Gotowe bibliografie tematyczne / Stem cell transplantation

Gotowa bibliografia na temat „Stem cell transplantation”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 29 lipca 2024

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Artykuły w czasopismach na temat "Stem cell transplantation"

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Ruutu, Tapani, Christian Koenecke i Grzegorz W. Basak. "Allogeneic hematopoietic stem cell transplantation and solid organ transplantation in the same patient". Cellular Therapy and Transplantation 4, nr 1-2 (2015): 14–18. http://dx.doi.org/10.18620/1866-8836-2015-4-1-2-14-18.

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Maurice, Catherine, Austin M. Pereira i Warren P. Mason. "Ataxia Following Allogenic Stem Cell Transplantation: No Stone Unturned". Neuroscience and Neurological Surgery 5, nr 2 (17.12.2019): 01–04. http://dx.doi.org/10.31579/2578-8868/108.

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A thirty-one year-old Sri Lankan man presented with a two-month history of progressive pan-cerebellar syndrome, following allogeneic stem cell transplantation. This curative-intent therapy was performed in the context of an underlying acute myeloid leukemia. During the post-transplant period, patients are extremely vulnerable, especially due to the immunologic fluctuations. Reaching equilibrium is crucial, preventing complications of both extremes of the immunologic response, such as opportunistic infections or graft versus host disease. Numerous aetiologies were considered in the differential diagnosis of this pan-cerebellar syndrome. Most of those conditions mandate a prompt management, because of their reversible or lethal nature. Our thorough investigation process was a race against time. Excluding “Red Flags” remains the priority. Mindfulness and time will eventually lead to the proper diagnosis. We discuss our structured investigation process emphasizing on the key element: a “Systematic Approach”.
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&NA;. "Stem cell transplantation". Inpharma Weekly &NA;, nr 1205 (wrzesień 1999): 8. http://dx.doi.org/10.2165/00128413-199912050-00012.

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Höglund, Martin. "Stem cell transplantation". HemaSphere 2 (czerwiec 2018): 159. http://dx.doi.org/10.1097/hs9.0000000000000120.

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&NA;. "Stem Cell Transplantation". Journal of Pediatric Hematology/Oncology 25, nr 4 (kwiecień 2003): S6—S7. http://dx.doi.org/10.1097/00043426-200304000-00027.

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&NA;. "Stem Cell Transplantation". Journal of Pediatric Hematology/Oncology 25, nr 4 (kwiecień 2003): S20—S21. http://dx.doi.org/10.1097/00043426-200304000-00039.

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Schaap, Nicolaas. "Stem cell transplantation". HemaSphere 3 (czerwiec 2019): 163. http://dx.doi.org/10.1097/hs9.0000000000000266.

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Marmont, AlbertoM. "Stem Cell Transplantation". Bone Marrow Transplantation 24, nr 10 (listopad 1999): 1155. http://dx.doi.org/10.1038/sj.bmt.1702036.

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Lejper, Alison D. "Stem-cell transplantation". Lancet 354, nr 9190 (listopad 1999): 1644–45. http://dx.doi.org/10.1016/s0140-6736(05)77130-0.

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Lennard, A. L. "Stem cell transplantation". Western Journal of Medicine 175, nr 1 (1.07.2001): 42–46. http://dx.doi.org/10.1136/ewjm.175.1.42.

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Rozprawy doktorskie na temat "Stem cell transplantation"

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Jansson, Monika. "Detection of donor cells in recipient tissues after stem cell transplantation using FISH and immunophenotypi Stem cell transplantationng /". Stockholm, 2007. http://diss.kib.ki.se/2007/978-91-7357-222-4/.

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Nadal-Melsio, Elisabet. "Regulatory T cells after allogeneic stem cell transplantation". Thesis, Imperial College London, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.523746.

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Mavin, Emily. "Regulatory T cells in haematopoietic stem cell transplantation". Thesis, University of Newcastle upon Tyne, 2014. http://hdl.handle.net/10443/2731.

