Rozprawy doktorskie na temat „Bone formation”
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Samizadeh, S. "Bone formation on calcium phosphate bone substitute materials". Thesis, University College London (University of London), 2010. http://discovery.ucl.ac.uk/19891/.
Pełny tekst źródłaChen, Jinbiao Prince of Wales Clinical School UNSW. "In vitro and in vivo bone formation - assessment and application". Awarded by:University of New South Wales. Prince of Wales Clinical School, 2006. http://handle.unsw.edu.au/1959.4/24922.
Pełny tekst źródłaHrit, Manuela. "Acceleration of bone formation in distraction osteogenesis by bone morphogenetic protein-7". Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=101142.
Pełny tekst źródłaBone morphogenetic proteins (BMPs) play an important role in bone formation. In this study, using a rabbit model of DO, the expressions of BMP's major intracellular signalling molecules, Smad proteins, was analyzed and correlated with the expression of BMP ligands and receptors. Based on these results, which confirmed post-receptor activity for the BMP signalling pathway during DO, we hypothesized that exogenous BMPs injected early in the distraction phase will accelerate bone formation in cases of DO. The cellular changes induced by local application of rhBMP-7 (OP-1) on bone formation were therefore investigated, as well as the possible pathways through which OP-1 was responsible for these effects.
The present study reveals that acceleration of bone formation can be attained after injection of OP-1 early during the distraction protocol. The enhanced bone formation, which occurs through the activation of numerous pathways, most likely depends on a non-vascular mechanism.
Hu, Kai. "VEGF-Dependent Mechanisms Controlling Osteoblast Differentiation and Bone Formation During Bone Repair". Thesis, Harvard University, 2015. http://nrs.harvard.edu/urn-3:HUL.InstRepos:17467316.
Pełny tekst źródłaBiological Sciences in Dental Medicine
Williams, Bristol Marie. "Effects of tricalcium phosphate coated titanium on adjacent early bone formation". View the abstract Download the full-text PDF version, 2007. http://etd.utmem.edu/ABSTRACTS/2007-005-Williams-index.html.
Pełny tekst źródłaTitle from title page screen (viewed on July 28, 2008). Research advisor: Joo L. Ong, Ph.D. Document formatted into pages (iv, 36 p. : ill.). Vita. Abstract. Includes bibliographical references (p. 33-36).
Lean, Jennifer Maree. "Mechanical stimulation of bone formation in the rat". Thesis, St George's, University of London, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.263682.
Pełny tekst źródłaMoroz, Adam. "Reduced order modelling of bone resorption and formation". Thesis, De Montfort University, 2011. http://hdl.handle.net/2086/5409.
Pełny tekst źródłaGundle, Roger. "Microscopical and biochemical studies of mineralised matrix production by bone-derived cells". Thesis, University of Oxford, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.282203.
Pełny tekst źródłaWang, Jason Lee. "Effects of aging and remodeling on bone microdamage formation". Thesis, Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/37114.
Pełny tekst źródłaLozano-Carrascal, Naroa. "Topical Application of Bisphosphonates to Enhance Alveolar New Bone Formation". Doctoral thesis, Universitat Internacional de Catalunya, 2017. http://hdl.handle.net/10803/456485.
Pełny tekst źródłaRivera, Jaime Rodrigo. "Bone formation around implants in adult transgenic mice with selective Runx2-II deficiency". Thesis, Birmingham, Ala. : University of Alabama at Birmingham, 2008. https://www.mhsl.uab.edu/dt/2008m/rivera.pdf.
Pełny tekst źródłaYoshida, Keiji. "Stimulation of bone formation and prevention of bone loss by prostaglandin E EP4 receptor activation". Kyoto University, 2002. http://hdl.handle.net/2433/149332.
Pełny tekst źródłaAlison, Susan Jean School of Medicine UNSW. "The control of bone formation by neuropeptide Y receptors". Awarded by:University of New South Wales. School of Medicine, 2006. http://handle.unsw.edu.au/1959.4/26188.
