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Zeitschriftenartikel zum Thema "Xia family"

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V. P., Thomas, M. SABU und E. SANOJ. „Amomum meghalayense (Zingiberaceae): a new species from northeast India“. Phytotaxa 245, Nr. 2 (25.01.2016): 178. http://dx.doi.org/10.11646/phytotaxa.245.2.9.

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Amomum Roxburgh (1820: 75) is the second largest genus in the ginger family with about 150–180 species, widely distributed in Southeast Asia (Xia et al. 2004). The genus is characterized by having radical inflorescences, an absence of involucre of sterile bracts, reduced lateral staminodes and well-developed anther crests.
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Zhang, Pingfan. „“A More Personal Look at Her Life”: Family Narrative, Gender, and Transnational Memories in The Girl and the Picture“. Camera Obscura: Feminism, Culture, and Media Studies 37, Nr. 2 (01.09.2022): 91–117. http://dx.doi.org/10.1215/02705346-9787028.

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Abstract Recent decades have witnessed a booming film industry portraying the Nanjing Massacre, both within and outside Mainland China, which is closely related to contemporary Chinese political, socioeconomic, and cultural transformations. This article examines the USC Shoah Foundation's 2018 documentary film The Girl and the Picture, featuring the well-known Nanjing Massacre female survivor Xia Shuqin. It argues that the cinematic rendition of Xia's family stories serves as a piercing incision into Nanjing Massacre historical memories and weaves together the personal with the national, and transgenerational with transnational memories. The Girl and the Picture radicalizes cinematic discourses on the Nanjing Massacre from multiple angles and not only sheds light on the emerging field of Nanjing Massacre studies but also contributes to our understanding of the ongoing memory boom of the Nanjing Massacre in the context of globalization. By delivering the stories of Xia along both family and transnational lines, The Girl and the Picture points out a new way to cope with the memory crisis of the Nanjing Massacre, and to take responsibility for transmitting the memories across generational, national, gender, and ethnic boundaries.
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Trappes-Lomax, John. „Trappes of Nidd: A Family History by Richard Trappes-Lomax“. Recusant History 27, Nr. 2 (Oktober 2004): 151–216. http://dx.doi.org/10.1017/s0034193200031319.

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In Ripon Liberty only one [Catholic] gentry family survived this period [the eighteenth century] (the Trappes of Nidd) and in their case the main line died out and a cadet branch from Carlton succeeded them’; this fact of mere survival both justifies and permits setting this account before the reader. Christopher Trappes (XIa), the founder of the Carlton branch, would probably have remained single, if he had not found an heiress with just sufficient income for marriage; had he remained single, the Trappes family would have died out in 1761, and this history would have remained unwritten. As it is, there survives just enough material to show something of how one recusant family contrived to retain its identity through and after the penal times.
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Nestell, Galina P., und Merlynd K. Nestell. „Late Capitanian (latest Guadalupian, Middle Permian) radiolarians from the Apache Mountains, West Texas“. Micropaleontology 56, Nr. 1-2 (2010): 7–68. http://dx.doi.org/10.47894/mpal.56.1.02.

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A diverse radiolarian fauna is described from strata of a road cut section of the uppermost part of the Bell Canyon Formation (Capitanian, Guadalupian, Middle Permian), Apache Mountains, West Texas. Fifteen new species are described: Campanulithus insuetus, Pseudoalbaillella apachensis, Astroentactinia capitanensis, Polyedroentactinia guadalupensis, Afanasievella apachensis, Copicyntra erinacea, Paracopicyntra snyderi, Klaengspongus planus, Copiellintra orbiculata, C. fastuosa, Shangella capitanensis, Rectotormentum wardlawi, Tetratormentum ormistoni, Quadrilobata? blomei, and Nazarovispongus globosum. The diagnoses of the species Follicucullus sphaericus Takemura in Takemura et al. 1999 and the genus Raciditor Sugiyama 2000 are emended. The rank of the subspecies Raphidociclicus gemellus americanus Nazarov and Ormiston 1985a is raised to species level. The genus Nazarovispongus Kozur 1980 is considered to be a valid genus and is reinstated. Established are one new genus, Afanasievella (assigned to the family Spongentactiniidae), one new subfamily Polyedroentactiniinae (in the composition of the family Orosphaeridae), and one new family Tetratormentidae (in the composition of the order Pyramidata). The radiolarian assemblage from the described section in the Apache Mountains is at least partly coeval with the radiolarian assemblage from the Reef Trail Member of the Bell Canyon Formation in the Guadalupe Mountains, allowing a straight correlation of this age strata between the Apache and Guadalupe mountains. This correlation is supported by the conodont species that define the latest Guadalupian conodont zones and that occur together with radiolarians in both areas. The radiolarian species Albaillella yamakitai in sense of Xia et al. (2005) present in the late Guadalupian J. altudaensis conodont Zone cannot be a marker for the Guadalupian – Lopingian boundary as was proposed by Xia et al. (2005).
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VU, QUANG NAM, NIAN-HE XIA, THI THO NGUYEN und THI HAI NINH KHUAT. „Magnolia quangninhensis (Magnoliaceae), a new species from northern Vietnam“. Phytotaxa 464, Nr. 2 (16.10.2020): 188–92. http://dx.doi.org/10.11646/phytotaxa.464.2.7.

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A new species of the family Magnoliaceae, Magnolia quangninhensis Q.N. Vu & N.H. Xia from Yen Tu National Forest, in the Quang Ninh Province, north of Vietnam is described and illustrated. It is most closely related to M. bawangensis and M. shangsiensis, but differs by having all parts of tree glabrous (except for dense brown sericeous tomentose to tomentulose brachyblasts), larger elliptic-obovate leaves, creamy-white to pink–purple tepals and stamens, and (6–)9–11 tepals.
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XIA, BIN. „A review of progress on the systematics and biology of the family Cheyletidae in China, with a checklist of the Chinese cheyletids“. Zoosymposia 4, Nr. 1 (30.06.2010): 158–64. http://dx.doi.org/10.11646/zoosymposia.4.1.11.

