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Results: 1-7 |
Results: 7
Genomic organization and refined mapping of the human nuclear corepressor 2 (NCOR2)/silencing mediator of retinoid and thyroid hormone receptor (SMRT) gene on chromosome 12q24.3
Authors: Jiang, Q Galiegue-Zoutina, S Roumier, C Hildebrand, MP Thomas, S Coignet, LJ
Citation: Q. Jiang et al., Genomic organization and refined mapping of the human nuclear corepressor 2 (NCOR2)/silencing mediator of retinoid and thyroid hormone receptor (SMRT) gene on chromosome 12q24.3, CYTOG C GEN, 92(3-4), 2001, pp. 217-220
Nonrandom 4p13 rearrangements of the RhoH/TTF gene, encoding a GTP-bindingprotein, in non-Hodgkin's lymphoma and multiple myeloma
Authors: Preudhomme, C Roumier, C Hildebrand, MP Dallery-Prudhomme, E Lantoine, D Lai, JL Daudignon, A Adenis, C Bauters, F Fenaux, P Kerckaert, JP Galiegue-Zouitina, S
Citation: C. Preudhomme et al., Nonrandom 4p13 rearrangements of the RhoH/TTF gene, encoding a GTP-bindingprotein, in non-Hodgkin's lymphoma and multiple myeloma, ONCOGENE, 19(16), 2000, pp. 2023-2032
High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21
Authors: Preudhomme, C Warot-Loze, D Roumier, C Grardel-Duflos, N Garand, R Lai, JL Dastugue, N Macintyre, E Denis, C Bauters, F Kerckaert, JP Cosson, A Fenaux, P
Citation: C. Preudhomme et al., High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21, BLOOD, 96(8), 2000, pp. 2762-2769
High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21
Authors: Preudhomme, C Warot-Loze, D Roumier, C Grardel-Duflos, N Garand, R Lai, JL Dastugue, N Macintyre, E Denis, C Bauters, F Kerckaert, JP Cosson, A Fenaux, P
Citation: C. Preudhomme et al., High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21, BLOOD, 96(8), 2000, pp. 2862-2869
Detection of BCR-ABL transcripts in chronic myeloid leukemia (CML) using a'real time' quantitative RT-PCR assay
Authors: Preudhomme, C Revillion, F Merlat, A Hornez, L Roumier, C Duflos-Grardel, N Jouet, JP Cosson, A Peyrat, JP Fenaux, P
Citation: C. Preudhomme et al., Detection of BCR-ABL transcripts in chronic myeloid leukemia (CML) using a'real time' quantitative RT-PCR assay, LEUKEMIA, 13(6), 1999, pp. 957-964
Detection of BCR-ABL transcripts in chronic myeloid leukemia (CML) using an in situ RT-PCR assay
Authors: Preudhomme, C Chams-Eddine, L Roumier, C Duflos-Grardel, N Denis, C Cosson, A Fenaux, P
Citation: C. Preudhomme et al., Detection of BCR-ABL transcripts in chronic myeloid leukemia (CML) using an in situ RT-PCR assay, LEUKEMIA, 13(5), 1999, pp. 818-823
p190 bcr-abl rearrangement: a secondary cytogenetic event in some chronic myeloid disorders?
Authors: Roumier, C Daudignon, A Soenen, V Dupriez, B Wetterwald, M Lai, JL Cosson, A Fenaux, P Preudhomme, C
Citation: C. Roumier et al., p190 bcr-abl rearrangement: a secondary cytogenetic event in some chronic myeloid disorders?, HAEMATOLOG, 84(12), 1999, pp. 1075-1080
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