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Results: 1 to 20 of 135

Similar articles for PubMed (Select 2818576)

2.

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 5;264(7):3773-80.

3.

Molecular characterization of erythrocyte glycophorin C variants.

Chang S, Reid ME, Conboy J, Kan YW, Mohandas N.

Blood. 1991 Feb 1;77(3):644-8.

5.
7.

Normal membrane function of abnormal beta-related erythrocyte sialoglycoproteins.

Reid ME, Anstee DJ, Jensen RH, Mohandas N.

Br J Haematol. 1987 Dec;67(4):467-72.

PMID:
3426964
8.

A novel gene member of the human glycophorin A and B gene family. Molecular cloning and expression.

Vignal A, Rahuel C, London J, Cherif Zahar B, Schaff S, Hattab C, Okubo Y, Cartron JP.

Eur J Biochem. 1990 Aug 17;191(3):619-25.

9.

Molecular analysis of glycophorin A and B gene structure and expression in homozygous Miltenberger class V (Mi. V) human erythrocytes.

Vignal A, Rahuel C, el Maliki B, London J, le van Kim C, Blanchard D, Andre C, d'Auriol L, Galibert F, Blajchman MA, et al.

Eur J Biochem. 1989 Sep 15;184(2):337-44.

10.

Co-presence of a point mutation and a deletion of exon 3 in the glycophorin C gene and concomitant production of a Gerbich-related antibody.

King MJ, Kosanke J, Reid ME, Poole J, Banks J, Hemming NJ, Smythe J, Martin PG.

Transfusion. 1997 Oct;37(10):1027-34.

PMID:
9354820
11.

Molecular basis of glycophorin C variants and their associated blood group antigens.

Reid ME, Spring FA.

Transfus Med. 1994 Jun;4(2):139-46.

PMID:
7921050
12.
13.

Glycophorin SAT of the human erythrocyte membrane is specified by a hybrid gene reciprocal to glycophorin Dantu gene.

Huang CH, Reid ME, Okubo Y, Daniels GL, Blumenfeld OO.

Blood. 1995 Apr 15;85(8):2222-7.

15.

Molecular analysis of a hybrid gene encoding human glycophorin variant Miltenberger V-like molecule.

Kudo S, Chagnovich D, Rearden A, Mattei MG, Fukuda M.

J Biol Chem. 1990 Aug 15;265(23):13825-9.

18.

Duplication of exon 3 in the glycophorin C gene gives rise to the Lsa blood group antigen.

Reid ME, Mawby W, King MJ, Sistonen P.

Transfusion. 1994 Nov-Dec;34(11):966-9.

PMID:
7526492
19.

Molecular analysis of glycophorin C deficiency in human erythrocytes.

Winardi R, Reid M, Conboy J, Mohandas N.

Blood. 1993 May 15;81(10):2799-803.

20.

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 15;172(1):147-53.

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