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Graft-versus-host disease (GvHD) remains the main complication associated with haematopoietic stem cell transplantation (HSCT). GvHD is caused by allo-reactive donor T cells mounting an attack against specific target tissues. CD4+CD25HiFoxp3+ regulatory T cells have been shown to modulate GvHD in vitro and also in vivo animal models. More recently early stage clinical trials have described the successful use of Treg to reduce the incidence of GvHD following HSCT. The aim of this study was to investigate further the suppressive mechanisms by which Treg are able to modulate GvHD and assess the influence of Treg on the beneficial graft-versus-leukaemia (GvL) effect therefore providing further insight into the use of Treg in the therapeutic management of GVHD. Data presented in this thesis demonstrates the successful isolation and expansion of a highly pure Treg population which maintained suppressive capacity throughout culture. We also confirmed that Treg retain suppressive capacity following cryopreservation resulting in reduced workload and increased consistency when used for in vitro functional studies. We also provide the first human in vitro evidence that Treg are able to prevent cutaneous GvH reaction by blocking the migration of effector T cells into the target tissues. The presence of Treg during allo-stimulation caused reduced effector cell activation, proliferation, IFNγ secretion and decreased skin homing receptor expression. Further investigation into the Treg modulation of dendritic cells demonstrated, for the first time in experimental in vitro human GvHD, that this was due to ineffective effector T cell priming in the presence of Treg caused by impairment of dendritic cell functions. Comprehensive phenotypic and functional analysis of Treg treated moDC showed their decreased antigen processing ability and allostimulatory capacity, resulting in a less severe GvH reaction in the skin explant model. Furthermore, this work has revealed that despite Treg impairing in vitro GvL mechanisms at a cellular level there was no association observed between increased Treg levels and the incidence of relapse in a small clinical cohort of HSCT patients. In conclusion this study has provided further insight into the mechanisms by which Treg are able to modulate GvHD. This would inform future clinical trials using Treg as a therapeutic alternative to current GvHD treatment and prophylaxis.
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Goodman, Reyna Suzanne. "Immunogenetics of haematopoietic stem cell transplantation". Thesis, Anglia Ruskin University, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.478885.

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Kahatapitiya, Prathibha C. "Enrichment of skeletal muscle stem cell transplantation using chemotherapeutic drugs a paradigm for enhanced stem cell transplantation /". Connect to full text, 2008. http://hdl.handle.net/2123/4050.

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Thesis (Ph. D.)--University of Sydney, 2009.
Title from title screen (viewed Apr. 24, 2008) Title from title screen (viewed Feb. 18, 2009) Submitted in fulfilment of the requirements for the degree of Doctor of Philosophy to the Discipline of Paediatrics and Child Health, Faculty of Medicine. Degree awarded 2009 ; thesis submitted 2008. Includes bibliographical references. Also available in print form.
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Szeto, Ching-ho. "Late complications of haemopoietic stem cell transplantation". Click to view the E-thesis via HKUTO, 2004. http://sunzi.lib.hku.hk/hkuto/record/B31972184.

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Trolle, Carl. "Stem Cell Transplantation in Dorsal Root Injury". Licentiate thesis, Uppsala universitet, Institutionen för neurovetenskap, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-218686.

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After traumatic injuries to the brachial plexus there is a risk that one or more of the spinal roots are torn from the spinal cord, known as avulsion injury. This often leads to paralysis and chronic pain, notoriously difficult to treat with current pharmacotherapy. Surgical treatment may improve motor function but sensory recovery is usually poor as sensory axons fail to establish functional connections inside the spinal cord. The aims of this thesis were to develop a model for dorsal root avulsion in rodents in order to investigate the potentials of stem cell therapy for enhancing sensory regeneration after spinal root avulsion. Two different types of stem cells, embryonic and neural crest stem cells, have been transplanted to the avulsion model and analysed using immunohistochemical methods. The results indicate that stem cells survive after transplantation to the avulsed dorsal root and associate with regenerating axons. Furthermore, the different stem cells display different phenotypes after transplantation where embryonic stem cells give rise to neurons located outside the spinal cord that could serve as projection neurons whereas the neural crest stem cells form elongated tubes outlining the avulsed dorsal root and are associated with regenerating neuronal fibers. We have also discovered that the neural crest stem cells migrate into the damaged spinal cord as single cells. The neural crest stem cells also display a diversity in generating both neuronal and glial cells that may have different beneficial effects in neural repair following dorsal root avulsion. To improve the survival of stem cell transplants, the potentials of co-transplanting embryonic stem cells together with nanoparticle delivered growth factor mimetics has been investigated. The results indicate that nanoparticle delivered growth factors improve both transplant survival and maturation in comparison to untreated controls and may be a promising strategy in stem cell transplantation.
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Szeto, Ching-ho, i 司徒精豪. "Late complications of haemopoietic stem cell transplantation". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2004. http://hub.hku.hk/bib/B31972184.

