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Auboyer, L., Monzo, C., Wallon, D., Rovelet-Lecrux, A., Gabelle, A., Gazagne, I., Cacheux, V., Lehmann, S., Crozet, C.
Published in Stem cell research (01.01.2019)
Published in Stem cell research (01.01.2019)
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Generation of induced pluripotent stem cells (iPSCs) IRMBi002-A from an Alzheimer's disease patient carrying a D694N mutation in the APP gene
Auboyer, L., Monzo, C., Wallon, D., Rovelet-Lecrux, A., Gabelle, A., Gazagne, I., Cacheux, V., Lehmann, S., Crozet, C.
Published in Stem cell research (01.05.2019)
Published in Stem cell research (01.05.2019)
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Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease
CACHEUX, Valère, DASTOT-LE MOAL, Florence, KÄÄRIÄINEN, Helena, BONDURAND, Nadège, RINTALA, Risto, BOISSIER, Brigitte, WILSON, Meredith, MOWAT, David, GOOSSENS, Michel
Published in Human molecular genetics (01.07.2001)
Published in Human molecular genetics (01.07.2001)
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Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice
Bruno, D L, Ganesamoorthy, D, Schoumans, J, Bankier, A, Coman, D, Delatycki, M, Gardner, R J M, Hunter, M, James, P A, Kannu, P, McGillivray, G, Pachter, N, Peters, H, Rieubland, C, Savarirayan, R, Scheffer, I E, Sheffield, L, Tan, T, White, S M, Yeung, A, Bowman, Z, Ngo, C, Choy, K W, Cacheux, V, Wong, L, Amor, D J, Slater, H R
Published in Journal of medical genetics (01.02.2009)
Published in Journal of medical genetics (01.02.2009)
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Retrospective study of allogeneic haematopoietic stem-cell transplantation for myelofibrosis
Lissandre, S, Bay, J-O, Cahn, J-Y, Porcher, R, Cacheux, V, Cabrespine, A, Cornillon, J, Cassinat, B, Peffault de Latour, R, Socie, G, Robin, M
Published in Bone marrow transplantation (Basingstoke) (01.04.2011)
Published in Bone marrow transplantation (Basingstoke) (01.04.2011)
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BONE MARROW INVOLVEMENT, BUT NO BLOOD INVOLVEMENT, IMPAIRS SURVIVAL IN ANGIOIMMUNOBLASTIC T CELL LYMPHOMA: AN ANCILLARY STUDY OF THE REVAIL TRIAL
Lemonnier, F., Safar, V., Ferchiou, A., Cottereau, A., Bachy, E., Cartron, G., Moles‐Moreau, M., Delmer, A., Bouabdallah, R., Voillat, L., Parrens, M., Casasnovas, O., Cacheux, V., Réguy, C., Tilly, H., Meignan, M., Gaulard, P., Leval, L., Delfau‐Larrue, M., Haioun, C.
Published in Hematological oncology (01.06.2019)
Published in Hematological oncology (01.06.2019)
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OBINUTUZUMAB PLUS DHAP FOLLOWED BY AUTOLOGOUS STEM CELL TRANSPLANTATION (ASCT) PLUS OBINUTUZUMAB MAINTENANCE PROVIDES A HIGH MRD RESPONSE RATE IN UNTREATED MCL PATIENTS. RESULTS OF LYMA‐101 TRIAL, A LYSA GROUP STUDY
Le Gouill, S., Beldi‐Ferchiou, A., Cacheux, V., Salles, G., Canioni, D., Bodet‐Milin, C., Alcantara, M., Delwail, V., Gastinne, T., Thieblemont, C., Maisonneuve, H., Lamy de la Chapelle, T., Oberic, l., Bouabdallah, K., Ribrag, V., Delfau‐Larue, M., Macintyre, E., Hermine, O.
