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Participer à un groupe selon Sartre: Agir « avec » ou « comme » les autres
Participer à un groupe selon Sartre: Agir « avec » ou « comme » les autres
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Participer à un groupe selon Sartre: Agir « avec » ou « comme » les autres

Malinge, Yoann

Archives de philosophie, 2022-05, Vol.Tome 85 (2), p.153-170 [Periódico revisado por pares]

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2
Participer à un groupe selon Sartre
Participer à un groupe selon Sartre
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Artigo 		Adicionar ao Meu Espaço

Participer à un groupe selon Sartre

Malinge, Yoann

Archives de philosophie, 2022, Vol.85 (2), p.153-170 [Periódico revisado por pares]

Centre Sèvres

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3
Triplication of a 21q22 region contributes to B cell transformation through HMGN1 overexpression and loss of histone H3 Lys27 trimethylation
Triplication of a 21q22 region contributes to B cell transformation through HMGN1 overexpression and loss of histone H3 Lys27 trimethylation
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Triplication of a 21q22 region contributes to B cell transformation through HMGN1 overexpression and loss of histone H3 Lys27 trimethylation

Lane, Andrew A ; Chapuy, Bjoern ; Lin, Charles Y ; Tivey, Trevor ; Li, Hubo ; Townsend, Elizabeth C ; van Bodegom, Diederik ; Day, Tovah A ; Wu, Shuo-Chieh ; Liu, Huiyun ; Yoda, Akinori ; Alexe, Gabriela ; Schinzel, Anna C ; Sullivan, Timothy J ; Malinge, Sébastien ; Taylor, Jordan E ; Stegmaier, Kimberly ; Jaffe, Jacob D ; Bustin, Michael ; te Kronnie, Geertruy ; Izraeli, Shai ; Harris, Marian H ; Stevenson, Kristen E ; Neuberg, Donna ; Silverman, Lewis B ; Sallan, Stephen E ; Bradner, James E ; Hahn, William C ; Crispino, John D ; Pellman, David ; Weinstock, David M

Nature genetics, 2014-06, Vol.46 (6), p.618-623 [Periódico revisado por pares]

United States: Nature Publishing Group

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4
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects
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Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects

Laquérriere, Annie ; Maluenda, Jérome ; Camus, Adrien ; Fontenas, Laura ; Dieterich, Klaus ; Nolent, Flora ; Zhou, Jié ; Monnier, Nicole ; Latour, Philippe ; Gentil, Damien ; Héron, Delphine ; Desguerres, Isabelle ; Landrieu, Pierre ; Beneteau, Claire ; Delaporte, Benoit ; Bellesme, Céline ; Baumann, Clarisse ; Capri, Yline ; Goldenberg, Alice ; Lyonnet, Stanislas ; Bonneau, Dominique ; Estournet, Brigitte ; Quijano-Roy, Susana ; Francannet, Christine ; Odent, Sylvie ; Saint-Frison, Marie-Hélène ; Sigaudy, Sabine ; Figarella-Branger, Dominique ; Gelot, Antoinette ; Mussini, Jean-Marie ; Lacroix, Catherine ; Drouin-Garraud, Valerie ; Malinge, Marie-Claire ; Attié-Bitach, Tania ; Bessieres, Bettina ; Bonniere, Maryse ; Encha-Razavi, Ferechte ; Beaufrère, Anne-Marie ; Khung-Savatovsky, Suonary ; Perez, Marie José ; Vasiljevic, Alexandre ; Mercier, Sandra ; Roume, Joelle ; Trestard, Laetitia ; Saugier-Veber, Pascale ; Cordier, Marie-Pierre ; Layet, Valérie ; Legendre, Marine ; Vigouroux-Castera, Adeline ; Lunardi, Joel ; Bayes, Monica ; Jouk, Pierre S ; Rigonnot, Luc ; Granier, Michèle ; Sternberg, Damien ; Warszawski, Josiane ; Gut, Ivo ; Gonzales, Marie ; Tawk, Marcel ; Melki, Judith

Human molecular genetics, 2014-05, Vol.23 (9), p.2279-2289 [Periódico revisado por pares]

England: Oxford University Press (OUP)

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5
Pressureless sintering of beta silicon carbide nanoparticles
Pressureless sintering of beta silicon carbide nanoparticles
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Pressureless sintering of beta silicon carbide nanoparticles

Malinge, Antoine ; Coupé, Aurélie ; Le Petitcorps, Yann ; Pailler, René

Journal of the European Ceramic Society, 2012-12, Vol.32 (16), p.4393-4400 [Periódico revisado por pares]

