Works matching AU Delattre, O.

Results: 27

MicroRNA-206 expression levels correlate with clinical behaviour of rhabdomyosarcomas.

Published in:

2010

By:

Missiaglia, E.;
Shepherd, C. J.;
Patel, S.;
Thway, K.;
Pierron, G.;
Pritchard-Jones, K.;
Renard, M.;
Sciot, R.;
Rao, P.;
Oberlin, O.;
Delattre, O.;
Shipley, J.

Publication type:

journal article

Chromosomal CGH identifies patients with a higher risk of relapse in neuroblastoma without MYCN amplification.

Published in:

2007

By:

Schleiermacher, G.;
Michon, J.;
Huon, I.;
d'Enghien, C. Dubois;
Klijanienko, J.;
Brisse, H.;
Ribeiro, A.;
Mosseri, V.;
Rubie, H.;
Munzer, C.;
Thomas, C.;
Valteau-Couanet, D.;
Auvrignon, A.;
Plantaz, D.;
Delattre, O.;
Couturier, J.;
Société Française des Cancers de l'Enfant (SFCE)

Publication type:

journal article

Incidence and prognostic value of tumour cells detected by RT–PCR in peripheral blood stem cell collections from patients with Ewing tumour.

Published in:

British Journal of Cancer, 2006, v. 95, n. 10, p. 1326, doi. 10.1038/sj.bjc.6603438

By:

Vermeulen, J.;
Ballet, S.;
Oberlin, O.;
Peter, M.;
Pierron, G.;
Longavenne, E.;
Laurence, V.;
Kanold, J.;
Chastagner, P.;
Lejars, O.;
Blay, J.-Y.;
Marec-Berard, P.;
Michon, J.;
Delattre, O.;
Schleiermacher, G.

Publication type:

Article

INI1 mutations in meningiomas at a potential hotspot in exon 9.

Published in:

2001

By:

Schmitz, U;
Mueller, W;
Weber, M;
Sévenet, N;
Delattre, O;
Deimling, A von;
von Deimling, A

Publication type:

journal article

Analyse de séries pluviométriques de longue durée en Afrique de l'Ouest et Centrale non sahélienne dans un contexte de variabilité climatique.

Published in:

Hydrological Sciences Journal/Journal des Sciences Hydrologiques, 1998, v. 43, n. 6, p. 937, doi. 10.1080/02626669809492188

By:

PATUREL, J. E.;
SERVAT, E.;
DELATTRE, M. O.;
LUBES-NIEL, H.

Publication type:

Article

VPREB3: cDNA characterization and expression in human and chromosome mapping in human and mouse.

Published in:

Cytogenetics & Cell Genetics, 1999, v. 87, n. 3/4, p. 205, doi. 10.1159/000015468

By:

Rosnet, O.;
Mattéi, M-G.;
Delattre, O.;
Schiff, C.

Publication type:

Article

Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity.

Published in:

Human Molecular Genetics, 1995, v. 4, n. 4, p. 551

By:

Demczuk, S.;
Aledo, R.;
Zucman, J.;
Delattre, O.;
Desmaze, C.;
Dauphinot, L.;
Jalbert, P.;
Rouleau, G.A.;
Thomas, G.;
Aurias, A.

Publication type:

Article

Association of ki- ras mutation with differentiation and tumor-formation pathways in colorectal carcinoma.

Published in:

International Journal of Cancer, 1991, v. 49, n. 2, p. 220, doi. 10.1002/ijc.2910490213

By:

Laurent-Puig, P.;
Olschwang, S.;
Delattre, O.;
Validire, P.;
Melot, T.;
Mosseri, V.;
Salmon, R. J.;
Thomas, G.

Publication type:

Article

Loss of alleles on chromosome 18 and on the short arm of chromosome 17 in polyploid colorectal carcinomas.

Published in:

International Journal of Cancer, 1988, v. 41, n. 3, p. 404, doi. 10.1002/ijc.2910410315

By:

Monpezat, J.-Ph.;
Delattre, O.;
Bernard, A;
Grunwald, D.;
Remvikos, Y.;
Muleris, M.;
Salmon, R. J.;
Frelat, G.;
Dutrillaux, B.;
Thomas, G.

Publication type:

Article

Two types of chromosome 1p losses with opposite significance in gliomas.