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Li, Pulin. "Chemical Genetics of Hematopoietic Stem Cell Transplantation". Thesis, Harvard University, 2012. http://dissertations.umi.com/gsas.harvard:10306.

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Hematopoietic stem and progenitor cells (HSPCs) repopulate the blood system upon transplantation. A large-scale genetic approach to understand the factors that participate in successful engraftment has not been undertaken. In this thesis, I present the development of a novel live imaging-based competitive marrow repopulation assay in adult zebrafish, which allows fast and quantitative measurement of HSPC engraftment capability. Using this assay, a transplantation-based chemical screen was performed, which led to the discovery of 10 compounds that can enhance the marrow engraftment capability in zebrafish. Among them, the arachidonic acid-derived epoxyeicosatrienoic acids (EET), had conserved effects on both short- and long-term bone marrow engraftment in mice. Genetic analysis in zebrafish embryos demonstrated that EET acts through a \(G\alpha12/13\)-mediated receptor, which activates PI3K and induces transcription factors of the AP-1 family. This PI3K/AP-1 pathway directly induced the transcription of HSC marker, runx1, in embryos. The activation of PI3K by EET promoted HSPC migration and interactions with niche cells. Our studies define a role for EETs in the development of blood stem cells during embryogenesis, and in engraftment in adult vertebrates. The other compounds discovered in the screen implicate additional novel signaling pathways involved in the HSPC engraftment process, which require further investigation. In summary, this thesis elucidated an important role of bioactive lipids in regulating HSC engraftment in adults and during embryo development. Systematically mapping out the regulatory network will tremendously benefit both the basic understanding of stem cell biology and the clinical manipulation to generate better stem cells for transplantation.
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Atarod, Sadaf. "MicroRNAs in haematopoietic stem cell transplantation outcome". Thesis, University of Newcastle upon Tyne, 2015. http://hdl.handle.net/10443/2936.

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Allogeneic haematopoietic stem cell transplantation (allo-HSCT) is a curative treatment for numerous haematological malignancies. Graft-versus-host disease (GVHD) is the major complication causing mortality and is classified into acute (aGVHD) and chronic. MicroRNAs play a significant role in inflammation and have reported potential as biomarkers of different diseases. This study has investigated the role of microRNAs in allo-HSCT outcomes and had two main aims; (1) identification of microRNAs specific to the aGVHD target organ, skin and (2) an investigation into the role of immune specific miRNAs (miR-146a and miR-155) in peripheral blood. Initially, pathway mining was performed on a list of 18 genes that were shown previously, to have deregulated expression levels with regards to GVHD. The pathway mining identified specific immunological pathways in relation to the genes and potential microRNA targets. Global microRNA profiling was performed on a discovery cohort that identified a signature microRNA list in skin biopsies obtained from patients at the time of cutaneous histopathological aGVHD onset (grades I-III) and healthy volunteers. Twelve microRNAs were selected for further validation and it was shown that miR-34a-5p, miR-34a-3p, miR-503-5p and let-7c-5p were elevated and significantly involved in allo-HSCT outcomes. There was an interaction between miR-34a-3p and miR-503-5p which was significantly diagnostic of aGVHD and let-7c-5p was significantly predictive of disease relapse. MiR-34a-5p protein targets; p53 and c-Myc were then evaluated in the same cohort. MiR-34a-5p expression levels and cells stained positively for p53 were significantly correlated in the epidermis. Preliminary optimization of miR-34a-5p knockdown study was successfully conducted which showed promising results in the reduction of T cell proliferation. The whole blood study showed that miR-146a-5p and its interaction with miR-155-5p was predictive of aGVHD incidence in pre-disease onset (Day+28) samples. Interestingly, the expression levels of miR-146a-5p and miR-155-5p negatively correlated with SPI1 (PU.1). In conclusion, these investigations showed that (1) the microRNAs studied in this investigation may regulate the expression levels of the selected 18 genes, (2) microRNA expression levels in clinical skin biopsies obtained at the time of aGVHD onset could potentially be used as diagnostic biomarkers for aGVHD and as predictive biomarkers for overall survival as well as relapse and (3) miR-146a-5p and miR-155-5p expression levels in whole blood could be used as predictive biomarkers for aGVHD incidence.
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Książki na temat "Stem cell transplantation"

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López-Larrea, Carlos, Antonio López-Vázquez i Beatriz Suárez-Álvarez, red. Stem Cell Transplantation. New York, NY: Springer US, 2012. http://dx.doi.org/10.1007/978-1-4614-2098-9.