Elsevier Ltd

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6
OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract
OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract
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OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract

Reynier, P ; Amati-Bonneau, P ; Verny, C ; Olichon, A ; Simard, G ; Guichet, A ; Bonnemains, C ; Malecaze, F ; Malinge, M C ; Pelletier, J B ; Calvas, P ; Dollfus, H ; Belenguer, P ; Malthièry, Y ; Lenaers, G ; Bonneau, D

Journal of medical genetics, 2004-09, Vol.41 (9), p.e110-e110 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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7
752P Novel CEAxCD3 (NILK-2301) and CEAxCD28 (NILK-3301) κλ bispecific antibodies for next generation immunotherapy of CEA-expressing cancer
752P Novel CEAxCD3 (NILK-2301) and CEAxCD28 (NILK-3301) κλ bispecific antibodies for next generation immunotherapy of CEA-expressing cancer
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752P Novel CEAxCD3 (NILK-2301) and CEAxCD28 (NILK-3301) κλ bispecific antibodies for next generation immunotherapy of CEA-expressing cancer

Seckinger, A. ; Majocchi, S. ; Moine, V. ; Nouveau, L. ; Daubeuf, B. ; Buatois, V. ; Gueneau, F. ; Ravn, U. ; Masternak, K. ; Poitevin, Y. ; Magistrelli, G. ; Malinge, P. ; Shang, L. ; Fischer, N. ; Strein, K. ; Ferlin, W.G. ; Hose, D.

Annals of oncology, 2022-09, Vol.33, p.S888 [Periódico revisado por pares]

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8
Modulation of MutS ATP-dependent Functional Activities by DNA containing a Cisplatin Compound Lesion (Base Damage and Mismatch)
Modulation of MutS ATP-dependent Functional Activities by DNA containing a Cisplatin Compound Lesion (Base Damage and Mismatch)
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Modulation of MutS ATP-dependent Functional Activities by DNA containing a Cisplatin Compound Lesion (Base Damage and Mismatch)

Sedletska, Yuliya ; Fourrier, Laurence ; Malinge, Jean-Marc

Journal of molecular biology, 2007-05, Vol.369 (1), p.27-40 [Periódico revisado por pares]

England: Elsevier Ltd

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9
Isatuximab Plus Pomalidomide/Low-Dose Dexamethasone Versus Pomalidomide/Low-Dose Dexamethasone in Patients with Relapsed/Refractory Multiple Myeloma (ICARIA-MM): Characterization of Subsequent Antimyeloma Therapies
Isatuximab Plus Pomalidomide/Low-Dose Dexamethasone Versus Pomalidomide/Low-Dose Dexamethasone in Patients with Relapsed/Refractory Multiple Myeloma (ICARIA-MM): Characterization of Subsequent Antimyeloma Therapies
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Isatuximab Plus Pomalidomide/Low-Dose Dexamethasone Versus Pomalidomide/Low-Dose Dexamethasone in Patients with Relapsed/Refractory Multiple Myeloma (ICARIA-MM): Characterization of Subsequent Antimyeloma Therapies

Richardson, Paul G. ; Perrot, Aurore ; San-Miguel, Jesús ; Beksac, Meral ; Spicka, Ivan ; Leleu, Xavier ; Schjesvold, Fredrik ; Moreau, Philippe ; Dimopoulos, Meletios A. ; Huang, Jeffrey SY ; Minarik, Jiri ; Cavo, Michele ; Prince, H. Miles ; Macé, Sandrine ; Malinge, Laure ; Dubin, Franck ; Morisse, Mony ; Anderson, Kenneth C.

Blood, 2022-11, Vol.140 (Supplement 1), p.608-610 [Periódico revisado por pares]

Elsevier Inc

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10
Integrative analysis of gene expression patterns predicts specific modulations of defined cell functions by estrogen and tamoxifen in MCF7 breast cancer cells
Integrative analysis of gene expression patterns predicts specific modulations of defined cell functions by estrogen and tamoxifen in MCF7 breast cancer cells
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Integrative analysis of gene expression patterns predicts specific modulations of defined cell functions by estrogen and tamoxifen in MCF7 breast cancer cells

Gadal, F ; Starzec, A ; Bozic, C ; Pillot-Brochet, C ; Malinge, S ; Ozanne, V ; Vicenzi, J ; Buffat, L ; Perret, G ; Iris, F ; Crepin, M

Journal of molecular endocrinology, 2005-02, Vol.34 (1), p.61-75 [Periódico revisado por pares]

England: BioScientifica

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