Relevant bibliographies by topics / XLQ

Academic literature on the topic 'XLQ'

Author: Grafiati
Published: 4 June 2021
Last updated: 9 February 2022

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Journal articles on the topic "XLQ"

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Cai, Hongcai, Guowei Zhang, Zechen Yan, and Xuejun Shang. "The Effect of Xialiqi Capsule on Testosterone-Induced Benign Prostatic Hyperplasia in Rats." Evidence-Based Complementary and Alternative Medicine 2018 (September 30, 2018): 1–9. http://dx.doi.org/10.1155/2018/5367814.

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Benign prostatic hyperplasia (BPH) is common among elderly men, of which inflammation, oxidative stress, proliferative, and apoptotic changes play important roles. Xialiqi (XLQ) capsule, a traditional Chinese herbal formula, is used as a potential drug in treating BPH. This study aims to evaluate the therapeutic effect of XLQ capsule on testosterone propionate- (TP-) induced BPH in rats. Fifty male Sprague-Dawley rats were randomly divided into 5 groups: sham control, BPH model, high and low dose of XLQ, and finasteride as a positive control group. All groups were treated with appropriate drugs/normal saline for 28 consecutive days. Prostate weights were recorded; histopathological changes and content of IL-8, TNF-α, DHT, SOD, MDA, caspase-3, and PCNA of the prostate were determined. Animals with BPH demonstrated significantly increased prostate weights and prostate index, higher levels of IL-8, TNF-α, DHT, MDA, and PCNA, but lower activity of SOD and reduced expression of caspase-3. After treatment with XLQ, significant reductions of prostate weights, prostate index, IL-8, TNF-α, DHT, MDA, and PCNA, increased activity of SOD, and higher level of caspase-3 were shown. The present study indicates that XLQ can effectively prevent the development of TP-induced BPH model through mechanisms of anti-inflammation, antioxidation, antiproliferation, and proapoptosis.
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Yang, Feiya, Lingquan Meng, Panpan Han, Dexi Chen, Mingshuai Wang, Yongguang Jiang, Yanqiao Wu, Yiling Wu, and Nianzeng Xing. "New therapy with XLQ ® to suppress chronic prostatitis through its anti‐inflammatory and antioxidative activities." Journal of Cellular Physiology 234, no. 10 (February 20, 2019): 17570–77. http://dx.doi.org/10.1002/jcp.28380.

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Vallejo, César. "Trilce XLI‐XLV." Review: Literature and Arts of the Americas 25, no. 45 (January 1991): 77–81. http://dx.doi.org/10.1080/08905769108594327.

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Pouzar, Vladimír, Hana Chodounská, Dalibor Sameš, Pavel Drašar, and Miroslav Havel. "Derivatives of 5α-androstan-3α- and 3β-ol with acrylate side chain." Collection of Czechoslovak Chemical Communications 55, no. 5 (1990): 1243–56. http://dx.doi.org/10.1135/cccc19901243.

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Hydroxy derivatives I, II, III, XVII and XX were oxidized to give the respective aldehydes IV, V, VI, XVIII and XXI which were further converted by Wittig-Horner reaction into unsaturated methyl and ethyl esters. Removal of the acetal protecting group in position 3 afforded methylesters X, XXIV and XXXVI and ethyl esters XIV, XXV and XXXVII. Compounds XXIV, XXV, XXXVI and XXXVII were converted into the corresponding hemisuccinates XXVIII, XXIX, XL and XLI and β-D-glucosides XXXII, XXXIII, XLIV and XLV.
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TURCAN, Doina, Lucia ANDRIES, Alexandr DORIF, and Victoria SACARA. "Analysis of clinical and molecular genetic characteristics of Wiskott-Aldrich syndrome and X-linked thrombocytopenia." One Health & Risk Management 2, no. 3 (June 17, 2021): 61–66. http://dx.doi.org/10.38045/ohrm.2021.3.10.

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Introduction. Wiskott-Aldrich syndrome is a rare X-linked disorder characterized by microthrombocytopenia, eczema, and recurrent infections. It is caused by mutations of the WAS gene which encodes the WAS protein (WASp) – a key regulator of actin polymerization in hematopoietic cells. Mutations within the WASp gene result in a wide heterogeneity of clinical disease, ranging from ‘classical WAS’ to mild asymptomatic thrombocytopenia (X-linked thrombocytopenia [XLT]), or congenital neutropenia (X-lined neutropenia [XLN]).Case presentation. This present paper reports a phenotypical and laboratory description of two children diagnosed with WAS and one child diagnosed with XLT. The first case was a six months old male with septicemia, thrombocytopenia, eczema and petechial rash. The second case was a 2 years old boy presenting with complaints of recurrent infections, eczema and thrombocytopenia with small platelet size. The third case was a 16 years old boy who presented with thrombocytopenia and recurrent sinopulmonary infections.Conclusions. Due to a wide spectrum of clinical findings, the diagnosis of WAS/XLT should be considered in any male patient presenting with petechiae, bruises, and congenital or early-onset thrombocytopenia associated with small platelet size.
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Luce, T. J., and John Briscoe. "Livius, Ab Urbe Condita libri XLI-XLV." American Journal of Philology 109, no. 3 (1988): 455. http://dx.doi.org/10.2307/294903.

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Summers, G. D. "An aerial Survey of Çevre Kale, Yaraşli." Anatolian Studies 42 (December 1992): 179–206. http://dx.doi.org/10.2307/3642957.

