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5. Structure of a neutral glycosphingolipid recognized by human antibodies in polyagglutinable erythrocytes from the rare NOR phenotype. Duk M; Reinhold BB; Reinhold VN; Kusnierz-Alejska G; Lisowska E J Biol Chem; 2001 Nov; 276(44):40574-82. PubMed ID: 11504714 [TBL] [Abstract][Full Text] [Related]
6. Defective glycosylation of erythrocyte membrane glycoconjugates in a variant of congenital dyserythropoietic anemia type II: association of low level of membrane-bound form of galactosyltransferase. Fukuda MN; Masri KA; Dell A; Thonar EJ; Klier G; Lowenthal RM Blood; 1989 Apr; 73(5):1331-9. PubMed ID: 2495036 [TBL] [Abstract][Full Text] [Related]
7. Red cell membrane diseases and blood group abnormalities. Cartron JP; Salmon C Rev Fr Transfus Immunohematol; 1983 Dec; 26(6):599-623. PubMed ID: 6426027 [No Abstract] [Full Text] [Related]
8. Isolation and characterization of poly-N-acetyllactosaminylceramides accumulated in the erythrocytes of congenital dyserythropoietic anemia type II patients. Fukuda MN; Bothner B; Scartezzini P; Dell A Chem Phys Lipids; 1986 Dec; 42(1-3):185-97. PubMed ID: 3829205 [TBL] [Abstract][Full Text] [Related]
9. Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II caused by a defect in the gene encoding alpha-mannosidase II. Fukuda MN; Masri KA; Dell A; Luzzatto L; Moremen KW Proc Natl Acad Sci U S A; 1990 Oct; 87(19):7443-7. PubMed ID: 2217175 [TBL] [Abstract][Full Text] [Related]
10. Structures of unique globoside elongation products present in erythrocytes with a rare NOR phenotype. Duk M; Singh S; Reinhold VN; Krotkiewski H; Kurowska E; Lisowska E Glycobiology; 2007 Mar; 17(3):304-12. PubMed ID: 17118951 [TBL] [Abstract][Full Text] [Related]
11. Heterozygosity of CDAN II (HEMPAS) gene may be detected by the analysis of erythrocyte membrane glycoconjugates from healthy carriers. Zdebska E; Mendek-Czajkowska E; Ploski R; Woêniewicz B; Koscielak J Haematologica; 2002 Feb; 87(2):126-30. PubMed ID: 11836161 [TBL] [Abstract][Full Text] [Related]
12. Primary structure of the oligosaccharide determinant of blood group Cad specificity. Blanchard D; Cartron JP; Fournet B; Montreuil J; van Halbeek H; Vliegenthart JF J Biol Chem; 1983 Jun; 258(12):7691-5. PubMed ID: 6190803 [TBL] [Abstract][Full Text] [Related]
13. Polylactosamines are not obligate receptors for invasion of Plasmodium falciparum malaria as shown in HEMPAS variant II-gal- erythrocytes. Dhume ST; Adams-Burton CR; Shumak KH; Laine RA Glycobiology; 1994 Dec; 4(6):903-8. PubMed ID: 7734852 [TBL] [Abstract][Full Text] [Related]
14. NOR polyagglutination and Sta glycophorin in one family: relation of NOR polyagglutination to terminal alpha-galactose residues and abnormal glycolipids. Kuśnierz-Alejska G; Duk M; Storry JR; Reid ME; Wiecek B; Seyfried H; Lisowska E Transfusion; 1999 Jan; 39(1):32-8. PubMed ID: 9920164 [TBL] [Abstract][Full Text] [Related]
15. Defect in glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia type II (HEMPAS). Fukuda MN; Papayannopoulou T; Gordon-Smith EC; Rochant H; Testa U Br J Haematol; 1984 Jan; 56(1):55-68. PubMed ID: 6538436 [TBL] [Abstract][Full Text] [Related]
16. Incompletely processed N-glycans of serum glycoproteins in congenital dyserythropoietic anaemia type II (HEMPAS). Fukuda MN; Gaetani GF; Izzo P; Scartezzini P; Dell A Br J Haematol; 1992 Dec; 82(4):745-52. PubMed ID: 1482662 [TBL] [Abstract][Full Text] [Related]
17. Glycophorin A in two patients with congenital dyserythropoietic anemia type I and type II is partly unglycosylated. Zdebska E; Adamczyk-Popławska M; Kościelak J Acta Biochim Pol; 2000; 47(3):773-9. PubMed ID: 11310976 [TBL] [Abstract][Full Text] [Related]
18. Gangliosides and sialoglycoproteins carrying a rare blood group antigen determinant, Cad, associated with human cancers as detected by specific monoclonal antibodies. Hiraiwa N; Tsuyuoka K; Li YT; Tanaka M; Seno T; Okubo Y; Fukuda Y; Imura H; Kannagi R Cancer Res; 1990 Sep; 50(17):5497-503. PubMed ID: 2167157 [TBL] [Abstract][Full Text] [Related]
19. Polyagglutination NOR: new glycosphingolipid antigens recognized by a new type of common human anti-alpha-galactosyl antibodies. Lisowska E; Duk M Arch Biochem Biophys; 2004 Jun; 426(2):142-7. PubMed ID: 15158664 [No Abstract] [Full Text] [Related]
20. A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)]. Parsons SF; Jones J; Anstee DJ; Judson PA; Gardner B; Wiener E; Poole J; Illum N; Wickramasinghe SN Blood; 1994 Feb; 83(3):860-8. PubMed ID: 7507739 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]