Dissertations / Theses on the topic 'GRP'
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Fox, David M. "Bolted joint studies in GRP." Thesis, Monterey, California. Naval Postgraduate School, 1994. http://hdl.handle.net/10945/25716.
Full textFox, David M. (David Michael). "Bolted joint studies in GRP." Thesis, Massachusetts Institute of Technology, 1994. http://hdl.handle.net/1721.1/37524.
Full textVita.
Includes bibliographical references (leaves ).
by David M. Fox.
M.S.
Nav.E.
McKillop, Jane Marie. "Studies with GRP and related peptides." Thesis, Queen's University Belfast, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.356949.
Full textHoffman, Timothy Joseph. "GRP receptor specific analogues of bombesin /." free to MU campus, to others for purchase, 1996. http://wwwlib.umi.com/cr/mo/fullcit?p9924958.
Full textFlaherty, Annette E. "Support of GRP vessels : a comparative study for the horizontal support of laminate construction GRP storage vessels." Thesis, University of Strathclyde, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.366892.
Full textHartshorn, Robert T. "The mechanical behaviour of cylindrical GRP panels." Thesis, Aston University, 1987. http://publications.aston.ac.uk/11895/.
Full textAfifi, Amal Afifi Mohamed. "Buckling of stiffened pultruded GRP plates and columns." Thesis, Lancaster University, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.497222.
Full textVelecela, Chuquilla Orlando Jonathan. "Energy absorption capability of GRP composite sandwich structures." Thesis, University of Sheffield, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.434504.
Full textCharlesworth, Amanda. "Signalling pathways mediated by the bombesin/GRP receptor." Thesis, University College London (University of London), 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.244267.
Full textEngstrand, Andreas. "Railway surveying - A case study of the GRP 5000." Thesis, KTH, Geoinformatik och Geodesi, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-31747.
Full textWang, Pu. "Structural integrity of bolted joints for pultruded GRP profiles." Thesis, Lancaster University, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.429955.
Full textFurniss, Jonathan P. "Testing and evaluation of GRP rockbolts for tunnel reinforcement." Thesis, University of Nottingham, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.395497.
Full textPrice, J. N. "The propagation of stress corrosion cracks in aligned GRP." Thesis, University of Liverpool, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.372730.
Full textEksik, Ömer. "Structural performance of GRP top hat stiffened marine structures." Thesis, University of Southampton, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.431952.
Full textChen, Fangping. "Study of blister formation in GRP laminates in water." Thesis, Loughborough University, 1989. https://dspace.lboro.ac.uk/2134/33055.
Full textLutz, Cyprien. "Structural integrity of bolted joints for pultruded GRP profiles." Thesis, University of Warwick, 2004. http://wrap.warwick.ac.uk/110311/.
Full textGray, Joseph. "The design, synthesis and biochemical application of bombesin/grp analogues." Thesis, Queen's University Belfast, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317440.
Full textAl-Rawe, Auday. "Design methodology for optimising the performance of underground GRP tanks." Thesis, Nottingham Trent University, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.263388.
Full textCornélio, Daniela Baumann. "Neuropeptídeos GRP e BDNF como alvos moleculares em neoplasias femininas." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2012. http://hdl.handle.net/10183/72309.
Full textNeuropeptide and neurotrophin receptors are increasingly important molecular targets in cancer. Growth factors as the gastrin-releasing peptide (GRP) and brain-derived neurotrophic factor (BDNF) are involved in cell proliferation and cancer progression, enhancing local invasion, angiogenesis, distant metastasis and apoptosis. The GRP receptor has been identified in many human malignancies, but no information regarding its expression in cervical cancer was found in the literature. Considering that cervical cancer is a very important cause of morbidity and mortality worldwide, we aimed to evaluate the GRPR expression profile in preinvasive and invasive cervical lesions. Our initial study demonstrated for the first time the aberrant GRPR expression in human cervical dysplasia and cancer, raising the hypothesis that GRPR could be implicated in the carcinogenic process of cervical tumors. To further exploit GRPR as a biomarker, in our second study we aimed to evaluate the diagnostic potential of GRPR immunocytochemistry in detecting cervical dysplasia and invasive cancer. This was the first immunocytochemical evaluation of GRPR expression in cervical epithelial cells. This receptor was strongly associated with cervical dysplasia and invasive cancers. Additionally, GRPR immunosignaling showed high accuracy in detecting dysplasias in cells classified as atypical squamous cells of undetermined significance (ASCUS). Based on these results, we concluded that immunocytochemistry for GRPR may be regarded as a valuable method for early detection of cervical intraepithelial neoplasia. Previous studies have indicated that compounds that act by blocking gastrin-releasing peptide receptors (GRPR) or tropomyosin receptor kinase B (TrkB) receptors can display antiproliferative activities against cancer cells. Here we show that GRPR activation can reduce, whereas its blockade can increase, the viability of breast, ovarian, and cervical cancer cell lines. In addition, we demonstrate that TrkB inhibition reduces the viability of these cells and BDNF increases the viability of ovarian cells. The results support the view that GRPR and BDNF/TrkB signaling regulate cancer cell viability. Most importantly, the findings provide the first evidence that, under certain conditions, GRPR activation can inhibit, rather than stimulate, breast, ovarian and cervical cancer cells.