Published in Hematological oncology (01.06.2019)
Published in Hematological oncology (01.06.2019)
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ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia
CAVE, H, CACHEUX, V, RAYNAUD, S, BRUNIE, G, BAKKUS, M, COCHAUX, P, PREUDHOMME, C, LAÏ, J. L, VILMER, E, GRANDCHAMP, B
Published in Leukemia (01.09.1997)
Published in Leukemia (01.09.1997)
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Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization
Cacheux, V, Tachdjian, G, Druart, L, Oury, J F, Sérero, S, Blot, P, Nessmann, C
Published in Prenatal diagnosis (01.02.1994)
Published in Prenatal diagnosis (01.02.1994)
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Detection of 47,XYY trophoblast fetal cells in maternal blood by fluorescence in situ hybridization after using immunomagnetic lymphocyte depletion and flow cytometry sorting
Cacheux, V, Milesi-Fluet, C, Tachdjian, G, Druart, L, Bruch, J F, Hsi, B L, Uzan, S, Nessmann, C
Published in Fetal diagnosis and therapy (1992)
Published in Fetal diagnosis and therapy (1992)
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Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency
Moers, Arpard v, Marcos, Elisabeth, Goossens, Michel, Schnabel, Dirk, Netchine, Irène, Maghnie, Mohamed, Amselem, Serge, Duriez, Bénédicte, Grüters, Annette, Sobrier, Marie-Laure, Krude, Heiko, Cacheux, Valère
Published in Nature genetics (01.06.2000)
Published in Nature genetics (01.06.2000)
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Loss-of-Function Mutations in a Human Gene Related to Chlamydomonas reinhardtii Dynein IC78 Result in Primary Ciliary Dyskinesia
Pennarun, Gaëlle, Escudier, Estelle, Chapelin, Catherine, Bridoux, Anne-Marie, Cacheux, Valère, Roger, Gilles, Clément, Annick, Goossens, Michel, Amselem, Serge, Duriez, Bénédicte
Published in American journal of human genetics (01.12.1999)
Published in American journal of human genetics (01.12.1999)
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S103 OBINUTUZUMAB PLUS DHAP FOLLOWED BY AUTOLOGOUS STEM CELL TRANSPLANTATION PLUS OBINUTUZUMAB MAINTENANCE PROVIDES A HIGH MRD RESPONSE RATE IN UNTREATED MCL PATIENTS, LYMA‐101 TRIAL ‐ A LYSA TRIAL
Legouill, S., Beldi‐Ferchiou, A., Cacheux, V., Alcantara, M., Salles, G., Canioni, D., Bodet‐Milin, C., Delwail, V., Gastinne, T., thieblemont, C., Moles, M.‐P., Damaj, G., Jaccard, A., Daguindau, N., Ribrag, V., Delfau‐Larue, M.‐H., Macintyre, E., Hermine, O.
Published in HemaSphere (01.06.2019)
Published in HemaSphere (01.06.2019)
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Allogeneic hematopoietic stem cell transplantation allows long-term complete remission and curability in high-risk Waldenström’s macroglobulinemia. Results of a retrospective analysis of the Société Française de Greffe de Moelle et de Thérapie Cellulaire
GARNIER, Alice, ROBIN, Marie, DREYFUS, Brigitte, DREGER, Peter, RIO, Bernard, MOLES-MOREAU, Marie-Pierre, BILGER, Karin, BAY, Jacques-Olivier, LEBLOND, Véronique, BLAISE, Didier, TOURNILHAC, Olivier, DHEDIN, Nathalie, LAROSA, Fabrice, GOLMARD, Jean-Louis, LE GOUILL, Steven, COITEUX, Valérie, TABRIZI, Reza, BULABOIS, Claude-Eric, CACHEUX, Victoria, KUENTZ, Mathieu
Published in Haematologica (Roma) (01.06.2010)
Published in Haematologica (Roma) (01.06.2010)
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The 12;21 translocation involving TEL and deletion of the other TEL allele : Two frequently associated alterations found in childhood acute lymphoblastic leukemia
RAYNAUD, S, CAVE, H, GRANDCHAMP, B, BAENS, M, BASTARD, C, CACHEUX, V, GROSGEORGE, J, GUIDAL-GIROUX, C, GUO, C, VILMER, E, MARYNEN, P
Published in Blood (01.04.1996)
Published in Blood (01.04.1996)
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Allogeneic haematopoietic stem cell transplantation as a curative therapy in primary and secondary myelofibrosis
Lissandre, S, Bay, J.-O, Cahn, J.-Y, Cacheux, V, Cabrespine, A, Cornillon, J, Cassinat, B, de Latour, R. Peffault, Socie, G, Robin, M
Published in Bone marrow transplantation (Basingstoke) (01.03.2009)
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Published in Bone marrow transplantation (Basingstoke) (01.03.2009)
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Human Prop-1: cloning, mapping, genomic structure: Mutations in familial combined pituitary hormone deficiency
Duquesnoy, Philippe, Roy, Anne, Dastot, Florence, Ghali, Isis, Teinturier, Cécile, Netchine, Irène, Cacheux, Valère, Hafez, Mona, Salah, Nermine, Chaussain, Jean-Louis, Goossens, Michel, Bougnères, Pierre, Amselem, Serge
Published in FEBS letters (23.10.1998)
Published in FEBS letters (23.10.1998)
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Techniques nouvelles en cytogénétique
Tachdjian, G, Cacheux, V, Romana, S
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (1996)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (1996)
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Further delineation of the phenotype associated with heterozygous mutations in ZFHX1B
Wilson, Meredith, Mowat, David, Dastot-Le Moal, Florence, Cacheux, Valère, Kääriäinen, Helena, Cass, Danny, Donnai, Dian, Clayton-Smith, Jill, Townshend, Sharron, Curry, Cynthia, Gattas, Michael, Braddock, Stephen, Kerr, Bronwyn, Aftimos, Salim, Zehnwirth, Harry, Barrey, Catherine, Goossens, Michel
Published in American journal of medical genetics. Part A (15.06.2003)
Published in American journal of medical genetics. Part A (15.06.2003)
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