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Thematische Bibliographien / Growth factors

Auswahl der wissenschaftlichen Literatur zum Thema „Growth factors“

Autor: Grafiati

Veröffentlicht am 4. Juni 2021

Zuletzt aktualisiert am 25. Mai 2024

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Inhaltsverzeichnis

Zeitschriftenartikel
Dissertationen
Bücher
Buchteile
Konferenzberichte
Berichte der Organisationen

Zeitschriftenartikel zum Thema "Growth factors":

1

Brattain, Michael G. „Growth and growth factors Growth factors in perinatal development“. Trends in Endocrinology & Metabolism 5, Nr. 3 (April 1994): 145. http://dx.doi.org/10.1016/1043-2760(94)90099-x.

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2

Bonazza, Veronica, Christopher Hajistilly, Dinker Patel, Jatan Patel, Rita Woo, Marco Angelo Cocchi, Barbara Buffoli et al. „Growth Factors Release From Concentrated Growth Factors“. Journal of Craniofacial Surgery 29, Nr. 8 (November 2018): 2291–95. http://dx.doi.org/10.1097/scs.0000000000004607.

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3

Dinsdale, Paul. „Growth factors“. Nursing Standard 16, Nr. 38 (05.06.2002): 12–13. http://dx.doi.org/10.7748/ns.16.38.12.s27.

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4

&NA;. „Growth factors“. Reactions Weekly &NA;, Nr. 520 (September 1994): 7. http://dx.doi.org/10.2165/00128415-199405200-00029.

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5

Allen, Garland E. „Growth factors“. Nature 436, Nr. 7054 (August 2005): 1089–90. http://dx.doi.org/10.1038/4361089a.

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6

Lloyd, Ricardo V. „Growth factors“. Endocrine Pathology 8, Nr. 2 (Juni 1997): 121–27. http://dx.doi.org/10.1007/bf02739940.

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7

Aloisi, F. „Growth factors“. Neurological Sciences 24 (01.12.2003): s291—s294. http://dx.doi.org/10.1007/s10072-003-0177-0.

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8

Edwall, Dan, Subburaman Mohan und David J. Baylink. „Growth factors“. Topics in Geriatric Rehabilitation 10, Nr. 4 (Juni 1995): 35–47. http://dx.doi.org/10.1097/00013614-199506000-00006.

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9

KLIJN, J. G. M., P. M. J. J. BERNS, M. BONTENBAL und J. A. FOEKENS. „Growth Factors.“ Annals of the New York Academy of Sciences 698, Nr. 1 Breast Cancer (November 1993): 85–101. http://dx.doi.org/10.1111/j.1749-6632.1993.tb17193.x.

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Nesbitt, Mark. „Growth factors“. Nature 375, Nr. 6529 (Mai 1995): 289. http://dx.doi.org/10.1038/375289a0.

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Dissertationen zum Thema "Growth factors":

1

Griffiths, Leigh. „Angiogenic growth factors in tumour growth“. Thesis, University of Oxford, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.312384.

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2

Robertson, James Gray. „Insulin-like growth factors and insulin-like growth factor binding proteins in wounds /“. Title page, contents and abstract only, 1999. http://web4.library.adelaide.edu.au/theses/09PH/09phr6509.pdf.

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Wahlgren, Aida. „Growth factors in spermatogenesis /“. Stockholm, 2003. http://diss.kib.ki.se/2003/91-7349-579-4/.

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4

Aase, Karin. „On vascular endothelial growth factor B and platelet-derived growth factor C : two members of the VEGF/PDGF family of growth factors /“. Stockholm : Karolinska Univ. Press, 2001. http://diss.kib.ki.se/2001/91-89428-14-5/.

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5

Martinez, Humberto Jose. „Nerve growth factor actions on the brain /“. Access full-text from WCMC, 1989. http://proquest.umi.com/pqdweb?did=744572291&sid=1&Fmt=2&clientId=8424&RQT=309&VName=PQD.

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6

Gillies, Peter John. „Modulation of dermal microvascular endithelial cell responses to growth factors and haemostatic factors in the presence of vitronectin“. Thesis, Queensland University of Technology, 2008. https://eprints.qut.edu.au/37176/1/Peter_Gillies_Thesis.pdf.

