Raynal V - Search Results

1

Structure and expression of the RH locus in the Rh-deficiency syndrome.

Chérif-Zahar B, Raynal V, Le Van Kim C, D'Ambrosio AM, Bailly P, Cartron JP, Colin Y. Chérif-Zahar B, et al. Among authors: raynal v. Blood. 1993 Jul 15;82(2):656-62. Blood. 1993. PMID: 8329719 Free article.

2

Multiple Rh messenger RNA isoforms are produced by alternative splicing.

Le Van Kim C, Chérif-Zahar B, Raynal V, Mouro I, Lopez M, Cartron JP, Colin Y. Le Van Kim C, et al. Among authors: raynal v. Blood. 1992 Aug 15;80(4):1074-8. Blood. 1992. PMID: 1379850 Free article.

3

Molecular cloning and primary structure of the human blood group RhD polypeptide.

Le van Kim C, Mouro I, Chérif-Zahar B, Raynal V, Cherrier C, Cartron JP, Colin Y. Le van Kim C, et al. Among authors: raynal v. Proc Natl Acad Sci U S A. 1992 Nov 15;89(22):10925-9. doi: 10.1073/pnas.89.22.10925. Proc Natl Acad Sci U S A. 1992. PMID: 1438298 Free PMC article.

4

Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysis.

Colin Y, Chérif-Zahar B, Le Van Kim C, Raynal V, Van Huffel V, Cartron JP. Colin Y, et al. Among authors: raynal v. Blood. 1991 Nov 15;78(10):2747-52. Blood. 1991. PMID: 1824267 Free article.

5

Molecular analysis of the structure and expression of the RH locus in individuals with D--, Dc-, and DCw- gene complexes.

Chérif-Zahar B, Raynal V, D'Ambrosio AM, Cartron JP, Colin Y. Chérif-Zahar B, et al. Among authors: raynal v. Blood. 1994 Dec 15;84(12):4354-60. Blood. 1994. PMID: 7994050 Free article.

6

Organization of the gene (RHCE) encoding the human blood group RhCcEe antigens and characterization of the promoter region.

Chérif-Zahar B, Le Van Kim C, Rouillac C, Raynal V, Cartron JP, Colin Y. Chérif-Zahar B, et al. Among authors: raynal v. Genomics. 1994 Jan 1;19(1):68-74. doi: 10.1006/geno.1994.1014. Genomics. 1994. PMID: 8188244

7

Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency.

Cherif-Zahar B, Raynal V, Gane P, Mattei MG, Bailly P, Gibbs B, Colin Y, Cartron JP. Cherif-Zahar B, et al. Among authors: raynal v. Nat Genet. 1996 Feb;12(2):168-73. doi: 10.1038/ng0296-168. Nat Genet. 1996. PMID: 8563755

8

Lack of RHCE-encoded proteins in the D--phenotype may result from homologous recombination between the two RH genes.

Cherif-Zahar B, Raynal V, Cartron JP. Cherif-Zahar B, et al. Among authors: raynal v. Blood. 1996 Aug 15;88(4):1518-20. Blood. 1996. PMID: 8695878 Free article. No abstract available.

9

RH gene structure: reassignment of two exon-exon junctions.

Cherif-Zahar B, Raynal V, Cartron JP. Cherif-Zahar B, et al. Among authors: raynal v. Blood. 1997 Jun 15;89(12):4661-2. Blood. 1997. PMID: 9192795 Free article. No abstract available.

10

A novel single missense mutation identified along the RH50 gene in a composite heterozygous Rhnull blood donor of the regulator type.

Hyland CA, Chérif-Zahar B, Cowley N, Raynal V, Parkes J, Saul A, Cartron JP. Hyland CA, et al. Among authors: raynal v. Blood. 1998 Feb 15;91(4):1458-63. Blood. 1998. PMID: 9454778 Free article.

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