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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Telomerase activity in human umbilical cord cell populations containing hematopoietic stem cells

Murthy, Vidya. January 2002 (has links)
Thesis (M.S.)--Worcester Polytechnic Institute. / Keywords: Hematopoietic stem cells; Umbilical cord blood. Includes bibliographical references.
2

Exploring the complications of hematopoietic stem cell transplantation : a laboratory and clinical study

Robles, Joseph Delano January 2014 (has links)
abstract / Paediatrics and Adolescent Medicine / Doctoral / Doctor of Philosophy
3

Late complications of haemopoietic stem cell transplantation

Szeto, Ching-ho., 司徒精豪. January 2004 (has links)
published_or_final_version / Medical Sciences / Master / Master of Medical Sciences
4

Analysis of telomerase activity and telomere lengths in human umbilical cord cell populations during ex vivo amplification of hematopoietic stem cells

Chomal, Manish R. January 2002 (has links)
Thesis (M.S.)--Worcester Polytechnic Institute. / Keywords: telomerase activity; telomere lengths; hematopoietic stem cells. Includes bibliographical references (p. 64-71).
5

Late complications of haemopoietic stem cell transplantation

Szeto, Ching-ho. January 2004 (has links)
Thesis (M. Med. Sc.)--University of Hong Kong, 2004. / Also available in print.
6

Immunologische Charakterisierung hämopoetischer Vorläuferzellen beim Hund

Hahn, Joachim. January 1993 (has links)
Thesis (doctoral)--Ludwig-Maximilians-Universität München, 1993.
7

Purification and characterization of the human hemopoietic stem cell

Sutherland, Heather Jeanine January 1991 (has links)
Previous studies in mice have suggested that some if not all hemopoietic stem cells with long-term in vivo repopulating ability are biologically, physically, and pharmacologically different from cells detectable by short-term colony assays. Since human hemopoietic stem cells cannot be assessed by expression of their in vivo repopulating potential, characterization of these cells requires an alternative endpoint. This thesis explores the use of clonogenic cell production in vitro in the presence of a competent stromal cell feeder layer for this purpose, based on the observation that this can continue for many weeks when unseparated human marrow cells are cultured under conditions that allow a stromal cell layer to form. Accordingly, a population of human clonogenic cell precursors referred to as long-term culture-initiating cells (LTC-IC) were postulated to exist as a biologically distinct compartment whose members could be quantitated by measuring the number of myeloid, erythroid and multi-lineage clonogenic progenitors present after 5 weeks of their culture on stromal feeder layers. LTC-IC in normal marrow assayed in this way were found to have a significantly lower forward light scatter, lower expression of HLA-DR, lower expression of CD 71 (transferrin receptor), and a higher expression of CD 34 as compared to clonogenic cells. Separation of marrow cells on the basis of these differences allowed a cell population enriched ~800 fold in LTC-IC to be obtained. This population contained only 0.06% of the marrow cells and 2% of the total clonogenic cells, but retained 50 - 60% of the LTC-IC present in the original marrow. Absolute numbers of LTC-IC and the proliferative and differentiative capability of individual LTC-IC were then determined by limiting dilution analysis following the demonstration that clonogenic cell output (at 5 weeks) is linearly related to input cell number over a wide range of cell concentrations. The frequency of LTC-IC in normal human marrow was determined to be ~1 per 2 x 10⁴ cells. Following purification this was increased to 1-2%. The proliferative capacity exhibited by individual LTC-IC as measured by the number of clonogenic cells per LTC-IC in 5 week-old cultures was found to range from 1 to 30 (the average being ~4). These studies also showed that a least some LTC-IC are multipotent as evident by their production of both erythroid and myeloid progeny. To study the effect of specific growth factors on LTC-IC maintenance and differentiation, highly purified LTC-IC were seeded onto irradiated murine marrow-derived stromal cells (from the M2-10B4 line) previously engineered to produce one of the human hemopoietic growth factors G-CSF, GM-CSF or IL-3. In the absence of any feeders, both the LTC-IC and their progeny in these purified suspensions decreased to very low levels within 5 weeks. However, in the presence of control M2-10B4 cells, LTC-IC maintenance and differentiation was supported as effectively as when standard human marrow feeders were present. The combined presence of G-CSF and IL-3-producing M2-10B4 cells further enhanced the maintenance and early differentiation of LTC-IC above levels obtained with control feeders, but only in the absence of GM-CSF producing feeders. In contrast, in the presence of GM-CSF-producing feeders the output of mature granulocytes and macrophages was maximal, and LTC-IC were inhibited. These studies describe and validate the use of the LTC-IC assay to selectively identify and quantitate a previously inaccessible population of very primitive human hemopoietic cells. Exploration of in vitro conditions and human growth factors able to influence their developmental behaviour points to G-CSF plus II-3 as the best candidates for future studies of LTC-IC activation and/or expansion in vitro. / Medicine, Faculty of / Pathology and Laboratory Medicine, Department of / Graduate
8

Telomerase Activity in Human Umbilical Cord Cell Populations Containing Hematopoietic Stem Cells

Murthy, Vidya 30 April 2002 (has links)
Hematopoietic cell populations exhibiting detectable telomerase activity and elongated telomere lengths display strong engraftment survivability in humans during transplants. We investigated telomerase activity and telomere length in umbilical cord blood hematopoietic cell populations obtained from ViaCell Inc. at various intervals of a two-week ex vivo stem cell amplification process. Telomerase activity is increased with time in ViaCell's amplification process, perhaps in response to the removal of differentiated cells and expansion of primitive hematopoietic stem cell populations in tissue culture media containing a mixture of growth factors. Two of ViaCell's cell culture fractions were analyzed for telomere length using a TLA. Our results showed relatively long telomere lengths for day-0 and day-14 cord populations, and that despite an upregulation of telomerase activity in Day-14 samples, a loss of about 2 kb of telomeric DNA occurs. Our data are consistent with a model in which the increase in telomerase activity in day-14 ex vivo amplified cord blood hematopoietic cells relative to fresh cord is sufficient to reduce, but not prevent, telomere shortening caused by cell proliferation. Lastly, we investigated various culture conditions that could potentially upregulate telomerase activity in the Day-14 amplified cells. However none of the treatments tested altered telomerase activity. Our detection of increased telomerase activity and relatively long telomere lengths in ViaCell's Day-14 ex vivo amplified cord blood stem cell fraction provides support for ViaCell's Selective Clonogenic AmplificationTM indicating a high engraftment potential for these cells.
9

The influence of osteoblasts and growth factors on the proliferation and differentiation of OMA-AML-1 cells a report submitted in partial fulfillment ... for the degree of Master of Science (School of Dentistry) ... /

Korsnes, Maria Isabel. January 1998 (has links)
Thesis (M.S.)--University of Michigan, 1998. / Includes bibliographical references.
10

Transcriptional regulation of Runx1 in the developing haematopoietic system

Nottingham, Wade January 2007 (has links)
No description available.

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