Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Stephanie van Straaten"'
Autor:
Annelies J. van Vuren, Alaa Sharfo, Simon T. Grootendorst, Stephanie van Straaten, Arjen M. Punt, Jesper B. Petersen, Daniel El Fassi, Wouter W. van Solinge, Marije Bartels, Richard van Wijk, Andreas Glenthøj, Eduard J. van Beers
Publikováno v:
HemaSphere, Vol 5, Iss 9, p e627 (2021)
Externí odkaz:
https://doaj.org/article/12447da937f6495b80a415abc7371f7b
Autor:
Annelies J. van Vuren, Stephanie van Straaten, Michal Mokry, Richard van Wijk, Eduard J. van Beers
Publikováno v:
HemaSphere, Vol 5, Iss 3, p e531 (2021)
Externí odkaz:
https://doaj.org/article/d09eb6d1e8e04d709ef446ff553f8121
Autor:
Minke A.E. Rab, Brigitte A. van Oirschot, Penelope A. Kosinski, Jeffrey Hixon, Kendall Johnson, Victor Chubukov, Lenny Dang, Gerard Pasterkamp, Stephanie van Straaten, Wouter W. van Solinge, Eduard J. van Beers, Charles Kung, Richard van Wijk
Publikováno v:
Haematologica, Vol 106, Iss 1 (2020)
Pyruvate kinase (PK) deficiency is a rare hereditary disorder affecting red cell (RBC) glycolysis, causing changes in metabolism including a deficiency in ATP. This affects red cell homeostasis, promoting premature removal of RBCs from the circulatio
Externí odkaz:
https://doaj.org/article/44b3ff13f934410f9834ac9556f1b87b
Autor:
Eduard J. van Beers, Stephanie van Straaten, D. Holmes Morton, Wilma Barcellini, Stefan W. Eber, Bertil Glader, Hassan M. Yaish, Satheesh Chonat, Janet L. Kwiatkowski, Jennifer A. Rothman, Mukta Sharma, Ellis J. Neufeld, Sujit Sheth, Jenny M. Despotovic, Nina Kollmar, Dagmar Pospíšilová, Christine M. Knoll, Kevin Kuo, Yves D. Pastore, Alexis A. Thompson, Peter E. Newburger, Yaddanapudi Ravindranath, Winfred C. Wang, Marcin W. Wlodarski, Heng Wang, Susanne Holzhauer, Vicky R. Breakey, Madeleine Verhovsek, Joachim Kunz, Melissa A. McNaull, Melissa J. Rose, Heather A. Bradeen, Kathryn Addonizio, Anran Li, Hasan Al-Sayegh, Wendy B. London, Rachael F. Grace
Publikováno v:
Haematologica, Vol 104, Iss 2 (2019)
Externí odkaz:
https://doaj.org/article/7c186564490a4bcea73e25b735945c6c
Autor:
Stephanie van Straaten, Marc Bierings, Paola Bianchi, Kensuke Akiyoshi, Hitoshi Kanno, Isabel Badell Serra, Jing Chen, Xiaohang Huang, Eduard van Beers, Supachai Ekwattanakit, Tayfun Güngör, Wijnanda Adriana Kors, Frans Smiers, Reinier Raymakers, Lucrecia Yanez, Julian Sevilla, Wouter van Solinge, Jose Carlos Segovia, Richard van Wijk
Publikováno v:
Haematologica, Vol 103, Iss 2 (2018)
Externí odkaz:
https://doaj.org/article/a1bb799c0c6748d08f56701f823ceb7e
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
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
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
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
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
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
https://curis.ku.dk/ws/files/298148076/A_Comprehensive_Analysis_of_the.4.pdf
Autor:
Gerard Pasterkamp, Minke A.E. Rab, Charles Kung, Stephanie van Straaten, Jeffrey Hixon, Kendall Johnson, Richard van Wijk, Lenny Dang, Victor Chubukov, Wouter W. van Solinge, Penelope A. Kosinski, Eduard J. van Beers, Brigitte A. van Oirschot
Publikováno v:
Haematologica
Pyruvate kinase (PK) deficiency is a rare hereditary disorder affecting red cell (RBC) glycolysis, causing changes in metabolism including a deficiency in ATP. This affects red cell homeostasis, promoting premature removal of RBCs from the circulatio
Autor:
Michele F Eisenga, Richard van Wijk, Carlo A. J. M. Gaillard, Eduard J. van Beers, Andreas Glenthøj, Stephan J. L. Bakker, Martin H. de Borst, Annelies J. Van Vuren, Stephanie van Straaten
Publikováno v:
Blood, 134(Supp. 1):4793. AMER SOC HEMATOLOGY
Background Recently, erythropoietin (EPO) was identified as an important regulator of production and cleavage of fibroblast growth factor 23 (FGF23). Since erythroid progenitor cells express high levels of FGF23 and carry the FGF receptor, they are i