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Results: 1-25 | 26-26
Results: 1-25/26
Ca2+-sensitive cytosolic nucleases prevent efficient delivery to the nucleus of injected plasmids
Authors: Pollard, H Toumaniantz, G Amos, JL Avet-Loiseau, H Guihard, G Behr, JP Escande, D
Citation: H. Pollard et al., Ca2+-sensitive cytosolic nucleases prevent efficient delivery to the nucleus of injected plasmids, J GENE MED, 3(2), 2001, pp. 153-164
High incidence of N and K-Ras activating mutations in multiple myeloma andprimary plasma cell leukemia at diagnosis
Authors: Bezieau, S Devilder, MC Avet-Loiseau, H Mellerin, MP Puthier, D Pennarun, E Rapp, MJ Harousseau, JL Moisan, JP Bataille, R
Citation: S. Bezieau et al., High incidence of N and K-Ras activating mutations in multiple myeloma andprimary plasma cell leukemia at diagnosis, HUM MUTAT, 18(3), 2001, pp. 212-224
Deletion of chromosomal region 13q14.3 in childhood acute lymphoblastic leukemia
Authors: Cave, H Avet-Loiseau, H Devaux, I Rondeau, G Boutard, P Lebrun, E Mechinaud, F Vilmer, E Grandchamp, B
Citation: H. Cave et al., Deletion of chromosomal region 13q14.3 in childhood acute lymphoblastic leukemia, LEUKEMIA, 15(3), 2001, pp. 371-376
Expression pattern, genomic structure and evaluation of the human SLC30A4 gene as a candidate for acrodermatitis enteropathica
Authors: Kury, S Devilder, MC Avet-Loiseau, H Dreno, B Moisan, JP
Citation: S. Kury et al., Expression pattern, genomic structure and evaluation of the human SLC30A4 gene as a candidate for acrodermatitis enteropathica, HUM GENET, 109(2), 2001, pp. 178-185
Characterization of adenovirus-induced inverted terminal repeat-independent amplification of integrated adeno-associated virus rep-cap sequences
Authors: Tessier, J Chadeuf, G Nony, P Avet-Loiseau, H Moullier, P Salvetti, A
Citation: J. Tessier et al., Characterization of adenovirus-induced inverted terminal repeat-independent amplification of integrated adeno-associated virus rep-cap sequences, J VIROLOGY, 75(1), 2001, pp. 375-383
Rearrangements of the c-myc oncogene are present in 15% of primary human multiple myeloma tumors
Authors: Avet-Loiseau, H Gerson, F Magrangeas, F Minvielle, S Harousseau, JL Bataille, R
Citation: H. Avet-loiseau et al., Rearrangements of the c-myc oncogene are present in 15% of primary human multiple myeloma tumors, BLOOD, 98(10), 2001, pp. 3082-3086
p16(INK4a) and p15(INK4b) gene methylations in plasma cells from monoclonal gammopathy of undetermined significance
Authors: Guillerm, G Gyan, E Wolowiec, D Facon, T Avet-Loiseau, H Kuliczkowski, K Bauters, F Fenaux, P Quesnel, B
Citation: G. Guillerm et al., p16(INK4a) and p15(INK4b) gene methylations in plasma cells from monoclonal gammopathy of undetermined significance, BLOOD, 98(1), 2001, pp. 244-246
Chromosome 13 abnormalities identified by FISH analysis and serum beta(2)-microglobulin produce a powerful myeloma staging system for patients receiving high-dose therapy
Authors: Facon, T Avet-Loiseau, H Guillerm, G Moreau, P Genevieve, F Zandecki, M Lai, JL Leleu, X Jouet, JP Bauters, F Harousseau, JL Bataille, R Mary, JY
Citation: T. Facon et al., Chromosome 13 abnormalities identified by FISH analysis and serum beta(2)-microglobulin produce a powerful myeloma staging system for patients receiving high-dose therapy, BLOOD, 97(6), 2001, pp. 1566-1571
Cytogenetic, interphase, and multicolor fluorescence in situ hybridizationanalyses in primary plasma cell leukemia: a study of 40 patients at diagnosis, on behalf of the Intergroupe Francophone du Myelome and the Groupe Francais de Cytogenetique Hematologique