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López-Larrea, Carlos. Stem Cell Transplantation. New York, NY: Springer US, 2012.

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J, Forman Stephen, Blume Karl G i Thomas E. Donnall, red. Hematopoietic cell transplantation. Wyd. 2. Oxford: Blackwell Science, 1999.

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Champlin, Richard, i Anthony Ho. Hematopoietic stem cell transplantation. New York: Marcel Dekker, 2000.

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Handelsman, Harry. Autologous peripheral stem-cell transplantation. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Agency for Health Care Policy and Research, 1995.

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Laughlin, Mary J., i Hillard M. Lazarus. Allogeneic Stem Cell Transplantation. New Jersey: Humana Press, 2002. http://dx.doi.org/10.1385/159259333x.

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Demirer, Taner, red. Haploidentical Stem Cell Transplantation. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-65319-8.

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Soiffer, Robert J., red. Hematopoietic Stem Cell Transplantation. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-438-4.

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Lazarus, Hillard M., i Mary J. Laughlin, red. Allogeneic Stem Cell Transplantation. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-59745-478-0.

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Bishop, Michael R., red. Hematopoietic Stem Cell Transplantation. Boston, MA: Springer US, 2009. http://dx.doi.org/10.1007/978-0-387-78580-6.

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Części książek na temat "Stem cell transplantation"

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Wingard, John R. "Stem Cell Transplantation". W Managing Infections in Patients With Hematological Malignancies, 211–31. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-59745-415-5_8.

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Durand, Christine, i Richard Ambinder. "Stem Cell Transplantation". W Encyclopedia of AIDS, 1–9. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-9610-6_24-1.

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Durand, Christine, i Richard Ambinder. "Stem Cell Transplantation". W Cancers in People with HIV and AIDS, 367–77. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-0859-2_28.

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Craddock, Charles, i Ronjon Chakraverty. "Stem Cell Transplantation". W Postgraduate Haematology, 651–75. Oxford, UK: John Wiley & Sons, Ltd, 2015. http://dx.doi.org/10.1002/9781118853771.ch35.

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Craddock, Charles, i Ronjon Chakraverty. "Stem Cell Transplantation". W Postgraduate Haematology, 722–45. Oxford, UK: Wiley-Blackwell, 2010. http://dx.doi.org/10.1002/9781444323160.ch38.

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Durand, Christine, i Richard Ambinder. "Stem Cell Transplantation". W Encyclopedia of AIDS, 1927–34. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7101-5_24.

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Ho, Anthony D., i Wolfgang Wagner. "Clinical Potentials of Stem Cells: Hype or Hope?" W Stem Cell Transplantation, 1–25. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527608745.ch1.

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Prósper, Felipe, i Catherine M. Verfaillie. "Testing the Limits: The Potential of MAPC in Animal Models". W Stem Cell Transplantation, 147–56. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527608745.ch10.

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Marini, Frank, Brett Hall, Jennifer Dembinski, Matus Studeny, A. Kate Sasser i Michael Andreeff. "Mesenchymal Stem Cells as Vehicles for Genetic Targeting of Tumors". W Stem Cell Transplantation, 157–75. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527608745.ch11.

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Fischer-Rasokat, Ulrich, i Stefanie Dimmeler. "Endothelial Progenitor Cells for Cardiac Regeneration". W Stem Cell Transplantation, 177–95. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527608745.ch12.

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Streszczenia konferencji na temat "Stem cell transplantation"

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Cassino, Theresa R., Masaho Okada, Lauren Drowley, Johnny Huard i Philip R. LeDuc. "Mechanical Stimulation Improves Muscle-Derived Stem Cell Transplantation for Cardiac Repair". W ASME 2008 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2008. http://dx.doi.org/10.1115/sbc2008-192941.