Published in:

2005

By:

Idbaih A;
Marie Y;
Pierron G;
Brennetot C;
Hoang-Xuan K;
Kujas M;
Mokhtari K;
Sanson M;
Lejeune J;
Aurias A;
Delattre O;
Delattre J

Publication type:

Journal Article

Studies on the Human Chromosome 3 Centromere with a Newly Cloned Alphoid DNA Probe.

Published in:

Human Heredity, 1988, v. 38, n. 3, p. 156, doi. 10.1159/000153777

By:

Delattre, O.;
Bernard, A.;
Malfoy, B.;
Marlhens, F.;
Viegas-Pequignot, E.;
Brossard, C.;
Haguenauer, O.;
Creau-Goldberg, N.;
Van Cong, N'Guyen;
Dutrillaux, B.;
Thomas, G.

Publication type:

Article

Rhabdoid component emerging as a subclonal evolution of paediatric glioneuronal tumours.

Published in:

Neuropathology & Applied Neurobiology, 2018, v. 44, n. 2, p. 224, doi. 10.1111/nan.12379

By:

Bertrand, A.;
Rondenet, C.;
Masliah‐Planchon, J.;
Leblond, P.;
de la Fourchardière, A.;
Pissaloux, D.;
Aït‐Raïs, K.;
Lequin, D.;
Jouvet, A.;
Freneaux, P.;
Sevestre, H.;
Ranchere‐Vince, D.;
Tauziede‐Espariat, A.;
Maurage, C.‐A.;
Silva, K.;
Pierron, G.;
Delattre, O.;
Varlet, P.;
Frappaz, D.;
Bourdeaut, F.

Publication type:

Article

CEB 29 detects a VNTR locus (Het: 80%) on chromosome XY.

Published in:

Human Molecular Genetics, 1992, v. 1, n. 1, p. 63

By:

Lauthier, V.;
Buard, J.;
Delattre, O.;
Zucman, J.;
Vergnaud, G.

Publication type:

Article

Comparative genomic hybridization (CGH) analysis of stage 4 neuroblastoma reveals high frequency of 11q deletion in tumors lacking MYCN amplification.

Published in:

International Journal of Cancer, 2001, v. 91, n. 5, p. 680, doi. 10.1002/1097-0215(200002)9999:9999<::AID-IJC1114>3.0.CO;2-R

By:

Plantaz, D.;
Vandesompele, J.;
Van Roy, N.;
Łastowska, M.;
Bown, N.;
Combaret, V.;
Favrot, M.C.;
Delattre, O.;
Michon, J.;
Bénard, J.;
Hartmann, O.;
Nicholson, J.C.;
Ross, F.M.;
Brinkschmidt, C.;
Laureys, G.;
Caron, H.;
Matthay, K.K.;
Feuerstein, B.G.;
Speleman, F.

Publication type:

Article

VPREB3: cDNA characterization and expression in human and chromosome mapping in human and mouse.

Published in:

Cytogenetic & Genome Research, 1999, v. 87, n. 3/4, p. 205, doi. 10.1159/000015468

By:

Rosnet, O.;
Mattéi, M-G.;
Delattre, O.;
Schiff, C.

Publication type:

Article

Predominant occurrence of somatic mutations of the NF2 gene in meningiomas and schwannomas.

Published in:

Genes, Chromosomes & Cancer, 1995, v. 13, n. 3, p. 211, doi. 10.1002/gcc.2870130311

By:

Mérel, P.;
Hoang-Xuan, K.;
Sanson, M.;
Moreau-Aubry, A.;
Bijlsma, E. K.;
Lazaro, C.;
Moisan, J. P.;
Resche, F.;
Nishisho, I.;
Estivill, X.;
Delattre, J. Y.;
Poisson, M.;
Theillet, C.;
Hulsebos, T.;
Delattre, O.;
Thomas, G.

Publication type:

Article

Unicolor and bicolor in situ hybridization in the diagnosis of peripheral neuroepithelioma and related tumors.

Published in:

Genes, Chromosomes & Cancer, 1992, v. 5, n. 1, p. 30, doi. 10.1002/gcc.2870050105

By:

Desmaze, C.;
Zucman, J.;
Delattre, O.;
Thomas, G.;
Aurias, A.

Publication type:

Article

MiR-30a-5p connects EWS-FLI1 and CD99, two major therapeutic targets in Ewing tumor.

