Rozprawy doktorskie na temat „Bone marrow”
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勞錦輝 i Kam-fai Simon Lo. "Cytomegalovirus and bone marrow transplantation". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1997. http://hub.hku.hk/bib/B31215609.
Pełny tekst źródłaLo, Kam-fai Simon. "Cytomegalovirus and bone marrow transplantation /". Hong Kong : University of Hong Kong, 1997. http://sunzi.lib.hku.hk/hkuto/record.jsp?B19471142.
Pełny tekst źródłaFadini, Gian Paolo. "Bone marrow dysfunction in diabetes". Doctoral thesis, Università degli studi di Padova, 2013. http://hdl.handle.net/11577/3422580.
Pełny tekst źródłaPresupposti. Il diabete mellito (DM) aumenta il rischio cardiovascolare e ciò viene attribuito almeno in parte alla riduzione delle cellule vasculo-rigenerative di origine midollare. Infatti il midollo osseo contiene precursori per cellule endoteliali, muscolari lisce e cardiomiociti, che derivano da un progenitore CD34+. Dati recenti ottenuti da modelli sperimentali di diabete tipo 1 e tipo 2 indicano l’esistenza di difetti midollari che includono microangiopatia, neuropatia, alterazione dell’espressione genica e disfunzione della nicchia staminale. Obiettivi. Questo set di esperimenti ha avuto l’obiettivo di descrivere in dettaglio le alterazioni della funzione midollare nel diabete clinico e sperimentale. Metodi. Gli approcci metodologici sono diversificati e comprendono: 1) un trial di stimolazione midollare diretta con G-CSF ricombinante umano in pazienti con e senza diabete; 2) un’analisi di meta-regressione dei trials in cui il G-CSF è stato somministrato per indurre rigenerazione cardiovascolare in pazienti con e senza diabete; 3) lo studio della compartimentalizzazione delle cellule staminali/progenitrici nel midollo e nel sangue periferico, in relazione al diabete; 4) un modello animale per la definizione del ruolo di DPP-4 nel difetto di mobilizzazione midollare associato al diabete. Risultati. Parte 1: in risposta al G-CSF, le cellule CD34+ circolanti aumentavano significativamente nel paziente non diabetico, ma non nel diabetico, che mostrava anche una difettosa mobilizzazione di cellule ematopoietiche CD133+ e CD34+CD133+, nonché di cellule progenitrici endoteliali CD133+KDR+, indipendentemente dai possibili fattori confondenti. La capacità angiogenica in vivo delle cellule mononucleate aumentava significativamente dopo G-CSF nei soggetti diabetici ma non nei non diabetici, rispetto al basale. Il diabete risultava associato ad una incapacità di upregolare DPP-4 sulle cellule CD34+ in risposta al G-CSF. Parte 2: per la meta-regressione sono stati individuati 227 articoli, recuperati 96 e trattenuti 24 per l’analisi primaria. È stata identificata una forte correlazione negativa tra prevalenza del diabete all’interno di ogni trial e livello delle cellule CD34+ raggiunte dopo mobilizzazione con G-CSF (r=-0.68; p<0.0001). Una analisi di regressione multipla ha confermato che il risultato era indipendente da possibili fattori confondenti. In 13 articoli contenenti dati sui livelli di cellule CD34+ pre- e post-G-CSF, la correlazione negativa tra prevalenza del diabete e mobilizzazione appariva ancora più stretta (r=-0.82; p<0.0001). Parte 3: i livelli delle cellule CD34+ nel midollo e nel sangue periferico risultano essere direttamente correlati e la maggior parte delle cellule CD34+ erano di origine midollare, non proliferanti e non apoptotiche. Lo studio della compartimentalizzazione delle cellule CD34+ in 72 pazienti con e senza malattia cardiovascolare mediante l’uso delle mappe auto-organizzanti ha permesso