Wahono, A. R. "Response of GRP sandwich panels to quasi-static and blast pressure." Thesis, University of Manchester, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.488320.
Full textBarber, Simon. "Industrial mediation in jazz production : A case study of GRP records." Thesis, University of Liverpool, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.511095.
Full textVarnam, Steven Michael. "Local loads on attachments and nozzles to GRP cylinders of varying thickness." Thesis, University of Manchester, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.320762.
Full textFrånlund, Ebba. "Exon sequencing of the gene encoding UCMA/GRP in healthy and clinical subjects." Thesis, Linköpings universitet, Institutionen för fysik, kemi och biologi, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-68647.
Full textJaved, Muhammad Afzal. "Stability analysis of P.F.R.P. box-sections." Thesis, University of Newcastle upon Tyne, 2003. http://hdl.handle.net/10443/3623.
Full textZhang, Xiangping. "Characterization of filament wound GRP pipes under lateral quasi-static and low velocity impact loads." Thesis, University of Aberdeen, 1998. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU551705.
Full textAbd, El-Galiel Wael Refat. "Studies on radiometal chelator-bombesin peptide-based radiopharmaceuticals for tumor GRP-receptor substype mediated radioimaging." Diss., Columbia, Mo. : University of Missouri-Columbia, 2007. http://hdl.handle.net/10355/5962.
Full textThe entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. Title from title screen of research.pdf file (viewed on March 12, 2009) Includes bibliographical references.
Carturan, Federico. "Seismic Risk Analysis of Revenue Losses, Gross Regional Product and transportation systems." Doctoral thesis, Università degli studi di Padova, 2013. http://hdl.handle.net/11577/3423071.
Full textGli eventi naturali quali terremoti, uragani, tsunami causano importanti impatti negativi nelle comunità. Gli eventi accaduti in passato, come il terremoto di Loma Prieta del 1989 o i più recenti eventi sismici come L’Aquila 2009 o Emilia Romagna 2012, hanno evidenziato la necessità e l’importanza di un’attiva preparazione pre-evento e la consapevolezza che sia necessario ridurre le conseguenze negative indotte da tali eventi. In tale ambito si inserisce l’attività di ricerca, focalizzandosi in particolar modo sulle conseguenze che eventi sismici hanno nel prodotto interno lordo della regione colpita. Nella letteratura scientifica non sono stati definiti scenari di scuotimento sismico ad uso ingegneristico in Italia. Il dipartimento di Protezione Civile ha pubblicato le mappe di pericolosità sismica, che sono state ricavate con analisi Probabilistic Seismic Hazard Analsys, tuttavia tali mappe non permettono la puntuale valutazione dei singoli scenari sismici che contribuiscono alla pericolosità. Risulta interessante, inoltre, determinare quali siano le conseguenze degli eventi sismici nei sistemi produttivi e quale sia il loro impatto nella riduzione del prodotto interno lordo. Infine, la riduzione di produttività nel sistema delle attività risulta legata alla presenza di un efficiente sistema dei trasporti. Il sistema dei trasporti viene danneggiato dall’evento sismico, pertanto è necessario determinare la relazione esistente tra questo ed il sistema produttivo. Inoltre, per effettuare analisi economiche di tipo Benefici-Costi è necessario sviluppare modelli di recupero e simulare gli effetti di aiuti statali nel processo di ricostruzione. Lo scopo della ricerca è stato pertanto la costruzione di scenari sismici utilizzando un approccio ingegneristico, tali scenari sono stati poi utilizzati per valutare le conseguenze economiche nelle regioni colpite da terremoto e l’interazione tra il sistema dei trasporti e quello produttivo. Per promuovere la consapevolezza degli effetti prodotti da un terremoto in una comunità intesa come un insieme unitario, è stata proposta una metodologia per lo sviluppo di scenari sismici. Tali scenari sono stati impiegati per valutare i danni agli edifici produttivi e ai ponti presenti nella rete di trasporto. La metodologia così sviluppata è stata applicata ad una regione test, l’area della città di Treviso nel Nord-Est d’Italia. Partendo dalle sorgenti sismogenetiche descritte nel progetto Zone Sismiche 9, impiegando la relazione di attenuazione di Sabetta e Pugliese del 1996 assieme al modello di occorrenza Gutenberg Ricther sono stati generati 8000 scenari sismici. Tale numero è stato ridotto tramite una procedura proposta per la rappresentazione della curva di pericolosità in corrispondenza di ogni singola posizione. Utilizzando il metodo di Montecarlo per il campionamento statistico della fragilità di edifici e di ponti sono state generati gli scenari di danno sismico ai sistemi produttivi ed alle infrastrutture di trasporto. Il rischio indotto dagli eventi sismici è stato poi calcolato e rappresentato tramite la curva di rischio del sistema. Nel corso del lavoro di ricerca sono stati proposti modelli innovativi per quanto riguarda il comportamento delle attività produttive successivamente ai danni causati da terremoti, un modello innovativo per descrivere il processo di ricostruzione degli edifici e quindi il recupero della produttività. Un ulteriore prodotto innovativo è la relazione tra il sistema produttivo e le infrastrutture di trasporto. I risultati ottenuti possono così essere riassunti: una procedura innovativa per la generazione di scenari sismici partendo dalla descrizione delle zone ad attività sismica, di utilizzo ingegneristico. Tale procedura può essere generalizzata per l’applicazione ad altre realtà. Un insieme di scenari di scuotimento sismico compatibili con la descrizione della pericolosità di sito è stata presentata per la prima volta Italia. Un modello innovativo per la valutazione della funzionalità post-evento in relazione alla fragilità degli edifici è stato proposto. Un innovativo modello per rappresentare il processo di ricostruzione post-terremoto è stato presentato per la prima volta. Sono stati esplorati gli effetti degli aiuti finanziari erogati dalle istituzioni. E’ stata valutata la relazione tra il sistema produttivo ed il sistema di trasporto.
