Search

Your search keyword '"Bayle, C."' showing total 253 results
Start Over Author "Bayle, C."
253 results on '"Bayle, C."'

9. Multicentric evaluation of the MDR phenotype in leukemia

Author

Marie, J-P, Huet, S, Faussat, A-M, Perrot, J-Y, Chevillard, S, Barbu, V, Bayle, C, Boutonnat, J, Calvo, F, Campos-Guyotat, L, Colosetti, P, Cazin, J-L, de Cremoux, P, Delvincourt, C, Demur, C, Drenou, B, Fenneteau, O, Feuillard, J, Garnier-Suillerot, A, Genne, P, Gorisse, M-C, Gosselin, P, Jouault, H, Lacave, R, Le Calvez, G, Léglise, M-C, Léonce, S, Manfait, M, Maynadié, M, Merle-Béral, H, Merlin, J-L, Mousseau, M, Morjani, H, Picard, F, Pinguet, F, Poncelet, P, Racadot, E, Raphael, M, Richard, B, Rossi, J-F, Schlegel, N, Vielh, P, Zhou, D-C, and Robert, J

Published
1997
Full Text
View/download PDF

10. French multicentric evaluation of mdr1 gene expression by RT-PCR in leukemia and solid tumours. Standardization of RT-PCR and preliminary comparisons between RT-PCR and immunohistochemistry in solid tumours

Author

Chevillard, S, Vielh, Ph, Validire, P, Marie, JP, Faussat, AM, Barbu, V, Bayle, C, Bénard, J, Bonnal, C, Boutonnat, J, Calvo, F, Charrier, J, Clary, A, Colosetti, P, Danel-Moore, L, Decrémoux, P, Delvincourt, C, Finat-Duclos, F, Genne, Ph, Kataki, A, Kouyoumdjian, JC, Lacave, R, Maugard, C, Merlin, JL, Mousseau, M, Pinguet, F, Quillien, V, Raphael, M, Richard, B, Verrelle, P, and Robert, J

Published
1997
Full Text
View/download PDF

19. Le musée au tournant du XXIe siècle (1998-2014)

Author

BERNADAC, M-L, BRESC-GAUTIER, G, Gombault, Anne, KREBS, A, MARDRUS, F, NAFFAH-BAYLE, C, TARDIVIER, N, and Kedge Business School (Kedge BS)

Subjects
ComputingMilieux_MISCELLANEOUS, [SHS]Humanities and Social Sciences
Abstract

National audience

Published
2016

21. A new classification scheme of European cold-water coral habitats: Implications for ecosystem-based management of the deep sea

Author

Davies, J.S., primary, Guillaumont, B., additional, Tempera, F., additional, Vertino, A., additional, Beuck, L., additional, Ólafsdóttir, S.H., additional, Smith, C.J., additional, Fosså, J.H., additional, van den Beld, I.M.J., additional, Savini, A., additional, Rengstorf, A., additional, Bayle, C., additional, Bourillet, J.-F., additional, Arnaud-Haond, S., additional, and Grehan, A., additional

Published
2017
Full Text
View/download PDF

23. The Congolobe project, a multidisciplinary study of Congo deep-sea fan lobe complex: Overview of methods, strategies, observations and sampling

Author

Rabouille, C., primary, Olu, K., additional, Baudin, F., additional, Khripounoff, A., additional, Dennielou, B., additional, Arnaud-Haond, S., additional, Babonneau, N., additional, Bayle, C., additional, Beckler, J., additional, Bessette, S., additional, Bombled, B., additional, Bourgeois, S., additional, Brandily, C., additional, Caprais, J.C., additional, Cathalot, C., additional, Charlier, K., additional, Corvaisier, R., additional, Croguennec, C., additional, Cruaud, P., additional, Decker, C., additional, Droz, L., additional, Gayet, N., additional, Godfroy, A., additional, Hourdez, S., additional, Le Bruchec, J., additional, Saout, J., additional, Le Saout, M., additional, Lesongeur, F., additional, Martinez, P., additional, Mejanelle, L., additional, Michalopoulos, P., additional, Mouchel, O., additional, Noel, P., additional, Pastor, L., additional, Picot, M., additional, Pignet, P., additional, Pozzato, L., additional, Pruski, A.M., additional, Rabiller, M., additional, Raimonet, M., additional, Ragueneau, O., additional, Reyss, J.L., additional, Rodier, P., additional, Ruesch, B., additional, Ruffine, L., additional, Savignac, F., additional, Senyarich, C., additional, Schnyder, J., additional, Sen, A., additional, Stetten, E., additional, Sun, Ming Yi, additional, Taillefert, M., additional, Teixeira, S., additional, Tisnerat-Laborde, N., additional, Toffin, L., additional, Tourolle, J., additional, Toussaint, F., additional, Vétion, G., additional, Jouanneau, J.M., additional, and Bez, M., additional

