Identification of the molecular and genetic basis of PX2, a glycosphingolipid blood group antigen lacking on globoside-deficient erythrocytes

Journal of Biological Chemistry

Volumn 290, Issue 30, 2015, Pages 18505-18518

  Westman, Julia S ^a   Benktander, John ^b   Storry, Jill R ^a,c   Peyrard, Thierry ^d,e   Hult, Annika K ^a,c   Hellberg, Åsa ^a,c   Teneberg, Susann ^b   Olsson, Martin L ^a,c  

^a LUND UNIVERSITY   (Sweden)

^b UNIVERSITY OF GOTHENBURG   (Sweden)

^c Diaverum Renal Services Group   (Sweden)

^d INSTITUT NATIONAL DE LA TRANSFUSION SANGUINE   (France)

^e Laboratory of Excellence GR Ex   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIGENS; MASS SPECTROMETRY; THIN LAYER CHROMATOGRAPHY;

BLOOD GROUP; BLOOD GROUP ANTIGEN; GENETIC BASIS; GLOBOTRIAOSYLCERAMIDE; GLYCOSPHINGOLIPIDS; NATURALLY OCCURRING; OVER-EXPRESSION; SYNTHASES;

BLOOD;

BLOOD GROUP ANTIBODY; BLOOD GROUP ANTIGEN; GLOBOSIDE; SMALL INTERFERING RNA; UDP N ACETYLGALACTOSAMINE:GLOBOTRIAOSYLCERAMIDE 3 BETA N ACETYLGALACTOSAMINYLTRANSFERASE; UNCLASSIFIED DRUG; URIDINE DIPHOSPHATE N ACETYLGALACTOSAMINE; X2 GLYCOSPHINGOLIPID; X2 GLYCOSPHINGOLIPID ANTIBODY; ANTIBODY; B3GALNT1 PROTEIN, HUMAN; DISACCHARIDE; GLYCOSPHINGOLIPID; N ACETYLGALACTOSAMINYLTRANSFERASE; N-ACETYLGALACTOSAMINYL-1-3-GALACTOSE;

ANTIGEN BINDING; ANTIGEN EXPRESSION; ARTICLE; B3GALNT1 GENE; CONTROLLED STUDY; ERYTHROCYTE; FLOW CYTOMETRY; GENE; GENE MUTATION; GENE OVEREXPRESSION; GENE SILENCING; HUMAN; HUMAN CELL; MASS SPECTROMETRY; MOLECULAR GENETICS; PHENOTYPE; PRIORITY JOURNAL; THIN LAYER CHROMATOGRAPHY; BIOSYNTHESIS; GENETICS; IMMUNOLOGY; METABOLISM; MUTATION; PATHOLOGY;

ANTIBODIES; BLOOD GROUP ANTIGENS; DISACCHARIDES; ERYTHROCYTES; GLOBOSIDES; GLYCOSPHINGOLIPIDS; HUMANS; MUTATION; N-ACETYLGALACTOSAMINYLTRANSFERASES; PHENOTYPE;

EID: 84937798145     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M115.655308     Document Type: Article

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