about
Identification of the Molecular and Genetic Basis of PX2, a Glycosphingolipid Blood Group Antigen Lacking on Globoside-deficient Erythrocytes.A and B antigen levels acquired by group O donor-derived erythrocytes following ABO-non-identical transfusion or minor ABO-incompatible haematopoietic stem cell transplantation.A novel RHCE*02 allele, containing the single-nucleotide change c.460A>G, encodes weakened expression of C and e antigens.Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry analysis of 36 blood group alleles among 396 Thai samples reveals region-specific variants.Disruption of a GATA1-binding motif upstream of XG/PBDX abolishes Xga expression and resolves the Xg blood group systemErythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes ProjectCharacterization of GYP*Mur and novel GYP*Bun-like hybrids in Thai blood donors reveals a qualitatively altered s antigenAutomatic for the people: a rapidly evolving movement for the future of genotypingA large deletion spanning XG and GYG2 constitutes a genetic basis of the Xgnull phenotype, underlying anti-Xga productionInternational Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology: Report of the Dubai, Copenhagen and Toronto meetings
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Q35883826-BAE2A950-1296-40C7-94D5-B9AE89607668Q38841008-EBCFBB11-BAF3-47AF-8ACC-23DB32A0FB5FQ48206482-E3431BC1-F78B-46FA-B2BC-10ED10F2948BQ52587770-85AAD445-5B65-4FDE-8CD8-69D27ACFBC37Q88633165-4952E1B4-262B-4B93-85E5-4B0EA56AE39CQ89777824-95A1EDEE-E84A-4F6F-8FC9-F573A3A4E27FQ90580766-C033F85C-6438-4F00-A6DE-FBAF14789D44Q91019776-13209EDB-240C-4C6C-B80A-C773451A6842Q92784672-11FEB355-C4F6-4EF5-9ECB-F8ECF1F94AD9Q93024009-3C08FAA1-E2F4-412E-BC48-7F688D6895F5
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description
investigador
@es
researcher
@en
name
Jill R Storry
@en
type
label
Jill R Storry
@en
prefLabel
Jill R Storry
@en
P31
P496
0000-0003-2940-2604