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About 1 km. north of the village of Yaraşlı on a natural hill that forms an extension of Karaca Daǧ, is a large and impressively defended site locally called Çevre Kale (Fig. 1). Pottery from the surface is Imperial Hittite and Phrygian in date. There is later material, Hellenistic to Byzantine, beneath and adjacent to the village. Yaraşlı is a large well watered village in the Kulu district (ilce) of Konya province (il). The map reference is 59-Ie on the 1:200,000 sheet for Katrancı (Harita Genel Müdürlüǧü 1945).The aims of the project were to produce a photographic record of the site from the air, using a helium filled blimp and remote controlled camera, from which plans could be drawn and relationships between the various elements of the site determined. Air photographs revealed outlines of buildings that could not be seen on the ground (Pls XLI–XLV(a)). An overall plan has been drawn (Fig. 3). In some cases it has been possible to draw stone for stone plans (Fig. 5 and Pl. XLIV(b), Fig. 6 and Pl. XLV(a)). The results are much superior to those that could have been achieved by traditional cadastral survey and were obtained in a short time. During the course of the day photographs can be taken in varying light so that changes in shadow highlight different features.
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Hannan, Khyle M. "Book Review: Encyclopedia of African American Business: Updated and Revised Edition, 2nd ed." Reference & User Services Quarterly 58, no. 1 (October 10, 2018): 62. http://dx.doi.org/10.5860/rusq.58.1.6853.

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The African American contribution to business and economic institutions in America is significant and spans “the period from 18th-century America to the present” (xlv). This encyclopedia is unique in being a reference work dedicated solely to exploring this contribution and its impact. In the preface, the editor, Jessie Carney Smith, Dean of the Library and Camille Cosby Distinguished Chair in the Humanities at Fisk University in Nashville, TN, mentions, “one subject that has been met with somewhat limited appeal is African American books on businesses, merely because the focus is narrow and unlike the wider scope of literary works” (xli). This explains the dearth of similar works in the field. It is this gap that motivated her to first publish this work in 2006 and prompted the publisher to reissue it eleven years later in 2017.
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Blundell, Michael P., Austen Worth, Gerben Bouma, and Adrian J. Thrasher. "The Wiskott-Aldrich Syndrome: The Actin Cytoskeleton and Immune Cell Function." Disease Markers 29, no. 3-4 (2010): 157–75. http://dx.doi.org/10.1155/2010/781523.

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Wiskott-Aldrich syndrome (WAS) is a rare X-linked recessive primary immunodeficiency characterised by immune dysregulation, microthrombocytopaenia, eczema and lymphoid malignancies. Mutations in the WAS gene can lead to distinct syndrome variations which largely, although not exclusively, depend upon the mutation. Premature termination and deletions abrogate Wiskott-Aldrich syndrome protein (WASp) expression and lead to severe disease (WAS). Missense mutations usually result in reduced protein expression and the phenotypically milder X-linked thrombocytopenia (XLT) or attenuated WAS [1-3]. More recently however novel activating mutations have been described that give rise to X-linked neutropenia (XLN), a third syndrome defined by neutropenia with variable myelodysplasia [4-6]. WASP is key in transducing signals from the cell surface to the actin cytoskeleton, and a lack of WASp results in cytoskeletal defects that compromise multiple aspects of normal cellular activity including proliferation, phagocytosis, immune synapse formation, adhesion and directed migration.
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Thrasher, Adrian J. "New insights into the biology of Wiskott-Aldrich syndrome (WAS)." Hematology 2009, no. 1 (January 1, 2009): 132–38. http://dx.doi.org/10.1182/asheducation-2009.1.132.

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Abstract The Wiskott-Aldrich syndrome (WAS) is an X-linked immunodeficiency disease with a characteristic clinical phenotype that includes thrombocytopenia with small platelets, eczema, recurrent infections due to immunodeficiency, and an increased incidence of autoimmune manifestations and malignancies. The identification of the molecular defect in the WAS gene has broadened the clinical spectrum of disease to include chronic or intermittent X-linked thrombocytopenia (XLT), a relatively mild form of WAS, and X-linked neutropenia (XLN) due to an arrest of myelopoiesis. The pathophysiological mechanisms relate to defective actin polymerization in hematopoietic cells as a result of deficient or dysregulated activity of the WAS protein (WASp). The severity of disease is variable and somewhat predictable from genotype. Treatment strategies therefore range from conservative through to early definitive intervention by using allogeneic hematopoietic stem cell transplantation and potentially somatic gene therapy. All aspects of the condition from clinical presentation to molecular pathology and basic cellular mechanisms have been reviewed recently.
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Dissertations / Theses on the topic "XLQ"

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Grisham, Tom, and tgrisham@tampabay rr com. "Cross cultural leadership." RMIT University. Property, Construction and Project Management, 2006. http://adt.lib.rmit.edu.au/adt/public/adt-VIT20061116.125205.