Published in:

Oncogene, 2013, v. 32, n. 33, p. 3915, doi. 10.1038/onc.2012.403

By:

Franzetti, G-A;
Laud-Duval, K;
Bellanger, D;
Stern, M-H;
Sastre-Garau, X;
Delattre, O

Publication type:

Article

P-cadherin is a direct PAX3-FOXO1A target involved in alveolar rhabdomyosarcoma aggressiveness.

Published in:

Oncogene, 2013, v. 32, n. 15, p. 1876, doi. 10.1038/onc.2012.217

By:

Thuault, S;
Hayashi, S;
Lagirand-Cantaloube, J;
Plutoni, C;
Comunale, F;
Delattre, O;
Relaix, F;
Gauthier-Rouvière, C

Publication type:

Article

The constitutive activity of the ALK mutated at positions F1174 or R1275 impairs receptor trafficking.

Published in:

Oncogene, 2011, v. 30, n. 17, p. 2017, doi. 10.1038/onc.2010.595

By:

Mazot, P;
Cazes, A;
Boutterin, M C;
Figueiredo, A;
Raynal, V;
Combaret, V;
Hallberg, B;
Palmer, R H;
Delattre, O;
Janoueix-Lerosey, I;
Vigny, M

Publication type:

Article

Molecular pathogenesis of peripheral neuroblastic tumors.

Published in:

Oncogene, 2010, v. 29, n. 11, p. 1566, doi. 10.1038/onc.2009.518

By:

Janoueix-Lerosey, I.;
Schleiermacher, G.;
Delattre, O.

Publication type:

Article

VIP hypersecretion as primary or secondary syndrome in neuroblastoma: a retrospective study by the Société Française des Cancers de l'Enfant (SFCE)

Published in:

2009

By:

Bourdeaut F;
de Carli E;
Timsit S;
Coze C;
Chastagner P;
Sarnacki S;
Delattre O;
Peuchmaur M;
Rubie H;
Michon J;
Neuroblastoma Committee of the Société Française des Cancers et Leucémies de l'Enfant et de l'Adolescent

Publication type:

Journal Article

Loss of SMARCB1 expression in colon carcinoma.

Published in:

Cancer Biomarkers, 2020, v. 27, n. 3, p. 399, doi. 10.3233/CBM-190287

By:

Melloul, S.;
Mosnier, J.-F.;
Masliah-Planchon, J.;
Lepage, C.;
Le Malicot, K.;
Gornet, J.-M.;
Edeline, J.;
Dansette, D.;
Texereau, P.;
Delattre, O.;
Laurent Puig, P.;
Taieb, J.;
Emile, J.-F.

Publication type:

Article

Mutations of the hSNF5/INI1 gene in renal rhabdoid tumors with second primary brain tumors.

Published in:

2000

By:

Savla, Jayshree;
Chen, Tina T.-Y.;
Savla, J;
Chen, T T;
Schneider, N R;
Timmons, C F;
Delattre, O;
Tomlinson, G E

Publication type:

journal article

In neuroblastic tumours, Schwann cells do not harbour the genetic alterations of neuroblasts but may nevertheless share the same clonal origin.

Published in:

Oncogene, 2008, v. 27, n. 21, p. 3066, doi. 10.1038/sj.onc.1210965

By:

Bourdeaut, F.;
Ribeiro, A.;
Paris, R.;
Pierron, G.;
Couturier, J.;
Peuchmaur, M.;
Delattre, O.

Publication type:

Article

The requirement for SNF5/INI1 in adipocyte differentiation highlights new features of malignant rhabdoid tumors.

Published in:

Oncogene, 2008, v. 27, n. 14, p. 2035, doi. 10.1038/sj.onc.1210847

By:

Caramel, J;
Medjkane, S;
Quignon, F;
Delattre, O

Publication type:

Article

hSNF5/INI1-deficient tumours and rhabdoid tumours are convergent but not fully overlapping entities.

Published in:

Journal of Pathology, 2007, v. 211, n. 3, p. 323, doi. 10.1002/path.2103

By:

Bourdeaut, F;
Fréneaux, P;
Thuille, B;
Lellouch-Tubiana, A;
Nicolas, A;
Couturier, J;
Pierron, G;
Sainte-Rose, C;
Bergeron, C;
Bouvier, R;
Rialland, X;
Laurence, V;
Michon, J;
Sastre-Garau, X;
Delattre, O

Publication type:

Article