Pełny tekst źródłaAllsopp, Richard Patrick. "The role of the vascular endothelium in bone formation". Thesis, University of Oxford, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.386827.
Pełny tekst źródłaPungchanchaikul, Patimaporn. "Palatal bone formation is regulated by palatal shelf fusion". Thesis, University College London (University of London), 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.500037.
Pełny tekst źródłaLi, Jun. "Indian hedgehog stimulates chondrocyte hypertrophic differentiation inendochondral bone formation". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2007. http://hub.hku.hk/bib/B39558009.
Pełny tekst źródłaDobson, Katharine Rebecca. "Studies into the effects of androgens on bone formation". Thesis, University of Sheffield, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.301007.
Pełny tekst źródłaTaylor, Amanda Faith. "The role of glutamate in bone formation in vitro". Thesis, University of York, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341824.
Pełny tekst źródłaBaba, Ismail Yanny Marliana. "Three-dimensional structured hybrid scaffolds for enhanced bone formation". Thesis, Keele University, 2016. http://eprints.keele.ac.uk/3215/.
Pełny tekst źródłaDeegan, Anthony John. "Novel tissue engineering approaches to enhance natural bone formation". Thesis, Keele University, 2016. http://eprints.keele.ac.uk/3224/.
Pełny tekst źródłaKimura, Hiroaki. "Cthrc1 is a positive regulator of osteoblastic bone formation". Kyoto University, 2009. http://hdl.handle.net/2433/124307.
Pełny tekst źródłaRetting, Kelsey Nicole. "Smad proteins and the regulation of endochondral bone formation". Diss., Restricted to subscribing institutions, 2008. http://proquest.umi.com/pqdweb?did=1666396551&sid=5&Fmt=2&clientId=1564&RQT=309&VName=PQD.
Pełny tekst źródłaMinaur, Nicola Jane. "Methotrexate and bone formation and turnover in rheumatoid arthritis". Thesis, University of Bath, 1998. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.285341.
Pełny tekst źródłaManitzky, Louise J. "Mathematical modelling of intramembranous bone formation during fracture healing". Thesis, Queensland University of Technology, 2014. https://eprints.qut.edu.au/78983/1/Louise_Manitzky_Thesis.pdf.
Pełny tekst źródłaLiu, Jin. "Increased CKIP-1 suppresses Smad-dependent BMP signaling to inhibit bone formation during aging". HKBU Institutional Repository, 2016. https://repository.hkbu.edu.hk/etd_oa/327.
Pełny tekst źródłaO'Connor, Rose Deeter. "MeCP2 deficiency decreases bone formation and reduces bone volume in a rodent model of Rett syndrome". Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 161 p, 2009. http://proquest.umi.com/pqdweb?did=1891570941&sid=6&Fmt=2&clientId=8331&RQT=309&VName=PQD.
Pełny tekst źródłaWei, Fei. "The osteoimmune effect of bone morphogenetic protein-2 in bone regeneration and biomaterial modification". Thesis, Queensland University of Technology, 2020. https://eprints.qut.edu.au/198148/1/Fei_Wei_Thesis.pdf.
Pełny tekst źródłaLi, Jun. "Indian hedgehog stimulates chondrocyte hypertrophic differentiation in endochondral bone formation". Click to view the E-thesis via HKUTO, 2007. http://sunzi.lib.hku.hk/HKUTO/record/B39558009.
Pełny tekst źródłaHamade, Fares. "Enhanced bone formation during distraction osteogenesis in FGFR3 deficient mice". Thesis, McGill University, 2008. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=112630.
Pełny tekst źródłaFibroblast Growth Factors (FGF) play a significant role in bone development and repair. FGF 18 has been shown to be the only FGF member to be expressed throughout both the distraction and the consolidation phases of DO. It was also reported that FGF18 is the physiological ligand of FGFR3. Therefore, we hypothesized that FGF18 and FGFR3 may have an important role in DO.
To test this hypothesis, we investigated DO in FGFR3 deficient mice (FGFR3-/-). (FGF18 deficient mice are not viable). A miniaturized DO apparatus was applied to the tibia followed by an osteotomy. Distraction began after a 5-day latency period at a rate of 0.2 mm/12 hours for 12 days.