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Global markets are increasingly taking advantage of the strength and economic advantages of a diverse global workforce. It is common on international projects to find multi-cultural teams located in multiple countries. It is also common to find such projects led by Project Managers who come from many different countries. So having a person raised in India managing a project in China, with a design team in the USA, procurement procurement teams in Japan and Mexico, and a drafting team in Albania is not unusual. Even in historically monolithic markets like the USA, it is far more common to have mulit-cultural teams and foreign competition. In addition, the pressure on the industry to increase productivity and reduce costs is unrelenting. This leads to flatter project structures, and the need for leadership at multiple levels. My experience in such markets, and the glaring need for a Cross-Cultural Leadership model that could be used to improve leadership skills in international markets were the reasons for undertaking this thesis. The hypothesis of this thesis is that there are of cross-cultural leadership dimensions that are effective and essential, regardless of culture. Those dimensions are Trust, Empathy, Transformation, Power, and Communication. The thesis first explores the cultural and leadership aspects of Cross-Cultural Leadership through a review of the published literature. The literature research was then subjected to an exegetical review of the themes that emerged, and used to construct the Descriptors, and Sub-Descriptors for each of the leadership dimensions. The thesis also explored the transfer of cultural knowledge with metaphors and storytelling. In a fast paced business environment, developing a richer understanding and sensitivity to other coulters, in general and specific, is a skill that Leaders must possess. Lastly, the thesis explored the connections between conflict management and Cross-Cultural Leadership. Conflict management skills are becoming ever more important due to the rapid changes that are common in the current business environment. Change, cultural mis-information, scarce resources, poor communication skills, contractual ambiguity and complexity are but a few of the reasons that managing conflict is a critical skill for leaders. IV The design of the testing protocols was bifurcated. One track evaluated the hypothesis, the other track evaluated the connection between the Leadership Dimensions hypothesized, and the GLOBE survey. The GLOBE survey was utilized to investigate if a viable connection existed between the Leadership Dimensions and a broad based international survey of cultural dimensions. The testing of the hypothesis was performed using a Delphi panel of experts in international cross-cultural leadership, through two sessions of questions with feedback after the end of the first session. Subsequently, the results were analyzed, studied, and evaluated with an eye toward my practical experience in the field - sense making. The results were that the hypothesis was confirmed, and the connection to the GLOBE Survey cultural dimensions was also confirmed. A model is presented to summarize the findings of the thesis, called the Cross-Cultural Leadership Intelligence (XLQ) Model. As discussed in the thesis, Project Management has not emphasized leadership in the current body of knowledge (PMBOK), and it only makes general reference to cultural considerations. Recognizing this, The Project Management Institute (PMI) has funded a study that recommends more research in the area of cross-cultural leadership, and a new grant to study the question of how global the PMBOK really is. Both of these issues are addressed by this thesis. The XLQ model provides a framework for assessing and training Project Managers in cross-cultural leadership skills. The model is a global one that can be used across cultures, business models, and markets. The model also points towards the need for further research into metrics, education, training techniques, and of course, further empirical testing of the model itself.
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Horn, Peter Christian. "Charakterisierung des XIAP-Gens bei zwei Familien mit X-chromosomalem lymphoproliferativem Syndrom." Doctoral thesis, Universitätsbibliothek Leipzig, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-179636.

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Dissertation zur Erlangung des akademischen Grades Dr. med. Charakterisierung des XIAP-Gens bei zwei Familien mit X-chromosomalem lymphoproliferativem Syndrom Eingereicht von: Peter Christian Horn geboren am 04.08.1982 in Freiburg Angefertigt an: Der Universitätsklinik und Poliklinik für Kinder und Jugendliche Leipzig und dem Zentrum für familiären Brust- und Eierstockkrebs der technischen Universität München Betreuer: Prof. Dr. med. Volker Schuster (Universität Leipzig) Prof. Dr. rer. nat. Alfons Meindl (TU München) Eingereicht im Dezember 2014 Das X-linked-inhibitor-of-apoptosis Protein XIAP nimmt eine zentrale Rolle in der Hemmung von Apoptoseprozessen beim Menschen ein. In Abwesenheit von XIAP kann eine defekte Immunabwehr gegenüber viralen Infektionen beobachtet werden. In Folge können lebensbedrohliche Immunreaktionen wie hämophagozytäre Lymphhistiozytose, aplastische Anämie und persistierende Hypogammaglobulinämie auftreten. Im Rahmen dieser Arbeit wurde untersucht, ob bei einem Patientenkollektiv mit lymphoproliferativem Syndrom Mutationen im XIAP-Gen Auslöser der Erkrankung sind. Es wurde eine molekulargenetische Sequenzierung und Auswertung des XIAP- 5 Zusammenfassung der Arbeit 53 Gens bei 36 Verdachtsfällen eines X-chromosomal vererbten lymphoproliferativen Syndroms durchgeführt. In allen Fällen wurde der gesamte exonische Abschnitt des Gens sequenziert und auf Polymorphismen und Mutationen untersucht. Bei zwei Proben wurden Mutationen im XIAP-Gen gefunden. Weiter konnten Mutter und Bruder eines der Betroffenen untersucht werden, so dass insgesamt drei Knaben mit XIAP-Gendefekt sowie eine heterozygote Konduktorin identifiziert wurden. Nach der Identifikation der Mutationsträger erfolgte eine Auswertung der Krankenge- schichte und ein Vergleich mit den verfügbaren Beschreibungen von XIAP-Defizienz. Die beiden neu identifizierten Mutationen verursachen ein Krankheitsbild, das mit den wenigen verfügbaren Beschreibungen von XIAP-Defizienz vereinbar ist. Die Auswer- tung der Klinik der drei Betroffenen unterstützt die Hypothese, dass bei XIAP- Defizienz keine Lymphome auftreten. Die Therapieentscheidung bei XIAP-Defizienz ist einzelfallabhängig. Die Arbeit ver- gleicht den Krankheitsverlauf der neu beschriebenen Patienten mit der Literatur und unterstreicht, dass die Entscheidung zu einer Knochenmarkstransplantation gut begrün- det werden muss. Es sind inzwischen mehr Patienten bekannt, die ohne Therapie oder unter IVIG-Gabe asymptomatisch sind, als solche, die eine Knochenmarkstransplantati- on überlebt haben. Alle hier beschriebenen Patienten konnten ohne Transplantation be- handelt werden. Eine Stammzelltransplantation kann jedoch erfolgreich sein. Bei kon- servativ behandelten Patienten können Rezidive auftreten. Kritisch zu sehen sind im Licht der Erfahrung mit den XIAP-defizenten Patienten An- strengungen, XIAP-Inhibitoren zur Tumortherapie am Menschen zu entwickeln – dies könnte als Nebenwirkung paradoxe Folgen wie Lymphoproliferation oder HLH haben. Die in der Arbeit beschriebenen Patienten waren die ersten Patienten mit XIAP- Defizienz, die im deutschsprachigen Raum identifiziert wurden. Die beiden Mutationen die bei den Familien gefunden wurden, waren bisher nicht beschrieben.
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Lam, Wai-Yeung. "XCQ : a framework for XML compression and querying /." View abstract or full-text, 2003. http://library.ust.hk/cgi/db/thesis.pl?COMP%202003%20LAM.

