kernel weights for the same hybrids were not different. Grain yields for the fertile hybrid genotypes were significantlydifferent. Hybrids which produced 100% waxy seed yielded significantly less than hybrids which produced 25% waxy seed. Upon further examination, hybrids that were produced from waxy F1 endosperm seed (wxwxwx) had significantly worse stand and panicle number per plot means than did hybrids from nonwaxy F1 endosperm seed (Wxwxwx). Grain yields adjusted for panicle number showed no significant differences. The average 500 kernel weights between hybrids with different amounts of waxy phenotype grain did not significantly differ. The yield effect seen in this population was the result of waxy endosperm hybrid seed displaying significantly poorer stand establishment than nonwaxy endosperm hybrid seed. These data do not support a xenia yield effect due to the waxy gene.
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Books on the topic "XENIX"

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Inside Xenix. H.W. Sams, 1986.

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UNIX & XENIX demystified. Tab Books, 1985.

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Dripke, Angelika, and Manfred Schumacher. SCO UNIX/XENIX. Edited by Andreas Dripke. Vieweg+Teubner Verlag, 1990. http://dx.doi.org/10.1007/978-3-663-13944-7.

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Xenix: Kino als Programm. Schüren, 2006.

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Kaare, Christian. The XENIX command reference guide. Wiley, 1989.

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Moore, Martin L. Working with Xenix System V. Scott, Foresman, 1986.

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R, Groff James, ed. Understanding XENIX: A conceptual guide. Que Corp., 1985.

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UNIX and XENIX for beginners. Abacus, 1989.

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Heck, Hans-Josef. Unix: Working with Unix and Xenix. McCarta, 1993.

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Brown, P. J. Introduction to PC/IX and PC XENIX. Addison-Wesley, 1985.

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Book chapters on the topic "XENIX"

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Dripke, Angelika, and Manfred Schumacher. "Befehle." In SCO UNIX/XENIX. Vieweg+Teubner Verlag, 1990. http://dx.doi.org/10.1007/978-3-663-13944-7_1.

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Topham, Douglas William. "Introduction to UNIX." In A System V Guide to UNIX and XENIX. Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3246-9_1.

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Topham, Douglas William. "Moving and Copying within a File." In A System V Guide to UNIX and XENIX. Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3246-9_10.

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Topham, Douglas William. "Working with More Than One File." In A System V Guide to UNIX and XENIX. Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3246-9_11.

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Topham, Douglas William. "Customizing vi." In A System V Guide to UNIX and XENIX. Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3246-9_12.

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Topham, Douglas William. "Searching and Sorting." In A System V Guide to UNIX and XENIX. Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3246-9_13.

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Topham, Douglas William. "Programming with awk." In A System V Guide to UNIX and XENIX. Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3246-9_14.

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Topham, Douglas William. "Programming with C." In A System V Guide to UNIX and XENIX. Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3246-9_15.

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Topham, Douglas William. "Introduction to mm." In A System V Guide to UNIX and XENIX. Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3246-9_16.

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Topham, Douglas William. "Formatting with mm." In A System V Guide to UNIX and XENIX. Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3246-9_17.

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Conference papers on the topic "XENIX"

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Gligor, V. D., E. L. Burch, G. S. Chandersekaran, et al. "On the Design and the Implementation of Secure Xenix Workstations." In 1986 IEEE Symposium on Security and Privacy. IEEE, 1986. http://dx.doi.org/10.1109/sp.1986.10016.

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Gligor, V. D., C. S. Chandersekaran, W. Cheng, et al. "A New Security Testing Method and its Application to the Secure Xenix Kernel." In 1986 IEEE Symposium on Security and Privacy. IEEE, 1986. http://dx.doi.org/10.1109/sp.1986.10021.

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Burrows, D. N., D. Hartmann, C. Kouvelioutou, L. Piro, J. W. den Herder, and T. Ohashi. "Xenia: cosmo-chemical evolution of the Universe." In SPIE Astronomical Telescopes + Instrumentation, edited by Monique Arnaud, Stephen S. Murray, and Tadayuki Takahashi. SPIE, 2010. http://dx.doi.org/10.1117/12.857099.

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Mougy, Amr El, Ahmed Khalaf, Hazem El Agaty, Mariam Mazen, Noureldin Saleh, and Mina Samir. "Xenia: Secure and interoperable smart home system with user pattern recognition." In 2017 International Conference on Internet of Things, Embedded Systems and Communications (IINTEC). IEEE, 2017. http://dx.doi.org/10.1109/iintec.2017.8325912.

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Korakakis, Michalis, Phivos Mylonas, and Evaggelos Spyrou. "Xenia: A context aware tour recommendation system based on social network metadata information." In 2016 11th International Workshop on Semantic and Social Media Adaptation and Personalization (SMAP). IEEE, 2016. http://dx.doi.org/10.1109/smap.2016.7753385.

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Lobok, Dmitrii Vladimirovich. "«We are not a numby-pumby!» (Xenia Institute during the First Russian revolution of 1905-1907)." In All-Russian scientific conference. Publishing house Sreda, 2019. http://dx.doi.org/10.31483/r-22251.

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