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This paper reviews the taxonomic research on the family Cheyletidae in China, with an updated checklist of 48 species belonging to 24 genera. The most important contributions to the Chinese fauna of these mites were made by Tseng Yi-Hsiung, who recognized and described ten species from Taiwan, Lin Jianzhen, who described seven species from Fujian, and Xia Bin, who added five new species. A few studies on the biology and ecology of Cheyletidae in China are briefly reviewed.
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Hamaguchi, Motohiro, Tadashi Matsushita, Mitsune Tanimoto, Isao Tekahashi, Kohji Yamamoto, Isamu Sugiura, Junki Takamatsu, Kanji Ogata, Tadashi Kamiya und Hidehiko Saito. „Three Distinct Point Mutations in the Factor IX Gene of Three Japanese CRM+ Hemophilia B Patients (Factor IX BMNagoya 2, Factor IX Nagoya 3 and 4)“. Thrombosis and Haemostasis 65, Nr. 05 (1991): 514–20. http://dx.doi.org/10.1055/s-0038-1648182.

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SummaryEnzymatic DNA amplification and complete sequence analysis were used to investigate human factor IX coding sequences in three CRM+ hemophilia B patients. In a patient with severe hemophilia B and a markedly prolonged ox-brain prothrombin time, a C to T transition in exon VI changed the codon for Argl80 to Trp (factor IX BMNagoya 2). This mutation would impair the cleavage by factor XIa required for activation of the zymogen. In a patient with mild hemophilia B, a G to A transition in exon VI changed the codon for Argl45 to His (factor IX Nagoya 3). This substitution also would be predicted to preclude the cleavage of factor IX by factor XIa at this peptide bond (Argl45-Alal46). Furthermore, this point mutation creates a new NlaIII restriction site which provides a quick and reliable method for carrier detection in the affected family members. A patient with severe hemophilia B (factor IX Nagoya 4) had a G to A transition in exon II changing the codon for Glu21 to Lys. This novel point mutation is assumed to impair the function of factor IX by disrupting the calcium binding of factor IX.
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Vázquez-García, J. Antonio, David A. Neill und Mercedes Asanza. „Magnolia vargasiana (Magnoliaceae), a new Andean species and a key to Ecuadorian species of subsection Talauma, with notes on its pollination biology“. Phytotaxa 217, Nr. 1 (22.06.2015): 26. http://dx.doi.org/10.11646/phytotaxa.217.1.2.

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Magnoliaceae Jussieu (1789: 280) consist of ca. 330 species worldwide, nearly half of them in the New World (Vázquez-García et al. 2014). There is no agreement on the internal classification, including the number of sections (0–11), genera (1–13), subgenera (0–9) and subfamilies (0–2) (Figlar & Nooteboom 2004; Xia et al. 2008, Romanov & Dilcher 2013) and despite various phylogenetic studies of Magnoliaceae in the last two decades, classification of the family has not reached a consensus (Qiu et al. 1993, 1995; Kim et al. 2001; Azuma et al. 2001, Li & Conran 2003, Nie et al. 2008, Kim & Suh 2013). Here we follow the classification of Figlar & Nooteboom (2004).
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Williams -Wheeler, Meeshay, Jawan M. Burwell, Gabrielle S. Gravely und Raleta Summers-Dawkins. „Experiential Learning in a Family Systems Course: Integrating the FCSfit KIDS Curriculum“. Journal of Family & Consumer Sciences 114, Nr. 1 (01.03.2022): 38–40. http://dx.doi.org/10.14307/jfcs114.1.38.

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Experiential learning is a pedagogical tool that aligns with the mission of family and consumer sciences (FCS) university programs because it emphasizes the role of formal education in the development of individuals, family members, and global citizens (Brooks & Simpson, 2014). College students benefit from experiential learning and field-based experiences through enhanced integration of course materials and enhanced perceptions of learning and actual learning (Langlais, 2018). There are many positive outcomes of experiential learning activities in the college classroom including high retention rates of students during and after these semesters (Darling & Cassidy, 2014), improved employability (Brooks & Simpson, 2014), and a broader global perspective (Smith & Yang, 2017). Within FCS courses, experiential learning often provides skills that prepare college students to succeed in their work with children, youth, and families (Brooks & Simpson, 2014; Taylor & Xia, 2018). This paper highlights an experiential activity provided in a Family Systems course in which students learn about family dynamics and the systematic approach of familial well-being. With its focus on the application, creativity, and linking theory to practice, the FCSfit KIDS curriculum was implemented in a Family Systems course to provide varied interactive learning activities to enhance students' understanding of the role of families on preschoolers' health and well-being.
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朱, 书艳. „The Development Dilemma and Promotion Path of Filial Piety in the Family with “En Wang Xia Liu”“. Advances in Social Sciences 11, Nr. 09 (2022): 3933–41. http://dx.doi.org/10.12677/ass.2022.119539.

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Dissertationen zum Thema "Xia family"

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Xia, Weiliang [Verfasser], und Ursula [Akademischer Betreuer] Seidler. „Regulation and functional significance of HCO3- transporters of the Slc4 and Slc26 family in mucosal protection, mucus layer build-up and small intestinal fluid absorption in the murine intestine in vivo / Weiliang Xia. Zentrum Innere Medizin Klinik für Gastroenterologie, Hepatologie und Endokrinologie Medizinische Hochschule Hannover. Betreuer: Ursula Seidler“. Hannover : Bibliothek der Medizinischen Hochschule Hannover, 2015. http://d-nb.info/1072588382/34.

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Zeberio, Blanca. „Derechos de propiedad y sistema normativo en la Argentina del siglo XIX“. Economía, 2012. http://repositorio.pucp.edu.pe/index/handle/123456789/117917.

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This paper aim to analyze the role that such a concepts like family, inheritance and property played for developing modern Argentine society. Especially how some principles were broken on, while others have been kept on, as the different legal criteria suggests. Rural Law of 1865, Civil Law of 1869 and juridical debates set the interaction rules among different notion of property rights and also different way for labor hiring, either into market rules or out of them. These kind of relations and their coexistent avoided to expand cattle business in a market way.
Este ensayo apunta a analizar el rol que conceptos como familia, herencia y propiedad jugaron para el desarrollo de la moderna sociedad argentina. Especialmente acerca de las rupturas y continuidades que sugieren los diferentes criterios. Los debates jurídicos y los Códigos Rurales de 1865 y Civil de 1869 buscaron resolver el problema de la convivencia en tierras pampeanas de formas diversas de propiedad, así como la existencia de una fuerza de trabajo que poseía formas de supervivencia extra mercado. Ambas situaciones dificultaban o entorpecían, las necesidades de un grupo social que apuntaba a la expansión ganadera.
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Cunha, Maisa Faleiros da 1980. „Demografia e familia escrava : Franca, SP, Seculo XIX“. [s.n.], 2009. http://repositorio.unicamp.br/jspui/handle/REPOSIP/280668.

