Authors:
RUAN J
PEYRUCHAUD O
ALBERIO L
VALLES G
CLEMETSON K
BOURRE F
NURDEN AT
Citation: J. Ruan et al., DOUBLE HETEROZYGOSITY OF THE GPIIB GENE IN A SWISS PATIENT WITH GLANZMANNS-THROMBASTHENIA, British Journal of Haematology, 102(4), 1998, pp. 918-925
Authors:
PEYRUCHAUD O
NURDEN AT
MILET S
MACCHI L
PANNOCHIA A
BRAY PF
KIEFFER N
BOURRE F
Citation: O. Peyruchaud et al., R-TO-Q AMINO-ACID SUBSTITUTION IN THE GFFKR SEQUENCE OF THE CYTOPLASMIC DOMAIN OF THE INTEGRIN ALPHA-IIB SUBUNIT IN A PATIENT WITH A GLANZMANNS-THROMBASTHENIA-LIKE SYNDROME, Blood, 92(11), 1998, pp. 4178-4187
Authors:
MILET S
BOURRE F
PEYRUCHAUD O
CAZES E
COMBRIE R
NURDEN P
NURDEN A
Citation: S. Milet et al., AMINO-ACID SUBSTITUTION CYS(457) TO TYR IN THE BETA(3) SUBUNIT OF ALPHA(IIIB)BETA(3) IS INVOLVED IN AN ATYPICAL CASE OF GLANZMANN THROMBASTHENIA, Thrombosis and haemostasis, 1997, pp. 1474-1474
Citation: O. Peyruchaud et al., EFFICIENT RT-PCR ON PLATELET MESSENGER-RNA AFTER LONG-TERM STORAGE, British Journal of Haematology, 96(1), 1997, pp. 183-185
Authors:
PEYRUCHAUD O
BOURRE F
MORELKOPP MC
REVIRON D
MERCIER P
NURDEN A
KAPLAN C
Citation: O. Peyruchaud et al., HPA-10W(B) (LA-A) - GENETIC DETERMINATION OF A NEW PLATELET-SPECIFIC ALLOANTIGEN ON GLYCOPROTEIN IIIA AND ITS EXPRESSION IN COS-7 CELLS, Blood, 89(7), 1997, pp. 2422-2428
Authors:
PEYRUCHAUD O
BOURRE F
MORELKOPP MC
REVIRON D
MERCIER P
NURDEN A
KAPLAN C
Citation: O. Peyruchaud et al., HPA-10W(B) (LA-A) - GENETIC DETERMINATION OF A NEW PLATELET-SPECIFIC ALLOANTIGEN ON GLYCOPROTEIN IIIA AND ITS EXPRESSION IN COS-7 CELLS, Blood, 88(10), 1996, pp. 1856-1856
Citation: O. Peyruchaud et al., USE OF PCR-SSCP TO SCREEN THE EXONS OF THE GP-IIB AND GP-IIIA GENES OF A VARIANT WITH GLANZMANNS-THROMBASTHENIA - A MUTATION IN THE NUCLEOTIDE-SEQUENCE FOR THE GFFKR CYTOPLASMIC DOMAIN OF THE INTEGRIN SUBUNIT ALPHA(IIB) (GP-IIB), Thrombosis and haemostasis, 73(6), 1995, pp. 1189-1189
Authors:
EVENO E
BOURRE F
QUILLIET X
CHEVALLIERLAGENTE O
ROZA L
EKER APM
KLEIJER WJ
NIKAIDO O
STEFANINI M
HOEIJMAKERS JHJ
BOOTSMA D
CLEAVER JE
SARASIN A
MEZZINA M
Citation: E. Eveno et al., DIFFERENT REMOVAL OF ULTRAVIOLET PHOTOPRODUCTS IN GENETICALLY RELATEDXERODERMA-PIGMENTOSUM AND TRICHOTHIODYSTROPHY DISEASES, Cancer research, 55(19), 1995, pp. 4325-4332
Citation: O. Peyruchaud et al., BILATERAL LINKAGE BETWEEN A NEW DELETION POLYMORPHISM IN INTRON-21 OFTHE GP-IIB GENE AND THE HPA-3B (BAK(B)) DETERMINANT, British Journal of Haematology, 91(3), 1995, pp. 747-751
Citation: O. Peyruchaud et al., NONRADIOACTIVE SSCP FOR GENOTYPING HUMAN PLATELET ALLOANTIGENS, British Journal of Haematology, 89(3), 1995, pp. 633-636
Authors:
BOURRE F
PEYRUCHAUD O
BRAY P
COMBRIE R
NURDEN P
NURDEN AT
Citation: F. Bourre et al., A POINT MUTATION IN THE GENE FOR PLATELET GPIIB LEADS TO A SUBSTITUTION IN A HIGHLY CONSERVED AMINO-ACID LOCATED BETWEEN THE 2ND AND THE 3RD CA++ BINDING DOMAIN, Blood, 86(10), 1995, pp. 1796-1796