di rilevare alterazioni della mobilizzazione in presenza di diabete ed elevato rischio cardiovascolare. Inoltre, un’elevata attività plasmatica di DPP-4 si associava ad alterata compartimentalizzazione delle cellule CD34+. In ratti diabetici rispetto ai controlli, l’attività di DPP-4 risultava significativamente aumentata nel sangue periferico e ridotta nel midollo osseo. Lo studio di ratti geneticamente deficienti dell’enzima DPP-4 ha permesso di stabilire che l’alterazione tessuto-specifica di DPP-4 nel diabete è responsabile del difetto di mobilizzazione post-G-CSF e post-ischemia. La delezione di DPP-4 ripristinava la mobilizzazione post-ischemica di cellule staminali ematopoietiche e progenitrici endoteliali e favoriva il recupero del tessuto ischemico nel diabete. Conclusioni. Diversi tipi di evidenze sperimentali indicano chiaramente che il diabete induce un difetto nella mobilizzazione delle cellule staminali/progenitrici midollari. Questo difetto primitivo del midollo osseo nel diabete è correlato ad una disregolazione tessuto-specifica dell’attività dell’enzima DPP-4
Fisher, Maya. "Bone marrow regeneration follwing tibial marrow ablation in rats is age dependent". Thesis, Atlanta, Ga. : Georgia Institute of Technology, 2008. http://hdl.handle.net/1853/26526.
Pełny tekst źródłaCommittee Chair: Boyan Barbara; Committee Member: Guldberg Robert; Committee Member: Lovachev Kiril; Committee Member: Schwartz Zvi. Part of the SMARTech Electronic Thesis and Dissertation Collection.
Jackson, G. H. "Long term bone marrow culture studies of patients with lymphoid malignancies undergoing autologous bone marrow transplantation". Thesis, University of Newcastle Upon Tyne, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.309068.
Pełny tekst źródłaSchmidt-Mende, Jan Georg. "Bone marrow apoptosis in myelodysplastic syndromes". [S.l.] : [s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=96939781X.
Pełny tekst źródłaMcIntosh, Bryan James. "Regulation of thrombopoietin in bone marrow". Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 2007. http://wwwlib.umi.com/cr/ucsd/fullcit?p3284334.
Pełny tekst źródłaTitle from first page of PDF file (viewed January 9, 2008). Available via ProQuest Digital Dissertations. Vita. Includes bibliographical references (p. 50-58).
Funaki, Hilde. "Psychological responses to bone-marrow-transplantation". Thesis, City University London, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283269.
Pełny tekst źródłaSebastian, Anil. "Recreating bone marrow tissues in vitro". Thesis, University of Manchester, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528263.
Pełny tekst źródłaDavison, Glenda Mary. "Immune reconstitution post bone marrow transplantation". Master's thesis, University of Cape Town, 2000. http://hdl.handle.net/11427/3376.
Pełny tekst źródłaThe aims of this project were therefore: to document the immune reconstitution following T-cell depleted bone marrow and peripheral blood stem cell transplantation and to compare this with the recovery following autologous grafts. to document the cell surface expression of CD95 in an attempt to comment on the role played by FAS mediated apoptosis in the post transplant immune deficiency.
Weber, Matthew Charles. "Engineering human bone marrow stromal cells". Case Western Reserve University School of Graduate Studies / OhioLINK, 1991. http://rave.ohiolink.edu/etdc/view?acc_num=case1055867071.
Pełny tekst źródłaAvera, Emily. "Transplant anxieties : discourses about bone marrow". Master's thesis, University of Cape Town, 2008. http://hdl.handle.net/11427/10038.
