Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

73 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variants.
Gueuning M, Thun GA, Wittig M, Galati AL, Meyer S, Trost N, Gourri E, Fuss J, Sigurdardottir S, Merki Y, Neuenschwander K, Busch Y, Trojok P, Schäfer M, Gottschalk J, Franke A, Gassner C, Peter W, Frey BM, Mattle-Greminger MP. Gueuning M, et al. Among authors: trost n. Blood Adv. 2023 Mar 28;7(6):878-892. doi: 10.1182/bloodadvances.2022007133. Blood Adv. 2023. PMID: 36129841 Free PMC article.
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: trost n. 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: trost n. 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.
Low-Frequency Blood Group Antigens in Switzerland.
Gassner C, Degenhardt F, Meyer S, Vollmert C, Trost N, Neuenschwander K, Merki Y, Portmann C, Sigurdardottir S, Zorbas A, Engström C, Gottschalk J, Amar El Dusouqui S, Waldvogel-Abramovski S, Rigal E, Tissot JD, Tinguely C, Mauvais SM, Sarraj A, Bessero D, Stalder M, Infanti L, Buser A, Sigle J, Weingand T, Castelli D, Braisch MC, Thierbach J, Heer S, Schulzki T, Krawczak M, Franke A, Frey BM. Gassner C, et al. Among authors: trost n. Transfus Med Hemother. 2018 Jul;45(4):239-250. doi: 10.1159/000490714. Epub 2018 Jul 10. Transfus Med Hemother. 2018. PMID: 30283273 Free PMC article.
Two Prevalent ∼100-kb GYPB Deletions Causative of the GPB-Deficient Blood Group MNS Phenotype S-s-U- in Black Africans.
Gassner C, Denomme GA, Portmann C, Bensing KM, Mattle-Greminger MP, Meyer S, Trost N, Song YL, Engström C, Jungbauer C, Just B, Storry JR, Forster M, Franke A, Frey BM. Gassner C, et al. Among authors: trost n. Transfus Med Hemother. 2020 Jul;47(4):326-336. doi: 10.1159/000504946. Epub 2020 Jan 21. Transfus Med Hemother. 2020. PMID: 32884505 Free PMC article.
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: trost n. Vox Sang. 2024 Apr;119(4):377-382. doi: 10.1111/vox.13580. Epub 2024 Jan 16. Vox Sang. 2024. PMID: 38226545
73 results