Authors: Avet-Loiseau, H Daviet, A Brigaudeau, C Callet-Bauchu, E Terre, C Lafage-Pochitaloff, M Desangles, F Ramond, S Talmant, P Bataille, R
Citation: H. Avet-loiseau et al., Cytogenetic, interphase, and multicolor fluorescence in situ hybridizationanalyses in primary plasma cell leukemia: a study of 40 patients at diagnosis, on behalf of the Intergroupe Francophone du Myelome and the Groupe Francais de Cytogenetique Hematologique, BLOOD, 97(3), 2001, pp. 822-825
Deletion of 5q31 is observed in megakaryocytic cells in patients with myelodysplastic syndromes and a del(5q), including the 5q-syndrome
Authors: Godon, C Talmant, P Garand, R Accart, F Bataille, R Avet-Loiseau, H
Citation: C. Godon et al., Deletion of 5q31 is observed in megakaryocytic cells in patients with myelodysplastic syndromes and a del(5q), including the 5q-syndrome, GENE CHROM, 29(4), 2000, pp. 350-352
Expression of cyclins D-type in B-chronic lymphoproliferative disorders
Authors: Sola, B Roue, G Duquesne, F Avet-Loiseau, H Macro, M Salaun, V Troussard, X
Citation: B. Sola et al., Expression of cyclins D-type in B-chronic lymphoproliferative disorders, LEUKEMIA, 14(7), 2000, pp. 1318-1319
Fluorescence in situ hybridization on peripheral-blood specimens is a reliable method to evaluate cytogenetic response in chronic myeloid leukemia
Authors: Le Gouill, S Talmant, P Milpied, N Daviet, A Ancelot, M Moreau, P Harousseau, JL Bataille, R Avet-Loiseau, H
Citation: S. Le Gouill et al., Fluorescence in situ hybridization on peripheral-blood specimens is a reliable method to evaluate cytogenetic response in chronic myeloid leukemia, J CL ONCOL, 18(7), 2000, pp. 1533-1538
Reactive plasmacytoses in multiple myeloma during hematopoietic recovery with G- or GM-CSF
Authors: Jego, G Avet-Loiseau, H Robillard, N Moreau, P Amiot, M Harousseau, JL Pellat-Deceunynck, C Bataille, R
Citation: G. Jego et al., Reactive plasmacytoses in multiple myeloma during hematopoietic recovery with G- or GM-CSF, LEUK RES, 24(7), 2000, pp. 627-630
Gene amplifications detected by fluorescence in situ hybridization in pureintraductal breast carcinomas: Relation to morphology, cell proliferation and expression of breast cancer-related genes
Authors: Fiche, M Avet-Loiseau, H Maugard, CM Sagan, C Heymann, MF Leblanc, M Classe, JM Fumoleau, P Dravet, F Mahe, M Dutrillaux, B
Citation: M. Fiche et al., Gene amplifications detected by fluorescence in situ hybridization in pureintraductal breast carcinomas: Relation to morphology, cell proliferation and expression of breast cancer-related genes, INT J CANC, 89(5), 2000, pp. 403-410
Chromosome 13 abnormalities in multiple myeloma are mostly monosomy 13
Authors: Avet-Loiseau, H Daviet, A Saunier, S Bataille, R
Citation: H. Avet-loiseau et al., Chromosome 13 abnormalities in multiple myeloma are mostly monosomy 13, BR J HAEM, 111(4), 2000, pp. 1116-1117
IgG-secreting lymphoplasmacytoid leukaemia: a B-cell disorder with extensively mutated V-H genes undergoing Ig isotype-switching frequently associated with trisomy 12
Authors: Garand, R Sahota, SS Avet-Loiseau, H Talmant, P Robillard, N Moreau, A Gaillard, F Stevenson, FK Bataille, R
Citation: R. Garand et al., IgG-secreting lymphoplasmacytoid leukaemia: a B-cell disorder with extensively mutated V-H genes undergoing Ig isotype-switching frequently associated with trisomy 12, BR J HAEM, 109(1), 2000, pp. 71-80