Pełny tekst źródłaThis minor dissertation examines the various discourses in the Bone Marrow Transplant (BMT) network in South Africa. The organisations in the network which were observed using participant observation were the South African Bone Marrow Registry and the Sunflower Fund to complement this, the researcher interviewed staff members at these organisations as well as at a public hospital haematology unit in the Cape Town area that conducts BMT. Additionally patients, donors, and their family members were interviewed. Some media related to the BMT network was also analysed. Informed heavily by Troy Duster's work on genetic and social feedback loops, it was found that the discourses reflect a complex interweaving of biological materiality, ethnicity, culture, mortality, health resource rationing, South African nationhood, and the limits of bodily integrity. There is extensive discussion of how the BMT discourses demonstrate the necessity of engagement with several issues: the hybridity of expert and lay intercultural communication, health inequalities, human rights, and the prioritisation of first and third world medicine, the meanings of race, culture, ethnicity, and nationhood in a diverse South Africa, conceptions of donor shortage, and the imperative of saving lives through medical practise.
Mancini, Richard Anthony. "Factors affecting beef bone marrow discoloration /". Search for this dissertation online, 2004. http://wwwlib.umi.com/cr/ksu/main.
Pełny tekst źródłaHussein, Hayam. "Cathepsin K Inhibition In Bone And Bone Marrow In Horses". The Ohio State University, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=osu1449218489.
Pełny tekst źródłaLACAVA, GIOVANNA. "A Comprehensive Study on Homeostatic Bone and Bone Marrow Mediators". Doctoral thesis, Università degli Studi di Camerino, 2019. http://hdl.handle.net/11581/428952.
Pełny tekst źródłaClutter, Suzanne Davis. "Chemotherapy disrupts bone marrow stromal cell function". Morgantown, W. Va. : [West Virginia University Libraries], 2006. https://eidr.wvu.edu/etd/documentdata.eTD?documentid=4528.
Pełny tekst źródłaTitle from document title page. Document formatted into pages; contains x, 180 p. : ill. (some col.). Vita. Includes abstract. Includes bibliographical references.
Baki, Mert. "Bone Marrow Targeted Liposomal Drug Delivery Systems". Master's thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12613251/index.pdf.
Pełny tekst źródła(SDF-1&alpha
) upon bone marrow transplantation (BMT). There is a need for increasing homing efficiency after BMT since only 10-15% of the transplanted cells can home to their own niches and a limited amount of donor marrow can be transplanted. In this study, we aimed to develop and characterize bone marrow targeted liposomal SDF-1&alpha
delivery system prepared by extrusion method. Alendronate conjugation was chosen to target the liposomes to bone marrow microenvironment, particularly the endosteal niche. Optimization studies were conducted with the model protein (
Fletcher, Joanne L. "Bone Marrow Progenitors in Vascular Tissue Engineering". Thesis, University of Manchester, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.518451.
Pełny tekst źródłaBågesund, Mats. "Salivary function after pediatric bone marrow transplantation /". Stockholm, 2000. http://diss.kib.ki.se/2000/91-628-4110-6/.
Pełny tekst źródłaAmofah, Eunice. "Bone marrow stem cells in liver disease". Thesis, Imperial College London, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.497234.
Pełny tekst źródła袁國勇 i Kwok-yung Yuen. "Infectious complications in bone marrow transplant recipients". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1998. http://hub.hku.hk/bib/B31981689.
Pełny tekst źródłaChandran, Priya. "Bone Marrow Microenvironment in Acute Myleoid Leukemia". Thèse, Université d'Ottawa / University of Ottawa, 2013. http://hdl.handle.net/10393/24301.
Pełny tekst źródłaMcWilliam, Nicola A. "The fibrinolytic system of human bone marrow". Thesis, University of Aberdeen, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.337476.
Pełny tekst źródłaElfer, Jane. "Emotional impact of sibling bone marrow donors". Thesis, University of East London, 2017. http://roar.uel.ac.uk/7137/.
Pełny tekst źródłaRehman, Haroon, Asha Chepkorir Segie, Kanishka Chakraborty i Devapiran Jaishankar. "Bone Marrow Wars: Attack of the Clones". Digital Commons @ East Tennessee State University, 2020. https://dc.etsu.edu/asrf/2020/presentations/33.