Francl, Jessica M. "Regulation of neuropeptide release in the SCN circadian clock: in vivo assessments of NPY, VIP, and GRP." Kent State University / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=kent1289328898.
Full textHeierli, Daniel. "Gefässspezifische Expression des Bohnengens grp 1.8 : modularer Aufbau des Promotors und Charakterisierung des bZIP-Proteins VSF-1 /." [S.l.] : [s.n.], 1993. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=10337.
Full textZiv, Michael. "A study of the behavior of the GRP hat-stiffened panel bondline under high strain rate loading." Thesis, Monterey, California. Naval Postgraduate School, 1995. http://hdl.handle.net/10945/26270.
Full textShah, Syed Iftikhar Hussain, and Syed Hassan Shaheed. "PERFORMANCE EVALUATION OF MANET ROUTING PROTOCOLS." Thesis, Blekinge Tekniska Högskola, Sektionen för datavetenskap och kommunikation, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:bth-1101.
Full textCzepielewski, Rafael Sanguinetti. "Investiga??o dos efeitos do pept?deo liberador de gastrina (GRP) e seu antagonista RC-3095 em c?lulas mieloides." Pontif?cia Universidade Cat?lica do Rio Grande do Sul, 2016. http://tede2.pucrs.br/tede2/handle/tede/7588.
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Tumor microenvironment and inflammatory diseases promote alterations in our immune system along with their development. Several molecules are implicated in this modulation and are therefore considered therapeutic targets. Gastrin-releasing peptide (GRP) is produced in tumors where it promotes cellular proliferation. It is also correlated with chronic diseases, as in rheumatoid arthritis and asthma, and in the acute condition of sepsis. Recently, our group found a direct GRP action over neutrophils, promoting migration. This work aimed to study the interface between GRP-producing tumors and the recruitment of immune cells, as well as extend the cellular studies about neutrophil activation and migration processes promoted by the peptide. In tumors, we observed that a lung adenocarcinoma cell line does not proliferate in response to GRP. Yet, it is induced to migrate when exposed to the peptide, indicating a potential role for GRP in metastasis of this type of cancer. In our tumor immunology studies, we established a novel in vivo model by overexpressing GRP in a melanoma cell line (B16F10). We observed the augment of infiltrating inflammatory monocytes in the tumor microenvironment of these tumors. In parallel, we verified that reactive oxygen species production and migration in response to GRP is dependent of the NADPH oxidase complex. GRP stimulation promotes an intense activation, which culminates in neutrophil extracellular traps (NETs) release. In addition, the GRP receptor (GRPR) antagonist RC-3095 presented anti-inflammatory potential, inhibiting neutrophil migration towards IL-8 and reducing the extent of acetaminophen-induced liver damage. This effect was due to motility alterations in infiltrating neutrophils within the tissue and reduction of cell adhesion molecules. The results presented herein demonstrate the wide panorama of GRP?s interactions in tumor and immune biology.