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Thesis (M.Phil.)--Hong Kong University of Science and Technology, 2003.
Includes bibliographical references (leaves 142-147). Also available in electronic version. Access restricted to campus users.
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AL, MOHAINI MOHAMMED. "XLF-Dependent Nonhomologous End Joining of Complex DNA Double-Strand Breaks with Proximal Thymine Glycol and Screening for XRCC4-XLF Interaction Inhibitors." VCU Scholars Compass, 2015. http://scholarscompass.vcu.edu/etd/3988.

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DNA double-strand breaks induced by ionizing radiation are often accompanied by ancillary oxidative base damage that may prevent or delay their repair. In order to better define the features that make some DSBs repair-resistant, XLF-dependent nonhomologous end joining of blunt-ended DSB substrates having the oxidatively modified nonplanar base thymine glycol (Tg) at the first (Tg1) , second (Tg2), third (Tg3) or fifth (Tg5) positions from one 3’ terminus was examined in human whole-cell extracts. Tg at the third position had little effect on end-joining even when present on both ends of the break. However, Tg as the terminal or penultimate base was a major barrier to end joining (>10-fold reduction in ligated products) and an absolute barrier when present at both ends. Dideoxy trapping of base excision repair intermediates indicated that Tg was excised from Tg1, Tg2 and Tg3 largely if not exclusively after DSB ligation. However, Tg was rapidly excised from the Tg5 substrate, resulting in a reduced level of DSB ligation, as well as slow concomitant resection of the opposite strand. XLFL115D mutant completely eliminates ligation of all five substrates and previous X‑ray crystallography shows that XLF binds to XRCC4 via a “leucine lock” motif wherein L115 of XLF slips into a hydrophobic pocket in XRCC4. This makes the XRCC4-XLF interaction a good target to develop peptide inhibitors in order to radiosensitize breast tumor cells that are dependent on NHEJ to repair their DSBs after ionizing radiation exposure. Using mRNA display, we created a diverse library of 870 billion unique peptide sequences. After seven rounds of in vitro selection, the eluted fusions were cloned and sequenced. The results showed homology of sequences of five main families. We have selected representative peptides from those families (Pep 7.1-7.5), and several were chemically synthesized. However, none of these significantly inhibited XLF-dependent end joining in whole-cell extracts. Overall, the results suggest that promoting ligation of DSBs with proximal base damage may be an important function of XLF, but that Tg can still be a major impediment to repair, being relatively resistant to both trimming and ligation. The effectiveness of XLF-XLRCC4 inhibitors in blocking nonhomologous end joining remains to be determined.
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Spencer, Stefan. "W XLV : structural and collisional atomic generation for fusion." Thesis, Queen's University Belfast, 2016. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.711906.

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Bacigalupo, Luis Eduardo. "Bernardo contra Abelardo: Moral y política en el siglo XlI." Pontificia Universidad Católica del Perú, 2012. http://repositorio.pucp.edu.pe/index/handle/123456789/119318.

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Una de las más célebres contiendas de la Edad Media es la que enfrentó en Sens (1140) a Pedro Abelardo y Bernardo de Claraval. El primero llegó a esa localidad como acusado; el segundo había reunido el concilio como acusador.
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DZWONKOWSKI, PIOTR. "Micro-generateur electrochimique li/b#2o#3+xli#2o/inse." Paris 6, 1990. http://www.theses.fr/1990PA066124.

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Des micro-generateurs en couches minces ont ete realises et etudies. Les structures sont constituees par l'empilement de couches minces: de lithium, d'electrolyte solide vitreux et d'inse. Les micro-generateurs ont une tension de l'ordre de 1. 5-2 v, un courant d'echange sur l'interface de l'ordre de 5. 10##9 a/cm#2. La valeur de coefficient de diffusion chimique du lithium dans la cathode est estimee a se situer entre 10##1#4-10##1#5 cm#2/s. Differents electrolytes solides du systeme b-o-li, b-o-li-cl et b-o-li-s ont ete envisages et les caracteristiques des micro-generateurs ont ete etudiees en fonction de la composition de l'electrolyte. La structure de l'electrolyte a ete etudiee par la spectroscopie d'absorption infrarouge. Une etude complete de l'impedance complexe des couches minces des verres alcalins a ete menee
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Santos, AndrÃa Feitosa dos. "Uma gramÃtica LFG-XLE para o processamento sintÃtico profunda do portuguÃs." Universidade Federal do CearÃ, 2014. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=13867.