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In order to effect permanent closure in burns patients suffering from full thickness wounds, replacing their skin via split thickness autografting, is essential. Dermal substitutes in conjunction with widely meshed split thickness autografts (+/- cultured keratinocytes) reduce scarring at the donor and recipient sites of burns patients by reducing demand for autologous skin (both surface area and thickness), without compromising dermal delivery at the wound face. Tissue engineered products such as Integra consist of a dermal template which is rapidly remodelled to form a neodermis, at which time the temporary silicone outer layer is removed and replaced with autologous split thickness skin. Whilst provision of a thick tissue engineered dermis at full thickness burn sites reduces scarring, it is hampered by delays in vascularisation which results in clinical failure. The ultimate success of any skin graft product is dependent upon a number of basic factors including adherence, haemostasis and in the case of viable tissue grafts, success is ultimately dependent upon restoration of a normal blood supply, and hence this study. Ultimately, the goal of this research is to improve the therapeutic properties of tissue replacements, through impregnation with growth factors aimed at stimulating migration and proliferation of microvascular endothelial cells into the donor tissue post grafting. For the purpose of my masters, the aim was to evaluate the responsiveness of a dermal microvascular endothelial cell line to growth factors and haemostatic factors, in the presence of the glycoprotein vitronectin. Vitronectin formed the backbone for my hypothesis and research due to its association with both epithelial and, more specifically, endothelial migration and proliferation. Early work using a platform technology referred to as VitroGro (Tissue Therapies Ltd), which is comprised of vitronectin bound BP5/IGF-1, aided keratinocyte proliferation. I hypothesised that this result would translate to another epithelium - endothelium. VitroGro had no effect on endothelial proliferation or migration. Vitronectin increases the presence of Fibroblast Growth Factor (FGF) and Vascular Endothelial Growth Factor (VEGF) receptors, enhancing cell responsiveness to their respective ligands. So, although Human Microvascular Endothelial Cell line 1 (HMEC-1) VEGF receptor expression is generally low, it was hypothesised that exposure to vitronectin would up-regulate this receptor. HMEC-1 migration, but not proliferation, was enhanced by vitronectin bound VEGF, as well as vitronectin bound Epidermal Growth Factor (EGF), both of which could be used to stimulate microvascular endothelial cell migration for the purpose of transplantation. In addition to vitronectin's synergy with various growth factors, it has also been shown to play a role in haemostasis. Vitronectin binds thrombin-antithrombin III (TAT) to form a trimeric complex that takes on many of the attributes of vitronectin, such as heparin affinity, which results in its adherence to endothelium via heparan sulfate proteoglycans (HSP), followed by unaltered transcytosis through the endothelium, and ultimately its removal from the circulation. This has been documented as a mechanism designed to remove thrombin from the circulation. Equally, it could be argued that it is a mechanism for delivering vitronectin to the matrix. My results show that matrix-bound vitronectin dramatically alters the effect that conformationally altered antithrombin three (cATIII) has on proliferation of microvascular endothelial cells. cATIII stimulates HMEC-1 proliferation in the presence of matrix-bound vitronectin, as opposed to inhibiting proliferation in its absence. Binding vitronectin to tissues and organs prior to transplant, in the presence of cATIII, will have a profound effect on microvascular infiltration of the graft, by preventing occlusion of existing vessels whilst stimulating migration and proliferation of endothelium within the tissue.

7

McMurray, Heather Forbes. „Macrophage growth factors in atherogenesis“. Thesis, University of Cambridge, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.306460.

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Sowter, Heidi Michelle. „Growth factors in ovarian cancer“. Thesis, Anglia Ruskin University, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299988.

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9

Martin, Christopher School of Biomedical Engineering UNSW. „Investigation of exogenous growth factors; platelet derived growth factor, insulin-like growth factor binding protein and fibroblast growth factor, and their influence on in vivo bone repair“. Awarded by:University of New South Wales. School of Biomedical Engineering, 2006. http://handle.unsw.edu.au/1959.4/30405.

