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A Bioinformatically Initiated Approach to Evaluate GATA1 Regulatory Regions in Samples with Weak D, Del, or D– Phenotypes Despite Normal RHD Exons.
- Published in:
- Transfusion Medicine & Hemotherapy, 2024, v. 51, n. 4, p. 252, doi. 10.1159/000538469
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- Publication type:
- Article
Evaluation of non-invasive prenatal RHD genotyping of the fetus.
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- Medical Journal of Australia, 2009, v. 191, n. 1, p. 21, doi. 10.5694/j.1326-5377.2009.tb02668.x
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- Publication type:
- Article
Frequency of Mi<sup>a</sup> (MNS7) and Classification of Mi<sup>a</sup>-Positive Hybrid Glycophorins in an Australian Blood Donor Population.
- Published in:
- Transfusion Medicine & Hemotherapy, 2020, v. 47, n. 4, p. 279, doi. 10.1159/000504026
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- Publication type:
- Article
Prevalence of hepatitis G virus in Queensland blood donors.
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- Medical Journal of Australia, 1996, v. 165, n. 7, p. 369, doi. 10.5694/j.1326-5377.1996.tb125019.x
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- Publication type:
- Article
Noninvasive fetal RHD genotyping of RhD negative pregnant women for targeted anti-D therapy in Australia: A cost-effectiveness analysis.
- Published in:
- 2017
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- Publication type:
- journal article
Strategy for managing maternal variant RHD alleles in Rhesus D negative obstetric populations during fetal RHD genotyping.
- Published in:
- Prenatal Diagnosis, 2014, v. 34, n. 1, p. 56, doi. 10.1002/pd.4253
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- Publication type:
- Article
Noninvasive fetal RHD genotyping by microfluidics digital PCR using maternal plasma from two alloimmunized women with the variant RHD(IVS3+1G>A) allele.
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- Prenatal Diagnosis, 2013, v. 33, n. 12, p. 1214, doi. 10.1002/pd.4230
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- Publication type:
- Article
Recurrent pregnancy loss in a patient with anti‐Rh17.
- Published in:
- Transfusion Medicine, 2024, v. 34, n. 1, p. 66, doi. 10.1111/tme.13014
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- Publication type:
- Article
A case of haemolytic disease of the fetus and newborn attributed to a novel antigen in the RHAG blood group system.
- Published in:
- Vox Sanguinis, 2023, v. 118, n. 12, p. 1095, doi. 10.1111/vox.13536
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- Publication type:
- Article
A new high‐prevalence LW antigen detected by an antibody in an Indigenous Australian homozygous for LW*A c.309C>A variant.
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- Vox Sanguinis, 2022, v. 117, n. 7, p. 958, doi. 10.1111/vox.13276
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- Publication type:
- Article
Recommendation for validation and quality assurance of non‐invasive prenatal testing for foetal blood groups and implications for IVD risk classification according to EU regulations.
- Published in:
- Vox Sanguinis, 2022, v. 117, n. 2, p. 157, doi. 10.1111/vox.13172
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- Publication type:
- Article
International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology: Report of the Dubai, Copenhagen and Toronto meetings.
- Published in:
- Vox Sanguinis, 2019, v. 114, n. 1, p. 95, doi. 10.1111/vox.12717
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- Publication type:
- Article
Targeted exome sequencing designed for blood group, platelet, and neutrophil antigen investigations: Proof-of-principle study for a customized single-test system.
- Published in:
- 2020
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- Publication type:
- journal article
Modified expression of the KEL2 (k) blood group antigen attributed to p.Leu196Val amino acid change three residues from the K/k antigen polymorphism site: implications for donor screening.
- Published in:
- 2019
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- Publication type:
- journal article
Comprehensive blood group antigen profile predictions for Western Desert Indigenous Australians from whole exome sequence data.
- Published in:
- 2019
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- Publication type:
- journal article
Severe hemolytic disease of the fetus and newborn due to allo-anti-D in a patient with a partial DEL phenotype arising from the variant allele described as RHD*148+1T (RHD*01EL.31).