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CoordenaÃÃo de AperfeiÃoamento de Pessoal de NÃvel Superior
A presente tese descreve a elaboraÃÃo de uma gramÃtica da frase do PortuguÃs Brasileiro, desenvolvida no quadro de um modelo teÃrico de sofisticado formalismo computacional, a Lexical Functional Grammar (LFG) e implementada no sistema que constitui o estado da arte em ambiente de processamento sintÃtico profundo no modelo gerativo da LFG, o robusto Xerox Linguistic Environment (XLE). A principal caracterÃstica da gramÃtica à que adota o sistema de anotaÃÃo do ParGram e a metodologia convencionada por desenvolvedores de gramÃtica XLE. No fragmento de gramÃtica estÃo modelados diversificados elementos da sintaxe frasal. Em nossa gramÃtica, foram modelados constituintes oracionais como IP e CP, elementos que encabeÃam as sentenÃas do portuguÃs. TambÃm foram modelados determinados aspectos da subcategorizaÃÃo verbal e da estrutura argumental. Dos elementos verbais, nossa gramÃtica contempla alguns casos de complexos verbais constituÃdos de verbos modais e verbos de controle. Os elementos nominais tratados na gramÃtica, de modo central, foram os pronomes expletivos e reflexivos, e os casos de sintagmas nominais e determinantes com pronomes demonstrativos e interrogativos. Os demais aspectos modelados na gramÃtica sÃo os sintagmas preposicionados, cuja complexidade se dà na distinÃÃo entre preposiÃÃes semÃnticas e nÃo semÃnticas; os sintagmas adjetivais, cuja projeÃÃo na sentenÃa pode ocorrer a partir de formas adjetivais atributivas, de formas ordinais ou cardinais e na forma de intensificadores; e os sintagmas adverbiais, cuja estrutura interna foi modelada levando-se em consideraÃÃo tanto advÃrbios intransitivos quanto transitivos com complemento PP. A nossa avaliaÃÃo demonstra que das 40 sentenÃas testadas, a nossa gramÃtica atribui, para todas elas, anÃlises consistentes e bem fundamentadas, ao passo que o parser Palavras, o atual estado da arte em processamento sintÃtico profundo do portuguÃs, atribui, a 9 sentenÃas, anÃlises incorretas. Uma outra avaliaÃÃo demonstra que, das 20 sentenÃas agramaticais testadas tanto em nossa gramÃtica, quanto no Palavras, somente 2 receberam anÃlises por parte de nossa gramÃtica, enquanto o Palavras fornece anÃlises para 19 sentenÃas. O trabalho tem, essencialmente, o objetivo de fazer uma descriÃÃo formal e fundamentada de um amplo leque de fenÃmenos do portuguÃs brasileiro, mas, sobretudo, tem o objetivo de contribuir com uma gramÃtica nÃo trivial da frase do portuguÃs no formalismo LFG-XLE, disponibilizando efetivamente um recurso gramatical do portuguÃs voltado para o processamento de linguagem natural.
The present thesis describes the development of a Brazilian Portuguese sentence grammar, developed in the framework of a sophisticated computational formalism, named Lexical Functional Grammar, and implemented on a system that is state of the art in deep parsing environment in LFG generative model, the robust XLE. The main feature of the grammar is that it adopts the ParGram annotation system and the methodology agreed by XLE grammar developers. In the grammar fragment are modeled diverse elements of phrasal syntax. In our grammar were modeled constituents as IP and CP, elements that are head the sentences of the Portuguese. Also were modeled certain aspects of verbal subcategorization and argument structure. In terms of verbal elements, our grammar includes some cases of verbal complex made up of modal verbs and control verbs. The nominal elements treated in grammar, centrally, were the expletives and reflexive pronouns, and cases of nominal and determiners phrases with demonstrative pronouns and interrogative. The other aspects modeled in the grammar are PPs, whose complexity is given the distinction between semantic and nonstandard prepositions; the adjectival phrases, whose projection in the sentence can occur from attributive adjectival forms of ordinal or cardinal forms and as intensifiers; and adverbial phrases, whose internal structure was modeled taking into account both adverbs as intransitive and as transitive, with PP complement. Our evaluation shows that of the 40 tested sentences, our grammar assigns, for all of them, consistent and well-founded analysis, while the parser Palavras, the current state of the art in deep syntactic processing of Portuguese, assigns incorrect analysis for 9 sentences. Another evaluation shows that, of the 20 ungrammatical sentences tested both in our grammar, as in Palavras, only 2 received analysis by our grammar, while the Palavras provides analysis to 19 sentences. The work has essentially the goal of making a formal and grounded description in a broad range of phenomena in Brazilian Portuguese, but mainly aims to collaborate with a not trivial grammar of the sentence in the LFG-XLE formalism, effectively contributing to a grammatical resource turned to the natural language processing.
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Sharifi, G. "Cellular studies on the pathogenesis of X-linked lymphoproliferative (XLP) syndrome." Thesis, University College London (University of London), 2005. http://discovery.ucl.ac.uk/1445057/.

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X-linked lymphoproliferative (XLP) disease is a severe primary immunodeficiency. Immunodysregulatory phenomena are observed following EBV infection suggesting that defects exist in these effector populations. The gene defective in XLP is SAP (SLAM-associated protein), an intracellular adaptor protein that mediates signals through SLAM and other immunoglobulin superfamily receptors including 2B4. Cytotoxic T cells (CTLs) and natural killer (NK) cells play a major role in the normal immune response to Epstein-Barr virus (EBV) infection. EBV specific T cell lines (EBV-T cell lines) were generated from normal individuals and XLP patients and examined for CTL function in response to different stimuli. It has been shown that XLP patients can generate EBV-T cell lines that are phenotypically similar to those from unaffected individuals. XLP patient derived EBV-T cell lines showed a significant decrease in interferon-gamma (IFN-gamma) production in response to 2B4 and autologous EBV transformed lymphoblastoid cell line (LCL) stimulation but not in response to SLAM. Furthermore, XLP EBV-T cell lines demonstrated markedly decreased cytotoxic activity against autologous LCLs. By retroviral gene transfer of the SAP gene into XLP patient derived EBV-T cell lines, reconstitution of EFN-gamma production and cytotoxic activity has been shown, confirming the defects are SAP dependent. These studies demonstrate that in XLP the lack of SAP affects specific signalling pathways resulting in severe disruption of CTL function. In addition, SLAM and 2B4 expression on immune cell lineages has been investigated, the results suggest a wider range of 2B4 expression and deserve further investigation in relation to XLP molecular and cellular pathogenesis.
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Groh, Stefan. "Die Insula XLI von Flavia Solva : Ergebnisse der Grabungen 1959 und 1989 bis 1992 /." Wien : Eingenverl. der Österreichischen Archäologischen Institutes, 1996. http://catalogue.bnf.fr/ark:/12148/cb39234694c.

