Found: 51
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PIGG defines the Emm blood group system.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98090-w
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- Article
3D analysis of CROMER (DAF) and a new antigen CRAG.
- Published in:
- Blood Transfusion (17232007), 2022, v. 20, n. 6, p. 483, doi. 10.2450/2022.0285-21
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- Article
Overcoming the challenges of interpreting complex and uncommon RH alleles from whole genomes.
- Published in:
- Vox Sanguinis, 2020, v. 115, n. 8, p. 790, doi. 10.1111/vox.12963
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- Article
Variant RHD alleles and Rh immunization in patients with sickle cell disease.
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- British Journal of Haematology, 2023, v. 201, n. 6, p. 1220, doi. 10.1111/bjh.18774
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- Article
SMIM1 variants rs1175550 and rs143702418 independently modulate Vel blood group antigen expression.
- Published in:
- Scientific Reports, 2017, p. 40451, doi. 10.1038/srep40451
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- Article
Anti-Emm, a rare specificity to the high-incidence antigen Emm in an Indian patient defining the new blood group system EMM (ISBT042).
- Published in:
- Asian Journal of Transfusion Science, 2021, v. 15, n. 2, p. 223, doi. 10.4103/ajts.ajts_59_21
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- Article
Mating Systems of Three Tropical Dry Forest Tree Species.
- Published in:
- Biotropica, 1998, v. 30, n. 4, p. 587, doi. 10.1111/j.1744-7429.1998.tb00098.x
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- Article
Three novel Er blood group system alleles and insights from protein modeling.
- Published in:
- Transfusion, 2024, v. 64, n. 9, p. 1633, doi. 10.1111/trf.17965
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- Article
RH genotypes and red cell alloimmunization rates in chronically transfused patients with sickle cell disease: A multisite study in the USA.
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- Transfusion, 2024, v. 64, n. 3, p. 526, doi. 10.1111/trf.17740
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- Article
Uncommon S–s–U+ phenotype encoded by two novel GYPB alleles.
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- Transfusion, 2023, v. 63, n. 12, p. E59, doi. 10.1111/trf.17592
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- Article
Evidence that donors with variant RH genotypes are associated with unexpected Rh antibodies.
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- Transfusion, 2023, v. 63, n. 10, p. 1962, doi. 10.1111/trf.17525
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- Article
Two novel variants that disrupt the RHCE start codon with varying effect on RhCE antigen expression.
- Published in:
- Transfusion, 2023, v. 63, n. 4, p. E12, doi. 10.1111/trf.17256
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- Article
A novel high‐prevalence antigen in the Lutheran system, LUGA (LU24), and an updated, full‐length 3D BCAM model.
- Published in:
- Transfusion, 2023, v. 63, n. 4, p. 798, doi. 10.1111/trf.17262
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- Article
Two new Scianna variants causing loss of high prevalence antigens: ERMAP model and 3D analysis of the antigens.
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- Transfusion, 2023, v. 63, n. 1, p. 230, doi. 10.1111/trf.17182
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- Article
Four novel ABO*AW alleles associated with weak antigen expression.
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- Transfusion, 2022, v. 62, n. 12, p. E76, doi. 10.1111/trf.17167
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- Article
YTGT: A new high-prevalence antigen in the Yt blood group system in two unrelated Native Americans and transfusion management.
- Published in:
- Transfusion, 2022, v. 62, n. 9, p. 1917, doi. 10.1111/trf.17001
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- Article
First report of a null allele on a GYPB*s background: GYPB*s(37 + 4_8delAGTGA).
- Published in:
- Transfusion, 2022, v. 62, n. 5, p. E24, doi. 10.1111/trf.16874
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- Article
An intron c.149‐2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype.
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- Transfusion, 2022, v. 62, n. 2, p. E14, doi. 10.1111/trf.16774
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- Article
Five novel silenced KEL*02 alleles.
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- Transfusion, 2021, v. 61, n. 11, p. E77, doi. 10.1111/trf.16681
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- Article
Five novel FY null alleles associated with typing discrepancies.
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- Transfusion, 2021, v. 61, n. 11, p. E80, doi. 10.1111/trf.16676
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- Article
Three new XK alleles; two associated with a McLeod RBC phenotype.
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- Transfusion, 2021, v. 61, n. 10, p. E69, doi. 10.1111/trf.16650
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- Article
A novel P1PK allele in two Bangladeshi sisters with a history of spontaneous abortion: A4GALT*02N(951C).
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- Transfusion, 2021, v. 61, n. 10, p. E71, doi. 10.1111/trf.16649
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- Article
An insertion/deletion polymorphism in the KLF1 gene resulting in an In(Lu) phenotype.
- Published in:
- Transfusion, 2021, v. 61, n. 10, p. E73, doi. 10.1111/trf.16648
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- Article
Screening of blood donors for sickle cell trait using a DNA‐based approach: Frequency in a multiethnic donor population.