Deletions of the p53 gene in multiple myeloma - Reply
Authors: Avet-Loiseau, H
Citation: H. Avet-loiseau, Deletions of the p53 gene in multiple myeloma - Reply, BR J HAEM, 108(4), 2000, pp. 887-887
Finding new human minisatellite sequences in the vicinity of long CA-rich sequences
Authors: Giraudeau, F Petit, E Avet-Loiseau, H Hauck, Y Vergnaud, G Amarger, V
Citation: F. Giraudeau et al., Finding new human minisatellite sequences in the vicinity of long CA-rich sequences, GENOME RES, 9(7), 1999, pp. 647-653
Amplification of the IIq23 region in acute myeloid leukemia
Authors: Avet-Loiseau, H Godon, C Li, JY Daviet, A Mellerin, MP Talmant, P Harousseau, JL Bataille, R
Citation: H. Avet-loiseau et al., Amplification of the IIq23 region in acute myeloid leukemia, GENE CHROM, 26(2), 1999, pp. 166-170
Genetic alterations in early-onset invasive breast carcinomas: Correlationof c-erbB-2 amplification detected by fluorescence in situ hybridization with p53 accumulation and tumor phenotype
Authors: Fiche, M Avet-Loiseau, H Heymann, MF Moussaly, F Digabel, C Joubert, M Classe, JM Dravet, F Fumoleau, P Ross, J Maugard, CM
Citation: M. Fiche et al., Genetic alterations in early-onset invasive breast carcinomas: Correlationof c-erbB-2 amplification detected by fluorescence in situ hybridization with p53 accumulation and tumor phenotype, INT J CANC, 84(5), 1999, pp. 511-515
14q32 translocations and monosomy 13 observed in monoclonal gammopathy of undetermined significance delineate a multistep process for the oncogenesisof multiple myeloma
Authors: Avet-Loiseau, H Facon, T Daviet, A Godon, C Rapp, MJ Harousseau, JL Grosbois, B Bataille, R
Citation: H. Avet-loiseau et al., 14q32 translocations and monosomy 13 observed in monoclonal gammopathy of undetermined significance delineate a multistep process for the oncogenesisof multiple myeloma, CANCER RES, 59(18), 1999, pp. 4546-4550
P53 deletion is not a frequent event in multiple myeloma
Authors: Avet-Loiseau, H Li, JY Godon, C Morineau, N Daviet, A Harousseau, JL Facon, T Bataille, R
Citation: H. Avet-loiseau et al., P53 deletion is not a frequent event in multiple myeloma, BR J HAEM, 106(3), 1999, pp. 717-719
Comparative genome hybridization detects many recurrent imbalances in central nervous system primitive neuroectodermal tumours in children
Authors: Avet-Loiseau, H Venuat, AM Terrier-Lacombe, MJ Lellouch-Tubiana, A Zerah, M Vassal, G
Citation: H. Avet-loiseau et al., Comparative genome hybridization detects many recurrent imbalances in central nervous system primitive neuroectodermal tumours in children, BR J CANC, 79(11-12), 1999, pp. 1843-1847
Monosomy 13 is associated with the transition of monoclonal gammopathy of undetermined significance to multiple myeloma
Authors: Avet-Loiseau, H Li, JY Morineau, N Facon, T Brigaudeau, C Harousseau, JL Grosbois, B Bataille, R
Citation: H. Avet-loiseau et al., Monosomy 13 is associated with the transition of monoclonal gammopathy of undetermined significance to multiple myeloma, BLOOD, 94(8), 1999, pp. 2583-2589
Detection of translocation t(11;14)(q13;q32) in mantle cell lymphoma by fluorescence in situ hybridization
Authors: Li, JY Gaillard, F Moreau, A Harousseau, JL Laboisse, C Milpied, N Bataille, R Avet-Loiseau, H
Citation: Jy. Li et al., Detection of translocation t(11;14)(q13;q32) in mantle cell lymphoma by fluorescence in situ hybridization, AM J PATH, 154(5), 1999, pp. 1449-1452
Risultati: 1-25 | 26-26