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- 2019
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Mark
Multiple miscarriages in two sisters of Thai origin with the rare Pk phenotype caused by a novel nonsense mutation at the B3GALNT1 locus
(
- Contribution to journal › Article
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Mark
A novel single-nucleotide substitution in the proximal ABO promoter gives rise to the B3 phenotype
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Automatic for the people : a rapidly evolving movement for the future of genotyping
(
- Contribution to journal › Debate/Note/Editorial
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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
Towards universally acceptable blood
(
- Contribution to journal › Article
- 2018
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Mark
Disruption of a GATA1-binding motif upstream of XG/PBDX abolishes Xga expression and resolves the Xg blood group system
(
- Contribution to journal › Article
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Mark
Allele-selective RUNX1 binding regulates P1 blood group status by transcriptional control of A4GALT
(
- Contribution to journal › Article
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Mark
ABO zygosity, but not secretor or Fc receptor status, is a significant risk factor for IVIG-Associated hemolysis
(
- Contribution to journal › Letter
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Mark
Vox Sanguinis International Forum on application of fetal blood grouping
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Vox Sanguinis International Forum on application of fetal blood grouping : summary
(
- Contribution to journal › Article
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Mark
Koden knäckt för det sista blodgruppssystemet
(
- Contribution to specialist publication or newspaper › Specialist publication article
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Mark
GBGT1 is allelically diverse but dispensable in humans and naturally occurring anti-FORS1 shows an ABO-restricted pattern
(
- Contribution to journal › Article
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Mark
Genetic Elucidation of Xg, the last unresolved blood group system
(
- Contribution to conference › Abstract
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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
Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry analysis of 36 blood group alleles among 396 Thai samples reveals region-specific variants
(
- Contribution to journal › Article
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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
FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon
(
- Contribution to journal › Article
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Mark
An update on the GLOB blood group system (and former GLOB collection)
(
- Contribution to journal › Article
-
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