A Single Point Mutation in the Gene Encoding Gb3/CD77 Synthase Causes a Rare Inherited Polyagglutination Syndrome-Reference-Cited by-同舟云学术

A Single Point Mutation in the Gene Encoding Gb3/CD77 Synthase Causes a Rare Inherited Polyagglutination Syndrome

Published:2012-11 Issue:45 Volume:287 Page:38220-38230
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Suchanowska Anna,Kaczmarek Radoslaw,Duk Maria,Lukasiewicz Jolanta,Smolarek Dorota,Majorczyk Edyta,Jaskiewicz Ewa,Laskowska Anna,Wasniowska Kazimiera,Grodecka Magdalena,Lisowska Elwira,Czerwinski Marcin

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference33 articles.

1. An inherited RBC characteristic, NOR, resulting in erythrocyte polyagglutination;Harris;Vox Sang.,1982

2. NOR polyagglutination and Sta glycophorin in one family. Relation of NOR polyagglutination to terminal α-galactose residues and abnormal glycolipids;Kuśnierz-Alejska;Transfusion,1999

3. Structure of a neutral glycosphingolipid recognized by human antibodies in polyagglutinable erythrocytes of the rare NOR phenotype;Duk;J. Biol. Chem.,2001

4. Structures of unique globoside elongation products present in erythrocytes with a rare NOR phenotype;Duk;Glycobiology,2007

5. Polyagglutinable NOR red blood cells found in an American family and a Polish family have the same unique glycosphingolipids;Duk;Transfusion,2006

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