Výsledky vyhledávání - "Fatima S. F. Aerts Kaya"

CXCR4 expression by mesenchymal stromal cells is lost after use of enzymatic dissociation agents, but preserved by use of non-enzymatic methods

Autor: Burcu, Pervin, Gözde, Aydın, Trudi, Visser, Duygu, Uçkan-Çetinkaya, Fatima S F, Aerts-Kaya

Publikováno v: International journal of hematology. 113(1)

In recent years, multipotent mesenchymal stromal cells (MSCs) have demonstrated tremendous potential for use in regenerative medicine. CXCR4, the receptor for CXCL12, is highly expressed by bone marrow (BM) MSCs and the CXCR4/CXCL12 axis has been sho

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cbf5579ee50497e19602e4114dc40e54
https://pubmed.ncbi.nlm.nih.gov/33389659

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Mobilization of hepatic mesenchymal stem cells from human liver grafts

Autor: Jaap Kwekkeboom, Fatima S. F. Aerts Kaya, Hugo W. Tilanus, Monique M A Verstegen, Suomi M. G. Fouraschen, Andrew P. Stubbs, Wilfred F. J. van IJcken, Geert Kazemier, Qiuwei Pan, Harry L.A. Janssen, Mario Pescatori, Herold J. Metselaar, Antoine van der Sloot, Jeroen de Jonge, Gerard Wagemaker, Luc J. W. van der Laan, Ron Smits

Publikováno v: Liver Transplantation, 17(5), 596-609. John Wiley & Sons Ltd.

Extensive studies have demonstrated the potential applications of bone marrow-derived mesenchymal stem cells (BM-MSCs) as regenerative or immunosuppressive treatments in the setting of organ transplantation. The aims of the present study were to expl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cf26fb293c4acc86ab2ce810766b0c0
https://doi.org/10.1002/lt.22260

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Lentiviral gene therapy of murine hematopoietic stem cells ameliorates the Pompe disease phenotype

Autor: Edwin H. Jacobs, Pascal van der Wegen, Fatima S. F. Aerts Kaya, Bob J. Scholte, Merel Stok, Trudi P. Visser, Ans T. van der Ploeg, Bart N. Lambrecht, Dirk J. Duncker, Arnold J. J. Reuser, Gerard Wagemaker, Monique Willart, Elnaz Farahbakhshian, Monique C. de Waard, Niek P. van Til, Marian A. Kroos, Monique M A Verstegen

Publikováno v: Blood, 115(26), 5329-5337. American Society of Hematology

Pompe disease (acid α-glucosidase deficiency) is a lysosomal glycogen storage disorder characterized in its most severe early-onset form by rapidly progressive muscle weakness and mortality within the first year of life due to cardiac and respirator

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c24f6d34f10c00552fc1c0ecec569ecb
https://doi.org/10.1182/blood-2009-11-252874

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5-Androstene-3b,17b-Diol Administration of Mice Exposed to Total Body Irradiation Results in Rapid Reconstitution of Immature Bone Marrow Progenitor Cells and Synergizes with Thrombopoietin but Not with Granulocyte-Colony Stimulating Factor

Autor: Trudi P. Visser, Dwight R. Stickney, Chris L. Reading, Fatima S. F. Aerts Kaya, Gerard Wagemaker, James M. Frincke

Publikováno v: Blood. 112:2327-2327

5-AED (5-androstene-3β,17β-diol) is a naturally occurring adrenal cortical steroid, which displays radioprotective effects in both rodents and non-human primates, resulting in accelerated multilineage hematopoiesis and enhanced survival after total

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::aeb8940fcfd9701aadc4338211d84cd0
https://doi.org/10.1182/blood.v112.11.2327.2327

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