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Muscle-derived stem cells (MDSCs) have been successfully transplanted into both skeletal (1) and cardiac muscle (2) of dystrophin-deficient (mdx) mice, and show potential for improving cardiac and skeletal dysfunction in diseases like Duchenne muscular dystrophy (DMD). Our previous study explored the regeneration of dystrophin-expressing myocytes following MDSC transplantation into environments with distinct blood flow and chemical/mechanical stimulation attributes. After MDSC transplantation within left ventricular myocardium and gastrocnemius (GN) muscles of the same mdx mice, significantly more dystrophin-positive fibers were found within the myocardium than in the GN. We hypothesized that the differences in mechanical loading of the two environments influenced the transplantation and explored whether using MDSCs exposed to mechanical stimulation prior to transplantation could improve transplantation. Our study shows increased engraftment into the heart and GN muscle for cells pretreated with mechanical stretch for 24 hours. This increase was significant for transplantation into the heart. These studies have implications in a variety of applications including mechanotransduction, stem cell biology, and Duchenne muscular dystrophy.
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Tent, Michiel. "Autologous haematopoietic stem cell transplantation versus DMTs". W ECTRIMS Congress 2022, redaktor Hans-Peter Hartung. Baarn, the Netherlands: Medicom Medical Publishers, 2022. http://dx.doi.org/10.55788/320f3185.

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Spyridonidis, Alexandros, Dionysia Kefala i Maria Liga. "Immunotherapeutic strategies after allogeneic stem cell transplantation". W The 4th European Congress Controversies in Leukemias Brussels, Belgium 20-21 November, 2023, redaktor Alessandro Isidori. Baarn, the Netherlands: Medicom Medical Publishers, 2024. http://dx.doi.org/10.55788/c34572ca.

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van Laar, Jacob M. "SP0113 STEM CELL TRANSPLANTATION – ALL SCIENTIFIC QUESTIONS ANSWERED?" W Annual European Congress of Rheumatology, EULAR 2019, Madrid, 12–15 June 2019. BMJ Publishing Group Ltd and European League Against Rheumatism, 2019. http://dx.doi.org/10.1136/annrheumdis-2019-eular.8611.

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Bergeron, Anne, Cendrine Godet, Sylvie Chevret, Gwenaël Lorillon, Régis Peffault de Latour, Marie Robin, Patricia Ribaud, Gérard Socié i Abdellatif Tazi. "Bronchial Disorders After Allogeneic Hematopoietic Stem Cell Transplantation". W American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a4666.

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Van Laar, JM, D. Farge i A. Tyndall. "FRI0185 Autologous stem cell transplantation international scleroderma trial". W Annual European Congress of Rheumatology, Annals of the rheumatic diseases ARD July 2001. BMJ Publishing Group Ltd and European League Against Rheumatism, 2001. http://dx.doi.org/10.1136/annrheumdis-2001.266.

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Cassino, Theresa R., Masaho Okada, Lauren M. Drowley, Joseph Feduska, Johnny Huard i Philip R. LeDuc. "Using Mechanical Environment to Enhance Stem Cell Transplantation in Muscle Regeneration". W ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-176545.

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Muscle-derived stem cell (MDSC) transplantation has shown potential as a therapy for cardiac and skeletal muscle dysfunction in diseases such as Duchenne muscular dystrophy (DMD). In this study we explore mechanical environment and its effects on MDSCs engraftment into cardiac and skeletal muscle in mdx mice and neoangiogenesis within the engraftment area. We first looked at transplantation of the same number of MDSCs into the heart and gastrocnemius (GN) muscle of dystrophic mice and the resulting dystrophin expression. We then explored neoangiogenesis within the engraftments through quantification of CD31 positive microvessels. This study is important to aid in determining the in vivo environmental factors leading to large graft size which may aid in determining optimum transplantation conditions for muscle repair.
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Yomota, Makiko, Tatsuru Okamura, Yusuke Ohkuma, Yukio Hosomi, Hirotoshi Horio, Kazuteri Ohashi i Tsunekazu Hishima. "Pulmonary veno-occlusive disease after hematopoietic stem cell transplantation". W Annual Congress 2015. European Respiratory Society, 2015. http://dx.doi.org/10.1183/13993003.congress-2015.pa813.

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Aribas, Zeynep, Meral Bosnak-Güçlü, Gülsah Bargi, Deniz Inal Ince, Zeynep Arzu Yegin, Sahika Zeynep Aki i Gülsan Sucak. "Effects of pulmonary rehabilitation during hematopoietic stem cell transplantation". W Annual Congress 2015. European Respiratory Society, 2015. http://dx.doi.org/10.1183/13993003.congress-2015.pa3539.