Samples were collected at 3 time points comparing the mutants (FGFR3-/-) to their wild type litter' sates: end of distraction (17 days post-surgery), mid-consolidation (34 days post-surgery), and end of consolidation (51 days post surgery). The samples were analyzed using X-ray, DEXA, microCT, histology, biomechanical testing and Real-Time PCR.
Our results revealed that FGFR3 deficient mice showed accelerated bone formation compared to the W.T. littermates at mid-consolidation where the parameters measured revealed increased bone mineral density, bone mineral content and trabecular number in the mutant tibial samples. The newly regenerated bone consolidated faster in the FGFR3 knock-out mice and the bone was of better quality as revealed by biomechanical tests in which more force was needed to break the mutant bone because it exhibited higher resistance than the age matched wild-type sample. The marker gene expression patterns revealed an up-regulation of chondrogenic markers that suggest that the knock-out mice follow the endochondral ossification pathway during DO. All results were statistically significant.
These results show that signaling through FGFR3 acts to decrease bone formation during DO. Consequently, blocking FGFR3 may lead to accelerated bone formation in DO. This may have important clinical implications in attempts to improve the functional outcome of DO by decreasing the long duration that the external fixator has to be kept on.
Gartland, Alison. "The role of the P2X7 receptor in bone cell formation". Thesis, University of Liverpool, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343968.
Pełny tekst źródłaGarcía, Gareta E. "Development of a bone tissue-engineered construct to enhance new bone formation in revision total hip replacement". Thesis, University College London (University of London), 2012. http://discovery.ucl.ac.uk/1338147/.
Pełny tekst źródłaKawai, Mariko. "Ectopic bone formation by human bone morphogenetic protein-2 gene transfer to skeletal muscle using transcutaneous electroporation". Kyoto University, 2004. http://hdl.handle.net/2433/147446.
Pełny tekst źródłaShekaran, Asha. "Beta 1 integrins in bone formation during development and engineering integrin-specific hydrogels for enhanced bone healing". Diss., Georgia Institute of Technology, 2013. http://hdl.handle.net/1853/51720.
Pełny tekst źródłaMiao, Dengshun. "Studies on the actions of bone anabolic drugs in vivo and in vitro". Thesis, University of Sheffield, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.300362.
Pełny tekst źródłaWeston, Darlene Adele. "Approaches to the investigation of periosteal new bone formation in palaeopathology". Thesis, University College London (University of London), 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.405263.
Pełny tekst źródłaSanghani-Kerai, Anita. "Do stem cells transfected with CXCR4 enhance bone formation in osteoporosis?" Thesis, University College London (University of London), 2018. http://discovery.ucl.ac.uk/10045319/.
Pełny tekst źródłaFerguson, James. "THE SPATIAL AND TEMPORAL ROLE OF EZH2 IN SKULL BONE FORMATION". Case Western Reserve University School of Graduate Studies / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=case1530898825341447.
Pełny tekst źródłaHorne, Jacqueline Avril. "Mathematical modelling of soft callus formation in early murine bone repair". Thesis, Queensland University of Technology, 2013. https://eprints.qut.edu.au/63823/1/Jacqueline_Avril_Horne_Thesis.pdf.
Pełny tekst źródłaLu, Luhui, i 陆璐慧. "Molecular control of osteo-chondroprogenitors formation". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2009. http://hub.hku.hk/bib/B44673966.
Pełny tekst źródłaClayton, Angela Ann. "Analysis of an Eocene Bone-bed, Contained within the Lower Lisbon Formation, Covington County, Alabama". Wright State University / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=wright1310391028.
Pełny tekst źródłaKim, Michael S. "Gene Expression in Bone Cells". Thesis, Griffith University, 2006. http://hdl.handle.net/10072/366180.
Pełny tekst źródłaThesis (PhD Doctorate)
Doctor of Philosophy (PhD)
School of Medical Science
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Walker, Katherine Elizabeth. "Studies on the effects of estrogen in human osteogenic cells". Thesis, University of Sheffield, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.245692.