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Orientadores: Maria Silvia Casagrande Beozzo Bassanezi, Robert Wayne Slenes
Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Filosofia e Ciencias Humanas
Made available in DSpace on 2018-08-12T20:34:55Z (GMT). No. of bitstreams: 1 Cunha_MaisaFaleirosda_D.pdf: 2541088 bytes, checksum: 6b506b74d5bfdb81b3b0d61217522b12 (MD5) Previous issue date: 2009
Resumo: O presente trabalho tem como objeto de análise a demografia e a família escrava no município de Franca-SP no decorrer do século XIX. Esse município caracterizou-se por uma economia baseada na atividade criatória (de gado vacum e suíno) e na produção de gêneros de subsistência destinados ao consumo local e ao comércio interno. A elaboração deste trabalho foi norteada pelo desafio de considerar a população escrava a partir do conceito de regime demográfico restrito. Para tanto, as principais fontes documentais utilizadas foram: a Lista Nominativa de Habitantes de 1836, o Recenseamento Geral do Império de 1872, os inventários post mortem (1811-1888) e os registros paroquiais de batismo, casamento e óbito (1806-1888). Dessa forma, apresentamos o contexto espacial e histórico do município de Franca-SP, onde a população escrava vivenciou os eventos vitais e estabeleceu relações sociais. Traçamos a evolução populacional e, de modo especial, caracterizamos a economia que se desenvolveu no período; focalizamos aspectos da demografia escrava e seus condicionantes. Refinando a análise através do cruzamento nominativo de fontes, resgatamos trajetórias demográficas e familiares de um segmento da população escrava pertencente a um grupo específico de senhores. Esse percurso permitiu evidenciar, ainda que em níveis de intensidade diferenciados, os mecanismos de controle demográfico (nupcialidade, fecundidade, mortalidade e manumissão), os arranjos familiares e as amplas relações e instituições sociais que marcaram o regime demográfico restrito da população escrava na localidade
Abstract: This work aims to analyze the demography and the slave family in Franca, Brazil during the nineteenth century. The characteristic of this town was an economy based on dairy cattle and swine breeding, and the production of first-necessity foods destined to local consumption and to the internal market. This work was guided by the challenge to consider the slave population as from the concept of a restricted demographic regime. For this purpose, the main sources used were the Lista Nominativa de Habitantes of 1836, the Recenseamento Geral do Império of 1872, post-mortem inventories from1811 to 1888 and the baptism, marriage and death parochial registers from 1806 to 1888. We have presented the spatial and historic context of Franca, where the slave population lived the vital events and established social relations. We have delineated the population evolution and, in special, characterized the economy developed in that period; focusing slave demography aspects and its conditionals. When refining the analysis through the nominal comparison of sources, we have recovered demographic and families trajectories of this slave population, belonging to a specific group of slave masters. The route has enabled us to provide evidence, although at different levels of intensity, to the mechanisms of demographic control (nuptiality, fertility, mortality and manumission), to family arrangements and to the wide social relations and institutions which have marked the restricted demographic regime of the local slave population
Doutorado
Demografia Historica
Doutor em Demografia
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Wang, Qinchuan. „The intercalated disc-associated Xin family of proteins in cardiac development and function“. Thesis, The University of Iowa, 2013. http://pqdtopen.proquest.com/#viewpdf?dispub=3568015.

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Intercalated discs (ICDs) are cardiac-specific structures located at the longitudinal termini of cardiomyocytes. Classically, the functions assigned to ICDs include mechanical and electrical communications among adjacent cardiomyocytes. More recently, it has been increasingly realized that ICDs also function in signal transduction and regulation of the surface expression of ion channels. Accordingly, defects of ICD components are shown to cause a number of human cardiac diseases and changes of ICDs are associated with cardiomyopathy, arrhythmias, and heart failure. The expansion of our knowledge about the development, function and maintenance of ICDs are promoted by identification, cataloging and characterization of the molecular components of the ICDs. In this thesis, I characterize a family of Xin repeat-containing proteins, which are striated muscle-specific and localized to the ICDs in the cardiomyocytes. This thesis provides novel insights into the mechanism of the formation, maintenance and functions of ICDs.

Our previous studies showed that the Xin repeat-containing proteins play critical role in cardiac morphogenesis and cardiac function. Knocking down the Xin in chicken embryo collapses the wall of developing heart chambers and leads to abnormal cardiac morphogenesis. In mammals, a pair of paralogous genes, Xinα and Xinβ , exists. Ablation of the mouse Xinα ( mXinα) does not affect heart development. Instead, the mXinα-deficient mice show adult late-onset cardiac hypertrophy and cardiomyopathy with conduction defects. The ICD structural defects in mXinα-null mice occur between 1 and 3 months of age and progressively worsen with aging. The mXinα-deficient hearts up-regulate mXinβ, suggesting a partial compensatory role of mXinβ.

In this thesis, I focus on two questions. First, what are the molecular mechanisms of mXinα's functions that account for the observed phenotypes in the mXinα-deficient hearts? And second, what are the functions of mXinβ? Through biochemical methods and electron microscopy, I demonstrated that mXinα binds and bundles actin filaments. In addition, a direct interaction between mXinα and the adherens junction protein β-catenin facilitates mXinα's interaction with the actin filaments. Based on this in vitro characterization of mXinα, we proposed that mXinα may act as a direct link between the adherens junctions and actin cytoskeleton, thus providing an important means to strengthening the intercellular adhesion at the ICDs. To characterize mXinβ's roles, I generated and characterized mXinβ-knockout mice. I showed that complete loss of mXinβ leads to cardiac morphological defects, diastolic dysfunction and heart failure, which lead to severe growth retardation and early postnatal lethality. I also showed that mXinβ might be involved in a number of cell signaling pathways and provide multiple lines of evidence to support mXinβ's roles in the formation of ICDs.

In summary, this thesis provides novel insights into the specialization of the adherens junctions at the ICDs to withstand the contractile forces, and the molecular mechanisms for the establishment, maintenance and function of ICDs. The knowledge gained from the roles of Xin proteins in cardiac development and function will likely provide new insights for improved therapeutic strategies for human cardiomyopathy, arrhythmias and heart failure.

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Wang, Qinchuan. „The intercalated disc-associated Xin family of proteins in cardiac development and function“. Diss., University of Iowa, 2011. https://ir.uiowa.edu/etd/2653.

