Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Michèle Milili"'
Autor:
M. Fougereau, S. Corbet, Jacques Thèze, J. Rocca-Serra, P. Ollier, C. Roth, C. Tonnelle, Gerard Somme, Michèle Milili, C. Schiff, G. Mazza, D. Moinier, C. Cambillau
Publikováno v:
Biological Applications of Anti-Idiotypes ISBN: 9781351070232
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1405f889fe251518b8d2a9cbe8e457f4
https://doi.org/10.1201/9781351070232-3
https://doi.org/10.1201/9781351070232-3
Autor:
Pierre Bordigoni, Danielle Canioni, Michèle Milili, Nathalie Lambert, Claire Galambrun, Marie Ouachée-Chardin, Filomeen Haerynck, Françoise Le Deist, Despina Moshous, Christelle Lenoir, Stephanie Rigaud, Lionel Galicier, Fabien Touzot, Capucine Picard, Mohamed Hamidou, Hirokazu Kanegane, Ester Mejstrikova, Helen Chapel, Eduardo López-Granados, Stéphane Blanche, Alain Dabadie, Jana Pachlopnik Schmid, Pierre-Simon Rohrlich, Fabian Hauck, Geneviève de Saint Basile, Claudin Schiff, Jean-Louis Stephan, Alain Fischer, Isabelle Pellier, Nizar Mahlaoui, Sylvain Latour, Alain Fourmaintraux, Vincent Barlogis
Publikováno v:
Blood
Blood, American Society of Hematology, 2011, 117 (5), pp.1522-9. ⟨10.1182/blood-2010-07-298372⟩
Blood, 2011, 117 (5), pp.1522-9. ⟨10.1182/blood-2010-07-298372⟩
Blood; Vol 117
Blood, American Society of Hematology, 2011, 117 (5), pp.1522-9. 〈10.1182/blood-2010-07-298372〉
Blood, American Society of Hematology, 2011, 117 (5), pp.1522-9. ⟨10.1182/blood-2010-07-298372⟩
Blood, 2011, 117 (5), pp.1522-9. ⟨10.1182/blood-2010-07-298372⟩
Blood; Vol 117
Blood, American Society of Hematology, 2011, 117 (5), pp.1522-9. 〈10.1182/blood-2010-07-298372〉
X-linked lymphoproliferative syndromes (XLP) are primary immunodeficiencies characterized by a particular vulnerability toward Epstein-Barr virus infection, frequently resulting in hemophagocytic lymphohistiocytosis (HLH). XLP type 1 (XLP-1) is cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fe9d22dee92c4a2e0ddda891a9b2537
https://doi.org/10.1182/blood-2010-07-298372
https://doi.org/10.1182/blood-2010-07-298372
Autor:
Laurent Gauthier, Michèle Milili, Valérie Guelpa-Fonlupt, Anne Marie Cuisinier, Cécile Tonnelle, Michel Fougereau, Claudine Schiff
Publikováno v:
Annals of the New York Academy of Sciences. 764:231-241
At the preB stage, when only the IGH locus has rearranged, mu chains become expressed in association with the psi L chains, lambda-like and VpreB, thus forming the preB receptor. By the use of a monoclonal anti VpreB antibody, preB cells were isolate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0fb4c6c51948c955dae8319ec999b16
https://doi.org/10.1111/j.1749-6632.1995.tb55833.x
https://doi.org/10.1111/j.1749-6632.1995.tb55833.x
Autor:
Claudine Schiff, Bertrand Montpellier, Julie Agopian, Bertrand Nadel, Michèle Milili, Sandrine Roulland, Pierre Grenot, Pascal Gauduchon, Jean Navarro, Pierre Lebailly
Publikováno v:
The Journal of Experimental Medicine
Journal of Experimental Medicine
Journal of Experimental Medicine, 2006, 203 (11), pp.2425-31. ⟨10.1084/jem.20061292⟩
Journal of Experimental Medicine, Rockefeller University Press, 2006, 203 (11), pp.2425-31. ⟨10.1084/jem.20061292⟩
Journal of Experimental Medicine
Journal of Experimental Medicine, 2006, 203 (11), pp.2425-31. ⟨10.1084/jem.20061292⟩
Journal of Experimental Medicine, Rockefeller University Press, 2006, 203 (11), pp.2425-31. ⟨10.1084/jem.20061292⟩
Follicular lymphoma (FL) is one of the most common B-cell lymphoma, and remains virtually incurable despite its relatively indolent nature. T(14;18)(q32;q21), the genetic hallmark and early initiating event of FL pathogenesis, is also present at low
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::271f5336f7db5bc723ce2a800c0e2979