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Books on the topic "XLQ"

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Livy. Titi Livi Ab vrbe condita libri XLI-XLV. Stvtgardiae: B.G. Tevbneri, 1986.

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Briscoe, John, ed. Titi Livi Ab Urbe Condita, Libri XLI-XLV. Berlin, Boston: DE GRUYTER, 1986. http://dx.doi.org/10.1515/9783110959543.

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Morlan, Michael. Clymer Harley-Davidson XL/XLH Sportster, 1986-2003. 5th ed. Overland Park, Kan: Clymer, 2007.

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Russia) Zimni︠a︡i︠a︡ shkola PII︠A︡F (40th 2007 Saint Petersburg. Fizika i tekhnika reaktorov: Materialy XL-XLI zimnikh shkol. Sankt-Peterburg: PiI︠A︡F, 2007.

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Kazımoğlu, Mukhtar. Xalq gülüşünün poetikası. Bakı: Elm, 2006.

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Naqī, Nāṣir al-Fuqarā Muḥammad, ed. Āz̲arbāycān xalq tarānahʹlarī. Tabrīz: Mihrān Nashr, 2000.

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Afzalov, Mansur, X. Rasulov, and Anatoliya Bobrov. O'zbek xalq ertaklari. Toshkent: G'afur G'ulom nomidagi Nashriyot-Matbaa Ijodiy Uyi, 2006.

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Mirzaev, Tŭra. Oʹzbek xalq maqollari. Toshkent: Gʹafur Gʹulom nomidagi Nashriyot-Matbaa Ijodiy Uyi, 2009.

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Afzalov, Mansur, and X. Rasulov. O'zbek xalq ertaklari. Toshkent: O'qituvchi, 2007.

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Kazımoğlu, Mukhtar. Xalq gülüşünün poetikası. Bakı: Elm, 2006.

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Book chapters on the topic "XLQ"

1

Bartholdi, Deborah, Albert Schinzel, Deborah Bartholdi, Albert Schinzel, Deborah Bartholdi, Albert Schinzel, Deborah Bartholdi, et al. "XLP." In Encyclopedia of Molecular Mechanisms of Disease, 2263. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_7242.

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Madaurensis], Apuleius [Lucius Apuleius. "XLI." In Oxford Classical Texts: Apulei: Metamorphoseon Libri XI, edited by Maaike Zimmerman, 227. Oxford University Press, 2012. http://dx.doi.org/10.1093/oseo/instance.00135287.

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Livius], Livy [Titus. "XLI." In Oxford Classical Texts: Titi Livi: Ab Vrbe Condita, Vol. 6: Libri XXXVI–XL, edited by Peter G. Walsh, 258. Oxford University Press, 1999. http://dx.doi.org/10.1093/oseo/instance.00093526.

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Livius], Livy [Titus. "XLV." In Oxford Classical Texts: Titi Livi: Ab Vrbe Condita, Vol. 6: Libri XXXVI–XL, edited by Peter G. Walsh, 263. Oxford University Press, 1999. http://dx.doi.org/10.1093/oseo/instance.00093530.

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Livius], Livy [Titus. "XLI." In Oxford Classical Texts: Titi Livi: Ab Vrbe Condita, Vol. 6: Libri XXXVI–XL, edited by Peter G. Walsh, 326. Oxford University Press, 1999. http://dx.doi.org/10.1093/oseo/instance.00093583.

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Livius], Livy [Titus. "XLV." In Oxford Classical Texts: Titi Livi: Ab Vrbe Condita, Vol. 6: Libri XXXVI–XL, edited by Peter G. Walsh, 330. Oxford University Press, 1999. http://dx.doi.org/10.1093/oseo/instance.00093587.

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Livius], Livy [Titus. "XLI." In Oxford Classical Texts: Titi Livi: Ab Vrbe Condita, Vol. 6: Libri XXXVI–XL, edited by Peter G. Walsh, 49. Oxford University Press, 1999. http://dx.doi.org/10.1093/oseo/instance.00093358.

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Livius], Livy [Titus. "XLV." In Oxford Classical Texts: Titi Livi: Ab Vrbe Condita, Vol. 6: Libri XXXVI–XL, edited by Peter G. Walsh, 54. Oxford University Press, 1999. http://dx.doi.org/10.1093/oseo/instance.00093362.

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Livius], Livy [Titus. "XLI." In Oxford Classical Texts: Titi Livi: Ab Vrbe Condita, Vol. 6: Libri XXXVI–XL, edited by Peter G. Walsh, 104. Oxford University Press, 1999. http://dx.doi.org/10.1093/oseo/instance.00093404.

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Livius], Livy [Titus. "XLV." In Oxford Classical Texts: Titi Livi: Ab Vrbe Condita, Vol. 6: Libri XXXVI–XL, edited by Peter G. Walsh, 108–10. Oxford University Press, 1999. http://dx.doi.org/10.1093/oseo/instance.00093408.

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Conference papers on the topic "XLQ"

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Laue, Thomas M., Arthur L. Anderson, and Bryan J. Weber. "Prototype fluorimeter for the XLA/XLI analytical ultracentrifuge." In BiOS '97, Part of Photonics West, edited by Gerald E. Cohn and Steven A. Soper. SPIE, 1997. http://dx.doi.org/10.1117/12.274351.

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Singh, Sundeep, and Ramjee Repaka. "Comparison of Ablation Volume Produced With Multi-Tine Dry Type and Wet Type Electrodes During Radio Frequency Ablation: An In Vitro Study." In ASME 2018 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/imece2018-88588.