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Intercalated discs (ICDs) are cardiac-specific structures located at the longitudinal termini of cardiomyocytes. Classically, the functions assigned to ICDs include mechanical and electrical communications among adjacent cardiomyocytes. More recently, it has been increasingly realized that ICDs also function in signal transduction and regulation of the surface expression of ion channels. Accordingly, defects of ICD components are shown to cause a number of human cardiac diseases and changes of ICDs are associated with cardiomyopathy, arrhythmias, and heart failure. The expansion of our knowledge about the development, function and maintenance of ICDs are promoted by identification, cataloging and characterization of the molecular components of the ICDs. In this thesis, I characterize a family of Xin repeat-containing proteins, which are striated muscle-specific and localized to the ICDs in the cardiomyocytes. This thesis provides novel insights into the mechanism of the formation, maintenance and functions of ICDs. Our previous studies showed that the Xin repeat-containing proteins play critical role in cardiac morphogenesis and cardiac function. Knocking down the Xin in chicken embryo collapses the wall of developing heart chambers and leads to abnormal cardiac morphogenesis. In mammals, a pair of paralogous genes, Xin&alpha and Xin&beta, exists. Ablation of the mouse Xin&alpha (mXin&alpha) does not affect heart development. Instead, the mXin&alpha-deficient mice show adult late-onset cardiac hypertrophy and cardiomyopathy with conduction defects. The ICD structural defects in mXin&alpha-null mice occur between 1 and 3 months of age and progressively worsen with aging. The mXin&alpha-deficient hearts up-regulate mXin&beta, suggesting a partial compensatory role of mXin&beta. In this thesis, I focus on two questions. First, what are the molecular mechanisms of mXin&alpha's functions that account for the observed phenotypes in the mXin&alpha-deficient hearts? And second, what are the functions of mXin&beta? Through biochemical methods and electron microscopy, I demonstrated that mXin&alpha binds and bundles actin filaments. In addition, a direct interaction between mXin&alpha and the adherens junction protein &beta-catenin facilitates mXin&alpha's interaction with the actin filaments. Based on this in vitro characterization of mXin&alpha, we proposed that mXin&alpha may act as a direct link between the adherens junctions and actin cytoskeleton, thus providing an important means to strengthening the intercellular adhesion at the ICDs. To characterize mXin&beta's roles, I generated and characterized mXin&beta-knockout mice. I showed that complete loss of mXin&beta leads to cardiac morphological defects, diastolic dysfunction and heart failure, which lead to severe growth retardation and early postnatal lethality. I also showed that mXin&beta might be involved in a number of cell signaling pathways and provide multiple lines of evidence to support mXin&beta's roles in the formation of ICDs. In summary, this thesis provides novel insights into the specialization of the adherens junctions at the ICDs to withstand the contractile forces, and the molecular mechanisms for the establishment, maintenance and function of ICDs. The knowledge gained from the roles of Xin proteins in cardiac development and function will likely provide new insights for improved therapeutic strategies for human cardiomyopathy, arrhythmias and heart failure.
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Phan, Cam Van Thi. „Family ties to Buddhist monks and nuns in medieval China : a biographical and hagiographical study of the Southern Xiao family branch“. Thesis, University of British Columbia, 2007. http://hdl.handle.net/2429/32228.

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The roles of kinship and family ties have recently become recognized as a vital yet unexplored area in the study of medieval Buddhism. This is especially critical in restructuring the relationship between political and religious spheres, which for the Sinologist have always been intricately linked to one another. Although there are studies noting the prominence of family connection in the study of monks and nuns, past studies have focused mainly on the manipulation and modification of religion by political figures for solely secular purposes. Not many studies have turned the tables to analyze the significance of a monk or nun's family background and its intimate influence throughout his or her religious life; nor have they considered how a layman or laywoman's spiritual devotion greatly shapes his or her social life and political career. It is my aim to extend such research and explore on a larger scale the intricate relationship between monastic and lay family members, in this case Xiao Yu, his daughters, sons and relatives, ten in all, from the Southern Xiao family branch during the late Sui to early Tang period. This research serves to prove that the life of a monk or nun, while determined by that individual's vocation and endeavor, is to a degree also conditioned by his or her family background, kinship ties and secular acquaintance. This research, based upon hagiography, epigraphy and relevant materials from canonical and secular sources substantiates the belief that comprehensive study of the monastic order should involve analysis of factors beyond the spiritual sphere.
Arts, Faculty of
Asian Studies, Department of
Graduate
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Eulitz, Stefan [Verfasser]. „Functional Analysis of the Xin-Repeat Protein Family in Cross-striated Muscle / Stefan Eulitz“. Bonn : Universitäts- und Landesbibliothek Bonn, 2011. http://d-nb.info/1044857749/34.

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Lachaud, Fabrice. „La structure familiale des Craon du XIè siècle à 1415 : le concept lignager en question“. Phd thesis, Université Michel de Montaigne - Bordeaux III, 2012. http://tel.archives-ouvertes.fr/tel-00724925.

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Le 25 octobre 1415, avec la disparition des derniers représentants du groupe par filiation directe, s'éteignait au combat le lignage de Craon dont la renommée et la fortune avaient été acquises, entre autres, sur les champs de bataille. Notre travail s'inscrit dans une perspective chronologique : la genèse du lignage des Craon au XIe siècle puis son fonctionnement jusqu'à sa disparition à Azincourt. À partir de l'étude sur la famille de Craon, nous proposons une réflexion sur le concept lignager. Pouvons-nous d'ailleurs parler sans nuance de lignage ? Le lignage du XIIe siècle ne ressemble pas à celui des siècles suivants : il s'agit d'une structure de parenté complexe recouvrant des réalités multiples. Si la nécessité d'une terminologie commune nous apparaît évidente, il convient cependant de rester prudent sur l'usage de " lignage ". Son emploi abusif en a appauvri le sens à tel point que nous avons l'impression que ce terme pose aujourd'hui un problème sémantique : peut-on opposer systématiquement deux structures de parenté - " carolingienne " et lignagère ? Le corpus documentaire des Craon nous met dans une position inconfortable puisqu'il nous oriente sur une structure de parenté particulière : le lignage. L'enjeu de ce travail consiste donc à formuler un questionnement sur le lignage à travers une documentation partielle et orientée qui en postule l'existence. L'emploi de ce terme ne nous offre qu'une vision simpliste de la parenté et ne prend pas assez en compte d'autres formes qui coexistent au même moment : sur une structure patrilinéaire de transmission des biens et des pouvoirs se plaque un système de filiation indifférenciée. Le monument funéraire des Craon, dans la chapelle des Cordeliers à Angers, réalisé par Maurice V de Craon à la fin du XIIIe siècle, est un document essentiel : il illustre une conception de la famille telle qu'elle se manifeste dans les actes de la pratique accordant une place essentielle aux alliances, au moins autant qu'à la filiation et dans laquelle la notion de lignage est difficile à cerner. Or, une telle représentation peut coexister avec d'autres, répondant à d'autres besoins et véhiculant d'autres messages : le lignage n'oblitère pas d'autres formes de parenté. Notre travail nous invite à remettre en cause les schémas modèles et à voir la parenté comme une intrication de systèmes diversement opératoires, par effet de sources ou selon le contexte, soumis au poids des normes canoniques omniprésentes à l'époque.
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Bujevičiūtė, Rasa. „Aukštesniųjų klasių (XI - XII) moksleivių streso tyrimas“. Master's thesis, Lithuanian Academic Libraries Network (LABT), 2005. http://vddb.library.lt/obj/LT-eLABa-0001:E.02~2005~D_20050610_123948-80690.

