Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Steve F. Parsons"'
Autor:
Kongtana Trakarnsanga, Marieangela C. Wilson, Winnie Lau, Belinda K. Singleton, Steve F. Parsons, Punthita Sakuntanaga, Ryo Kurita, Yukio Nakamura, David J. Anstee, Jan Frayne
Publikováno v:
Haematologica, Vol 99, Iss 11 (2014)
A major barrier to the clinical use of erythrocytes generated in vitro from pluripotent stem cells or cord blood progenitors is failure of these erythrocytes to express adult hemoglobin. The key regulators of globin switching KLF1 and BCL11A are abse
Externí odkaz:
https://doaj.org/article/fa9914930d7a4284b64ccca182c292dc
Autor:
Kongtana Trakarnsanga, Marieangela C Wilson, Rebecca E Griffiths, Ashley M Toye, Lee Carpenter, Kate J Heesom, Steve F Parsons, David J Anstee, Jan Frayne
Publikováno v:
PLoS ONE, Vol 9, Iss 7, p e100874 (2014)
Induced pluripotent stem cells (iPSC) are an attractive progenitor source for the generation of in vitro blood products. However, before iPSC-derived erythroid cells can be considered for therapeutic use their similarity to adult erythroid cells must
Externí odkaz:
https://doaj.org/article/a5c97a43397a4584ad42b90d3800431e
Autor:
David J. Anstee, Marieangela C. Wilson, Nicola Cogan, Steve F. Parsons, Kongtana Trakarnsanga, Jan Frayne, Carole Green, Ashley M. Toye, Kate J. Heesom
Publikováno v:
Wilson, M, Trakarnsanga, K, Heesom, K, Toye, A & Frayne, J 2016, ' Comparison of the proteome of adult and cord erythroid cells, and changes in the proteome following reticulocyte maturation ', Molecular and Cellular Proteomics, vol. 15, no. 6, pp. 1938-1946 . https://doi.org/10.1074/mcp.M115.057315
Cord blood stem cells are an attractive starting source for the production of red blood cells in vitro for therapy because of additional expansion potential compared with adult peripheral blood progenitors and cord blood banks usually being more repr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c547dbbf9a8800f561c9e719e8e8ceb
https://hdl.handle.net/1983/b273f2a3-b8e1-462d-8f78-de4e5a905735
https://hdl.handle.net/1983/b273f2a3-b8e1-462d-8f78-de4e5a905735
Autor:
Jan Frayne, Marieangela C. Wilson, Winnie W. Y. Lau, R. Leo Brady, Ben M. Richardson, Nicholas M. Burton, David J. Anstee, Belinda K. Singleton, Victoria Fairweather, Steve F. Parsons, Kongtana Trakarnsanga
Publikováno v:
Blood. 118:3137-3145
Mutations in the human erythroid Krüppel-like factor (EKLF) can lead to either anemia or the benign InLu phenotype. To elucidate the relationship between these mutations and the differing phenotypes, we prepared recombinant forms of wild-type and 5
Autor:
Jan Frayne, Rebecca E. Griffiths, David J. Anstee, Marieangela C. Wilson, Kate J. Heesom, Ashley M. Toye, Steve F. Parsons, Kongtana Trakarnsanga, Lee Carpenter
Publikováno v:
PLoS ONE
PLoS ONE, Vol 9, Iss 7, p e100874 (2014)
PLoS ONE, Vol 9, Iss 7, p e100874 (2014)
Induced pluripotent stem cells (iPSC) are an attractive progenitor source for the generation of in vitro blood products. However, before iPSC-derived erythroid cells can be considered for therapeutic use their similarity to adult erythroid cells must
Publikováno v:
Proteomics. Clinical applications. 3(9)
In the present study we have used an in vitro culture system that induces differentiation of human CD34(+) cells down the erythroid lineage along with 2-D DIGE to determine the differential proteome of erythroblasts at specific developmental stages d
Publikováno v:
Blood. 118:2096-2096
Abstract 2096 We have formulated a robust culture system simulating human erythropoiesis, producing mature reticulocytes from adult peripheral blood CD34+ progenitor cells in 20 days. Expansion of cell numbers over the course of the culture exceeded
Autor:
Jon D. Lane, Virginie M S Betin, Rebecca E. Griffiths, Steve F. Parsons, David J. Anstee, Nicola Cogan, Sabine Kupzig, Tosti J. Mankelow
Publikováno v:
Blood. 118:177-177
Abstract 177 The erythrocyte is one of the best characterized human cells. However, studies of the process whereby human reticulocytes mature to erythrocytes have been hampered by the difficulty of obtaining sufficient numbers of cells for analysis.