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The present in vitro study aims at comparing the ablation volume obtained with commercially available RITA’s StarBurst® XL (dry type) and StarBurst® Xli-e (wet type) multi-tine electrodes during radiofrequency ablation (RFA) procedure. The experiments have been conducted on polyacrylamide based tissue-mimicking phantom gel whose thermo-electric properties are similar to that of the soft tissues. A temperature-controlled RFA has been performed utilizing AngioDynamics RITA 1500X® radiofrequency generator. The maximal longitudinal and maximal transverse dimensions of the coagulated phantom gels have been measured from which the derived ablation volume has been calculated. Further, the temperature distribution and power delivered with the dry type and wet type electrodes have been compared. The in vitro study revealed that the efficacy of wet type electrode is more pronounced as compared to the dry type electrode. Moreover, it has been found that both the electrodes are capable enough of producing ablation volume up to 5 cm in diameter.
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Scott, Cheryl F., John L. Brash, Pauline ten Hove, Peter Wojciechowaki, and Robert W. Colman. "PLASMA-ARTIFICIAL SURFACE INTERACTIONS; ROLE OF CONTACT AND FIBRINOLYTIC SYSTEMS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642919.

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The transient adsorption of fibrinogen (Fg) to artificial surfaces (Vroman Effect) is modulated principally by the procofactor, high molecular weight kininogen (HK). We investigated which form of HK was responsible for Fg displacement and also whether other proteins participated in the Vroman Effect. Experiments were performed at 23°C with a 5 min surface exposure to various concentrations of either normal plasma or plasma deficient in specific proteins to which 125I Fg had been added. Typically, Fg adsorption reached a maximum at 1% plasma and decreased at higher plasma concentrations. On all surfaces tested, Fg displacement was greatly reduced in HK-deficient plasma. Normal plasma,when exposed to the contact system activator, dextran sulfate, prior to its interaction with glass, displayed Fg displacement similar to untreated HK-deficient plasma.However, if Factor Xl-deficient plasma was incubated with dextran sulfate prior to exposure to glass, the Fg displacement pattern resembled normal, untreated plasma. These results suggest that the inactive cofactor form of HK (HMWKi) generated by Factor XIa (formed during extensive contact activation) does not displace Fg. Furthermore, Fg displacement was also reduced in untreated Factor Xll-deficient plasma exposed to glass, suggesting that the active cofactor form of HK (HMWKa) generated by exposure to kallikrein (during Factor Xll-dependent contact activation) may be the active participant in the Vroman Effect. The cofactor function of HK and its ability to displace Fg, therefore, appear to parallel. We also found that plasminogen or plasminogen activators were minimally involved in the Vroman Effect. Fg adsorption to glass in plasminogen-depleted HK-deficent plasma resembled Fg adsorption in a single protein system since more Fg was adsorbed and desorption failed to occur. A synergism may therefore exist between plasminogen and HK in the Vroman Effect. A better understanding of the mechanism of blood-artificial surface interaction is essential for the design of less thrombogenic biomaterials.
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Baroux, C., M. Detrilleaux, and G. Demazy. "Operational Experience of TN 24 Dual Purpose Spent Fuel Storage Casks at the DOEL Nuclear Power Plants in Belgium." In ASME 2001 8th International Conference on Radioactive Waste Management and Environmental Remediation. American Society of Mechanical Engineers, 2001. http://dx.doi.org/10.1115/icem2001-1217.

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Abstract Spent nuclear fuel has been stored at the DOEL power station in Belgium in dual-purpose metal casks since 1995. The casks were procured from TRANSNUCLEAIRE by SYNATOM to meet the operational demands for on-site dry storage solutions for fuel arising from the four PWR reactors at DOEL. The TN 24 type of cask was chosen and a range of different cask types were developed. The initial requirement was for dual purpose cask to contain fuel from the DOEL units 3 and 4, these having similar fuel types but different lengths, and thus two new members of the TN 24 family were developed; the TN 24 D and TN 24 XL with capacities of 28 and 24 SFA’s. These casks were licensed as B(U) fissile packagings with approval certificates granted by the French and validated by the Belgium competent authorities for the transport configurations. Both cask designs were also analyzed by TRANSNUCLEAIRE in their storage configurations to ensure that the criteria for safe interim storage could be met. Since 1995, a total of 18 TN 24 D and TN 24 XL casks have been loaded with spent fuel assemblies with an average burn-up of 40,000 MWd/tU. SYNATOM subsequently decided to purchase further casks for DOEL 3 and 4 fuels with higher enrichments, higher burn-ups and shorter cooling times. TRANSNUCLEAIRE developed the TN 24 DH and TN 24 XLH casks within the similar envelope size and weight limits. The increase in performance was achieved by an in-depth optimization of each design in terms of radiation shielding, heat transfer and criticality safety. This paper shows how this optimization process was undertaken for the TN 24 DH and TN 24 XLH casks, 16 of which have been ordered by SYNATOM. DOEL 1 and 2 units use much shorter PWR fuel and it was decided to ship the fuel to unit 3 with an internal transfer cask because the handling limitations in the DOEL 1 and 2 pool prohibited the loading of a high capacity dual purpose transport/storage cask. The TN 24 SH cask was subsequently designed for DOEL 1 and 2 PWR fuel with a capacity of 37 assemblies and nine of there casks have been ordered by SYNATOM. The casks are fitted with monitoring devices to detect any change in the performance of the double metal O ring closure system and none of the casks has shown any deterioration in leaktightness. This paper examines the operation experience of loading and storing more than 30 TN 24 dual purpose casks and compares the performance with design expectations.
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Xuhui Li and Mengchi Liu. "Design issues of XTQ language." In 2008 8th IEEE International Conference on Computer and Information Technology (CIT). IEEE, 2008. http://dx.doi.org/10.1109/cit.2008.4594667.