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Goal of the paper: examine and evaluate stress and stressors of the senior pupils (that attend the 11th-12th forms). Objectives: Identify stressors of the urban and regional pupils and evaluate possible territorial differences. Learn about pupils’ subjective evaluation of their health state. Set recommendations for the prophylaxis of pupils’ stress. Research material and methods: 521 senior pupils - 286 from Kaunas and 235 from Birzai - were selected at random and questioned. The stress-evaluating questionnaire covered two parts: scale of subjectively perceived stress (10 points) and stress-evaluating scale for the juvenile. The pupils were also questioned about the issues of smoking, use of strong drinks. They were asked to mark all the symptoms that bothered them through the past 12 months. The statistical data analysis was performed by means of a statistical package “SSPS 11.5”. Results: 29.9% out of 521 pupils that were questioned experience slight stress, 46.3 % - great stress, and 23.8%- enormous stress. The major stressors of the aforementioned pupils are lack of sleep (70.6%), arguments with family and friends (62.2%), problems at school (39.0%), use of alcohol and drugs (36.5%). Girls usually pinpoint arguments with family and friends, separation, alteration of living conditions. Boys distinguish more often the use of strong drinks and drugs or a misdemeanor. It has been noticed that the more pupils use strong drinks (starting with abstinence and continuing with... [to full text]
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Agnew, Christopher S. „Culture and power in the making of the descendents of Confucius, 1300-1800 /“. Thesis, Connect to this title online; UW restricted, 2006. http://hdl.handle.net/1773/10360.

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Bücher zum Thema "Xia family"

1

Kong, Xiangmin. Tian xia di yi jia. Beijing: Xin hua chu ban she, 1995.

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Xia, Shengqian. 湖南夏姓人物志. Yiyang Shi: [s.n.], 2006.

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Garwood, Julie. Xia yi bu, ai qing. Taibei Shi: Guo shu chu ban she you xian gong si, 2015.

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ill, Williams Garth, und Wang Zongwen, Hrsg. Qiao xia yi jia ren: The family under the bridge. Tianjin Shi: Xin lei chu ban she, 2013.

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Hannah, Kristin. Xia zhi dao. Taibei shi: Gao bao guo ji you xian gong si Taiwan fen gong si, 2004.

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Luo, Yu'an. Cui yu ying dan xia: Mile Xiong Qinglai jia zu wen hua ping zhuan. Zhengzhou Shi: Zhengzhou da xue chu ban she, 2015.

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McCloskey, Robert. Xia ri hai wan: Time of wonder. Taibei Shi: Guo yü ri bao she, 1995.

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Law Reform Commission of Hong Kong. Yi zhu, wei liu yi zhu qing kuang xia de ji cheng yi ji si zhe jia shu he shou gong yang ren shi de gong yang wen ti yan jiu bao bao shu. Xianggang: Xianggang fa lü gai ge wei yuan hui, 1990.

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author, Xiao Limei, und Pan Zhiyu 1980 author, Hrsg. Bi jiao fa shi ye xia de xian dai jia ting cai chan guan xi gui zhi yu chong gou: Regulation and reconstruction of modern family property relations under the perspective of comparative law. Beijing Shi: Beijing da xue chu ban she, 2014.

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Wu, Weifeng Tan. Xian dai jia ting xin pai cai =: New-style family dishes. Xianggang: Wan li ji gou, Yin shi tian di chu ban she, 2001.

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Buchteile zum Thema "Xia family"

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Wong, Yee Lam Elim, und Tai Wei Lim. „The Xie Family in Yokohama Chinatown“. In Contemporary History of Cantonese Migrants in Yokohama Chinatown, 103–32. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-9980-4_4.

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Wong, Yee Lam Elim, und Tai Wei Lim. „The Xie Family and Cantonese Cultural Heritage“. In Contemporary History of Cantonese Migrants in Yokohama Chinatown, 193–251. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-9980-4_6.

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AL-Hussaini, Essam K., und Mohammad Ahsanullah. „Family of Exponentiated Burr Type XII Distributions“. In Atlantis Studies in Probability and Statistics, 103–22. Paris: Atlantis Press, 2015. http://dx.doi.org/10.2991/978-94-6239-079-9_5.

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Sullivan, Susan L., Kerry J. Ressler und Linda B. Buck. „Olfactory Receptor Family: Diversity and Spatial Patterning“. In Olfaction and Taste XI, 127–31. Tokyo: Springer Japan, 1994. http://dx.doi.org/10.1007/978-4-431-68355-1_55.

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Akiyama, Chihiro, T. Yuguchi, M. Nishio, T. Fujinaka, M. Taniguchi, Y. Nakajima und T. Yoshimine. „Src family kinase inhibitor PP1 improves motor function by reducing edema after spinal cord contusion in rats“. In Brain Edema XII, 421–23. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-0651-8_87.

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Wong, Yee Lam Elim, und Tai Wei Lim. „The Xie Family and Making of Overseas Chinese Associations“. In Contemporary History of Cantonese Migrants in Yokohama Chinatown, 133–92. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-9980-4_5.

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Murata, Yuko, Hikaru Henmi und Fujio Nishioka. „Comparison of Extracts from Species of the Mackerel Family“. In Olfaction and Taste XI, 279. Tokyo: Springer Japan, 1994. http://dx.doi.org/10.1007/978-4-431-68355-1_107.