Published
2017
Full Text
View/download PDF

25. T cell repertoire in patients with B chronic lymphocytic leukemia. Evidence for multiple in vivo T cell clonal expansions

Author

Farace, F., Orlanducci, F., Dietrich, P. -Y, Gaudin, C., Eric ANGEVIN, Courtier, M. -H, Bayle, C., Hercend, T., and Triebel, F.

Subjects
Immunology, Immunology and Allergy
Abstract

To characterize circulating T cell subpopulations in B chronic lymphocytic leukemia patients, TCR V alpha and V beta gene-segment use was analyzed by PCR using a panel of V gene-segment subfamily-specific oligonucleotide primers (V alpha 1-29/V beta 1-24). Virtually all V alpha and V beta subfamily specificities were expressed in these patients (nine stage A and four stage C), and the mean values obtained for each specificity were similar to those of a group of 13 healthy donors. Nonetheless, individual analysis revealed that unique V alpha or V beta gene-segment transcripts were overrepresented in patients compared with the control group. Overrepresentation of some TCR V beta chains was also detected by cytofluorometric analysis using a panel of 18 anti-V beta-specific mAbs. To further characterize these T cell subpopulations, we sequenced five different V beta-C beta PCR products in two selected stage A patients and found highly predominant recurrent transcripts in each of the five V beta specificities (50% to 100% of the analyzed sequences with identical V(D)J regions). These results were confirmed on bulk cDNA (i.e., without cloning) and extended to other V beta specificities (up to nine clonal expansions of 24 V beta specificities in one patient) and two other patients using a PCR-based method that determines V(D)J junction size patterns. Finally, it was observed that a V beta 19+ T cell subpopulation was clonally expanded in one patient to up to 30% of circulating T cells. This V beta 19+ CD8+ T cell clone was shown to specifically recognize the autologous tumor cells in vitro, as determined in cytokine release assays. Together, these results support the view that multiple expansions of unique T cell clones may derive in vivo from B chronic lymphocytic leukemia tumor-associated Ag stimulation.

Published
1994

26. A gene candidate approach to study the control of recurrent blooming in rose

Author

Foucher, Fabrice, Lalanne, David, Soufflet-Freslon, Vanessa, Bayle, C., Hibrand-Saint Oyant, Laurence, Génétique et Horticulture (GenHort), Institut National de la Recherche Agronomique (INRA)-AGROCAMPUS OUEST, GenHort, Institut National de la Recherche Agronomique (INRA), and Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)

Subjects
clone, congenital, hereditary, and neonatal diseases and abnormalities, rosa, déterminant de la floraison, [SDV]Life Sciences [q-bio], fungi, approche gène candidat, food and beverages, nutritional and metabolic diseases, hip rose, cartographie de clones, librairie de clones
Abstract

A gene candidate approach to study the control of recurrent blooming in rose. Plant genomics European meetings

Published
2004

29. Prise en charge thérapeutique de la démence

Author

Rigaud, A.-S., primary, Latour, F., additional, Lenoir, H., additional, Bayle, C., additional, Seux, M.-L., additional, Hanon, O., additional, Péquignot, R., additional, Cantegreil, I., additional, Wenisch, E., additional, Moulin, F., additional, and de Rotrou, J., additional

Published
2006
Full Text
View/download PDF

30. Tratamiento de la demencia

Author

Rigaud, A.-S., primary, Latour, F., additional, Lenoir, H., additional, Bayle, C., additional, Seux, M.-L., additional, Hanon, O., additional, Péquignot, R., additional, Cantegreil, I., additional, Wenisch, E., additional, Moulin, F., additional, and de Rotrou, J., additional

Published
2005
Full Text
View/download PDF

31. Actualités cliniques et thérapeutiques dans les démences

Author

Seux, M.-L., primary, Bayle, C., additional, Lenoir, H., additional, Latour, F., additional, Pequignot, R., additional, Hanon, O., additional, Artaz, M.-A., additional, Wenisch, E., additional, Cantegreil, I., additional, Moulin, F., additional, De Rotrou, J., additional, and Rigaud, A.-S., additional

Published
2004
Full Text
View/download PDF

37. Burkitt-like lymphomas in AIDS patients: characterization within a series of 103 human immunodeficiency virus-associated non-Hodgkin's lymphomas. Burkitt's Lymphoma Study Group.

