227 related articles for article (PubMed ID: 2390989)
21. Alteration of the genes for glycophorin A and B in glycophorin-A-deficient individuals.
Rahuel C; London J; Vignal A; Cherif-Zahar B; Colin Y; Siebert P; Fukuda M; Cartron JP
Eur J Biochem; 1988 Nov; 177(3):605-14. PubMed ID: 3197721
[TBL] [Abstract][Full Text] [Related]
22. Molecular genetics of glycophorin MNS variants.
Blumenfeld OO; Huang CH
Transfus Clin Biol; 1997 Jul; 4(4):357-65. PubMed ID: 9269716
[TBL] [Abstract][Full Text] [Related]
23. Evolution of the glycophorin gene family in the hominoid primates.
Rearden A; Phan H; Kudo S; Fukuda M
Biochem Genet; 1990 Apr; 28(3-4):209-22. PubMed ID: 2383247
[TBL] [Abstract][Full Text] [Related]
24. The major integral proteins of the human red cell.
Tanner MJ
Baillieres Clin Haematol; 1993 Jun; 6(2):333-56. PubMed ID: 8043929
[TBL] [Abstract][Full Text] [Related]
25. Critical glycosylated residues in exon three of erythrocyte glycophorin A engage Plasmodium falciparum EBA-175 and define receptor specificity.
Salinas ND; Paing MM; Tolia NH
mBio; 2014 Sep; 5(5):e01606-14. PubMed ID: 25205096
[TBL] [Abstract][Full Text] [Related]
26. Molecular genetics of the glycophorin gene family, the antigens for MNSs blood groups: multiple gene rearrangements and modulation of splice site usage result in extensive diversification.
Blumenfeld OO; Huang CH
Hum Mutat; 1995; 6(3):199-209. PubMed ID: 8535438
[TBL] [Abstract][Full Text] [Related]
27. Characterization of cDNA clones for human glycophorin A. Use for gene localization and for analysis of normal of glycophorin-A-deficient (Finnish type) genomic DNA.
Rahuel C; London J; d'Auriol L; Mattei MG; Tournamille C; Skrzynia C; Lebouc Y; Galibert F; Cartron JP
Eur J Biochem; 1988 Feb; 172(1):147-53. PubMed ID: 3345758
[TBL] [Abstract][Full Text] [Related]
28. Erythrocyte glycophorin B deficiency may occur by two distinct gene alterations.
Rahuel C; London J; Vignal A; Ballas SK; Cartron JP
Am J Hematol; 1991 May; 37(1):57-8. PubMed ID: 2024643
[TBL] [Abstract][Full Text] [Related]
29. Genomic organization of glycophorin A gene family revealed by yeast artificial chromosomes containing human genomic DNA.
Onda M; Kudo S; Fukuda M
J Biol Chem; 1994 Apr; 269(17):13013-20. PubMed ID: 8175721
[TBL] [Abstract][Full Text] [Related]
30. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
Zhang DL; Ji L; Li YD
Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
[TBL] [Abstract][Full Text] [Related]
31. Complete structure of the human alpha-albumin gene, a new member of the serum albumin multigene family.
Nishio H; Dugaiczyk A
Proc Natl Acad Sci U S A; 1996 Jul; 93(15):7557-61. PubMed ID: 8755513
[TBL] [Abstract][Full Text] [Related]
32. Human erythrocyte glycophorin C. Gene structure and rearrangement in genetic variants.
Colin Y; Le Van Kim C; Tsapis A; Clerget M; d'Auriol L; London J; Galibert F; Cartron JP
J Biol Chem; 1989 Mar; 264(7):3773-80. PubMed ID: 2917976
[TBL] [Abstract][Full Text] [Related]
33. Genomic organization and mutational analysis of the human UCP2 gene, a prime candidate gene for human obesity.
Lentes KU; Tu N; Chen H; Winnikes U; Reinert I; Marmann G; Pirke KM
J Recept Signal Transduct Res; 1999; 19(1-4):229-44. PubMed ID: 10071761
[TBL] [Abstract][Full Text] [Related]
34. Rearrangements of the red-cell membrane glycophorin C (sialoglycoprotein beta) gene. A further study of alterations in the glycophorin C gene.
High S; Tanner MJ; Macdonald EB; Anstee DJ
Biochem J; 1989 Aug; 262(1):47-54. PubMed ID: 2818576
[TBL] [Abstract][Full Text] [Related]
35. Hypobetalipoproteinemia due to an apolipoprotein B gene exon 21 deletion derived by Alu-Alu recombination.
Huang LS; Ripps ME; Korman SH; Deckelbaum RJ; Breslow JL
J Biol Chem; 1989 Jul; 264(19):11394-400. PubMed ID: 2567736
[TBL] [Abstract][Full Text] [Related]
36. Gerbich blood groups and minor glycophorins of human erythrocytes.
Colin Y
Transfus Clin Biol; 1995; 2(4):259-68. PubMed ID: 8542024
[TBL] [Abstract][Full Text] [Related]
37. Post-transcriptional regulation of the cell surface expression of glycophorins A, B, and E.
Rahuel C; Elouet JF; Cartron JP
J Biol Chem; 1994 Dec; 269(52):32752-8. PubMed ID: 7806496
[TBL] [Abstract][Full Text] [Related]
38. Nucleotide sequence of the gene for the b subunit of human factor XIII.
Bottenus RE; Ichinose A; Davie EW
Biochemistry; 1990 Dec; 29(51):11195-209. PubMed ID: 2271707
[TBL] [Abstract][Full Text] [Related]
39. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
Lee PL; Gelbart T; West C; Halloran C; Beutler E
Blood Cells Mol Dis; 1998 Jun; 24(2):199-215. PubMed ID: 9642100
[TBL] [Abstract][Full Text] [Related]
40. Glycophorin He(Sta) of the human red blood cell membrane is encoded by a complex hybrid gene resulting from two recombinational events.
Huang CH; Lomas C; Daniels G; Blumenfeld OO
Blood; 1994 Jun; 83(11):3369-76. PubMed ID: 8193374
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