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Hinckley, Jane. „Clara Reeve, ‘Letter XIV’ (‘The Plan of a Female Community’)“. In Family Life in England and America, 1690–1820, 445–55. London: Routledge, 2021. http://dx.doi.org/10.4324/9781003113058-70.

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Kandyel, E., X. J. Wu, S. Adachi und S. Tajima. „A New Family of 2223-Type Superconductors, (Tl1-x Hg x )2Sr2Ca2Cu3O y Synthesized Under High Pressure“. In Advances in Superconductivity XII, 116–18. Tokyo: Springer Japan, 2000. http://dx.doi.org/10.1007/978-4-431-66877-0_26.

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Rosemont, Henry, und Roger T. Ames. „Family Reverence (xiao) as the Source of Consummatory Conduct (ren)“. In Confucian Role Ethics, 59–72. Göttingen: V&R unipress, 2016. http://dx.doi.org/10.14220/9783737006057.59.

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Konferenzberichte zum Thema "Xia family"

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Volinia, S., P. Patracchini, F. Vannini, L. Felloni, F. Panicucci und F. Beranardi. „HAGEMAN TRAIT INVESTIGATED BY FACTOR XII cDNA PROBES“. In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643299.

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The presence of gene lesions and of restriction fragment length polymorphisms (RFLPs) has been investigated by means of cDNA probes for the coagulation factor XII (FXII).A TaqI additional fragment (2.1Kb) has been found in two brothers with Hageman trait and in 11 members of their paternal lineage. Digestions with different enzymes exclude that FXII gene deletion is responsible for Hageman trait in this family. A point mutation originating an additional TaqI site is likely.The abnormal pattern (not present in 40 normal subjects) is correlated with a reduced FXII activity and identifies the heterozygous subjects in the paternal lineage. The presence of two different gene lesions causing Hageman trait in this family can be inferred.The TaqI additional site has been mapped within the 5 portion of the gene.Data suggest the presence of one FXII gene per aploid genome and disagree with previous localization of FXII gene on chromosome 6.Work supported by P.F. Ing. Gen. e Basi Mol. Mai. Ered. contratto CNR N.8400877
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Iegoroff, Renan, Rafael Herlan Terceros Vaca, Gustavo Araújo Pinheiro, Alvaro Marcelo Huchani Huanca, Matheus Henrique de Souza Coradini und Leonardo Mariano Inácio Medeiros. „Cadasil, atypical and familial presentation – family case report“. In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.318.

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Introduction: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), is a non-atherosclerotic, nonamyloid, hereditary cerebral disease of small vessels and capillaries caused by mutations in the NOTCH-3 gene located on chromosome 19. The presence of granular osmophilic material (GOM) deposition in the smooth muscle cells of vessel walls is the pathological hallmark of arteriopathy in CADASIL. GOM deposits in the basal lamina of smooth muscle of small vessels are pathognomonic for CADASIL. The presence of GOM in capillary blood vessels of the skin and muscle in biopsy and genetic studies (NOTCH-3 analysis) plays a key diagnostic role. Biopsy tests have high specificity (up to 100%) and low sensitivity (less than 50%). The NOTCH-3 test has been proposed as the primary diagnostic approach, allowing detection of 90% of affected individuals. CADASIL has an estimated prevalence between 2 and 5 in 100,000, and the phenotypic study demonstrates different clinical symptoms in the course of the disease within the same family. The average age of onset of clinical symptoms varies between 48.3 years in men and 52.2 years in women. Characteristic symptoms of migraine, stroke or TIA (transient ischemic attack), behavioral changes, early and progressive cognitive changes associated with leukoencephalopathy on imaging studies. The large association of symptoms often causes the diagnosis of CADASIL to be delayed. In this case, we had an association of gait ataxia within the framework of motor alterations, demonstrating the wide range of symptomatology of the pathology. This case report presents a familial course that started outside the most prevalent age group in the studies described and with an atypical presentation in an affected generation. Case reports: Case 01: woman, 68 years old, started progressively forgetting to perform household activities after the age of fifty, associated with primarily generalized myoclonic epileptic seizures, evolving rapidly within five years to walking apraxia with the use of a wheelchair and tonic-tonic epileptic seizures. bilateral clonic disorders, comprehension aphasia and bradypsychism. Relatives report previous migraine without chronic aura and REM (rapid eye movement sleep) sleep behavior disorder (RMSD). On neurological examination, severe ataxia with bilateral dysdiadochokinesia associated with bilateral hypometric index-index. Bilateral ROT 4+/4+ with bilateral Hoffman and Babinski signs. MMSS and MMII with FGM 4/5 proximal and distal. Case 02: woman, 36 years old, pastry chef, had episodes of forgetting about everyday activities of her work, progressive in the last three years (cake recipes, budget accounts, orders placed) associated with confusion for spatial location on the way home/ work, evolving to apraxia in writing letters and words and difficulty with calculations associated with monoparesis of the right lower limb for twelve months with progression to paresis of the lower limbs after six months and evolution to paresthesia of the upper limbs for three months. Associated with the condition, he has migraine without chronic aura and RMSD. The neurological examination showed Mini-Mental State Examination 22/30 (expected score of 29), list of animals in one minute: 09 animals; list of words starting with “F”: 03 words; clock test: 2/4; difficulty with calculations and digital agnosia with right/left apraxia; Upper limbs: eutrophic, FMG 4/5, bilateral distal; FMG 5/5 bilateral proximal; Lower limbs: eutrophic, bilateral FMG 4/5 distal and proximal with positive Mingazini; atypical gait with evidenced weakness in heel, toe and tandem gait; Bilateral dysdiadochokinesia with eumetric, slowed indexindex; ROT 4+/4+ in the right side with positive Hoffman and Babinski signs. MRI Brain (17/09/2020): extensive area of hypersignal on T2 and FLAIR (T2- weighted-Fluid-Attenuated Inversion Recovery) involving the periventricular white matter in all lobes without atrophic or expansive effect; Case 03: woman, 45 years old, started behavioral arrest epileptic seizures at the age of thirty-two, progressing to focal dysperceptive seizures with progression to bilateral tonic clonic seizures after eight months and multiple episodes of anterograde amnesia, presenting forgetfulness related to everyday work activities (exchanged worksheets , payments, calculation errors and budgets); associated with the condition presented migraine without chronic aura and RMSD. Genetic Test (04/06/2017): Heterozygous alteration in exon 8 of the NOTHC – 3 gene. Discussion: CADASIL presents a rare cause of cognitive decline and is often overlooked in diagnosis, except in cases of high clinical suspicion in a familial course. Access to imaging tests becomes fundamental for the diagnostic segment and the primordial genetic test for etiological elucidation and family planning, in the report described the family presentation with the same course of satellite symptoms (migraine without aura, and RMSD) associated with cognitive alteration with anticipation of age of onset are hallmarks of clinical thinking. Cases described in the literature show that the clinical symptomatology is not necessarily related to the level of brain injury observed in the imaging exam, which could be explained by personal factors and which exon is affected. The NOTCH-3 gene has 24 exons, in which the literature reports exon 4 as the most common mutation, followed by 3, 5 and 6, mainly in the Caucasian population. In an Asian population, the most affected exon is 4 and 11, which is also found in Italian descendants. The mutation in exon 8, described in the clinical case, is found in a population of Portuguese origin, being the second most common mutation in this nationality, behind the mutation in exon 4. Brain MRI studies have tried to elucidate the most affected brain regions, aiming to trace a line of evolution. Involvement of the temporal lobe, external capsule and corpus callosum are described as probable markers of CADASIL, and can be used as an aid in the diagnosis due to its specificity of 86% and sensitivity of 89%. Studies also show that the frontoparietal area has frequent findings of hyperintensity (100%), followed by the temporal lobe (83%), less frequently affecting the brainstem, occipital lobe and cerebellum. Despite the great advances in the specialized literature, the causes of the important cognitive dysfunction presented in the course of the evolution of CADASIL remain unclear. However, studies have suggested that the process of cognitive decline is more related to the loss of cortico-subcortical connections than to brain atrophy itself, with these disconnections resulting from repeated transient ischemic accidents. Science has been looking for ways to change the prognosis of CADASIL, recent studies in gene therapy and neurogenetics show the importance of thinking about this pathology as a genetic disease of great importance to change the prognosis of this pathology.
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Cool, D. E., und R. T. A. MacGillivray. „CHARACTERIZATION OF THe HUMAN FACTOR XII GENE“. In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642800.

