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- 2024
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Mark
Epigenetic dissection of human blood group genes reveals regulatory elements and detailed characteristics of KEL and four other loci
2024) In Transfusion(
- Contribution to journal › Article
- 2022
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Mark
Novel or not? Reference alleles, genes, and genomes to unmask the true nature of the ABO*AW.10 allele associated with weak A phenotype
(
- Contribution to journal › Debate/Note/Editorial
- 2020
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Mark
The Xg blood group system : no longer forgotten
(
- Contribution to journal › Letter
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Mark
May the FORS be with you : a system sequel
(
- Contribution to journal › Scientific review
- 2019
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Mark
Missense mutations in the C-terminal portion of the B4GALNT2-encoded glycosyltransferase underlying the Sd(a−) phenotype
(
- Contribution to journal › Article
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Mark
A large deletion spanning XG and GYG2 constitutes a genetic basis of the Xgnull phenotype, underlying anti-Xga production
(
- Contribution to journal › Article
- 2018
-
Mark
Identification of human glycosyltransferase genes expressed in erythroid cells predicts potential carbohydrate blood group loci
(
- Contribution to journal › Article
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Mark
Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project
(
- Contribution to journal › Article
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Mark
A molecular mechanism underlying the P1/P2 phenotypes: allele-selective RUNX1 binding regulates P1 blood group status by transcriptional control of A4GALT
2018) 35th international congress of the International Society of Blood Transfusion, ISBT, 2018 In Vox Sanguinis 113(S1). p.251-252(
- Contribution to journal › Published meeting abstract
-
Mark
Disruption of a GATA-1 binding motif 3.7 KB upstream of the XG/PBDX gene abolishes erythroid Xga expression and elucidates the last unresolved blood group system
2018) 35th international congress of the International Society of Blood Transfusion, ISBT, 2018 In Vox Sanguinis 113(S1). p.62-63(
- Contribution to journal › Published meeting abstract