Zobrazeno 1 - 10
of 94
pro vyhledávání: '"H, Hustinx"'
Akademický článek
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Autor:
K. M. K. de Vooght, E. Zhiburt, A Alarcón, Laura Infanti, H. Hustinx, D Brilhante, Christine Cserti-Gazdewich, Ashish Jain, R.R. Sharma, Miquel Lozano, K Suzuki, Jacob Pendergrast, Paolo Perseghin, Jill R. Storry, Janice Hawes, Neelam Marwaha, Véronique Deneys, Julie Staves, M Dassi, Jose Mauro Kutner, Andreas Buser, J Bueno, C Bonet Bub, Andreas Greinacher, Kathleen Selleng, M E Colling, Michael F. Murphy, Claire Thiry, Arianna Incontri, A Frélik, M N Lundgren, L Castilho, Richard M. Kaufman, A Macédo, I Romera, Andreas Holbro
Publikováno v:
Vox Sanguinis, 113(5), e36. Wiley-Blackwell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b66f3ba5408eb533dd40b4985280e096
https://dspace.library.uu.nl/handle/1874/372713
https://dspace.library.uu.nl/handle/1874/372713
Autor:
Miquel Lozano, Andreas Greinacher, Andreas Buser, Arianna Incontri, Jill R. Storry, D Brilhante, Paolo Perseghin, Richard M. Kaufman, Christine Cserti-Gazdewich, C Thiry, Janice Hawes, Michael F. Murphy, K Suzuki, M Dassi, Laura Infanti, Jose Mauro Kutner, Jacob Pendergrast, Véronique Deneys, H. Hustinx, Neelam Marwaha, A Alarcón, R.R. Sharma, L Castilho, A Macédo, I Romera, Andreas Holbro, J Bueno, Kathleen Selleng, M E Colling, K. M. K. de Vooght, A Frélik, C Bonet Bub, Ashish Jain, M N Lundgren, Julie Staves, E. Zhiburt
Publikováno v:
Vox sanguinis.
Publikováno v:
Transfusion Medicine. 26:150-152
Publikováno v:
Geburtshilfe und Frauenheilkunde. 76
Autor:
Bahram Hosseini-Maaf, Annika K. Hult, H. Hustinx, Britt Thuresson, Martin L. Olsson, M. Alan Chester
Publikováno v:
Vox Sanguinis. 102:55-64
Background and Objectives Weak expression of A/B histo-blood group antigens is often explained by single nucleotide substitutions at the ABO locus. However, hybrid alleles containing segments from different ABO alleles can result in unexpected phenot
Autor:
D. Gounder, M. A. de Brito, K. Barotine-Toth, C. C. Folman, S. Wendel, J. Matilainen, Vered Yahalom, H. Hustinx, Pertti Sistonen, M. de Haas, Orna Asher, Geralyn M. Meny, Maria Antonietta Villa, P.Y. Le Pennec, Rita Fontão-Wendel, Harald Schennach, S. R. Joshi, W. C. Tsoi, K. Vasantha, I. von Zabern, Peter Flanagan, M. M. W. Koopman, C. P. Engelfriet, Maurizio Marconi, Christoph Niederhauser, Erik A M Beckers, I. Hoffer, C. K. Lin, Nicoletta Revelli, N. Greppi, Cyril Levene, Christoph Gassner, E. Aranburu Urtasun, Lorna Wall, Henk W. Reesink, Philippe Rouger, Willy A. Flegel, Bach-Nga Pham, Sandra Nance, Yoshihiko Tani, T. Peyrard, C. Flickinger
Publikováno v:
Vox sanguinis, 95(3), 236-253. Wiley-Blackwell
Autor:
Pierre‐Yves Lepennec, Martin L. Olsson, Monica M. Palcic, Elizabeth Smart, Mattias Persson, Stephen V. Evans, H. Hustinx, Bahram Hosseini-Maaf, M. Alan Chester, Zhihon Zhao, James A. Letts
Publikováno v:
Transfusion. 47:864-875
BACKGROUND: Four amino-acid-changing polymorphisms differentiate the blood group A and B alleles. Multiple missense mutations are associated with weak expression of A and B antigens but the structural changes causing subgroups have not been studied.
Autor:
H. Hustinx, Ursula Bauerfeind, Hubert Schrezenmeier, Eduard K. Petershofen, Ingeborg Von Zabern, Andrea Doescher, Willy A. Flegel, Peter Gowland, Nicole I. Eicher, Behrouz Mansouri Taleghani, Franz F. Wagner, Manfred Ernst
Publikováno v:
Transfusion. 46:2156-2161
BACKGROUND: The deletion of three adjacent nucleotides in an exon may cause the lack of a single amino acid, while the protein sequence remains otherwise unchanged. Only one such in-frame deletion is known in the two RH genes, represented by the RHCE
Autor:
Stefano Fontana, H. Hustinx, Peter Gowland, Sonja Sigurdardottir, Martin Stolz, Andreas Maier, Christoph Gassner, Beat M. Frey, Jutta Thierbach, Franziska Still, Jochen Gottschalk, Christoph Niederhauser, Jean-Daniel Tissot
Publikováno v:
Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis. 50(2)
This work aims to assess the value of a generalized molecular RHD screening strategy which could replace routine serological screening of weak D by indirect antiglobulin test. Three independent studies were performed at the two Blood Transfusion Serv