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This research investigated if exogenous growth factors (GFs), in particular platelet derived growth factor (PDGF), has an in vivo effect on the healing response of normal healthy bone. The research was orientated to study whether a clinical beneficial effect could be demonstrated. To achieve this two animal models were utilised, namely, a rabbit tibial osteotomy model and an ovine tibial defect and porous implant ingrowth model. The rabbit model comprised of a unilateral V-shaped tibial osteotomy, stabilised with an absorbable intramedullary pin and figure-of-eight tension band suture, with a 3 week survival period. The GFs tested in this model were 3 concentrations of PDGF, a single dose of insulin-like growth factor binding protein (IGF-BP) and a combination of the two. Each osteotomy was injected with a single bolus of collagen (control) or collagen containing GF (treatment) during surgery. After sacrifice tibiae were CT-scanned in situ, harvested and subject to 4-point bend testing. The callus, underlying bone and contralateral bone's greyscales and mechanical testing results were used for comparative analysis. The ovine model consisted of implanting 6 small rectangular shaped titanium alloy porous implants and one empty defect bilaterally in sheep's tibiae, for 4 and 6 weeks. The sheep were injected with tetracycline bone marker at 2 week intervals. The model's characteristics and any positional effects were initially investigated. Followed by an investigation into the influence of various exogenous GFs on the healing response and ingrowth characteristics of bone into the porous implants. The GFs investigated were PDGF, IGF-BP and fibroblast growth factor impregnated into the porous implants in a collagen carrier. Comparative analysis was done on results from 3-point bend testing of the bone/implant interface, image analysis to quantify percentage of bone, from scanning electron microscopy images of implant sections and confocal microscopy images of tibial defect sections. Analyses indicate that the GFs investigated have a direct and quantifiable positive in vivo effect. The more significant finding is that the growth factors have a potent systemic effect. These results were confirmed by both the sheep porous bone plug model and the rabbit tibial osteotomy model used within this research.

10

Olofsson, Susanne. „Design, synthesis, structure, and dynamics of a polypeptide with supersecondary structure a helix-loop-helix dimer /“. Göteborg : Dept. of Organic Chemistry, University of Göteborg, 1994. http://books.google.com/books?id=6AdrAAAAMAAJ.

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Bücher zum Thema "Growth factors":

1

D, Waterfield M., Hrsg. Growth factors. Edinburgh: Churchill Livingstone for the British Council, 1989.

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2

Heath, John K. Growth factors. Oxford: IRL Press at Oxford University Press, 1993.

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3

D, Waterfield Michael, und British Medical Bulletin, Hrsg. Growth factors. Edinburgh: Churchill Livingstone, 1989.

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4

A, Rush Robert, Hrsg. Nerve growth factors. Chichester [England]: Wiley, 1989.

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5

K, MacIntire Guy, Hrsg. Nerve growth factor: New research. New York: Nova Science Publishers, 2008.

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6

Bothwell, Mark, Hrsg. Neuronal Growth Factors. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-75747-1.

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7

W, Barnes David, und Sirbasku David A, Hrsg. Peptide growth factors. Orlando: AcademicPress, 1987.

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8

Habenicht, Andreas, Hrsg. Growth Factors, Differentiation Factors, and Cytokines. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-74856-1.

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9

1948-, Habenicht A., Hrsg. Growth factors, differentiation factors, and cytokines. Berlin: Springer-Verlag, 1990.

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10

Franz, Hefti, Fondation IPSEN pour la recherche thérapeutique. und Colloque médecine et recherche (6th : 1990 : Strasbourg, France), Hrsg. Growth factors and Alzheimer's disease. Berlin: Springer-Verlag, 1991.

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Buchteile zum Thema "Growth factors":

1

Sausville, Edward A., und Dan L. Longo. „Growth Factors and Growth Factor Inhibitors“. In Cancer Therapeutics, 337–70. Totowa, NJ: Humana Press, 1997. http://dx.doi.org/10.1007/978-1-59259-717-8_16.

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2

Savgan-Gurol, Eray. „Growth Factors“. In Endocrine Conditions in Pediatrics, 145–47. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-52215-5_24.

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3

diZerega, Gere S., und Kathleen E. Rodgers. „Growth Factors“. In The Peritoneum, 57–121. New York, NY: Springer New York, 1992. http://dx.doi.org/10.1007/978-1-4613-9235-4_3.

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4

Bradshaw, R. A. „Growth Factors“. In Comprehensive Human Physiology, 431–50. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-60946-6_22.

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5

LeRoith, Derek, und William L. Lowe. „Growth Factors“. In Endocrinology, 85–91. Totowa, NJ: Humana Press, 2005. http://dx.doi.org/10.1007/978-1-59259-829-8_6.