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Murayama, H., and N. U. Bang. "INCORPORATION OF PLASMINOGEN ACTIVATOR INHIBITOR INTO FIBRIN, AN ALTERNATIVE REGULATORY PATHWAY OF FIBRINOLYSIS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644442.

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A plasminogen activator inhibitor (PAI-1) Mj, 50 kd is normally found in plasma at low concentrations. Plasma levels increase sharply upon stimulation of endothelial cells with endotoxin or monokines and activated platelets secrete significant quantities of PAI-1. It is possible that high levels of PAI-1 may be achieved at the local sites of intravascular thrombi. Semipurified PAI-1 was therefore prepared from human platelets to study its affinity for fibrin (F). Approximately 50% PAI-1 adsorbed to F monomer immobilized on sepharose and desorbed under conditions of acidic pH and high ionic strength suggesting hydrogen bonding as the mode of interaction. Wells of 96-well microtiter plates were each coated with 50 yg [125I] plasminogen (P)-free fibrinogen and clotted with thrombin in the presence and absence of different concentrations of PAI-1. After extensive washing of the wells, they were incubated with 5 mU of tissue plasminogen activator (t-PA) and 5 mU of P for 6 h. Appropriate calibration curves utilizing different concentrations of t-PA and different concentrations of PAI-1 added to the supernatant rather than to F established that 8-15% of 21-166 mU PAI-1 incorporated into crosslinked (XL) F or noncrosslinked (NXL) F. Incorporated PAI strikingly inhibited fibrinolysis (FL). Percent inhibition of FL of XL or NXLF (Mean±S.D., N=5) plotted in the presence of 166, 83, 42 and 21 mU of PAI were: 83±3.3, 59.5±1.8, 29.7±5.2 and 15.2±6.14 for XLF and 78±5.3, 31±8.1, 14.5±10.5 and 0 Tor NXL F. As demonstrated by radioautography on SDS PAGE PAI-1 incorporated into F readily formed complexes with [125I] urokinase (u-PA). In these experiments, no evidence for crosslinking of PAI-1 into F has been obtained to date. In experiments utilizing agarose immobilized proteins, it was evident that not only F but also fibrinogen binds PAI-1; PAI-1 associated with F as well as fibrinogen is capable of forming complexes with [1251] u-PA.In contrast, fibronectin, collagen, gelatin and albumin did not bind PAI-1. Thus, PAI-1 in analogy with alpha-2 plasmin inhibitor may modulate physiological fibrinolysis through incorporation into fibrin.
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Li, Xuhui, and Mengchi Liu. "Query XML Documents Using XTQ Language." In 2008 IEEE International Workshop on Semantic Computing and Systems (WSCS). IEEE, 2008. http://dx.doi.org/10.1109/wscs.2008.26.

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Vanessa, Armel, Clemente Jacky, Jeremy Hyvert, Godon Aurelie, Peres Jean Paul, Remy Stephane, and Borthomieu Yannick. "MP XLR battery range for constellation." In 2019 European Space Power Conference (ESPC). IEEE, 2019. http://dx.doi.org/10.1109/espc.2019.8932000.

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Wood, K. S. "The X-ray large array (XLA)." In High−Energy Astrophysics in the 21st Century. AIP, 1990. http://dx.doi.org/10.1063/1.39659.

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Levchenko, Kirill, Geoffrey M. Voelker, Ramamohan Paturi, and Stefan Savage. "Xl." In the ACM SIGCOMM 2008 conference. New York, New York, USA: ACM Press, 2008. http://dx.doi.org/10.1145/1402958.1402962.

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Reports on the topic "XLQ"

1

Tremaine, Aaron. XL5 Klystron. Office of Scientific and Technical Information (OSTI), December 2014. http://dx.doi.org/10.2172/1165898.

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Bozoki, E., and H. Halama. Ion related problems for the XLS ring. Office of Scientific and Technical Information (OSTI), July 1989. http://dx.doi.org/10.2172/5606165.

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Tremaine, Aaron. XL4 Klystron (Top level drawing AD-700-924-00). Office of Scientific and Technical Information (OSTI), December 2014. http://dx.doi.org/10.2172/1165899.

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Coates, B. The Xl Deposit. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1991. http://dx.doi.org/10.4095/132322.

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Blumberg, L., ed. Superconducting x-ray lithography source Phase 1 (XLS) safety analysis report. Office of Scientific and Technical Information (OSTI), July 1990. http://dx.doi.org/10.2172/6609783.

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Hunt, G. BT's eXtended Network Quality RTP Control Protocol Extended Reports (RTCP XR XNQ). RFC Editor, December 2007. http://dx.doi.org/10.17487/rfc5093.

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Simpkins, A. A. VENTSAR XL User`s Manual. Office of Scientific and Technical Information (OSTI), May 1996. http://dx.doi.org/10.2172/401725.

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Duewer, David L., Sam A. Margolis, Katherine E. Sharpless, Jeanice B. Thomas, and Margaret C. Kline. NIST micronutrients measurement quality assurance program winter, spring, and fall 1997 comparability studies : results for round robin XXXIX, XL, and XLI fat-soluble vitamins and carotenoids in human serum and round robin 10 ascorbic acid in human serum. National Institute of Standards and Technology, July 2013. http://dx.doi.org/10.6028/nist.ir.7880-27.

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Simpkins, A. A. Verification of VENTSAR XL - a spreadsheet version of VENTSAR. Office of Scientific and Technical Information (OSTI), May 1996. http://dx.doi.org/10.2172/405720.

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Tremaine, Aaron. XL Magnet (Top level drawing SA-700-897-10). Office of Scientific and Technical Information (OSTI), December 2014. http://dx.doi.org/10.2172/1165897.

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