http://europepmc.org/articles/PMC2118129
http://europepmc.org/articles/PMC2118129
Autor:
Yun Liang Jiang, Bertrand Roquelaure, Claudine Schiff, Isabelle Thuret, Carla Blanco-Betancourt, Anne Moncla, Evani M. Viegas-Péquignot, Michèle Milili
Publikováno v:
Blood. 103:2683-2690
Immunodeficiency, centromeric region instability, and facial anomalies (ICF) syndrome is a rare autosomal recessive disease. Mutations in the DNA methyltransferase 3B (DNMT3B) gene are responsible for most ICF cases reported. We investigated the B-ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e18e2535b80dbe5497f6744284c544c5
https://doi.org/10.1182/blood-2003-08-2632
https://doi.org/10.1182/blood-2003-08-2632
Autor:
Eric Meffre, Michel C. Nussenzweig, Claudine Schiff, Carla Blanco-Betancourt, Michèle Milili, Henedina Antunes
Publikováno v:
Journal of Clinical Investigation. 108:879-886
Developing B cells must pass a series of checkpoints that are regulated by membrane-bound Ig(mu) through the Igalpha-Igbeta signal transducers. To determine how Ig(mu) expression affects B cell development and Ab selection in humans we analyzed Ig ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a272a33e2221f48651d304237ef8c09
https://doi.org/10.1172/jci13051
https://doi.org/10.1172/jci13051
Publikováno v:
Mammalian Genome. 7:598-602
The surrogate light chain, composed of the VpreB and the λ-like proteins, plays a critical role in controlling the early stages of B lymphocyte development. The λ -@#@ like locus, located on the q11.2–q11.3 region of human Chromosome (Chr) 22, co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a65cbf58cfd8a1a179e034fdf2c4c21f
https://doi.org/10.1007/s003359900177
https://doi.org/10.1007/s003359900177
Autor:
David Bossy, Claudine Schiff, Patrice Mannoni, Antonio Tabilio, Jean Gabert, Michèle Milili, Franca Falzetti, Michel Fougereau
Publikováno v:
Blood. 78:1516-1525
V pre-B and lambda-like genes are selectively expressed in human pre-B cells and encode polypeptide chains that associate in a mu-pseudolight chain complex that may regulate some crucial steps of early B-cell differentiation. We have followed by poly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3eb2c3b687354ca965f12698b6811e5
https://doi.org/10.1182/blood.v78.6.1516.1516
https://doi.org/10.1182/blood.v78.6.1516.1516
Autor:
Michel Fougereau, Gilles Thomas, Michèle Milili, Claudine Schiff, David Bossy, Jessica Zucman
Publikováno v:
International Immunology. 3:1081-1090
Lambda-like genes encode a polypeptide chain that associates with VpreB and mu chain in the so-called mu-psi light chain complex specifically expressed in pre-B cells. In humans, the lambda-like gene cluster contains three genes, termed 14.1, 16.1, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::137b16a82011d008b00e53999c03ae74
https://doi.org/10.1093/intimm/3.11.1081
https://doi.org/10.1093/intimm/3.11.1081
Autor:
Leila Talby, Michèle Milili, Christophe Picard, Pierre Chiappetta, Gérard Michel, Marie-Christine Roubaud, Catherine Nguyen, Béatrice Loriod, Hervé Chambost, Claudine Schiff, Jean Gabert, Chantal Fossat
Publikováno v:
Leukemia Research
Leukemia Research, Elsevier, 2006, 30, pp.665-676
Leukemia Research, 2006, 30, pp.665-676
Leukemia Research, Elsevier, 2006, 30, pp.665-676
Leukemia Research, 2006, 30, pp.665-676
We have identified genes differentially expressed in childhood early B acute lymphoblastic leukemia at diagnosis, according to chemosensitivity. Chemosensitive (M1) and chemoresistant (M3) patients present5% and25% of residual leukemic blasts at 21 d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91b20d40c25b7f23cccb82b0b24183ba
https://hal.archives-ouvertes.fr/hal-00080179
https://hal.archives-ouvertes.fr/hal-00080179