- Published in:
- 2018
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- Publication type:
- case study
Investigation of the variable In(Lu) phenotype caused by KLF1 variants.
- Published in:
- 2018
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- Publication type:
- journal article
Genotyping analysis of MNS blood group GP(B-A-B) hybrid glycophorins in the Chinese Southern Han population using a high-resolution melting assay.
- Published in:
- 2018
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- Publication type:
- journal article
A proposed new low-frequency antigen in the Augustine blood group system associated with a severe case of hemolytic disease of the fetus and newborn.
- Published in:
- 2018
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- Publication type:
- journal article
A DEL phenotype attributed to RHD Exon 9 sequence deletion: slipped-strand mispairing and blood group polymorphisms.
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- 2018
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- Publication type:
- journal article
Targeted exome sequencing defines novel and rare variants in complex blood group serology cases for a red blood cell reference laboratory setting.
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- 2018
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- Publication type:
- journal article
Genotyping by sequencing defines independent novel RHD variants for an antenatal patient and a blood donor.
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- 2017
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- Publication type:
- journal article
Anti-D in a mother, hemizygous for the variant RHD*DNB gene, associated with hemolytic disease of the fetus and newborn.
- Published in:
- 2017
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- Publication type:
- case study
Evaluation of targeted exome sequencing for 28 protein-based blood group systems, including the homologous gene systems, for blood group genotyping.
- Published in:
- 2017
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- Publication type:
- journal article
An alloantibody in a homozygous GYP*Mur individual defines JENU (MNS49), a new high-frequency antigen on glycophorin B.
- Published in:
- 2017
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- Publication type:
- journal article
A D+ blood donor with a novel RHD*D-CE(5-6)-D gene variant exhibits the low-frequency antigen RH23 (D(W) ) characteristic of the partial DVa phenotype.
- Published in:
- 2016
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- Publication type:
- journal article
GYP*Kip, a novel GYP(B-A-B) hybrid allele, encoding the MNS48 (KIPP) antigen.
- Published in:
- 2016
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- Publication type:
- journal article
Identification of six new RHCE variant alleles in individuals of diverse racial origin.
- Published in:
- 2016
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- Publication type:
- journal article
SARA: a 'new' low-frequency MNS antigen ( MNS47) provides further evidence of the extreme diversity of the MNS blood group system.
- Published in:
- Transfusion, 2015, v. 55, n. 6pt2, p. 1451, doi. 10.1111/trf.12973
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- Publication type:
- Article
The RHD(1227G>A)DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes.
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- 2014
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- Publication type:
- Journal Article
The RHD(1227 G> A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes.
- Published in:
- Transfusion, 2014, v. 54, n. 11, p. 2931, doi. 10.1111/trf.12701
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- Publication type:
- Article
Anti-D in pregnant women with the RHD(IVS3+1G>A)-associated DEL phenotype.
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- Transfusion, 2012, v. 52, n. 9, p. 2016, doi. 10.1111/j.1537-2995.2011.03538.x
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- Publication type:
- Article
The risk of dengue transmission by blood during a 2004 outbreak in Cairns, Australia.
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- Transfusion, 2009, v. 49, n. 7 Part 1, p. 1482, doi. 10.1111/j.1537-2995.2009.02159.x
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- Publication type:
- Article
Dengue viremia in blood donors from Honduras, Brazil, and Australia.
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- Transfusion, 2008, v. 48, n. 7, p. 1355, doi. 10.1111/j.1537-2995.2008.01772.x
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- Publication type:
- Article
Sensitivity of HCV RNA and HIV RNA blood screenings assays.
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- Transfusion, 2002, v. 42, n. 5, p. 527, doi. 10.1046/j.1537-2995.2002.00101.x
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- Publication type:
- Article
The role of non‐invasive prenatal testing (NIPT) for fetal blood group typing in Australia.
