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Results: 1-25 | 26-34 |
Results: 26-34/34
CYS209 SER MUTATION IN THE PLATELET MEMBRANE GLYCOPROTEIN IB-ALPHA GENE IS ASSOCIATED WITH BERNARD-SOULIER SYNDROME
Authors: SIMSEK S NORIS P LOZANO M PICO M VONDEMBORNE AEGK RIBERA A GALLARDO D
Citation: S. Simsek et al., CYS209 SER MUTATION IN THE PLATELET MEMBRANE GLYCOPROTEIN IB-ALPHA GENE IS ASSOCIATED WITH BERNARD-SOULIER SYNDROME, British Journal of Haematology, 88(4), 1994, pp. 839-844
HUMAN PLATELET ANTIGEN-5 (BR) GENOTYPING BY ASPA - ALLELE-SPECIFIC PRIMER AMPLIFICATION (PCR-SSP) (VOL 88, PG 659, 1994)
Authors: SIMSEK S BLEEKER PMM HEEREMANS J VONDEMBORNE AEGK
Citation: S. Simsek et al., HUMAN PLATELET ANTIGEN-5 (BR) GENOTYPING BY ASPA - ALLELE-SPECIFIC PRIMER AMPLIFICATION (PCR-SSP) (VOL 88, PG 659, 1994), British Journal of Haematology, 88(4), 1994, pp. 898-898
HUMAN PLATELET ANTIGEN-5 (BR) GENOTYPING BY ASPA - ALLELE-SPECIFIC PRIMER AMPLIFICATION (PCR-SSP)
Authors: SIMSEK S BLEEKER PMM HEEREMANS J VONDEMBORNE AEGK
Citation: S. Simsek et al., HUMAN PLATELET ANTIGEN-5 (BR) GENOTYPING BY ASPA - ALLELE-SPECIFIC PRIMER AMPLIFICATION (PCR-SSP), British Journal of Haematology, 88(3), 1994, pp. 659-661
THE HUMAN PLATELET ALLOANTIGENS, HPA-5(A-) AND HPA-5(A-,B+), ARE ASSOCIATED WITH A GLU(505)(,B)LYS(505) POLYMORPHISM OF GLYCOPROTEIN IA (THE ALPHA(2) SUBUNIT OF VLA-2)/
Authors: SIMSEK S GALLARDO D RIBERA A VONDEMBORNE AEGK
Citation: S. Simsek et al., THE HUMAN PLATELET ALLOANTIGENS, HPA-5(A-) AND HPA-5(A-,B+), ARE ASSOCIATED WITH A GLU(505)(,B)LYS(505) POLYMORPHISM OF GLYCOPROTEIN IA (THE ALPHA(2) SUBUNIT OF VLA-2)/, British Journal of Haematology, 86(3), 1994, pp. 671-674
IDENTIFICATION OF A NEW GENETIC IGG-FC RECEPTOR POLYMORPHISM PRESENT ON NK CELL AND MACROPHAGE FC-GAMMA-RIIIA
Authors: DEHAAS M KLEIJER M SIMSEK S ROOS D VONDEMBORNE AEGK
Citation: M. Dehaas et al., IDENTIFICATION OF A NEW GENETIC IGG-FC RECEPTOR POLYMORPHISM PRESENT ON NK CELL AND MACROPHAGE FC-GAMMA-RIIIA, Blood, 84(10), 1994, pp. 10000184-10000184
A HOMOZYGOUS POINT MUTATION IN A LEUCINE-RICH MOTIF OF PLATELET GLYCOPROTEIN-IX ASSOCIATED WITH BERNARD-SOULIER SYNDROME (BSS)
Authors: NORIS P SIMSEK S STIBBE J VONDEMBORNE AEGK
Citation: P. Noris et al., A HOMOZYGOUS POINT MUTATION IN A LEUCINE-RICH MOTIF OF PLATELET GLYCOPROTEIN-IX ASSOCIATED WITH BERNARD-SOULIER SYNDROME (BSS), Blood, 84(10), 1994, pp. 10000320-10000320
NEONATAL ALLOIMMUNE THROMBOCYTOPENIA (NATP) CAUSED BY A NEW LOW-FREQUENCY PLATELET-SPECIFIC ALLOANTIGEN, MAXA, LOCATED ON GPIIB
Authors: NORIS P SIMSEK S DEBRUIJNEADMIRAAL LG PORCELIIN L HUISKES E VANDERVLIST G VANLEEUWEN EF VANDERSCHOOT CE VONDEMBORNE AEGK
Citation: P. Noris et al., NEONATAL ALLOIMMUNE THROMBOCYTOPENIA (NATP) CAUSED BY A NEW LOW-FREQUENCY PLATELET-SPECIFIC ALLOANTIGEN, MAXA, LOCATED ON GPIIB, Blood, 84(10), 1994, pp. 10000527-10000527
IDENTIFICATION OF A HOMOZYGOUS SINGLE-BASE PAIR DELETION IN THE GENE CODING FOR THE HUMAN PLATELET GLYCOPROTEIN IB-ALPHA CAUSING BERNARD-SOULIER SYNDROME
Authors: SIMSEK S ADMIRAAL LG MODDERMAN PW VANDERSCHOOT CE VONDEMBORNE AEGK
Citation: S. Simsek et al., IDENTIFICATION OF A HOMOZYGOUS SINGLE-BASE PAIR DELETION IN THE GENE CODING FOR THE HUMAN PLATELET GLYCOPROTEIN IB-ALPHA CAUSING BERNARD-SOULIER SYNDROME, Thrombosis and haemostasis, 69(6), 1993, pp. 963-963
GLANZMANN THROMBASTHENIA CAUSED BY HOMOZYGOSITY FOR A SPLICE DEFECT THAT LEADS TO DELETION OF THE 1ST CODING EXON OF THE GLYCOPROTEIN-IIIA MESSENGER-RNA
Authors: SIMSEK S HEYBOER H DEBRUIJNEADMIRAAL LG GOLDSCHMEDING R CUIJPERS HTM VONDEMBORNE AEGK
Citation: S. Simsek et al., GLANZMANN THROMBASTHENIA CAUSED BY HOMOZYGOSITY FOR A SPLICE DEFECT THAT LEADS TO DELETION OF THE 1ST CODING EXON OF THE GLYCOPROTEIN-IIIA MESSENGER-RNA, Blood, 81(8), 1993, pp. 2044-2049
Risultati: 1-25 | 26-34 |