Author

Davi, F, primary, Delecluse, H J, additional, Guiet, P, additional, Gabarre, J, additional, Fayon, A, additional, Gentilhomme, O, additional, Felman, P, additional, Bayle, C, additional, Berger, F, additional, Audouin, J, additional, Bryon, P A, additional, Diebold, J, additional, and Raphaël, M, additional

Published
1998
Full Text
View/download PDF

42. Carcinoma cell leukemia [letter]

Author

Nasr, F, primary, Corti, C, additional, Carde, P, additional, Ribrag, V, additional, Valensi, F, additional, Bayle, C, additional, Turhan, AG, additional, and Bosq, J, additional

Published
1996
Full Text
View/download PDF

44. Recherche d'un envahissement de la moelle osseuse lors du diagnostic de tumeur solide chez l'enfant. Méthodes, résultats et interprétation

Author

Pein, F, primary, Hartmann, O, additional, Sakiroglu, C, additional, Bayle, C, additional, Terrier-Lacombe, MJ, additional, Valteau-Couanet, D, additional, Lumbroso, J, additional, Oberlin, O, additional, Couanet, D, additional, Patte, C, additional, Brugières, L, additional, and Lemerle, J, additional

Published
1995
Full Text
View/download PDF

46. CD2+ CD19+ acute lymphoblastic leukaemia in 16 children and adults: clinical and biological features. The Groupe d'Etude Immunologique des Leucémies (G.E.I.L.)

Author

Lenormand, B., primary, Vannier, J. P., additional, Bene, M. C., additional, Falkenrodt, A., additional, Bayle, C., additional, Favre, M., additional, Garand, R., additional, Griveau, A. M., additional, Briquet, M. T., additional, Reman, O., additional, Boutard, P., additional, Tilly, H., additional, Faure, G., additional, and Monconduit, M., additional

Published
1993
Full Text
View/download PDF

49. Unfractionated peripheral blood stem cell autografts and CD34+-enriched autografts have similar long-term culture initiating capacity in multiple myeloma.

Author

Turhan, A.G., Bourhis, J.H., Bonnet, M.L., Novault, S., Bayle, C., Bennaceur, A., Vainchenker, W., Pico, J.L., and Beaujean, F.

Abstract

CD34+-enriched peripheral blood stem cells (PBSC) are increasingly being used as an autograft in patients with multiple myeloma (MM). The rationale for the use of the CD34+-enriched fraction in MM is the ability to obtain a graft with a significant reduction of contamination by plasma cells. However, the effect of such a manipulation on the proliferating potential of the engrafted cells is not known. We wished to study, as part of a randomized trial comparing the outcome in MM patients transplanted with either CD34+- enriched cells or unfractionated PBSC, the primitive hematopoietic cell content of the autografts using long-term culture initiating cell (LTC-IC) assays in 7 MM patients. In 3 patients CD34+cell-enriched fraction was compared to unfractionated PBSC whereas in the remaining 4 patients the LTC-IC assay was performed on total PBSC. The mean percentage of CD34+ cells of the CD34+ selected fraction in three patients was 82% (range 71%-96%) whereas the same percentage in PBSC varied from 0.6% to 10% in 4 patients (mean: 4.2%). Out of three patients transplanted with CD34+ cell fraction, two patients were found to have a very similar LTC-IC generating potential in their CD34+ versus PBSC fractions as this was assessed by the clonogenic cell output at week+5 per 104 CD34+ cells initiating the culture (PBSC: 92 and 168 and CD34+ fraction: 102 and 161, respectively) whereas one patient had a slightly different values (PBSC: 51 and CD34+ fraction: 103). When the PBSC fraction was compared in all 7 patients, the LTC-IC generation potential was very heterogenous, varying from 1.4 to 168. To determine if the selection procedure influences the numbers of LTC-IC’s in both fractions, we have performed limiting dilution assays to determine both the frequency of distribution of hematopoietic colonies and the frequency of LTC-IC’s in two patients. The frequency of distribution of hematopoietic colonies was linear in both CD34+ and PBSC fractions as was the frequency of LTC-IC when the corrections were made with regard to the CD34+ cell-content of the cultures (1/20). Our results indicate that the CD34+ selection procedure used in all three patients (Ceprate) is not deleterious for the generation of LTC-IC’s and these findings support the rationale for the use of this procedure in multiple myeloma for the purposes of tumor depletion. [ABSTRACT FROM AUTHOR]

Published
2000
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results