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6

Wagner, Peter, Frank C. Mooren, Hidde J. Haisma, Stephen H. Day, Alun G. Williams, Julius Bogomolovas, Henk Granzier et al. „Growth Factors“. In Encyclopedia of Exercise Medicine in Health and Disease, 379. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-540-29807-6_2460.

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7

Thiriet, Marc. „Growth Factors“. In Control of Cell Fate in the Circulatory and Ventilatory Systems, 177–277. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4614-0329-6_3.

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8

Forbes, Ian J., und Anthony S.-Y. Leong. „Growth Factors“. In Essential Oncology of the Lymphocyte, 77–89. London: Springer London, 1987. http://dx.doi.org/10.1007/978-1-4471-1467-3_7.

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9

Gooch, Jan W. „Growth Factors“. In Encyclopedic Dictionary of Polymers, 897. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_13871.

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10

Schliephake, Henning, und Florian Böhrnsen. „Growth Factors“. In Tissue Engineering in Oral and Maxillofacial Surgery, 53–69. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-24517-7_5.

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Konferenzberichte zum Thema "Growth factors":

1

Ciftcioglu, Neva, und E. Olavi Kajander. „Growth factors for nanobacteria“. In SPIE's International Symposium on Optical Science, Engineering, and Instrumentation, herausgegeben von Richard B. Hoover. SPIE, 1999. http://dx.doi.org/10.1117/12.375069.

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2

BOCKMAN, DALE E. „GROWTH FACTORS AND CHRONIC PANCREATITIS“. In Proceedings of the 92nd Course of the International School of Medical Sciences. WORLD SCIENTIFIC, 1999. http://dx.doi.org/10.1142/9789814447249_0004.

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3

Denton, CP. „SP0136 Multifactorial tissue growth factors“. In Annual European Congress of Rheumatology, 14–17 June, 2017. BMJ Publishing Group Ltd and European League Against Rheumatism, 2017. http://dx.doi.org/10.1136/annrheumdis-2017-eular.2532.

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4

Poliduts, Aleksey, und Yuner Kapkaev. „Economic Growth: Types and Factors“. In International Conference on Eurasian Economies. Eurasian Economists Association, 2015. http://dx.doi.org/10.36880/c06.01404.

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The article deals with the content of economic growth as an economic category through determining its type, indicators and factors. It proposed grading factors based on the various existing theoretical approaches. With all the variety of growth factors and options for sorting the basic separation occurs in the direct and indirect factors, internal and external, intensive and extensive, the factors of supply, demand and distribution, controlled and uncontrolled factors, factors of economic and non-economic, interchangeable and supplemented growth factors. The author points out the main trends and features of economic growth, determining the pace and quality of economic growth in Russia at the present stage of development. The methodological basis of the study is the dialectical method of knowledge, which allows to study economic phenomena and processes in their constant interaction and development. Sources of data in the study is an analytical and statistical materials the IMF, the World Bank and the Federal State Statistics Service. Formulate a set of restrictions for sustainable economic growth in Russia, due to the influence of various kinds of factors. As highlighted in its basic elements: the raw structure of Russian exports, weak competitiveness of downstream industries, the economic sanctions imposed in 2014 by the Western countries, reducing the purchasing power of the ruble against the reserve currencies. The results may help to improve the efficiency of stimulating the development and maintenance of high economic growth in the implementation of measures of state regulation both in Russia and in other countries.

5

Sharma, Vishal, Anupriya Tuli, Asra Sakeen Wani, Anjali Karol Mohan, Bonnie Nardi, Marc Hassenzahl, Morgan Vigil-Hayes, Rikke Hagensby Jensen, Shaowen Bardzell und Neha Kumar. „Post-growth HCI: Co-Envisioning HCI Beyond Economic Growth“. In CHI '24: CHI Conference on Human Factors in Computing Systems. New York, NY, USA: ACM, 2024. http://dx.doi.org/10.1145/3613905.3636292.

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6

Lee Cheng Choo und Roslan Md Nor. „Factors Affecting the Growth of Carbon Nanotubes“. In 2006 IEEE International Conference on Semiconductor Electronics. IEEE, 2006. http://dx.doi.org/10.1109/smelec.2006.381037.

