Molecular basis of the Dombrock null phenotype

Transfusion

Volumn 41, Issue 11, 2001, Pages 1405-1407

  Rios, Maria ^a,b   Hue Roye, Kim ^a,b   Storry, Jill R ^a,b   Lee, Terry ^a,b   Miller, Jeffery L ^a,b   Reid, Marion E ^a,b  

^a NEW YORK BLOOD CENTER   (United States)

^b NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD GROUP ANTIGEN; GLYCOPROTEIN; GLYCOSYLPHOSPHATIDYLINOSITOL; NUCLEOTIDE;

ARTICLE; BLOOD GROUP DOMBROCK SYSTEM; BLOOD GROUP SYSTEM; CONTROLLED STUDY; DNA FLANKING REGION; DNA SEQUENCE; ERYTHROCYTE; EXON; FRAMESHIFT MUTATION; GENE MUTATION; HUMAN; HUMAN CELL; INTRON; NUCLEOTIDE SEQUENCE; PHENOTYPE; POLYMERASE CHAIN REACTION; STOP CODON;

AMINO ACID SEQUENCE; BASE SEQUENCE; BLOOD GROUP ANTIGENS; DNA; DNA, COMPLEMENTARY; DNA, RECOMBINANT; EXONS; FRAMESHIFT MUTATION; GENOME; HUMANS; ISOANTIGENS; MOLECULAR SEQUENCE DATA; PHENOTYPE;

EID: 0035180240     PISSN: 00411132     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1537-2995.2001.41111405.x     Document Type: Article

References (12)

1. a
2. b
3. Evidence that several high-frequency human blood group antigens reside on phosphatidylinositol-linked erythrocyte membrane proteins
4. a/Hy-active glycoprotein
5. a and Hy are carried on a novel glycosylphosphatidylinositol-linked erythrocyte membrane glycoprotein
6. a antigens belong to the Dombrock blood group system
7. Identification of the Dombrock blood group glycoprotein as a polymorphic member of the ADP-ribosyltransferase gene family
8. DNA analysis for the Dombrock polymorphism
9. a (Gregory)
10. Prospective identification of erythroid elements in cultured peripheral blood
11. Defects in RNA splicing and the consequence of shortened translational reading frames
12. null individuals