- Published in:
- Transfusion, 2021, v. 61, n. 7, p. 2008, doi. 10.1111/trf.16403
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- Article
A pair of S-silencing single nucleotide variants cis-linked on GYPB.
- Published in:
- 2021
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- Publication type:
- journal article
ABO maternal‐child discordance: Evidence of variable allelic expression and considerations for investigation.
- Published in:
- Transfusion, 2021, v. 61, n. 3, p. 979, doi. 10.1111/trf.16263
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- Article
Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles.
- Published in:
- Transfusion, 2021, v. 61, n. 1, p. 256, doi. 10.1111/trf.16100
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- Article
A novel RHD*DAU allele with c.1136C>T (p.Thr379Met) and c.17C>T (p. Pro6Leu).
- Published in:
- Transfusion, 2020, v. 60, n. 12, p. E51, doi. 10.1111/trf.16135
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- Article
RHCE*02 (c.148G>A, p.Val50Ile) allele with silenced RHCE*Ce expression.
- Published in:
- 2020
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- journal article
Multiple GYPB gene deletions associated with the U- phenotype in those of African ancestry.
- Published in:
- 2020
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- Publication type:
- journal article
Reliability of labeling red cell units with minor antigen historical results and process considerations.
- Published in:
- 2020
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- Publication type:
- journal article
Automated typing of red blood cell and platelet antigens from whole exome sequences.
- Published in:
- 2019
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- Publication type:
- journal article
A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xg<sup>a</sup>.
- Published in:
- 2019
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- journal article
Four novel silenced RHCE.
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- 2018
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- journal article
Novel JK allele background associated with production of anti-JK3 during pregnancy.
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- 2018
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- journal article
Novel mutations in KLF1 encoding the In(Lu) phenotype reflect a diversity of clinical presentations.
- Published in:
- 2018
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- journal article
Two novel ABCG2 alleles resulting in a Jr(a-) phenotype.
- Published in:
- 2017
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- journal article
RHCE*ceAG (254C>G, Ala85Gly) is prevalent in blacks, encodes a partial ce-phenotype, and is associated with discordant RHD zygosity.
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- 2015
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- journal article
Changing practice: red blood cell typing by molecular methods for patients with sickle cell disease.
- Published in:
- Transfusion, 2015, v. 55, n. 6pt2, p. 1388, doi. 10.1111/trf.12987
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- Article
Changing practice: red blood cell typing by molecular methods for patients with sickle cell disease.
- Published in:
- 2015
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- Publication type:
- journal article
RHCE*ceMO is frequently in cis to RHD*DAU0 and encodes a hr(S) -, hr(B) -, RH:-61 phenotype in black persons: clinical significance.
- Published in:
- 2013
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- Publication type:
- journal article
RHCE*ceMO is frequently in cis to RHD*DAU0 and encodes a hr<sup>S</sup>-, hr<sup>B</sup>-, RH:-61 phenotype in black persons: clinical significance.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2983, doi. 10.1111/trf.12271
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- Publication type:
- Article
Expansion of the Kell blood group system: two new high-prevalence antigens and two novel K<sub>0</sub> ( Kell<sub>null</sub>) phenotypes.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2887, doi. 10.1111/trf.12377
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- Article
RHCE* ceTI encodes partial c and partial e and is often in cis to RHD* DIVa.
- Published in:
- Transfusion, 2013, v. 53, n. 4, p. 741, doi. 10.1111/j.1537-2995.2012.03800.x
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- Article
A novel JKA allele, nt561C>A, associated with silencing of Kidd expression.
- Published in:
- Transfusion, 2012, v. 52, n. 5, p. 1092, doi. 10.1111/j.1537-2995.2011.03399.x
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- Article
Nucleotide deletion in RHCE* cE (907delC) is responsible for a D- - haplotype in Hispanics.
- Published in:
- Transfusion, 2011, v. 51, n. 10, p. 2142, doi. 10.1111/j.1537-2995.2011.03144.x
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- Article
RHCE*ceCF encodes partial c and partial e but not CELO, an antigen antithetical to Crawford.
- Published in:
- 2011
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- Publication type:
- journal article
RHCE* ceCF encodes partial c and partial e but not CELO, an antigen antithetical to Crawford.
- Published in:
- Transfusion, 2011, v. 51, n. 1, p. 25, doi. 10.1111/j.1537-2995.2010.02764.x
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- Article
DIIIa and DIII Type 5 are encoded by the same allele and are associated with altered RHCE*ce alleles: clinical implications.
- Published in:
- Transfusion, 2010, v. 50, n. 6, p. 1303, doi. 10.1111/j.1537-2995.2009.02573.x
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- Article
The JAL antigen (RH48) is the result of a change in RHCE that encodes Arg114Trp.
- Published in:
- Transfusion, 2009, v. 49, n. 4, p. 725, doi. 10.1111/j.1537-2995.2008.02034.x
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- Publication type:
- Article