O microambiente tumoral e as doen?as inflamat?rias promovem altera??es nas c?lulas do nosso sistema imune ? medida que progridem. Diversas mol?culas est?o envolvidas nessa modula??o, e por isso s?o alvos terap?uticos. O pept?deo liberador de gastrina (GRP) ? produzido por tumores, onde promove prolifera??o celular. Este tamb?m est? correlacionado com doen?as cr?nicas como a artrite reumatoide e asma, e em doen?as agudas, como a sepse. Recentemente, nosso grupo descobriu a??o direta do GRP em neutr?filos, promovendo indu??o de migra??o. O presente trabalho se prop?s a estudar a interface entre tumores produtores de GRP e o recrutamento celular, assim como aprofundar os estudos celulares sobre os processos de ativa??o e migra??o de neutr?filos promovidos pelo pept?deo. Em tumores, observamos que uma linhagem de adenocarcinoma pulmonar n?o prolifera quando exposto ao GRP, por?m ? induzida a migrar quando exposta ao pept?deo, estabelecendo um potencial papel deste na promo??o de met?stases para esse tipo tumoral. Na interface da imunologia tumoral, atrav?s do desenvolvimento de um modelo in vivo de superexpress?o de GRP em melanoma murino (B16F10), observamos que esse aumento do GRP induz a infiltra??o de mon?citos inflamat?rios no microambiente tumoral. Em paralelo, verificamos que a produ??o de esp?cies reativas de oxig?nio e a migra??o em dire??o ao GRP s?o dependentes do complexo NADPH oxidase. Esse est?mulo promove ativa??o intensa, culminando na produ??o de redes extracelulares de neutr?filos (NETs). J? o antagonista do seu receptor, GRPR, apresentou potencial antiinflamat?rio, sendo capaz de inibir a migra??o neutrof?lica via modula??o de IL-8 e reduzindo a extens?o da les?o hep?tica induzida por paracetamol (acetaminofeno), alterando a motilidade dos neutr?filos no tecido e a express?o de mol?culas de ades?o. Assim, os resultados aqui apresentados demonstram um panorama amplo da fun??o do GRP na biologia tumoral e no sistema imune.
Hajjaj, Bouchra. "Conception, synthèse et évaluation biologique d’antagonistes de la bombésine pour la visualisation de cancers par imagerie médicale." Thesis, Montpellier 1, 2013. http://www.theses.fr/2013MON13517.
Full textThe abundant expression of the GRP receptor in many frequently occurring cancers that inflict humans provides the opportunity to use radiolabeled bombesin analogs for their diagnosis and treatment. This postgraduate work is dedicated to the design, synthesis and biological evaluation of new radiopharmaceuticals. These are made up of a GRP receptor antagonist, a spacer and the cyclic metal chelating agent DOTA. We first determined the spacer length which has optimal biological properties. Moving forward from this study, different radio-ligands containing new bombesin antagonists have been synthesized and biologically evaluated. Those antagonists are based on compound JMV 594, a powerful bombesin antagonist synthesized in our laboratory. Besides modifications of this peptide also dimers have been made to obtain more stable bombesin antagonist with more affinity to the GRP receptor
Kleinspehn, Edgar Verfasser], and Eike Sebastian [Akademischer Betreuer] [Debus. "Kombinatorische Anwendung von TRH und GRP in einem humanen in-vitro-Wundheilungsmodell / Edgar Kleinspehn ; Betreuer: E. Sebastian Debus." Hamburg : Staats- und Universitätsbibliothek Hamburg, 2016. http://d-nb.info/1121783074/34.
Full textChile, Thais. "Análise da expressão dos genes CRABP1, CRABP2, GRP e RERG em adenomas hipofisários funcionantes e clinicamente não funcionantes." Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/5/5135/tde-05032010-171210/.
Full textPituitary tumors account for approximately 10%-15% of the intracranial neoplasms. Although the pathogenesis is not fully characterized, many molecular mechanisms involved in pituitary tumorigenesis have been unraveled. Using the methodology of cDNA microarray containing approximately 20000 genes, our group recently compared the expression of two distinct conditions: a pool of four clinically nonfunctioning pituitary adenomas and a spinal cord metastasis of a nonfunctioning pituitary carcinoma. Several genes were shown to be differentially expressed, among them, CRABP1 (cellular retinoic acid binding protein 1), CRABP2 (cellular retinoic acid binding protein 2), GRP (gastrin-releasing peptide) and RERG (RAS-like, estrogen-regulated, growth inhibitor). This study aimed to evaluate the expression of these four genes in a series of 59 pituitary adenomas (30 nonfunctioning, 13 GH-secreting, 8 ACTH-secreting and 8 PRL-secreting adenomas), comparing each tumor group with a set of normal pituitary tissues. While PRL-secreting adenomas showed lower expression of CRABP1 and CRABP2 mRNA when compared with normal tissues, GH-secreting adenomas had only lower expression of CRABP2 mRNA. Clinically nonfunctioning adenomas showed lower expression of GRP mRNA and higher expression of RERG mRNA when compared with the normal pituitary glands. Therefore, it was observed that not only the CRABP1 gene but also the CRABP2, GRP and RERG genes showed differences in transcript expression between the groups of pituitary adenomas. However, their role in pituitary tumorigenesis remains to be investigated.
Jaeger, Natália. "Investigação do efeito proliferativo e migratório do peptídeo liberador de gastrina (GRP) sobre uma linhagem de adenocarcinoma pulmonar." Pontifícia Universidade Católica do Rio Grande do Sul, 2014. http://hdl.handle.net/10923/6965.