Pełny tekst źródłaMorrison, Matthew Sam. "Osteoclast function : role of extracellular pH and ATP". Thesis, University College London (University of London), 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.369218.
Pełny tekst źródłaRoberts, Ellen. "Investigations into a novel osteoclastic antigen". Thesis, University of Liverpool, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.263794.
Pełny tekst źródłaSimmons, Craig Alexander. "Modelling and characterization of mechanically regulated tissue formation around bone-interfacing implants". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape3/PQDD_0022/NQ49943.pdf.
Pełny tekst źródłaEijken, Hermanus Johannes Marco. "Human osteoblast differentiation and bone formation: growth factors, hormones & regulatory networks". [S.l.] : Rotterdam : [The Author] ; Erasmus University [Host], 2007. http://hdl.handle.net/1765/10597.
Pełny tekst źródłaHusseini, Abdallah. "Bone formation during fracture repair in mice deficient for the cyp24a1 gene". Thesis, McGill University, 2012. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=106532.
Pełny tekst źródłaLa vitamine D est un régulateur important de l'homéostasie minérale et osseuse. L'enzyme CYP24A1 métabolise la vitamine D en 24,25(OH)2D. L'activité biologique de la 24,25(OH)2D demeure imprécise. Des études ont démontré que la 24,25(OH)2D est un métabolite important pour la réparation des fractures chez le poulet. Notre laboratoire a conçu un modèle de souris déficientes pour le gène Cyp24a1 afin d'étudier le rôle de la 24,25(OH)2D. Nous avons entrepris d'étudier le rôle de ce métabolite dans l'ossification endochondrale et intramembranaire pendant la réparation des fractures dans ce modèle de souris. Méthodes: les souris sauvages et Cyp24a1-mutantes ont été soumises à deux différentes procédures chirurgicales pour simuler la formation d'os pendant la réparation des fractures. Pour imiter l'ossification endochondrale, nous avons utilisé un clou intramédullaire afin de stabiliser le tibia après la fracture. Pour évaluer l'ossification intramembranaire, nous avons appliqué l'ostéogénèse par distraction sur le tibia à l'aide d'un appareil de fixation externe. Les paramètres histomorphométriques et l'expression génique au cours de la réparation de la fracture chez les souris mutantes et sauvages ont été mesurés par microtomographie, histologie et PCR quantitative (qRT-PCR), respectivement. Résultats: l'analyse histomorphométrique démontre un retard dans la réparation des fractures stabilisée par clou intramédullaire chez les souris mutantes par rapport au type sauvage. Dans le même modèle, l'expression du collagène de type X était plus élevée chez les souris de type sauvage. Ces différences significatives ont été entièrement corrigées par l'injection de 24,25(OH)2D exogène chez les souris mutantes. Dans le modèle d'ostéogénèse par distraction, nous avons trouvé une tendance vers la formation osseuse réduite chez les souris mutantes comparativement aux souris de type sauvage. Cependant, les différences observées n'étaient pas statistiquement significatives. Conclusion: Nos résultats suggèrent un rôle pour CYP24A1 et la 24,25(OH)2D dans la réparation des fractures par ossification endochondrale. Une étude plus approfondie du rôle de la 24,25(OH)2D pourrait conduire à l'utilisation de ce métabolite afin d'accélérer la formation osseuse et la réparation des fractures.
Rapp, Anna Elise [Verfasser]. "Effect of MSC-administration on bone formation and repair / Anna Elise Rapp". Ulm : Universität Ulm. Medizinische Fakultät, 2015. http://d-nb.info/1067924396/34.
Pełny tekst źródłaMalik, Ghada. "The role of Heparin in BMP2-induced osteoblast differentiation and bone formation". Thesis, University of Newcastle Upon Tyne, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.446237.
Pełny tekst źródłaAlthnaian, Thnaian Ali. "Factors that regulate osteoclast formation and bone resorption in regenerating deer antlers". Thesis, Royal Veterinary College (University of London), 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.439832.
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