Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Puspa Batten"'
Autor:
Ryszard T. Smolenski, Ewa M. Slominska, Kameljit K. Kalsi, Ada H. Yuen, Joanna Karbowska, Maria Laura Bacci, Massimo Macherini, Zdzislaw Kochan, Marialuisa Lavitrano, Monica Forni, Magdi H. Yacoub, Zain Khalpey, Puspa Batten
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1741:191-198
The endothelial cell Surface expression of ecto-5-nucleotidase (E5'N, CD73) is thought to be essential for the extracellular formation of cytoprotective, anti-thrombotic and immunosuppressive adenosine. Decreased E5'N activity may play a role in xeno
Autor:
Puspa Batten, Monica Forni, Zdzislaw Kochan, A. H. Y. Yuen, Zain Khalpey, Ryszard T. Smolenski, M. Macherini, Joanna Karbowska, Kameljit K. Kalsi, Ewa M. Slominska, Magdi H. Yacoub, Marialuisa Lavitrano, Maria Laura Bacci
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 24:271-274
Ecto-5'-nucleotidase (E5'N) is an extracellular enzyme forming anti-inflammatory and immunosuppressive adenosine. We evaluated whether confrontation of pig heart and endothelial cells with human blood changes the activity of E5'N. Pig hearts were per
Publikováno v:
The International Journal of Biochemistry & Cell Biology. 35:113-118
Cardiac valve interstitial cells (ICs) are a heterogeneous and dynamic population of specific cell types that have many unique characteristics. They are responsible for maintaining the extracellular scaffold that provides the mechanical characteristi
Publikováno v:
The Journal of Thoracic and Cardiovascular Surgery. 122:129-135
Objectives: Valve allografts produce an immune response, which can influence their performance. The exact role of the interaction between recipient T cells and the different cellular components of the donor valve in stimulating an immune response is
Publikováno v:
Transplantation. 68:1552-1560
Background. Human T cells proliferate in response to both human umbilical vein endothelial cells (HUVEC) and porcine aortic endothelial cells (PAEC) via the second signals LFA-3/CD2 and B7-2 (CD86), respectively. Previous studies have shown that stim
Publikováno v:
Transplantation. 64:1175-1180
BACKGROUND Immunocytochemical analysis of human organs in situ reveals differential expression of MHC class II antigens by microvascular endothelial cells (MVEC) and endothelial cells (EC) from large vessels. In view of the role of EC as initiators o
Publikováno v:
Transplantation. 60:1024-1032
To investigate whether human T cells can directly recognize pig xenoantigens, highly purified human CD4+ and CD8+ T cells were incubated with pig aortic endothelial cells (PAEC). The response was measured by [3H]thymidine uptake and release of bioact
Although recent progress in cardiovascular tissue engineering has generated great expectations for the exploitation of stem cells to restore cardiac form and function, the prospects of a common mass-produced cell resource for clinically viable engine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5daae293d7179b84b44fd4d0e8a29c2
https://europepmc.org/articles/PMC2440400/
https://europepmc.org/articles/PMC2440400/
Autor:
Najma, Latif, Padmini, Sarathchandra, Penny S, Thomas, Joe, Antoniw, Puspa, Batten, Adrian H, Chester, Patricia M, Taylor, Magdi H, Yacoub
Publikováno v:
The Journal of heart valve disease. 16(1)
Human mesenchymal stem cells (MSCs) are a potential cell source for the tissue engineering of biological structures, including cardiac valves. A comprehensive, phenotypic analysis of MSCs and, for the latter, their comparison with valve interstitial
Autor:
Sajiram Sarvananthan, Eleftherios Sachlos, Jan T. Czernuszka, Puspa Batten, Patricia M. Taylor, David N. Firmin, Adrian H. Chester, Magdi H. Yacoub, John V. Terrovitis, Jeff W.M. Bulte, Padmini Sarathchandra, Lindsey A. Crowe
Publikováno v:
Tissue engineering 3rd Biennial Meeting of Society-for-Heart-Valve-Disease. 12(10)
Mesenchymal stem cells (MSCs) are a promising candidate cell for tissue engineering. Magnetic resonance imaging (MRI) has been proven effective in visualizing iron-labeled stem cells; however, the efficiency of this approach for visualization of cell