Full textLung cancer is the most commonly diagnosed type of cancer and the leading cause of cancer related mortality in the world, causing nearly one million deaths per year. Among all histological types, adenocarcinoma is the most frequent one (75-80%). Gastrin-releasing peptide (GRP) is considered to be a mitogen, capable of inducing cell proliferation, since it is involved in fetal lung development. This neuropeptide had its effect on tumor growth first identified in human cells of small cell lung cancer, acting as an autocrine growth factor for tumor tissues by binding to its receptor GRPR. The receptor has been found in many tumor types such as prostate, breast, stomach, pancreas and colon. Moreover, this peptide acts as a morphogen, in angiogenesis and is related to inflammatory processes and in the regulation of cells of the immune system. Furthermore, asymptomatic smokers have high levels of GRP in bronchoalveolar lavage and urine. However, little is known about its effects in tumorigenesis and metastasis, and which molecular mechanisms and signaling pathways are responsible for the effects found. Our group demonstrated recently that GRP could act as a chemotactic molecule for neutrophils. Thus, we hypothesized that GRP could be also a chemotactic stimulus to tumor cells expressing the GRPR. In this study, we tested this hypothesis by examining the effect of GRP on proliferation, survival and migration of cells from the adenocarcinoma cell line A549, seeking to identify the mechanisms of action of this peptide. These cells express high levels of GRPR and treatment with GRP leads to activation of kinases such as AKT and ERK1/2 that are involved in the cellular processes mentioned. Our results suggest that GRP is a migratory stimulus to these cells without evidence of significant effect on their proliferation or survival to treatment with the chemotherapy drug cisplatin (CDDP). Nonetheless, they become more sensitive to CDDP when the drug is combined with a GRPR antagonist. Thus, we believe that future studies should consider a possible role for GRP in metastasis of NSCLC.
O câncer de pulmão é o tipo de câncer que mais comumente diagnosticado e o que mais mata no mundo levando a quase 1 milhão de mortes por ano. Entre todos os tipos histológicos, o adenocarcinoma é o mais frequente (75-80%). O peptídeo liberador de gastrina (GRP) é considerado um agente mitogênico, capaz de induzir a proliferação celular, uma vez que está envolvido no desenvolvimento fetal dos pulmões. Este peptídeo teve sua ação sobre o crescimento tumoral primeiramente identificada em células humanas de câncer de pulmão de pequenas células, atuando como fator autócrino de crescimento de tecidos e tumores através da ligação ao seu receptor GRPR. Este receptor foi encontrado em diversos tipos de tumores como próstata, mama, estômago, pâncreas e cólon. Além disso, este peptídeo atua como um morfógeno, na angiogênese e, está relacionado a processos inflamatórios e na regulação de células do sistema imune. E, fumantes assintomáticos possuem altos níveis de GRP no lavado broncoalveolar e na urina. No entanto, pouco se conhece sobre os seus efeitos na tumorigênese e metástase e, quais os mecanismos moleculares e as vias de sinalização que são responsáveis pelos efeitos encontrados. Nosso grupo demonstrou, recentemente, que o GRP pode atuar como uma molécula quimiotática para neutrófilos. Desta forma, hipotetizamos que o GRP poderia constituir num estimulo quimiotático também para as células tumorais que expressão o GRPR. Neste trabalho, testamos essa hipótese, analisando o efeito do GRP sobre a proliferação, sobrevivência e migração de células da linhagem de adenocarcinoma A549, buscando identificar mecanismos de ação desse peptídeo. Esta linhagem expressa altos níveis de GRPR.O tratamento com GRP leva a ativação de quinases como a AKT e ERK1/2 que estão envolvidas nestes processos celulares. Nossos resultados sugerem que o GRP é principalmente um estímulo migratório para estas células, sem evidências de efeito significativo sobre a sua proliferação ou sobrevivência ao tratamento com a droga quimioterápica cisplatina, mas tornam-se mais sensíveis quando a droga é combinada com um antagonista do GRPR. Dessa forma, acreditamos que estudos futuros devam considerar um possível papel para o GRP na metástase.
Wei, Lixia. "Development of a Novel Protein Based MRI Contrast Agent for Molecular Imaging of Prostate Cancer." Digital Archive @ GSU, 2010. http://digitalarchive.gsu.edu/biology_diss/75.
Full textFilali, Bilal. "Caractérisation des ondes radar de surface par la simulation numérique et les mesures GRP pour l'auscultation en génie civil." Thèse, Université de Sherbrooke, 2014. http://hdl.handle.net/11143/6635.
Full textOliveira, Sílvia Helena Soares. "Mecanismos moleculares envolvidos na ação modulatória do receptor GRP sobre a consolidação da memória na área Ca1 do hipocampo." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2006. http://hdl.handle.net/10183/17318.