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Surface activation of the plasma systems involved with coagulation, fibrinolysis, renin formation and kinin generation involves factor XII (Hageman factor). This protein is a 76,000 dalton glycoprotein which circulates in plasma as an inactive form of a serine protease. A human liver cDNA coding for factor XII was used to screen a human genomic phage library. Two overlapping clones were isolated, XHXII27 and XHXII76, and contain the entire gene for human factor XII. The gene is 13.5 Kbp in length and consists of 14 exons and 13 introns. The transcriptional start site of the mRNA was determined using S1 mapping and primer extension analysis. The results indicate that the 5′ untranslated end of the mRNA has a leader sequence of 47 bp and is not interrupted by an intron in the gene. DNA sequence analysis of the region upstream of the transcriptional start site does not contain TATA or CAAT sequences, which are often found in other genes transcribed by RNA polymerase II. The positions of the introns in the coding sequence separate the protein into domains which are homologous to similar regions found in fibronectin and tissue-type plasminogen activator. Furthermore, wherever protein homologies are found, the positions of the introns in the triplet codon occur in the same reading frame as in the tissue-type plasminogen activator, urokinase plasminogen activator and factor XII genes. The intron/exon organization of the factor XII gene is different to the organization of other coagulation genes such as prothrombin, factor IX and factor X. Therefore, factor XII appears to have evolved as a member of the plasminogen activator family of genes rather than as a member of the clotting factor gene family.
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„Ural Urban Family in the All-Union Census of 1959“. In XII Ural Demographic Forum “Paradigms and models of demographic development”. Institute of Economics of the Ural Branch of the Russian Academy of Sciences, 2021. http://dx.doi.org/10.17059/udf-2021-1-17.

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Analysis of the Russian urban family in the second half of the 20th century is important for assessing the consequences of the demographic transition of the 1930s–1980s. The use of official census materials, in particular, the All-Union Census of 1959, is limited due to both the census form and the selective publication of the obtained results. In part, this problem is solved by using fragmentary census forms. The article aims to clarify the possibility of using, along with the published data, the primary materials of the 1959 census to study urban family in the city of Sverdlovsk. To systematize the information of the census forms, the database “Family of the city of Sverdlovsk. 1959” was created. It combines the principles of individual and family registration. Based on the analysis of the obtained data, the Ural urban family was examined from the point of view of the second demographic transition, which significantly influenced the size of the family, the distribution of intra-family roles, and the strategies of marriage behaviour.
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Leontyeva, T. V. „THE FORMATION OF THE IMAGE OF THE FAMILY IN MODERN RUSSIAN ANIMATED FILMS“. In XIV International Social Congress. Russian State Social University, 2015. http://dx.doi.org/10.15216/rgsu-xiv-250.

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Chicheva, V. A. „THE YOUNG FAMILY AS AN OBJECT OF SOCIAL SECURITY OF THE RUSSIAN SOCIETY“. In XIV International Social Congress. Russian State Social University, 2015. http://dx.doi.org/10.15216/rgsu-xiv-462-1.

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Murzina, Julia, Albert Brand, Daniel Pavlov und Svetlana Shvab. „Career preferences for university students from Russia and Bulgaria“. In XIX International May Conference on Strategic Management – IMCSM24 Proceedings. University of Belgrade, Technical Faculty in Bor, 2024. http://dx.doi.org/10.5937/imcsm24024m.

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The development of family companies can become a driver of the national economy and form mechanisms that overcome foreign economic barriers and political challenges. The purpose of the presented work was to study the dynamics of career preferences of students from Russia and Bulgaria (the comparison was made in 2021 and 2023). This empirical study was conducted within the framework of the InterGen project. The results of the statistical analysis showed that the most desirable thing for students in the two countries is to build their own business. The second most popular is working in a large company. The least attractive is the prospect of creating or continuing a family business. Comparison by year showed that for the University of Ruse the statistical differences are not significant. For University of Tyumen the career orientation "opening a family business" shows a significant decrease. This empirical result may indicate the ineffectiveness of government programs to popularize family businesses in Russia.
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Puiu, Silvia. „The interest of students and graduates in family businesses“. In XIX International May Conference on Strategic Management – IMCSM24 Proceedings. University of Belgrade, Technical Faculty in Bor, 2024. http://dx.doi.org/10.5937/imcsm24015p.

