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Novel regulatory variant in ABO intronic RUNX1 binding site inducing A3 phenotype.
Thun GA, Gueuning M, Sigurdardottir S, Meyer E, Gourri E, Schneider L, Merki Y, Trost N, Neuenschwander K, Engström C, Frey BM, Meyer S, Mattle-Greminger MP. Thun GA, et al. Among authors: frey bm. Vox Sang. 2024 Apr;119(4):377-382. doi: 10.1111/vox.13580. Epub 2024 Jan 16. Vox Sang. 2024. PMID: 38226545
Implementation of a mandatory donor RHD screening in Switzerland.
Crottet SL, Henny C, Meyer S, Still F, Stolz M, Gottschalk J, Neuenschwander K, Taleghani BM, Gowland P, Frey BM, Fontana S, Hustinx H, Niederhauser C, Gassner C. Crottet SL, et al. Among authors: frey bm. Transfus Apher Sci. 2014 Apr;50(2):169-74. doi: 10.1016/j.transci.2014.02.011. Epub 2014 Mar 6. Transfus Apher Sci. 2014. PMID: 24679597 Review.
High-throughput Kell, Kidd, and Duffy matrix-assisted laser desorption/ionization, time-of-flight mass spectrometry-based blood group genotyping of 4000 donors shows close to full concordance with serotyping and detects new alleles.
Meyer S, Vollmert C, Trost N, Brönnimann C, Gottschalk J, Buser A, Frey BM, Gassner C. Meyer S, et al. Among authors: frey bm. Transfusion. 2014 Dec;54(12):3198-207. doi: 10.1111/trf.12715. Epub 2014 May 21. Transfusion. 2014. PMID: 24845979 Clinical Trial.
MNSs genotyping by MALDI-TOF MS shows high concordance with serology, allows gene copy number testing and reveals new St(a) alleles.
Meyer S, Vollmert C, Trost N, Sigurdardottir S, Portmann C, Gottschalk J, Ries J, Markovic A, Infanti L, Buser A, Amar El Dusouqui S, Rigal E, Castelli D, Weingand B, Maier A, Mauvais SM, Sarraj A, Braisch MC, Thierbach J, Hustinx H, Frey BM, Gassner C. Meyer S, et al. Among authors: frey bm. Br J Haematol. 2016 Aug;174(4):624-36. doi: 10.1111/bjh.14095. Epub 2016 Apr 13. Br J Haematol. 2016. PMID: 27072601 Free article.
238 results