• No results found

Megakarocyte formation in vitro to expand and explore - Contents

N/A
N/A
Protected

Academic year: 2021

Share "Megakarocyte formation in vitro to expand and explore - Contents"

Copied!
3
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

UvA-DARE is a service provided by the library of the University of Amsterdam (https://dare.uva.nl)

UvA-DARE (Digital Academic Repository)

Megakarocyte formation in vitro to expand and explore

van den Oudenrijn, S.

Publication date

2001

Link to publication

Citation for published version (APA):

van den Oudenrijn, S. (2001). Megakarocyte formation in vitro to expand and explore.

General rights

It is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), other than for strictly personal, individual use, unless the work is under an open content license (like Creative Commons).

Disclaimer/Complaints regulations

If you believe that digital publication of certain material infringes any of your rights or (privacy) interests, please let the Library know, stating your reasons. In case of a legitimate complaint, the Library will make the material inaccessible and/or remove it from the website. Please Ask the Library: https://uba.uva.nl/en/contact, or a letter to: Library of the University of Amsterdam, Secretariat, Singel 425, 1012 WP Amsterdam, The Netherlands. You will be contacted as soon as possible.

(2)

Contents

Chapter 1. Scope of this thesis

Chapter 2. Thrombopoietin and ex vivo expansion of megakaryocytes.

In: Platelet Therapy: Current Status and Future Trends: Elsevier,

2000: 337-362 13

Chapter 3. A combination of Megakaryocyte Growth and Development Factor and interleukin-1 is sufficient to culture large numbers of megakaryocyte progenitors and megakaryocytes for transfusion purposes.

British Journal of Haematology, 1999; 106: 553-563 43

Chapter 4. Differences in megakaryocyte expansion potential between CD34+ stem cells derived from cord blood, peripheral blood

and bone marrow from adults and children.

Experimental Hematology, 2000; 28: 1054-1061 63

Chapter 5. Influence of medium components on ex vivo megakaryocyte expansion.

Journal of Hematotherapy and Stem Cell Research, in press 81

Chapter 6. Mutations in the thrombopoietin receptor, Mpl, in children with congenital amegakaryocytic thrombocytopenia.

British Journal of Haematology, 2000; 110: 441-448 97

Chapter 7. Three parameters: plasma thrombopoietin levels, plasma glycocahcin levels and megakaryocyte culture, distinguish between different causes of congenital thrombocytopenia.

Submitted for publication 113

Chapter 8. Aberrant processing and folding of Mpl due to mutations associated with congenital amegakaryocytic thrombocytopenia.

1 n

Manuscript in preparation l J '

Chapter 9. Summary and general discussion 145

Chapter 10. Samenvatting 167

1 nn

(3)

Referenties

GERELATEERDE DOCUMENTEN

In the current study we show that specific T-bet and Eomes expression states relate to distinct expression patterns of IL-7R α , granzyme K, KLRG1 and granzyme B expression,

Using the unique TCRß sequence of each virus specific clones, they were identified within the total CD8 population during the early response (50 most abundant CD8+ T-cell clones

In summary, with regard to cytolytic function, LN-derived hCMV- and EBV-specific and total CD8 + T cells contain fewer effector-type cells.. More polyfunctional hCMV-specific CD8 +

Here we studied whether IL-7R α -expressing cells obtained from peripheral blood (PB) or lymph nodes (LNs) sustain the circulating effector-type hCMV-specific pool..

In this study, we show that the percentage of CD28 ⁻ CD27 ⁻ granzyme B-expressing CD4 + T cells in the circulation largely increases after primary hCMV

new naive T cells also might be primed during the latency phase, as has been reported in mice.15 In any case, it is apparent that the virus-specific cells late in infection are

Het lijkt echter niet plausibel om dit als verklaring te gebruiken voor de verschillen op de voor- en nameting van de N-back taak, want er waren geen ‘pure’

Als interne standaard werd Thiamphenicol gebruikt welke bij het gebruik van de "electron capture" detector goed terugge- vonden werd, bij de GC-MS kon de