Zobrazeno 1 - 10
of 336
pro vyhledávání: '"F A, Kuypers"'
Autor:
S. Saraf, R. C. Brown, R. W. Hagar, M. Idowu, I. Osunkwo, T. A. Kalfa, F. A. Kuypers, J. Geib, P. Schroeder, E. Wu, P. Kelly, M. J. Telen
Publikováno v:
HemaSphere, Vol 6, Pp 1377-1378 (2022)
Externí odkaz:
https://doaj.org/article/262dc9b8e6cf4b478ba5910bcd26a386
Publikováno v:
Journal of Lipid Research, Vol 36, Iss 2, Pp 322-331 (1995)
Cigarette smokers have reduced levels of plasma high density lipoprotein (HDL) compared to nonsmokers and are at risk of premature cardiovascular disease. Previous work from this laboratory has shown that exposure of human plasma to gas-phase cigaret
Externí odkaz:
https://doaj.org/article/0268688121d04c8598d65cc53252845b
Autor:
Lu, Haojiang1 (AUTHOR), Jiang, Hong1 (AUTHOR), Li, Congru1 (AUTHOR), Derisoud, Emilie1 (AUTHOR), Zhao, Allan1 (AUTHOR), Eriksson, Gustaw1 (AUTHOR), Lindgren, Eva1 (AUTHOR), Pui, Han‐Pin1 (AUTHOR), Risal, Sanjiv1 (AUTHOR), Pei, Yu1 (AUTHOR), Maxian, Theresa2 (AUTHOR), Ohlsson, Claes3 (AUTHOR), Benrick, Anna4,5 (AUTHOR), Haider, Sandra2 (AUTHOR), Stener‐Victorin, Elisabet1 (AUTHOR) elisabet.stener-victorin@ki.se, Deng, Qiaolin1 (AUTHOR) qiaolin.deng@ki.se
Publikováno v:
Advanced Science. 9/25/2024, Vol. 11 Issue 36, p1-15. 15p.
Autor:
Wang K; Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA., Olave N; Department of Pediatrics, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA., Aggarwal S; Department of Cellular and Molecular Medicine, Herbert Wertheim College of Medicine, Florida International University, Miami, Florida, USA., Oh JY; Department of Pathology, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA., Patel RP; Department of Pathology, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA., Rahman AKMF; Department of Biostatistics, School of Public Health, University of Alabama at Birmingham, Birmingham, Alabama, USA., Lebensburger J; Department of Pediatrics, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA., Alishlash AS; Department of Pediatrics, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Publikováno v:
European journal of haematology [Eur J Haematol] 2024 Nov 05. Date of Electronic Publication: 2024 Nov 05.
Publikováno v:
Journal of Lipid Research, Vol 36, Iss 2, Pp 322-331 (1995)
Cigarette smokers have reduced levels of plasma high density lipoprotein (HDL) compared to nonsmokers and are at risk of premature cardiovascular disease. Previous work from this laboratory has shown that exposure of human plasma to gas-phase cigaret
Autor:
B, Kanathezhath, F K, Hazard, H, Guo, J, Kidd, M, Azimi, F A, Kuypers, E P, Vichinsky, A, Lal
Publikováno v:
Pediatric bloodcancer. 54(2)
Certain beta globin gene mutations produce a thalassemia major phenotype in the heterozygous state. While most such patients have thalassemia intermedia, we describe a young Guatemalan child with a de novo mutation in the beta globin gene, codon 31 T
Autor:
F A, Kuypers, K, de Jong
Publikováno v:
Cellular and molecular biology (Noisy-le-Grand, France). 50(2)
During the time that erythrocytes (RBC) spend in the circulation, a series of progressive events take place that lead to their removal and determine their apparent aging and limited survival. In addition, a fraction of RBC precursors will be removed
Autor:
F A, Kuypers, L A, Styles
Publikováno v:
Cellular and molecular biology (Noisy-le-Grand, France). 50(1)
Acute chest syndrome (ACS) is the leading cause of death in sickle cell disease. Severe ACS often develops in the course of a vasoocclusive crisis (VOC), and frequently involves pulmonary fat embolism. Secretory phospholipase A2 (sPLA2), a potent inf
Publikováno v:
British journal of haematology. 111(2)
To determine the effects of L-arginine (L-Arg) supplementation on nitric oxide metabolite (NOx) production, oral L-Arg was given to normal controls, sickle cell disease (SCD) patients at steady state and SCD patients hospitalized with a vaso-occlusiv
Publikováno v:
Blood. 96(10)
The development of hemolytic alloantibodies and erythrocyte autoantibodies complicates transfusion therapy in thalassemia patients. The frequency, causes, and prevention of this phenomena among 64 transfused thalassemia patients (75% Asian) were eval