Pełny tekst źródłaYuen, Kwok-yung. "Infectious complications in bone marrow transplant recipients". Hong Kong : University of Hong Kong, 1998. http://sunzi.lib.hku.hk/hkuto/record.jsp?B19929614.
Pełny tekst źródłaLloyd, Brandon R. "Comparison of Bone Marrow Mesenchymal Stem Cells from Limb and Jaw Bones". The Ohio State University, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=osu1458678153.
Pełny tekst źródłaHall, Brett Matthew. "Effects of high dose chemotherapy on the bone marrow microenvironment". Morgantown, W. Va. : [West Virginia University Libraries], 2002. http://etd.wvu.edu/templates/showETD.cfm?recnum=2558.
Pełny tekst źródłaTitle from document title page. Document formatted into pages; contains ix, 173 p. : ill. (some col.). Vita. Includes abstract. Includes bibliographical references (p. 163-169).
Lu, King-hei Crosby. "A single centre, randomised trial on harvest cell yield and marrow engraftment using haemopoietic growth-factor primed bone marrow". Hong Kong : University of Hong Kong, 2002. http://sunzi.lib.hku.hk/hkuto/record.jsp?B25176481.
Pełny tekst źródłaBailey, Amy. "A systemic approach to paediatric bone marrow transplantation". Thesis, University of Birmingham, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.408830.
Pełny tekst źródłaGray, Caroline J. "Distress and emotional state throughout bone marrow transplantation". Thesis, University of British Columbia, 1991. http://hdl.handle.net/2429/29729.
Pełny tekst źródłaApplied Science, Faculty of
Nursing, School of
Graduate
Barron, Mary Anne. "Vitamin K deficiency in paediatric bone marrow transplantation". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape11/PQDD_0008/MQ40822.pdf.
Pełny tekst źródłaRodriguez, Francisco Jose. "Oral mucositis in children receiving bone marrow transplantation". Thesis, Birmingham, Ala. : University of Alabama at Birmingham, 2008. https://www.mhsl.uab.edu/dt/2008m/rodriguez.pdf.
Pełny tekst źródłaAl-Khaldi, Abdulaziz A. "Therapeutic angiogenesis using autologous bone marrow stromal cells". Thesis, McGill University, 2002. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=32749.
Pełny tekst źródłaMethods and result. Using murine Matrigel angiogenesis model, we compared MSCs related angiogenesis to that produced by vascular endothelial growth factor (VEGF) and basic fibroblast growth factor. We found that MSCs result in an efficient and organized angiogenesis, arteriogenesis and vasculogenesis. MSC-related angiogenesis is VEGF dependent. MSCs in vivo produce VEGF that through paracrine effect induces local angiogenesis and through an autocrine loop stimulates FLK1+MSCs to differentiate into endothelial cells. MSCs implanted into ischemic hind limb resulted in marked improvement in blood flow and collateral vessels formation.
Conclusion. MSCs spontaneously induce efficient and mature angiogenesis in ischemic/hypoxic tissues with significant arteriolar component resulting in increased blood flow. They are also capable of spontaneous differentiation into endothelium. VEGF appears to be necessary for MSC-related angiogenesis and vasculogenesis.
Vig, Pamela. "Bone marrow stem cell contribution to liver regeneration". Thesis, Imperial College London, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.427949.
Pełny tekst źródłaBurdon, Peter Charles Edward. "Regulation of neutrophil mobilisation from the bone marrow". Thesis, Imperial College London, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.289739.
Pełny tekst źródłaPowell, Timothy Jack. "Characterisation of rat bone marrow derived dendritic cells". Thesis, University of Oxford, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.298613.
Pełny tekst źródłaKallis, Yiannis Nicolaou. "The bone marrow in liver fibrosis and regeneration". Thesis, Imperial College London, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528283.
Pełny tekst źródłaPorter, Christopher John Hamilton. "Targeting collodial drug carriers to the bone marrow". Thesis, University of Nottingham, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315061.
