Bourre F - Search Results

1

HPA-10w(b) (La(a)): genetic determination of a new platelet-specific alloantigen on glycoprotein IIIa and its expression in COS-7 cells.

Peyruchaud O, Bourre F, Morel-Kopp MC, Reviron D, Mercier P, Nurden A, Kaplan C. Peyruchaud O, et al. Among authors: bourre f. Blood. 1997 Apr 1;89(7):2422-8. Blood. 1997. PMID: 9116286 Free article.

2

Non-radioactive SSCP for genotyping human platelet alloantigens.

Peyruchaud O, Nurden A, Bourre F. Peyruchaud O, et al. Among authors: bourre f. Br J Haematol. 1995 Mar;89(3):633-6. doi: 10.1111/j.1365-2141.1995.tb08376.x. Br J Haematol. 1995. PMID: 7734366

3

Bilateral linkage between a new deletion polymorphism in intron 21 of the GP IIb gene and the HPA-3b (Bakb) determinant.

Peyruchaud O, Nurden A, Bourre F. Peyruchaud O, et al. Among authors: bourre f. Br J Haematol. 1995 Nov;91(3):747-51. doi: 10.1111/j.1365-2141.1995.tb05380.x. Br J Haematol. 1995. PMID: 8555087

4

Efficient RT-PCR on platelet mRNA after long-term storage.

Peyruchaud O, Nurden A, Bourre F. Peyruchaud O, et al. Among authors: bourre f. Br J Haematol. 1997 Jan;96(1):183-5. doi: 10.1046/j.1365-2141.1997.d01-2004.x. Br J Haematol. 1997. PMID: 9012707 Free article.

5

Linkage of four polymorphisms on the alphaIIb gene.

Ruan J, Peyruchaud O, Nurden A, Bourre F. Ruan J, et al. Among authors: bourre f. Br J Haematol. 1998 Jul;102(2):622-5. doi: 10.1046/j.1365-2141.1998.00810.x. Br J Haematol. 1998. PMID: 9695983 Free article.

6

R to Q amino acid substitution in the GFFKR sequence of the cytoplasmic domain of the integrin IIb subunit in a patient with a Glanzmann's thrombasthenia-like syndrome.

Peyruchaud O, Nurden AT, Milet S, Macchi L, Pannochia A, Bray PF, Kieffer N, Bourre F. Peyruchaud O, et al. Among authors: bourre f. Blood. 1998 Dec 1;92(11):4178-87. Blood. 1998. PMID: 9834222 Free article.

7

Double heterozygosity of the GPIIb gene in a Swiss patient with Glanzmann's thrombasthenia.

Ruan J, Peyruchaud O, Alberio L, Valles G, Clemetson K, Bourre F, Nurden AT. Ruan J, et al. Among authors: bourre f. Br J Haematol. 1998 Sep;102(4):918-25. doi: 10.1046/j.1365-2141.1998.00852.x. Br J Haematol. 1998. PMID: 9734640 Free article.

8

Two different beta3 cysteine substitutions alter alphaIIb beta3 maturation and result in Glanzmann thrombasthenia.

Milet-Marsal S, Breillat C, Peyruchaud O, Nurden P, Combrié R, Nurden A, Bourre F. Milet-Marsal S, et al. Among authors: bourre f. Thromb Haemost. 2002 Jul;88(1):104-10. Thromb Haemost. 2002. PMID: 12152649

9

Homozygous Cys542-->Arg substitution in GPIIIa in a Swiss patient with type I Glanzmann's thrombasthenia.

Ruan J, Schmugge M, Clemetson KJ, Cazes E, Combrie R, Bourre F, Nurden AT. Ruan J, et al. Among authors: bourre f. Br J Haematol. 1999 May;105(2):523-31. Br J Haematol. 1999. PMID: 10233432 Free article.

10

Analysis of the amino acid requirement for a normal alphaIIbbeta3 maturation at alphaIIbGlu324 commonly mutated in Glanzmann thrombasthenia.

Milet-Marsal S, Breillat C, Peyruchaud O, Nurden P, Combrié R, Nurden AT, Bourre F. Milet-Marsal S, et al. Among authors: bourre f. Thromb Haemost. 2002 Oct;88(4):655-62. Thromb Haemost. 2002. PMID: 12362239

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