Zobrazeno 1 - 10 of 21 pro vyhledávání: '"Annelies J. Van Vuren"'
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Akademický článek
The EPO-FGF23 Signaling Pathway in Erythroid Progenitor Cells: Opening a New Area of Research
Autor: Annelies J. van Vuren, Carlo A. J. M. Gaillard, Michele F. Eisenga, Richard van Wijk, Eduard J. van Beers
Publikováno v: Frontiers in Physiology, Vol 10 (2019)
We provide an overview of the evidence for an erythropoietin-fibroblast growth factor 23 (FGF23) signaling pathway directly influencing erythroid cells in the bone marrow. We outline its importance for red blood cell production, which might add, amon
Externí odkaz: https://doaj.org/article/617cbd2a12e14294abc3f5c130ac9e2d
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Transfusion burden in early childhood plays an important role in iron overload in Diamond-Blackfan anaemia
Autor: Jonathan R. A. de Wilde, Birgit van Dooijeweert, Annelies J. van Vuren, Elise J. Huisman, Frans J. Smiers, Arian van der Veer, Richard van Wijk, Wouter W. van Solinge, Edward E. S. Nieuwenhuis, Eduard J. van Beers, Marije Bartels
Publikováno v: eJHaem, 3(4), 1300-1304. John Wiley & Sons Inc.
eJHaem, 3, 1300-1304. Wiley
In Diamond-Blackfan anaemia (DBA), iron overload (IO) is common in transfusion-dependent patients, yet has also been reported in non-transfusion-dependent patients. We explored the incidence of IO in transfusion-dependent and non-transfusion-dependen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd483b2a66f339220296b60801b1af58
https://doi.org/10.1002/jha2.524
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Interplay of erythropoietin, fibroblast growth factor 23, and erythroferrone in patients with hereditary hemolytic anemia
Autor: Stephanie van Straaten, Stephan J. L. Bakker, Michele F Eisenga, Richard van Wijk, Martin H. de Borst, Andreas Glenthøj, Annelies J. Van Vuren, Carlo A. J. M. Gaillard, Eduard J. van Beers
Publikováno v: van Vuren, A J, Eisenga, M F, van Straaten, S, Glenthøj, A, Gaillard, C A J M, Bakker, S J L, de Borst, M H, van Wijk, R & van Beers, E J 2020, ' Interplay of erythropoietin, fibroblast growth factor 23, and erythroferrone in patients with hereditary hemolytic anemia ', Blood advances, vol. 4, no. 8, pp. 1678-1682 . https://doi.org/10.1182/bloodadvances.2020001595
Blood, 4(8), 1678-1682. AMER SOC HEMATOLOGY
Recently, erythropoietin (EPO) was identified as regulator of fibroblast growth factor 23 (FGF23). Proteolytic cleavage of biologically active intact FGF23 (iFGF23) results in the formation of C-terminal fragments (cFGF23). An increase in cFGF23 rela
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ca45755baf1eec5e044c495f788e2da
https://doi.org/10.1182/bloodadvances.2020001595
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A Unique Monocyte Transcriptome Discriminates Sickle Cell Disease From Other Hereditary Hemolytic Anemias and Shows the Particular Importance of Lipid and Interferon Signaling
Autor: Stephanie van Straaten, Michal Mokry, Richard van Wijk, Eduard J. van Beers, Annelies J. Van Vuren
Publikováno v: HemaSphere, Vol 5, Iss 3, p e531 (2021)
HemaSphere
Introduction Sickle cell disease (SCD) is a hereditary hemolytic disease characterized by a complex pathophysiology including inflammation and oxidative stress. Intravascular hemolysis leads to release of heme, an erythrocyte-derived Danger Associate
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c2230ee4521f87f294f1b0554814f4f
http://journals.lww.com/10.1097/HS9.0000000000000531
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A Proposed Concept for Defective Mitophagy Leading to Late Stage Ineffective Erythropoiesis in Pyruvate Kinase Deficiency
Autor: Annelies J. Van Vuren, Eduard J. van Beers, Richard van Wijk
Publikováno v: Frontiers in Physiology, Vol 11 (2021)
Frontiers in Physiology
Pyruvate kinase deficiency (PKD) is a rare congenital hemolytic anemia caused by mutations in the PKLR gene. Here, we review pathophysiological aspects of PKD, focusing on the interplay between pyruvate kinase (PK)-activity and reticulocyte maturatio
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09f5897e59bec4cfca96b7bf5330dc6f
https://doi.org/10.3389/fphys.2020.609103
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A Comprehensive Analysis of the Erythropoietin-erythroferrone-hepcidin Pathway in Hereditary Hemolytic Anemias
Autor: Marije Bartels, Daniel El Fassi, Richard van Wijk, Jesper Petersen, Arjen M Punt, Andreas Glenthøj, Eduard J. van Beers, Wouter W. van Solinge, Alaa Sharfo, Simon T. Grootendorst, Stephanie van Straaten, Annelies J. Van Vuren
Publikováno v: Van Vuren, A J, Sharfo, A, Grootendorst, S T, Van Straaten, S, Punt, A M, Petersen, J B, El Fassi, D, Van Solinge, W W, Bartels, M, Van Wijk, R, Glenthøj, A & Van Beers, E J 2021, ' A Comprehensive Analysis of the Erythropoietin-erythroferrone-hepcidin Pathway in Hereditary Hemolytic Anemias ', HemaSphere, vol. 5, no. 9, e627 . https://doi.org/10.1097/HS9.0000000000000627
HemaSphere, Vol 5, Iss 9, p e627 (2021)
HemaSphere
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63b7f3d7d5bf7cae24b27e6b3dc17f2e
https://curis.ku.dk/ws/files/298148076/A_Comprehensive_Analysis_of_the.4.pdf
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