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The main aim of this paper is to highlight if there is an interest of the younger generation towards starting a family business with members in the first or second generation. The data were collected by applying an online questionnaire in 2023 on 201 students and graduates of University of Craiova in Romania. The structure of the survey was established within the INTERGEN international project and follows the intentions of youngsters in time, by applying the survey each year. The results show that even if there is an interest in starting a business, the respondents would prefer to be independent and not be too linked with their families. The findings are useful for academic management in orienting the curricula towards the interests exhibited by young generations, but also for adjusting national strategies meant to support small businesses.
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Istomina, Yelena Alexandrovna, und Julia Valeryevna Ivanchina. „Labor and Family Responsibilities: Updated Approaches in Law“. In XIV European-Asian Congress "The value of law" (EAC-LAW 2020). Paris, France: Atlantis Press, 2020. http://dx.doi.org/10.2991/assehr.k.201205.023.

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Yershova, O. N., und N. V. Makarova. „A STUDY OF THE CONDITIONS AND LIFESTYLE OF A MODERN FAMILY RAISING A DISABLED CHILD“. In XIV International Social Congress. Russian State Social University, 2015. http://dx.doi.org/10.15216/rgsu-xiv-167.

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Berichte der Organisationen zum Thema "Xia family"

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Sadot, Einat, Christopher Staiger und Mohamad Abu-Abied. Studies of Novel Cytoskeletal Regulatory Proteins that are Involved in Abiotic Stress Signaling. United States Department of Agriculture, September 2011. http://dx.doi.org/10.32747/2011.7592652.bard.

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In the original proposal we planned to focus on two proteins related to the actin cytoskeleton: TCH2, a touch-induced calmodulin-like protein which was found by us to interact with the IQ domain of myosin VIII, ATM1; and ERD10, a dehydrin which was found to associate with actin filaments. As reported previously, no other dehydrins were found to interact with actin filaments. In addition so far we were unsuccessful in confirming the interaction of TCH2 with myosin VIII using other methods. In addition, no other myosin light chain candidates were found in a yeast two hybrid survey. Nevertheless we have made a significant progress in our studies of the role of myosins in plant cells. Plant myosins have been implicated in various cellular activities, such as cytoplasmic streaming (1, 2), plasmodesmata function (3-5), organelle movement (6-10), cytokinesis (4, 11, 12), endocytosis (4, 5, 13-15) and targeted RNA transport (16). Plant myosins belong to two main groups of unconventional myosins: myosin XI and myosin VIII, both closely related to myosin V (17-19). The Arabidopsis myosin family contains 17 members: 13 myosin XI and four myosin VIII (19, 20). The data obtained from our research of myosins was published in two papers acknowledging BARD funding. To address whether specific myosins are involved with the motility of specific organelles, we cloned the cDNAs from neck to tail of all 17 Arabidopsis myosins. These were fused to GFP and used as dominant negative mutants that interact with their cargo but are unable to walk along actin filaments. Therefore arrested organelle movement in the presence of such a construct shows that a particular myosin is involved with the movement of that particular organelle. While no mutually exclusive connections between specific myosins and organelles were found, based on overexpression of dominant negative tail constructs, a group of six myosins (XIC, XIE, XIK, XI-I, MYA1 and MYA2) were found to be more important for the motility of Golgi bodies and mitochondria in Nicotiana benthamiana and Nicotiana tabacum (8). Further deep and thorough analysis of myosin XIK revealed a potential regulation by head and tail interaction (Avisar et al., 2011). A similar regulatory mechanism has been reported for animal myosin V and VIIa (21, 22). In was shown that myosin V in the inhibited state is in a folded conformation such that the tail domain interacts with the head domain, inhibiting its ATPase and actinbinding activities. Cargo binding, high Ca2+, and/or phosphorylation may reduce the interaction between the head and tail domains, thus restoring its activity (23). Our collaborative work focuses on the characterization of the head tail interaction of myosin XIK. For this purpose the Israeli group built yeast expression vectors encoding the myosin XIK head. In addition, GST fusions of the wild-type tail as well as a tail mutated in the amino acids that mediate head to tail interaction. These were sent to the US group who is working on the isolation of recombinant proteins and performing the in vitro assays. While stress signals involve changes in Ca2+ levels in plants cells, the cytoplasmic streaming is sensitive to Ca2+. Therefore plant myosin activity is possibly regulated by stress. This finding is directly related to the goal of the original proposal.
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Jindal-Snape, Divya, Chris Murray, Andrew Keiller, Lynn Kelly, Judith Langlands-Scott, Anj Snape, Jonathan B. Snape et al. AĦNA U L-FiBROMiLAĠJA. UniVerse, Mai 2022. http://dx.doi.org/10.20933/100001245.

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Milux, psikologu li jispeċjalizza fl-uġigħ qalli li għandu jsir ħafna aktar sabiex iktar professjonisti li jaħdmu fis-saħħa jsiru konxji dwar il-fibromijalġja. Meta tqabbel ma’ dak li konna nafu saħansitra sentejn ilu, bil-progress li sar fir-riċerka, issa nistgħu nifhmu aħjar x’inhi l-fibromijalġja. Madankollu, m’hemmx ċertezza sakemm it-tabib, il-fiżjoterapista, jew professjonisti oħra jkollhom għarfien sħiħ ta’ din il-kundizzjoni kumplessa. Kultant qisha lotterija. Darba kont fis-sodda nsofri bl-uġigħ u bdejt naħseb kif nista’ noħloq komik dwar din il-kundizzjoni. Bgħatt emails lil xi wħud li kont naf, u dawn kitbuli lura, jgħiduli li jridu jaħdmu miegħi fuq dan il-proġett. Dan il-komik huwa miktub u ddisinjat bl-għan li jqajjem kuxjenza dwar il-fibromijalġja fost professjonisti, familji, u komunitajiet. Jagħtina stampa tal-bidliet kontinwi fil-ħajja ta’ dawk li għandhom il-fibromijalġja u kif ukoll dwar l-impatt li dan iħalli fuq dawk qrib tagħhom. Jitfa’ dawl u jenfasizza l-importanza ta’ gruppi u netwerks ta’ appoġġ li jgħinu n-nies jadattaw għal ħafna bidliet li ġġib il-fibromijalġja, u sabiex dawn xorta jkomplu jiffjorixxu minkejja l-isfidi u l-konsegwenzi sostanzjali li jaffaċċjaw.
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