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Mykytiuk, Oksana, und Kateryna Petrenko. „CONCEPTUAL APPROACHES TO DETERMINING ECONOMIC GROWTH FACTORS“. In PUBLIC COMMUNICATION IN SCIENCE: PHILOSOPHICAL, CULTURAL, POLITICAL, ECONOMIC AND IT CONTEXT. European Scientific Platform, 2020. http://dx.doi.org/10.36074/15.05.2020.v1.02.

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Yuan, Jiaojiao, Xuefang Wang, Zhicheng Lv, Shuai Shi, Yuzhe Wang und Sheng Liu. „Study of factors influencing tin whisker growth“. In 2012 13th International Conference on Electronic Packaging Technology & High Density Packaging (ICEPT-HDP). IEEE, 2012. http://dx.doi.org/10.1109/icept-hdp.2012.6474763.

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Zhou, Xiaodi. „The literature review on firm growth factors“. In 2011 International Conference on E-Business and E-Government (ICEE). IEEE, 2011. http://dx.doi.org/10.1109/icebeg.2011.5886983.

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Eschbach, Florence, Daniel Selassie, Peter Sanchez, Daniel Tanzil, Vikram Tolani, Mahmood Toofan, Huiying Liu, Barbara Greenebaum, Michael Murray und Raul Villacorta. „ArF lithography reticle crystal growth contributing factors“. In Photomask Technology, herausgegeben von Wolfgang Staud und J. Tracy Weed. SPIE, 2004. http://dx.doi.org/10.1117/12.569272.

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Berichte der Organisationen zum Thema "Growth factors":

1

Fischer, Stanley. The Role of Macroeconomic Factors in Growth. Cambridge, MA: National Bureau of Economic Research, Dezember 1993. http://dx.doi.org/10.3386/w4565.

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Boven, Van, Jack und King. L51965 Environmental Factors-Effect of SCC Growth. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), September 2002. http://dx.doi.org/10.55274/r0011264.

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Stress corrosion cracking (SCC) is an established threat to the integrity of gas transmission pipelines and is a significant concern to pipeline operators. In line inspection (ILI) tools are actively being developed to detect SCC. This project combined the implementation of new ILI tools with the environmental characterization of identified SCC sites. Characterization of sites included site and soil parameters traditionally derived from surface inspection as well as the measurement of pipe depth soil parameters (electrical resistance, oxidation reduction potential, temperature, pipe to soil potential). The intent was to relate environmental parameters to the incidence of SCC features with the hope of developing predictive models for the probability of SCC. Such models would be useful in direct assessment or in prioritizing sections of line for hydrotests or ILI.

3

Brown, Gregory L. Enhancement of Wound Healing by Biosynthetic Growth Factors. Fort Belvoir, VA: Defense Technical Information Center, November 1995. http://dx.doi.org/10.21236/ada303777.

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4

Bloom, Nicholas, Paul Romer, Stephen Terry und John Van Reenen. Trapped Factors and China's Impact on Global Growth. Cambridge, MA: National Bureau of Economic Research, März 2014. http://dx.doi.org/10.3386/w19951.

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Yueh, Linda. China’s growth hindered by cyclical and structural factors. East Asia Forum, Mai 2024. http://dx.doi.org/10.59425/eabc.1715767200.

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Nusse, Roel. Isolation of a Receptor for WNT/Wingless Growth Factors. Fort Belvoir, VA: Defense Technical Information Center, September 1998. http://dx.doi.org/10.21236/ada366728.

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Eisinger, Magdalena. Wound Healing by Cultured Skin Cells and Growth Factors. Fort Belvoir, VA: Defense Technical Information Center, Juni 1994. http://dx.doi.org/10.21236/ada284593.

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Nusse, Roel. Isolation of a Receptor for WNT/Wingless Growth Factors. Fort Belvoir, VA: Defense Technical Information Center, September 1996. http://dx.doi.org/10.21236/ada319774.

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Nusse, Roel. Isolation of a Receptor for WNT/Wingless Growth Factors. Fort Belvoir, VA: Defense Technical Information Center, September 1995. http://dx.doi.org/10.21236/ada301701.

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Nusse, Roel. Isolation of a Receptor for WNT/Wingless Growth Factors. Fort Belvoir, VA: Defense Technical Information Center, September 1999. http://dx.doi.org/10.21236/ada382531.

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