Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Peter Ligthart"'
Autor:
Jesse Eernstman, Barbera Veldhuisen, Peter Ligthart, Marieke von Lindern, C. Ellen van der Schoot, Emile van den Akker
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract Beta-hemoglobinopathies become prominent after birth due to a switch from γ-globin to the mutated β-globin. Haploinsufficiency for the erythroid specific indispensable transcription factor Krueppel-like factor 1 (KLF1) is associated with h
Externí odkaz:
https://doaj.org/article/9ee3cf0d7bf745ada041de96f847e1a5
Autor:
Inge Baas, Laura Delvasto-Nuñez, Peter Ligthart, Conny Brouwer, Claudia Folman, Edimara S. Reis, Daniel Ricklin, John D. Lambris, Diana Wouters, Masja de Haas, Ilse Jongerius, Sacha S. Zeerleder
Publikováno v:
Haematologica, Vol 105, Iss 2 (2020)
Externí odkaz:
https://doaj.org/article/080d337720a34853a8f979a034075c99
Autor:
Christoph Gassner, Lilian Castilho, Qing Chen, Frederik Banch Clausen, Gregory A. Denomme, Willy A. Flegel, Nick Gleadall, Åsa Hellberg, Yanli Ji, Margaret A. Keller, William J. Lane, Peter Ligthart, Christine Lomas‐Francis, Nuria Nogues, Martin L. Olsson, Thierry Peyrard, Jill R. Storry, Yoshihiko Tani, Nicole Thornton, Ellen van der Schoot, Barbera Veldhuisen, Franz Wagner, Christof Weinstock, Silvano Wendel, Connie Westhoff, Vered Yahalom, Catherine A. Hyland
Publikováno v:
Vox Sanguinis. 117:1332-1344
Under the ISBT, the Working Party (WP) for Red Cell Immunogenetics and Blood Group Terminology is charged with ratifying blood group systems, antigens and alleles. This report presents the outcomes from four WP business meetings, one located in Basel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e687413664adcce47bca056071f1c180
https://doi.org/10.1111/vox.13361
https://doi.org/10.1111/vox.13361
Autor:
Yanli, Ji, Barbera, Veldhuisen, Peter, Ligthart, Lonneke, Haer-Wigman, John, Jongerius, Mohamed, Boujnan, Aicha, Ait Soussan, Guangping, Luo, Yongshui, Fu, C Ellen, van der Schoot, Masja, de Haas
Publikováno v:
Transfusion. 55(2)
Alloantibodies directed against antigens of the Kell blood group system are clinically significant. In the Netherlands, the KEL1 antigen is determined in all blood donors. In this study, after phenotyping of KEL:1-positive donors, genotyping analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0c7985c404d977069c4f4d6b3d476c77
https://pubmed.ncbi.nlm.nih.gov/25156717
https://pubmed.ncbi.nlm.nih.gov/25156717
Autor:
Rick, Kapur, Luciana, Della Valle, Onno J H M, Verhagen, Agnes, Hipgrave Ederveen, Peter, Ligthart, Masja, de Haas, Belinda, Kumpel, Manfred, Wuhrer, C Ellen, van der Schoot, Gestur, Vidarsson
Publikováno v:
Transfusion. 55(3)
RhIG is obtained from hyperimmunized healthy anti-D donors (HIDs) boosted with D+ red blood cells (RBCs). One hypothesis for its mechanism of action is fast clearance of opsonized D+ RBCs through Fcγ receptor (FcγR)III. Levels of immunoglobulin (Ig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::803a848fe0f1d1a9c7a66c27a47b94d3
https://pubmed.ncbi.nlm.nih.gov/25234110
https://pubmed.ncbi.nlm.nih.gov/25234110
Autor:
Lonneke, Haer-Wigman, Tamara C, Stegmann, Shabnam, Solati, Aïcha, Ait Soussan, Erik, Beckers, Pim, van der Harst, Marga, van Hulst-Sundermeijer, Peter, Ligthart, Dick, van Rhenen, Hein, Schepers, Masja, de Haas, C Ellen, van der Schoot
Publikováno v:
Transfusion. 55(6 Pt 2)
Serologic determination of the Vel- phenotype is challenging due to variable Vel expression levels. In this study we investigated the genetic basis for weak Vel expression levels and developed a high-throughput genotyping assay to detect Vel- donors.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7dff330577a2b8ef7a2b2f7f71d50696
https://pubmed.ncbi.nlm.nih.gov/25647324
https://pubmed.ncbi.nlm.nih.gov/25647324
Autor:
Rick, Kapur, Luciana, Della Valle, Myrthe, Sonneveld, Agnes, Hipgrave Ederveen, Remco, Visser, Peter, Ligthart, Masja, de Haas, Manfred, Wuhrer, C Ellen, van der Schoot, Gestur, Vidarsson
Publikováno v:
British Journal of Haematology
Haemolytic disease of the fetus and newborn (HDFN) may occur when maternal IgG antibodies against red blood cells (RBCs), often anti-RhD (anti-D) antibodies, cross the placenta and mediate the destruction of RBCs via phagocytic IgG-Fc-receptors (Fcγ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6f95ad918e0b3db9c04e0c7840e4f141
https://pubmed.ncbi.nlm.nih.gov/24909983
https://pubmed.ncbi.nlm.nih.gov/24909983
Autor:
Lonneke, Haer-Wigman, Aïcha, Ait Soussan, Peter, Ligthart, Masja, de Haas, C Ellen, van der Schoot
Publikováno v:
Transfusion. 54(7)
Individuals with anti-Jr(a) or anti-Lan are ideally transfused with rare Jr(a-) or Lan- red blood cells. We characterized mutations in Dutch Jr(a-) and Lan- individuals and developed a high-throughput genotyping assay to detect Jr(a-) and Lan- donors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9fcb244ea59f6504a5cb2dd9d3af30e5
https://pubmed.ncbi.nlm.nih.gov/24456066
https://pubmed.ncbi.nlm.nih.gov/24456066