Full textGastrin-releasing peptide (GRP), a bombesin-like peptide, and their receptors are gifts in all the central nervous system, particular in cerebral limbic areas as hippocampus and amigdala, which are involved in an important way in the emotional regulation, cognitive function and neurodegenerative and neuropsychiatric disorders. Studies suggest that GRPR can act in synaptic plasticity regulation, emotional answers and memory formation. Although this, this system has been relatively little studied how much its paper in the cerebral function and the involved cellular mechanisms in the transdução of signal are not known activated for receivers GRP in the nervous system. Studies in other cell types suggest that activation of GRPR can active signal transduction pathways mediated by protein cinase C (protein kinase C, PKC) and mitogen-activated protein kinase (MAPK). The envolvement of protein kinase A (PKA) pathways are controversial. Already it is established that PKC, MAPK and PKA signal pathways are involved of crucial form in emotional memory formation in CA1 area of dorsal hippocampus. Thus, it is possible that the activation of GRPR modulates the memory through the activation of one or more than these ways. In present study, we propose an pharmacological investigation, using an established emotional memory model in rodents, to analyze the interactions between GRPRs and the biological events following to the receptores activation in other words, the neuronal sign cascades activation mediated by proteins kinases, in CA1 hippocampus area. Male Wistar rats received bilateral infusions of the GRPR agonist bombesin into the dorsal hippocampus immediately after inhibitory avoidance training. Intermediate doses of bombesin enhanced, whereas a higher doses impaired 24-h memory retention. The bombesin-induced memory enhancement was prefented by pretraining infusions of a GRPR antagonist or inhibitors of PKC, MAPK and PKA, but not a neuromedin B (NMB) antagonist. We conclude that memory modulation by hippocampal GRPRs is mediated by the PKC, MAPK and PKA pathways.
Giacchetti, Sylvie. "Facteurs de croissance et cancers du sein : étude du récepteur à la bombesine-GRP (Gastrin Releasing Peptide) in vitro." Paris 6, 1990. http://www.theses.fr/1990PA062036.
Full textTsai, Liren. "SHOCK WAVE STRUCTURE AND SPALL STRENGTH OF LAYERED HETEROGENEOUS GLASS/POLYMER COMPOSITE." Case Western Reserve University School of Graduate Studies / OhioLINK, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=case1138377998.
Full textJaeger, Nat?lia. "Investiga??o do efeito proliferativo e migrat?rio do pept?deo liberador de gastrina (GRP) sobre uma linhagem de adenocarcinoma pulmonar." Pontif?cia Universidade Cat?lica do Rio Grande do Sul, 2014. http://tede2.pucrs.br/tede2/handle/tede/5511.
Full textLung cancer is the most commonly diagnosed type of cancer and the leading cause of cancer related mortality in the world, causing nearly one million deaths per year. Among all histological types, adenocarcinoma is the most frequent one (75-80%). Gastrin-releasing peptide (GRP) is considered to be a mitogen, capable of inducing cell proliferation, since it is involved in fetal lung development. This neuropeptide had its effect on tumor growth first identified in human cells of small cell lung cancer, acting as an autocrine growth factor for tumor tissues by binding to its receptor GRPR. The receptor has been found in many tumor types such as prostate, breast, stomach, pancreas and colon. Moreover, this peptide acts as a morphogen, in angiogenesis and is related to inflammatory processes and in the regulation of cells of the immune system. Furthermore, asymptomatic smokers have high levels of GRP in bronchoalveolar lavage and urine. However, little is known about its effects in tumorigenesis and metastasis, and which molecular mechanisms and signaling pathways are responsible for the effects found. Our group demonstrated recently that GRP could act as a chemotactic molecule for neutrophils. Thus, we hypothesized that GRP could be also a chemotactic stimulus to tumor cells expressing the GRPR. In this study, we tested this hypothesis by examining the effect of GRP on proliferation, survival and migration of cells from the adenocarcinoma cell line A549, seeking to identify the mechanisms of action of this peptide. These cells express high levels of GRPR and treatment with GRP leads to activation of kinases such as AKT and ERK1/2 that are involved in the cellular processes mentioned. Our results suggest that GRP is a migratory stimulus to these cells without evidence of significant effect on their proliferation or survival to treatment with the chemotherapy drug cisplatin (CDDP). Nonetheless, they become more sensitive to CDDP when the drug is combined with a GRPR antagonist. Thus, we believe that future studies should consider a possible role for GRP in metastasis of NSCLC.
