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DYRK1A controls the transition from proliferation to quiescence during lymphoid development by destabilizing Cyclin D3
DYRK1A controls the transition from proliferation to quiescence during lymphoid development by destabilizing Cyclin D3
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DYRK1A controls the transition from proliferation to quiescence during lymphoid development by destabilizing Cyclin D3

Thompson, Benjamin J ; Bhansali, Rahul ; Diebold, Lauren ; Cook, Daniel E ; Stolzenburg, Lindsay ; Casagrande, Anne-Sophie ; Besson, Thierry ; Leblond, Bertrand ; Désiré, Laurent ; Malinge, Sébastien ; Crispino, John D

The Journal of experimental medicine, 2015-06, Vol.212 (6), p.953-970 [Periódico revisado por pares]

United States: Rockefeller University Press

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2
Kisspeptin Directly Stimulates Gonadotropin-Releasing Hormone Release via G Protein-Coupled Receptor 54
Kisspeptin Directly Stimulates Gonadotropin-Releasing Hormone Release via G Protein-Coupled Receptor 54
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Kisspeptin Directly Stimulates Gonadotropin-Releasing Hormone Release via G Protein-Coupled Receptor 54

Messager, Sophie ; Chatzidaki, Emmanouella E. ; Ma, Dan ; Hendrick, Alan G. ; Zahn, Dirk ; Dixon, John ; Thresher, Rosemary R. ; Malinge, Isabelle ; Lomet, Didier ; Mark B. L. Carlton ; Colledge, William H. ; Caraty, Alain ; Samuel A. J. R. Aparicio ; Brenner, Sydney

Proceedings of the National Academy of Sciences - PNAS, 2005-02, Vol.102 (5), p.1761-1766 [Periódico revisado por pares]

United States: National Academy of Sciences

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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
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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6
Activating mutations in human acute megakaryoblastic leukemia
Activating mutations in human acute megakaryoblastic leukemia
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Activating mutations in human acute megakaryoblastic leukemia

Malinge, Sébastien ; Ragu, Christine ; Della-Valle, Veronique ; Pisani, Didier ; Constantinescu, Stefan N. ; Perez, Christelle ; Villeval, Jean-Luc ; Reinhardt, Dirk ; Landman-Parker, Judith ; Michaux, Lucienne ; Dastugue, Nicole ; Baruchel, André ; Vainchenker, William ; Bourquin, Jean-Pierre ; Penard-Lacronique, Virginie ; Bernard, Olivier A.

Blood, 2008-11, Vol.112 (10), p.4220-4226 [Periódico revisado por pares]

Washington, DC: Elsevier Inc

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7
Isatuximab plus pomalidomide and dexamethasone in relapsed/refractory multiple myeloma patients with renal impairment: ICARIA-MM subgroup analysis
Isatuximab plus pomalidomide and dexamethasone in relapsed/refractory multiple myeloma patients with renal impairment: ICARIA-MM subgroup analysis
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Isatuximab plus pomalidomide and dexamethasone in relapsed/refractory multiple myeloma patients with renal impairment: ICARIA-MM subgroup analysis

Dimopoulos, Meletios A ; Leleu, Xavier ; Moreau, Philippe ; Richardson, Paul G ; Liberati, Anna Marina ; Harrison, Simon J ; Miles Prince, H ; Ocio, Enrique M ; Assadourian, Sylvie ; Campana, Frank ; Malinge, Laure ; Sémiond, Dorothée ; van de Velde, Helgi ; Yong, Kwee

Leukemia, 2021-02, Vol.35 (2), p.562-572 [Periódico revisado por pares]

England: Nature Publishing Group

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8
DYRK1A regulates B cell acute lymphoblastic leukemia through phosphorylation of FOXO1 and STAT3
DYRK1A regulates B cell acute lymphoblastic leukemia through phosphorylation of FOXO1 and STAT3
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DYRK1A regulates B cell acute lymphoblastic leukemia through phosphorylation of FOXO1 and STAT3

Bhansali, Rahul S ; Rammohan, Malini ; Lee, Paul ; Laurent, Anouchka P ; Wen, Qiang ; Suraneni, Praveen ; Yip, Bon Ham ; Tsai, Yi-Chien ; Jenni, Silvia ; Bornhauser, Beat ; Siret, Aurélie ; Fruit, Corinne ; Pacheco-Benichou, Alexandra ; Harris, Ethan ; Besson, Thierry ; Thompson, Benjamin J ; Goo, Young Ah ; Hijiya, Nobuko ; Vilenchik, Maria ; Izraeli, Shai ; Bourquin, Jean-Pierre ; Malinge, Sébastien ; Crispino, John D

The Journal of clinical investigation, 2021-01, Vol.131 (1), p.1-18 [Periódico revisado por pares]

United States: American Society for Clinical Investigation

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9
Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease
Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease
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Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease

Loiseau, Dominique ; Chevrollier, Arnaud ; Verny, Christophe ; Guillet, Virginie ; Gueguen, Naïg ; Pou De Crescenzo, Marie-Anne ; Ferré, Marc ; Malinge, Marie-Claire ; Guichet, Agnès ; Nicolas, Guillaume ; Amati-Bonneau, Patrizia ; Malthièry, Yves ; Bonneau, Dominique ; Reynier, Pascal

Annals of neurology, 2007-04, Vol.61 (4), p.315-323 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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10
Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France
Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France
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Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France

Claustres, Mireille ; Guittard, Caroline ; Bozon, Dominique ; Chevalier, Françoise ; Verlingue, Claudine ; Ferec, Claude ; Girodon, Emanuelle ; Cazeneuve, Cécile ; Bienvenu, Thierry ; Lalau, Guy ; Dumur, Viviane ; Feldmann, Delphine ; Bieth, Eric ; Blayau, Martine ; Clavel, Christine ; Creveaux, Isabelle ; Malinge, Marie-Claire ; Monnier, Nicole ; Malzac, Perrine ; Mittre, Hervé ; Chomel, Jean-Claude ; Bonnefont, Jean-Paul ; Iron, Albert ; Chery, Michèle ; Georges, Marie Des

Human mutation, 2000-08, Vol.16 (2), p.143-156 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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