Pełny tekst źródłaCavanagh, Gary. "The role of CD31 in bone marrow transplantation". Thesis, University of Newcastle Upon Tyne, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.404955.
Pełny tekst źródłaFegan, C. D. "The gut mucosal barrier following bone marrow transplantation". Thesis, University of Newcastle Upon Tyne, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.308776.
Pełny tekst źródłaWadoodi, Ashar. "The role of bone marrow in thrombus resolution". Thesis, King's College London (University of London), 2012. https://kclpure.kcl.ac.uk/portal/en/theses/the-role-of-bone-marrow-in-thrombus-resolution(2983faec-0618-4c4f-8897-7816419c55bd).html.
Pełny tekst źródłaDavies, Julie Theresa. "Activation of adhesion of bone marrow stromal cells". Thesis, St George's, University of London, 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.656858.
Pełny tekst źródłaBennett, Jonathan Hilary. "The differentiation of osteogenic cells from bone marrow". Thesis, University of Oxford, 1991. http://ora.ox.ac.uk/objects/uuid:3460f26e-a124-4605-8601-2e300241de14.
Pełny tekst źródłaRoulson, Jo-An. "Bone marrow endothelial transmigration of prostate carcinoma cells". Thesis, University of Manchester, 2008. https://www.research.manchester.ac.uk/portal/en/theses/bone-marrow-endothelial-transmigration-of-prostate-carcinoma-cells(997acbf2-bbbc-455b-bb84-b439ffb9f839).html.
Pełny tekst źródłaLyndina, Yu. "Histological features of red bone marrow in rats". Thesis, Sumy State University, 2016. http://essuir.sumdu.edu.ua/handle/123456789/46296.
Pełny tekst źródłaGowers, Kate Hayley Christine. "Characterisation of bone marrow progenitor cells in disease". Thesis, Imperial College London, 2013. http://hdl.handle.net/10044/1/11068.
Pełny tekst źródłaLangford-Smith, Kia Jane. "Non-myeloablative bone marrow transplantation for Mucopolysaccharide diseases". Thesis, University of Manchester, 2012. https://www.research.manchester.ac.uk/portal/en/theses/nonmyeloablative-bone-marrow-transplantation-for-mucopolysaccharide-diseases(5d3fd9c5-01f2-42aa-81ed-a2ce6ef140fe).html.
Pełny tekst źródłaTandy, Corinne B. "Time line of decomposition of porcine bone marrow". Thesis, Boston University, 2011. https://hdl.handle.net/2144/38104.
Pełny tekst źródłaPLEASE NOTE: Boston University Libraries did not receive an Authorization To Manage form for this thesis or dissertation. It is therefore not openly accessible, though it may be available by request. If you are the author or principal advisor of this work and would like to request open access for it, please contact us at open-help@bu.edu. Thank you.
The postmortem interval, or time since death, is a significant factor in medicolegal death investigations. Currently, the techniques used to assess time since death are subjective, phase-based qualitative methods. Recently, legal decisions and best practice recommendations have encouraged increasing quantitative assessment of forensic techniques. The purpose of this research is to determine ifbone marrow biopsy can be used as a quantifiable predictive indicator of time since death. Bone marrow plug biopsies were acquired from six pigs (Sus scrofa) during decomposition through skeletonization (28 days) and examined microscopically. The appearance of 122 marrow sections were scored and analyzed in light of time since death and accumulated degree-days. This pilot study suggests that there is a strong relationship between bone marrow appearance and the postmortem interval and the results encourage further research into a potential quantitative predictive tool to be utilized in medicolegal death investigations.
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Porter, Ryan Michael. "Examination of Glucocorticoid Treatment on Bone Marrow Stroma: Implications for Bone Disease and Applied Bone Regeneration". Thesis, Virginia Tech, 2002. http://hdl.handle.net/10919/36365.
Pełny tekst źródłaMaster of Science