O c?ncer de pulm?o ? o tipo de c?ncer que mais comumente diagnosticado e o que mais mata no mundo levando a quase 1 milh?o de mortes por ano. Entre todos os tipos histol?gicos, o adenocarcinoma ? o mais frequente (75-80%). O pept?deo liberador de gastrina (GRP) ? considerado um agente mitog?nico, capaz de induzir a prolifera??o celular, uma vez que est? envolvido no desenvolvimento fetal dos pulm?es. Este pept?deo teve sua a??o sobre o crescimento tumoral primeiramente identificada em c?lulas humanas de c?ncer de pulm?o de pequenas c?lulas, atuando como fator aut?crino de crescimento de tecidos e tumores atrav?s da liga??o ao seu receptor GRPR. Este receptor foi encontrado em diversos tipos de tumores como pr?stata, mama, est?mago, p?ncreas e c?lon. Al?m disso, este pept?deo atua como um morf?geno, na angiog?nese e, est? relacionado a processos inflamat?rios e na regula??o de c?lulas do sistema imune. E, fumantes assintom?ticos possuem altos n?veis de GRP no lavado broncoalveolar e na urina. No entanto, pouco se conhece sobre os seus efeitos na tumorig?nese e met?stase e, quais os mecanismos moleculares e as vias de sinaliza??o que s?o respons?veis pelos efeitos encontrados. Nosso grupo demonstrou, recentemente, que o GRP pode atuar como uma mol?cula quimiot?tica para neutr?filos. Desta forma, hipotetizamos que o GRP poderia constituir num estimulo quimiot?tico tamb?m para as c?lulas tumorais que express?o o GRPR. Neste trabalho, testamos essa hip?tese, analisando o efeito do GRP sobre a prolifera??o, sobreviv?ncia e migra??o de c?lulas da linhagem de adenocarcinoma A549, buscando identificar mecanismos de a??o desse pept?deo. Esta linhagem expressa altos n?veis de GRPR. O tratamento com GRP leva a ativa??o de quinases como a AKT e ERK1/2 que est?o envolvidas nestes processos celulares. Nossos resultados sugerem que o GRP ? principalmente um est?mulo migrat?rio para estas c?lulas, sem evid?ncias de efeito significativo sobre a sua prolifera??o ou sobreviv?ncia ao tratamento com a droga quimioter?pica cisplatina, mas tornam-se mais sens?veis quando a droga ? combinada com um antagonista do GRPR. Dessa forma, acreditamos que estudos futuros devam considerar um poss?vel papel para o GRP na met?stase.
Cruz, Luciane Beitler da. "Efeitos do antagonista dos receptores Gastrin-Releasing Peptide (GRP) sobre peso, alimentação, parâmetros metabólicos, bioquímicos e composição corporal de ratos wistar." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2014. http://hdl.handle.net/10183/110313.
Full textIntroduction and Objective: Gastrin-releasing peptide (GRP) is involved in several brain and gastrointestinal functions, including pancreatic secretion, gastrointestinal peptide hormone release, and reduction of food intake. We tested the effects of an intraperitoneal injection of the GRP receptor (GRPR) antagonist RC-3095 on weight, food intake, biochemical metabolic parameters, and body composition. Methods: Thirty-five young adult male Wistar rats, submitted to a minimal weight loss of 7%, were divided into four groups: the control group (G0) received saline; Group 1 (G1) received 0.1 mg/kg RC-3095; Group 2 (G2) received 0.3 mg/kg RC-3095; and Group 3 (G3) received 1.0 mg/kg RC-3095 for 14 days. Results: The mean daily variation of food intake was statistically different between the groups (F: 3.139; df: 3; P = 0.039); and G2, which received the intermediate dose of 0.3 mg/kg RC-3095, showed a greater food intake than G0 (P = 0.041). There was a similar increase in weight, approximately 22% (F: 0.572; df: 3; P = 0.638), as well as a similar mean animal weight (F: 1.145; df: 9.685; P = 0.338) between the groups during the study period. However, the mean weight of G2 animals was more than the mean weight of G0 animals (P = 0.042). At the end of the study, no difference was observed between the groups in terms of the total lean mass or fat mass from the rat carcass, liver, and skin. Comparing the serum levels of albumin, amylase, glucose, total cholesterol, high-density lipoprotein (HDL) cholesterol, and interleukin (IL)-6 from day 1 (D1) to D14, there were no statistically relevant differences between the groups. However, the mean triglyceride level in G2 compared to G0 showed a greater increase (P = 0.038). Conclusion: In this study, the injection of an intermediate dose of GRPR antagonist RC- 3095 (0.3 mg/kg/day) into healthy young adult Wistar rats submitted to weight loss affected food intake and the mean weight. No effects on weight gain, body composition, or biochemical metabolic parameters were observed, except for a great increase in the serum triglyceride levels. These results demonstrate some physiological effects of GRP on food intake and weight, expanding the possibilities of future studies on hunger/satiety and macronutrient metabolism as well as highly stressful conditions like cancer.
Elder, David James, and d. elder@crc-acs com au. "Optimisation of parametric equations for shock transmission through surface ships from underwater explosions." RMIT University. Aerospace, Mechanical and Manufacturing Engineering, 2006. http://adt.lib.rmit.edu.au/adt/public/adt-VIT20080212.105012.
Full textAlibabaei, Navid. "Wireless Mesh Networks: a comparative study of Ad-Hoc routing protocols toward more efficient routing." Thesis, Blekinge Tekniska Högskola, Institutionen för kommunikationssystem, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:bth-1023.