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- Australian & New Zealand Journal of Obstetrics & Gynaecology, 2022, v. 62, n. 1, p. 33, doi. 10.1111/ajo.13446
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- Publication type:
- Article
Implications of Dengue Outbreaks for Blood Supply, Australia.
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- Emerging Infectious Diseases, 2013, v. 19, n. 5, p. 787, doi. 10.3201/eid1905.121664
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- Publication type:
- Article
Next generation sequencing to identify iron status and individualise blood donors' experience.
- Published in:
- Blood Transfusion (17232007), 2023, v. 21, n. 6, p. 463, doi. 10.2450/BloodTransfus.499
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- Publication type:
- Article
Aggregates in blood filter chambers used from the plasma donations of anti-D donors: evaluation for monoclonal antibody discovery using phage display.
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- Blood Transfusion (17232007), 2021, v. 19, n. 1, p. 64, doi. 10.2450/2020.0093-20
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- Publication type:
- Article
Genetic factors associated with iron storage in Australian blood donors.
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- Blood Transfusion (17232007), 2018, v. 16, n. 2, p. 123, doi. 10.2450/2016.0138-16
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- Publication type:
- Article
Non‐invasive prenatal testing (NIPT) for fetal Kell, Duffy and Rh blood group antigen prediction in alloimmunised pregnant women: power of droplet digital PCR.
- Published in:
- British Journal of Haematology, 2020, v. 189, n. 3, p. e90, doi. 10.1111/bjh.16500
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- Publication type:
- Article
Developments beyond blood group serology in the genomics era.
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- British Journal of Haematology, 2019, v. 184, n. 6, p. 897, doi. 10.1111/bjh.15747
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- Publication type:
- Article
Genotyping confirms inheritance of the rare At(a−) type in a case of haemolytic disease of the newborn.
- Published in:
- Journal of Pathology: Clinical Research, 2016, v. 2, n. 1, p. 53, doi. 10.1002/cjp2.33
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- Publication type:
- Article
Feasibility for non‐invasive prenatal fetal blood group and platelet genotyping by massively parallel sequencing: A single test system for multiple atypical red cell, platelet and quality control markers.
- Published in:
- British Journal of Haematology, 2024, v. 204, n. 2, p. 694, doi. 10.1111/bjh.19197
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- Publication type:
- Article
RHD Gene Mutations and the Weak D Phenotype: An Australian Blood Donor Study.
- Published in:
- Vox Sanguinis, 2000, v. 79, n. 4, p. 252, doi. 10.1159/000056745
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- Publication type:
- Article
A Single Point Mutation at a Splice Site Generates a Silent RH50 Gene in a Composite Heterozygous Rh<sub>null</sub> Blood Donor.
- Published in:
- Vox Sanguinis, 1999, v. 76, n. 4, p. 247, doi. 10.1159/000031060
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- Publication type:
- Article
A cold case of hemolytic disease of the fetus and newborn resolved by genomic sequencing and population studies to define a new antigen in the Rh system.
- Published in:
- Transfusion, 2024, v. 64, n. 6, p. 1171, doi. 10.1111/trf.17205
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- Publication type:
- Article
Hemolytic disease of the fetus and newborn caused by anti-s<sup>D</sup> antibody in a GP.Mur/Mur Thai mother and review of the prevalence of s<sup>D</sup> in Thai blood donors.
- Published in:
- 2022
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- Publication type:
- case study
Novel or not? Reference alleles, genes, and genomes to unmask the true nature of the ABO*AW.10 allele associated with weak A phenotype.
- Published in:
- 2022
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- Publication type:
- editorial
Genotyping for Glycophorin GYP(B- A- B) Hybrid Genes Using a Single Nucleotide Polymorphism-Based Algorithm by Matrix-Assisted Laser Desorption/Ionisation, Time-of-Flight Mass Spectrometry.
- Published in:
- Molecular Biotechnology, 2016, v. 58, n. 10, p. 665, doi. 10.1007/s12033-016-9966-6
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- Publication type:
- Article