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Lahzami, S., R. Schoeffel, C. Reid, M. Greenwood, C. Salome, N. Berend i GG King. "Peripheral Airway Function Declines Following Allogeneic Hematopoietic Stem Cell Transplantation." W American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a5081.

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Raporty organizacyjne na temat "Stem cell transplantation"

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Cohen, Isaac. Megakaryocytopoiesis in Stem Cell Transplantation. Fort Belvoir, VA: Defense Technical Information Center, październik 1997. http://dx.doi.org/10.21236/adb233503.

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Reshef, Ran. Chemokine Receptor Signatures in Allogeneic Stem Cell Transplantation. Fort Belvoir, VA: Defense Technical Information Center, sierpień 2014. http://dx.doi.org/10.21236/ada610688.

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Reshef, Ran. Chemokine Receptor Signatures in Allogeneic Stem Cell Transplantation. Fort Belvoir, VA: Defense Technical Information Center, sierpień 2015. http://dx.doi.org/10.21236/ada620593.

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Jin, Dachuan, Zhongfeng Cui, Tao Zhou, Baoqiang Guo, Shunqin Jin, Guangming Li i Chunming Zhang. Comparison of therapeutic effects of various stem cell types, sources, and routes of administration on chronic decompensated cirrhosis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, styczeń 2023. http://dx.doi.org/10.37766/inplasy2023.1.0050.

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Review question / Objective: The aim of this study was to compare the therapeutic effects of various stem cell types, sources and routes of administration on chronic decompensated cirrhosis by using network meta-analysis. Condition being studied: Liver cirrhosis is an important public health problem that puzzles the world. It is divided into compensatory stage and decompensated stage. Once the patient enters decompensated stage, the treatment is very limited, and liver transplantation is currently the best and only approach to improve the survival rate of decompensated cirrhosis4. However, liver transplantation is difficult to be widely applied due to the lack of donor organs and high cost. Therefore, it is very important to study the alternative treatment of liver transplantation. Stem cell therapy as a promising frontier treatment for decompensated cirrhosis, is becoming one of the best feasible alternatives to liver transplantation in recent 20 years. It is very important and necessary to optimize the factors such as cell sources, types, and delivery route, etc. before taking stem cell therapy as a routine clinical treatment. It is believed that the network meta-analysis of the efficacy of various types of stem cells from different sources and routes of administration in the treatment of chronic decompensated cirrhosis can provide useful very clues for clinical practice.
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Lewis, Michael T. Unmasking Stem/Progenitor Cell Properties in Differentiated Epithelial Cells Using Short-term Transplantation. Fort Belvoir, VA: Defense Technical Information Center, sierpień 2006. http://dx.doi.org/10.21236/ada462432.

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Lewis, Michael T. Unmasking Stem/Progenitor Cell Properties in Differentiated Epithelial Cells Using Short-term Transplantation. Fort Belvoir, VA: Defense Technical Information Center, sierpień 2007. http://dx.doi.org/10.21236/ada482708.

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Maragakis, Nicholas J., i Hongjun Song. Preclinical Studies of Induced Pluripotent Stem Cell-Derived Astrocyte Transplantation in ALS. Fort Belvoir, VA: Defense Technical Information Center, grudzień 2014. http://dx.doi.org/10.21236/ada613757.

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Maragakis, Nicholas J., i Hongjun Song. Preclinical Studies of Induced Pluripotent Stem Cell-Derived Astrocyte Transplantation in ALS. Fort Belvoir, VA: Defense Technical Information Center, październik 2012. http://dx.doi.org/10.21236/ada568166.

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Maragakis, Nicholas J., i Hongjun Song. Preclinical Studies of Induced Pluripotent Stem Cell-Derived Astrocyte Transplantation in ALS. Fort Belvoir, VA: Defense Technical Information Center, październik 2011. http://dx.doi.org/10.21236/ada555307.

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Avigan, David. Vaccination with Dendritic Cell Myeloma Fusions in Conjunction with Stem Cell Transplantation and PD-1 Blockade. Fort Belvoir, VA: Defense Technical Information Center, maj 2012. http://dx.doi.org/10.21236/ada565007.

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