Found: 14
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Allele‐specific long‐range sequencing as a method for ABO haplotyping in clinical blood group diagnosis and immunohematology research.
- Published in:
- Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 1, p. 1, doi. 10.1002/mgg3.2286
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- Article
Immunoglobulin Class Profiles of ABO Antibodies in Saliva and Serum of Healthy Individuals.
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- Transfusion Medicine & Hemotherapy, 2023, v. 50, n. 4, p. 294, doi. 10.1159/000527233
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- Article
Impact of allogeneic red blood cell transfusion on prognosis in soft tissue sarcoma patients. A single‐centre study.
- Published in:
- Cancer Medicine, 2023, v. 12, n. 2, p. 1237, doi. 10.1002/cam4.4989
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- Article
Membrane Properties of Human Induced Pluripotent Stem Cell-Derived Cultured Red Blood Cells.
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- Cells (2073-4409), 2022, v. 11, n. 16, p. 2473, doi. 10.3390/cells11162473
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- Article
Lewis and ABO histo‐blood types and the secretor status of patients hospitalized with COVID‐19 implicate a role for ABO antibodies in susceptibility to infection with SARS‐CoV‐2.
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- Transfusion, 2021, v. 61, n. 9, p. 2736, doi. 10.1111/trf.16567
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- Article
Ethical Issues and Management of Fetal Hemolytic Anemia Caused by Anti-Rh17 in a Multipara with Rare –D– Phenotype.
- Published in:
- Transfusion Medicine & Hemotherapy, 2021, v. 48, n. 3, p. 183, doi. 10.1159/000513124
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- Article
A 24-base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O.
- Published in:
- 2020
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- Publication type:
- journal article
The Effect of Parenteral or Oral Iron Supplementation on Fatigue, Sleep, Quality of Life and Restless Legs Syndrome in Iron-Deficient Blood Donors: A Secondary Analysis of the IronWoMan RCT.
- Published in:
- Nutrients, 2020, v. 12, n. 5, p. 1313, doi. 10.3390/nu12051313
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- Publication type:
- Article
Aberrant ABO B Phenotype with Irregular Anti-B Caused by a Para-Bombay FUT1 Mutation.
- Published in:
- Transfusion Medicine & Hemotherapy, 2020, v. 47, n. 1, p. 94, doi. 10.1159/000499724
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- Article
RHD del28Phe (DMW) encoded by a novel in-frame deletion resulting in reduced D antigen expression.
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- 2019
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- Publication type:
- journal article
A novel variant B allele at the ABO gene locus characterized by a duplication-based insertion of 27 nucleotides identified in an Iraqi male with a weak B subgroup phenotype.
- Published in:
- 2018
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- Publication type:
- journal article
RHD Tyr311Stop encoded by a novel nonsense mutation.
- Published in:
- 2016
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- Publication type:
- journal article
A novel factor V mutation causes a normal activated protein C ratio despite the presence of a heterozygous F5 R506 Q (factor V Leiden) mutation.
- Published in:
- British Journal of Haematology, 2013, v. 163, n. 3, p. 414, doi. 10.1111/bjh.12506
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- Publication type:
- Article
Identification of 14 new alleles at the fucosyltransferase 1, 2, and 3 loci in Styrian blood donors, Austria.
- Published in:
- Transfusion, 2009, v. 49, n. 10, p. 2097, doi. 10.1111/j.1537-2995.2009.02293.x
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- Article