Full textZahir, Aishath Zehereen. "Degradation of e-glass fibre in selected organic acids." Thesis, Curtin University, 2008. http://hdl.handle.net/20.500.11937/1654.
Full textGhazanfar, Katrina. "BIOINFORMATIC ANALYSIS OF A MAMMALIAN BIP GENE FOR INSERTION INTO GREEN ALGAE AND COMPARISON OF ITS POSSIBLE EFFECTS ON THE SYNTHESIS OF A MAMMALIAN ANTIBODY." VCU Scholars Compass, 2004. http://scholarscompass.vcu.edu/etd/36.
Full textZahir, Aishath Zehereen. "Degradation of e-glass fibre in selected organic acids." Curtin University of Technology, Department of Applied Chemistry, 2008. http://espace.library.curtin.edu.au:80/R/?func=dbin-jump-full&object_id=128425.
Full textExcept for the last section of the research (analysis using a kinetic approach) where glass fibre was cut out to weigh approximately 1.0g, standard sized specimens were soaked in the required acid solutions of desired concentrations for varying temperatures and time frames. Wherever tensile strength retention was measured, LLOYD instrument was employed. Leaching of the cations were analysed using Inductively Coupled Plasma – Optical Emission Spectroscopy (ICP-OES and also know and ICP-AES).
The scope of this project can be divided in to four sections; first section involved investigating the effects of malonic acid. The study of malonic acid was narrowed to investigating the trend in strength retention. A rapid strength loss was observed initially followed by a much steady decline in the strength. However the continuation of the loss of strength was unmistakable throughout the time period of exposure. Furthermore, temperature can be observed as a facilitating factor in this degradation reaction.
Secondly the corrosive effect of glyoxylic acid on E-glass fibre was studied. This was explored at two different temperatures for two specific time frames using various concentrations of the acid of interest. The influence of this acid on the glass fibre was found out in terms of strength retention and loss of cations from the glass matrix. The mildness of this acid was accentuated by the fact that 70% or more of the strength was retained at all the conditions employed. A minima in strength retention was observed at 2M acid concentration similar to the trends observed in the past (Betz and Jones 2003 and Jones and Chandler 1986). Leaching of cations reflected this trend. The large strength retention could be related to the fewer amounts of Ca and K leached from the glass matrix (Kumosa and Qui, 1997). Similar to malonic acid, an unusually large amount of B was leached out that could be due to the favourable orientation of the anion with the trivalent ions during the complex formation. Yet again temperature was found to enhance the degradation process.
Next the extent of passivation (if any) showed by malonic acid was investigated using E-glass fibre pre-treated in 5M malonic acid and post treated in known corrosive acids hydrochloric acid and oxalic acid. Passivation of malonic acid was put to test through examination of strength retention of the fibres under these conditions. This segment was carried out as an extension of a finding (a behaviour synonymous to passivation) shown by malonic that surfaced the previous year by the present researcher. Increasing the pre-treatment time showed a great improvement in the retained strength for all the post-treatment acid mediums. Furthermore, while Jones and Betz (2004) featured 20-40% strength retention within a short time frame in 3M HCl, the immense amount of strength retention (60-70%) preceding pre-treatment should definitely be noted. Similarly strength retention of about 80% was observed when post-treated with the severely corrosive oxalic acid. Hence its is clear that passivation can be induced through prolonged pre-treatment in 5M malonic acid that could inhibit the attack of corrosive acid at least for a period of time.
The last fragment of the study focussed on understanding and working out the mechanism behind the reactions between the E-glass fibre and acid medium in terms of kinetics. The acids utilized were 1.5M malonic acid and 3M glyoxylic acid and the assessments were made through the analysis of the weight changes brought about by the acid medium at various temperatures and time frames. In addition leaching patterns of cations were evaluated as this could contribute in achieving the objective. Maximum weight loss reached 4% in glyoxylic acid while that for malonic acid exceeded 20%. The general trend was that the glass fibres lost weight in both acids for a period of time followed by an evident weight gain. Furthermore the weight loss results fit the first order rate law. While the leaching of cations reflects the weight loss for the shorter time frames, steady loss of ions was visible even for the longer time frames where the weight has increased. The weight gain could be explained in terms of binding of anions to certain cations on the glass surface, accounting for the hindrance in the loss of cations at the longer time frames as well. About 50% of weight loss was associated to Ca while 20% was to Al, leaving 6% to B where as the rest of the ions had shown almost insignificant contribution to the weight loss.
Åström, Erik. "Is there an economic value for elite sports? : The case of Swedish Hockey League." Thesis, Linnéuniversitetet, Institutionen för nationalekonomi och statistik (NS), 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:lnu:diva-65826.
Full textYuan, Fuping. "PLATE IMPACT EXPERIMENTS TO INVESTIGATE DYNAMIC SLIP, DEFORMATION AND FAILURE OF MATERIALS." Case Western Reserve University School of Graduate Studies / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=case1193161550.
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