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Effect of antimalarial drugs on DNA synthesis in the bone morrow cells /Saisanom Tampitag. January 1969 (has links) (PDF)
Thesis (M.Sc. (Biochemistry))--Mahidol University, 1969.
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Chloramphenicol-induced toxicity on haemopoiesis /Kong, Cheuk-ting. January 1998 (has links)
Thesis (M. Phil.)--University of Hong Kong, 1999. / Includes bibliographical references (leaves 126-137).
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Generation and functional characterization of dendritic cells from bone marrow of patients with leukaemia diseases and various haemato-oncological conditionsChan, Shing. January 2002 (has links)
Thesis (M.Med.Sc.)--University of Hong Kong, 2002. / Includes bibliographical references (leaves 61-64). Also available in print.
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Combining Erythropoietin Infusion With Intramyocardial Delivery of Bone Marrow Cells Is More Effective for Cardiac RepairZhang, Dingguo, Zhang, Fumin, Zhang, Yuqing, Gao, Xiang, Li, Chuanfu, Yang, Naiquan, Cao, Kejiang 01 February 2007 (has links)
We postulated that combining erythropoietin (EPO) infusion with bone marrow mesenchymal stem cells (MSC) delivery may give better prognosis in a rat infarcted heart. Acute myocardial infarction (MI) model was developed by coronary artery ligation. Animals were grouped (n = 18) to receive intramyocardial injection of 30 μl saline solution without cells (EPO and control groups) or with 3 × 106 MSC from transgenic green fluorescent protein (GFP)+ male mice (MSC and MSC-EPO groups). The animals received either 5000 U/kg body weight EPO (EPO and MSC-EPO groups) or saline solution (MSC and control groups) for 7 days after MI. Cardiac functions were measured by echocardiography and cardiac tissue was harvested for immunohistological studies 3 weeks after surgery. We observed regeneration of MSC in and around the infarcted myocardium in MSC and MSC-EPO groups. Capillary density was markedly enhanced with significantly smaller infarct size and reduced fibrotic area in MSC-EPO group as compared with other three groups. A smaller left ventricular (LV) diastolic dimension and a higher LV fractional shortening were observed in MSC-EPO group than in other three groups. Transplantation of MSC combined with cytokine EPO is superior to either of the monotherapy approach for angiomyogenesis and cardiac function recovery.
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Expression and regulation of c-myb in B-lymphocyte developmentDamiani, Candice LaShawn. January 1900 (has links)
Thesis (Ph. D.)--West Virginia University, 2002. / Title from document title page. Document formatted into pages; contains viii, 168 p. : ill. (some col.). Includes abstract. Includes bibliographical references.
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Prion Protein is Expressed on Long-term Repopulating Hematopoietic Stem Cells and is Necessary for their Self-renewalLodish, Harvey F., Zhang, Cheng Cheng, Steele, Andrew D., Lindquist, Susan L. 01 1900 (has links)
We show that the prion protein (PrP) is expressed on the surface of bone marrow cell populations enriched in long-term repopulating hematopoietic stem cells. Affinity purification of the PrP-positive and PrP-negative fractions from these populations, followed by competitive reconstitution assays, show that all long-term repopulating hematopoietic stem cells express PrP. Hematopoietic stem cells from PrP null bone marrow exhibit impaired self-renewal in serial competitive transplantation experiments, and premature exhaustion when exposed to cell cycle-specific myelotoxic injury. Therefore, PrP is a novel marker for hematopoietic stem cells and regulates their self-renewal. / Singapore-MIT Alliance (SMA)
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Characteristics and differentiation of cells involved in bone formationMaybee, Sarah Helen January 1984 (has links)
No description available.
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Radon decay in bone marrow fat cells and the possible induction of leukaemia /Utteridge, Tammy Debra. Unknown Date (has links)
Thesis (PhD in AppSc)--University of South Australia, 1996
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Ovine bone marrow mesenchymal stem cells : isolation, characterisation, and developmental potential for application in growth plate cartilage regeneration.McCarty, Rosa Clare January 2008 (has links)
Title page, contents and abstract only. The complete thesis in print form is available from the University of Adelaide Library. / The growth plate is a cartilaginous structure located at the proximal and distal ends of immature long bones, which contributes to longitudinal growth through the process of endochondral ossification. Cartilage has a limited ability to regenerate and in children, injury to the the growth plate can result in limb length discrepancies and angular deformity, due to formation of a bone bridge at the damaged site which disturbs structure and function of the growth plate. Current treatments of the abnormalities arising from growth plate arrest involve surgical correction once the deformities have manifested. To date, there is no biological based therapy for the repair of injured/damaged growth plate cartilage. Mesenchymal stem cells (MSC) are self renewable mulitpotential progenitor cells with the capacity to differentiate toward the chondrogenic lineage. Since their discovery, significant interest has been generated in the potential application of these cells for cartilage regeneration. In this study, the ability of autologous bone marrow mesenchymal stem cells to regenerate growth plate cartilage in a sheep model was examined. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1330837 / Thesis (Ph.D.) -- University of Adelaide, School of Paediatrics and Reproductive Health, 2008
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Stromal precursor cells : purification and the development of bone tissue / Stan Gronthos.Gronthos, Stan January 1998 (has links)
Bibliography: leaves 152-223. / xxiii, 223, [137] leaves, [27] leaves of plates : ill. (chiefly col.) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Experiments were designed to identify and purify human bone marrow stromal precursor cells by positive immunoselection, based on the cell surface expression of the VCAM-1 and STRO-1 antigens. The data presented demonstrates a hierarchy of bone cell development in vitro. / Thesis (Ph.D.)--University of Adelaide, Dept. of Orthopaedics Surgery and Trauma, 1998
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